Fan Weiguo, Liu Hualong, Shen Yang, Hong Kui
Department of Cardiovascular Medicine, the Second Affiliated Hospital of Nanchang University, NO 1 Mingde Road, Nanchang, Jiangxi, China.
Jiangxi Key Laboratory of Molecular Medicine, Nanchang, Jiangxi, China.
Cardiovasc Drugs Ther. 2024 Jun;38(3):517-525. doi: 10.1007/s10557-023-07425-4. Epub 2023 Jan 10.
Drug-induced QT interval prolongation has been reported to be related to life-threatening polymorphic ventricular tachycardia (torsade de pointes). Proton pump inhibitors (PPIs) are prescribed widely for hospitalized patients; the QT interval prolongation and torsade de pointes caused by PPIs were reported. We conducted a study to determine the association between PPI treatment and QT interval prolongation in critically ill patients.
This study included patients with electrocardiography (ECG) reports from the Medical Information Mart for Intensive Care III database (MIMIC-III). Patients younger than 18 years, missing baseline laboratories and with QT interval prolongation before intensive care unit (ICU) admission were excluded. The end point was the diagnosis of QT interval prolongation reported by ECG.
This study included 24,512 ICU patients. Of them, 11,327 patients were treated with PPIs, 4181 with histamine 2 receptor antagonists (HRAs) and 6351 without acid suppression therapy (non-AST); the incidence of QT interval prolongation were 8.5%, 3.3% and 3.4% respectively. After adjustment for demographics, electrolytes, comorbidities and medications, PPIs were associated a higher risk of QT interval prolongation compared with HRAs (OR 1.66, 95% CI 1.36 - 2.03) and non-AST (OR 1.54, 95% CI 1.31 - 1.82), while there was not significant difference between HRAs and non-AST (OR 0.93, 95% CI 0.73 - 1.17). In the propensity score matching population, the results were consistent. Pantoprazole (OR 2.14, 95% CI 1.52 - 3.03) and lansoprazole (OR 1.80, 95% CI: 1.18 - 2.76) showed a higher QT prolongation risk than omeprazole. Several drugs caused higher QT prolongation risk when used in combination with PPIs.
In ICU patients, the association between PPI prescription and increased risk of QT interval prolongation was independent of known QT-prolonging factors; pantoprazole and lansoprazole had a higher risk compared with omeprazole. The combination of PPIs and other QT-prolonging drugs should be avoided.
据报道,药物引起的QT间期延长与危及生命的多形性室性心动过速(尖端扭转型室速)有关。质子泵抑制剂(PPI)在住院患者中广泛使用;有报道称PPI可导致QT间期延长和尖端扭转型室速。我们开展了一项研究,以确定PPI治疗与危重症患者QT间期延长之间的关联。
本研究纳入了来自重症监护医学信息数据库三期(MIMIC-III)且有心电图(ECG)报告的患者。排除年龄小于18岁、缺少基线实验室检查结果以及在重症监护病房(ICU)入院前有QT间期延长的患者。终点是ECG报告的QT间期延长诊断。
本研究纳入了24512例ICU患者。其中,11327例患者接受了PPI治疗,4181例接受了组胺2受体拮抗剂(HRA)治疗,6351例未接受抑酸治疗(非AST);QT间期延长的发生率分别为8.5%、3.3%和3.4%。在对人口统计学、电解质、合并症和药物进行调整后,与HRA(比值比1.66,95%置信区间1.36 - 2.03)和非AST(比值比1.54,95%置信区间1.31 - 1.82)相比,PPI与更高的QT间期延长风险相关,而HRA和非AST之间无显著差异(比值比0.93,95%置信区间0.73 - 1.17)。在倾向评分匹配人群中,结果一致。泮托拉唑(比值比2.14,95%置信区间1.52 - 3.03)和兰索拉唑(比值比1.80,95%置信区间:1.18 - 2.76)显示出比奥美拉唑更高的QT延长风险。几种药物与PPI联合使用时导致更高的QT延长风险。
在ICU患者中,PPI处方与QT间期延长风险增加之间的关联独立于已知的QT延长因素;与奥美拉唑相比,泮托拉唑和兰索拉唑风险更高。应避免PPI与其他QT延长药物联合使用。