Literature DB >> 14962215

An economic model of haemophilia in Mexico.

C Martínez-Murillo1, S Quintana, R Ambriz, H Benitez, A Berges, J Collazo, A Esparza, T Pompa, C Taboada, S Zavala, M R Larochelle, J D Bentkover.   

Abstract

A model was developed to assess the lifetime costs and outcomes associated with haemophilia in Mexico. A retrospective chart review of 182 type A haemophiliacs was conducted for patients aged 0-34 years receiving one of three treatments: (i) cryoprecipitate at clinic; (ii) concentrate at home; or (iii) concentrate at clinic. Patients treated at home experienced 30% less joint damage, used 13-54% less factor VIII, had four times fewer clinic visits, and utilized half as many hospital days than those treated at a clinic. For cryoprecipitate at clinic patients, the annual incidence rates of HCV and HIV were calculated to be 3.6% and 1.4% respectively. The life expectancy for patients receiving cryoprecipitate and those receiving concentrate was estimated to be 49 years and 69 years respectively, with 58% of cryoprecipitate patients predicted to die of AIDS before age 69. Across the lifespan, the average annual cost of care was US$11,677 (MN$110,464) for cryoprecipitate at clinic patients, US$10,104 (M$95,580) for concentrate at home patients and US$18,819 (MN$178,027) for concentrate at clinic patients. Using a 5% discount rate, the incremental lifetime cost per year of life added for treatment with concentrate at home compared with cryoprecipitate at a clinic was US$738 (MN$6981). Rank order stability analysis demonstrated that the model was most sensitive to the cost of fVIII. These results indicate that treatment with concentrate at home compared with cryoprecipitate at a clinic substantially improves clinical outcomes at reduced annual cost levels.

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Year:  2004        PMID: 14962215     DOI: 10.1046/j.1365-2516.2003.00811.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  3 in total

1.  Transfusion-transmitted infections in haemophilia patients.

Authors:  Bukurije Zhubi; Ymer Mekaj; Zana Baruti; Ilirijane Bunjaku; Mazllum Belegu
Journal:  Bosn J Basic Med Sci       Date:  2009-11       Impact factor: 3.363

Review 2.  Care models in the management of haemophilia: a systematic review.

Authors:  C H T Yeung; N Santesso; M Pai; C Kessler; N S Key; M Makris; T Navarro-Ruan; J M Soucie; H J Schünemann; A Iorio
Journal:  Haemophilia       Date:  2016-07       Impact factor: 4.287

3.  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

  3 in total

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