Short-term usage of proton pump inhibitors during admission was associated with increased risk of rehospitalization in critically ill patients with myocardial infarction: a cohort study.

IF 2.7 3区 医学 Q3 PHARMACOLOGY & PHARMACY European Journal of Clinical Pharmacology Pub Date : 2024-11-01 Epub Date: 2024-08-14 DOI:10.1007/s00228-024-03737-y
Jia-De Zhu, Li-Juan Yang, Jian-Nan Zhao, Ping Wang, Yi-Hua Li, Xue-Sha Zhang, Jian-Mei Pan, Meng-Han Jiang, Hai-Ying Yang, Sun-Jun Yin, Gong-Hao He
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Abstract

Purpose: Previous studies showed that long-term use of proton pump inhibitors (PPIs) was associated with cardiovascular events. However, the impact of short-term PPI exposure on intensive care unit (ICU) patients with myocardial infarction (MI) remains largely unknown. This study aims to determine the precise correlation between short-term PPI usage during hospitalization and prognostic outcomes of ICU-admitted MI patients using Medical Information Mart for Intensive Care IV database (MIMIC-IV).

Methods: Propensity score matching (PSM) was applied to adjust confounding factors. The primary study outcome was rehospitalization with mortality and length of stay as secondary outcomes. Binary logistic, multivariable Cox, and linear regression analyses were employed to estimate the impact of short-term PPI exposure on ICU-admitted MI patients.

Results: A total of 7249 patients were included, involving 3628 PPI users and 3621 non-PPI users. After PSM, 2687 pairs of patients were matched. The results demonstrated a significant association between PPI exposure and increased risk of rehospitalization for MI in both univariate and multivariate [odds ratio (OR) = 1.157, 95% confidence interval (CI) 1.020-1.313] analyses through logistic regression after PSM. Furthermore, this risk was also observed in patients using PPIs > 7 days, despite decreased risk of all-cause mortality among these patients. It was also found that pantoprazole increased the risk of rehospitalization, whereas omeprazole did not.

Conclusion: Short-term PPI usage during hospitalization was still associated with higher risk of rehospitalization for MI in ICU-admitted MI patients. Furthermore, omeprazole might be superior to pantoprazole regarding the risk of rehospitalization in ICU-admitted MI patients.

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入院期间短期使用质子泵抑制剂与心肌梗死重症患者再住院风险增加有关:一项队列研究。
目的:以往的研究表明,长期使用质子泵抑制剂(PPI)与心血管事件有关。然而,短期服用质子泵抑制剂对重症监护病房(ICU)心肌梗死(MI)患者的影响在很大程度上仍是未知数。本研究旨在利用重症监护医学信息市场IV数据库(MIMIC-IV)确定住院期间短期服用PPI与ICU收治的心肌梗死患者预后结果之间的精确相关性:方法:采用倾向得分匹配法(PSM)调整混杂因素。研究的主要结果是再次入院,次要结果是死亡率和住院时间。采用二元逻辑分析、多变量 Cox 分析和线性回归分析来估计短期 PPI 暴露对入住 ICU 的心肌梗死患者的影响:共纳入 7249 例患者,其中 3628 例使用 PPI,3621 例未使用 PPI。经过PSM后,2687对患者进行了配对。结果显示,通过 PSM 后的逻辑回归分析,单变量和多变量[比值比 (OR) = 1.157,95% 置信区间 (CI) 1.020-1.313]分析均显示 PPI 暴露与心肌梗死再住院风险增加之间存在明显关联。此外,在使用 PPIs > 7 天的患者中也观察到了这种风险,尽管这些患者的全因死亡风险有所降低。研究还发现,泮托拉唑会增加再次住院的风险,而奥美拉唑不会:结论:ICU收治的心肌梗死患者在住院期间短期使用PPI仍与较高的心肌梗死再住院风险有关。此外,就ICU收治的心肌梗死患者再次入院的风险而言,奥美拉唑可能优于泮托拉唑。
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CiteScore
5.40
自引率
3.40%
发文量
170
审稿时长
3-8 weeks
期刊介绍: The European Journal of Clinical Pharmacology publishes original papers on all aspects of clinical pharmacology and drug therapy in humans. Manuscripts are welcomed on the following topics: therapeutic trials, pharmacokinetics/pharmacodynamics, pharmacogenetics, drug metabolism, adverse drug reactions, drug interactions, all aspects of drug development, development relating to teaching in clinical pharmacology, pharmacoepidemiology, and matters relating to the rational prescribing and safe use of drugs. Methodological contributions relevant to these topics are also welcomed. Data from animal experiments are accepted only in the context of original data in man reported in the same paper. EJCP will only consider manuscripts describing the frequency of allelic variants in different populations if this information is linked to functional data or new interesting variants. Highly relevant differences in frequency with a major impact in drug therapy for the respective population may be submitted as a letter to the editor. Straightforward phase I pharmacokinetic or pharmacodynamic studies as parts of new drug development will only be considered for publication if the paper involves -a compound that is interesting and new in some basic or fundamental way, or -methods that are original in some basic sense, or -a highly unexpected outcome, or -conclusions that are scientifically novel in some basic or fundamental sense.
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