{"title":"Proton pump inhibitors in cirrhosis: a retrospective five-year analysis of increased risks of hepatic decompensation and infections.","authors":"Abhimati Ravikulan, Natalie Russell, Christin Coomarasamy, Ashok Raj","doi":"10.26635/6965.6838","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Proton pump inhibitors (PPIs) are widely used in cirrhotic patients, often without a clear indication. Evidence links PPI use to adverse outcomes such as hepatic encephalopathy and spontaneous bacterial peritonitis. This study analyses outcomes associated with PPI use in cirrhosis over 5 years at a New Zealand tertiary centre.</p><p><strong>Methods: </strong>This retrospective study included all patients diagnosed with liver cirrhosis at Counties Manukau Health in 2014. Patients were divided into two groups: those taking PPIs and those not taking PPIs. Demographic data, relevant blood tests and cumulative PPI doses were recorded. Outcomes such as mortality, liver-related events (hepatic encephalopathy, spontaneous bacterial peritonitis, variceal bleeding and ascites) and infections were monitored over 5 years. Logistic regression analyses calculated odds ratios (ORs) for the association of PPI usage with outcomes, adjusting for age, comorbidities, medications, aetiology of cirrhosis and liver disease severity.</p><p><strong>Results: </strong>Of 392 patients, 304 (77%) received PPIs and 88 (23%) did not. Only 31% had a clear indication for PPI use. PPI users had higher comorbidity and liver disease severity. Adjusted analysis showed no significant difference in all-cause mortality (29.9% vs 19.3%, p=0.67) or liver-related mortality (35.2% vs 17.6%, p=0.37). However, there were higher liver-related events (30.9% vs 10%, OR 2.9, p=0.046) and all-cause infections (30.9% vs 11.2%, OR 2.4, p=0.024).</p><p><strong>Conclusion: </strong>PPI use in cirrhosis is linked to hepatic decompensation and higher infection risk. Judicious PPI use with clear indications is essential.</p>","PeriodicalId":48086,"journal":{"name":"NEW ZEALAND MEDICAL JOURNAL","volume":"138 1614","pages":"70-80"},"PeriodicalIF":1.2000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NEW ZEALAND MEDICAL JOURNAL","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26635/6965.6838","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: Proton pump inhibitors (PPIs) are widely used in cirrhotic patients, often without a clear indication. Evidence links PPI use to adverse outcomes such as hepatic encephalopathy and spontaneous bacterial peritonitis. This study analyses outcomes associated with PPI use in cirrhosis over 5 years at a New Zealand tertiary centre.
Methods: This retrospective study included all patients diagnosed with liver cirrhosis at Counties Manukau Health in 2014. Patients were divided into two groups: those taking PPIs and those not taking PPIs. Demographic data, relevant blood tests and cumulative PPI doses were recorded. Outcomes such as mortality, liver-related events (hepatic encephalopathy, spontaneous bacterial peritonitis, variceal bleeding and ascites) and infections were monitored over 5 years. Logistic regression analyses calculated odds ratios (ORs) for the association of PPI usage with outcomes, adjusting for age, comorbidities, medications, aetiology of cirrhosis and liver disease severity.
Results: Of 392 patients, 304 (77%) received PPIs and 88 (23%) did not. Only 31% had a clear indication for PPI use. PPI users had higher comorbidity and liver disease severity. Adjusted analysis showed no significant difference in all-cause mortality (29.9% vs 19.3%, p=0.67) or liver-related mortality (35.2% vs 17.6%, p=0.37). However, there were higher liver-related events (30.9% vs 10%, OR 2.9, p=0.046) and all-cause infections (30.9% vs 11.2%, OR 2.4, p=0.024).
Conclusion: PPI use in cirrhosis is linked to hepatic decompensation and higher infection risk. Judicious PPI use with clear indications is essential.
目的:质子泵抑制剂(PPIs)广泛用于肝硬化患者,通常没有明确的适应症。有证据表明使用PPI与肝性脑病和自发性细菌性腹膜炎等不良后果有关。本研究分析了新西兰某三级医疗中心5年以上肝硬化患者使用PPI的相关结果。方法:本回顾性研究纳入2014年在Manukau县卫生院诊断为肝硬化的所有患者。患者被分为两组:服用质子泵抑制剂组和未服用质子泵抑制剂组。记录人口统计数据、相关血液检查和PPI累积剂量。结果如死亡率,肝脏相关事件(肝性脑病,自发性细菌性腹膜炎,静脉曲张出血和腹水)和感染监测超过5年。Logistic回归分析计算了PPI使用与结果相关的比值比(or),调整了年龄、合并症、药物、肝硬化病因和肝病严重程度。结果:392例患者中,304例(77%)接受了ppi治疗,88例(23%)未接受ppi治疗。只有31%的患者有明确的PPI适应症。PPI使用者有更高的合并症和肝脏疾病严重程度。校正分析显示,全因死亡率(29.9% vs 19.3%, p=0.67)或肝脏相关死亡率(35.2% vs 17.6%, p=0.37)无显著差异。然而,肝脏相关事件(30.9% vs 10%, OR 2.9, p=0.046)和全因感染(30.9% vs 11.2%, OR 2.4, p=0.024)较高。结论:肝硬化患者使用PPI与肝功能失代偿和感染风险增高有关。明智地使用PPI并明确适应症是必要的。