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A pilot study of 1 versus 3 days of dexamethasone as add-on therapy in children with streptococcal pharyngitis. | LitMetric

A pilot study of 1 versus 3 days of dexamethasone as add-on therapy in children with streptococcal pharyngitis.

Pediatr Infect Dis J

Department of Pediatrics, Section of Emergency Medicine, Children's Hospital, The Ohio State University, Columbus, OH 43205, USA.

Published: June 2006

AI Article Synopsis

  • A study evaluated the effectiveness of one versus three doses of dexamethasone in children aged 4-21 with group A beta-hemolytic streptococcal pharyngitis, focusing on throat pain and overall improvement.
  • Despite both dexamethasone treatments showing quicker recovery compared to a placebo, the difference in symptom resolution was minimal, with most improvements seen in just one day.
  • The findings suggest that dexamethasone may aid faster recovery for children with GABHS pharyngitis, particularly for those receiving three doses, though no major complications were reported during the study.

Article Abstract

Background: Studies in adults, but not in children, have shown a beneficial effect of one dose of steroid on the severity and duration of throat pain in acute pharyngitis. The effectiveness of longer steroid treatment has not been evaluated in children.

Methods: We performed a randomized, double-blind, 3-arm, placebo-controlled trial to estimate the effectiveness of one dose versus 3 daily doses of oral dexamethasone in the treatment of 4- to 21-year-old patients with group A beta-hemolytic streptococcal (GABHS) pharyngitis. Participants used the Wong-Baker FACES scale to rate their symptoms at enrollment and twice daily for 5 days. Patient-completed diaries and telephone interviews provided follow-up data. Primary end points-severity of throat pain, improvement in general condition and improvement in activity level-were evaluated by survival analysis.

Results: Ninety patients were enrolled. For each end point, we rejected the null hypothesis of a common survival experience for the 3 study arms. With the exception of 2 days for throat pain in participants receiving one dose of dexamethasone, the median time to improvement for all end points was 1 day for both arms of dexamethasone and 2 days for placebo. There was no difference between study arms in return to a clinical setting for symptoms related to GABHS pharyngitis or absenteeism from work/school. No patient experienced complications related to GABHS pharyngitis in the 30 days after enrollment.

Conclusions: In this pilot study, children with GABHS pharyngitis who receive dexamethasone as add-on therapy have a more rapid improvement in general condition and level of activity and, for those receiving 3 daily doses of dexamethasone, in resolution of throat pain.

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Source
http://dx.doi.org/10.1097/01.inf.0000219469.95772.3fDOI Listing

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