Literature DB >> 29774392

Cost-Effectiveness of Ventricular Assist Device Destination Therapy for Advanced Heart Failure in Duchenne Muscular Dystrophy.

Defne A Magnetta1, JaHyun Kang2,3, Peter D Wearden4, Kenneth J Smith5, Brian Feingold6,7.   

Abstract

Destination ventricular assist device therapy (DT-VAD) is well accepted in select adults with medically refractory heart failure (HF) who are not transplant candidates; however, its use in younger patients with progressive diseases is unclear. We sought to evaluate the cost-effectiveness of DT-VAD in Duchenne muscular dystrophy (DMD) patients with advanced HF. We created a Markov-state transition model (5-year horizon) to compare survival, costs, and quality of life (QOL) between medical management and DT-VAD in DMD with advanced HF. Model input parameters were derived from the literature. We used sensitivity analyses to explore uncertainty around model assumptions. DT-VAD had higher costs ($435,602 vs. $125,696), survival (3.13 vs. 0.60 years), and quality-adjusted survival (1.99 vs. 0.26 years) than medical management. The incremental cost-effectiveness ratio (ICER) for DT-VAD was $179,086 per quality-adjusted life year (QALY). In sensitivity analyses that were widely varied to account for uncertainty in model assumptions, the DT-VAD strategy generally remained more costly and effective than medical management. Only when VAD implantation costs were <$113,142 did the DT-VAD strategy fall below the $100,000/QALY willingness-to-pay threshold commonly considered to be "cost-effective." In this exploratory analysis, DT-VAD for patients with DMD and advanced HF exceeded societal expectations for cost-effectiveness but had an ICER similar to the accepted practice of DT-VAD in adult HF patients. While more experience and research in this population is needed, our analysis suggests that DT-VAD for advanced HF in DMD should not be dismissed solely based on cost.

Entities:  

Keywords:  Cardiomyopathy; Cost effectiveness; Heart failure; Mechanical circulatory support; Neuromuscular disease; Quality of life

Mesh:

Year:  2018        PMID: 29774392     DOI: 10.1007/s00246-018-1889-5

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  34 in total

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Journal:  Circulation       Date:  2010-07-13       Impact factor: 29.690

2.  Sixth INTERMACS annual report: a 10,000-patient database.

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Journal:  J Heart Lung Transplant       Date:  2014-04-21       Impact factor: 10.247

3.  Advanced heart failure treated with continuous-flow left ventricular assist device.

Authors:  Mark S Slaughter; Joseph G Rogers; Carmelo A Milano; Stuart D Russell; John V Conte; David Feldman; Benjamin Sun; Antone J Tatooles; Reynolds M Delgado; James W Long; Thomas C Wozniak; Waqas Ghumman; David J Farrar; O Howard Frazier
Journal:  N Engl J Med       Date:  2009-11-17       Impact factor: 91.245

4.  Health care utilization and expenditures for children and young adults with muscular dystrophy in a privately insured population.

Authors:  Lijing Ouyang; Scott D Grosse; Aileen Kenneson
Journal:  J Child Neurol       Date:  2008-04-10       Impact factor: 1.987

5.  Health-related quality of life in children and adolescents with Duchenne muscular dystrophy.

Authors:  Karen Uzark; Eileen King; Linda Cripe; Robert Spicer; Jackie Sage; Kathleen Kinnett; Brenda Wong; Jesse Pratt; James W Varni
Journal:  Pediatrics       Date:  2012-11-05       Impact factor: 7.124

6.  Cost-effectiveness of continuous-flow left ventricular assist devices.

Authors:  Mattias Neyt; Ann Van den Bruel; Yolba Smit; Nicolaas De Jonge; Michiel Erasmus; Diederik Van Dijk; Joan Vlayen
Journal:  Int J Technol Assess Health Care       Date:  2013-06-14       Impact factor: 2.188

7.  Utility estimates for decision-analytic modeling in chronic heart failure--health states based on New York Heart Association classes and number of rehospitalizations.

Authors:  Alexander Göhler; Benjamin P Geisler; Jennifer M Manne; Mikhail Kosiborod; Zefeng Zhang; William S Weintraub; John A Spertus; G Scott Gazelle; Uwe Siebert; David J Cohen
Journal:  Value Health       Date:  2008-07-18       Impact factor: 5.725

8.  Paying for the Orphan Drug System: break or bend? Is it time for a new evaluation system for payers in Europe to take account of new rare disease treatments?

Authors:  Wills Hughes-Wilson; Ana Palma; Ad Schuurman; Steven Simoens
Journal:  Orphanet J Rare Dis       Date:  2012-09-26       Impact factor: 4.123

9.  Effect of left ventricular assist device implantation and heart transplantation on habitual physical activity and quality of life.

Authors:  Djordje G Jakovljevic; Adam McDiarmid; Kate Hallsworth; Petar M Seferovic; Vladan M Ninkovic; Gareth Parry; Stephan Schueler; Michael I Trenell; Guy A MacGowan
Journal:  Am J Cardiol       Date:  2014-04-18       Impact factor: 2.778

10.  Cost-effectiveness of enzyme replacement therapy with alglucosidase alfa in classic-infantile patients with Pompe disease.

Authors:  Tim A Kanters; Iris Hoogenboom-Plug; Maureen P M H Rutten-Van Mölken; W Ken Redekop; Ans T van der Ploeg; Leona Hakkaart
Journal:  Orphanet J Rare Dis       Date:  2014-05-16       Impact factor: 4.123

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  1 in total

1.  Characterizing health state utilities associated with Duchenne muscular dystrophy: a systematic review.

Authors:  Shelagh M Szabo; Ivana F Audhya; Daniel C Malone; David Feeny; Katherine L Gooch
Journal:  Qual Life Res       Date:  2019-12-06       Impact factor: 4.147

  1 in total

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