Use of proton pump inhibitors is associated with increased risk of out-of-hospital cardiac arrest in the general population: a nested case-control study.

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS European Heart Journal - Cardiovascular Pharmacotherapy Pub Date : 2024-08-14 DOI:10.1093/ehjcvp/pvae020
Talip E Eroglu, Ruben Coronel, Gunnar H Gislason
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引用次数: 0

Abstract

Aims: Proton pump inhibitors (PPIs) impair cardiac repolarization, prolong the QT interval, and may potentially be pro-arrhythmic. However, the risk of out-of-hospital cardiac arrest (OHCA) is scarcely investigated. We studied whether past or current PPI use is associated with OHCA in the general population.

Methods and results: We conducted a nationwide nested case-control study with OHCA-cases of presumed cardiac causes and age/sex/OHCA-date-matched non-OHCA-controls from the general population. Exposure to PPI was categorized into three mutually exclusive groups of current-, past-, and non-use. Conditional logistic regression analyses with adjustments for risk factors of OHCA were used to calculate the odds ratio (OR) of OHCA comparing PPI use with non-users. We identified 46 578 OHCA cases and 232 890 matched non-OHCA controls (mean: 71 years, 68.8% men). PPI was used by 8769 OHCA-cases and 21 898 non-OHCA controls, and current use of PPI was associated with increased odds of OHCA compared with non-users [OR: 1.32 (95% CI: 1.28-1.37)], while past use conferred no increase in the odds of OHCA [OR: 1.01 (95% CI: 0.98-1.04)]. This increased odds of OHCA occurred in both sexes. Finally, the ORs remained elevated when we repeated the analyses in individuals without registered ischaemic heart disease [OR: 1.36 (95% CI: 1.31-1.41)], without heart failure [OR: 1.33 (95% CI: 1.29-1.38)], or without any cardiovascular comorbidities [OR: 1.84 (95% CI: 1.70-2.00)]. Also, the OR remained elevated when H2-antagonists served as the reference group [OR: 1.28 (95% CI: 1.11-1.47)].

Conclusion: PPI use is associated with an increased risk of OHCA in the general population. Considering the widespread use of PPIs, this study raises concerns and the need for awareness to balance the benefit and risk of treatment.

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使用质子泵抑制剂与普通人群院外心脏骤停风险增加有关:一项巢式病例对照研究。
目的:质子泵抑制剂(PPIs)会损害心脏复极化,延长 QT 间期,并可能导致心律失常。然而,院外心脏骤停(OHCA)的风险却鲜有研究。我们研究了在普通人群中,过去或现在使用 PPI 是否与 OHCA 相关:我们在全国范围内开展了一项巢式病例对照研究,研究对象为推测为心脏原因导致的 OHCA 病例以及与年龄/性别/OHCA 日期相匹配的非 OHCA 病例。PPI暴露分为三个相互排斥的组别,即当前使用、过去使用和未使用。在对 OHCA 风险因素进行调整后,采用条件逻辑回归分析计算使用 PPI 与未使用 PPI 的 OHCA 机率比 (OR)。我们发现了 46578 例 OHCA 病例和 232890 例匹配的非 OHCA 对照者(平均 71 岁,68.8% 为男性)。有 8769 例 OHCA 患者和 21898 例非 OHCA 对照者使用了 PPI,与未使用 PPI 的患者相比,当前使用 PPI 与 OHCA 发生几率增加有关(OR:1.32 [95%-CI:1.28-1.37]),而过去使用 PPI 不会增加 OHCA 发生几率(OR:1.01 [95%-CI:0.98-1.04])。OHCA几率的增加在男女两性中均有发生。最后,当我们对无登记缺血性心脏病(OR:1.36 [95%-CI:1.31-1.41])、无心力衰竭(OR:1.33 [95%-CI:1.29-1.38])或无任何心血管合并症(OR:1.84 [95%-CI:1.70-2.00])的个体重复进行分析时,OR 值仍然升高。此外,以 H2-拮抗剂作为参照组时,OR 值仍然升高(OR:1.28 [95%-CI:1.11-1.47]):结论:在普通人群中,使用 PPI 与 OHCA 风险增加有关。考虑到 PPIs 的广泛使用,本研究引起了人们的关注,需要提高人们的认识,以平衡治疗的益处和风险。
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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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