Literature DB >> 30312032

Chronic inflammatory demyelinating polyneuropathy: considerations for diagnosis, management, and population health.

Melody Ryan1, Stephen J Ryan2.   

Abstract

First described almost 50 years ago, chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare autoimmune disorder characterized by progressive peripheral neuropathy. CIDP is difficult to diagnose, but early diagnosis can be crucial to prevent permanent nerve damage. Initial treatment options include corticosteroids, immunoglobulin given by intravenous administration, and therapeutic plasma exchange. Subcutaneous administration of immunoglobulin provides a new option for patients with CIDP that has the potential to increase independence and improve tolerability. This article reviews the epidemiology, diagnosis, treatment options for first- and second-line therapy, treatment guidelines, and monitoring parameters for CIDP.

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Year:  2018        PMID: 30312032

Source DB:  PubMed          Journal:  Am J Manag Care        ISSN: 1088-0224            Impact factor:   2.229


  2 in total

Review 1.  The Role of the Complement System in Chronic Inflammatory Demyelinating Polyneuropathy: Implications for Complement-Targeted Therapies.

Authors:  Luis A Querol; Hans-Peter Hartung; Richard A Lewis; Pieter A van Doorn; Timothy R Hammond; Nazem Atassi; Miguel Alonso-Alonso; Marinos C Dalakas
Journal:  Neurotherapeutics       Date:  2022-04-04       Impact factor: 6.088

Review 2.  Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP).

Authors:  Luis Querol; M Crabtree; M Herepath; E Priedane; I Viejo Viejo; S Agush; P Sommerer
Journal:  J Neurol       Date:  2020-06-24       Impact factor: 4.849

  2 in total

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