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替卡格雷在链激酶治疗后 STE-ACS 患者中的安全性结局:一项回顾性观察研究。

Safety outcomes of ticagrelor among patients with STE-ACS post streptokinase therapy-a retrospective observational study.

机构信息

Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.

Pharmacy Department, Nakornping Hospital, Chiang Mai, Thailand.

出版信息

PLoS One. 2023 Aug 4;18(8):e0289721. doi: 10.1371/journal.pone.0289721. eCollection 2023.

Abstract

From the restriction of access to primary percutaneous coronary intervention, about 46% of patients with ST-elevation acute coronary syndrome (STE-ACS) received fibrinolytic therapy as a reperfusion strategy; streptokinase is frequently used in Thailand. Despite the guidelines recommending potent P2Y12 inhibitors among these patients, the data are limited, especially among patients with STE-ACS post streptokinase therapy. The study was proposed to describe factors for P2Y12 inhibitors selection and evaluate outcomes of pharmacoinvasively treated STE-ACS receiving ticagrelor compared with clopidogrel in Thailand. We performed a retrospective observational study of patients with STE-ACS post streptokinase therapy followed by percutaneous coronary intervention (PCI) with coronary stent placement and receiving ticagrelor or clopidogrel as P2Y12 inhibitor treatment from January 2017 to June 2021. The primary outcomes described factors for P2Y12 inhibitor selection and evaluated safety outcomes with inverse probability weight (IPW) adjustment. The secondary outcome was a composite of all-cause death, myocardial infarction and stroke. The median time from streptokinase therapy to initiating ticagrelor in the switch group was 25.7 (IQR, 1.9-4.4) hours. The factors related to switching from clopidogrel to ticagrelor included young age, history of coronary artery disease (CAD), dose of streptokinase and use of intravascular imaging. Any bleeding events occurred among 83 patients (41.71%) in the switch group and 83 patients (41.09%) in the no switch group (adjusted HR 1.04, 95% CI 0.75-1.44; p = 0.826). The composite of efficacy outcomes occurred in 6 patients in the switch group (3.02%) and 12 patients (5.94%) in the no switch group (adjusted HR 0.57, 95% CI 0.21-1.57; p = 0.279). Conclusion: In real practice, ticagrelor switching among patients with STE-ACS post streptokinase therapy did not differ regarding safety outcomes and composite of efficacy outcomes compared with clopidogrel.

摘要

从直接经皮冠状动脉介入治疗的限制来看,约有 46%的 ST 段抬高型急性冠状动脉综合征(STE-ACS)患者接受了溶栓治疗作为再灌注策略;链激酶在泰国经常使用。尽管指南建议在这些患者中使用强效 P2Y12 抑制剂,但数据有限,尤其是在接受链激酶治疗后的 STE-ACS 患者中。该研究旨在描述选择 P2Y12 抑制剂的因素,并评估在泰国接受替格瑞洛治疗的经皮冠状动脉介入治疗(PCI)后接受 STE-ACS 患者的治疗效果与氯吡格雷相比。我们对 2017 年 1 月至 2021 年 6 月接受链激酶治疗后行 PCI 并置入冠状动脉支架且接受替格瑞洛或氯吡格雷作为 P2Y12 抑制剂治疗的 STE-ACS 患者进行了回顾性观察性研究。主要结局描述了选择 P2Y12 抑制剂的因素,并通过逆概率加权(IPW)调整评估了安全性结局。次要结局是全因死亡、心肌梗死和中风的复合终点。在转换组中,从链激酶治疗开始转换为替格瑞洛的中位时间为 25.7(IQR,1.9-4.4)小时。从氯吡格雷转换为替格瑞洛的相关因素包括年龄较小、冠心病史、链激酶剂量和血管内成像的使用。在转换组的 83 例患者(41.71%)和未转换组的 83 例患者(41.09%)中均发生了任何出血事件(调整后的 HR 1.04,95%CI 0.75-1.44;p=0.826)。在转换组的 6 例患者(3.02%)和未转换组的 12 例患者(5.94%)中发生了疗效复合终点(调整后的 HR 0.57,95%CI 0.21-1.57;p=0.279)。结论:在实际实践中,与氯吡格雷相比,STE-ACS 患者接受链激酶治疗后,替格瑞洛的转换在安全性结局和疗效复合终点方面没有差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c2b/10403104/9b6cc2adbb8c/pone.0289721.g001.jpg

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