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DOI 10.1159/000279306

Медицинская библиотека · Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2010

Effects of medications on post-endoscopic retrograde cholangiopancreatography pancreatitis.

Li N, Tieng A, Novak S, Fernandes A, Jalal P K, Akerman M, Sideridis K, Bank S

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Аннотация

BACKGROUND AND AIMS: Drug-induced pancreatitis accounts for about 2% of acute pancreatitis. The aim of this study is to determine whether propofol and other medications are associated with increased risk for post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis.

METHODS

A retrospective study was conducted at a single tertiary care hospital. All patients who underwent ERCP from 2001 to 2004 were included. Diagnosis of acute post-ERCP pancreatitis was based on a consensus definition.

RESULTS

A total of 506 patients underwent ERCP. The total incidence of post-ERCP pancreatitis was 7.1%. There was no significant difference in post-ERCP pancreatitis between patients who received propofol compared to patients who received midazolam and fentanyl (9.0 vs. 5.9%, p = 0.18). Patients receiving an angiotensin receptor blocker were approximately 4 times more likely to develop post-ERCP pancreatitis (OR = 4.1, 95% CI 1.6-10.9). Patients younger than 65 years and smokers also had higher risk of developing acute post-ERCP pancreatitis than those who were older than 65 years (OR = 3.9, 95% CI 1.7-9.1) and non-smokers (OR = 2.8, 95% CI 1.3-6.2).

CONCLUSIONS

Propofol is a safe sedative drug for ERCP without additional risk of developing acute post-ERCP pancreatitis. Use of angiotensin receptor blockers, smoking and younger age are independent risk factors for post-ERCP pancreatitis.

Для цитирования: Li N, Tieng A, Novak S, Fernandes A, Jalal P K, Akerman M, Sideridis K, Bank S. Effects of medications on post-endoscopic retrograde cholangiopancreatography pancreatitis.. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]. 2010. DOI: 10.1159/000279306.

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