Abstract

Idiopathic inflammatory myopathies (IIM) are progressive, debilitating diseases that can lead to severe impairment. The aim of the study was to evaluate the level of disability and compare it between different subtypes of IIM as well as to estimate clinical symptoms associated with greater risk of disability and distinguish the most troublesome activities in this group of patients. A online form concerning clinical symptoms, comorbidities and limitations in daily living was created and distributed to online support groups for patients with IIM. Health Assessment Questionnaire was used to estimate disability and physical limitations while visual analogue scales enabled to assess the intensity of clinical symptoms. 361 out of 377 responders were included for further evaluation. High prevalence of disability was observed in each subtype yet predominantly in patients with inclusion body myositis (IBM) as 51.43% of them fulfilled the criteria of severe to very severe disability. Level of disability correlated with muscle weakness, tolerance of physical activity and level of fatigue. 45.62% of responders in general required walking devices and 43.50% of participants declared using facilitating devices for maintaining hygiene. Patients with IIM encounter multitude physical limitations that can be partially compensated by usage of facilitating devices or aid of the caregivers. IBM seems to be the most disabling subtype.

Highlights

  • Idiopathic inflammatory myopathies (IIM) are rare, heterogeneous, autoimmune collagen vascular diseases [1]

  • The aim of the study was to assess the level of disability in different subtypes of IIM and to analyse the possible factors leading to progressive loss of physical function

  • Sporadic inclusion body myositis (IBM) is considered as the most distinctive and severe out of IIM subtypes, usually associated with poorer prognosis and greater risk of disability, the lifespan is comparable to general population [1, 9]

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Summary

Introduction

Idiopathic inflammatory myopathies (IIM) are rare, heterogeneous, autoimmune collagen vascular diseases [1].

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