Published online Aug 27, 2024. doi: 10.4240/wjgs.v16.i8.2662
Revised: June 8, 2024
Accepted: July 1, 2024
Published online: August 27, 2024
Processing time: 101 Days and 3.9 Hours
Patients with rectal cancer undergoing radical resection often have poor post
To analyze the effects of goal-directed fluid therapy (GDFT) with a preoperative glucose load regimen on postoperative recovery and complications in patients undergoing radical resection for rectal cancer.
Patients with rectal cancer who underwent radical resection (n = 184) between January 2021 and December 2023 at our hospital were randomly divided into either a control group or an observation group (n = 92 in each group). Both groups received a preoperative glucose load regimen, and routine fluid replacement and GDFT were additionally implements in the control and observation groups, res
The colloidal fluid dosage, total infusion, and urine volume, as well as time to first exhaust, time to food intake, and postoperative length of hospital stay, were lower in the observation group (P < 0.05). No significant differences were observed between the two groups in terms of operation time, bleeding volume, crystalloid liquid consumption, time to tracheal extubation, complication rate, heart rate, or mean arterial pressure (P > 0.05). Compared with the control group, in the ob
GDFT combined with the preoperative glucose load regimen is a safe and effective treatment strategy for im
Core Tip: The application of goal-directed fluid therapy combined with a preoperative glucose load regimen in patients with rectal cancer undergoing radical resection can not only significantly improve the postoperative recovery and brain tissue oxygen metabolism, but also alleviate inflammatory reactions, and improve cognitive function, hemodynamics, and blood lactate levels. This study observed the postoperative recovery of patients undergoing radical resection for rectal cancer, and confirmed the effectiveness of goal-directed fluid therapy combined with a preoperative glucose load regimen in patients undergoing radical resection for rectal cancer.
- Citation: Xia LC, Zhang K, Wang CW. Effects of fluid therapy combined with a preoperative glucose load regimen on postoperative recovery in patients with rectal cancer. World J Gastrointest Surg 2024; 16(8): 2662-2670
- URL: https://www.wjgnet.com/1948-9366/full/v16/i8/2662.htm
- DOI: https://dx.doi.org/10.4240/wjgs.v16.i8.2662
The incidence of rectal cancer, a primary malignant tumor involving the rectal mucosal epithelium, has been frequently reported in 40-80-year-old men. Rectal cancer does not present with any obvious symptoms during the early stage; however, tumor metastasis, accompanied by jaundice, dyspnea, dizziness, headache, and pain at the site of bone me
Goal-directed fluid therapy (GDFT) facilitates the monitoring of the hemodynamic status of patients in real time. The fluid replacement method is adjusted according to the detected conditions to maintain the hemodynamic stability and improve the tissue supply. Few studies have investigated the effects of GDFT combined with a preoperative glucose load regimen on postoperative recovery in patients with rectal cancer undergoing radical resection. Based on these results, patients with rectal cancer undergoing radical resection (n = 184) were included in this study to evaluate the effects of GDFT combined with a preoperative glucose load regimen on their postoperative recovery.
Patients with rectal cancer who underwent radical resection (n = 184) at our hospital between January 2021 and December 2023 were randomly divided into either a control group or an observation group (n = 92 cases in each group). The in
A preoperative glucose load regimen was implemented in both groups. The patients in both groups fasted for 8 h before the surgery. Water deprivation was implemented for 6 h before the surgery. Oral carbohydrates (4 mL/kg; 10% glucose) were administered orally 2 h before the surgery, and the total volume was < 300 mL.
Midazolam (0.05 mg/kg; intravenous administration) was administered after the patient entered the operating room. Routine monitoring of blood pressure and electrocardiography were commenced after inducing local anesthesia. A catheter was inserted into the artery to monitor the mean arterial pressure (MAP) and pulse pressure variability (PPV).
For anesthesia induction, etomidate (0.3 mg/kf), sufentanil (0.3-0.4 μg/kg), and rocuronium (0.6 mg/kg) were administered intravenously. Tracheal intubation and mechanical ventilation were performed subsequently. The res
Sodium lactate solution (3 mL/kg/h) was administered intravenously to all participants. Ephedrine (6 mg) was administered intravenously during the surgery if the MAP was < 60 mmHg for > 15 min. The crystalloid solution used was a mixture of sodium lactate Ringer's solution and a colloid mixed at a 3:1 ratio.
Routine fluid replacement and traditional infusion were implemented in the control group. Norepinephrine (0.03 μg/kg/min) was infused intravenously if the systolic blood pressure had a decrease of > 20% compared with the preope
GDFT and the monitoring of PPV and systolic blood pressure were implemented in the observation group. Fluid replacement (3 mL/kg) was performed for 5 min when the systolic blood pressure increased by > 20% or the PPV reached or exceeded 13% of the preoperative values. The patients were re-evaluated subsequently. Fluid replacement was discontinued when the systolic blood pressure returned to the normal range or the PPV was < 13%; only real-time monitoring was performed. Fluid replacement was performed at 3 mL/kg for less than 5 min when the systolic blood pressure was < 20% and the PPV was > 13% of the preoperative values. Norepinephrine (0.03 μg/kg/min) was infused intravenously when the PPV was < 13% and > 10 mL/kg. The dose of norepinephrine was adjusted according to the systolic blood pressure.
Operative conditions: The operation time and urine volume in the two groups were recorded.
Blood lactic acid levels: Peripheral venous blood samples were collected immediately after entering the operating room and immediately after the surgery. Blood lactic acid levels were detected using ultraviolet spectrophotometry.
Postoperative recovery: Time to first exhaust time, time to tracheal extubation, time to food intak, and postoperative length of hospital stay in the two groups were recorded.
Cognitive status: The patients were evaluated using the Mini-Mental State Examination (MMSE) before and 3 d after the surgery. The MMSE comprises 30 items, with a total score ranging from 0 to 30 points. MMSE scores of 27-30, 21-26, 10-20, and 0-9 points indicated normal state, mild cognitive impairment, moderate cognitive impairment, and severe cognitive impairment, respectively.
Hemodynamic indicators: The heart rate (HR), MAP, and PPV were recorded 1 d before the surgery (T0), before the induction of anesthesia (T1), immediately after the surgery (T2), 30 min after pneumoperitoneum (T3), and immediately after the surgery (T4).
Inflammatory factors: Venous blood samples were collected before and 3 d after the surgery in the fasting state. TNF-α and IL-6 levels were measured by ELISA.
Oxygen metabolism in brain tissue: Left and right regional cerebral oxygen saturation (rScO2) was measured using a brain oxygen saturation monitor at T1, T2, and T3.
Complications: The incidence of complications, such as nausea, vomiting, wound infection, pulmonary infection, and urinary system infection, was recorded.
All statistical analyses were performed using SPSS 22.0. Measurement data were tested for normality by the Shapiro-Wilk test. Count data are presented as n (%), and inter-group comparisons were performed using the χ2 test or the corrected χ2 test when n was > 30 or < 5. Measurement data are presented as the mean ± SD, and inter-group comparisons were performed using the t test. Statistical significance was set at P < 0.05.
The colloid fluid dosage, total infusion volume, and urine volume were lower in the observation group (P < 0.05). In contrast, the operation time, intraoperative bleeding volume, and crystalloid liquid dosage did not differ significantly between the two groups (P > 0.05; Table 1).
Group | Number of cases | Operation time (minute) | Intraoperative bleeding volume (mL) | Crystalloid liquid (mL) | Colloid fluid (mL) | Total infusion volume (mL) | Urine volume (mL) |
Observation group | 92 | 183.61 ± 8.52 | 249.25 ± 10.22 | 1134.69 ± 20.98 | 521.06 ± 10.52 | 1908.25 ± 20.66 | 321.58 ± 10.52 |
Control group | 92 | 183.67 ± 8.55 | 248.63 ± 10.36 | 1129.87 ± 20.55 | 532.05 ± 10.56 | 1915.58 ± 20.32 | 522.14 ± 10.777 |
t value | 0.048 | 0.409 | 1.574 | 7.072 | 2.426 | 127.733 | |
P value | 0.962 | 0.683 | 0.117 | < 0.001 | 0.016 | < 0.001 |
No significant differences were observed between the two groups in terms of blood lactic acid levels measured immediately after entering the operating room (P > 0.05). However, blood lactic acid level was lower immediately after the surgery in the observation group than in the control group (P < 0.05; Table 2).
Group | Number of cases | Blood lactic acid level (mmol/L) | |
Immediately after entering operating room | Immediately after surgery | ||
Observation group | 92 | 1.09 ± 0.22 | 1.24 ± 0.24 |
Control group | 92 | 1.10 ± 0.25 | 1.38 ± 0.29 |
t value | 0.288 | 3.567 | |
P value | 0.774 | < 0.001 |
The time to first exhaust, time to food intake, and postoperative length of hospital stay were shorter in the observation group (P < 0.05), though no significant difference was observed in the time to tracheal extubation between the two groups (P > 0.05; Table 3).
Group | Number of cases | Time to first exhaust (h) | Time to tracheal extubation (h) | Time to food intake (h) | Postoperative hospital stay (d) |
Observation group | 92 | 72.63 ± 6.88 | 0.66 ± 0.16 | 67.58 ± 4.28 | 11.14 ± 1.22 |
Control group | 92 | 90.51 ± 6.40 | 0.69 ± 0.17 | 77.25 ± 4.63 | 14.78 ± 1.40 |
t value | 18.251 | 1.233 | 14.710 | 18.801 | |
P value | < 0.001 | 0.219 | < 0.001 | < 0.001 |
No significant differences were observed between the groups in terms of the MMSE scores before the surgery (P > 0.05). The MMSE score on postoperative day 3 was higher in the observation group than in the control group (P < 0.05; Table 4).
Group | Number of cases | Mini-Mental State Examination score | |
Preoperatively | 3 d after surgery | ||
Observation group | 92 | 27.42 ± 1.05 | 26.77 ± 1.15 |
Control group | 92 | 27.33 ± 1.11 | 25.01 ± 1.25 |
t value | 0.565 | 9.939 | |
P value | 0.573 | < 0.001 |
No significant differences were observed between the groups at any time point in terms of HR and MAP (P > 0.05). PPV at T3 in the observation group was significantly lower that of the control group (P < 0.05). However, PPV did not differ significantly in the two groups at T0, T1, T2, and T4 (P > 0.05; Table 5).
Group | Number of cases | HR (times/min) | Mean arterial pressure (mmHg) | Pulse pressure variability (%) | ||||||||||||
T0 | T1 | T2 | T3 | T4 | T0 | T1 | T2 | T3 | T4 | T0 | T1 | T2 | T3 | T4 | ||
Observation group | 92 | 66.41 ± 4.55 | 67.25 ± 5.66 | 68.69 ± 4.60 | 68.99 ± 4.05 | 70.11 ± 4.05 | 76.02 ± 4.05 | 78.10 ± 6.25 | 80.01 ± 6.11 | 81.98 ± 6.40 | 83.99 ± 6.24 | - | 11.75 ± 1.02 | 9.87 ± 0.98 | 12.79 ± 1.13 | 8.82 ± 0.76 |
Control group | 92 | 66.78 ± 4.25 | 67.05 ± 5.14 | 68.25 ± 4.05 | 68.11 ± 4.14 | 70.25 ± 4.22 | 76.27 ± 5.60 | 77.89 ± 6.11 | 80.25 ± 6.45 | 82.66 ± 6.52 | 84.14 ± 6.66 | - | 12.01 ± 1.25 | 9.89 ± 0.94 | 14.96 ± 1.35 | 9.02 ± 0.77 |
t value | 0.570 | 0.251 | 0.689 | 1.457 | 0.230 | 0.347 | 0.230 | 0.259 | 0.714 | 0.158 | 1.546 | 0.141 | 11.823 | 1.773 | ||
P value | 0.569 | 0.802 | 0.492 | 0.147 | 0.819 | 0.729 | 0.818 | 0.796 | 0.476 | 0.875 | 0.124 | 0.888 | < 0.001 | 0.078 |
No significant differences were observed between the groups in terms of the inflammatory factor levels before the surgery (P > 0.05). TNF-α and IL-6 levels on postoperative day 3 were lower in the observation group than in the control group (P < 0.05; Table 6).
Group | Number of cases | TNF-α (mg/L) | IL-6 (ng/L) | ||
Preoperatively | 3 d after surgery | Preoperative | 3 d after surgery | ||
Observation group | 92 | 60.14 ± 4.03 | 32.53 ± 3.06 | 80.25 ± 8.79 | 41.26 ± 4.03 |
Control group | 92 | 60.22 ± 4.14 | 38.77 ± 3.14 | 80.36 ± 8.41 | 52.06 ± 4.19 |
t value | 0.133 | 13.651 | 0.087 | 17.819 | |
P value | 0.894 | < 0.001 | 0.931 | < 0.001 |
No significant differences were observed between the two groups in terms of brain tissue oxygen metabolism indices at T1 (P > 0.05). The rScO2 levels on the left and right sides at T2 and T3 were significantly higher in the observation group than in the control group (P < 0.05; Table 7).
Group | Number of cases | Left rScO2 (%) | Right rScO2 (%) | ||||
T1 | T2 | T3 | T1 | T2 | T3 | ||
Observation group | 92 | 72.05 ± 6.25 | 68.41 ± 5.05 | 66.10 ± 6.31 | 70.22 ± 6.37 | 67.08 ± 5.40 | 65.11 ± 4.06 |
Control group | 92 | 72.11 ± 6.45 | 64.25 ± 5.11 | 62.08 ± 6.16 | 70.40 ± 6.49 | 64.99 ± 5.19 | 61.78 ± 4.27 |
t value | 0.064 | 5.554 | 4.373 | 0.190 | 2.677 | 5.421 | |
P value | 0.949 | < 0.001 | < 0.001 | 0.850 | 0.008 | < 0.001 |
No significant differences were observed between the groups in terms of the incidence of complications (P > 0.05; Table 8).
Group | Number of cases | Nausea and vomiting | Wound infection | Pulmonary infection | Urinary system infection | Total incidence |
Observation group | 92 | 1 (1.09) | 1 (1.09) | 0 | 0 | 2 (2.17) |
Control group | 92 | 2 (2.17) | 3 (3.26) | 0 | 0 | 5 (5.43) |
χ2 | 0.594 | |||||
P value | 0.441 |
The etiology of rectal cancer is relatively complex and is often the result of a combination of environmental, diet, lifestyle, and genetic factors. Radical resection remains the treatment of choice for rectal cancer. Resection involves the complete excision of the tumor and part of the surrounding tissues during surgery; it is mainly used for the treatment of early- and middle-stage rectal cancer. Surgical technology has advanced with the developments in the field of medical technology. This has led to a reduction in morbidity. Nevertheless, blood loss and body fluid loss occur during surgery. Thus, maintaining the body fluid balance intraoperatively is necessary. Fasting and water deprivation are often implemented before radical resection of rectal cancer. In addition to causing disorders of glucose metabolism and imbalance of ho
The colloid fluid dose, total infusion volume, and urine volume, as well as time to first exhaust, time to food intake, and postoperative length of hospital stay were lower in the observation group than in the present study (P < 0.05). This finding indicates that implementing GDFT combined with a preoperative glucose load regimen improved the surgical outcome of radical resection and postoperative recovery. GDFT facilitates the improvement of cardiac output, tissue and organ perfusion, and oxygen supply by enabling the monitoring of the changes in body volume in real time and guiding fluid replacement according to the condition of the patients[13,14]. The fluid infusion measures implemented as a part of GDFT address the phenomenon of insufficient circulation volume during the surgery, maintain tissue perfusion, and reduce the incidence of adverse effects (such as intraoperative blood loss and body fluid loss).
Blood lactic acid levels reflect the intraoperative oxygen supply and consumption. Patients with rectal cancer under
The MMSE score was higher in the observation group than in the control group 3 d after the surgery in the present study (P < 0.05), suggesting that the implementation of GDFT combined with the preoperative glucose load regimen could improve the postoperative cognitive status of patients with rectal cancer undergoing radical resection. GDFT faci
Owing to the effect of factors such as fluid loss and hypothermia, patients undergoing radical resection for rectal cancer have abnormal hemodynamics, leading to changes in the levels of relevant hemodynamic indicators. The data in this study showed that PPV was lower in the observation group at T3 (P < 0.05). This finding indicates that the imple
IL-6 is a common indicator of acute inflammation. TNF-α can mediate the production of other inflammatory factors in the body and aggravate the inflammatory response. Owing to the effect of factors such as hypotension, intraoperative fluid loss, and insufficient energy, patients with rectal cancer undergoing radical resection are prone to developing stress responses and inflammatory reactions. The TNF-α and IL-6 Levels were lower in the observation group 3 d after the surgery (P < 0.05; Table 6). This finding indicates that the implementation of GDFT combined with the preoperative glucose load regimen could improve the inflammatory status of patients with rectal cancer undergoing radical resection. The preoperative glucose load regimen instructs patients to consume oral carbohydrates before surgery to supplement body fluid and energy and reduce the impact of body fluid loss and insufficient capacity on the inflammatory response. In contrast, GDFT enables the monitoring of the changes in PPV and systolic blood pressure in patients in real time and supplementation of body fluids, thereby improving cardiac function. In addition, it can achieve fluid replacement rapidly, improve the oxygen supply, and reduce the risk of hypotension. Combined with the preoperative glucose load regimen, GDFT further alleviated the inflammatory state of the patients.
Clinical research has shown that hypoxia in brain tissue is characterized by poor tolerance and high metabolism. The oxygen demand status of brain tissue can reflect brain injury and metabolism and can be used to assess the oxygen supply balance of brain tissue by observing changes in rScO2 levels[17]. Radical resection of rectal cancer causes damage to the body and stress reactions, resulting in increased brain oxygen consumption and functional brain metabolism abnormalities. Therefore, the rScO2 Levels declined to a certain extent at the beginning of surgery. However, the rScO2 Levels on the left and right sides were higher in the observation group than in the control group at T2 and T3 (P < 0.05; Table 7). GDFT facilitates the adjustment of the fluid replacement method at any time by enabling the monitoring of PPV. Fluid replacement can also reduce the probability of excessive fluid replacement and the load of excessive fluid re
This study found no significant differences between the two groups in terms of the incidence of complications (P > 0.05). This finding indicates that the implementation of GDFT combined with the preoperative glucose load regimen had a relatively small effect on the risk of complications in patients with rectal cancer undergoing radical resection; moreover, its safety was high. However, due to the limited sample size of this study, the results may be biased. In the future, we need to expand the sample size and conduct multi-center cooperative research to obtain more robust and generalizable evidence.
The implementation of GDFT combined with a preoperative glucose load regimen in patients with rectal cancer under
1. | Oh SY, Park IJ, Kim YI, Lee JL, Kim CW, Yoon YS, Lim SB, Yu CS, Kim JC. Comparison between Local Excision and Radical Resection for the Treatment of Rectal Cancer in ypT0-1 Patients: An Analysis of the Clinicopathological Factors and Survival Rates. Cancers (Basel). 2021;13. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis (0)] |
2. | Hrebinko KA, Reitz KM, Mohammed MK, Nassour I, Watson AR, Cunningham KE, Medich DS, Celebrezze JP, Holder-Murray JM. Transanal excision with adjuvant therapy for pT1N0 rectal tumors with high-risk features offers equivalent survival to radical resection: A National Cancer Database analysis. J Surg Oncol. 2022;125:475-483. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis (0)] |
3. | Chen S, Hao Y, Huang S, Leng D, Ma Y. Resection of rectal metastasis after previous radical surgery for pancreatic cancer: Case report and literature review. Medicine (Baltimore). 2023;102:e36365. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (0)] |
4. | Motamedi MAK, Mak NT, Brown CJ, Raval MJ, Karimuddin AA, Giustini D, Phang PT. Local versus radical surgery for early rectal cancer with or without neoadjuvant or adjuvant therapy. Cochrane Database Syst Rev. 2023;6:CD002198. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Reference Citation Analysis (0)] |
5. | Osman MM, Huynh LM, El-Khatib FM, Towe M, Su HW, Andrianne R, Barton G, Broderick G, Burnett AL, Campbell JD, Clavell-Hernandez J, Connor J, Gross M, Guillum R, Guise AI, Hatzichristodoulou G, Henry GD, Hsieh TC, Jenkins LC, Koprowski C, Lee KB, Lentz A, Munarriz RM, Osmonov D, Pan S, Parikh K, Park SH, Patel AS, Perito P, Sadeghi-Nejad H, Sempels M, Simhan J, Wang R, Yafi FA. Immediate preoperative blood glucose and hemoglobin a1c levels are not predictive of postoperative infections in diabetic men undergoing penile prosthesis placement. Int J Impot Res. 2021;33:296-302. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis (0)] |
6. | Castro MJ, Jiménez JM, López M, Cao MJ, Santos-Torres J, López A, Moreno A, Ruiz-Tovar J. Impact of Preoperative Total Proteins and Glycated Hemoglobin on Recurrences after Early Colorectal Cancer. Nutrients. 2021;13. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (0)] |
7. | National Health Commission of the People′s Republic of China; Chinese Society of Oncology. [Chinese Protocol of Diagnosis and Treatment of Colorectal Cancer (2023 edition)]. Zhonghua Wai Ke Za Zhi. 2023;61:617-644. [PubMed] [DOI] [Cited in This Article: ] [Cited by in F6Publishing: 3] [Reference Citation Analysis (0)] |
8. | Hu D, Peng F, Lin X, Zhang H, Xia Y, Lin J, Zheng X, Niu W. The risk trajectory between preoperative fasting glucose and common digestive tract cancer-specific mortality in the FIESTA cohort involving 6865 Chinese patients. J Cancer. 2019;10:4596-4602. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis (0)] |
9. | Shi M, Hu Z, Yang D, Cai Q, Zhu Z. Preoperative Oral Carbohydrate Reduces Postoperative Insulin Resistance by Activating AMP-Activated Protein Kinase after Colorectal Surgery. Dig Surg. 2020;37:368-375. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis (0)] |
10. | Virág M, Rottler M, Gede N, Ocskay K, Leiner T, Tuba M, Ábrahám S, Farkas N, Hegyi P, Molnár Z. Goal-Directed Fluid Therapy Enhances Gastrointestinal Recovery after Laparoscopic Surgery: A Systematic Review and Meta-Analysis. J Pers Med. 2022;12. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 9] [Reference Citation Analysis (0)] |
11. | Kan CFK, Skaggs JD. Current Commonly Used Dynamic Parameters and Monitoring Systems for Perioperative Goal-Directed Fluid Therapy: A Review. Yale J Biol Med. 2023;96:107-123. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (0)] |
12. | Li X, Zhang Q, Zhu Y, Yang Y, Xu W, Zhao Y, Liu Y, Xue W, Fang Y, Huang J. Effect of perioperative goal-directed fluid therapy on postoperative complications after thoracic surgery with one-lung ventilation: a systematic review and meta-analysis. World J Surg Oncol. 2023;21:297. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (0)] |
13. | Ma H, Li X, Wang Z, Qiao Q, Gao Y, Yuan H, Guan B, Guan Z. The effect of intraoperative goal-directed fluid therapy combined with enhanced recovery after surgery program on postoperative complications in elderly patients undergoing thoracoscopic pulmonary resection: a prospective randomized controlled study. Perioper Med (Lond). 2023;12:33. [PubMed] [DOI] [Cited in This Article: ] [Cited by in F6Publishing: 1] [Reference Citation Analysis (0)] |
14. | Xu C, Peng J, Liu S, Huang Y, Guo X, Xiao H, Qi D. Goal-directed fluid therapy versus conventional fluid therapy in colorectal surgery: A meta analysis of randomized controlled trials. Int J Surg. 2018;56:264-273. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 17] [Cited by in F6Publishing: 22] [Article Influence: 3.7] [Reference Citation Analysis (0)] |
15. | Zorrilla-Vaca A, Mena GE, Ripolles-Melchor J, Abad-Motos A, Aldecoa C, Lorente JV, Ramirez-Rodriguez JM, Grant MC. Goal-Directed Fluid Therapy and Postoperative Outcomes in an Enhanced Recovery Program for Colorectal Surgery: A Propensity Score-Matched Multicenter Study. Am Surg. 2021;87:1189-1195. [PubMed] [DOI] [Cited in This Article: ] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis (0)] |
16. | Gopal J, Srivastava S, Singh N, Haldar R, Verma R, Gupta D, Mishra P. Pulse Pressure Variance (PPV)-Guided Fluid Management in Adult Patients Undergoing Supratentorial Tumor Surgeries: A Randomized Controlled Trial. Asian J Neurosurg. 2023;18:508-515. [PubMed] [DOI] [Cited in This Article: ] [Reference Citation Analysis (0)] |
17. | Chin K, Joo H, Jiang H, Lin C, Savinova I, Joo S, Alli A, Sklar MC, Papa F, Simpson J, Baker AJ, Mazer CD, Darrah W, Hare GMT. Importance of assessing biomarkers and physiological parameters of anemia-induced tissue hypoxia in the perioperative period. Braz J Anesthesiol. 2023;73:186-197. [PubMed] [DOI] [Cited in This Article: ] [Cited by in F6Publishing: 4] [Reference Citation Analysis (0)] |