Myotonic dystrophy type 1: surveillance
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Myotonic dystrophy type 1: surveillance. Speech and swallowing, Mobility, Balance, Falls, Activities of daily living. Fully referenced neurology checklist.
General clinical monitoring indices
- Speech and swallowing
- Mobility
- Balance
- Falls
- Activities of daily living
- Self-care
- School and social activities
- Work activities
Respiratory clinical monitoring indices
Locked: subscribe to see this section.
Cardiac clinical monitoring indices
Locked: subscribe to see this section.
Laboratory monitoring indices
Locked: subscribe to see this section.
Indications for neuromuscular respiratory specialist referral
Locked: subscribe to see this section.
Indications for more frequent cardiac surveillance
Locked: subscribe to see this section.
Indications for sleep studies
Locked: subscribe to see this section.
Acronym
Locked: subscribe to see this section.
References
- Ashizawa T, Gagnon C, Groh WJ, et al. Consensus-based care recommendations for adults with myotonic dystrophy type 1. Neurol Clin Pract 2018; 8:507-520.
- Pelargonio G, Russo AD, Sanna T, De Martino G, Bellocci F. Myotonic dystrophy and the heart. Heart 2002; 88:665-670.
- Boentert M, Cao M, Mass D, et al. Consensus-based care recommendations for pulmonologists treating adults with myotonic dystrophy type 1. Respiration 2020; 99:360-368.
- McNally EM, Mann DL, Pinto Y, et al. Clinical care recommendations for cardiologists treating adults with myotonic dystrophy. J Am Heart Assoc 2020; 9:e014006.
Related checklists
- Myotonic dystrophy type 1: genetics
- Myotonic dystrophy type 1: neurological features
- Myotonic dystrophy type 1: systemic features
- Myotonic dystrophy type 1 and cancer
- Myotonic dystrophy type 1: investigations
- Myotonic dystrophy type 1: anaesthetic management
- Myotonic dystrophy type 1: treatments
- Myotonic dystrophy type 1: outcome