Dartmouth Health and The Dartmouth Institute, Lebanon, NH (E.P.Z.).
Boston Scientific, Marlborough, MA (B.B., D.J.A., T.C., K.R.).
Circ Cardiovasc Qual Outcomes. 2024 Oct;17(10):e011007. doi: 10.1161/CIRCOUTCOMES.124.011007. Epub 2024 Oct 4.
Long-term outcomes following left atrial appendage occlusion outside clinical trials and small registries are largely unknown. Collecting these data was a condition of US market authorization of the WATCHMAN device. The aim of this analysis was to evaluate the rates of stroke, bleeding, and death among Medicare beneficiaries following left atrial appendage occlusion implantation during initial commercial availability of the WATCHMAN left atrial appendage occlusion device overall and in important subgroups.
All Medicare fee-for-service beneficiaries ≥65 years of age who underwent left atrial appendage occlusion from April 1, 2016, to August 31, 2020, were included based on the , and Current Procedural Terminology codes. Over a 5-year follow-up period, the cumulative incidence over time of mortality, ischemic stroke, and major bleeding were calculated using the , diagnosis codes for the full study cohort and within important prespecified subgroups.
WATCHMAN recipients (n=48 763) were a median of 77 (interquartile range, 72-82) years of age, 42% female, and mostly White (93%). The median CHADSVASc score was 4 (interquartile range, 3-5) with prior major bleeding in 42% and prior stroke in 12%. At 5 years, death occurred in 44%, bleeding in 15% (with higher risk early following implantation), and ischemic stroke in 7%. Each of these end points was more common with greater baseline age. Male patients had greater 5-year mortality than female patients (46.9% versus 40.6%), but there was no difference between sexes in the rates of ischemic stroke (6.6% versus 7.5%) or major bleeding (14.9% for both). WATCHMAN recipients with prior ischemic stroke or a major bleeding event were older and frailer; these groups had higher rates of ischemic stroke, major bleeding, and death.
Compared with patients enrolled in the pivotal clinical trials, Medicare beneficiaries undergoing WATCHMAN implantation were older, more female, and had more comorbid conditions. Substantial long-term mortality and major bleeding following WATCHMAN reflect the high-risk nature of the patient population, while the ischemic stroke rate was relatively low (<1.5% per year).
在临床试验和小型注册研究之外,左心耳封堵术的长期结果在很大程度上尚不清楚。收集这些数据是美国 Watchman 设备市场授权的一个条件。本分析的目的是评估在 Watchman 左心耳封堵装置首次商业应用期间,医疗保险受益人的中风、出血和死亡发生率,总体以及在重要亚组中。
所有 2016 年 4 月 1 日至 2020 年 8 月 31 日期间根据医疗保险费用服务受益人的 ≥65 岁患者,均采用 和当前程序术语代码纳入研究。在 5 年的随访期间,使用 和全研究队列以及重要预设亚组内的诊断代码,计算死亡率、缺血性卒中和主要出血的随时间累积发生率。
Watchman 接受者(n=48763)的中位年龄为 77 岁(四分位距,72-82),42%为女性,大多数为白人(93%)。中位 CHADSVASc 评分为 4 分(四分位距,3-5),42%有既往大出血史,12%有既往卒史。在 5 年内,44%的患者死亡,15%的患者发生出血(植入后早期风险较高),7%的患者发生缺血性卒中。这些终点在基线年龄较大的患者中更为常见。男性患者的 5 年死亡率高于女性患者(46.9%比 40.6%),但在缺血性卒中和大出血的发生率方面,性别之间没有差异(分别为 6.6%和 7.5%)。有既往缺血性卒史或大出血史的 Watchman 接受者年龄较大,身体较脆弱;这些人群的缺血性卒史、大出血和死亡率较高。
与纳入关键临床试验的患者相比,接受 Watchman 植入术的医疗保险受益人年龄较大,女性较多,合并症较多。Watchman 植入术后的长期高死亡率和大出血反映了患者人群的高风险性质,而缺血性卒的发生率相对较低(<1.5%/年)。