Suppr超能文献

比较接受经皮冠状动脉介入治疗的年轻人群中普拉格雷和氯吡格雷的安全性和有效性:使用日本索赔数据库的回顾性研究。

A comparison of the safety and effectiveness of prasugrel and clopidogrel in younger population undergoing percutaneous coronary intervention: A retrospective study using a Japanese claims database.

机构信息

Department of Medical Innovation, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan; Clinical Research Management Center, Nagoya City University Hospital, Nagoya, Japan.

Clinical Research Management Center, Nagoya City University Hospital, Nagoya, Japan; Core Laboratory, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

出版信息

J Cardiol. 2021 Mar;77(3):285-291. doi: 10.1016/j.jjcc.2020.10.001. Epub 2020 Oct 21.

Abstract

BACKGROUND

Prasugrel inhibits platelet aggregation more potently than clopidogrel. In the global phase III trial, prasugrel [loading dose/maintenance dose (LD/MD), 60/10 mg] reduced the incidence of ischemic events but involved a higher risk of hemorrhage than clopidogrel in patients with acute coronary syndromes who were scheduled to undergo percutaneous coronary intervention (PCI). In the Japanese phase III trial for similar patients wherein the prasugrel dose regimen was adjusted (LD/MD, 20/3.75 mg), the efficacy of prasugrel and clopidogrel were comparable to that in the global trial; however, the safety could not be determined due to limited power. Given the strict enrollment criteria, the results of the Japanese phase III trial may not be applicable to routine clinical practice. We compared the safety and effectiveness of prasugrel and clopidogrel in the real-world setting in Japanese patients.

METHODS

With an analysis of a large claims database prepared during the post-marketing stages in Japan, we identified patients undergoing PCI and compared the incidence of bleeding and ischemic coronary events between patients who received prasugrel and those receiving clopidogrel.

RESULTS

Between January 1, 2014 and December 31, 2018, we identified 1977 patients who were scheduled to undergo urgent PCI (urgent PCI cohort) and 1922 who were scheduled to undergo elective PCI (elective PCI cohort). After propensity-score matching, there were no significant differences in the baseline clinical characteristics of the prasugrel and clopidogrel groups in the urgent (n = 1080) and elective PCI (n = 1626) cohorts. In Cox proportional hazard analyses, there were no significant differences in the incidence of bleeding or ischemic coronary events during the median 8-month follow-up in both cohorts.

CONCLUSIONS

The safety and effectiveness of prasugrel was comparable to that of clopidogrel in real-world Japanese patients scheduled to undergo PCI.

摘要

背景

普拉格雷比氯吡格雷更能抑制血小板聚集。在全球三期临床试验中,普拉格雷[负荷剂量/维持剂量(LD/MD),60/10mg]降低了急性冠状动脉综合征患者行经皮冠状动脉介入治疗(PCI)的缺血事件发生率,但出血风险高于氯吡格雷。在类似患者的日本三期临床试验中,普拉格雷剂量方案进行了调整(LD/MD,20/3.75mg),普拉格雷和氯吡格雷的疗效与全球试验相当;然而,由于效力有限,安全性无法确定。鉴于严格的入组标准,日本三期临床试验的结果可能不适用于常规临床实践。我们比较了日本患者真实世界中普拉格雷和氯吡格雷的安全性和有效性。

方法

利用日本上市后阶段准备的大型理赔数据库进行分析,我们确定了接受 PCI 的患者,并比较了接受普拉格雷和氯吡格雷治疗的患者出血和缺血性冠状动脉事件的发生率。

结果

2014 年 1 月 1 日至 2018 年 12 月 31 日,我们确定了 1977 例计划行紧急 PCI 的患者(紧急 PCI 队列)和 1922 例计划行择期 PCI 的患者(择期 PCI 队列)。经倾向评分匹配后,紧急(n=1080)和择期 PCI(n=1626)队列中普拉格雷和氯吡格雷组的基线临床特征无显著差异。在 Cox 比例风险分析中,在中位 8 个月的随访期间,两组均未发生出血或缺血性冠状动脉事件。

结论

在计划接受 PCI 的日本真实世界患者中,普拉格雷的安全性和有效性与氯吡格雷相当。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验