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

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.
AuthorsCharles T Quinn, Marie J Stuart, Karen Kesler, Kenneth I Ataga, Winfred C Wang, Lori Styles, Kim Smith-Whitley, Ted Wun, Ashok Raj, Lewis L Hsu, Suba Krishnan, Frans A Kuypers, Yamaja Setty, Seungshin Rhee, Nigel S Key, George R Buchanan, Investigators of the Comprehensive Sickle Cell Centers
JournalBritish journal of haematology (Br J Haematol) Vol. 155 Issue 2 Pg. 263-7 (Oct 2011) ISSN: 1365-2141 [Electronic] England
PMID21848879 (Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, N.I.H., Extramural)
Copyright© 2011 Blackwell Publishing Ltd.
Chemical References
  • Cell Adhesion Molecules
  • Nitric Oxide
  • Dexamethasone
  • C-Reactive Protein
Topics
  • Acute Chest Syndrome (blood, drug therapy, etiology, therapy)
  • Adolescent
  • Adult
  • Anemia, Sickle Cell (complications)
  • C-Reactive Protein (analysis)
  • Cell Adhesion Molecules (blood)
  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Dexamethasone (administration & dosage, therapeutic use)
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nitric Oxide (blood)
  • Oxygen Inhalation Therapy
  • Sickle Cell Trait (complications)
  • Treatment Outcome
  • Young Adult
  • beta-Thalassemia (complications)

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