• J Am Heart Assoc · Sep 2020

    Multicenter Study Clinical Trial

    Atrial Arrhythmias in Clinically Manifest Cardiac Sarcoidosis: Incidence, Burden, Predictors, and Outcomes.

    • Willy Weng, Christiane Wiefels, Santabhanu Chakrabarti, Pablo B Nery, Emel Celiker-Guler, Jeff S Healey, Tomasz W Hruczkowski, F Russell Quinn, Steven Promislow, Maria C Medor, Stewart Spence, Roupen Odabashian, Wael Alqarawi, Daniel Juneau, Rob de Kemp, Eugene Leung, Rob Beanlands, and David Birnie.
    • Division of Cardiology University of Ottawa Heart Institute Ottawa ON Canada.
    • J Am Heart Assoc. 2020 Sep 1; 9 (17): e017086.

    AbstractBackground Recent data have suggested a substantial incidence of atrial arrhythmias (AAs) in cardiac sarcoidosis (CS). Our study aims were to first assess how often AAs are the presenting feature of previously undiagnosed CS. Second, we used prospective follow-up data from implanted devices to investigate AA incidence, burden, predictors, and response to immunosuppression. Methods and Results This project is a substudy of the CHASM-CS (Cardiac Sarcoidosis Multicenter Prospective Cohort Study; NCT01477359). Inclusion criteria were presentation with clinically manifest cardiac sarcoidosis, treatment-naive status, and implanted with a device that reported accurate AA burden. Data were collected at each device interrogation visit for all patients and all potential episodes of AA were adjudicated. For each intervisit period, the total AA burden was obtained. A total of 33 patients met the inclusion criteria (aged 56.1±7.7 years, 45.5% women). Only 1 patient had important AAs as a part of the initial CS presentation. During a median follow-up of 49.1 months, 11 of 33 patients (33.3%) had device-detected AAs, and only 2 (6.1%) had a clinically significant AA burden. Both patients had reduced burden after CS was successfully treated and there was no residual fluorodeoxyglucose uptake on positron emission tomography scan. Conclusions First, we found that AAs are a rare presenting feature of clinically manifest cardiac sarcoidosis. Second, AAs occurred in a minority of patients at follow-up; the burden was very low in most patients. Only 2 patients had clinically significant AA burden, and both had a reduction after CS was treated. Registration URL: https://www.clini​caltr​ials.gov; unique identifier NCT01477359.

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