Wu Yang, Bi Wen-Tao, Qu Li-Ping, Fan Jun, Kong Xiang-Jun, Ji Cheng-Cheng, Chen Xu-Miao, Yao Feng-Juan, Liu Li-Juan, Cheng Yun-Jiu, Wu Su-Hua
Department of Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
NHC Key Laboratory of Assisted Circulation, Sun Yat-sen University, Guangzhou, China.
Front Cardiovasc Med. 2023 Feb 23;10:1117254. doi: 10.3389/fcvm.2023.1117254. eCollection 2023.
The increased risk of cardiovascular events in patients prescribed macrolides has been subject to debate for decades.
Medline, EMBASE databases and ClinicalTrials.gov were searched from inception until August 31, 2022 for studies investigating the link between macrolides and cardiovascular risk. A meta-analysis was performed using a random-effects model.
A total of 80 studies involving 39,374,874 patients were included. No association was found between macrolides and all-cause death. However, compared with the non-macrolide group, macrolides were associated with a significantly increased risk of ventricular arrhythmia or sudden cardiac death (VA or SCD) (azithromycin, relative ratio [RR]: 1.53; 95% confidence interval [CI]: 1.19 to 1.97; clarithromycin, RR: 1.52; 95% CI: 1.07 to 2.16). Besides, administration of macrolides was associated with a higher risk of cardiovascular disease (CVD) death (azithromycin, RR: 1.63; 95% CI: 1.17 to 2.27) and a slightly increased risk of myocardial infarction (MI) (azithromycin, RR: 1.08; 95% CI: 1.02 to 1.15). Interestingly, no association was observed between roxithromycin and adverse cardiac outcomes. Increased risk of VA or SCD was observed for recent or current use of macrolides, MI for former use, and CVD death for current use.
Administration of macrolide antibiotics and timing of macrolide use are associated with increased risk for SCD or VTA and cardiovascular death, but not all-cause death.
几十年来,服用大环内酯类药物的患者心血管事件风险增加一直存在争议。
检索Medline、EMBASE数据库和ClinicalTrials.gov,检索时间从建库至2022年8月31日,以查找研究大环内酯类药物与心血管风险之间联系的研究。使用随机效应模型进行荟萃分析。
共纳入80项研究,涉及39374874例患者。未发现大环内酯类药物与全因死亡之间存在关联。然而,与非大环内酯类药物组相比,大环内酯类药物与室性心律失常或心源性猝死(VA或SCD)风险显著增加相关(阿奇霉素,相对比率[RR]:1.53;95%置信区间[CI]:1.19至1.97;克拉霉素,RR:1.52;95%CI:1.07至2.16)。此外,服用大环内酯类药物与心血管疾病(CVD)死亡风险较高相关(阿奇霉素,RR:1.63;95%CI:1.17至2.27),与心肌梗死(MI)风险略有增加相关(阿奇霉素,RR:1.08;95%CI:1.02至1.15)。有趣的是,未观察到罗红霉素与不良心脏结局之间存在关联。近期或当前使用大环内酯类药物会增加VA或SCD风险,既往使用会增加MI风险,当前使用会增加CVD死亡风险。
服用大环内酯类抗生素及大环内酯类药物的使用时机与SCD或VTA风险及心血管死亡风险增加相关,但与全因死亡无关。