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Prevalence of fatigue in Guillain-Barre syndrome in neurological rehabilitation setting. | LitMetric

Prevalence of fatigue in Guillain-Barre syndrome in neurological rehabilitation setting.

Ann Indian Acad Neurol

Department of Medical Epidemiologist (Independent), Bangalore, Karnataka, India.

Published: July 2014

Background: Fatigue contributes significantly to the morbidity and affects the quality of life adversely in Guillain-Barre Syndrome (GBS).

Objective: To determine the prevalence of fatigue in GBS in neurological rehabilitation setting and to study its clinical correlates.

Materials And Methods: We performed secondary analysis of data of patients with GBS admitted in neurological rehabilitation ward of a tertiary care centre, recorded at both admission and discharge. Assessment of fatigue was done by Fatigue Severity Scale (FSS), disability-status by Hughe's Disability Scale (HDS), functional-status by Barthel Index, anxiety/depression by Hospital Anxiety Depression Scale, sleep disturbances by Pittsburgh Sleep Quality Index and muscle weakness by Medical Research Council sum scores.

Results: A total of 90 patients (62 men) with mean age 34 years (95% CI 32.2, 37.7) were included. Median duration of, stay at neurological rehabilitation ward was 30 days, while that of symptoms was 18.5 days. Presence of fatigue at admission (FSS ≥ 4 in 39% patients) was associated with ventilator requirement (P = 0.021) and neuropathic pain (P = 0.03). Presence of fatigue at discharge (FSS ≥ 4 in 12% patients) was associated with disability- HDS (≥3) (P = 0.008), presence of anxiety (P = 0.042) and duration of stay at rehabilitation ward (P = 0.02). Fatigue did not correlate with age, gender, antecedent illness, muscle weakness, depression and sleep disturbances.

Conclusion: Fatigue is prevalent in GBS during early recovery phase of illness. Despite motor recovery fatigue may persist. Knowledge about fatigue as burden of disease in these patients will improve patient care.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162023PMC
http://dx.doi.org/10.4103/0972-2327.138521DOI Listing

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