Cardiology Division, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Via del Pozzo, 71, Modena 41124, Italy.
Division of Cardiology, Cardiocentro Ticino, Lugano, Switzerland.
Europace. 2023 Aug 2;25(9). doi: 10.1093/europace/euad212.
After an ischaemic stroke, atrial fibrillation (AF) detection allows for improved secondary prevention strategies. This study aimed to compare AF detection and oral anticoagulant (OAC) initiation in patients with an insertable cardiac monitor (ICM) vs. external cardiac monitor (ECM) after ischaemic stroke.
Medicare Fee-for-Service (FFS) insurance claims and Abbott Labs device registration data were used to identify patients hospitalized with an ischaemic stroke in 2017-2019 who received an ICM or ECM within 3 months. Patients with continuous Medicare FFS insurance and prescription drug enrolment in the prior year were included. Patients with prior AF, atrial flutter, cardiac devices, or OAC were excluded. Insertable cardiac monitor and ECM patients were propensity score matched 1:4 on demographics, comorbidities, and stroke hospitalization characteristics. The outcomes of interest were AF detection and OAC initiation evaluated with Kaplan-Meier and Cox proportional hazard regression analyses. A total of 5702 Medicare beneficiaries (ICM, n = 444; ECM, n = 5258) met inclusion criteria. The matched cohort consisted of 2210 Medicare beneficiaries (ICM, n = 442; ECM, n = 1768) with 53% female, mean age 75 years, and mean CHA₂DS₂-VASc score 4.6 (1.6). Insertable cardiac monitor use was associated with a higher probability of AF detection [(hazard ratio (HR) 2.88, 95% confidence interval (CI) (2.31, 3.59)] and OAC initiation [HR 2.91, CI (2.28, 3.72)] compared to patients monitored only with ECM.
Patients with an ischaemic stroke monitored with an ICM were almost three times more likely to be diagnosed with AF and to be prescribed OAC compared to patients who received ECM only.
发生缺血性卒中后,检测心房颤动(房颤)可改善二级预防策略。本研究旨在比较缺血性卒中后使用植入式心脏监测仪(ICM)与外部心脏监测仪(ECM)患者的房颤检测和口服抗凝剂(OAC)起始情况。
使用医疗保险费用制(FFS)保险理赔和雅培实验室设备注册数据,确定 2017 年至 2019 年因缺血性卒中住院且在 3 个月内接受 ICM 或 ECM 的患者。纳入在前一年有持续医疗保险 FFS 保险和处方药参保的患者。排除有既往房颤、房扑、心脏设备或 OAC 的患者。采用倾向评分匹配法对 ICM 和 ECM 患者的人口统计学、合并症和卒中住院特征进行 1:4 匹配。主要观察指标为通过 Kaplan-Meier 分析和 Cox 比例风险回归分析评估房颤检测和 OAC 起始情况。共有 5702 名医疗保险受益人(ICM,n=444;ECM,n=5258)符合纳入标准。匹配队列包括 2210 名医疗保险受益人(ICM,n=442;ECM,n=1768),其中 53%为女性,平均年龄 75 岁,平均 CHA₂DS₂-VASc 评分为 4.6(1.6)。与仅使用 ECM 监测的患者相比,使用 ICM 的患者发生房颤的概率更高[风险比(HR)2.88,95%置信区间(CI)(2.31,3.59)],并且更有可能开始使用 OAC[HR 2.91,CI(2.28,3.72)]。
与仅接受 ECM 监测的患者相比,缺血性卒中患者使用 ICM 监测发生房颤和处方 OAC 的可能性几乎高出三倍。