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Barker KL, Hannink E, Room J, Toye F. The impact of physical changes to appearance on people with vertebral fragility fracture: a qualitative study. Physiotherapy 2025; 127:101771. [PMID: 40120571 DOI: 10.1016/j.physio.2025.101771] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/24/2024] [Revised: 02/03/2025] [Accepted: 02/04/2025] [Indexed: 03/25/2025]
Abstract
OBJECTIVES The aim of this study was to explore the experiences of people with Vertebral Fragility Fracture (VFF) due to osteoporosis and the impact of the physical changes resulting from their condition. DESIGN Interpretive qualitative research using semi-structured individual interviews PARTICIPANTS: Eighteen people with VFF were interviewed; nine men and nine women. Participants ranged in age from 55 to 92 years and had between 1 and 10 previous vertebral fragility fractures. SETTING Interviews were offered in participants own homes, at the hospital or by Microsoft TEAMS or telephone. These were audio-recorded, transcribed verbatim, and analysed through reflexive thematic analysis. RESULTS Results are presented within four themes: loss of height; finding spinal curvature upsetting, the impact on looking good and whether having a stoop was inevitable or could be prevented by active engagement. CONCLUSION The findings show the negative impact on self-image caused by the physical manifestations of a VFF and that these can be as significant and distressing as pain and functional limitations. This information is useful for physiotherapists treating people with vertebral fragility fractures offering insight into the patients' experiences of these physical changes. CONTRIBUTION OF THE PAPER.
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Affiliation(s)
- Karen L Barker
- Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Botnar Research Centre, Oxford OX3 7LD, UK; Physiotherapy Research Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
| | - Erin Hannink
- Physiotherapy Research Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
| | - Jon Room
- Physiotherapy Research Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK; Faculty of Health, Oxford Brookes University, Oxford OX3 0BP, UK
| | - Francine Toye
- Physiotherapy Research Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
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Dona DJS, Peters MEWJ, Senden TF, Bloem S, Bartstra H, Jacobs MT, Schaafsma FG, Jeurissen P. Including 'Work as a Treatment Goal' in the Care for Patients with Chronic Diseases : The Development of a Generic Care Model-A Descriptive Study. JOURNAL OF OCCUPATIONAL REHABILITATION 2025; 35:411-422. [PMID: 38896400 PMCID: PMC12089200 DOI: 10.1007/s10926-024-10215-w] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Accepted: 05/29/2024] [Indexed: 06/21/2024]
Abstract
BACKGROUND The Netherlands faces 60% prevalence of chronic conditions by 2040, impacting societal participation and quality of life. Current clinical care inadequately addresses these consequences, and most hospitals do not integrate occupational health in their care. OBJECTIVES To develop a generic person- and work-oriented medical care model (WMCM) based on real life experiences with work-oriented care and supporting the chronically ill in active societal participation. METHODS A qualitative research project with a participative approach in one hospital (November 2019 until March 2020). In an expert meeting, a schematic representation of a work-oriented care model was developed. Subsequent discussion rounds, with professionals from different patient groups, iteratively refined the model to a WMCM. RESULTS Consensus was reached after seven rounds of discussion, defining the model's core elements (1) a combination of biomedical and biopsychosocial approaches, (2) involvement of a clinical occupational physician in the treatment team, (3) a coordinating role for nursing specialists, and (4) incorporation of a work-oriented intervention plan (WoIP) into the treatment plan. Advocating early attention to societal participation, the model emphasises the WoIP and consensus on monitoring indicators. The final goal is a sustainable return to societal participation, considering both quality of life and work. CONCLUSION It is feasible to develop a generic person- and work-oriented care model for patients with chronic illness within a hospital care setting. Collaboration between healthcare professionals and a specialised occupational physician, with a central role for nurses, is deemed crucial.
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Affiliation(s)
- Desiree J S Dona
- Department of Primary and Community Care, Radboud University Medical Center, Geert Grooteplein 21, 6525, Nijmegen, EZ, The Netherlands.
| | - Marlies E W J Peters
- Department of Primary and Community Care, Radboud University Medical Center, Geert Grooteplein 21, 6525, Nijmegen, EZ, The Netherlands
| | - Theo F Senden
- Department of Primary and Community Care, Radboud University Medical Center, Geert Grooteplein 21, 6525, Nijmegen, EZ, The Netherlands
| | - Sjaak Bloem
- Center for Marketing & Supply Chain Management, Nyenrode Business University, 3621, Breukelen, BG, The Netherlands
| | - Herman Bartstra
- Department of Primary and Community Care, Radboud University Medical Center, Geert Grooteplein 21, 6525, Nijmegen, EZ, The Netherlands
| | - Marieke T Jacobs
- Department of Primary and Community Care, Radboud University Medical Center, Geert Grooteplein 21, 6525, Nijmegen, EZ, The Netherlands
| | - Frederieke G Schaafsma
- Department of Public and Occupational Health, Amsterdam UMC, Amsterdam Public Health Research Institute, Amsterdam, The Netherlands
| | - Patrick Jeurissen
- Department of IQ Health, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525, Nijmegen, GA, The Netherlands
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Pu J, Li D, Luo X, Wang J, Li Y, Lei L, Zhao X, Du H, Yang X, Du X. Wrist-ankle acupuncture alleviates pain in the acute phase of herpes zoster: A randomized controlled trial. PLoS One 2025; 20:e0318386. [PMID: 40440263 PMCID: PMC12121775 DOI: 10.1371/journal.pone.0318386] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/05/2025] [Accepted: 04/28/2025] [Indexed: 06/02/2025] Open
Abstract
Alternative therapeutic strategies for herpes zoster, especially for acute phase pain relief, are still largely unexplored. This study aimed to compare the effects of wrist-ankle acupuncture combined with standard pharmacological treatment versus standard pharmacological treatment alone in relieving pain in the acute phase of herpes zoster. An open-label, randomized, controlled clinical trial was conducted, enrolling patients diagnosed with acute-phase herpes zoster with pain visual analog scale (VAS) scores greater than or equal to 2. The participants were randomly assigned to either the control group receiving standard pharmacological treatment (antiviral therapy combined with pain relievers) alone or the experimental group receiving wrist-ankle acupuncture plus standard pharmacological treatment. VAS pain scores were recorded on days 1-7 and on day 28 after treatment began. Dermatology Life Quality Index scores were assessed both during the pre-treatment phase and at hospital discharge. A total of 106 patients completed the trial protocol and were included in the analysis, with 52 and 54 patients in the control and experimental groups, respectively. The clinical cure rates of pain (the rate of complete absence of pain) in the experimental group was statistically higher than control group on days 7 after treatment began(87.04% vs 65.38%, p < 0.005). The average pain VAS scores of the experimental group were lower than the control group on days 2-6 after treatment began, and they are statistically significant (all p < 0.05). No significant difference was observed between day 7 and day 28 after treatment began (p > 0.05). The Dermatology Life Quality Index scores significantly differed at hospital discharge (p < 0.05). Side effects did not significantly differ between the two groups (all p > 0.05). Wrist-ankle acupuncture combined with standard pharmacological treatment may potentially improve the pain cure rate at 7 days post-treatment. This suggests a potential new strategy for alleviating pain in patients in the acute phase of herpes zoster. Trial registration: ChiCTR2300071795.
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Affiliation(s)
- Jing Pu
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Daiwen Li
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Xia Luo
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Juan Wang
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Yanxia Li
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Li Lei
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Xiankun Zhao
- Dermatological department, Mianyang Central Hospital, Mianyang, PR China
| | - Huan Du
- Department of medicine, University of Electronic Science and Technology of China, Chengdu, PR China
- Department of oncology, Mianyang Central Hospital, Mianyang, PR China
| | - Xiyue Yang
- Department of oncology, Mianyang Central Hospital, Mianyang, PR China
- Sichuan Clinical Research Center for Radiation and Therapy, Mianyang, China
| | - Xiaobo Du
- Department of oncology, Mianyang Central Hospital, Mianyang, PR China
- Sichuan Clinical Research Center for Radiation and Therapy, Mianyang, China
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Yang Y, Hou L, Zeng W, Gan X, Qian Z, Zhao X. Emotions and experiences of head and neck cancer survivors returning to work: A meta-synthesis of qualitative studies. J Psychosoc Oncol 2025:1-20. [PMID: 40424631 DOI: 10.1080/07347332.2025.2496642] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/29/2025]
Abstract
PURPOSE Head and neck cancer (HNC) survivors may face several challenges when returning to work. Although there are some qualitative studies on the return-to-work experiences of HNC survivors, a comprehensive review of these studies is lacking. This study aimed to systematically evaluate the emotions, experiences, and needs of HNC survivors returning to work. METHODS This review was conducted in accordance with the PRISMA statement of systematic reviews. Databases including PubMed, Embase, Web of Science, MEDLINE, Cochrane Library, CINAHL, and APA PsycInfo were searched from inception to December 2023 to identify qualitative studies on the emotions and experiences of HNC survivors returning to work. The quality of the included studies was independently assessed by two investigators using the Joanna Briggs Institute Critical Appraisal Tool for Qualitative Research (2016). RESULTS Eleven studies were included in this review. A total of 54 key findings were extracted and synthesized into three overarching themes and 10 subthemes: stress perception, regulatory mechanisms, and external support. CONCLUSION HNC survivors faced many challenges in returning to work, including symptomatic burden and psychological challenges. Efforts should focus on enhancing symptom management, addressing psychological well-being, and strengthening social support systems. Additionally, targeted interventions and support strategies should be developed to facilitate the timely reintegration of HNC survivors into the workplace.
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Affiliation(s)
- Ying Yang
- School of Nursing, Chengdu University of Traditional Chinese Medicine, Chengdu, China
| | - Lili Hou
- Department of Nursing, Shanghai JiaoTong University School of Medicine Affiliated Ninth People's Hospital, Shanghai, China
| | - Weisi Zeng
- School of Nursing, Chengdu University of Traditional Chinese Medicine, Chengdu, China
| | - Xing Gan
- School of Nursing, Chengdu University of Traditional Chinese Medicine, Chengdu, China
| | - Zhen Qian
- Department of Oral Maxillofacial & Head and Neck Oncology, Shanghai JiaoTong University School of Medicine Affiliated Ninth People's Hospital, Shanghai, China
| | - Xiaomei Zhao
- Department of Oral Maxillofacial & Head and Neck Oncology, Shanghai JiaoTong University School of Medicine Affiliated Ninth People's Hospital, Shanghai, China
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Israr S, Javed R, Fawad Z. Letter to Editor: The Impact of Body Mass Index on Breast Reduction Outcomes: A Multi-Institutional Data Analysis of 45,000 Cases over 15 Years. Aesthetic Plast Surg 2025:10.1007/s00266-025-04990-x. [PMID: 40425888 DOI: 10.1007/s00266-025-04990-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/14/2025] [Accepted: 05/01/2025] [Indexed: 05/29/2025]
Abstract
We commend Knoedler et al. for their comprehensive study, "The impact of body mass index on breast reduction outcomes," which leverages a robust sample size and a reputable dataset to address an important topic in plastic surgery. While the study successfully highlights the relevance of BMI in breast reduction outcomes, we identify several methodological limitations that could affect the generalizability and depth of its findings. Crucially, the omission of confounding variables such as smoking, diabetes, immunologic and mental health status may limit the accuracy of the reported outcomes. Unlike previous work by the same authors on gynecomastia surgery, which incorporated more comprehensive factors, this study does not fully explore the relationship between BMI, reoperation, and complication rates. Moreover, the limited 30-day post-operative follow-up may overlook long-term complications such as fat necrosis and scarring, which are critical to patient satisfaction. The exclusion of male, non-binary patients, and those undergoing simultaneous procedures, while controlling variability, restricts the study's applicability to broader populations. Additionally, reliance on NSQIP, though valuable, omits nuances like surgical techniques and patient compliance. We suggest future studies incorporate a broader range of variables and follow-up periods to enhance the scope and precision of surgical outcome research.Level of Evidence V This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .
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Affiliation(s)
- Syed Israr
- Bolan University of Medical and Health Sciences, Quetta, Pakistan
| | - Ruba Javed
- Karachi Medical and Dental College, Block M, North Nazimabad Town, Karachi, 74700, Pakistan.
| | - Zauha Fawad
- Peoples University of Medical and Health Sciences for Women Shaheed Benazirabad, Benazirabad, Pakistan
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Zhang J, Qin S, Huang X, Hilmayanti E, Hu F, Luan X, Ye T, Li F, Yang Y, Liu N, Kabayama K, Fukase K, Yu F. Preclinical evaluation of [ 211At]At-AuNP-ABDMPL16 for targeted alpha therapy in Melanoma. Eur J Nucl Med Mol Imaging 2025:10.1007/s00259-025-07238-7. [PMID: 40394402 DOI: 10.1007/s00259-025-07238-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/21/2025] [Accepted: 03/19/2025] [Indexed: 05/22/2025]
Abstract
PURPOSE The aim of this study is to overcome the challenges of poor tumor penetration and systemic toxicity in targeted alpha therapy (TAT) while also evaluating its immunomodulatory effects to enhance antitumor immune responses in melanoma treatment. METHODS This study developed a 211At-labeled single-domain antibody agent ([211At]At-AuNP-ABDMPL16) targeting PD-L1, a protein overexpressed in melanoma cells. The binding affinity and internalization of [211At]At-AuNP-ABDMPL16 were evaluated in vitro using melanoma cell lines. In vivo studies in melanoma-bearing mice were conducted to assess biodistribution, pharmacokinetics, therapeutic efficacy, and the immune response induced by the treatment. RESULTS [211At]At-AuNP-ABDMPL16 demonstrated high binding affinity and efficient internalization in melanoma cells, resulting in significant tumor cell death through α-particle radiation. In vivo, [211At]At-AuNP-ABDMPL16 preferentially accumulated in tumors, inhibited tumor growth, and prolonged survival in melanoma-bearing mice. The treatment also triggered a robust anti-tumor immune response, marked by increased cytotoxic T lymphocytes and reduced regulatory T cells within the tumor microenvironment, with minimal systemic toxicity. CONCLUSION [211At]At-AuNP-ABDMPL16 shows promise as a novel therapeutic for melanoma, combining effective tumor targeting with potent cytotoxic and immune-activating effects. These findings support further investigation of this 211At-labeled single-domain antibodies in clinical applications.
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Affiliation(s)
- Jiajia Zhang
- Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
- Institute of Nuclear Medicine, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
| | - Shanshan Qin
- Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
- Institute of Nuclear Medicine, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
| | - Xuhao Huang
- Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560 - 0043, Japan
- Laboratory of Molecular Immunology, Immunology Frontier Research Center (Ifrec), Osaka University, Suita, Osaka, 565 - 0871, Japan
| | - Erina Hilmayanti
- Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560 - 0043, Japan
| | - Fan Hu
- Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
- Institute of Nuclear Medicine, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
| | - Xiaohui Luan
- Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
- Institute of Nuclear Medicine, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China
| | - Tianzhen Ye
- Key Laboratory of Radiation Physics and Technology of the Ministry of Education, Institute of Nuclear Science and Technology, Sichuan University, Chengdu, 610064, People's Republic of China
| | - Feize Li
- Key Laboratory of Radiation Physics and Technology of the Ministry of Education, Institute of Nuclear Science and Technology, Sichuan University, Chengdu, 610064, People's Republic of China
| | - Yuanyou Yang
- Key Laboratory of Radiation Physics and Technology of the Ministry of Education, Institute of Nuclear Science and Technology, Sichuan University, Chengdu, 610064, People's Republic of China
| | - Ning Liu
- Key Laboratory of Radiation Physics and Technology of the Ministry of Education, Institute of Nuclear Science and Technology, Sichuan University, Chengdu, 610064, People's Republic of China
| | - Kazuya Kabayama
- Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560 - 0043, Japan
- Institute for Radiation Sciences, Osaka University, Suita, Japan
- Forefront Research Center, Graduate School of Science, Osaka University, Toyonaka, Japan
| | - Koichi Fukase
- Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560 - 0043, Japan
- Institute for Radiation Sciences, Osaka University, Suita, Japan
- Forefront Research Center, Graduate School of Science, Osaka University, Toyonaka, Japan
| | - Fei Yu
- Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China.
- Institute of Nuclear Medicine, Tongji University School of Medicine, No. 301 Yan-Chang-Zhong Road, Shanghai, 200072, China.
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Brouwer AM, Karr TM, Russell EJ. Community Mental Health in the Time of COVID-19: A Qualitative Assessment of Rural Providers' Experiences. SOCIAL WORK IN PUBLIC HEALTH 2025; 40:198-215. [PMID: 39992259 DOI: 10.1080/19371918.2025.2467395] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 02/25/2025]
Abstract
The experiences of social and community mental health (SCMH) workers serving in rural communities during the COVID-19 pandemic are understudied. Therefore, nine SCMH workers were interviewed about challenges and strategies for providing mental health services in rural communities in the wake of COVID-19. Through qualitative analyses three primary themes emerged; challenges, needed resources and strategies for addressing mental health needs. Challenges included lack of resources, stigma, and policy barriers, but collaborating with local organizations, providing individualized services, and improving communication were suggested strategies to overcome challenges. The resilience and flexibility of SCMH workers was advantageous in adapting to the changing mental health landscape post-COVID-19, yet advocacy for funding, resources, and training for practitioners in rural mental health is still needed. Findings suggest offering individualized services, forging community connections and maximizing use of existing resources through local collaborations. Moreover, utilizing online mental health services and peer community-building may improve effective services.
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Affiliation(s)
- Amanda M Brouwer
- Psychology Department, Winona State University, Winona, Minnesota, USA
| | - Trisha M Karr
- Psychology Department, Winona State University, Winona, Minnesota, USA
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Liu X, Yu J, Liu K. Retrospective analysis of mini-implant assisted micro-osteoperforation for accelerating canine movement in adult orthodontics. BMC Oral Health 2025; 25:695. [PMID: 40340783 PMCID: PMC12063301 DOI: 10.1186/s12903-025-05751-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/17/2025] [Accepted: 03/04/2025] [Indexed: 05/10/2025] Open
Abstract
BACKGROUND Traditional orthodontic treatment methods are associated with long treatment durations and patient discomfort. The mini-implant assisted micro-osteoperforation (MOP) has shown great potential in clinical practice, but systematic research on this technology remains limited. METHODS A retrospective analysis of 106 adult patients requiring extraction of both maxillary first premolars were conducted, with patients randomly grouped: experimental group (EG, mini-implant assisted MOP) and control group (CG, conventional orthodontic treatment), with 53 cases in each. Tooth movement distances, root resorption amounts, craniofacial relationship measurement angles (SNA, SNB, ANB), maxillary anterior tooth positions and angles (U1-X, U1-Y, U1-SN), maxillary first molar positions and angles (U6-X, U6-Y, U6-X), and soft tissue angles (NLA) were compared. RESULTS The distance of canine movement in the EG was (1.89±0.28) mm after 1 month of force application, and (3.67±0.54) mm after 2 months of force application. In the CG, the distance of canine movement was (0.96±0.32) mm after 1 month of force application, and (1.88±0.34) mm after 2 months of force application. The EG suggested visibly greater canine movement distances one month and two months after force application as against the CG, with visibly lower U1-X and U1-Y angles, and visibly lower U6-X and U6-Y angles (P<0.05). No visible distinctions were noted in soft tissue angles between the EG and the CG one month and two months after force application (P>0.05). CONCLUSION Compared to existing orthodontic treatment methods, implant-supported mini-screw perforation surgery, as an auxiliary approach to accelerate orthodontic treatment, can significantly accelerate tooth movement without significantly increasing the risk of root resorption, and has minimal impact on craniofacial relationships and soft tissues. This finding provides a new and effective adjunct for orthodontic treatment, with the potential to shorten treatment duration and improve the patient experience in clinical practice, making it of significant importance for advancing the development of orthodontic techniques.
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Affiliation(s)
- Xiaoyan Liu
- Department of Stomatology, Wuwei Hospital of Traditional Chinese Medicine, Wuwei, Gansu Province, 733000, China
| | - Jinbing Yu
- Department of Stomatology, The Second People'S Hospital of Wuwei, Wuwei, Gansu Province, 733000, China
| | - Kang Liu
- Department of Stomatology, Wuwei Hospital of Traditional Chinese Medicine, Wuwei, Gansu Province, 733000, China.
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Haldar AK, Dhar R, Maity S, Krishnan S, Bhattacharya A, Sovani M. A comparative cloud-based view of adherence data over 1 year of CPAP versus APAP uses in OSA patients: Adherence depends on PAP device. Lung India 2025; 42:186-190. [PMID: 40296388 PMCID: PMC12097661 DOI: 10.4103/lungindia.lungindia_572_24] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/17/2024] [Revised: 11/19/2024] [Accepted: 11/27/2024] [Indexed: 04/30/2025] Open
Abstract
INTRODUCTION Compliance or adherence with positive airway pressure (PAP) therapy is a major issue in obstructive sleep apnea (OSA). The telemonitoring gives an opportunity to track a group of patients on cloud-based devices. In this study, we followed up patients with this cloud-based method for more than a year and followed up two different cohorts who are on continuous PAP (CPAP) and auto adjusting PAP (APAP) devices. The main objective was to judge whether one device scores over the other. METHODS This was a retrospective study. We included 60 patients in the CPAP group and 80 patients in the APAP group in the study who are using the device for 1 year or more; they all were on cloud-based devices, and for them, we had data of completed 1 year at least. The data were reviewed periodically for compliance, AHI (Apnea-Hypopnea Index), and leak and compared. RESULTS Both the groups were matched in terms of age, BMI, and AHI. Adherence at 365 days was significantly more (P < 0.001) for CPAP than APAP. Overall adherence was not lesser than 60% for CPAP in any patient. The mean AHI was 1.48 in CPAP group and 2.30 in APAP group. When we measured the leak in CPAP versus APAP group, it was 0.53 liter/minute more in CPAP group than in APAP group, but it was statistically non-significant (P = 0.8553). The mean pressure level between APAP and CPAP was 11.11 cmH2O in CPAP group and 11.62 cm H2O in APAP group, and it was again statistically non-significant (P = 0.1960). CPAP group used the machine 5.77 hours average, while APAP group used it for 4.51 hours average. CONCLUSION CPAP adherence at 1 year was better over APAP in this study, which has a large cost implication.
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Affiliation(s)
- Arup K. Haldar
- Department of Pulmonary Medicine, CMRI Hospital, Kolkata, West Bengal, India
| | - Raja Dhar
- Department of Pulmonary Medicine, CMRI Hospital, Kolkata, West Bengal, India
| | - Somnath Maity
- Department of Physiotherapy, Myofunctional Therapist, Institute of Sleep Sciences, Kolkata, West Bengal, India
| | - Shyam Krishnan
- Department of Pulmonary Medicine, CMRI Hospital, Kolkata, West Bengal, India
| | - Amrita Bhattacharya
- Department of Pulmonary Medicine, CMRI Hospital, Kolkata, West Bengal, India
| | - Milind Sovani
- Department of Pulmonology, Consultant Respiratory Physician, Nottingham University Hospital NHS Trust, UK
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Dhankhar S, Sharma P, Chauhan S, Saini M, Garg N, Singh R, Kamal MA, Sharma SK, Rani N. Cognitive Rehabilitation For Early-Stage Dementia: A Review. CURRENT PSYCHIATRY RESEARCH AND REVIEWS 2025; 21:109-122. [DOI: 10.2174/0126660822275618231129073551] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/15/2023] [Revised: 10/26/2023] [Accepted: 11/14/2023] [Indexed: 05/04/2025]
Abstract
:
In the primary phases of Alzheimer's disease (AD) and vascular dementia,
memory impairments and cognitive abnormalities are common. Because of the rising
prevalence of dementia among the elderly, it is critical to promote healthy habits that
can delay the onset of cognitive decline. Cognitive training (CT) and cognitive rehabilitation
(CR) are particular treatments aimed to resolve memory and further areas of cognitive
working in order to overcome these challenges. These are some of the different
kinds of non-pharmacological treatments like reality orientation and skills training programs
that can be used to deal with the cognitive and non-cognitive repercussions. The
purpose of this review is to assess the efficacy and influence of cognitive training and
cognitive rehabilitation in patients who are in their early phases of Alzheimer's disease or
vascular dementia. These interventions are geared toward improving the patients'
memory, in addition to other aspects of their cognitive functioning.
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Affiliation(s)
- Sanchit Dhankhar
- Chitkara College of Pharmacy, Chitkara University, Punjab, India
| | - Prerna Sharma
- Guru Gobind Singh College of
Pharmacy, Yamunanagar, 135001, Haryana, India
| | - Samrat Chauhan
- Chitkara College of Pharmacy, Chitkara University, Punjab, India
| | - Monika Saini
- Maharishi Markandeshwar (Deemed to be
University), Mullana, Ambala, 133207, India
| | - Nitika Garg
- Ganpati Institute of Pharmacy, Bilaspur, 135102,
Haryana, India
| | - Randhir Singh
- Central University of Punjab, Bathinda, 151401, Punjab, India
| | - Mohammad Amjad Kamal
- West China
School of Nursing / Institutes for Systems Genetics, Frontiers Science Center for
Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, 610041,
Sichuan, China
- King Fahd Medical Research Center, King Abdulaziz University, P. O. Box,
80216, Jeddah, 21589, Saudi Arabia,
- Novel Global Community Educational Foundation,
Australia
| | | | - Nidhi Rani
- Chitkara College of Pharmacy, Chitkara University, Punjab, India
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Barnard-Mayers R, Declercq E, Murray EJ, Yarrington TD, Werler MM. Using linked data to explore medical complications associated with Robson classification of cesarean deliveries in Massachusetts, 2011 to 2018. AJOG GLOBAL REPORTS 2025; 5:100470. [PMID: 40201619 PMCID: PMC11976233 DOI: 10.1016/j.xagr.2025.100470] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/10/2025] Open
Abstract
Background Cesarean delivery rates in the United States far exceed the World Health Organization (WHO)'s recommended population cesarean rate of 15%. This has resulted in calls from experts to reduce cesarean delivery rates. However, crude cesarean delivery rates are not necessarily comparable across populations since different birthing populations have different distributions of underlying cesarean delivery risk factors. WHO recommends using the Robson classification system to compare standardized cesarean delivery rates across populations, though it has been rarely used within the U.S. Objective The objectives of this study were to understand the distribution of cesarean deliveries using the Robson Classification system and to identify associated conditions (and potential drivers) of cesarean delivery across Robson groups. Study Design Our data comes from the Pregnancy and Early Life Longitudinal Data System from the Massachusetts Department of Health, which contains all birth certificate records for Massachusetts from 2011 to 2018. Using the WHO Robson Classification System Implementation guide, we categorized births into one of its 10 categories based on data from birth certificate records and ICD-9 and ICD-10 codes from billing records. Using the linked birth certificate records and hospital discharge records we went beyond the Robson classifications and examined patterns in maternal comorbidities and labor and delivery complications of cesarean deliveries across Robson groups. Results Among the 25% of birthing people who had singleton, term, vertex births with spontaneous labor, the cesarean delivery rate was 15% for nulliparous and 3% for multiparous (with no prior cesarean). The prevalence of maternal risk factors was 28% in the former and 30% in the latter. Labor and delivery complications were present in 46% and 35% of births, respectively. Birthing people with breech or transverse fetal presentation had the highest cesarean delivery rates around 95%. Multiparous birthing people with a prior cesarean delivery and cephalic, singleton, term births were the largest contributor to the cesarean delivery rate (38% of all cesareans). Almost all births for malpresentation or malposition of fetus had at least one labor and delivery complication but much lower rates of risk factors (between 25% and 46%). Conclusion While cesarean delivery rates, maternal risk factors, and labor and delivery complications followed similar patterns across Robson groups, there were notable discrepancies, especially in births with noncephalic presentations where maternal comorbidity rates matched lower cesarean-risk groups like the nulliparous single-term cephalic births.
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Affiliation(s)
- Ruby Barnard-Mayers
- Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA (Barnard-Mayers, Murray, and Werler)
| | - Eugene Declercq
- Department of Community Health Sciences, Boston University School of Public Health, Boston, MA, USA (Declercq)
| | - Eleanor J. Murray
- Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA (Barnard-Mayers, Murray, and Werler)
| | - Tina D. Yarrington
- Department of Obstetrics and Gynecology, Division of Maternal and Fetal Medicine, University of New Mexico, Albequerque, NM, USA (Yarrington)
| | - Martha M. Werler
- Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA (Barnard-Mayers, Murray, and Werler)
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Saadah OI, AlAmeel T, Al Sarkhy A, Hasosah M, Al-Hussaini A, Almadi MA, Al-Bawardy B, Altuwaijri TA, AlEdreesi M, Bakkari SA, Alharbi OR, Azzam NA, Almutairdi A, Alenzi KA, Al-Omari BA, Almudaiheem HY, Al-Jedai AH, Mosli MH. Saudi consensus guidance for the diagnosis and management of inflammatory bowel disease in children and adolescents. Saudi J Gastroenterol 2025; 31:107-136. [PMID: 39215473 DOI: 10.4103/sjg.sjg_171_24] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 05/13/2024] [Accepted: 07/20/2024] [Indexed: 09/04/2024] Open
Abstract
ABSTRACT The management of inflammatory bowel disease (IBD) in children and adolescents is challenging. Clear evidence-based guidelines are required for this population. This article provides recommendations for managing IBD in Saudi children and adolescents aged 6-19 years, developed by the Saudi Ministry of Health in collaboration with the Saudi Society of Clinical Pharmacy and the Saudi Gastroenterology Association. All 57 guideline statements are based on the most up-to-date information for the diagnosis and management of pediatric IBD.
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Affiliation(s)
- Omar I Saadah
- Department of Pediatrics, Faculty of Medicine, King Abdulaziz University, Inflammatory Bowel Disease Unit, King Abdulaziz University Hospital, Jeddah, Saudi Arabia
| | - Turki AlAmeel
- Department of Medicine, King Fahad Specialist Hospital, Dammam, Saudi Arabia
| | - Ahmed Al Sarkhy
- Gastroenterology Unit, Pediatrics Department, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia
| | - Mohammed Hasosah
- Department of Pediatrics, Gastroenterology Unit, King Abdulaziz Medical City, National Guard Hospital, Jeddah, Saudi Arabia
- Department of Pediatric Gastroenterology, King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia
- Department of Pediatric Gastroenterology, King Abdullah International Medical Research Center, Jeddah, Saudi Arabia
| | - Abdulrahman Al-Hussaini
- Children's Specialized Hospital, King Fahad Medical City, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
| | - Majid A Almadi
- Division of Gastroenterology, Department of Medicine, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia
| | - Badr Al-Bawardy
- Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia, Department of Internal Medicine, Section of Digestive Diseases, Yale School of Medicine, New Haven, CT, USA
| | - Talal A Altuwaijri
- Department of Surgery, Division of Vascular Surgery, College of Medicine, King Saud University, Riyadh, Saudi Arabia
| | - Mohammed AlEdreesi
- Gastroenterology Unit, Pediatric Department, Al Habib Medical Group, Khobar, Saudi Arabia
| | - Shakir A Bakkari
- Department of Gastroenterology, King Saud Medical City, Riyadh, Saudi Arabia
| | - Othman R Alharbi
- Division of Gastroenterology, Department of Medicine, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia
| | - Nahla A Azzam
- Division of Gastroenterology, Department of Medicine, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia
| | - Abdulelah Almutairdi
- Department of Medicine, King Faisal Specialist Hospital and Research Center, Alfaisal University, Riyadh, Saudi Arabia
| | - Khalidah A Alenzi
- Executive Management of Transformation, Planning, and Business Development, Tabuk Health Cluster, Tabuk, Saudi Arabia
| | - Bedor A Al-Omari
- Department of Pharmaceutical Care Services, Prince Sultan Military Medical City, Riyadh, Saudi Arabia
| | | | - Ahmed H Al-Jedai
- Deputyship of Therapeutic Affairs, Ministry of Health, Riyadh, Saudi Arabia
- Colleges of Medicine and Pharmacy, Alfaisal University, Riyadh, Saudi Arabia
| | - Mahmoud H Mosli
- Department of Internal Medicine, King Abdulaziz University, Inflammatory Bowel Disease Unit, King Abdulaziz University Hospital, Jeddah, Saudi Arabia
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13
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Di Buono G, Romano G, Rodolico V, Amato G, Zanghì G, Romano G, Calò PG, Agrusa A. Progrip versus ProFlor: two fixation-free devices for laparoscopic inguinal hernia repair-the Pro/Pro study, a randomized clinical trial. Surg Endosc 2025; 39:3113-3126. [PMID: 40167608 PMCID: PMC12041049 DOI: 10.1007/s00464-025-11680-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/24/2024] [Accepted: 03/14/2025] [Indexed: 04/02/2025]
Abstract
TRIAL DESIGN This randomized, multicenter clinical trial evaluates laparoscopic bilateral inguinal hernia repair outcomes by comparing the Progrip self-fixating mesh to the ProFlor 3D dynamic regenerative scaffold. METHODS Adults aged 18-85 years with clinically diagnosed bilateral primary inguinal hernias were enrolled and randomized into two treatment groups (Progrip or ProFlor) using block randomization. Operative time, intra- and postoperative complications, recurrence rates, postoperative pain, and quality of life were assessed over a 24-month follow-up. The allocation was not blinded to investigators or patients. RESULTS From January 2021 to June 2022, 150 patients underwent laparoscopic TAPP repair. Eighteen were lost to follow-up (5 in the ProFlor group, 13 in the Progrip group). A total of 132 patients (67 ProFlor, 65 Progrip) were analyzed. The ProFlor group demonstrated shorter operative times, fewer intra- and postoperative complications, and reduced early postoperative pain compared to the Progrip group. Patients in the ProFlor arm achieved faster recovery and earlier return to daily activities. Notably, none of the ProFlor patients experienced chronic pain, whereas 10.8% of Progrip patients developed this complication. Hernia recurrence was observed in 2 Progrip patients, while no recurrences were reported in the ProFlor™ group. CONCLUSION In this randomized trial, both devices proved feasible and effective for laparoscopic repair of bilateral inguinal hernias. However, the ProFlor scaffold was associated with reduced postoperative pain, absence of chronic pain, and no recurrences during follow-up compared to Progrip. While these findings are encouraging, further studies with larger cohorts and longer-term follow-up are warranted to confirm the potential benefits of the ProFlor scaffold and its role in routine clinical practice. TRIAL REGISTRATION This study was registered at ClinicalTrials.gov with number NCT06556498.
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Affiliation(s)
- Giuseppe Di Buono
- Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Via del Vespro, 129, 90127, Palermo, Italy.
| | - Giorgio Romano
- Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Via del Vespro, 129, 90127, Palermo, Italy
| | - Vito Rodolico
- Department PROMISE, Section Pathological Anatomy University of Palermo, Palermo, Italy
| | - Giuseppe Amato
- Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Via del Vespro, 129, 90127, Palermo, Italy
| | - Guido Zanghì
- Department of General Surgery, University of Catania, Catania, Italy
| | - Giorgio Romano
- Postgraduate School of General Surgery, University of Palermo, Palermo, Italy
| | | | - Antonino Agrusa
- Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Via del Vespro, 129, 90127, Palermo, Italy
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Tang D, Tran Y, Bennett RJ, Lo C, Lee JN, Turner J, Gopinath B. The Benefits of Hearing Aids for Adults: A Systematic Umbrella Review. Ear Hear 2025; 46:563-570. [PMID: 39849317 DOI: 10.1097/aud.0000000000001620] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/25/2025]
Abstract
OBJECTIVES This umbrella review aims to summarize the major benefits of hearing aid usage in adults by synthesizing findings from published review articles. DESIGN A comprehensive search of databases, including MEDLINE, EMBASE, PsycINFO, and Google Scholar, was conducted. The search was limited to English-language review articles published between 1990 and 2023, focusing on hearing aid outcomes in at least 5 adults (aged ≥18 years). Two researchers independently screened titles, abstracts, and full-text articles, and conducted a quality assessment using the Joanna Briggs Checklist for Systematic Reviews and Research Syntheses. A third researcher was involved in discussions with the 2 researchers to resolve conflicts during the screening and quality assessment stages. RESULTS Eleven articles were included in this review. There were three systematic reviews with meta-analysis and eight systematic reviews without meta-analysis. The quality assessment indicated that articles scored between 6 and 11 out of a total of 11 criteria. Three articles met all quality criteria. Study participants tended to be middle-aged (≥40 years) or older adults (≥65 years). Participant gender was less clear as this was not consistently reported but appeared to favor men. This umbrella review found that speech perception, communication function, hearing handicap, and self-assessed hearing aid benefit were consistently positively associated with hearing aid use in the analysis of included studies. Hearing handicap was the most frequently reported outcome with evidence from four different studies supporting its mitigation with hearing aid use. There was insufficient evidence in terms of benefit on balance, cognitive function, depression, tinnitus, loneliness, and social isolation. There was conflicting evidence on the impact of hearing aid use on quality of life. Among eligible studies, there were no reports of negative impacts of hearing aid use. CONCLUSIONS There are a number of potential benefits associated with hearing aid use. However, this review found that there was a clear lack of high-quality evidence and limited use of robust study design to support the benefits of hearing aids on other outcomes such as quality of life and cognition. Inconsistent use and interpretation of various outcome measures makes it difficult to produce homogenous data which is needed to make more conclusive statements about the benefits of hearing aids.
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Affiliation(s)
- Diana Tang
- Department of Health Sciences, Faculty of Medicine Health and Human Sciences, Macquarie University, North Ryde, New South Wales, Australia
| | - Yvonne Tran
- Department of Health Sciences, Faculty of Medicine Health and Human Sciences, Macquarie University, North Ryde, New South Wales, Australia
| | - Rebecca J Bennett
- National Acoustic Laboratories, Australian Hearing Hub, Sydney, New South Wales, Australia
| | - Charles Lo
- Department of Management, Australian College of Applied Professions, Sydney, New South Wales, Australia
| | - Jien Nien Lee
- Department of Health Sciences, Faculty of Medicine Health and Human Sciences, Macquarie University, North Ryde, New South Wales, Australia
| | - Jessica Turner
- Department of Health Sciences, Faculty of Medicine Health and Human Sciences, Macquarie University, North Ryde, New South Wales, Australia
| | - Bamini Gopinath
- Department of Health Sciences, Faculty of Medicine Health and Human Sciences, Macquarie University, North Ryde, New South Wales, Australia
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15
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Lara-Palomo IC, Capel-Alcaraz AM, García-López H, Castro-Sánchez AM, Querol-Zaldívar MDLÁ, Fernández-Sánchez M. Effectiveness of monopolar diathermy by radiofrequency combined with exercise in patients with chronic low back pain: A randomized clinical trial. J Back Musculoskelet Rehabil 2025; 38:420-433. [PMID: 39392597 DOI: 10.3233/bmr-240118] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 10/12/2024]
Abstract
BackgroundChronic low back pain can severely affect quality of life. While several treatments are available, the combination of therapies often results in better outcomes.ObjectiveThis study delves into the comparative effectiveness of combining monopolar dielectric diathermy radiofrequency (MDR) with supervised therapeutic exercise against the latter treatment alone.MethodsA randomized single-blind controlled trial was conducted. The intervention group (( n = 30 ) 30) received MDR with supervised therapeutic exercises for eight weekly sessions for four weeks. The control group (n = 30) received only the same exercise protocol. The following self-report measures were assessed before the first treatment session, at four, and 12 weeks: disability, pain, kinesiophobia, quality of life, sleep quality, emotional distress, isometric trunk strength, and trunk flexion range.ResultsRepeated ANOVA measures revealed significant time*group interactions for the McQuade test (p = 0.003), the physical role (p = 0.011), vitality (p = 0.023), social function (p = 0.006), and mental health subscales (p = 0.042). Between-group analyses showed significant differences for all outcomes at each follow-up: RMDQ (post-treatment, p = 0.040), ODI (post-treatment and 12-week, p = 0.040), VAS (p < 0.001), TSK (p < 0.001), and McQuade Test (p < 0.020).ConclusionThe combination of diathermy radiofrequency with supervised therapeutic exercise significantly surpasses the efficacy of supervised therapeutic exercise alone, showcasing improvements in pain, disability, kinesiophobia, lumbar mobility in flexion, and overal quality of life in patients with chronic low back pain.
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Affiliation(s)
- Inmaculada Carmen Lara-Palomo
- Department of Nursing, Physical Therapy and Medicine, University of Almeria, La Cañada de San Urbano, Almería, Spain
| | - Ana María Capel-Alcaraz
- Department of Nursing, Physical Therapy and Medicine, University of Almeria, La Cañada de San Urbano, Almería, Spain
| | - Héctor García-López
- Department of Nursing, Physical Therapy and Medicine, University of Almeria, La Cañada de San Urbano, Almería, Spain
| | - Adelaida María Castro-Sánchez
- Department of Nursing, Physical Therapy and Medicine, University of Almeria, La Cañada de San Urbano, Almería, Spain
| | | | - Manuel Fernández-Sánchez
- Department of Nursing, Physical Therapy and Medicine, University of Almeria, La Cañada de San Urbano, Almería, Spain
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16
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Lottermann NC, Andreazza NL, de Araújo Moura Cavalcante M, Fernandez LA, Vitola Gonçalvez C, Zhang L. Efficacy of tranexamic acid application in gynecology and obstetrics procedures: a umbrella review of systematic reviews of randomized trials. REVISTA BRASILEIRA DE GINECOLOGIA E OBSTETRÍCIA 2025; 47:e-rbgo18. [PMID: 40406479 PMCID: PMC12097445 DOI: 10.61622/rbgo/2025rbgo18] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/03/2024] [Accepted: 01/31/2025] [Indexed: 05/26/2025] Open
Abstract
Objective This umbrella review aimed to synthesize evidence from systematic reviews of clinical trials on the efficacy of tranexamic acid in gynecology and obstetrics procedures. Methods We searched Medline, Embase, SciELO and Cochrane Database of Systematic Reviews on March 11, 2024, using the term "tranexamic acid". Four reviewers independently select studies and extract data. We assessed the quality of systematic review and the quality of evidence, using AMSTAR 2 and GRADE tools, respectively. Results Of 651 systematic reviews identified, 16 reviews with 96663 patients were included. The surgical procedures were cesarean section, myomectomy, hysterectomy, and cervical intraepithelial neoplasia surgery. All reviews showed a statistically significant and clinically relevant reduction in intraoperative and post-procedure blood loss, associated with intravenous or topical use of tranexamic acid. Tranexamic acid resulted in a significant reduction in the need for blood transfusions and a less pronounced drop in postoperative hematocrit and hemoglobin levels in cesarean section. Several reviews addressed the same question, but the number of included trials varied substantially, which might indicate flaws in search and selection of studies of these reviews. The quality of systematic reviews was low or critically low, and the quality of evidence was moderate. Conclusions This umbrella review shows that tranexamic acid can reduce blood loss and hemorrhage in gynecology and obstetrics procedures. High quality systematic reviews are still needed.
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Affiliation(s)
- Nicole Cristina Lottermann
- Universidade Federal do Rio GrandeRio GrandeRSBrazilUniversidade Federal do Rio Grande, Rio Grande, RS, Brazil.
| | - Nathalia Luiza Andreazza
- Universidade Federal do Rio GrandeRio GrandeRSBrazilUniversidade Federal do Rio Grande, Rio Grande, RS, Brazil.
| | | | - Laura Andrade Fernandez
- Universidade Federal do Rio GrandeRio GrandeRSBrazilUniversidade Federal do Rio Grande, Rio Grande, RS, Brazil.
| | - Carla Vitola Gonçalvez
- Universidade Federal do Rio GrandeRio GrandeRSBrazilUniversidade Federal do Rio Grande, Rio Grande, RS, Brazil.
| | - Linjie Zhang
- Universidade Federal do Rio GrandeRio GrandeRSBrazilUniversidade Federal do Rio Grande, Rio Grande, RS, Brazil.
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17
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Jones ASK, Seaton N, Brown A, Jenkinson E, Carroll S, Dietz KC, Hudson JL, Wroe A, Moss-Morris R. The Illness-Related Distress Scale: development and psychometric evaluation of a new transdiagnostic measure. Psychol Med 2025; 55:e122. [PMID: 40289643 PMCID: PMC12094643 DOI: 10.1017/s003329172500090x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/27/2024] [Revised: 03/14/2025] [Accepted: 03/24/2025] [Indexed: 04/30/2025]
Abstract
BACKGROUND Individuals with long-term physical health conditions (LTCs) experience higher rates of depression and anxiety. Conventional self-report measures do not distinguish distress related to LTCs from primary mental health disorders. This difference is important as treatment protocols differ. We developed a transdiagnostic self-report measure of illness-related distress, applicable across LTCs. METHODS The new Illness-Related Distress (IRD) scale was developed through thematic coding of interviews, systematic literature search, think-aloud interviews with patients and healthcare providers, and expert-consensus meetings. An internet sample (n = 1,398) of UK-based individuals with LTCs completed the IRD scale for psychometric analysis. We randomly split the sample (1:1) to conduct: (1) an exploratory factor analysis (EFA; n = 698) for item reduction, and (2) iterative confirmatory factor analysis (CFA; n = 700) and exploratory structural equation modeling (ESEM). Here, further item reduction took place to generate a final version. Measurement invariance, internal consistency, convergent, test-retest reliability, and clinical cut-points were assessed. RESULTS EFA suggested a 2-factor structure for the IRD scale, subsequently confirmed by iteratively comparing unidimensional, lower order, and bifactor CFAs and ESEMs. A lower-order correlated 2-factor CFA model (two 7-item subscales: intrapersonal distress and interpersonal distress) was favored and was structurally invariant for gender. Subscales demonstrated excellent internal consistency, very good test-retest reliability, and good convergent validity. Clinical cut points were identified (intrapersonal = 15, interpersonal = 12). CONCLUSION The IRD scale is the first measure that captures transdiagnostic distress. It may aid assessment within clinical practice and research related to psychological adjustment and distress in LTCs.
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Affiliation(s)
- Annie S. K. Jones
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Natasha Seaton
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Ashley Brown
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Emma Jenkinson
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Susan Carroll
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Kristina C. Dietz
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Joanna L. Hudson
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Abigail Wroe
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
| | - Rona Moss-Morris
- Health Psychology Section, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
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18
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Krieger A. Benzos (as) needed: research into as-needed and intermittent benzodiazepines for anxiety is required for comprehensive best prescribing practices. Front Psychiatry 2025; 16:1569416. [PMID: 40357517 PMCID: PMC12066482 DOI: 10.3389/fpsyt.2025.1569416] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/31/2025] [Accepted: 04/04/2025] [Indexed: 05/15/2025] Open
Abstract
The medical and public health communities are divided around the use of benzodiazepine ("benzo") pharmacotherapy for anxiety disorders. Recent years have seen increased attention to benzo overprescription and its risks, leading to a pervasive emphasis on deprescribing. Some have resisted this trend, arguing that the balance of evidence supports the safety and efficacy of benzo pharmacotherapy for both short-term and long-term treatment of anxiety disorders. Given that rising rates of anxiety disorders and benzo misuse are both serious public health concerns, there is an urgent need for comprehensive evidence-based best practices for the prescription of benzos for anxiety. At present, however, major scientific gaps make it impossible to formulate such guidance. Most concerning is the lack of research into as-needed and intermittent prescription and use, which are both what benzos are best suited for, and likely, how they are most commonly administered. Further research into the safety and efficacy of both long-term daily and intermittent, as-needed benzo prescription and use are badly needed. But a roundly "anti-benzo" sentiment may be causing problematic underprescription of benzos, particularly when superior alternatives like cognitive-behavioral therapy are not widely available.
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Affiliation(s)
- Arthur Krieger
- Department of Philosophy, Temple University, Philadelphia, PA, United States
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19
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Collins H, Wittkowski A, Gregg L. The Parenting Practices of Parents with Psychosis: A Systematic Integrative Review. Clin Child Fam Psychol Rev 2025:10.1007/s10567-025-00518-6. [PMID: 40268853 DOI: 10.1007/s10567-025-00518-6] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 03/23/2025] [Indexed: 04/25/2025]
Abstract
Parental psychosis has been reliably associated with adverse outcomes for both parents and children. Despite this, support for these families remains limited. Understanding the everyday parenting practices of parents with psychosis, and whether they differ from parents without psychosis is crucial for developing suitable, evidence-based interventions. We therefore aimed to synthesise quantitative and qualitative research to answer two research questions: (1) 'What are the parenting practices of parents who experience psychosis?' and (2) 'Are the parenting practices of parents who experience psychosis the same as the parenting practices of parents without serious mental illness (SMI)?' Five databases were searched for terms associated with parenting, psychosis and parenting practices, following the Preferred Reporting Items for Systematic Review and Meta-Analysis guidelines. The Mixed Methods Appraisal Tool was used for quality appraisal prior to an integrative narrative synthesis being conducted. Twelve studies (n = 9 quantitative; n = 3 qualitative) containing 1115 parents with psychosis were included. The synthesis revealed that parents with psychosis frequently use positive authoritative parenting strategies, but sometimes this can be difficult to sustain, with parents resorting to permissive and inconsistent parenting practices. They appear to do so more frequently than parents without SMI but because only four studies utilised a control group, more comparative research is needed. The review recommends further support, and use of parenting interventions for parents with psychosis, alongside systemic practice change initiatives within adult mental health services.
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Affiliation(s)
- Hannah Collins
- Division of Psychology and Mental Health, School of Health Sciences, University of Manchester, Manchester, UK
- Greater Manchester Mental Health NHS Foundation Trust, Manchester, UK
| | - Anja Wittkowski
- Division of Psychology and Mental Health, School of Health Sciences, University of Manchester, Manchester, UK
- Greater Manchester Mental Health NHS Foundation Trust, Manchester, UK
- Manchester Academic Health Science Centre, Manchester, M13 9NQ, UK
| | - Lynsey Gregg
- Division of Psychology and Mental Health, School of Health Sciences, University of Manchester, Manchester, UK.
- Manchester Academic Health Science Centre, Manchester, M13 9NQ, UK.
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20
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Zaki J. Mesh-assisted regenerated site for alveolar ridge preservation: A case report. Clin Adv Periodontics 2025. [PMID: 40254793 DOI: 10.1002/cap.10356] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/06/2024] [Revised: 03/01/2025] [Accepted: 03/23/2025] [Indexed: 04/22/2025]
Abstract
BACKGROUND The proposed technique utilizes the osteoconductive regenerative properties of bone-substitute materials (BSMs) and the space-maintaining function of titanium mesh to restore the alveolar ridge at extraction sites with lost labial plates in a single procedure. This approach may reduce the need for extensive ridge augmentation procedures, shorten treatment duration, minimize complications, and potentially lower overall costs for patients. METHODS Both patients presented with hopeless dentition, characterized by chronic infection and loss of the labial plates. To regenerate the alveolar ridge, a titanium mesh was utilized in combination with a layered application of xenograft and allograft BSMs. The success of this technique depended on mesh stabilization, thorough site debridement, and the absence of soft-tissue tension. RESULTS The technique effectively restored the lost labial plates and regenerated sufficient bone to accommodate dental implants. Significant bone regeneration was achieved in both cases, with minimal complications. In one case, a minor mesh exposure occurred; however, it did not affect the healing and was managed during the re-entry surgery. CONCLUSION The presented technique effectively regenerated the lost labial plates. It represents a novel alveolar ridge preservation approach to restore the alveolar ridge at extraction sites with lost labial bone plates, even in the presence of chronic infection. However, future studies with sound methodology, larger sample sizes, and long follow-up periods are recommended to validate these findings. KEY POINTS The Mesh-Assisted Regenerated Site (MARS) technique restores the alveolar ridge at sites with lost labial plates by combining the osteoconductive properties of bone substitutes with the space-maintaining function of titanium mesh in a single procedure. This approach may reduce the need for extensive augmentation, shorten treatment duration, minimize complications, and potentially lower long-term treatment costs. The success of this approach depends on minimally traumatic extraction, meticulous socket debridement, careful soft tissue management, and precise placement of titanium mesh and bone substitutes under optimal magnification. Although effective, this technique has limitations, including potential vertical bone loss, time-consuming procedures, possible need for additional augmentation, occasional challenges with mesh retrieval, and infection risk, all of which may compromise regeneration and implant success. Proper case selection and precise application of the technique are essential to mitigate these challenges and optimize clinical outcomes. PLAIN LANGUAGE SUMMARY When teeth are removed, the surrounding bone can shrink. Techniques to preserve this area, known as alveolar ridge preservation, help prevent this shrinkage. This novel technique uses specialized bone materials and a titanium mesh to rebuild the bone in areas where the front portion is missing. The author used a combination of bone materials and a titanium mesh to rebuild the lost bone. Key steps included stabilizing the mesh, thoroughly cleaning out any infection, layering the bone materials, and ensuring the gum tissue was not overly tight. The technique successfully reconstructed the missing bone, making it possible to place standard dental implants. Both cases showed significant bone growth with minimal issues. In one case, a small part of the mesh was exposed but did not impact healing and was addressed during follow-up surgery. This technique effectively rebuilt the lost bone, even with the presence of a long-standing infection. It shows promise for preserving and regenerating bone in these areas, but more extensive studies are needed to confirm the results and improve the method.
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Affiliation(s)
- John Zaki
- Private Practice, Salmiya Block 2, Hawalli, Kuwait
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21
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Frees M, Ward CM. Outcomes of Corticosteroid Injection for Lacertus Syndrome. Hand (N Y) 2025:15589447251331103. [PMID: 40219767 PMCID: PMC11993550 DOI: 10.1177/15589447251331103] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 04/14/2025]
Abstract
BACKGROUND Lacertus syndrome is a proximal median nerve compression neuropathy characterized by weakness of flexor pollicis longus (FPL), index finger flexor digitorum profundus (FDP), and flexor carpi radialis (FCR) and pain with compression of the median nerve at the lacertus fibrosus. The purpose of this study was to investigate the efficacy of corticosteroid injection (CSI) for symptom management in lacertus syndrome. METHODS A retrospective review of patients with lacertus syndrome who underwent lacertus CSI between 2016 and 2021 was performed. Patient demographics, history, and physical examination were extracted from the electronic medical record. Outcomes included subjective improvement in symptoms, physical examination findings, incidence of repeat lacertus CSI, and/or subsequent surgical lacertus fibrosus release. RESULTS A total of 64 patients met the inclusion criteria. Chief complaint included hand/forearm pain in 44 patients (69%), median nerve paresthesias in 49 patients (77%), and hand weakness in 9 patients (14%). On examination, 63 (98%) had tenderness at the lacertus fibrosus. Manual motor testing identified weakness of the index FDP in 50 patients, FPL weakness in 42 patients, and FCR weakness in 23 patients. Forty-eight (75%) patients had subjective improvement in symptoms following CSI. Seventeen patients who had an initial response to CSI subsequently underwent surgical lacertus release, with 16 of 17 surgical patients reporting postoperative symptom relief. DISCUSSION Seventy-five percent of patients with lacertus syndrome who underwent CSI at the lacertus fibrosus experienced at least temporary subjective symptomatic relief. Of the 35% of patients who had recurrent symptoms after CSI and underwent surgery, the vast majority experienced symptom relief.
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Affiliation(s)
| | - Christina M. Ward
- University of Minnesota, Minneapolis, USA
- Regions Hospital, Saint Paul, MN, USA
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22
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Lu F, Lu G, Wang Z, Wei W, Chen J, Zheng H, Liu X, Ye Y, Liu S, Lin Y, Liu Y, Bi Z, Zou Q, Zhang G, Sun H, Tong Y. Improved antibacterial activity of a sustained-release biocompatible nanofilm for treating Pseudomonas aeruginosa wound infection in vitro and in vivo. Front Microbiol 2025; 16:1548106. [PMID: 40270824 PMCID: PMC12015611 DOI: 10.3389/fmicb.2025.1548106] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/08/2025] [Accepted: 03/24/2025] [Indexed: 04/25/2025] Open
Abstract
Objectives The primary goal of this research was to design a useful and biocompatible nanofilm system (CNF) encapsulating chlorhexidine acetate (CHX) for wounds that is endowed with antibacterial and anti-inflammatory activities and promotes wound healing. Methods The nanofilm system was developed on the basis of the successful preparation of its nanoemulsion and PVA-CS film system and then important properties of the nanofilm system, including its morphological and physicochemical characteristics, stability and safety, its antimicrobial efficacy against P. aeruginosa was also evaluated in vitro and in vivo. The antibacterial effect, wound healing effect and inflammatory factor change in vivo were evaluated. Results These results of this nanofilm system revealed a good particle size (59.27 nm) and stable zeta potential (-15.2 mV) that are suitable for wound healing applications. Additionally, it was stable, exhibited long-term stability (24 months) and sustained release in simulated wound fluid. Results showed that this nanofilm does not induce dose-related toxic effects and displays a better antibacterial effect that occurs more quickly, two times greater than that of CHX in vitro. This safe nanofilm enhances antibacterial activity against P. aeruginosa for 14 days, modulates the immune response, and accelerates skin wound healing in vivo. Conclusions These insights into multifunctional nanofilm designs for improved antibacterial effects and sustained release suggest promising clinical applications.
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Affiliation(s)
- Feifei Lu
- College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, Liaoning, China
| | - Guoxiu Lu
- College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, Liaoning, China
| | - Zhiguo Wang
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
| | - Wenzhua Wei
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Jingjing Chen
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Hailin Zheng
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Xuesong Liu
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Yan Ye
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Shuling Liu
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Yuxiang Lin
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
| | - Yuxin Liu
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
| | - Zhanhua Bi
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
| | - Quanming Zou
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Guoxu Zhang
- College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, Liaoning, China
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
| | - Hongwu Sun
- National Engineering Research Centre of Immunological Products, Department of Microbiology and Biochemical Pharmacy, College of Pharmacy, Third Military Medical University, Chongqing, China
| | - Yanan Tong
- Department of Nuclear Medicine, General Hospital of Northern Theater Command, Shenyang, China
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Ng QJ, Ee TX, Goh CSY, Lee SH, Low JEH, Lin J, Phoon JWL, Chan JJ, Chin FHX. Oncofertility care and fertility preservation in gynaecological cancer: experience from Singapore's largest tertiary centre. Singapore Med J 2025:00077293-990000000-00189. [PMID: 40205745 DOI: 10.4103/singaporemedj.smj-2024-094] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/08/2024] [Accepted: 09/23/2024] [Indexed: 04/11/2025]
Abstract
INTRODUCTION Fertility-sparing management is an option for young patients with gynaecological cancers, conferring comparable oncological and favourable reproductive outcomes as standard treatment. With delayed childbearing, the need for fertility-sparing treatment and demand for fertility preservation have increased. We describe the development of an oncofertility model of care at a tertiary hospital, along with our experiences. METHODS This was a retrospective audit of patients who attended the OncoFertility Clinic, KK Women's and Children's Hospital, Singapore, from 9 September 2020 to 9 March 2023, focusing on the epidemiology and short-term outcomes. RESULTS A total of 144 women (median age 31 years) attended the OncoFertility Clinic, of whom 69 (47.9%) had uterine conditions, 65 (45.1%) had ovarian conditions, six (4.2%) had cervical conditions and four (2.8%) had synchronous uterine and ovarian conditions. Among the 45 women on fertility-sparing management for endometrial cancer, 66.7% had complete regression, 11.1% had persistent carcinoma and 22.2% regressed to endometrial hyperplasia. Fourteen women underwent in vitro fertilisation (IVF), resulting in three live births and one miscarriage. Thirty-two women had ovarian cancer, 23 had borderline ovarian tumours, one had Krukenberg tumour and nine had benign ovarian tumours. Fertility-sparing surgery was performed in 90.6% of the ovarian cancer cases. Fertility preservation was offered to twenty women, four of whom proceeded with fertility-preserving procedures. Three patients underwent assisted reproductive therapy. Four patients had surgery for suspected recurrences, but histologies were benign. CONCLUSION A multidisciplinary OncoFertility Clinic provides comprehensive counselling for young women with gynaecological cancers or precancers, addresses their reproductive health concerns, supports their decision-making and ensures timely access to fertility services.
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Affiliation(s)
- Qiu Ju Ng
- Department of Gynaecological Oncology, KK Women's and Children's Hospital, Singapore
| | - Tat Xin Ee
- Department of Reproductive Medicine, KK Women's and Children's Hospital, Singapore
| | | | - Shi Hui Lee
- Department of Obstetrics and Gynecology, KK Women's and Children's Hospital, Singapore
| | - Jasmine Earn Huay Low
- Department of Gynaecological Oncology, KK Women's and Children's Hospital, Singapore
| | - Jinlin Lin
- Department of General Surgery, Changi General Hospital, Singapore
| | | | - Jack Junjie Chan
- Division of Medical Oncology, National Cancer Centre Singapore, Singapore
| | - Felicia Hui Xian Chin
- Department of Gynaecological Oncology, KK Women's and Children's Hospital, Singapore
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24
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Ye Z, Yuan Y, Kuang G, Qiu L, Tan X, Wen Z, Lu M. Platelet-rich plasma and corticosteroid injection for tendinopathy: a systematic review and meta-analysis. BMC Musculoskelet Disord 2025; 26:339. [PMID: 40200209 PMCID: PMC11980122 DOI: 10.1186/s12891-025-08566-3] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/07/2024] [Accepted: 03/20/2025] [Indexed: 04/10/2025] Open
Abstract
OBJECTIVE In this systematic review and meta-analysis, we evaluated and compared the efficacy and safety of platelet-rich plasma injection into corticosteroid injection in the treatment of tendinopathy. METHODS We searched PUBMED, EMBASE, Cochrane Library, SCOPUS, and Web of Science to identify randomized controlled trials on the PRP injection versus CS injection in treatment of tendinopathy.The meta-analysis was performed using the Revman 5.4 software. RESULT We found 27 RCT studies with a total of 1779 patients enrolled. 8 rotator cuff injuries, 7 humeral external epicondylitis, 10 plantar fasciitis, and 2 tenosynovitis. The results of the meta-analysis showed that there were no significant group differences in the results of patients with rotator cuff injury comparing the pain visual analog scale score and functional measures at 1 month after receiving injection treatment. After three months of receiving PRP treatment, the VAS scores showed greater improvement compared to the CS group(OR = -1.64,95%CI [-2.97,-0.31],P = 0.02), while there was no statistically significant difference in shoulder joint function between the two groups at the 3-6 month post-treatment mark. Patients with plantar fasciitis showed no significant differences in VAS and AOFAS scores after receiving PRP or CS injections at 1 and 3 months. However, at the 6-month mark, the PRP group demonstrated significantly better VAS and AOFAS scores compared to the CS group(OR = -1.41,95%CI [-1.88,-0.44],P < 0.00001; OR = 7.19,95%CI [2.41,11.91],P = 0.003). 1 month after CS injection in patients with tenosynovitis, the VAS score was lower than that of the PRP group; patients with elbow epicondylitis had better improved upper limb function rating scale scores 1 month after CS injection compared to the PRP group. In patients with tenosynovitis, the VAS scores were superior to the CS group six months after PRP treatment(OR = -0.72,95%CI [-1.04,-0.40],P < 0.00001); similarly, patients with lateral epicondylitis exhibited better VAS, DASH scores than the CS group three and twelve months post-PRP treatment(OR = -9.76,95%CI [-10.89,-8.63],P = 0.0002; OR = -0.97,95%CI [-1.87,-0.06],P < 0.0001; OR = -18.03,95%CI [-31.61,-4.46],P = 0.009). CONCLUSION PRP can effectively improve pain and functional impairment in patients with tendinopathy, and its mid-term efficacy is superior to that of corticosteroids. However, the long-term efficacy remains to be further clinically verified.
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Affiliation(s)
- Zifeng Ye
- Hunan University of Chinese Medicine, Changsha, 410208, China
- The First Hospital of Hunan University of Chinese Medicine, Changsha, 410007, China
| | - Yiwei Yuan
- Hunan University of Chinese Medicine, Changsha, 410208, China
| | - Gaoyan Kuang
- The First Hospital of Hunan University of Chinese Medicine, Changsha, 410007, China
| | - Liguo Qiu
- Hunan University of Chinese Medicine, Changsha, 410208, China
- The First Hospital of Hunan University of Chinese Medicine, Changsha, 410007, China
| | - Xuyi Tan
- Affiliated Hospital of Hunan Academy of Traditional Chinese Medicine, Changsha, 410006, China
| | - Zhi Wen
- Hunan University of Chinese Medicine, Changsha, 410208, China
- The First Hospital of Hunan University of Chinese Medicine, Changsha, 410007, China
| | - Min Lu
- The First Hospital of Hunan University of Chinese Medicine, Changsha, 410007, China.
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25
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Biswas I, Adebusoye B, Lewis S, Chattopadhyay K. Clinical knowledge, experiences, and perceptions of yoga providers in arthritis treatment: a UK-based qualitative study. Rheumatol Int 2025; 45:88. [PMID: 40183922 PMCID: PMC11971125 DOI: 10.1007/s00296-025-05843-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/01/2025] [Accepted: 03/19/2025] [Indexed: 04/05/2025]
Abstract
This study explored yoga providers' clinical knowledge of arthritis, experiences of delivering yoga to people with arthritis, their perceived role in arthritis treatment, and perceived yoga training needs. Qualitative semi-structured interviews with 20 United Kingdom (UK)-based yoga providers were conducted. The interviews were digitally recorded, transcribed verbatim, and analysed thematically. The analysis generated eight themes. Yoga providers were generally aware of their attendees' health conditions and had clinical knowledge of arthritis through their yoga training. They were reasonably confident in delivering yoga to attendees with arthritis and felt that they had an important role in supporting these attendees. Gentle yoga practices were considered appropriate by the yoga providers, with a perception that a potential interplay between major components of yoga including yogic poses (asana), breathing practices (pranayama), and meditation (dhyana) and relaxation practices could help impart mind-body benefits in arthritis. Creating a safe and supportive environment in yoga sessions, being empathetic towards attendees' needs, and offering tailored modifications were perceived to be important for delivering yoga in arthritis treatment. Major system-level challenges to yoga delivery in arthritis treatment included the inadequate promotion of yoga, the unregulated nature of yoga delivery, and the absence of evidence-based arthritis-specific yoga training. Yoga providers felt they could play a key role in arthritis treatment in the UK, provided yoga is adequately promoted and made accessible to people with arthritis, yoga delivery is regulated, and arthritis-specific yoga training using the best available scientific evidence is made accessible to them.
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Affiliation(s)
- Isha Biswas
- Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG5 1PB, UK.
| | - Busola Adebusoye
- Centre for Medical Imaging, University College London, London, W1W 7TS, UK
| | - Sarah Lewis
- Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG5 1PB, UK
| | - Kaushik Chattopadhyay
- Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG5 1PB, UK
- The Nottingham Centre for Evidence-Based Healthcare: A JBI Centre of Excellence, Nottingham, NG5 1PB, UK
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26
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Berg T, Flunkert S, Brenner E. [Systematic review of individual biopsychosocial aspects of interventions during a physiological birth in primiparous women]. Z Geburtshilfe Neonatol 2025; 229:131-146. [PMID: 39938571 DOI: 10.1055/a-2506-9511] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 02/14/2025]
Abstract
The birth process involves biopsychosocial aspects, the identification of which has been little researched. This systematic review aims to identify biopsychosocial aspects of interventions during physiological birth in first-time mothers and to assess the effectiveness of these interventions on birth outcomes.A systematic guideline search resulted in the definition of a physiological birth of first-time mothers with a singleton from the cephalic position at 37+0 to 42+0 weeks' gestation. A systematic literature search assessed intervention studies for evidence quality using the GRADE methodology. Structured content analysis according to Mayring was used to identify biopsychosocial aspects.18 bio-organic, psychological and sociological aspects were identified from 20 studies. The quality of evidence was mostly low to very low due to inadequate reporting of fetal and maternal outcomes and characteristics. Moderate confidence was shown for midwifery care and aromatherapy in increasing spontaneous labor, and transcutaneous electrical nerve stimulation in improving satisfaction, subjective pain perception and APGAR score. Identified biopsychosocial aspects enable a multidimensional assessment of physiological birth and could lead to a biopsychosocial care model. Insufficient quality of evidence does not allow the derivation of specific interventions. Studies in obstetrics should use defined endpoints and characteristics to improve the quality of evidence.
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Affiliation(s)
- Tina Berg
- fhg - Zentrum für Gesundheitsberufe, Innsbruck, Austria
| | | | - Erich Brenner
- fhg - Zentrum für Gesundheitsberufe, Innsbruck, Austria
- Institut für Klinisch-Funktionelle Anatomie, Medizinische Universität Innsbruck, Innsbruck, Austria
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27
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Zhang Y, Li Y, Wu X, Wang S, Wei X, Sun X. Recombinant Humanized Collagen: A Promising Treatment for Pelvic Organ Prolapse via Enhanced Fibroblast Function and Angiogenesis. Int Urogynecol J 2025; 36:881-893. [PMID: 40116904 DOI: 10.1007/s00192-025-06117-x] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/07/2024] [Accepted: 03/03/2025] [Indexed: 03/23/2025]
Abstract
INTRODUCTION AND HYPOTHESIS The treatment of pelvic organ prolapse (POP) presents significant challenges. It is important to explore safer and more effective treatment modalities. Recombinant humanized collagen (rhCol) is a promising biomaterial with excellent biocompatibility and pro-regenerative properties. Therefore, this study aims to evaluate the potential applications of rhCol in POP treatment. METHODS Vaginal wall tissues were collected from three non-POP and five POP patients to analyze extracellular matrix (ECM) changes via histological staining. Primary fibroblasts isolated from POP vaginal tissues were treated with rhCol III. Cell proliferation, migration, senescence, and ECM synthesis were assessed. A simulated birth injury (SBI) rat model was used to evaluate ECM remodeling following rhCol injection into the vaginal wall. Additionally, the angiogenic potential of rhCol III was examined in vivo and in vitro. RESULTS POP patient tissues and fibroblasts exhibited lower expression levels of type I and III collagen compared to non-POP samples. At a 1 mg/ml concentration, rhCol III promoted fibroblast proliferation and migration, reduced cellular senescence, and enhanced ECM synthesis. In the vaginal wall, the expression of COL1A1 and COL3A1 in the rhCol group was significantly higher than that in the SBI group, with a marked increase in the levels of CD31, CD34, and VEGFA. Furthermore, rhCol III improved the proliferation, migration, and tubule formation capacities of HUVECs. CONCLUSIONS rhCol III may promote ECM remodeling in an injured vaginal wall by restoring fibroblast function and stimulating angiogenesis, offering a novel biomaterial-based strategy for POP treatment.
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Affiliation(s)
- Yue Zhang
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China
| | - Yaqin Li
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China
| | - Xiaotong Wu
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China
| | - Shiyan Wang
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China
| | - Xiaoting Wei
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China
| | - Xiuli Sun
- Department of Obstetrics and Gynecology, Peking University People's Hospital, No.11, Xi-Zhi-Men South Street, Xicheng District, Beijing, 100044, China.
- Pelvic Floor Disorders Research Center of Peking University Health Science Center, Beijing, 100044, China.
- Research Center of Female Pelvic Floor Disorders of Peking University, Beijing, 100044, China.
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Mugyenyi GR, Tumuhimbise W, Ntayi JM, Byamugisha JK, Musimenta A, Kayondo M, Ngonzi J, Tornes Y, Atukunda EC. Opportunities, Challenges, and Lessons Learned From Partograph Utilization for Labor Monitoring in Sub-Saharan Africa: A Systematic Review. Cureus 2025; 17:e82295. [PMID: 40376328 PMCID: PMC12081134 DOI: 10.7759/cureus.82295] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/15/2025] [Indexed: 05/18/2025] Open
Abstract
Despite decades of healthcare provider training and investment, rates of utilization and capacity to appropriately plot the partograph and use it to make critical decisions remain sub-optimal in Sub-Saharan Africa. The objective of this review was to synthesize evidence of existing challenges and opportunities of partograph utilization in labor monitoring in Sub-Saharan Africa from existing literature. PUBMED, Cochrane Library of Trials, Google Scholar, and ScienceDirect databases published between January 1, 2013, and July 31, 2023, for studies reporting opportunities and challenges of utilizing the partograph in labor monitoring in Sub-Saharan Africa, were searched. Preferred Reporting Items for Systematic Reviews and Meta-Analyses guided the identification of eligible studies. We utilized a Consolidated Framework for Implementation Research to interpret findings. The review protocol was registered under PROSPERO-CRD42023452882. Twenty-eight high-quality studies identified from a total of 452 in eight countries in Sub-Saharan Africa were analyzed in this review. Opportunities identified included 1) the partograph's uncontested potential to reduce maternal and neonatal mortality facilitated by good support supervision, formal and on-the-job training, active mentorships, and ongoing supervision, and the availability of enabling policies, standards, and protocols on partograph use; 2) the availability of partographs in health facilities. Gaps and challenges identified included 1) lack of inadequate training and tool complexity, 2) availability of different labor monitoring tools other than the partograph, 3) lack of motivation and feedback, 4) unavailability of the partograph in some health facilities, 5) shortage of staff in busy facilities, 6) lack of support supervision, 7) lack of protocols, 8) inappropriate motivation leading to 9) lack of commitment, negative attitude, negligence, careless partograph completion, or non-use. The challenges, opportunities, and lessons learned from this review on partograph utilization in labor monitoring will help develop suitable implementation strategies to guide the introduction and scale-up of the labor care guide in Sub-Saharan Africa if we are to avoid similar challenges.
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Affiliation(s)
- Godfrey R Mugyenyi
- Obstetrics and Gynecology, Mbarara University of Science and Technology, Mbarara, UGA
| | - Wilson Tumuhimbise
- Computing and Informatics, Mbarara University of Science and Technology, Mbarara, UGA
| | - Joseph M Ntayi
- Procurement, Logistics, and Supply Management, Makerere University Business School, Kampala, UGA
| | - Josaphat K Byamugisha
- Obstetrics and Gynecology, Makerere University College of Health Sciences, Kampala, UGA
| | - Angella Musimenta
- Computing and Informatics, Mbarara University of Science and Technology, Mbarara, UGA
| | - Musa Kayondo
- Obstetrics and Gynecology, Mbarara University of Science and Technology, Mbarara, UGA
| | - Joseph Ngonzi
- Obstetrics and Gynecology, Mbarara University of Science and Technology, Mbarara, UGA
| | - Yarine Tornes
- Obstetrics and Gynecology, Mbarara University of Science and Technology, Mbarara, UGA
| | - Esther C Atukunda
- Pharmacy, Mbarara University of Science and Technology, Mbarara, UGA
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Zetterberg L, Niemi Andersson E, Åsenlöf P, Nyholm D, de Roos P, Bring A. "I'm still the person I am. Not the body it has become." An active but challenging life with cervical dystonia. Physiother Theory Pract 2025; 41:763-771. [PMID: 38814175 DOI: 10.1080/09593985.2024.2359495] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/23/2023] [Revised: 04/13/2024] [Accepted: 05/20/2024] [Indexed: 05/31/2024]
Abstract
BACKGROUND Improvement of activity and participation for the disabled and chronically ill is an important aim of rehabilitation. Cervical dystonia is a neurological movement disorder characterized by involuntary contractions of the neck muscles. Until now, research has identified factors contributing to disability rather than factors which may make it easier to be active and participate in the community. OBJECTIVE Explore and describe perceived experiences of activity and participation in daily life as experienced by persons with cervical dystonia. METHODS Sixteen informants participated in this semi-structured interview study. Inductive qualitative content analysis was performed to understand and interpret experiences shared by the informants. RESULTS Results from the analysis generated two themes "An active life" and "A challenging life" and six sub-themes: Using helpful coping strategies, Accepting a new life situation, Adhering to BT treatment, Facing the negative impact of stress, Experiencing a negative self-image and Suffering from pain and fatigue. CONCLUSIONS Our results support the importance of actions using a rehabilitation approach that consider both motor and non-motor symptoms. Future studies should compare the effects of physiotherapy taking into account wishes and challenges in patients' everyday life versus traditional physiotherapy addressing mostly the motor disorder.
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Affiliation(s)
- Lena Zetterberg
- Department of Women's and Children's Health, Physiotherapy, Uppsala University, Uppsala, Sweden
| | | | - Pernilla Åsenlöf
- Department of Women's and Children's Health, Physiotherapy, Uppsala University, Uppsala, Sweden
| | - Dag Nyholm
- Department of Medical Sciences, Neurology, Uppsala University, Uppsala, Sweden
| | - Paul de Roos
- Department of Medical Sciences, Neurology, Uppsala University, Uppsala, Sweden
| | - Annika Bring
- Department of Women's and Children's Health, Physiotherapy, Uppsala University, Uppsala, Sweden
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Cordeiro JFC, Dos Santos AP, Bohn L, Sebastião E, Marchiori GF, Gomide EBG, Castro-Piñero J, Florindo AA, Mota J, Machado DRL. Exploring the relationship between daily sedentary time and occurrence of multimorbidity in middle-aged and older adults: results from ELSI-Brazil. Arch Public Health 2025; 83:84. [PMID: 40170110 PMCID: PMC11959999 DOI: 10.1186/s13690-024-01469-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/05/2024] [Accepted: 12/02/2024] [Indexed: 04/03/2025] Open
Abstract
AIM To explore the relationship between varying durations of sedentary time (ST) in hours per day and multimorbidity, while considering covariates such as non-compliance to moderate to vigorous physical activity (MVPA) recommendations, age, sex, and smoking in middle-aged and older adults. METHODS Data from the first wave (2015-2016) of the nationally-representative Brazilian Longitudinal Study of Aging (ELSI-Brazil) were analyzed. Ordinary regression analysis was utilized to assess the odds ratio for individuals with varying daily ST durations concerning the escalation in the number of diseases while accounting for covariates such as failure to meet MVPA recommendations, age, sex, and smoking status. RESULTS A cohort of 7,314 individuals aged 50-105 years (56,3% females) participated in the study. The most prevalent occurrence of multimorbidity was having 2 conditions (1521/19.3%). A clear trend emerges, showing a rise in the number of multimorbidities as ST increase. Notably, individuals engaging in less than 4 h of daily ST exhibited a significantly lower likelihood of experiencing an increase in the total number of multimorbidity cases, with an odds ratio of 0.842 and a confidence interval of 0.764 to 0.928, even after adjusting for potential covariables. CONCLUSIONS Our findings indicate a progressive increase in multimorbidity with longer durations of ST. Moreover, limiting ST to less than 4 h daily was associated with a lower chance of multimorbidity.
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Affiliation(s)
| | - André Pereira Dos Santos
- Faculty of Sport of the University of Porto, Street Dr. Plácido da Costa 91, 4200-450, Porto, Portugal
- College of Nursing of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- School of Physical Education and Sport of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- Study and Research Group in Anthropometry, Training and Sport, Ribeirão Preto. School of Physical Education and Sport of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- Human Exposome and Infectious Diseases Network (HEID), Ribeirão Preto, Brazil
- Department of Child, Family and Population Health Nursing, University of Washington, Seattle, WA, USA
| | - Lucimere Bohn
- Research Center in Physical Activity, Health and Leisure (CIAFEL)-Faculty of Sports, University of Porto (FADEUP) and Laboratory for Integrative and Translational Research in Population Health (ITR), Porto, Portugal
- Research Center in Sport, Physical Education, and Exercise and Health, Lusófona University, Porto, Portugal
| | - Emerson Sebastião
- Department of Health and Kinesiology, University of Illinois Urbana-Champaign, Illinois, USA
| | - Gianna Fiori Marchiori
- Department of Nursing in Hospital Care, Federal University of Triângulo Mineiro, Uberaba, Brazil
| | - Euripedes Barsanulfo Gonçalves Gomide
- Study and Research Group in Anthropometry, Training and Sport, Ribeirão Preto. School of Physical Education and Sport of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- Claretiano University Center of Batatais, São Paulo, Brazil
| | | | - Alex Antonio Florindo
- School of Arts, Sciences, and Humanities, University of São Paulo, São Paulo, Brazil
| | - Jorge Mota
- Research Center in Physical Activity, Health and Leisure (CIAFEL)-Faculty of Sports, University of Porto (FADEUP) and Laboratory for Integrative and Translational Research in Population Health (ITR), Porto, Portugal
| | - Dalmo Roberto Lopes Machado
- Faculty of Sport of the University of Porto, Street Dr. Plácido da Costa 91, 4200-450, Porto, Portugal
- College of Nursing of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- School of Physical Education and Sport of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- Study and Research Group in Anthropometry, Training and Sport, Ribeirão Preto. School of Physical Education and Sport of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
- Research Center in Physical Activity, Health and Leisure (CIAFEL)-Faculty of Sports, University of Porto (FADEUP) and Laboratory for Integrative and Translational Research in Population Health (ITR), Porto, Portugal
- School of Education and Communication (ESEC), University of Algarve. Penha Campus, Faro, Portugal
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Fu F, Yan W, Yu X. Management Process of Fear of Falling Among Hospitalized Older Patients with Fall Experience. JOURNAL OF GERONTOLOGICAL SOCIAL WORK 2025; 68:360-377. [PMID: 39655813 DOI: 10.1080/01634372.2024.2435894] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 03/25/2024] [Accepted: 11/26/2024] [Indexed: 03/20/2025]
Abstract
This study sought to explore the management process of FOF among the older adults patients hospitalized due to falls. Semi-structured in-depth interviews were performed with 21 older patients. Three types of coping strategies were developed by hospitalized older adults: primary management of explaining the reason of falls by attributing it to inevitable consequence of aging as well as accidental events; secondary management of fear including self-consolation, downstairs comparison and distraction from fear, as well as confronting and reflecting fear; and tertiary management of the consequences of falling such as active rehabilitation, food therapy, seeking emotional support etc.
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Affiliation(s)
- Fang Fu
- School of Social Development and Public Policy, Fudan University, Shanghai, China
| | - Weiting Yan
- Medical Social Work Department, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
| | - Xinbei Yu
- School of Social Development and Public Policy, Fudan University, Shanghai, China
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Costanzo A, Vescovi L, Rampulla V, Caprioli M, Marini M, Rigamonti A, Passannanti D, Crisafulli V, Floridi A. Oncological and Functional Outcomes After Minimally Invasive Surgery for Mid and Low Rectal Adenocarcinoma: A Review. Cureus 2025; 17:e82238. [PMID: 40231297 PMCID: PMC11996004 DOI: 10.7759/cureus.82238] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/14/2025] [Indexed: 04/16/2025] Open
Abstract
In this study, we analyze the oncological and functional outcomes after minimally invasive surgery (laparoscopic and robotic) for mid and low rectal adenocarcinoma. This is a narrative review of articles published from January 2019 to December 2024 in which we analyzed the rate of short-term oncological outcomes (quality of surgical samples), long-term oncological outcomes (recurrence rate, overall survival, and disease-free survival), and functional disorders (urinary, sexual, and bowel function) after minimally invasive surgery. The rates of complete mesorectum are 67.7%-92.8%, the rate of free circumferential resection margin is 94%-98.2%, and the rate of free distal resection margin is 99.4%-100%. The local recurrence rate is 2.3%-7.3%, the overall survival rate is 80%-95.6%, and the disease-free survival rate is 70%-86.4%. The rate of urinary disorders is 25%-26.5%, sexual disorders are 35%-80%, and bowel disorders are 17%-44.6%. This review demonstrates that minimally invasive surgery yields favorable oncological and functional outcomes. The continuous evolution in robotic surgery will increasingly lead to interesting implications for rectal surgery, thanks to less surgical trauma and better intraoperative visualization of nerves.
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Affiliation(s)
- Antonio Costanzo
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Lorenzo Vescovi
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Valentina Rampulla
- General Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Ovest, Ospedale di Treviglio-Caravaggio, Treviglio, ITA
| | - Michela Caprioli
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Michele Marini
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Andrea Rigamonti
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Daniele Passannanti
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Valentina Crisafulli
- Pathology, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
| | - Antonio Floridi
- General and Emergency Surgery, Azienda Socio Sanitaria Territoriale (ASST) Bergamo Est, Seriate, ITA
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Selsjord AR, Leren L, Irgens I. Pressure Injury Recurrence After Flap Surgery in Home-Dwelling Patients With Spinal Cord Injury in Norway: A Retrospective Study. Int Wound J 2025; 22:e70211. [PMID: 40234086 PMCID: PMC11999728 DOI: 10.1111/iwj.70211] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/19/2024] [Revised: 01/09/2025] [Accepted: 01/27/2025] [Indexed: 04/17/2025] Open
Abstract
A retrospective single-centre study. To investigate the period prevalence of pressure injury recurrence (PIR) and characteristics associated with PIR in the population of persons with spinal cord injury (SCI) who were treated with flap surgery between 2008 and 2019. A spinal cord unit (SCU) in Norway. The study is based on analysis of patient data from the electronic medical record. Crosstabs and logistic regression were used to investigate the potential correlations between the odds of PIR and potential risk characteristics. We identified 54 patients who were treated with flap surgery in the period of interest, and 47 (87%) were men. The mean age for flap surgery was 51 years (SD = 12.7). The occurrence of PIR post-flap surgery was 46% (n = 25). Factors associated with increased risk of PIR were use of manual wheelchair (65% vs. 32%, odds ratio [OR] = 3.9, 95% confidence interval [CI] = 1.06-14.33, p = 0.04) when compared with powered wheelchair, and history of PI and flap surgery at the ischial tuberosity (sit bones) (68% vs. 24%, OR = 3.67, 95% CI = 1.01-13.40, p = 0.04) compared with all other body locations. Factors associated with decreased risk of PIR were independence in position changes (29% vs. 58%, OR = 0.29, 95% CI = 0.91-0.95, p = 0.04) compared with not needing assistance with position changes, tetraplegia (C5-C8) (21% vs. 60%, OR = 0.18, CI = 0.04-0.83, p = 0.02) compared with paraplegia, and postoperative follow-up by the SCU (15% vs. 55%, OR = 0.28, 95% CI 0.03-0.76, p = 0.04) compared with no follow-up from the SCU, as well assistance from personal assistant follow-up (PAF) (26% vs. 56%, OR = 0.15, 95% CI = 0.03-0.76, p = 0.01) compared with not receiving assistance from PAF. The period prevalence of PIR post-flap surgery in the Norwegian population of people with SCI is high and increased odds of PIR were related to flap surgery on the sit bones. Reduced odds of PIR were related to tetraplegia, powered wheelchair use, follow up by PAF and the SCU. The study is registered in the Open science framework.
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Affiliation(s)
- Anne Riisøen Selsjord
- Oslo Metropolitan UniversityOsloNorway
- Sunnaas Rehabilitation HospitalBjørnemyrNorway
| | - Lena Leren
- University of South‐Eastern NorwayDrammenNorway
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Feng Y, Wen F, Ahmad I, Chen Y, Ye W, Jiang H, Li H, Dai J, Li L, Hu R, Teng C, Yin Y. Does exercise training combined with blood flow restriction improve muscle mass, lower extremity function, and walking capacity in hemiplegic patients? A randomized clinical trial. Top Stroke Rehabil 2025:1-10. [PMID: 40159947 DOI: 10.1080/10749357.2025.2482390] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/17/2024] [Accepted: 03/17/2025] [Indexed: 04/02/2025]
Abstract
BACKGROUND Blood flow restriction creates a state with increased motor function that permits treatment modalities to induce muscle hypertrophy. Blood flow-restricted exercise training (BFRET) may induce motor learning and boost the facilitatory effect of exercise training (ET). OBJECTIVE This study investigated the effects of BFRET on post-stroke hemi paretic lower extremity function and walking capacity recovery. METHODOLOGY This randomized clinical trial was conducted from September 2021 to October 2022 at the Department of Rehabilitation Medicine of the Second Affiliated Hospital of Chongqing Medical University in China. Participants were randomized 1:1 to BFRET or ET, each involving 30 minutes of training twice per day for 4 weeks. MAIN OUTCOMES MEASURES The main outcomes were manual muscle testing (MMT) and Fugl-Meyer assessment scale-lower extremity (FMA-LE), the timed up and go test (TUGT), Outcomes were assessed by blinded raters after 4 weeks of training. RESULTS 40 participants mean [SD] age 48.79[12.58] years, 30 males [75%], 20 were randomized to BFRET and 20 to ET. The mean (SD) time since stroke was 2.5 (1.3) years. The MMT scores showed greater strength by within-group comparisons and superior changes in hip flexion and plantar flexion in the BFRET group. CONCLUSIONS BFRET is superior to ET alone in enhancing muscle mass and strength in the lower extremities. BFRET may improve the function of the lower extremities through physiological adaptations for muscle hypertrophy. REGISTRATION URL: https://www.clinicaltrials.gov; Unique identifier: ChiCTR2100050206.
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Affiliation(s)
- Yali Feng
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Fanglin Wen
- Department of Rehabilitation Medicine, the Chongqing Medical University, Chongqing, China
| | - Irfan Ahmad
- Department of Rehabilitation Medicine, the Chongqing Medical University, Chongqing, China
| | - Yuanyuan Chen
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Wenwen Ye
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Hang Jiang
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Hao Li
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Jinshan Dai
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Le Li
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Rui Hu
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
| | - Can Teng
- Department of Pain Rehabilitation, The Second Affiliated Hospital of the Chinese People's Liberation Army Army Medical University, Chongqing, China
| | - Ying Yin
- Department of Rehabilitation Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
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Wu Q, Feng X, Shen C, Liu Y, Yang S, Su N. Global research trends of home pharmaceutical care: a bibliometric analysis via CiteSpace. Front Med (Lausanne) 2025; 12:1489720. [PMID: 40224623 PMCID: PMC11985810 DOI: 10.3389/fmed.2025.1489720] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/01/2024] [Accepted: 03/17/2025] [Indexed: 04/15/2025] Open
Abstract
Background This study aimed to systematically review the research on home pharmaceutical care and to identify emerging trends and research hotspots using bibliometric methods. Methods Publications related to home pharmaceutical care, published from inception to 6 February 2025, were extracted from the Web of Science Core Collection (WoSCC). The bibliometric tool CiteSpace was employed to analyze various metrics, including the number of publications, contributing countries, institutions, authors, keywords, cited references, and research trends in the field of home pharmaceutical care. Results A total of 812 relevant articles were retrieved from the WoSCC. The most prolific contributors were Hughes CM, Nishtala, PS, and Lapane KL. The United States emerged as the leading country in the field, with Queen's University Belfast identified as the most productive institution. The keyword with the highest frequency was "pharmaceutical care." The research hotspots in this field were centered around "polypharmacy," "medication reconciliation," and "drug-related problems." Conclusion This study utilized CiteSpace to analyze research trends and hotspots in the field of home pharmaceutical care. The findings suggest that "polypharmacy" and "care homes" are likely to become focal points of future research. Additionally, the development of research in developing countries lags behind that in developed countries. Therefore, it is crucial for developing countries to learn from the advances made by developed nations in this field, and to foster greater international collaboration and research efforts.
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Affiliation(s)
- Qingfang Wu
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
- Department of Pharmacy, The First People's Hospital of Shuangliu District, West China (Airport) Hospital of Sichuan University, Chengdu, China
| | - Xiaorong Feng
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
- Department of Pharmacy, Shangjin Hospital, West China Hospital, Sichuan University, Chengdu, China
| | - Chao Shen
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
| | - Ying Liu
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
| | - Shiwen Yang
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
| | - Na Su
- Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China
- West China School of Pharmacy, Sichuan University, Chengdu, China
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Aiello A, Calabrò A, Ligotti ME, Accardi G, Azgomi MS, Caccamo N, Caruso C, Dieli F, Manna MPL, Procopio A, Candore G. Enhancing flu vaccine responses in older adults: preliminary insights from the ISOLDA study on immunosenescence and antioxidant and anti-inflammatory approaches. Immun Ageing 2025; 22:13. [PMID: 40140897 PMCID: PMC11938677 DOI: 10.1186/s12979-025-00506-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/06/2024] [Accepted: 03/05/2025] [Indexed: 03/28/2025]
Abstract
Aging is frequently characterized by an inadequate primary vaccine response, likely due to immunosenescence and inflamm-aging, a low-level, chronic inflammatory state. Both aspects increase the susceptibility of older adults to viral and bacterial infections, resulting in a higher frequency and severity of infectious diseases. In this preliminary study, a cohort of 52 individuals was recruited and divided into two groups: young (age range 21-35) and older adults (> 60 years old). Peripheral blood mononuclear cells (PBMCs) were collected before (time 0, T0) and after (time 1, T1) the immunization with a tetravalent influenza vaccine. Then, T cell immunophenotyping analysis was conducted to investigate how aging and influenza vaccination influence T cell responses. Additionally, the anti-inflammatory and antioxidant effects of oleuropein (OLE), a secoiridoid extracted from extra virgin olive oil, alone or in combination with BIRB 796, a potent inhibitor of p38 MAPK, were explored to enhancing the impact of influenza virus on T cell activation, aiming to identify potential alternatives or complementary strategies to improve traditional flu-vaccine formulations. Statistically significant observations were noted for a decrement in CD8 + T naïve and an increase of effector memory between the young and older adults after flu-vaccination. Moreover, preliminary findings indicate anti-inflammatory and antioxidant properties of OLE and BIRB 796 on T cell responses, particularly regarding Reactive Oxygen Species/Reactive Nitrogen Species modulation, with a trend toward the decrease of pro-inflammatory cytokines (i.e., Interferon-γ (INF-γ), Tumor Necrosis Factor-α (TNF-α)), αalthough without statistical significance.
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Affiliation(s)
- Anna Aiello
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy
| | - Anna Calabrò
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy
| | - Mattia Emanuela Ligotti
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy
- Department of Research, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IRCCS-ISMETT), 90127, Palermo, Italy
| | - Giulia Accardi
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy.
| | - Mojtaba Shekarkar Azgomi
- Department of Biomedicine, Neuroscience and Advanced Diagnosis, University of Palermo, 90127, Palermo, Italy
- Central Laboratory of Advanced Diagnosis and Biomedical Research (CLADIBIOR), AOUP Paolo Giaccone, 90127, Palermo, Italy
| | - Nadia Caccamo
- Department of Biomedicine, Neuroscience and Advanced Diagnosis, University of Palermo, 90127, Palermo, Italy
- Central Laboratory of Advanced Diagnosis and Biomedical Research (CLADIBIOR), AOUP Paolo Giaccone, 90127, Palermo, Italy
| | - Calogero Caruso
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy
| | - Francesco Dieli
- Department of Biomedicine, Neuroscience and Advanced Diagnosis, University of Palermo, 90127, Palermo, Italy
- Central Laboratory of Advanced Diagnosis and Biomedical Research (CLADIBIOR), AOUP Paolo Giaccone, 90127, Palermo, Italy
| | - Marco Pio La Manna
- Department of Biomedicine, Neuroscience and Advanced Diagnosis, University of Palermo, 90127, Palermo, Italy
- Central Laboratory of Advanced Diagnosis and Biomedical Research (CLADIBIOR), AOUP Paolo Giaccone, 90127, Palermo, Italy
| | - Antonio Procopio
- Department of Health Sciences, University Magna Graecia of Catanzaro, Viale Europa - Campus Universitario S. Venuta - Loc. Germaneto, 88100, Cosenza, Italy
| | - Giuseppina Candore
- Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy
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Parfenov AI, Indejkina LK, Sabelnikova EA, Leontiev AV, Makarova AA. [Radiation-induced intestinal injury]. TERAPEVT ARKH 2025; 97:101-108. [PMID: 40237744 DOI: 10.26442/00403660.2025.02.203116] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/08/2024] [Accepted: 02/19/2025] [Indexed: 04/18/2025]
Abstract
This article addresses theoretical and clinical aspects of radiation-induced intestinal injuries, which complicate radiation therapy for malignant neoplasms of the abdominal and pelvic organs. Many clinical aspects of this issue remain unknown due to the lack of awareness among doctors and patients. Further study of radiation-induced intestinal injuries and the development of personalized approaches to their prevention and treatment represent a relevant direction in internal medicine.
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Affiliation(s)
| | - L K Indejkina
- Loginov Moscow Clinical Scientific Center
- Research Institute for Healthcare and Medical Management
| | - E A Sabelnikova
- Loginov Moscow Clinical Scientific Center
- Russian University of Medicine
| | - A V Leontiev
- Loginov Moscow Clinical Scientific Center
- Moscow University for Industry and Finance "Synergy"
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Sommer I, Harlfinger J, Toromanova A, Affengruber L, Dobrescu A, Klerings I, Griebler U, Kien C. Stakeholders' perceptions and experiences of factors influencing the commissioning, delivery, and uptake of general health checks: a qualitative evidence synthesis. Cochrane Database Syst Rev 2025; 3:CD014796. [PMID: 40110911 PMCID: PMC11924333 DOI: 10.1002/14651858.cd014796.pub2] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 03/22/2025]
Abstract
BACKGROUND General health checks are integral to preventive services in many healthcare systems. They are offered, for example, through national programmes or commercial providers. Usually, general health checks consist of several screening tests to assess the overall health of clients who present without symptoms, aiming to reduce the population's morbidity and mortality. A 2019 Cochrane review of effectiveness studies suggested that general health checks have little or no effect on either all-cause mortality, cancer or cardiovascular mortality or cardiovascular morbidity. These findings emphasise the need to explore the values of different stakeholder groups associated with general health checks. OBJECTIVES To identify how stakeholders (i.e. healthcare managers or policymakers, healthcare providers, and clients) perceive and experience general health checks and experience influencing factors relevant to the commissioning, delivery and uptake of general health checks. Also, to supplement and contextualise the findings and conclusions of a 2019 Cochrane effectiveness review by Krogsbøll and colleagues. SEARCH METHODS We searched MEDLINE (Ovid) and CINAHL (EBSCO) and conducted citation-based searches (e.g. reference lists, effectiveness review-associated studies and cited references in our included studies). The original searches cover the period from inception to August 2022. The results from the update search in September 2023 have not yet been incorporated. SELECTION CRITERIA We included primary studies that utilised qualitative methods for data collection and analysis. Included studies explored perceptions and experiences of commissioning, delivery and uptake of general health checks. Stakeholders of interest were healthcare managers, policymakers, healthcare providers and adults who participate (clients) or do not participate (potential clients) in general health checks. The general health check had to include screening tests for at least two diseases or risk factors. We considered studies conducted in any country, setting, and language. DATA COLLECTION AND ANALYSIS We applied a prespecified sampling frame to purposefully sample a variety of eligible studies. This sampling approach allowed us to capture conceptually rich studies that described the viewpoints of different stakeholder groups from diverse geographical regions and different settings. Using the framework synthesis approach, we developed a framework representing individual, intervention and contextual factors, which guided data extraction and synthesis. We assessed the methodological limitations of each study using an adapted version of the Critical Appraisals Skills Programme (CASP) tool. We applied the GRADE-CERQual (Confidence in the Evidence from Reviews of Qualitative Research) approach to assess our confidence in each finding. MAIN RESULTS One hundred and forty-six studies met the inclusion criteria, and we sampled 36 of these for our analysis. While most of the studies were set in high-income countries in Europe, nearly a third (11/36) were set in culturally diverse middle-income countries across Eastern Europe, South and Southeast Asia, and Latin America. Sixteen sampled studies were conducted in primary and community healthcare settings, four in workplace settings and four in community settings. Included studies explored the perceptions and experiences of clients (n = 25), healthcare providers (n = 15) and healthcare managers or commissioners (n = 9). We grouped the findings at the individual level, intervention level and surrounding context. The findings at the individual level mainly reflect the client's perspective. General health checks helped motivate most clients to change their lifestyles. They were trusted to assess their health objectively, finding reassurance through professional confirmation (moderate confidence). However, those who feared negative results or relied on symptom-based care were more reluctant to attend (moderate confidence). Perceptions of disease, risk factors and prevention affected uptake (high confidence). Some clients felt an obligation to their families and society to maintain and improve their health through general health checks (moderate confidence). Healthcare providers played a crucial role in motivating participation, but negative experiences with unqualified providers discouraged attendance (moderate confidence). The availability and accessibility of general health checks and awareness systems played significant roles in clients' decision-making. Factors such as time and concerns that health insurance may not cover potential treatment costs influenced attendance (moderate confidence). The findings at the intervention level drew on the perspectives of all three stakeholder groups, with a strong focus on the healthcare provider's perspective. Healthcare providers and clients considered it essential that general health check providers were skilled and culturally competent (high confidence). Barriers to delivery included time competition with curative care, staff changes and shortages, resource limitations, technical issues, and reimbursement challenges (moderate confidence). Stakeholders thought innovative and diverse settings might improve access (moderate confidence). The evidence suggests that clients appreciated a comprehensive approach, with various tests. At the same time, healthcare providers deemed individualised approaches tailored to clients' health risks suitable, focusing on improving rather than abandoning general health checks (low confidence). The perspectives on the effectiveness of general health checks differed among healthcare commissioners, managers, providers, and clients (moderate confidence). Healthcare providers and clients recognised the importance of information, invitation systems, and educational approaches to create awareness of general health check availability and their respective advantages or disadvantages (moderate confidence). Clients considered explaining test results and providing recommendations as key elements of general health checks (low confidence). We have low or very low confidence in findings related to the contextual level and reasons for commissioning general health checks. The evidence suggests that cultural background, social norms, religion, gender, and language shape the perception of prevention and disease, thereby influencing the uptake of general health checks. Policymakers thought that a favourable political climate and support from various stakeholders are needed to establish general health checks. AUTHORS' CONCLUSIONS Despite the lack of effectiveness in the quantitative review, our findings showed that general health checks remain popular amongst clients, healthcare providers, managers and policymakers across countries and settings. Our data did not offer strong evidence on why these are commissioned, but it did point to these interventions being valued in contexts where general health checks have long been established. General health checks fulfil specific wants and needs, and de-implementation strategies may need to offer alternatives before a constructive debate can take place about fundamental changes to this widely popular or, at least, accepted service.
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Affiliation(s)
- Isolde Sommer
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Julia Harlfinger
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Ana Toromanova
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Lisa Affengruber
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Andreea Dobrescu
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Irma Klerings
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Ursula Griebler
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
| | - Christina Kien
- Cochrane Austria, Department for Evidence-based Medicine and Evaluation, University for Continuing Education Krems (Danube University Krems), Krems, Austria
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Cai LY, Yuan Y, Huang H, Zhang J, Zou XY, Zhang XM. Mechanism of LCN2 in cerebral ischemia-reperfusion injury. Front Neurosci 2025; 19:1536055. [PMID: 40182140 PMCID: PMC11965685 DOI: 10.3389/fnins.2025.1536055] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/28/2024] [Accepted: 03/10/2025] [Indexed: 04/05/2025] Open
Abstract
Cerebral ischemia-reperfusion injury (CIRI) is a complex pathophysiological process faced by brain tissues after ischemic stroke treatment, which involves mechanisms of inflammatory response, oxidative stress and apoptosis, and severely affects treatment outcome. Lipocalin-2 (LCN2), an acute-phase protein, is significantly up-regulated after CIRI and promotes neural repair by enhancing astrocyte phagocytosis, but its over-activation may also trigger secondary inflammation and demyelination injury. LCN2 also plays a key role in neuroinflammation regulation by regulating the polarization state of astrocytes and the release of inflammatory factors, and may affect the integrity of the blood-brain barrier and a variety of pathologic injury processes. In view of the important role of LCN2 in CIRI, this article reviews the mechanism of LCN2, aiming to provide new ideas and methods for the treatment of ischemic stroke.
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Affiliation(s)
- Luo-yang Cai
- School of Acupuncture-Moxibustion and Orthopedics, Hubei University of Chinese Medicine, Wuhan, China
| | - Ying Yuan
- Hubei Shizhen Laboratory, Wuhan, China
- Hubei University of Chinese Medicine, Wuhan, China
| | - Hai Huang
- Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan, China
- Affiliated Hospital of Hubei University of Traditional Chinese Medicine, Wuhan, China
| | - Jin Zhang
- School of Acupuncture-Moxibustion and Orthopedics, Hubei University of Chinese Medicine, Wuhan, China
| | - Xin-yi Zou
- School of Acupuncture-Moxibustion and Orthopedics, Hubei University of Chinese Medicine, Wuhan, China
| | - Xiao-ming Zhang
- School of Acupuncture-Moxibustion and Orthopedics, Hubei University of Chinese Medicine, Wuhan, China
- Sub-Health Institute Hubei University of Chinese Medicine, Wuhan, China
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Wang Y, Li M, Hou C, Wang Y, Guo J, Wang X. IL-36RN gene: key insights into its role in pediatric pustular psoriasis pathogenesis and treatment. Front Pediatr 2025; 13:1520804. [PMID: 40176872 PMCID: PMC11964088 DOI: 10.3389/fped.2025.1520804] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 10/31/2024] [Accepted: 02/25/2025] [Indexed: 04/05/2025] Open
Abstract
Pediatric pustular psoriasis (PPP) is an autoimmune skin disease that seriously affects the physical and mental health of children. The IL-36RN (Interleukin-36 Receptor Antagonist) gene plays a key role in the pathogenesis of PPP. This review comprehensively elaborates on the research progress of IL-36RN in the context of the pathogenesis and treatment of PPP, covering the basic structure, function, mutation sites and types, and inheritance patterns of the gene and its role in the pathogenesis of PPP. In addition, we discussed the frequency of IL-36RN mutations in patients with different types of PPP and the treatment methods for these patients, aiming to provide a valuable reference for further research and treatment of this disease.
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Affiliation(s)
- Ye Wang
- School of Medicine, University of Electronic Science and Technology of China, Chengdu, China
| | - Mingyue Li
- Health Care Department, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
| | - Changcheng Hou
- Department of Chinese Medicine Surgery, Jiangsu Province Hospital of Traditional Chinese Medicine Chongqing Hospital, Chongqing, China
| | - Yueyue Wang
- Department of Chinese Medicine Surgery, Jiangsu Province Hospital of Traditional Chinese Medicine Chongqing Hospital, Chongqing, China
| | - Jing Guo
- Dermatological Department, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
| | - Xurui Wang
- Department of Chinese Medicine Surgery, Sichuan Provincial People’s Hospital, University of Electronic Science and Technology of China, Chengdu, China
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Eluwa GIE, Geibel S, Callens S, Vu L, Iyortim I. Evaluation of differentiated service delivery models on HIV treatment retention among key populations in Nigeria: a prospective cohort analysis. BMC Public Health 2025; 25:1066. [PMID: 40108577 PMCID: PMC11924709 DOI: 10.1186/s12889-025-21630-w] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/13/2024] [Accepted: 01/24/2025] [Indexed: 03/22/2025] Open
Abstract
INTRODUCTION Differentiated Service Delivery models (DSD) that cater to the needs of key populations (KP) have shown promise in providing KP-sensitive and KP-tailored care and treatment services. We evaluated the effect of two DSD models on linkage to and retention in treatment in Nigeria. METHODS Between December 2017 and June 2018, newly-diagnosed men who have sex with men (MSM) and female sex workers (FSWs) were enrolled into treatment through two DSD models and followed prospectively for one year. Model 1 was a fully integrated one-stop-shop (OSS) while model 2 was a hybrid HIV prevention and treatment site (DIC). Retention was estimated from drug pick-up records and was defined as being on treatment within 90 days one-year post ART initiation. Cox regression was used to identify the independent effect of the DSD models on retention while probability of being retained in treatment at 1-year was estimated with Kaplan-Meier product limit. RESULTS A total of 605 newly-diagnosed clients were enrolled into the study (340 in OSS and 265 in DIC; 342 were FSWs, while 263 were MSM). Median age was 26 years for MSM and 30 years for FSWs. Among those linked to treatment, retention was higher in the OSS than in DIC (63% vs. 48%; p = 0.002). Among those not retained, mean days to be lost-to-follow up (LFTU) was 60 days. Controlling for educational level, population type and age, clients who received treatment in M2 were 6 times more likely not to be retained in treatment at the end of 1 year (Hazard ratio 5.89; 95% CI: 1.04-33.16). The Kaplan Meier estimates of the probability of being retained in 6 months, 9 months and 12 months was 0.97, 0.92, 0.80 for the DIC and 1.00, 0.96, 0.91 for the OSS. CONCLUSION Linkage to treatment was suboptimal across both models with less than 90% of newly-diagnosed positives initiated on treatment and suggests that facilitated linkage is required to achieve at least 95%. Though retention was higher in the OSS model, both models had an alarmingly short time frame for LTFU and thus intensive monitoring during this phase of treatment is recommended irrespective of the type of DSD. Addressing these gaps will improve service delivery by one stop shops for HIV care and treatment.
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Affiliation(s)
| | - Scott Geibel
- Population Council, HIV/AIDS, Washington, D.C., USA
| | - Steven Callens
- Faculty of Medicine and Health Sciences, University of Gent., Gent, Belgium
| | - Lung Vu
- Health, Nutrition and Population, World Bank, Washington, D.C., USA
| | - Isa Iyortim
- United States Agency for International Development, Abuja, Nigeria
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Bynum JPW. Challenges and Innovations in Dementia Care-Evaluating Comprehensive Models. JAMA 2025; 333:943-945. [PMID: 39878988 DOI: 10.1001/jama.2024.28066] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 01/31/2025]
Affiliation(s)
- Julie P W Bynum
- Department of Internal Medicine, University of Michigan Medical School, Ann Arbor
- Institute for Healthcare Policy and Innovation, University of Michigan, Ann Arbor
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Almutairi MN, Alshehri AM, Alhoumaily AY, Alnahdi O, Taha MA, Gangadharan S. Meta-analysis: clinical outcomes of laser-assisted in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) in hyperopia. BMC Ophthalmol 2025; 25:140. [PMID: 40102791 PMCID: PMC11917003 DOI: 10.1186/s12886-025-03956-6] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/07/2024] [Accepted: 03/03/2025] [Indexed: 03/20/2025] Open
Abstract
BACKGROUND To evaluate differences in clinical outcome, safety, and efficacy of photorefractive keratectomy (PRK) and laser-assisted in situ keratomileusis (LASIK) in the correction of hyperopic refractive errors. METHODS We have adhered to PRISMA criteria in this systematic review, which is registered with PROSPERO (CRD42023469543). Our search with studies comparing PRK and LASIK for hyperopia was conducted through the databases PubMed, EMBASE, Web of Science, and the Cochrane Library. We used the Cochrane method to assess bias and evaluated variables like uncorrected distance visual acuity and mean spherical equivalent. Using fixed- or random-effects models, a meta-analysis was performed using RevMan 5.4 for evaluating heterogeneity and significance. Sensitivity analysis addressed the causes of heterogeneity to assure stability. RESULTS We included 6 articles (419 participants, 585 eyes) in this review five were retrospective and 1 case-series. The final mean refractive SE (WMD, -0.05; 95% confidence interval [CI], 0.42 to 0.31; P = 0.06). patients achieving uncorrected distance visual acuity (UDVA) of 20/20 or better (OR, 0.58; 95% CI, 0.39-0.78; P = 0.33). final UDVA of 20/40 or better (OR, 1.40; 95% CI, 0.65-3.02; P = 0.81) were analyzed. CONCLUSIONS In this meta-analysis, LASIK had no significant benefits over PRK in relation to clinical outcomes. Less corneal haze was observed in LASIK-treated eyes at 1 to 3 months after surgery.
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Affiliation(s)
- Mohammed Naji Almutairi
- College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
| | - Abdullrahman M Alshehri
- College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia
| | | | - Osamah Alnahdi
- College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia
| | - Mohammed A Taha
- King Saud Bin Abdulaziz University for Health Sciences, Riyadh, 11426, Saudi Arabia
- King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
- Department of Ophthalmology, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, 11426, Saudi Arabia
| | - Shiji Gangadharan
- King Saud Bin Abdulaziz University for Health Sciences, Riyadh, 11426, Saudi Arabia
- King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
- Department of Ophthalmology, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, 11426, Saudi Arabia
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Xiangyun Y, Hongmin X, Liangliang L, Weigang L, Lili M, Xianghong L. Pulmonary artery thrombosis in preterm infants born to a diabetic mother: a case report. J Med Case Rep 2025; 19:120. [PMID: 40102909 PMCID: PMC11916993 DOI: 10.1186/s13256-025-05155-9] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/01/2023] [Accepted: 02/19/2025] [Indexed: 03/20/2025] Open
Abstract
BACKGROUND Pulmonary artery thrombosis in neonates is a rare entity. We describe a neonate with this diagnosis as well as his presentation, evaluation, and management. This case highlights the importance of cardiac ultrasound screening for neonates with high risk factors for pulmonary artery thrombosis without clinical symptoms, as it is not easily detected. CASE PRESENTATION Here, we present an unusual case of a Chinese premature infant, born to a diabetic mother, in whom thrombosis developed in the main pulmonary artery 12 days after an exploratory laparotomy. The preterm infant had no clinical manifestations of pulmonary artery thrombosis, which was found by reexamination of cardiac ultrasound before discharge; after treatment with low-molecular-weight heparin sodium, the embolus became smaller, and follow-up examination was conducted after discharge, and the baby is now developing well. CONCLUSION Pulmonary artery thrombosis is rare in newborns, and asymptomatic manifestations are even rarer in this age group. For newborns with high risk factors, early cardiac ultrasound screening is very important.
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Affiliation(s)
- Yin Xiangyun
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China
| | - Xi Hongmin
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China
| | - Li Liangliang
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China
| | - Liu Weigang
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China
| | - Ma Lili
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China
| | - Li Xianghong
- Department of the Affiliated Hospital of Qingdao University, Qingdao, China.
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Yue F, Shi X, Ji R, Wei Y, Xiao H, Zhang H, Fu M, Ji F. Anesthesia effects of different doses of fospropofol disodium for painless colonoscopy diagnosis and treatment. Front Med (Lausanne) 2025; 12:1562592. [PMID: 40160329 PMCID: PMC11949946 DOI: 10.3389/fmed.2025.1562592] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/17/2025] [Accepted: 03/03/2025] [Indexed: 04/02/2025] Open
Abstract
Purpose To explore the clinical anesthesia effect of different doses of fospropofol disodium for painless colonoscopy. Patients and methods A total of 69 patients undergoing colonoscopy under general intravenous anesthesia were included in this study. They were divided into three groups: fospropofol disodium 10 mg/kg group (P1 group, n = 23), fospropofol disodium 12.5 mg/kg group (P2 group, n = 23), and fospropofol disodium 15 mg/kg group (P3 group, n = 23). All patients were first injected with 5 μg/kg of alfentanil intravenously at the time of anesthesia induction, 1 min later, group P1, group P2 and group P3 were given 10 mg/kg, 12.5 mg/kg and 15 mg/kg of fospropofol disodium, respectively. The success rate of the first sedation, the time of sedation start, the time of awakening, hemodynamic changes and adverse reactions were recorded. Results The success rate of first sedation in the P2 and P3 groups was significantly higher than that in the P1 group (p < 0.05). The onset time of sedation was significantly shorter in the P2 and P3 groups than in the P1 group (p < 0.05). The awakening time of the P2 group and the P3 group (9 min vs. 7 min) was significantly longer than that of the P1 group (5 min) (p < 0.05). The incidence of hypotension in the P3 group was significantly higher than that in the P1 and P2 groups (p < 0.05). At T2, the MAP of the P3 group decreased significantly compared with the P1 and P2 groups (p < 0.05). There were no significant differences in adverse reactions such as injection pain, abnormal sensation/itching between the three groups (p > 0.05). Conclusion In painless colonoscopy, fospropofol disodium 12.5 mg/kg combined with alfentanil 5 μg/kg has a high success rate of first-time sedation and low hemodynamic impact, which has some clinical advantages. Clinical trial registration ChiCTR2400090788.
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Affiliation(s)
- Fangli Yue
- Department of Anesthesiology, Weifang People’s Hospital, Weifang, China
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Xinyuan Shi
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Ruoyi Ji
- School of Psychology and Cognitive Sciences, Peking University, Beijing, China
| | - Yaxin Wei
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Hongyi Xiao
- Department of Anesthesiology, Weifang People’s Hospital, Weifang, China
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Huan Zhang
- Department of Anesthesiology, Weifang People’s Hospital, Weifang, China
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Min Fu
- Department of Anesthesiology, Weifang People’s Hospital, Weifang, China
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
| | - Fanceng Ji
- Department of Anesthesiology, Weifang People’s Hospital, Weifang, China
- School of Anaesthesiology, Shandong Second Medical University, Weifang, China
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Lu M, Saeys W, Maryam M, Gjeleshi I, Nazarahari H, Truijen S, Scataglini S. Using 3D and 4D digital human modeling in extended reality-based rehabilitation: a systematic review. Front Bioeng Biotechnol 2025; 13:1496168. [PMID: 40144388 PMCID: PMC11937100 DOI: 10.3389/fbioe.2025.1496168] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/13/2024] [Accepted: 02/06/2025] [Indexed: 03/28/2025] Open
Abstract
Introduction Extended reality (XR) is increasingly used in rehabilitation, showing potential to enhance clinical outcomes. Recently, integrating digital human modeling (DHM) with XR has gained attention. This systematic review aimed to evaluate the effectiveness of combining 3D and 4D DHM with XR in rehabilitation. Methods A systematic literature search was conducted according to PRISMA 2020 guidelines on the 28th of May 2024 in five databases (PubMed, IEEE Database, Cochrane Library, Web of Science, and Science Direct). All types of experimental studies investigating the effectiveness of XR using 3D and 4D DHM in rehabilitation were included. Consensus-based Standards for the selection of health Measurement Instruments (COSMIN) and Evidence-Based Guideline Development (EBRO) were used to evaluate the methodological quality of the studies included. Results Of the 1048 articles found, 16 were included in this review. These studies focused on 3D DHM in XR-based rehabilitation across various conditions and demonstrated superior effectiveness, especially in individuals with neglect, anorexia nervosa, bulimia nervosa, and type 2 diabetes in comparison with conventional therapy. DHM, captured via 3D cameras and combined with motion analysis or Wii remotes, was integrated into XR systems like VR games and avatar therapy. The studies reveal positive impacts on functional (e.g., upper limb function, gait, balance, quality of life), physical (e.g., pain reduction, spasticity, joint range), psychological (e.g., depression, emotional regulation, body image), and general health outcomes (e.g., body composition, metabolic health). Conclusion Despite variability in study parameters, limited evidence suggests that 3D DHM in XR-based rehabilitation may enhance physical and psychological recovery across various pathologies. This review highlights the potential of DHM and XR integration but underscores the need for further research with larger samples, longer follow-ups, and standardized measures to confirm these technologies' reliability and effectiveness in rehabilitation. Systematic Review Registration https://www.crd.york.ac.uk/PROSPERO/view/CRD42024553551, identifier CRD42024553551.
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Affiliation(s)
- Mengdi Lu
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
| | - Wim Saeys
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
- Department of Neurological Rehabilitation, Rehabilitation Hospital Revarte, Edegem, Belgium
| | - Maria Maryam
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
| | - Inva Gjeleshi
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
| | - Hoda Nazarahari
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
| | - Steven Truijen
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
| | - Sofia Scataglini
- 4D4ALL Laboratory, Department of Rehabilitation Sciences and Physiotherapy, Center for Health and Technology (CHaT), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
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Fontijn J, Engel C, Kreutzer KB, Poets C, Bassler D. Influence of antenatal steroids on the effect of early inhaled postnatal corticosteroids: a post-hoc analysis of the NEuroSIS trial. BMC Pediatr 2025; 25:172. [PMID: 40050762 PMCID: PMC11887233 DOI: 10.1186/s12887-025-05512-z] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/30/2024] [Accepted: 02/17/2025] [Indexed: 03/09/2025] Open
Abstract
BACKGROUND Few data are available on the interplay of antenatal and early inhaled postnatal corticosteroids. The NEuroSIS trial randomized extremely preterm infants to receive either early inhaled budesonide or placebo and analyzed the effect of study medication on bronchopulmonary dysplasia or death, as well as the effect on neurodevelopmental outcome at 18-22 months corrected age. Application of antenatal steroids may have had an influence on these outcomes. OBJECTIVE To analyze if antenatal corticosteroids (ANS) influenced the short- (BPD and death before 36 weeks PMA) and long-term (disability at 18-22 months corrected age or death before time of assessment) effects of early inhaled postnatal budesonide in NEuroSIS study participants. METHODS Post-hoc analysis of the intention-to-treat population of the NEuroSIS study. Generalized logits models were used to (1) predict risk of BPD, death before 36 weeks PMA and survival without BPD with application of ANS, NEuroSIS study treatment and gestational age as independent variables and (2) predict the risk of disability at 18-22 months corrected age, death before time of neurodevelopmental assessment and survival without disability, with ANS and gestational age as independent variables. RESULTS Application of ANS, added as an independent variable, did not change the effect of study medication on developing BPD (OR 0.79, 95% CI 0.67-0.93) and there was no association with the risk of death (OR 1.03, 95% CI 0.84-1.27) at 36 weeks PMA. ANS added as an independent variable showed an association with a reduced risk of death before time of completion of neurodevelopmental assessment (OR 0.60, 95% CI 0.44-0.81) and was associated with a reduced risk of disability at 18-22 months corrected age(OR 0.63, 95% CI 0.49-0.81). CONCLUSION ANS did not alter the reduction of BPD risk by study medication and there was no association with increased mortality in NEuroSIS study participants.
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Affiliation(s)
- Jehudith Fontijn
- Department of Neonatology, University Hospital Zurich and University of Zurich, Frauenklinikstrasse 10, Zurich, 8091, Switzerland.
| | - Corinna Engel
- Center for Pediatric Clinical Studies (CPCS), University Children's Hospital Tübingen, Tübingen, Germany
| | - Karen B Kreutzer
- Department of Neonatology, University Children's Hospital Tübingen, Tübingen, Germany
| | - Christian Poets
- Department of Neonatology, University Children's Hospital Tübingen, Tübingen, Germany
| | - Dirk Bassler
- Department of Neonatology, University Hospital Zurich and University of Zurich, Frauenklinikstrasse 10, Zurich, 8091, Switzerland
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Brakus RB, Brakus I, Carek A, Galić T, Alajbeg IZ. Evaluating amitriptyline's role in chronic TMD management: a placebo-controlled trial. BMC Oral Health 2025; 25:334. [PMID: 40038711 PMCID: PMC11877830 DOI: 10.1186/s12903-025-05670-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/17/2024] [Accepted: 02/14/2025] [Indexed: 03/06/2025] Open
Abstract
BACKGROUND To assess the effectiveness of low-dose amitriptyline in reducing pain and improving oral health-related quality of life in individuals with chronic temporomandibular disorders (TMD) over a 2-month period, compared to placebo. METHODS Forty participants were randomly assigned to receive either 25 mg of amitriptyline or a placebo pill for 2 months. The primary outcome was pain intensity, measured using a visual analogue scale (VAS). The secondary outcome was the impact of pain on oral health-related quality of life, assessed by the Oral Health Impact Profile questionnaire (OHIP-14). Evaluations were conducted at baseline and after the 1st and 2nd months of treatment. RESULTS No statistically significant differences were observed between the treatment groups at baseline (p > 0.05). After 2 months of treatment participants in amitriptyline group experienced a significantly greater reduction in spontaneous pain, with a 63.3% decrease in VAS scores. Participants in placebo group showed a much smaller reduction in spontaneous pain, with only a 16.2% decrease in VAS scores. Additionally, the amitriptyline group demonstrated a significant improvement in OHIP-14 scores (p < 0.001), whereas the placebo group showed no significant change in oral health-related quality of life (p = 0.184). CONCLUSION This study highlights low-dose amitriptyline as an effective treatment for chronic TMD, showing significant pain reduction and improved quality of life, underscoring its value in a multimodal approach despite the need for further research to personalize care. TRIAL REGISTRATION This study was registered retrospectively in ISRCTNregistry under the number ISRCTN17622685, on 01/10/2024.
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Affiliation(s)
| | - Ivan Brakus
- Department of Oral Surgery, University of Split School of Medicine, 21000, Split, Croatia.
| | - Andreja Carek
- Department of Fixed Prosthodontics, University of Zagreb School of Dental Medicine, 10000, Zagreb, Croatia
| | - Tea Galić
- Department of Prosthodontics, University of Split School of Medicine, 21000, Split, Croatia
| | - Iva Z Alajbeg
- Department of Removable Prosthodontics, University of Zagreb School of Dental Medicine, 10000, Zagreb, Croatia.
- Department of Dentistry, Clinical Hospital Center Zagreb, 10000, Zagreb, Croatia.
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Kelini KIS, Saleh MSM, Abbas MAM, Bayoumi MBI, Ahmed SM. High-intensity laser therapy can improve pain, health status and quality of life in women with fibromyalgia: a single blinded-randomized controlled trial. Lasers Med Sci 2025; 40:123. [PMID: 40032695 DOI: 10.1007/s10103-025-04351-9] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/16/2024] [Accepted: 01/29/2025] [Indexed: 03/05/2025]
Abstract
This study was conducted to explore the influence of High-Intensity Laser Therapy (HILT) on health status, pain intensity, Pain Pressure Threshold (PPT), and Quality of Life (QoL) in Fibromyalgia (FM) women. Fifty-two women with FM were randomly divided into either the HILT group (n = 26) or the control group (n = 26). Those in the HILT group underwent HILT alongside an exercise program consisted of low-impact aerobics training and stretching exercises, while the control group received the exercise program only. Treatments were administered three times per week for six weeks. Fibromyalgia symptoms and health status (Revised Fibromyalgia Impact Questionnaire (RFIQ), Pain intensity (visual analog scale), PPT (pressure algometer), and QoL (Short Form 36 Questionnaire) were measured pre and post six-week intervention timeframe. Regarding baseline data, insignificant differences were identified between groups (p > 0.05). Comparing groups after 6-week intervention reveals statistically significant differences in favor of the HILT group across all measured aspects (p < 0.001). HILT may be an effective treatment for women with FM, potentially enhancing pain management, reducing the impact of FM, and improving their QoL.
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Affiliation(s)
- Kerolous Ishak Shehata Kelini
- Department of Physical Therapy, Faculty of Applied Medical Sciences, Al-Zaytoonah University of Jordan, Amman, Jordan
| | - Marwa Shafiek Mustafa Saleh
- Department of Physical Therapy, Faculty of Applied Medical Sciences, Al-Zaytoonah University of Jordan, Amman, Jordan.
- Department of Basic Science for Physical Therapy, Faculty of Physical Therapy, Cairo University, Giza, Egypt.
| | - Menna Allah Mohammed Abbas
- Lecturer of Physical Therapy for women's health, Faculty of Physical Therapy, October 6 University, Giza, Egypt
| | - Mohamed Bayoumi Ibrahim Bayoumi
- Lecturer in Department of Physical Therapy for Surgery, Faculty of Physical Therapy, Cairo University, Giza, Egypt
- Department of Physiotherapy, Faculty of Allied Medical Sciences, Middle East University, Amman, Jordan
| | - Sara M Ahmed
- Department of Physical Therapy for Women Health, Faculty of Physical Therapy, Cairo University, Giza, Egypt
- Lecturer in Department of Physical Therapy for Women's Health, MSA University, Giza, Egypt
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Chen X, Zuo Z, Li L, Liu L, Bao X, Song R, Wang Y, Wang L, Zhu M, Wang Y. The effect of Time-Acupoints-Space Acupuncture on fatigue in postoperative chemotherapy patients with breast cancer: a randomized controlled trial. Front Oncol 2025; 15:1518278. [PMID: 40098703 PMCID: PMC11911492 DOI: 10.3389/fonc.2025.1518278] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/28/2024] [Accepted: 02/03/2025] [Indexed: 03/19/2025] Open
Abstract
Background Breast cancer (BC) is a common malignant tumor in women, and cancer-related fatigue (CRF) is prevalent among breast cancer patients. Time-Acupoints-Space Acupuncture (ATAS) is an acupuncture method different from traditional acupuncture. It combines time acupoints with space acupoints, proposing a new treatment approach. This randomized controlled trial aims to evaluate whether ATAS can improve fatigue in postoperative chemotherapy patients with breast cancer. Objective This randomized controlled trial focuses on survivors of postoperative chemotherapy for breast cancer, primarily assessing whether ATAS can reduce fatigue in these patients. Additionally, it reports on the effects of ATAS on sleep, anxiety, depression, and inflammatory factors. Methods The researchers randomly assigned 90 postoperative breast cancer patients to the ATAS group (n=30), the sham acupuncture group (n=30), and the waitlist control group (n=30). The primary outcome was the Piper Fatigue Scale (PFS), and the secondary outcomes were the Insomnia Severity Index (ISI), Hospital Anxiety and Depression Scale (HADS), Interleukin-2 (IL-2), Interleukin-6 (IL-6), CD3+T, and CD4+T. Data analysis was performed using the statistical software SPSS, utilizing descriptive statistics and analytic statistics. The significance level was set at less than 0.05. Results The baseline differences in PFS scores among the three groups were not statistically significant (P > 0.05). ATAS treatment is superior to sham acupuncture and the waitlist control in improving fatigue (mean difference 4.98, 95% CI 3.96 to 6.00, P<0.05). Additionally, secondary outcome analysis shows that the ATAS group has positive effects on ISI, HADS, and inflammatory factors. After the treatment ended, ISI (mean difference 15.17, 95% CI 12.28 to 18.06, P<0.05), HADS-A (mean difference 8.63, 95% CI 5.18 to 12.08, P<0.05), HADS-D (mean difference 7.80, 95% CI 4.73 to 10.87, P<0.05). IL-2(mean difference 20.18, 95% CI 11.51 to 28.85, P<0.05), IL-6(mean difference 24.56, 95% CI 7.57 to 41.55, P<0.05), CD3+T(mean difference 79.03, 95% CI 68.56 to 89.50, P<0.05), CD4+T(mean difference 42.89, 95% CI 35.14 to 50.64, P<0.05). Conclusions Our preliminary findings indicate that ATAS effectively improves fatigue in postoperative chemotherapy patients with breast cancer. It also has positive effects on sleep, anxiety, depression, and inflammatory factors. These results suggest that ATAS intervention may be an effective method for alleviating fatigue in breast cancer patients. Clinical Trial Registration https://www.chictr.org.cn/showproj.html?proj=21999, identifier ChiCTR17013652.
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Affiliation(s)
- Xin Chen
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Zheng Zuo
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Li Li
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Liangxian Liu
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Xiongying Bao
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Ran Song
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | - Yinghao Wang
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
| | | | - Miansheng Zhu
- First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, China
- ARIATAS, Association Pour la Recherche et I’Information de I’Acupuncture Time-Acupoints-Space, College of Acupuncture, Paris, France
| | - Yan Wang
- Second Department of Acupuncture and Moxibustion, Dali Bai Autonomous Prefecture Chinese Medicine Hospital, Dali, China
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