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Aug 4, 2015 (publication date) through Apr 19, 2024
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Journal Information of This Article
Publication Name
World Journal of Critical Care Medicine
ISSN
2220-3141
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Reeves EP, McCarthy C, McElvaney OJ, Vijayan MSN, White MM, Dunlea DM, Pohl K, Lacey N, McElvaney NG. Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function. World J Crit Care Med 2015; 4(3): 179-191 [PMID: 26261770 DOI: 10.5492/wjccm.v4.i3.179] |
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| URL: | https://www.wjgnet.com/1948-5182/full/v4/i3/179.htm |
| Number | Citing Articles |
| 1 |
Sanchayita Mitra, Daran Schiller, Cameron Anderson, Fabia Gamboni, Angelo D’Alessandro, Margeurite Kelher, Christopher C. Silliman, Anirban Banerjee, Kenneth L. Jones, Nades Palaniyar. Hypertonic saline attenuates the cytokine-induced pro-inflammatory signature in primary human lung epithelia. PLOS ONE 2017; 12(12): e0189536 doi: 10.1371/journal.pone.0189536
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| 2 |
Xiaojie Luan, Julian S. Tam, George Belev, Santosh Jagadeeshan, Brendan Murray, Noman Hassan, Terry E. Machen, L. Dean Chapman, Juan P. Ianowski. Nebulized hypertonic saline triggers nervous system-mediated active liquid secretion in cystic fibrosis swine trachea. Scientific Reports 2019; 9(1) doi: 10.1038/s41598-018-36695-4
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| 3 |
Rex B. Keith, Douglas Lewis. Cystic Fibrosis in Primary Care. 2020; : 47 doi: 10.1007/978-3-030-25909-9_6
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| 4 |
Miriam Frankenthal Figueira, Carla M.P. Ribeiro, Brian Button. Mucus-targeting therapies of defective mucus clearance for cystic fibrosis: A short review. Current Opinion in Pharmacology 2022; 65: 102248 doi: 10.1016/j.coph.2022.102248
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| 5 |
Massimo Conese, Stefano Castellani, Susanna D’Oria, Sante Di Gioia, Pasqualina Montemurro. Role of Neutrophils in Disease Pathogenesis. 2017; doi: 10.5772/67798
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| 6 |
Sejal Saglani, Clare M. Lloyd, Andrew Bush. Kendig's Disorders of the Respiratory Tract in Children. 2019; : 101 doi: 10.1016/B978-0-323-44887-1.00007-9
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| 7 |
R. L. Blackmon, S. M. Kreda, P. R. Sears, B. S. Chapman, D. B. Hill, J. B. Tracy, L. E. Ostrowski, A. L. Oldenburg. Direct monitoring of pulmonary disease treatment biomarkers using plasmonic gold nanorods with diffusion-sensitive OCT. Nanoscale 2017; 9(15): 4907 doi: 10.1039/C7NR00376E
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| 8 |
Angela Sepe, Valeria R. Villella, Chiara Cimbalo, Alice Castaldo, Francesco Nunziata, Adele Corcione, Gianni Bona, Luigi Maiuri, Valeria Raia. Inhaled medications in cystic fibrosis beyond antibiotics. Minerva Pediatrica 2019; 71(4) doi: 10.23736/S0026-4946.19.05509-9
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| 9 |
Patrick A. Flume, Elena Amelina, Cori L. Daines, Brett Charlton, Joanna Leadbetter, Alessandro Guasconi, Moira L. Aitken. Efficacy and safety of inhaled dry-powder mannitol in adults with cystic fibrosis: An international, randomized controlled study. Journal of Cystic Fibrosis 2021; 20(6): 1003 doi: 10.1016/j.jcf.2021.02.011
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| 10 |
Natalia Galaz Souza, Andrew Bush, Hui-Leng Tan. Exploratory study of the effectiveness of nebulised saline in children with neurodisability. European Respiratory Journal 2021; 57(3): 2001407 doi: 10.1183/13993003.01407-2020
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| 11 |
Franz Tatzber, Ulrike Resch, Meinrad Lindschinger, Gerhard Cvirn, Willibald Wonisch. Improved protection of filtering facepiece through inactivation of pathogens by hypertonic salt solutions – A possible COVID-19 prevention device. Preventive Medicine Reports 2020; 20: 101270 doi: 10.1016/j.pmedr.2020.101270
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| 12 |
Seyed-Ahmad Tabatabaei, Gholamreza Panahandeh, Ghamartaj Khanbabaei, Saeid Sadr. The Acute Effect of Inhaled NaCl 5%, Per CF TRUST Protocol, on Spirometry Indices in Patients Over Six Years with Cystic Fibrosis. Archives of Pediatric Infectious Diseases 2018; 6(2) doi: 10.5812/pedinfect.12063
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| 13 |
Kata Csekő, Dóra Hargitai, Lilla Draskóczi, Adrienn Kéri, Pongsiri Jaikumpun, Beáta Kerémi, Zsuzsanna Helyes, Ákos Zsembery. Safety of chronic hypertonic bicarbonate inhalation in a cigarette smoke-induced airway irritation guinea pig model. BMC Pulmonary Medicine 2022; 22(1) doi: 10.1186/s12890-022-01919-x
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| 14 |
Tracey Bonfield, James F. Chmiel. Impaired innate immune cells in cystic fibrosis: Is it really a surprise?. Journal of Cystic Fibrosis 2017; 16(4): 433 doi: 10.1016/j.jcf.2017.06.001
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| 15 |
O. I. Simonova, Yu. V. Gorinova, O. V. Vysokolova, M. A. Mukhina, E. E. Yakushina. Mannitol therapy for children with cystic fibrosis: efficacy and safety. Meditsinskiy sovet = Medical Council 2022; 16(18): 56 doi: 10.21518/2079-701X-2022-16-18-56-63
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| 16 |
Alejandro Teper, Carlos Kofman, Jessica Alchundia Moreira, Teresa Köhler, Facundo García Bournissen. Bronchodilator response to albuterol nebulized with hypertonic saline in asthmatic children. Pediatric Pulmonology 2021; 56(12): 3714 doi: 10.1002/ppul.25653
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