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. 2020 Jan 14;9(2):e014004. doi: 10.1161/JAHA.119.014004

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© 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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Cardiac assessment of patients with muscular dystrophy (MD) in the Neuromuscular Multidisciplinary (NMMD) clinic. Cardiac assessment and intervention applied through the NMMD clinic care pathway (A). Prevalence of cardiomyopathy in patients with MD (B). Heart failure diagnosed in patients at their initial NMMD clinic visit (C). Arrhythmia burden as captured by ECG, Holter monitoring, and device interrogation (D). DM1 indicates type 1 myotonic dystrophy; FSHD, facioscapulohumeral muscular dystrophy; LGMD, limb‐girdle muscular dystrophy; ND, not detected.