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Infections and the relationship to treatment in neuromuscular autoimmunity.


ABSTRACT: INTRODUCTION:This study aimed to identify infections in patients with myasthenia gravis, dermatomyositis, and chronic inflammatory demyelinating polyradiculoneuropathy, and to investigate the relationship between infection and immunomodulation. METHODS:A retrospective chart review examined 631 patients with myasthenia gravis (n?=?358), chronic inflammatory demyelinating polyradiculoneuropathy (n?=?124), and dermatomyositis (n?=?149) patients over a 10-year time period. RESULTS:Infection rates were similar at approximately 19% in all 3 diseases. Of the infections in which a causative organism was identified, pneumonia, sepsis, and opportunistic infections were the leading diagnoses. A multivariate model demonstrated a significant association between infection and an increased dose of plasma exchange, mycophenolate mofetil, and corticosteroid therapy. DISCUSSION:There are few large studies investigating rates of infections in patients with autoimmune neuromuscular disorders and the relationship to immunomodulation. This study not only demonstrates the remarkably similar infection rates across the 3 diseases studied, but also shows their relationship to commonly used immunotherapies. Muscle Nerve 57: 927-931, 2018.

SUBMITTER: Prior DE 

PROVIDER: S-EPMC5951723 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

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Infections and the relationship to treatment in neuromuscular autoimmunity.

Prior Devin E DE   Nurre Emily E   Roller Stephanie L SL   Kline David D   Panara Ramit R   Stino Amro M AM   Davis John A JA   Freimer Miriam L ML   Arnold W David WD  

Muscle & nerve 20171220 6


<h4>Introduction</h4>This study aimed to identify infections in patients with myasthenia gravis, dermatomyositis, and chronic inflammatory demyelinating polyradiculoneuropathy, and to investigate the relationship between infection and immunomodulation.<h4>Methods</h4>A retrospective chart review examined 631 patients with myasthenia gravis (n = 358), chronic inflammatory demyelinating polyradiculoneuropathy (n = 124), and dermatomyositis (n = 149) patients over a 10-year time period.<h4>Results<  ...[more]

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