Su Hu, Li Menghuan, Hao Lijun, Wang Hui
Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 210000 Nanjing, Jiangsu, China.
Department of Cardiology, Sir Run Run Hospital, Nanjing Medical University, 210000 Nanjing, Jiangsu, China.
Rev Cardiovasc Med. 2022 May 31;23(6):203. doi: 10.31083/j.rcm2306203. eCollection 2022 Jun.
The most optimal strategy for ST-segment elevation myocardial infarction (STEMI) between drug-eluting stents (DES) and drug-coated balloons (DEB) is still unknown. This meta-analysis aims to compare the short-term outcomes of both methods in patients with STEMI.
We searched PubMed, Web of Science, EMBASE, and the Cochrane Library Databases for eligible studies with publication data from 2015 to Jan 2022. Four trials with 360 patients were included. The study was conducted by following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statements.
There were no significant differences in major adverse cardiac events between DCB and DES during 6 to 12 months of follow-up (RR 1.38, 95% CI: 0.65 to 2.93; = 0.41). Similar risks of myocardial infarction (RR 0.48, 95% CI: 0.11 to 2.11, = 0.33), all causes of death (RR 1.55, 95% CI: 0.32 to 7.62, = 0.59), and target lesion revascularization (RR 1.29, 95% CI: 0.55 to 3.04, = 0.55) were observed. The pooled results indicated that DCB was comparable to DES in terms of late lumen loss with a mean difference (MD) of -0.06 mm with significant heterogeneity (95% CI: -0.25 to 0.13, = 0.54, = 85%). Subsequent subgroup analysis based on the study design revealed that late lumen loss was significantly lower in the drug-coated balloon group in randomized controlled trials (MD -0.16, 95% CI: -0.26 to -0.05, = 0.003).
Drug-coated balloons were associated with similar risks of MACE compared with drug-eluting stents in the setting of STEMI. However, a larger randomized controlled trial is required to confirm these observations.
药物洗脱支架(DES)与药物涂层球囊(DEB)治疗ST段抬高型心肌梗死(STEMI)的最佳策略仍不明确。本荟萃分析旨在比较这两种方法在STEMI患者中的短期疗效。
我们在PubMed、Web of Science、EMBASE和Cochrane图书馆数据库中检索了2015年至2022年1月有发表数据的符合条件的研究。纳入了四项试验,共360例患者。本研究按照系统评价和荟萃分析的首选报告项目声明的指南进行。
在6至12个月的随访期间,药物涂层球囊(DCB)与药物洗脱支架(DES)在主要不良心脏事件方面无显著差异(风险比[RR]1.38,95%置信区间[CI]:0.65至2.93;P = 0.41)。观察到心肌梗死(RR 0.48,95% CI:0.11至2.11,P = 0.33)、全因死亡(RR 1.55,95% CI:0.32至7.62,P = 0.59)和靶病变血运重建(RR 1.29,95% CI:0.55至3.04,P = 0.55)的风险相似。汇总结果表明,DCB在晚期管腔丢失方面与DES相当,平均差值(MD)为-0.06 mm,具有显著异质性(95% CI:-0.25至0.13,P = 0.54,I² = 85%)。基于研究设计的后续亚组分析显示,在随机对照试验中,药物涂层球囊组的晚期管腔丢失显著更低(MD -0.16, 95% CI: -0.26至-0.05, P = 0.003)。
在STEMI患者中,与药物洗脱支架相比,药物涂层球囊发生主要不良心血管事件的风险相似。然而,需要更大规模的随机对照试验来证实这些观察结果。