Literature DB >> 36243834

Cost-effectiveness of miglustat versus symptomatic therapy of Niemann-Pick disease type C.

Medo Gutić1, Miloš N Milosavljević2, Slobodan M Janković1.   

Abstract

BACKGROUND: Niemann-Pick disease type C (NP-C) is a progressive neurodegenerative disorder with early infantile (< 2 years), late infantile (2-6 years), juvenile (7-15 years) and adolescent (> 15 years) onset. The mainstay of therapy for NP-C patients with neurological symptoms is miglustat, a drug that may modify the course of the disease. AIM: Our aim was to evaluate the cost-effectiveness of miglustat in comparison to symptomatic therapy in patients with NP-C in the socio-economic settings of the Republic of Serbia, an upper-middle-income European economy.
METHOD: The perspective of the Serbian Republic Health Insurance Fund was chosen for this study, and the time horizon was eighty years. The main outcomes of the study were quality-adjusted life years gained with miglustat and comparator, and direct costs of treatment. The study was conducted through the generation and simulation of the Discrete-Event Simulation model. The model results were obtained after Monte Carlo microsimulation of a sample with 1000 virtual patients.
RESULTS: Treatment with miglustat was not cost-effective when compared with symptomatic therapy and was associated with negative values of net monetary benefit regardless of the onset of neurological manifestations (- 110,447,627.00 ± 701,614.00 RSD, - 343,871,695.00 ± 2,577,441.00 RSD, - 1,397,908,502.00 ± 23,084,235.00 RSD and - 2,953,680,879.00 ± 33,297,412.00 RSD) for early infantile, late infantile, juvenile and adolescent cohorts, respectively).
CONCLUSION: When traditional pharmacoeconomic evaluation is employed, miglustat is not a cost-effective option in comparison to symptomatic therapy for the treatment of NP-C. However, given the proven efficacy of miglustat, there is a need to find ways to make this drug available to all patients with NP-C.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Entities:  

Keywords:  Cost-benefit analysis; Health; Insurance; Miglustat; Niemann–Pick disease; Type C

Year:  2022        PMID: 36243834     DOI: 10.1007/s11096-022-01491-8

Source DB:  PubMed          Journal:  Int J Clin Pharm


  47 in total

Review 1.  Neuropsychological assessment in Niemann-Pick disease type C: a systematic review.

Authors:  Giuseppa Maresca; Caterina Formica; Vanessa Nocito; Desiree Latella; Simona Leonardi; Maria Cristina De Cola; Giuseppe Triglia; Placido Bramanti; Francesco Corallo
Journal:  Neurol Sci       Date:  2021-05-22       Impact factor: 3.307

2.  NPC2 facilitates bidirectional transfer of cholesterol between NPC1 and lipid bilayers, a step in cholesterol egress from lysosomes.

Authors:  Rodney E Infante; Michael L Wang; Arun Radhakrishnan; Hyock Joo Kwon; Michael S Brown; Joseph L Goldstein
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-04       Impact factor: 11.205

3.  Structure of N-terminal domain of NPC1 reveals distinct subdomains for binding and transfer of cholesterol.

Authors:  Hyock Joo Kwon; Lina Abi-Mosleh; Michael L Wang; Johann Deisenhofer; Joseph L Goldstein; Michael S Brown; Rodney E Infante
Journal:  Cell       Date:  2009-06-26       Impact factor: 41.582

Review 4.  [High cost drugs for rare diseases in Brazil: the case of lysosomal storage disorders].

Authors:  Mônica Vinhas de Souza; Bárbara Corrêa Krug; Paulo Dornelles Picon; Ida Vanessa Doederlein Schwartz
Journal:  Cien Saude Colet       Date:  2010-11

Review 5.  Niemann-Pick disease type C.

Authors:  Marie T Vanier
Journal:  Orphanet J Rare Dis       Date:  2010-06-03       Impact factor: 4.123

6.  Cost of illness associated with Niemann-Pick disease type C in the UK.

Authors:  Jackie Imrie; Carmen Galani; Kerry Gairy; Kevin Lock; Elke Hunsche
Journal:  J Med Econ       Date:  2009-09       Impact factor: 2.448

7.  Cost-effectiveness of enzyme replacement therapy with alglucosidase alfa in adult patients with Pompe disease.

Authors:  Tim A Kanters; Ans T van der Ploeg; Michelle E Kruijshaar; Dimitris Rizopoulos; W Ken Redekop; Maureen P M H Rutten-van Mӧlken; Leona Hakkaart-van Roijen
Journal:  Orphanet J Rare Dis       Date:  2017-12-13       Impact factor: 4.123

Review 8.  Consensus clinical management guidelines for Niemann-Pick disease type C.

Authors:  Tarekegn Geberhiwot; Alessandro Moro; Andrea Dardis; Uma Ramaswami; Sandra Sirrs; Mercedes Pineda Marfa; Marie T Vanier; Mark Walterfang; Shaun Bolton; Charlotte Dawson; Bénédicte Héron; Miriam Stampfer; Jackie Imrie; Christian Hendriksz; Paul Gissen; Ellen Crushell; Maria J Coll; Yann Nadjar; Hans Klünemann; Eugen Mengel; Martin Hrebicek; Simon A Jones; Daniel Ory; Bruno Bembi; Marc Patterson
Journal:  Orphanet J Rare Dis       Date:  2018-04-06       Impact factor: 4.123

Review 9.  Miglustat in Niemann-Pick disease type C patients: a review.

Authors:  Mercè Pineda; Mark Walterfang; Marc C Patterson
Journal:  Orphanet J Rare Dis       Date:  2018-08-15       Impact factor: 4.123

Review 10.  Treatment trials in Niemann-Pick type C disease.

Authors:  Dominika Sitarska; Anna Tylki-Szymańska; Agnieszka Ługowska
Journal:  Metab Brain Dis       Date:  2021-10-01       Impact factor: 3.584

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