Authors
Woo Hyun Paik, Gunn Huh, Young Hoon Choi, Jin Ho Choi, In Rae Cho, Sang Hyub Lee, Ji Kon Ryu, Hwa Jung Kim, Taehyung Lee, Ce Hwan Park, Yoonchan Lee, Sung Hyun Cho, Dong-Wan Seo, Kwang Hyuck Lee, Kyu Taek Lee, Jong Kyun Lee, Sunguk Jang, John Vargo, Steven Edmundowicz, Joo Kyung Park, Do Hyun Park
Published in
United European gastroenterology journal. Volume 14. Issue 7. Pages e70281.
Abstract
Aggressive peri-procedural intravenous fluid (IVF) therapy with lactated Ringer's solution (LR) reduces the risk of post-ERCP pancreatitis (PEP), but the standard 8-h protocol is impractical in outpatient settings and the optimal fluid type remains uncertain. We compared LR with an acetate-buffered balanced crystalloid (AC) using a symptom-guided 4-h aggressive IVF protocol.
This multicentre, double-blind, randomized superiority trial was conducted at three academic hospitals in Korea where rectal NSAIDs are unavailable. Adults with native papillae and moderate-to-high PEP risk were randomized to receive LR or AC. The IVF protocol comprised 10 mL/kg boluses before and after ERCP, followed by 3 mL/kg/h for 4 hours and extended to 8 hours if abdominal pain developed or worsened. The primary outcome was PEP incidence; secondary outcomes included early post-ERCP pain and adverse events.
Of 813 patients (404 LR, 409 AC), PEP occurred in 12.4% of the LR group and 11.5% of the AC group (relative risk [RR] 0.93; 95% CI, 0.64-1.35; P = 0.70). Rates of mild (7.9% vs. 7.1%) and moderate (4.5% vs. 4.4%) PEP were similar, and no severe PEP or fluid overload occurred. Among the 68.3% of patients who remained asymptomatic at 4 hours and required only 4-h IVF, PEP occurred in 7.4%, with no cases of severe PEP.
In this superiority trial, acetate-buffered crystalloid did not reduce PEP compared with lactated Ringer's solution, and no significant safety differences were observed between the two agents. Lactated Ringer's remains the recommended first-line crystalloid for aggressive hydration when rectal NSAIDs are unavailable.
ClinicalTrials.gov (NCT05832047).
PMID:
42640715
Bibliographic data and abstract were imported from PubMed on 26 Aug 2026.
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