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Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease
Authors:Quinn Charles T,Stuart Marie J,Kesler Karen,Ataga Kenneth I,Wang Winfred C,Styles Lori,Smith-Whitley Kim,Wun Ted,Raj Ashok,Hsu Lewis L,Krishnan Suba,Kuypers Frans A,Setty Yamaja,Rhee Seungshin,Key Nigel S,Buchanan George R  Investigators of the Comprehensive Sickle Cell Centers
Affiliation:Cincinnati Children's Hospital Medical Center, Hematology/Oncology, Cincinnati, OH 45220, USA. charles.quinn@cchmc.org
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 17·3 years) before early study termination. Dexamethasone decreased duration of hospitalization for ACS by 20·8 h 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 24 h of treatment (dexamethasone or placebo). This ACS assessment tool was feasibly applied, and sL-selectin is a promising biomarker of ACS therapy.
Keywords:sickle cell disease  acute chest syndrome  corticosteroid  biomarkers  L‐selectin
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