Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
28 05 2019
Historique:
received: 01 11 2018
accepted: 12 04 2019
entrez: 19 5 2019
pubmed: 19 5 2019
medline: 7 7 2020
Statut: ppublish

Résumé

The health effects of sickle cell trait among children are unknown. We compared select health outcomes and health services utilization among children with sickle cell trait, sickle cell anemia (SCA), and normal hemoglobin. Newborn screening records were used to identify children with sickle cell trait and SCA born in Michigan (1997-2014) who were enrolled in Michigan Medicaid for ≥1 year from 2012 to 2014. Each select health outcome (acute otitis media, acute respiratory infections, fever, invasive pneumococcal disease, pneumonia and influenza, renal complications, spleen problems, stroke) was defined as ≥1 claim with a diagnosis code for the respective outcome within a study year. Health services utilization was summarized as counts of emergency department, inpatient, and outpatient encounters. The relationship between hemoglobin status and each health outcome or utilization was assessed by logistic or negative binomial regression with generalized estimating equations. The study population consisted of 18 257 children with sickle cell trait, 368 with SCA, and 74 523 with normal hemoglobin (227 188 total person-years). Compared with those with normal hemoglobin, children with sickle cell trait had lower odds of acute otitis media (odds ratio [OR], 0.88; 95% confidence interval [CI], 0.84-0.91), acute respiratory infections (OR, 0.94; 95% CI, 0.92-0.97), pneumonia and influenza (OR, 0.93; 95% CI, 0.87-0.99), and outpatient visits (incidence rate ratio, 0.95; 95% CI, 0.93-0.97). Children with SCA had higher or nonsignificant odds of all outcomes and types of health services utilization. These results indicate that children with sickle cell trait may not be at additional health risk for these outcomes. However, additional case-control studies may be necessary to identify rare events.

Identifiants

pubmed: 31101648
pii: bloodadvances.2018028043
doi: 10.1182/bloodadvances.2018028043
pmc: PMC6538867
doi:

Substances chimiques

Hemoglobins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1574-1580

Informations de copyright

© 2019 by The American Society of Hematology.

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Auteurs

Sarah L Reeves (SL)

Susan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, and.
Department of Epidemiology, University of Michigan, Ann Arbor, MI; and.

Hannah K Jary (HK)

Susan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, and.

Jennifer P Gondhi (JP)

Susan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, and.

Mary Kleyn (M)

Michigan Department of Health and Human Services, Lansing, MI.

Kevin J Dombkowski (KJ)

Susan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, and.

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