Socioeconomic Status, Smoke Exposure, and Health Outcomes in Young Children With Cystic Fibrosis

Author:

Ong Thida1,Schechter Michael2,Yang Jing3,Peng Limin3,Emerson Julia1,Gibson Ronald L.1,Morgan Wayne4,Rosenfeld Margaret1,

Affiliation:

1. Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Washington, Seattle, Washington;

2. Division of Pulmonary Medicine, Department of Pediatrics, Virginia Commonwealth University, Children’s Hospital of Richmond at VCU, Richmond, Virginia;

3. Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia; and

4. Departments of Pediatrics and Physiology, Pediatric Pulmonary Center, University of Arizona, Tucson, Arizona

Abstract

BACKGROUND: Lower socioeconomic status (SES) and environmental tobacco smoke (ETS) exposure are both associated with poorer disease outcomes in cystic fibrosis (CF), and children with low SES are disproportionately exposed to ETS. We analyzed a large cohort of young children with CF to distinguish the impact of SES and ETS on clinical outcomes. METHODS: The Early Pseudomonas Infection Control Observational study enrolled Pseudomonas-negative young children with CF <13 years of age. An enrollment survey assessed SES and ETS exposures. Forced expiratory volume in 1 second (FEV1), crackles and wheezes, and weight-for-age percentile were assessed at each clinical encounter over at least 4 years. Repeated measures analyses estimated the association of SES and ETS exposures with longitudinal clinical outcomes, adjusting for confounders. RESULTS: Of 1797 participants, 1375 were eligible for analysis. Maternal education was high school or less in 28.1%, 26.8% had household income <$40 000, and 43.8% had Medicaid or no insurance. Maternal smoking after birth was present in 24.8%, more prevalent in household with low SES. In separate models, lower SES and ETS exposure were significantly associated with lower FEV1% predicted, presence of crackles or wheezes, and lower weight percentile. In combined models, effect estimates for SES changed minimally after adjustment for ETS exposures, whereas estimates for ETS exposures were attenuated after adjusting for SES. CONCLUSIONS: ETS exposure was disproportionately high in low SES families in this cohort of children with CF. Lower SES and ETS exposure had independent adverse effects on pulmonary and nutritional outcomes. Estimated effect of SES on FEV1 decreased minimally after ETS adjustment, suggesting health disparity risks independent of ETS exposure.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

Reference45 articles.

1. Cystic Fibrosis Foundation Patient Registry . Annual data report to the center directors, 2013. Available at: https://www.cff.org/2013_CFF_Annual_Data_Report_to_the_Center_Directors.pdf. Accessed September 10, 2015

2. The effect of social deprivation on clinical outcomes and the use of treatments in the UK cystic fibrosis population: a longitudinal study.;Taylor-Robinson;Lancet Respir Med,2013

3. The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States.;Schechter;Am J Respir Crit Care Med,2001

4. Effect of ambient air pollution on pulmonary exacerbations and lung function in cystic fibrosis.;Goss;Am J Respir Crit Care Med,2004

5. Key findings of the US Cystic Fibrosis Foundation’s clinical practice benchmarking project.;Boyle;BMJ Qual Saf,2014

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