Richard A. and Susan F. Smith Center for Outcomes Research in Cardiology, Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston MA (N.M,B., H.T., J.B.S., Y.S., C.S., E.A.S., C.M.G., R.W.Y.).
Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston (N.M.B.).
Circulation. 2022 Jan 11;145(2):97-106. doi: 10.1161/CIRCULATIONAHA.121.056878. Epub 2021 Nov 8.
Differences in patient characteristics, changes in treatment algorithms, and advances in medical technology could each influence the applicability of older randomized trial results to contemporary clinical practice. The DAPT Study (Dual Antiplatelet Therapy) found that longer-duration DAPT decreased ischemic events at the expense of greater bleeding, but subsequent evolution in stent technology and clinical practice may attenuate the benefit of prolonged DAPT in a contemporary population. We evaluated whether the DAPT Study population is different from a contemporary population of US patients receiving percutaneous coronary intervention and estimated the treatment effect of extended-duration antiplatelet therapy after percutaneous coronary intervention in this more contemporary cohort.
We compared the characteristics of drug-eluting stent-treated patients randomly assigned in the DAPT Study to a sample of more contemporary drug-eluting stent-treated patients in the National Cardiovascular Data Registry CathPCI Registry from July 2016 to June 2017. After linking trial and registry data, we used inverse-odds of trial participation weighting to account for patient and procedural characteristics and estimated a contemporary real-world treatment effect of 30 versus 12 months of DAPT after coronary stent procedures.
The US drug-eluting stent-treated trial cohort included 8864 DAPT Study patients, and the registry cohort included 568 540 patients. Compared with the trial population, registry patients had more comorbidities and were more likely to present with myocardial infarction and receive 2nd-generation drug-eluting stents. After reweighting trial results to represent the registry population, there was no longer a significant effect of prolonged DAPT on reducing stent thrombosis (reweighted treatment effect: -0.40 [95% CI, -0.99% to 0.15%]), major adverse cardiac and cerebrovascular events (reweighted treatment effect, -0.52 [95% CI, -2.62% to 1.03%]), or myocardial infarction (reweighted treatment effect, -0.97% [95% CI, -2.75% to 0.18%]), but the increase in bleeding with prolonged DAPT persisted (reweighted treatment effect, 2.42% [95% CI, 0.79% to 3.91%]).
The differences between the patients and devices used in contemporary clinical practice compared with the DAPT Study were associated with the attenuation of benefits and greater harms attributable to prolonged DAPT duration. These findings limit the applicability of the average treatment effects from the DAPT Study in modern clinical practice.
患者特征的差异、治疗方案的变化和医疗技术的进步都可能影响到旧的随机试验结果在当代临床实践中的适用性。DAPT 研究(双联抗血小板治疗)发现,延长 DAPT 时间可降低缺血事件的发生率,但代价是出血增加,但随后支架技术和临床实践的发展可能会削弱延长 DAPT 在当代人群中的获益。我们评估了 DAPT 研究人群与接受经皮冠状动脉介入治疗的当代美国患者人群是否存在差异,并估计了在这个更现代的队列中,经皮冠状动脉介入治疗后延长抗血小板治疗的疗效。
我们比较了 DAPT 研究中接受药物洗脱支架治疗的患者与 2016 年 7 月至 2017 年 6 月国家心血管数据注册中心 CathPCI 注册中心中接受药物洗脱支架治疗的更现代的患者样本的特征。在将试验和注册数据链接后,我们使用试验参与的逆概率加权来解释患者和手术特征,并估计在冠状动脉支架手术后,30 个月与 12 个月 DAPT 的实际治疗效果。
美国接受药物洗脱支架治疗的试验队列包括 8864 名 DAPT 研究患者,注册队列包括 568540 名患者。与试验人群相比,登记人群的合并症更多,更有可能因心肌梗死就诊,并接受第二代药物洗脱支架治疗。对试验结果进行重新加权以代表登记人群后,延长 DAPT 对降低支架血栓形成的影响不再显著(重新加权的治疗效果为-0.40[95%CI,-0.99%至 0.15%])、主要不良心脑血管事件(重新加权的治疗效果为-0.52[95%CI,-2.62%至 1.03%])或心肌梗死(重新加权的治疗效果为-0.97%[95%CI,-2.75%至 0.18%]),但延长 DAPT 引起的出血增加仍然存在(重新加权的治疗效果为 2.42%[95%CI,0.79%至 3.91%])。
与 DAPT 研究相比,当代临床实践中患者和器械的差异与延长 DAPT 持续时间所带来的获益减少和更大的危害有关。这些发现限制了 DAPT 研究中平均治疗效果在现代临床实践中的应用。