Westman Peter C, Lipinski Michael J, Torguson Rebecca, Waksman Ron
MedStar Heart and Vascular Institute, MedStar Washington Hospital Center, Washington, DC.
MedStar Heart and Vascular Institute, MedStar Washington Hospital Center, Washington, DC.
Cardiovasc Revasc Med. 2017 Mar;18(2):79-85. doi: 10.1016/j.carrev.2016.10.005. Epub 2016 Oct 21.
Newer P2Y12 inhibitors have more rapid onset of platelet inhibition compared with clopidogrel, especially the intravenous P2Y12 inhibitor cangrelor. Direct comparisons between cangrelor and oral P2Y12 inhibitors ticagrelor and prasugrel do not exist. Thus, we performed a network meta-analysis to directly and indirectly compare different P2Y12 inhibitors in patients undergoing percutaneous coronary intervention (PCI).
MEDLINE/PubMed and ClinicalTrials.gov were searched for randomized controlled trials (RCTs) that compared at least two P2Y12 inhibitors including cangrelor, clopidogrel, prasugrel, and ticagrelor. Network meta-analysis with a Bayesian approach was performed to directly and indirectly compare the effects of the aforementioned P2Y12 inhibitors on clinical outcomes. Odds ratios with credible intervals (OR [CrIs]) were generated with random-effects models to compare outcomes.
This analysis included 15 RCTs with 54,025 patients randomized to cangrelor (n=12,475), clopidogrel (n=26,903), prasugrel (n=7455), or ticagrelor (n=7192) at time of PCI. Patients had a mean age of 63±10, 74% were male, and 82% underwent PCI for acute coronary syndrome. No significant differences between cangrelor and clopidogrel were found with respect to cardiovascular death (OR 1.01 [CrI 0.23-4.39]), myocardial infarction (OR 0.94 [CrI 0.69-1.25]), major adverse cardiac events (OR 0.91 [CrI 0.69-1.18]), stent thrombosis (OR 0.66 [CrI 0.37-1.19]), or major bleeding (OR 1.52 [CrI 0.79-2.98]). Rank probability data suggested that ticagrelor and prasugrel were better than cangrelor for reducing ischemic events, though these differences were not significant.
Despite rapid platelet inhibition provided by cangrelor, newer oral P2Y12 inhibitors such as ticagrelor and prasugrel have comparable clinical outcomes.
与氯吡格雷相比,新型P2Y12抑制剂对血小板的抑制起效更快,尤其是静脉用P2Y12抑制剂坎格雷洛。坎格雷洛与口服P2Y12抑制剂替格瑞洛和普拉格雷之间尚无直接比较。因此,我们进行了一项网状Meta分析,以直接和间接比较经皮冠状动脉介入治疗(PCI)患者中不同P2Y12抑制剂的效果。
检索MEDLINE/PubMed和ClinicalTrials.gov,查找比较至少两种P2Y12抑制剂(包括坎格雷洛、氯吡格雷、普拉格雷和替格瑞洛)的随机对照试验(RCT)。采用贝叶斯方法进行网状Meta分析,以直接和间接比较上述P2Y12抑制剂对临床结局的影响。采用随机效应模型生成具有可信区间的比值比(OR[CrIs])来比较结局。
该分析纳入了15项RCT,共54025例患者在PCI时被随机分配至坎格雷洛组(n = 12475)、氯吡格雷组(n = 26903)、普拉格雷组(n = 7455)或替格瑞洛组(n = 7192)。患者的平均年龄为63±10岁,74%为男性,82%因急性冠状动脉综合征接受PCI。在心血管死亡(OR 1.01[CrI 0.23 - 4.39])、心肌梗死(OR 0.94[CrI 0.69 - 1.25])、主要不良心脏事件(OR 0.91[CrI 0.69 - 1.18])、支架血栓形成(OR 0.66[CrI 0.37 - 1.19])或大出血(OR 1.52[CrI 0.79 - 2.98])方面,未发现坎格雷洛与氯吡格雷之间存在显著差异。排序概率数据表明,在减少缺血事件方面,替格瑞洛和普拉格雷优于坎格雷洛,尽管这些差异并不显著。
尽管坎格雷洛能迅速抑制血小板,但替格瑞洛和普拉格雷等新型口服P2Y12抑制剂具有相当的临床结局。