Literature DB >> 28093464

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

Thida Ong1, Michael Schechter2, Jing Yang3, Limin Peng3, Julia Emerson4, Ronald L Gibson4, Wayne Morgan5, Margaret Rosenfeld4.   

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.
Copyright © 2017 by the American Academy of Pediatrics.

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Year:  2017        PMID: 28093464      PMCID: PMC5260155          DOI: 10.1542/peds.2016-2730

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  44 in total

1.  Disparities in Cystic Fibrosis Care and Outcome: Socioeconomic Status and Beyond.

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2.  Spirometric reference values from a sample of the general U.S. population.

Authors:  J L Hankinson; J R Odencrantz; K B Fedan
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3.  Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort.

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Journal:  Pediatr Pulmonol       Date:  2010-09

Review 4.  Key findings of the US Cystic Fibrosis Foundation's clinical practice benchmarking project.

Authors:  Michael P Boyle; Kathryn A Sabadosa; Hebe B Quinton; Bruce C Marshall; Michael S Schechter
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Authors:  Benjamin T Kopp; Lisa Sarzynski; Sabrina Khalfoun; Don Hayes; Rohan Thompson; Lisa Nicholson; Frederick Long; Robert Castile; Judith Groner
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Review 6.  Cystic fibrosis genetics: from molecular understanding to clinical application.

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10.  The effect of social deprivation on clinical outcomes and the use of treatments in the UK cystic fibrosis population: a longitudinal study.

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  21 in total

1.  Is It Acceptable to Assess Prenatal Smoking Risk to Infants without Considering Socioeconomic Status?

Authors:  Thida Ong; Michael S Schechter
Journal:  Am J Respir Crit Care Med       Date:  2018-04-01       Impact factor: 21.405

2.  Poor recovery from cystic fibrosis pulmonary exacerbations is associated with poor long-term outcomes.

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3.  Tobacco smoke exposure in pediatric cystic fibrosis: A qualitative study of clinician and caregiver perspectives on smoking cessation.

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5.  Neighborhood Poverty and Pediatric Intensive Care Use.

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6.  Tobacco smoke exposure and socioeconomic factors are independent predictors of pulmonary decline in pediatric cystic fibrosis.

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Review 7.  The Equitable Implementation of Cystic Fibrosis Personalized Medicines in Canada.

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Review 8.  Influences of environmental exposures on individuals living with cystic fibrosis.

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9.  Metabolomics profiling of tobacco exposure in children with cystic fibrosis.

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10.  Association between insurance variability and early lung function in children with cystic fibrosis.

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