Continuous Infusion of Fluid Hydration Over 24 Hours Does Not Prevent Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis
dc.contributor.author | Chang A. | |
dc.contributor.author | Pausawasdi N. | |
dc.contributor.author | Charatcharoenwitthaya P. | |
dc.contributor.author | Kaosombatwattana U. | |
dc.contributor.author | Sriprayoon T. | |
dc.contributor.author | Limsrivilai J. | |
dc.contributor.author | Prachayakul V. | |
dc.contributor.author | Leelakusolvong S. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-06-18T16:46:24Z | |
dc.date.available | 2023-06-18T16:46:24Z | |
dc.date.issued | 2022-08-01 | |
dc.description.abstract | Background: Aggressive intravenous fluid hydration, by administering 3500 mL of lactated Ringer’s solution (LRS) in 9 h with a peri-procedural bolus, reduces post-ERCP pancreatitis (PEP) incidence. A concern of this strategy is adverse events related to volume overload; however, the impact of fluid hydration over an extended period without a bolus on PEP is unknown. Aim: To assess the effect of continuous infusion of high-volume fluid at a constant rate over 24 h on PEP incidence and severity. Methods: Two-hundred patients were randomly assigned (1:1) to receive either 3600 mL of LRS in 24 h starting 2 h before the ERCP (high-volume group) or maintenance fluid hydration calculated by the Holliday-Segar method (control group). Results: The mean age of the patients was 50.6 ± 11.6 years. The predominant indications were choledocholithiasis (48%) and malignancies (32%). Patient demographics and PEP risk factors were similar in both groups. Patients in the high-volume group received significantly more fluid than the control group (3600 vs. 2413 ml, P < 0.001). PEP incidence was not different between the high-volume and the control group (14% vs. 15%; relative risk 0.93: 95% CI 0.48–1.83, P = 0.84). There were no differences in moderate to severe PEP (3% vs. 4%; relative risk 0.75: 95% CI, 0.17–3.27, P = 1.00). Subgroup analysis did not show a benefit in high-risk patients. Only one patient in the control group developed peripheral edema. Conclusions: An infusion of high-volume hydration over 24 h is not sufficient to provide optimal hydration for PEP prevention. Clinical Trial Registry Number: No. NCT 02821546. | |
dc.identifier.citation | Digestive Diseases and Sciences Vol.67 No.8 (2022) , 4122-4130 | |
dc.identifier.doi | 10.1007/s10620-021-07256-z | |
dc.identifier.eissn | 15732568 | |
dc.identifier.issn | 01632116 | |
dc.identifier.pmid | 34655014 | |
dc.identifier.scopus | 2-s2.0-85117126659 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/83667 | |
dc.rights.holder | SCOPUS | |
dc.subject | Biochemistry, Genetics and Molecular Biology | |
dc.title | Continuous Infusion of Fluid Hydration Over 24 Hours Does Not Prevent Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85117126659&origin=inward | |
oaire.citation.endPage | 4130 | |
oaire.citation.issue | 8 | |
oaire.citation.startPage | 4122 | |
oaire.citation.title | Digestive Diseases and Sciences | |
oaire.citation.volume | 67 | |
oairecerif.author.affiliation | Siriraj Hospital | |
oairecerif.author.affiliation | Hatyai Hospital |