Department of Cardiovascular and Thoracic Sciences, Fondazione Policlinico Universitario A Gemelli IRCCS, Catholic University of the Sacred Heart, Rome, Italy; Division of Cardiology, University of Florida College of Medicine, Jacksonville, FL, USA.
Department of Internal Medicine and Medical Specialties (DIMI) Chair of Cardiovascular Diseases, University of Genoa, Genoa, Italy.
Lancet. 2021 Apr 17;397(10283):1470-1483. doi: 10.1016/S0140-6736(21)00533-X.
Whether guided selection of antiplatelet therapy in patients undergoing percutaneous coronary intervention (PCI) is effective in improving outcomes compared with standard antiplatelet therapy remains controversial. We assessed the safety and efficacy of guided versus standard selection of antiplatelet therapy in patients undergoing PCI.
For this systematic review and meta-analysis, from Aug 20 to Oct 25, 2020, we searched MEDLINE (via PubMed), Cochrane, Embase, and Web of Science databases for randomised controlled trials and observational studies published in any language that compared guided antiplatelet therapy, by means of platelet function testing or genetic testing, versus standard antiplatelet therapy in patients undergoing PCI. Two reviewers independently assessed study eligibility, extracted the data, and assessed risk of bias. Risk ratios (RRs) and 95% CIs were used with random-effects or fixed-effect models according to the estimated heterogeneity among studies assessed by the I index. Coprimary endpoints were trial-defined primary major adverse cardiovascular events and any bleeding. Key secondary endpoints were all-cause death, cardiovascular death, myocardial infarction, stroke, definite or probable stent thrombosis, and major and minor bleeding. This study is registered with PROSPERO (CRD42021215901).
3656 potentially relevant articles were screened. Our analysis included 11 randomised controlled trials and three observational studies with data for 20 743 patients. Compared with standard therapy, guided selection of antiplatelet therapy was associated with a reduction in major adverse cardiovascular events (RR 0·78, 95% CI 0·63-0·95, p=0·015) and reduced bleeding, although not statistically significant (RR 0·88, 0·77-1·01, p=0·069). Cardiovascular death (RR 0·77, 95% CI 0·59-1·00, p=0·049), myocardial infarction (RR 0·76, 0·60-0·96, p=0·021), stent thrombosis (RR 0·64, 0·46-0·89, p=0·011), stroke (RR 0·66, 0·48-0·91, p=0·010), and minor bleeding (RR 0·78, 0·67-0·92, p=0·0030) were reduced with guided therapy compared with standard therapy. Risks of all-cause death and major bleeding did not differ between guided and standard approaches. Outcomes varied according to the strategy used, with an escalation approach associated with a significant reduction in ischaemic events without any trade-off in safety, and a de-escalation approach associated with a significant reduction in bleeding, without any trade-off in efficacy.
Guided selection of antiplatelet therapy improved both composite and individual efficacy outcomes with a favourable safety profile, driven by a reduction in minor bleeding, supporting the use of platelet function or genetic testing to optimise the choice of agent in patients undergoing PCI.
None.
经皮冠状动脉介入治疗(PCI)患者中,与标准抗血小板治疗相比,抗血小板治疗的有指导选择是否能改善结局仍存在争议。我们评估了 PCI 患者中抗血小板治疗有指导选择与标准选择的安全性和疗效。
在本次系统评价和荟萃分析中,我们于 2020 年 8 月 20 日至 10 月 25 日,通过 MEDLINE(通过 PubMed)、Cochrane、Embase 和 Web of Science 数据库,以任何语言检索了比较有指导的抗血小板治疗(通过血小板功能检测或基因检测)与标准抗血小板治疗的随机对照试验和观察性研究,这些研究纳入了行 PCI 的患者。两位评审员独立评估了研究的纳入标准、提取了数据,并评估了偏倚风险。根据 I 指数评估的研究间异质性,采用随机效应或固定效应模型计算风险比(RR)和 95%置信区间。主要复合终点为试验定义的主要不良心血管事件和任何出血。关键次要终点为全因死亡、心血管死亡、心肌梗死、卒中和确定或可能的支架血栓形成以及大出血和小出血。本研究已在 PROSPERO(CRD42021215901)上注册。
筛选出了 3656 篇可能相关的文章。我们的分析纳入了 11 项随机对照试验和 3 项观察性研究,共纳入了 20743 例患者的数据。与标准治疗相比,抗血小板治疗的有指导选择与主要不良心血管事件减少相关(RR 0·78,95%CI 0·63-0·95,p=0·015),且出血减少,但无统计学意义(RR 0·88,0·77-1·01,p=0·069)。心血管死亡(RR 0·77,95%CI 0·59-1·00,p=0·049)、心肌梗死(RR 0·76,95%CI 0·60-0·96,p=0·021)、支架血栓形成(RR 0·64,95%CI 0·46-0·89,p=0·011)、卒中和(RR 0·66,95%CI 0·48-0·91,p=0·010)和小出血(RR 0·78,0·67-0·92,p=0·0030)减少与标准治疗相比,抗血小板治疗的有指导选择。有指导和标准治疗的全因死亡和大出血风险无差异。根据所使用的策略,结果存在差异,强化策略可显著降低缺血性事件,且不影响安全性,而降级策略可显著减少出血,且不影响疗效。
抗血小板治疗的有指导选择改善了复合和单个疗效结局,且具有良好的安全性,这主要归因于轻微出血减少,支持使用血小板功能或基因检测来优化行 PCI 患者的药物选择。
无。