4.7 Review

Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP)

Journal

JOURNAL OF NEUROLOGY
Volume 268, Issue 10, Pages 3706-3716

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-020-09998-8

Keywords

CIDP; Burden; QoL; Epidemiology; Treatment; Cost

Funding

  1. CSL Behring GmbH
  2. Good Publication Practice (GPP3) guidelines

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CIDP is a rare neurological disorder characterized by muscle weakness and impaired sensory function. Patients with CIDP experience high physical and psychosocial burden, including physical function impairment, pain, and depression. Treatment of CIDP can be burdensome, with direct costs driven by treatment and hospitalization, as well as indirect costs associated with impaired productivity.
Background Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare neurological disorder characterised by muscle weakness and impaired sensory function. The present study provides a comprehensive literature review of the burden of illness of CIDP. Methods Systematic literature search of PubMed, Embase, and key conferences in May 2019. Search terms identified studies on the epidemiology, humanistic burden, current treatment, and economic burden of CIDP published since 2009 in English. Results Forty-five full texts and nineteen conference proceedings were identified on the epidemiology (n = 9), humanistic burden (n = 7), current treatment (n = 40), and economic burden (n = 8) of CIDP. Epidemiological studies showed incidence and prevalence of 0.2-1.6 and 0.8-8.9 per 100,000, respectively, depending on geography and diagnostic criteria. Humanistic burden studies revealed that patients experienced physical and psychosocial burden, including impaired physical function, pain and depression. Publications on current treatments reported on six main types of therapy: intravenous immunoglobulins, subcutaneous immunoglobulins, corticosteroids, plasma exchange, immunosuppressants, and immunomodulators. Treatments may be burdensome, due to adverse events and reduced independence caused by treatment administration setting. In Germany, UK, France, and the US, CIDP economic burden was driven by direct costs of treatment and hospitalisation. CIDP was associated with indirect costs driven by impaired productivity. Conclusions This first systematic review of CIDP burden of illness demonstrates the high physical and psychosocial burden of this rare disease. Future research is required to fully characterise the burden of CIDP, and to understand how appropriate treatment can mitigate burden for patients and healthcare systems.

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