Literature DB >> 27212083

Respiratory syncytial virus immunoprophylaxis in high-risk infants and development of childhood asthma.

Kecia N Carroll1, Tebeb Gebretsadik2, Gabriel J Escobar3, Pingsheng Wu4, Sherian Xu Li5, Eileen M Walsh5, Ed Mitchel6, Chantel D Sloan7, William D Dupont2, Tina V Hartert8.   

Abstract

BACKGROUND: Respiratory syncytial virus (RSV) lower respiratory tract infection is implicated in asthma development. RSV immunoprophylaxis during infancy is efficacious in preventing RSV-related hospitalizations and has been associated with decreased wheezing in the first years of life.
OBJECTIVE: We investigated whether greater adherence to immunoprophylaxis in infants at high risk for severe RSV would be associated with decreased childhood asthma.
METHODS: We conducted a retrospective cohort investigation including children born from 1996-2003 who were enrolled in Kaiser Permanente Northern California or Tennessee Medicaid and eligible to receive RSV immunoprophylaxis. Asthma was defined at 4.5 to 6 years of age by using asthma-specific health care visits and medication fills. We classified children into immunoprophylaxis eligibility groups and calculated adherence (percentage receipt of recommended doses). We used a set of statistical strategies (multivariable logistic regression and propensity score [PS]-adjusted and PS-matched analyses) to overcome confounding by medical complexity because infants with higher adherence (≥70%) have higher prevalence of chronic lung disease, lower birth weight, and longer nursery stays.
RESULTS: By using multivariable logistic regression and PS-adjusted models in the combined group, higher adherence to RSV immunoprophylaxis was not associated with decreased asthma. However, in PS-matched analysis, treated children with 70% or greater adherence had decreased odds of asthma compared with those with 20% or less adherence (odds ratio, 0.62; 95% CI, 0.50-0.78).
CONCLUSIONS: This investigation of RSV immunoprophylaxis in high-risk children primarily found nonsignificant associations on prevention of asthma in specific preterm groups. Our findings highlight the need for larger studies and prospective cohorts and provide estimates of potential preventive effect sizes in high-risk children.
Copyright © 2016 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Respiratory syncytial virus; asthma; bronchiolitis; lower respiratory tract infection; palivizumab; primary prevention; respiratory syncytial virus immunoprophylaxis; wheezing

Mesh:

Year:  2016        PMID: 27212083      PMCID: PMC5074917          DOI: 10.1016/j.jaci.2016.01.055

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  37 in total

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5.  Adherence to Immunoprophylaxis Regimens for Respiratory Syncytial Virus Infection in Insured and Medicaid Populations.

Authors:  Gabriel J Escobar; Tebeb Gebretsadik; Kecia Carroll; Sherian Xu Li; Eileen M Walsh; Pingsheng Wu; Ed Mitchel; Chantel Sloan; Tina Hartert
Journal:  J Pediatric Infect Dis Soc       Date:  2013-03-21       Impact factor: 3.164

6.  Methodological issues in evaluating expanded Medicaid coverage for pregnant women.

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7.  Respiratory syncytial virus in early life and risk of wheeze and allergy by age 13 years.

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Authors:  Nandini Krishnamoorthy; Anupriya Khare; Timothy B Oriss; Mahesh Raundhal; Christina Morse; Manohar Yarlagadda; Sally E Wenzel; Martin L Moore; R Stokes Peebles; Anuradha Ray; Prabir Ray
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2.  Preventing Respiratory Syncytial Virus Infection to Prevent Asthma: The Missing Link.

Authors:  Tebeb Gebretsadik; Pingsheng Wu; Kecia Carroll; William Dupont; Tina Hartert
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4.  Effectiveness of Respiratory Syncytial Virus Immunoprophylaxis in Reducing Bronchiolitis Hospitalizations Among High-Risk Infants.

Authors:  Pingsheng Wu; Gabriel J Escobar; Tebeb Gebretsadik; Kecia N Carroll; Sherian X Li; Eileen M Walsh; Edward F Mitchel; Chantel Sloan; William D Dupont; Chang Yu; Jeffrey R Horner; Tina V Hartert
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Review 10.  Early-Life Respiratory Syncytial Virus Infection, Trained Immunity and Subsequent Pulmonary Diseases.

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