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Aliment Pharmacol Ther. 2024;59(8):973-983.

High-dose proton pump inhibitor treatment is associated with a higher mortality in cirrhotic patients: A multicentre study.

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제1저자 윤준식, 홍지훈, 박수영, 김승업, 김휘영 · 교신저자 이정훈

PMID 38389319 DOI 10.1111/apt.17909 IF 6.8 소화기내과
소속 (7)
  1. Department of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Republic of Korea.
  2. Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
  3. Department of Internal Medicine, School of Medicine, Kyungpook National University, Kyungpook National University Hospital, Daegu, Republic of Korea.
  4. Department of Internal Medicine and Yonsei Liver Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
  5. Department of Internal Medicine, College of Medicine, Ewha Womans University, Seoul, Republic of Korea.
  6. Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
  7. Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Abstract

BACKGROUND Proton pump inhibitors (PPI) are frequently used in patients with cirrhosis.

AIMS This study aimed to determine whether PPI use is associated with the prognosis of cirrhotic patients.

METHODS We conducted a multicentre retrospective cohort study involving 1485 patients who had experienced hepatic encephalopathy (HE) from 7 referral centres in Korea. The primary outcome was overall survival and secondary outcomes included the development of cirrhotic complications, including recurrent HE, spontaneous bacterial peritonitis (SBP), hepatorenal syndrome (HRS), and gastrointestinal bleeding. Patients treated with PPI with a mean defined daily dose (mDDD) ≥0.5 (high-dose PPI group) were compared to those treated with PPI of an mDDD < 0.5 (No or low-dose PPI group) for each outcome.

RESULTS Among 1485 patients (median age, 61 years; male, 61%), 232 were assigned to the high-dose PPI group. High-dose PPI use was independently associated with a higher risk of death (adjusted HR [aHR] = 1.71, 95% confidence interval [CI] = 1.38-2.11, p < 0.001). This result was reproducible after propensity score-matching (PSM) (aHR = 1.90, 95% CI = 1.49-2.44, p < 0.001). High-dose PPI use was an independent risk factor of recurrent HE (before PSM: aHR = 2.04, 95% CI = 1.66-2.51, p < 0.001; after PSM: aHR = 2.16, 95% CI = 1.70-2.74, p < 0.001), SBP (before PSM: aHR = 1.87, 95% CI = 1.43-2.43, p < 0.001; after PSM: aHR = 1.76, 95% CI = 1.31-2.36, p = 0.002), HRS (before PSM: aHR = 1.48, 95% CI = 1.02-2.15, p = 0.04; after PSM: aHR = 1.47, 95% CI = 0.95-2.28, p = 0.09), and gastrointestinal bleeding (before PSM: aHR = 1.46, 95% CI = 1.12-1.90, p = 0.006; after PSM: aHR = 1.74, 95% CI = 1.28-2.37, p < 0.001).

CONCLUSIONS The use of high-dose PPI was independently associated with increased risks of mortality and cirrhotic complications.

© 2024 John Wiley & Sons Ltd.

Keywords

bacterial translocationhepatic encephalopathymean defined daily dosespontaneous bacterial peritonitis

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그 밖의 정보
출판 형태
Multicenter Study, Journal Article
저널
Alimentary pharmacology & therapeutics · eISSN 1365-2036
전자 출판
2024-02-22
MeSH
Humans · Male · Middle Aged · Gastrointestinal Hemorrhage / drug therapy · Hepatic Encephalopathy* / etiology · Liver Cirrhosis / complications / drug therapy · Proton Pump Inhibitors* / adverse effects · Retrospective Studies · Risk Factors · Female
Substances
Proton Pump Inhibitors
참고문헌
40편