Small-nerve-fiber pathology in critical illness documented by serial skin biopsies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25307783
DOI
10.1002/mus.24489
Knihovny.cz E-resources
- Keywords
- critical illness, myopathy, polyneuropathy, skin biopsy, small fibers,
- MeSH
- Biopsy methods MeSH
- Electromyography MeSH
- Erythromelalgia diagnosis physiopathology MeSH
- Glasgow Coma Scale MeSH
- Critical Illness * MeSH
- Skin pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Longitudinal Studies MeSH
- Neural Conduction physiology MeSH
- Neurologic Examination MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
INTRODUCTION: Small-fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in critical care survivors. METHODS: Eleven adult ischemic stroke patients in a neurocritical care unit were enrolled in an observational cohort study. Intraepidermal nerve fiber density (IENFD) in the distal leg was assessed on admission to the intensive care unit and 10-14 days later, together with electrophysiological testing. RESULTS: Of the 11 patients recruited, 9 (82%) had sepsis or multiple-organ failure. Median IENFD on admission (5.05 fibers/mm) decreased significantly to 2.18 fibers/mm (P < 0.001), and abnormal IENFD was found in 6 patients (54.5%). Electrodiagnostic signs of large-fiber neuropathy and/or myopathy were found in 6 patients (54.5%), and autonomic dysfunction was found in 2 patients (18.2%). CONCLUSION: Serial IENFD measurements confirmed the development of small-fiber sensory involvement in the acute phase of critical illness.
Central European Institute of Technology Masaryk University Kamenice 5 62500 Brno Czech Republic
Department of Neurology University Hospital Brno Brno Czech Republic
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