Serum potassium is a critical risk factor for cardiac arrhythmias in acute heart failure patients treated with levosimendan: A retrospective study in a cohort of 250 patients.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Wenguang Liu, Xiaowu Wang, Dong Wu, Zhen Ma, Bin Ning
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Abstract

Objectives: This study aimed to investigate the risk factors associated with developing cardiac arrhythmias in patients with acute heart failure treated with levosimendan.

Materials and methods: A retrospective analysis was conducted in patients diagnosed with acute heart failure or acute exacerbation of chronic heart failure treated with levosimendan. The patients were divided into arrhythmia and non-arrhythmia groups based on the presence of rapid-type arrhythmias. Logistic regression analysis was used to identify independent risk factors for levosimendan-induced arrhythmias.

Results: Among the 250 patients, 49 (19.60%) experienced nine types of cardiac arrhythmias, the most common being atrial fibrillation (28.57%). The highest incidence of arrhythmias occurred within 48 hours of levosimendan infusion (77.6%). Multivariate analysis indicated that the lowest serum potassium concentration within 5 days after drug administration (odds ratio (OR) 0.410, p = 0.010, 95% confidence interval (CI) 0.209 - 0.805), micro-pump speed of > 0.2 μg/kg/min (OR 3.106, p = 0.039, 95% CI 1.584 - 11.789), and concomitant use of drugs that prolong the QT interval (OR 4.226, p = 0.001, 95% CI 1.850 - 9.657) were independent risk factors for levosimendan-induced arrhythmias. The incidence of arrhythmias increased when the lowest serum potassium concentration within 5 days after drug administration was below 3.94 mmol/L.

Conclusion: This study identified risk factors associated with levosimendan-induced arrhythmias. Clinicians should monitor at-risk patients when administering levosimendan. When using levosimendan in clinical practice, it is necessary to maintain a serum potassium concentration above 3.94 mmol/L.

血清钾是左西孟旦治疗急性心力衰竭患者心律失常的关键危险因素:一项250例患者的回顾性研究。
目的:本研究旨在探讨左西孟旦治疗急性心力衰竭患者发生心律失常的相关危险因素。材料和方法:回顾性分析诊断为急性心力衰竭或慢性心力衰竭急性加重的患者使用左西孟旦治疗。根据有无快速型心律失常分为心律失常组和非心律失常组。采用Logistic回归分析确定左西孟旦诱发心律失常的独立危险因素。结果:250例患者中,49例(19.60%)发生9种心律失常,以房颤(28.57%)最为常见。左西孟旦输注48小时内心律失常发生率最高(77.6%)。多因素分析显示,给药后5 d内最低血钾浓度(比值比(OR) 0.410, p = 0.010, 95%可信区间(CI) 0.209 ~ 0.805)、微泵速度>.2 μg/kg/min (OR 3.106, p = 0.039, 95% CI 1.584 ~ 11.789)、同时使用延长QT间期的药物(OR 4.226, p = 0.001, 95% CI 1.850 ~ 9.657)是左西门丹诱发心律不整的独立危险因素。当给药后5 d内最低血钾浓度低于3.94 mmol/L时,心律失常发生率增高。结论:本研究确定了左西孟旦诱发心律失常的相关危险因素。临床医生在使用左西孟旦时应监测高危患者。在临床上使用左西孟旦时,需要维持血清钾浓度在3.94 mmol/L以上。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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