Health Technologies Assessment for Orphan Diseases. Example of Social and Economic Burden of Spinal Muscular Atrophy
https://doi.org/10.15690/pf.v18i5.2333
Abstract
Background. Studies of the economic impact of disease on society or the social and economic burden, known as developmental disease cost analysis, are equivalent to public health epidemiological studies. Spinal muscular atrophy (SMA) has significant social and economic burden according to various studies.
Objective. The aim of the study is to compare Russian and international methodological approaches and results of health technology assessment (HTA) of SMA from the perspective of social and economic burden. Materials and methods. Literature searches were conducted using the Medline, PubMed, ClinicalTrials.gov, and Cochrane Library databases. Keywords and criteria for inclusion and exclusion have been used. The following parameters were used: costs, year of calculation, assessment method, primary and secondary results, type of economic assessment, perspective, time horizon, intervention, analysis of the sensitivity of the results. Both direct medical and non-medical costs were taken into account, as well as indirect costs.
Results. The analysis of SMA burden the USA, Germany, Spain, Australia, France, Great Britain, and the Russian Federation was carried out based on 8 international studies and one Russian study that described the costs of SMA. All costs, including indirect ones, were estimated only in 4 international studies and in Russian one. The main source of information was either patient registers or cross-sectional retrospective studies of patients diagnosed with SMA. The costs were higher for type I SMA in all countries. The highest total SMA costs were in the United States, and the lowest in Russian Federation and Spain. Costs excluded new disease-modifying drugs such as nusinersen, risdiplam, and onasemogen abeparvovec in all conducted studies.
Conclusions. The social and economic burden of SMA in Russian Federation in 2020 before the introduction of pathogenetic therapy into practice was 2.38 billion RUR/year. The costs of inpatient treatment and rehabilitation were 30.8 and 32.3% of total costs, respectively. These costs, before the introduction of pathogenetic therapy into practice, are lower than in Western Europe and United States, which is most likely since domestic studies used the standards of primary health care for children with SMA implemented in 2012, as well as low indirect costs for SMA in Russian Federation. Unified methodology for assessing the socio-economic significance of orphan diseases is required to carry out HTA of orphan diseases in Russian Federation. It should be based on domestic registries, otherwise on valid data, including those based on data from real clinical practice (RWD /RWE).
About the Authors
Aleksei S. KolbinRussian Federation
Aleksei S. Kolbin
6/8 Lva Tolstogo Str., 197089, St. Petersburg, +7 (921) 759-04-49; eLibrary SPIN: 7966-0845
Disclosure of interest:
Not declared
Dmitriy V. Vlodavets
Russian Federation
Dmitry V. Vlodavets
eLibrary SPIN: 2657-4710
Disclosure of interest:
Not declared
Aleksei A. Kurylev
Russian Federation
Aleksey A. Kurylev
1 Ostrovityanova Str., 117997 Moscow, eLibrary SPIN: 2657-4710
Disclosure of interest:
Not declared
Olga Yu. Germanenko
Russian Federation
Olga Y. Germanenko
Moscow
Disclosure of interest:
Not declared
Natalia Yu. Kolbina
Russian Federation
Natalia Yu. Kolbina
2 Akkuratova Str., 197341, Saint-Petersburg
Disclosure of interest:
Not declared
References
1. Verhaart IEC, Robertson A, Wilson IJ, et al. Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy — a literature review. Orphanet J Rare Dis. 2017;12(1):124. doi: 10.1186/s13023-017-0671-8
2. Zerres K, Rudnik-Schoneborn S. Natural history in proximal spinal muscular atrophy, Clinical analysis of 445 patients and suggestions for a modification of existing classifications. Arch Neurol. 1995;52(5):518–523. doi: 10.1001/archneur.1995.00540290108025
3. Sokolova MG, Aleksandrov NYu, Lobzin SV. Spinal muscular atrophy in children: etiology, pathogenesis, diagnostics and tretment guidelines. Herald of North-Western State Medical University named after I.I. Mechnikov. 2013;5(4):108–113. (In Russ).
4. Wijngaarde CA, Stam M, Otto LAM, et al. Populationbased analysis of survival in spinal muscular atrophy. Neurology. 2020;94(15):e1634–e1644. doi: 10.1212/WNL.0000000000009248
5. Gillingwater TH. Counting the cost of spinal muscular atrophy. J Med Econ. 2016;19(8):827–828. doi: 10.1080/13696998.2016.1202833
6. Armstrong EP, Malone DC, Yeh WS, et al. The economic burden of spinal muscular atrophy. J Med Econ. 2016;19(8):822–826. doi: 10.1080/13696998.2016.1198355
7. Droege M, Sproule D, Arjunji R, et al. Economic burden of spinal muscular atrophy in the United States: a contemporary assessment. J Med Econ. 2020;23(1):70–79. doi: 10.1080/13696998.2019.1646263
8. Dangouloff T, Botty C, Beaudartet C, et al. Systematic literature review of the economic burden of spinal muscular atrophy and economic evaluations of treatments. Orphanet J Rare Dis. 2021;16(1):47. doi: 10.1186/s13023-021-01695-7
9. Landfeldt E, Pechmann A, McMillan H, et al. Costs of Illness of Spinal Muscular Atrophy: A Systematic Review. Appl Health Econ Health Policy. 2021;19(4):501–520. doi: 10.1007/s40258-020-00624-2
10. Kolbin АS, Kurylev АА, Balykina YuЕ, et al. Health economic evaluation of risdiplam in patients with spinal muscular atrophy. FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology. 2021;14(3):299-310. (In Russ). doi: 10.17749/2070-4909/farmakoekonomika.2021.101
11. Kolbin AS, Vlodavets DV, Kurylev AA, et al. The social-economic burden of spinal muscular atrophy in Russia. FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology. 2020;13(4):337-354. (In Russ). doi: 10.17749/2070-4909/farmakoekonomika.2020.068
12. Klug C, Schreiber-Katz O, Thiele S, et al. Disease burden of spinal muscular atrophy in Germany. Orphanet J Rare Dis. 2016;11(1):58. doi: 10.1186/s13023-016-0424-0
13. Lopez-Bastida J, Pena-Longobardo LM, Aranda-Reneo I, et al. Social/economic costs and health-related quality of life in patients with spinal muscular atrophy (SMA) in Spain. Orphanet J Rare Dis. 2017;12(1):141. doi: 10.1186/s13023-017-0695-0
14. Lee M Jr, França U, Graham R, et al. Pre-Nusinersen Hospitalization Costs of Children With Spinal Muscular Atrophy. Iatr Neurol. 2019;92:3–5. doi: 10.1016/j.pediatrneurol.2018.11.002
15. Chambers GM, Settumba SN, Carey KA, et al. Prenusinersen economic and health-related quality of life burden of spinal muscular atrophy. Neurology. 2020;95(1):e1–e10. doi: 10.1212/WNL.0000000000009715
16. Darbà J. Direct medical costs of spinal muscular atrophy in the Catalonia region: a population-based analysis. Clin Drug Investig. 2020;40(4):335–341. doi: 10.1007/s40261-020-00897-4
17. Peña-Longobardo LM, Aranda-Reneo I, Oliva-Moreno J, et al. The economic impact and health-related quality of life of spinal muscular atrophy. An analysis across Europe. Int J Environ Res Public Health. 2020;17(16):5640. doi: 10.3390/ijerph17165640
18. Order of the Ministry of Health of the Russian Federation dated December 29, 2012 N 1741н “Ob utverzhdenii standarta pervichnoi mediko-sanitarnoi pomoshchi detyam pri spinal’nykh myshechnykh atrofiyakh”. (In Russ).
19. General Tariff Agreement for Compulsory Health Insurance of St. Petersburg, 2020. Official website of the Territorial Fund for Compulsory Health Insurance of St. Petersburg. (In Russ). Доступно по: https://spboms.ru/page/docs. Ссылка активна на 20.07.2020.
20. State register of maximum selling prices for medicines. (In Russ). Доступно по: http://grls.rosminzdrav.ru. Ссылка активна на 20.07.2020.
21. Unified procurement information system. (In Russ). Доступно по: https://zakupki.gov.ru/epz/main/public/home.html. Ссылка активна на 20.07.2020.
22. Darbà J. Management and current status of spinal muscular atrophy: a retrospective multicentre claims database analysis. Orphanet J Rare Dis. 2020;15(1):8. doi: 10.1186/s13023-019-1287-y
23. Vlodavets DV, Kharlamov DA, Artem’eva SB, Belousova ED. Federal’nye klinicheskie rekomendatsii (protokoly) po diagnostike i lecheniyu spinal’nykh myshechnykh atrofii u detei. (In Russ). Доступно по: http://ulgb3.ru/doc/211218_10-58.pdf. Ссылка активна на 20.07.2020.
24. Oskoui M, Levy G, Garland CJ, et al. The changing natural history of spinal muscular atrophy type 1. Neurology. 2007;69(20):1931–1936. doi: 10.1212/01.wnl.0000290830.40544.b9
25. Decree of the President of the Russian Federation dated March 7, 2019 N 95 “O vnesenii izmeneniya v Ukaz Prezidenta Rossiiskoi Federatsii ot 26 fevralya 2013 g. № 175 “O ezhemesyachnykh vyplatakh litsam, osushchestvlyayushchim ukhod za det’mi-invalidami i invalidami s detstva I gruppy”. (In Russ).
26. Kolbin AS, Belousov DYu, Zyryanov SK, et al. Issledovaniya real’noi klinicheskoi praktiki. Kolbin AS, ed. Moscow: Izd-vo OKI Buki Vedi; 2020. 208 p. (In Russ).
27. Schieppati A, Henter JI, Daina E, Aperia A. Why rare diseases are an important medical and social issue. Lancet. 2008;371(9629):2039–2041. doi: 10.1016/S0140-6736(08)60872-7
28. The Federal Health Monitoring System: Health expenditures in Germany as share of GDP and in millions of Euro (absolute and per inhabitant). https://www.destatis.de/EN/Themes/Society-Environment/Health/Health-Expenditure/_node.html
29. Qian Y, McGraw S, Henne J, et al. Understanding the experiences and needs of individuals with spinal muscular atrophy and their parents: a qualitative study. BMC Neurol. 2015;15:217. doi: 10.1186/s12883-015-0473-3
Review
For citations:
Kolbin A.S., Vlodavets D.V., Kurylev A.A., Germanenko O.Yu., Kolbina N.Yu. Health Technologies Assessment for Orphan Diseases. Example of Social and Economic Burden of Spinal Muscular Atrophy. Pediatric pharmacology. 2021;18(5):408-415. (In Russ.) https://doi.org/10.15690/pf.v18i5.2333