About this item:

407 Views | 334 Downloads

Author Notes:

Correspondence: Susan A. Berry (berry002@umn.edu)

The authors thank the investigators at the following institutions: University of Minnesota Amplatz Children’s Hospital (Kristi Bentler); Cincinnati Children’s Hospital Medical Center (Nancy Leslie); Emory University (Mary Brauchla); Greenwood Genetics Center (Melinda Whetsell and Neena Champaigne); University of Florida (Helen McCune and Robert Zori); University of North Carolina–Chapel Hill (Dianne Frazier); University of Tennessee (Darla Henderson Smith); Vanderbilt University Medical Center (Gina Wey); Mount Sinai Medical Center (Roberta Salveson); Children’s Hospital at Albany Medical Center (Katherine Marra); Children’s Hospital of Pittsburgh (Judith Henry); Golisano Children’s Hospital at Strong (Eileen Blakely); Maria Fareri Children’s Hospital at Westchester Medical Center (Shideh Mofidi); University of Maryland Hospital for Children (Megan Skinner).

The authors declare no conflict of interest.

Subjects:

Research Funding:

The project was supported through a Cooperative Agreement between the Maternal and Child Health Bureau (MCHB), Genetic Services Branch, and the University of Texas Health Science Center at San Antonio, National Newborn Screening and Genetics Resource Center, Health Resources and Services Administration (HRSA) grant no. U32MC00148 and by HRSA-MCHB Regional Genetic and Newborn Screening Services Collaboratives, Heritable Disorders Program: Region 2 New York—Mid-Atlantic Consortium for Genetic and Newborn Screening Services, Cooperative Agreement No. U22MC03956; Region 3 Southeast Newborn Screening and Genetics Collaborative, Cooperative Agreement No. U22MC10979; and Region 4 Midwest Genetics Collaborative, Cooperative Agreement No. U22MC03963.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Genetics & Heredity
  • diet therapy
  • inborn errors of metabolism
  • insurance coverage
  • neonatal screening

Insurance coverage of medical foods for treatment of inherited metabolic disorders

Show all authors Show less authors

Tools:

Journal Title:

Genetics in Medicine

Volume:

Volume 15, Number 12

Publisher:

, Pages 978-982

Type of Work:

Article | Final Publisher PDF

Abstract:

Purpose:Treatment of inherited metabolic disorders is accomplished by use of specialized diets employing medical foods and medically necessary supplements. Families seeking insurance coverage for these products express concern that coverage is often limited; the extent of this challenge is not well defined. Methods:To learn about limitations in insurance coverage, parents of 305 children with inherited metabolic disorders completed a paper survey providing information about their use of medical foods, modified low-protein foods, prescribed dietary supplements, and medical feeding equipment and supplies for treatment of their child's disorder as well as details about payment sources for these products. Results:Although nearly all children with inherited metabolic disorders had medical coverage of some type, families paid "out of pocket" for all types of products. Uncovered spending was reported for 11% of families purchasing medical foods, 26% purchasing supplements, 33% of those needing medical feeding supplies, and 59% of families requiring modified low-protein foods. Forty-two percent of families using modified low-protein foods and 21% of families using medical foods reported additional treatment-related expenses of $100 or more per month for these products. Conclusion:Costs of medical foods used to treat inherited metabolic disorders are not completely covered by insurance or other resources.

Copyright information:

© American College of Medical Genetics and Genomics.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommerical-NoDerivs 3.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/3.0/).

Creative Commons License

Export to EndNote