Incidence of bleeding and performance of the PRECISE-DAPT score in predicting bleeding in patients on dual antiplatelet therapy after treatment for acute coronary syndrome in Kenya.

IF 2.3 3区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS BMC Cardiovascular Disorders Pub Date : 2025-02-28 DOI:10.1186/s12872-024-04434-5
Peter Mugo, Mohamed Jeilan, Miriam Msunza, James Orwa, Mzee Ngunga
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Abstract

Introduction: Dual Antiplatelet Therapy (DAPT) plays an important role in the secondary prevention of ischemic events after treatment for acute coronary syndrome (ACS). The long-term use of DAPT is associated with an increased risk of bleeding, which affects morbidity and mortality. Risk stratification scores have been developed to predict this risk and provide a balance against the risk of ischemic events. The aim of this study was to determine the incidence of bleeding in a cohort of patients in Kenya on DAPT and assess the performance of the PRECISE-DAPT Score in predicting the risk of bleeding.

Methods: This was a retrospective study conducted in three hospitals in Kenya among patients on DAPT after ACS between January 2019 and April 2022. We reviewed medical records for demographic and clinical characteristics and conducted telephone interviews to assess bleeding for patients on DAPT for a minimum period of one year. Bleeding events were categorized according to the TIMI criteria for bleeding, and the PRECISE-DAPT Score was calculated using an online calculator. The cumulative one-year incidence of bleeding was calculated and presented as frequencies and percentages. Receiver operating characteristic (ROC) analysis and C-statistics were used to quantify the ability of the PRECISE-DAPT Score to predict bleeding events, whereas calibration was estimated using the Hosmer‒Lemeshow goodness-of-fit test.

Results: A total of 202 patients were enrolled in the study. The study population was predominantly male (n = 156, 77.2%) and African (n = 141, 69.8%), with a median age of 61 years (IQR 52-72). Majority were admitted with ST-Elevation Myocardial infarction (STEMI) (n = 126, 62.4%) and had a mildly reduced left ventricle ejection fraction (n = 124, 61.4%). Fourteen patients (6.9%) met the TIMI criteria for bleeding, of whom 11 (5.4%) had minimal bleeding and 3 (1.5%) had minor bleeding. There was no incidence of major bleeding. The discrimination and calibration of the PRECISE-DAPT Score was good {ROC curve 0.699 (95% CI: 0.564-0.835)} and the Hosmer-Lemeshow goodness-of-fit test (Chi-square, 6.53; p = 0.588), respectively.

Conclusion: The incidence of bleeding was low, with the majority of patients having minimal bleeding that did not require medical intervention. The PRECISE-DAPT Score performed well in predicting bleeding in patients on DAPT.

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肯尼亚急性冠状动脉综合征治疗后接受双重抗血小板治疗的患者出血发生率和precision - dapt评分预测出血的表现
简介:双重抗血小板治疗(DAPT)在急性冠脉综合征(ACS)治疗后缺血性事件的二级预防中起着重要作用。长期使用DAPT与出血风险增加相关,从而影响发病率和死亡率。风险分层评分已经发展到预测这种风险,并提供一个平衡对缺血性事件的风险。本研究的目的是确定肯尼亚一组DAPT患者的出血发生率,并评估precision -DAPT评分在预测出血风险方面的表现。方法:这是一项回顾性研究,于2019年1月至2022年4月在肯尼亚三家医院对ACS术后DAPT患者进行研究。我们回顾了人口统计学和临床特征的医疗记录,并进行了电话访谈,以评估DAPT患者至少一年的出血情况。根据出血的TIMI标准对出血事件进行分类,使用在线计算器计算precision - dapt评分。计算1年累计出血发生率,并以频率和百分比表示。使用受试者工作特征(ROC)分析和c统计来量化precision - dapt评分预测出血事件的能力,而使用Hosmer-Lemeshow拟合优度检验来估计校准。结果:共有202例患者入组。研究人群以男性(n = 156, 77.2%)和非洲人(n = 141, 69.8%)为主,中位年龄61岁(IQR 52-72)。大多数患者入院时伴有st段抬高型心肌梗死(STEMI) (n = 126, 62.4%),左心室射血分数轻度降低(n = 124, 61.4%)。14例患者(6.9%)符合TIMI出血标准,其中轻度出血11例(5.4%),轻度出血3例(1.5%)。无大出血发生。precision - dapt评分的判别和校准良好(ROC曲线0.699 (95% CI: 0.564-0.835)), Hosmer-Lemeshow拟合优度检验(χ 2, 6.53;P = 0.588)。结论:出血发生率低,大多数患者出血轻微,不需要医疗干预。precision -DAPT评分在预测DAPT患者出血方面表现良好。
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来源期刊
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.50
自引率
0.00%
发文量
480
审稿时长
1 months
期刊介绍: BMC Cardiovascular Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the heart and circulatory system, as well as related molecular and cell biology, genetics, pathophysiology, epidemiology, and controlled trials.
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