Influence of severity of anemia on clinical findings in infants with sickle cell anemia: analyses from the BABY HUG study
- PMID: 22190441
- PMCID: PMC3337342
- DOI: 10.1002/pbc.24037
Influence of severity of anemia on clinical findings in infants with sickle cell anemia: analyses from the BABY HUG study
Abstract
Background: Clinical complications of sickle cell anemia begin in infancy. BABY HUG (ClinicalTrials.gov, NCT00006400) was a NHLBI-NICHD supported randomized phase III placebo-controlled trial of hydroxyurea (HU) in infants (recruited at 9-18 months) unselected for clinical severity with sickle cell anemia. This secondary analysis of data from BABY HUG examines the influence of anemia on the incidence of sickle cell related complications, and the impact of hydroxyurea therapy in altering these events by comparing children with lower (<25th percentile) and higher (>75th percentile) hemoglobin concentrations at study entry.
Procedure: Infants were categorized by: (1) age-adjusted hemoglobin quartiles as determined by higher (Hi) and lower (Lo) hemoglobin concentrations at study entry (9-12 months old: <8.0 and >10.0 gm/dL; 12-18 months old: <8.1 and >9.9 gm/dL) and (2) treatment arm (hydroxyurea or placebo). Four subgroups were created: placebo (PL) LoHb (n = 25), PL HiHb (n = 27), hydroxyurea (HU) LoHb (n = 21), and HU HiHb (n = 18). The primary and secondary endpoints of BABY HUG were analyzed by subgroup.
Results: Infants with lower hemoglobin at baseline were more likely to have a higher incidence of clinical events (acute chest syndrome, pain crisis, fever) as well as higher TCD velocities and lower neuropsychological scores at study exit. Hydroxyurea reduced the incidence of these findings.
Conclusion: Infants with more severe anemia are at risk for increased clinical events that may be prevented by early initiation of hydroxyurea.
Copyright © 2011 Wiley Periodicals, Inc.
References
-
- Powars DR, Chan LS, Hiti A, et al. Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients. Medicine (Baltimore) 2005;84(6):363–376. - PubMed
-
- Halasa NB, Shankar SM, Talbot TR, et al. Incidence of invasive pneumococcal disease among individuals with sickle cell disease before and after the introduction of the pneumococcal conjugate vaccine. Clin Infect Dis. 2007;44(11):1428–1433. - PubMed
-
- Telfer P, Coen P, Chakravorty S, et al. Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London. Haematologica. 2007;92(7):905–912. - PubMed
-
- Wang WC, Pavlakis SG, Helton KJ, et al. MRI abnormalities of the brain in one-year-old children with sickle cell anemia. Pediatr Blood Cancer. 2008;51(5):643–646. - PubMed
-
- Wang WC, Langston JW, Steen RG, et al. Abnormalities of the central nervous system in very young children with sickle cell anemia. J Pediatr. 1998;132(6):994–998. - PubMed
Publication types
MeSH terms
Substances
Associated data
Grants and funding
- N01-HB-07150/HB/NHLBI NIH HHS/United States
- N01-HB-07159/HB/NHLBI NIH HHS/United States
- N01 HB007160/HB/NHLBI NIH HHS/United States
- N01-HB-07160/HB/NHLBI NIH HHS/United States
- N01-HB-07153/HB/NHLBI NIH HHS/United States
- N01-HB-07156/HB/NHLBI NIH HHS/United States
- N01-HB-07157/HB/NHLBI NIH HHS/United States
- N01-HB-07152/HB/NHLBI NIH HHS/United States
- N01-HB-07155/HB/NHLBI NIH HHS/United States
- N01 HB007150/HL/NHLBI NIH HHS/United States
- N01-HB-07158/HB/NHLBI NIH HHS/United States
- N01-HB-07151/HB/NHLBI NIH HHS/United States
- N01-HB-07154/HB/NHLBI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
