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Practice Variation in Anticoagulation Prescription and Outcomes After Device-Detected Atrial Fibrillation.

Perino AC, Fan J, Askari M, Heidenreich PA, Keung E, Raitt MH, Piccini JP, Ziegler PD, Turakhia MP. Practice Variation in Anticoagulation Prescription and Outcomes After Device-Detected Atrial Fibrillation. Circulation. 2019 May 28; 139(22):2502-2512.

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Abstract:

BACKGROUND: Device-detected atrial fibrillation (AF) is associated with increased risk of stroke; however, there are no clearly defined thresholds of AF burden at which to initiate oral anticoagulation (OAC). We sought to describe OAC prescription practice variation in response to new device-detected AF and the association with outcomes. METHODS: We performed a retrospective cohort study using data from the Veterans Health Administration linked to remote monitoring data that included day-level AF burden. We included patients with cardiac implantable electronic devices and remote monitoring from 2011 to 2014, CHADS-VASc score = 2, and no prior stroke or OAC receipt in the preceding 2 years. We determined the proportion of patients prescribed OAC within 90 days after new device-detected AF across a range of AF thresholds ( = 6 minutes to > 24 hours) and examined site variation in OAC prescription. We used multivariable Cox proportional hazards regressions to determine the association of OAC prescription with stroke by device-detected AF burden. RESULTS: Among 10?212 patients with cardiac implantable electronic devices, 4570 (45%), 3969 (39%), 3263 (32%), and 2469 (24%) had device-detected AF > 6 minutes, > 1 hour, > 6 hours, and > 24 hours, respectively. For device-detected AF > 1 hour, 1712 patients met inclusion criteria (72±10 years; 1.5% female; CHADS-VASc score 4.0±1.4; HAS-BLED score 2.6±1.1). The proportion receiving OAC varied based on device-detected AF burden ( = 6 minutes: 272/2101 [13%]; > 1 hour: 273/1712 [16%]; > 6 hours: 263/1279 [21%]; > 24 hours: 224/818 [27%]). Across 52 sites (N = 1329 patients), there was substantial site-level variation in OAC prescription after device-detected AF > 1 hour (median, 16%; range, 3%-67%; median odds ratio, 1.56 [95% credible interval, 1.49-1.71]). In adjusted models, OAC prescription after device-detected AF > 24 hours was associated with reduced stroke risk (hazard ratio, 0.28; 95% CI, 0.10-0.81; P = 0.02), although the propensity-adjusted model was significant when AF lasted at least 6 minutes. CONCLUSIONS: Among veterans with cardiac implantable electronic devices, device-detected AF is common. There is large practice variation in 90-day OAC initiation after new device-detected AF, with low rates of treatment overall, even for episodes that last > 24 hours. The strongest association of OAC with reduction in stroke was observed after device-detected AF > 24 hours. Randomized trials are needed to confirm these observational findings.





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