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Volume 155, Issue 5, Pages 634-639.e4 (November 2009)


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Association of Socioeconomic Status with the Use of Chronic Therapies and Healthcare Utilization in Children with Cystic Fibrosis

Michael S. Schechter, MD, MPHaCorresponding Author Informationemail address, Susanna A. McColley, MDb, Stefanie Silva, MSc, Tmirah Haselkorn, PhDd, Michael W. Konstan, MDe, Jeffrey S. Wagener, MDf, Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis and the North American Scientific Advisory Group for ESCF

Received 1 December 2008; received in revised form 20 February 2009; accepted 24 April 2009. published online 17 July 2009.

Refers to erratum:
Errata
The Journal of Pediatrics
March 2010 (Vol. 156, Issue 3, Page 515)
Full Text | Full-Text PDF (30 KB)
Objective

To determine whether previously reported socioeconomic status (SES)-related disparities in cystic fibrosis (CF) health outcomes vary by the indicator used (median household income by zip code [MIZ], maternal educational attainment [MEA], and state insurance coverage [MA]), and whether these disparities can be explained by differences in medical treatment.

Study design

A cross-sectional analysis of data on patients age <18 years from the Epidemiologic Study of Cystic Fibrosis (ESCF).

Results

Disease severity showed a similar inverse correlation with all 3 SES measures. The number of stable clinic visits was unrelated to SES. Patients with MA had more sick outpatient visits and more courses of intravenous (IV) antibiotics for pulmonary exacerbations, and were more likely to be prescribed all chronic therapies. Low-MIZ patients had slightly fewer sick visits and more courses of IV antibiotics, and were more likely to receive oral nutrition supplements but less likely to receive macrolide prescriptions. Low-MEA patients were less likely to receive IV antibiotics at home, more likely to receive oral nutrition supplements, but less likely to receive macrolide prescriptions.

Conclusions

CF health outcomes are correlated with the SES spectrum, but these disparities are not explained by differential use of health services or prescription of chronic therapy. Future investigations should focus on the possible impact of environmental exposures and differences in disease self-management.

a Division of Pulmonary, Allergy/Immunology, Cystic Fibrosis and Sleep, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA

b Northwestern University Feinberg School of Medicine, Denver, CO

c ICON Clinical Research, Denver, CO

d EpiMetrix, Inc

e Rainbow Babies and Children's Hospital and Case Western Reserve University School of Medicine, Denver, CO

f University of Colorado Denver School of Medicine, Denver, CO

Corresponding Author InformationReprint requests: Michael S. Schechter, MD, MPH, Emory University School of Medicine, 1547 Clifton Road, Atlanta, GA 30322.

 Funding and conflict of interest disclosure information is available at www.jpeds.com (Appendix 2).

 A list of the members of the ESCF and the North American Scientific Advisory Group for ESCF is available at www.jpeds.com (Appendix 1).

PII: S0022-3476(09)00455-7

doi:10.1016/j.jpeds.2009.04.059


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