Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease

32Citations
Citations of this article
52Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Tapered oral dexamethasone for acute chest syndrome (ACS) in sickle cell anaemia was studied using a novel ACS assessment tool and investigational biomarkers. Twelve participants were randomized (mean age 17·3years) before early study termination. Dexamethasone decreased duration of hospitalization for ACS by 20·8h compared to placebo (P=0·024). Rebound pain occurred in both groups (3 dexamethasone versus 1 placebo). Overall, dexamethasone decreased the leucocyte activation biomarker, sL-selectin; however, participants with rebound pain had higher sL-selectin within 24h of treatment (dexamethasone or placebo). This ACS assessment tool was feasibly applied, and sL-selectin is a promising biomarker of ACS therapy. © 2011 Blackwell Publishing Ltd.

Cite

CITATION STYLE

APA

Quinn, C. T., Stuart, M. J., Kesler, K., Ataga, K. I., Wang, W. C., Styles, L., … Buchanan, G. R. (2011). Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease. British Journal of Haematology, 155(2), 263–267. https://doi.org/10.1111/j.1365-2141.2011.08827.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free