| Literature DB >> 28193112 |
Carmen Yea1, Ari Bitnun2,3, Joan Robinson4, Aleksandra Mineyko5, Michelle Barton6, Jean K Mah5, Jiri Vajsar1,3, Susan Richardson7,8, Christoph Licht3,9, Jason Brophy10, Megan Crone5, Shalini Desai11, Juliette Hukin12, Kevin Jones11, Katherine Muir12, Jeffrey M Pernica13, Robert Pless14, Daniela Pohl15, Mubeen F Rafay16, Kathryn Selby12, Sunita Venkateswaran15, Geneviève Bernard17,18,19, E Ann Yeh1,3.
Abstract
We describe the presenting features and long-term outcome of an unusual cluster of pediatric acute flaccid paralysis cases that occurred in Canada during the 2014 enterovirus D68 outbreak. Children (n = 25; median age 7.8 years) presenting to Canadian centers between July 1 and October 31, 2014, and who met diagnostic criteria for acute flaccid paralysis were evaluated retrospectively. The predominant presenting features included prodromal respiratory illness (n = 22), cerebrospinal fluid lymphocytic pleocytosis (n = 18), pain in neck/back (n = 14) and extremities (n = 10), bowel/bladder dysfunction (n = 9), focal central gray matter lesions found in all regions of the spinal cord within the cohort (n = 16), brain stem lesions (n = 8), and bulbar symptoms (n = 5). Enterovirus D68 was detectable in nasopharyngeal specimens (n = 7) but not in cerebrospinal fluid. Acute therapies (corticosteroids, intravenous immunoglobulins, plasmapheresis) were well tolerated with few side effects. Fourteen of 16 patients who were followed beyond 12 months post onset had neurologic deficits but showed ongoing clinical improvement and motor recovery.Entities:
Keywords: North America; enterovirus D68; limb weakness; outbreak; pediatric
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Year: 2016 PMID: 28193112 DOI: 10.1177/0883073816680770
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987