缺血性心脏病双联抗血小板治疗最佳时长:随机对照试验的系统评价与网状Meta分析
结果显示1个月DAPT的净不良临床事件(NACE)风险显著低于其他时长,出血风险亦显著低于12个月及>12个月DAPT,但心肌梗死风险高于>12个月DAPT。结论提示1个月DAPT可能提供最优的缺血与出血风险平衡,需个体化应用。
要点
- 1个月DAPT的NACE风险显著低于3、6、12及>12个月DAPT。
- 1个月DAPT出血风险显著低于12个月和>12个月DAPT。
- 1个月DAPT心肌梗死风险高于>12个月DAPT,需个体化权衡。
核心结论
- 1个月DAPT可能提供缺血与出血风险间最低的净风险平衡。
- 研究结果应在个体化、患者特异性风险管理框架内应用。
研究设计与样本
- 系统评价与网状Meta分析,检索Medline、Scopus和Cochrane Library的随机对照试验。
- 比较1个月、3个月、6个月、12个月和>12个月五种DAPT时长。
- 主要结局为NACE,即死亡、心肌梗死、卒中、支架血栓和出血事件的复合终点。
主要发现
- 1个月DAPT的NACE风险显著低于3个月DAPT(RR 0.74,95%CI 0.58-0.93)。
- 1个月DAPT的NACE风险显著低于6个月DAPT(RR 0.63,95%CI 0.50-0.80)。
- 1个月DAPT的NACE风险显著低于12个月DAPT(RR 0.64,95%CI 0.53-0.78)。
- 1个月DAPT的NACE风险显著低于>12个月DAPT(RR 0.67,95%CI 0.51-0.87)。
- 1个月DAPT出血风险显著低于12个月DAPT(RR 0.57,95%CI 0.40-0.83)和>12个月DAPT(RR 0.47,95%CI 0.29-0.77)。
关键数值与推荐
- 1个月DAPT相比>12个月DAPT心肌梗死风险更高(RR 1.53,95%CI 1.02-2.30)。
- 死亡、心肌梗死、卒中或支架血栓在1个月DAPT与其他时长间无显著差异(心肌梗死与>12个月比较除外)。
- NACE的SUCRA值:1个月为99.8,3个月为65.4,6个月为24.6,12个月为21.9,>12个月为38.3。
临床怎么用
- 对于缺血性心脏病患者,可考虑1个月DAPT以降低NACE和出血风险。
- 需结合患者个体缺血与出血风险,尤其关注心肌梗死风险可能升高的情况。
以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。
原文
BACKGROUND: Shorter dual antiplatelet therapy (DAPT) regimens may offer a more favourable risk-benefit profile compared with longer treatment. The aim of this study was to determine the optimal duration by assessing net adverse clinical events (NACE). METHODS: We searched for randomised controlled trials that compared clinical outcomes of different DAPT durations in patients with ischaemic heart disease from Medline, Scopus and the Cochrane Library. A network meta-analysis was subsequently conducted for DAPT durations of 1 month, 3 months, 6 months, 12 months and >12 months. The primary outcome was defined as NACE, a composite of death, myocardial infarction, stroke, stent thrombosis and bleeding events. Individual components of NACE served as secondary outcomes. Five DAPT durations were ranked for each outcome using surface under the cumulative ranking. RESULTS: This analysis included 31 randomised controlled trials comprising 95 910 patients. 1-month DAPT was associated with a significantly lower risk of NACE compared with 3-month, 6-month, 12-month and >12 month DAPT (risk ratio (CI): 0.74 (0.58 to 0.93); 0.63 (0.50 to 0.80); 0.64 (0.53 to 0.78); and 0.67 (0.51 to 0.87), respectively). There were no significant differences in death, myocardial infarction, stroke or stent thrombosis with 1-month DAPT, except for a higher risk of myocardial infarction compared with >12 month DAPT (risk ratio (CI): 1.53 (1.02 to 2.30)). Notably, 1-month DAPT was associated with a significantly lower risk of bleeding events compared with 12-month and >12 month DAPT (risk ratio (CI): 0.57 (0.40 to 0.83) and 0.47 (0.29 to 0.77), respectively). The SUCRA value for NACE was the highest for the 1-month regimen (99.8, 65.4, 24.6, 21.9 and 38.3 for 1 month, 3 months, 6 months, 12 months and >12 months, respectively). CONCLUSIONS: 1-month DAPT may offer the lowest risk balance between ischaemic and bleeding risks; however, these findings should be applied within an individualised, patient-specific risk management framework.
引用
- Fujii T, Kasai S, Kawamura Y, et al. Optimal duration of dual antiplatelet therapy in ischaemic heart disease: a systematic review and network meta-analysis of randomised controlled trials. Heart. 2026. PMID: 42225402. doi:10.1136/heartjnl-2025-327720
供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。