Literature DB >> 17123398

Assessing the costs for clinical care of patients with high-responding factor VIII and IX inhibitors.

M Ullman1, W K Hoots.   

Abstract

The costs of haemophilia-related care and the impact of unusually expensive, or outlier, patients on these costs have been explored in numerous European, American and Canadian studies during the last decade. In particular, antibodies that neutralize infused factor VIII or IX (high-responding inhibitors) make treatment responses, and thereby costs, much less predictable. There is little debate that the health care costs of haemophilic patients with high-responding inhibitors are routinely higher and more variable than those of non-inhibitor patients. However, the extent to which this is attributable to the few outlier inhibitor patients whose expenditures tend to skew the data is not as clear. To compare the variation and range in health care expenditures among patients with inhibitors and those without, we reviewed data originally gathered during a 24-month period in 1995-1997 from a prospectively created cohort as part of a broader cost and utilization study conducted at a large haemophilia treatment centre. We conclude that although the use of outpatient factor replacement products was not significantly greater or more expensive among inhibitor patients, their hospital-related costs greatly increased overall expenditures. Among our study population, the overall costs associated with inhibitor patients are not only higher in absolute monetary terms, but also in terms of the degree of variation. This variation was demonstrated by: (i) the extremely wide range of costs over an extended timeframe among individual inhibitor patients when compared with those without inhibitors, and (ii) the much larger year-to-year variation in costs among the inhibitor group.

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Year:  2006        PMID: 17123398     DOI: 10.1111/j.1365-2516.2006.01370.x

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


  8 in total

1.  Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008.

Authors:  S Guh; S D Grosse; S McAlister; C M Kessler; J M Soucie
Journal:  Haemophilia       Date:  2011-12-12       Impact factor: 4.287

2.  A study of prospective surveillance for inhibitors among persons with haemophilia in the United States.

Authors:  J M Soucie; C H Miller; F M Kelly; A B Payne; M Creary; P L Bockenstedt; C L Kempton; M J Manco-Johnson; A T Neff
Journal:  Haemophilia       Date:  2013-11-22       Impact factor: 4.287

3.  Economic analysis of not running tenders for recombinant Factor VIII procurement: a simplified analysis to estimate an otherwise unknown pharmacoeconomic index.

Authors:  Dario Maratea; Valeria Fadda; Sabrina Trippoli; Andrea Messori
Journal:  Eur J Hosp Pharm       Date:  2015-12-23

4.  Costs and utilization of treatment in patients with hemophilia.

Authors:  Patrícia Rocha; Manuela Carvalho; Manuela Lopes; Fernando Araújo
Journal:  BMC Health Serv Res       Date:  2015-10-26       Impact factor: 2.655

Review 5.  Haemophilia A: pharmacoeconomic review of prophylaxis treatment versus on-demand.

Authors:  Brigid Unim; Maria Assunta Veneziano; Antonio Boccia; Walter Ricciardi; Giuseppe La Torre
Journal:  ScientificWorldJournal       Date:  2015-01-05

Review 6.  Bridging the Missing Link with Emicizumab: A Bispecific Antibody for Treatment of Hemophilia A.

Authors:  Georg Gelbenegger; Christian Schoergenhofer; Paul Knoebl; Bernd Jilma
Journal:  Thromb Haemost       Date:  2020-07-27       Impact factor: 5.249

7.  Barriers and perceived limitations to early treatment of hemophilia.

Authors:  Kapil Saxena
Journal:  J Blood Med       Date:  2013-05-16

8.  Economic burden of high-responding inhibitors in patients with hemophilia A in Taiwan.

Authors:  Tsu-Chiang Tu; Shin-Nan Cheng; Jye-Daa Chen; Thau-Ming Cham; Mei-Ing Chung
Journal:  Yonsei Med J       Date:  2013-03-01       Impact factor: 2.759

  8 in total

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