Sex-Based Outcomes of Dual-Antiplatelet Therapy After Percutaneous Coronary Intervention: A Pairwise and Network Meta-Analysis.

IF 13 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Drugs Pub Date : 2024-06-01 Epub Date: 2024-05-29 DOI:10.1007/s40265-024-02034-3
Thomas A Agbaedeng, Jean Jacques Noubiap, Kirsty A Roberts, Derek P Chew, Peter J Psaltis, Azmeraw T Amare
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引用次数: 0

Abstract

Background: Although dual antiplatelet therapy (DAPT) improves the outcomes of patients undergoing percutaneous coronary intervention (PCI), sex-specific differences in efficacy and safety of DAPT remain unresolved. We compared sex differences for DAPT outcomes and DAPT durations (1-3 months [short-term], 6 months [mid-term], and >12 months [extended] vs. 12 months).

Methods: We searched databases through 31 December 2023 for trials reporting DAPT after PCI. The endpoints were major adverse cardiovascular and cerebrovascular events (MACCE), net adverse clinical and cerebrovascular events (NACCE), and any bleeding. Extracted data were pooled in a frequentist network and pairwise, random-effects meta-analysis.

Results: Twenty-two trials (99,591 participants, 25.2% female) were included. Female sex was significantly associated with a higher 1-year MACCE risk (hazard ratio 1.14 [95% confidence interval 1.02-1.28]) and bleeding (1.13 [1.00-1.28]), but not NACCE (1.12 [0.96-1.31]). In sub-analyses, the association between female sex and MACCE was related to use of clopidogrel as the second antiplatelet agent (1.11 [1.03-1.20]), whereas higher bleeding events were related to newer P2Y12 inhibitors (P2Y12i) (1.58 [1.01-2.46]). For DAPT duration, short-term DAPT followed by P2Y12i monotherapy was non-inferior for MACCE in females and males (0.95 [95% CI 0.83-1.10; and 0.96 [0.80-1.16]) but tended to be superior in males for NACCE versus 12-month DAPT (0.96 [0.91-1.01]); mid-term DAPT tended to be associated with a lower bleeding risk in males (0.43 [0.17-1.09]).

Conclusions: Female sex is associated with higher MACCE and bleeding when newer P2Y12i agents are used. Short-term DAPT followed by P2Y12i monotherapy is safe and effective in both sexes undergoing PCI.

Clinical trials registration: PROSPERO ID: CRD42021278663.

Abstract Image

经皮冠状动脉介入术后基于性别的双抗血小板疗法结果:配对和网络 Meta 分析
背景:尽管双联抗血小板疗法(DAPT)可改善经皮冠状动脉介入治疗(PCI)患者的预后,但DAPT在疗效和安全性方面的性别差异仍未得到解决。我们比较了DAPT疗效和DAPT持续时间(1-3个月[短期]、6个月[中期]、>12个月[延长]与12个月)的性别差异:方法:我们检索了截至 2023 年 12 月 31 日的数据库,以查找报告 PCI 后 DAPT 的试验。终点为主要不良心脑血管事件(MACCE)、净不良临床和脑血管事件(NACCE)以及任何出血。提取的数据通过频数网络和配对随机效应荟萃分析进行汇总:共纳入 22 项试验(99,591 名参与者,25.2% 为女性)。女性性别与较高的 1 年 MACCE 风险(危险比 1.14 [95% 置信区间 1.02-1.28])和出血(1.13 [1.00-1.28])明显相关,但与 NACCE(1.12 [0.96-1.31])无关。在子分析中,女性性别与MACCE之间的关系与使用氯吡格雷作为第二种抗血小板药物有关(1.11 [1.03-1.20]),而较高的出血事件与较新的P2Y12抑制剂(P2Y12i)有关(1.58 [1.01-2.46])。就DAPT持续时间而言,短期DAPT后P2Y12i单药治疗对女性和男性的MACCE无劣效(0.95 [95% CI 0.83-1.10;0.96 [0.80-1.16]),但对男性而言,NACCE往往优于12个月的DAPT(0.96 [0.91-1.01]);中期DAPT往往与男性较低的出血风险有关(0.43 [0.17-1.09]):结论:使用新型 P2Y12i 药物时,女性与较高的 MACCE 和出血相关。临床试验注册:临床试验注册:PROSPERO ID:CRD42021278663。
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来源期刊
Drugs
Drugs 医学-毒理学
CiteScore
22.70
自引率
0.90%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Drugs is a journal that aims to enhance pharmacotherapy by publishing review and original research articles on key aspects of clinical pharmacology and therapeutics. The journal includes: Leading/current opinion articles providing an overview of contentious or emerging issues. Definitive reviews of drugs and drug classes, and their place in disease management. Therapy in Practice articles including recommendations for specific clinical situations. High-quality, well designed, original clinical research. Adis Drug Evaluations reviewing the properties and place in therapy of both newer and established drugs. AdisInsight Reports summarising development at first global approval. Moreover, the journal offers additional digital features such as animated abstracts, video abstracts, instructional videos, and podcasts to increase visibility and educational value. Plain language summaries accompany articles to assist readers with some knowledge of the field in understanding important medical advances.
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