Literature DB >> 27283463

The High Direct Medical Costs of Prader-Willi Syndrome.

Andrew J Shoffstall1, Julia A Gaebler2, Nerissa C Kreher3, Timothy Niecko4, Diah Douglas2, Theresa V Strong5, Jennifer L Miller6, Diane E Stafford7, Merlin G Butler8.   

Abstract

OBJECTIVE: To assess medical resource utilization associated with Prader-Willi syndrome (PWS) in the US, hypothesized to be greater relative to a matched control group without PWS. STUDY
DESIGN: We used a retrospective case-matched control design and longitudinal US administrative claims data (MarketScan) during a 5-year enrollment period (2009-2014). Patients with PWS were identified by Classification of Diseases, Ninth Revision, Clinical Modification diagnosis code 759.81. Controls were matched on age, sex, and payer type. Outcomes included total, outpatient, inpatient and prescription costs.
RESULTS: After matching and application of inclusion/exclusion criteria, we identified 2030 patients with PWS (1161 commercial, 38 Medicare supplemental, and 831 Medicaid). Commercially insured patients with PWS (median age 10 years) had 8.8-times greater total annual direct medical costs than their counterparts without PWS (median age 10 years: median costs $14 907 vs $819; P < .0001; mean costs: $28 712 vs $3246). Outpatient care comprised the largest portion of medical resource utilization for enrollees with and without PWS (median $5605 vs $675; P < .0001; mean $11 032 vs $1804), followed by mean annual inpatient and medication costs, which were $10 879 vs $1015 (P < .001) and $6801 vs $428 (P < .001), respectively. Total annual direct medical costs were ∼42% greater for Medicaid-insured patients with PWS than their commercially insured counterparts, an increase partly explained by claims for Medicaid Waiver day and residential habilitation.
CONCLUSION: Direct medical resource utilization was considerably greater among patients with PWS than members without the condition. This study provides a first step toward quantifying the financial burden of PWS posed to individuals, families, and society.
Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  administrative claims; burden of illness; cost of illness; orphan conditions; rare disorders

Mesh:

Year:  2016        PMID: 27283463     DOI: 10.1016/j.jpeds.2016.05.018

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  13 in total

Review 1.  Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study.

Authors:  Merlin G Butler; Virginia Kimonis; Elisabeth Dykens; June A Gold; Jennifer Miller; Roy Tamura; Daniel J Driscoll
Journal:  Am J Med Genet A       Date:  2017-12-22       Impact factor: 2.802

2.  How adequate is measles surveillance in the United States? Investigations of measles-like illness, 2010-2017.

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3.  Demographics and medical comorbidities among hospitalized patients with Prader-Willi Syndrome: A National Inpatient Sample analysis.

Authors:  James Luccarelli
Journal:  Am J Med Genet A       Date:  2022-07-15       Impact factor: 2.578

4.  The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia.

Authors:  Emma K Baker; Sheena Arora; David J Amor; Perrin Date; Meagan Cross; James O'Brien; Chloe Simons; Carolyn Rogers; Stephen Goodall; Jennie Slee; Chris Cahir; David E Godler
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5.  Valganciclovir Use Among Commercially and Medicaid-insured Infants With Congenital CMV Infection in the United States, 2009-2015.

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6.  [Clinical screening and genetic diagnosis for Prader-Willi syndrome].

Authors:  Guo-Qing Dong; Yue-Yue Su; Xiao-Ying Qiu; Xi-Yan Lu; Jian-Xu Li; Miao Huang; Xiao-Ping Luo
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2020-09

7.  Prevalence of Granulomas in Patients With Primary Immunodeficiency Disorders, United States: Data From National Health Care Claims and the US Immunodeficiency Network Registry.

Authors:  Jessica Leung; Kathleen E Sullivan; Ludmila Perelygina; Joseph P Icenogle; Ramsay L Fuleihan; Tatiana M Lanzieri
Journal:  J Clin Immunol       Date:  2018-07-24       Impact factor: 8.317

8.  Guillain-Barré syndrome and antecedent cytomegalovirus infection, USA 2009-2015.

Authors:  Jessica Leung; James J Sejvar; Jesus Soares; Tatiana M Lanzieri
Journal:  Neurol Sci       Date:  2019-12-11       Impact factor: 3.307

9.  Characteristics and relationship between hyperphagia, anxiety, behavioral challenges and caregiver burden in Prader-Willi syndrome.

Authors:  Nathalie Kayadjanian; Caroline Vrana-Diaz; Jessica Bohonowych; Theresa V Strong; Josée Morin; Diane Potvin; Lauren Schwartz
Journal:  PLoS One       Date:  2021-03-25       Impact factor: 3.240

10.  Analysis of economic burden and its associated factors of twenty-three rare diseases in Shanghai.

Authors:  Xiaoshu Cai; Hui Yang; Georgi Z Genchev; Hui Lu; Guangjun Yu
Journal:  Orphanet J Rare Dis       Date:  2019-10-22       Impact factor: 4.123

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