Literature DB >> 16195512

Decreased attendance at cystic fibrosis centers by children covered by managed care insurance.

Ian Nathanson1, Gabriela Ramírez-Garnica, Stacey Armatti Wiltrout.   

Abstract

OBJECTIVE: The evolution of managed care has raised concerns about differential access to care for children with cystic fibrosis (CF). We tested the hypothesis that children with CF with managed care attended CF centers less frequently compared with children with non-managed care.
METHODS: We conducted a prospective cohort study by telephone every 4 months to measure access to care at CF centers among 630 randomly selected patients aged 6-18 years from 15 US CF centers. We analyzed data with unconditional logistic regression and generalized estimating equations.
RESULTS: Attendance at CF centers was significantly reduced among children with managed care (odds ratio [OR] = 0.74; 95% confidence interval [CI] = 0.57, 0.98; P=0.03) and among girls (OR=0.68; 95% CI=0.48, 0.97; P=0.04).
CONCLUSIONS: Children with CF with managed care attended CF centers significantly less frequently than those with non-managed care. These findings suggest that children with CF with managed care may not have equal access to experts in CF as children with non-managed care. Families should consider this when selecting their medical insurance plan. These findings may apply to other children with special health care needs.

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Year:  2005        PMID: 16195512      PMCID: PMC1449468          DOI: 10.2105/AJPH.2004.059089

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  27 in total

1.  Racial and ethnic differences in access to medical care in managed care plans.

Authors:  J L Hargraves; P J Cunningham; R G Hughes
Journal:  Health Serv Res       Date:  2001-10       Impact factor: 3.402

2.  Effects of Medicaid managed care on health care use: infant emergency department and ambulatory services.

Authors:  E A Alessandrini; K N Shaw; W B Bilker; K A Perry; M D Baker; D F Schwarz
Journal:  Pediatrics       Date:  2001-07       Impact factor: 7.124

3.  International comparison of median age at death from cystic fibrosis.

Authors:  A Fogarty; R Hubbard; J Britton
Journal:  Chest       Date:  2000-06       Impact factor: 9.410

4.  Predictive 5-year survivorship model of cystic fibrosis.

Authors:  T G Liou; F R Adler; S C Fitzsimmons; B C Cahill; J R Hibbs; B C Marshall
Journal:  Am J Epidemiol       Date:  2001-02-15       Impact factor: 4.897

5.  Patterns of medical practice in cystic fibrosis: part I. Evaluation and monitoring of health status of patients. Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis.

Authors:  M W Konstan; S M Butler; D V Schidlow; W J Morgan; J R Julius; C A Johnson
Journal:  Pediatr Pulmonol       Date:  1999-10

6.  The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States.

Authors:  M S Schechter; B J Shelton; P A Margolis; S C Fitzsimmons
Journal:  Am J Respir Crit Care Med       Date:  2001-05       Impact factor: 21.405

7.  What people really know about their health insurance: a comparison of information obtained from individuals and their insurers.

Authors:  D E Nelson; B L Thompson; N J Davenport; L J Penaloza
Journal:  Am J Public Health       Date:  2000-06       Impact factor: 9.308

8.  Effects of medicaid managed care on quality: childhood immunizations.

Authors:  E A Alessandrini; K N Shaw; W B Bilker; D F Schwarz; L M Bell
Journal:  Pediatrics       Date:  2001-06       Impact factor: 7.124

9.  Parents' perceptions of pediatric primary care quality: effects of race/ethnicity, language, and access.

Authors:  Michael Seid; Gregory D Stevens; James W Varni
Journal:  Health Serv Res       Date:  2003-08       Impact factor: 3.402

10.  Factors influencing outcomes in cystic fibrosis: a center-based analysis.

Authors:  Charles Johnson; Steven M Butler; Michael W Konstan; Wayne Morgan; Mary Ellen B Wohl
Journal:  Chest       Date:  2003-01       Impact factor: 9.410

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  2 in total

1.  Genetic counseling, insurance status, and elements of medical home: analysis of the national survey of children with special health care needs.

Authors:  Grace Wang; Cindy Watts
Journal:  Matern Child Health J       Date:  2007-02-27

Review 2.  Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy.

Authors:  Edith T Zemanick; J Kirk Harris; Steven Conway; Michael W Konstan; Bruce Marshall; Alexandra L Quittner; George Retsch-Bogart; Lisa Saiman; Frank J Accurso
Journal:  J Cyst Fibros       Date:  2009-10-14       Impact factor: 5.482

  2 in total

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