Acute flaccid myelitis: cause, diagnosis, and management

AFM working group

Research output: Contribution to journalReview articlepeer-review

103 Scopus citations

Abstract

Acute flaccid myelitis (AFM) is a disabling, polio-like illness mainly affecting children. Outbreaks of AFM have occurred across multiple global regions since 2012, and the disease appears to be caused by non-polio enterovirus infection, posing a major public health challenge. The clinical presentation of flaccid and often profound muscle weakness (which can invoke respiratory failure and other critical complications) can mimic several other acute neurological illnesses. There is no single sensitive and specific test for AFM, and the diagnosis relies on identification of several important clinical, neuroimaging, and cerebrospinal fluid characteristics. Following the acute phase of AFM, patients typically have substantial residual disability and unique long-term rehabilitation needs. In this Review we describe the epidemiology, clinical features, course, and outcomes of AFM to help to guide diagnosis, management, and rehabilitation. Future research directions include further studies evaluating host and pathogen factors, including investigations into genetic, viral, and immunological features of affected patients, host–virus interactions, and investigations of targeted therapeutic approaches to improve the long-term outcomes in this population.

Original languageEnglish (US)
Pages (from-to)334-346
Number of pages13
JournalThe Lancet
Volume397
Issue number10271
DOIs
StatePublished - Jan 23 2021

Funding

We are grateful for the support provided by the Siegel Rare Neuroimmune Association (SRNA) for facilitating administrative support to the AFM Working Group, and the Bart McLean Fund for Neuroimmunology Research for AFM research. We thank Janell A Routh and Sarah E Kidd at the Centers for Disease Control and Prevention for sharing their expertise. OCM was funded through the SRNA James T Lubin Fellowship. CAP is supported by National Institutes of Health (R01 NS108358) and the Bart McLean Fund for Neuroimmunology Research. KM is supported by National Institutes of Health (K23 AI128069). KTT is supported by National Institutes of Health (1K23NS105935).

ASJC Scopus subject areas

  • General Medicine

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