Channeling effects in the prescription of new therapies: the case of emicizumab for hemophilia A

被引:2
|
作者
Mahajerin, Arash [1 ,2 ,3 ]
Faghmous, Imi [4 ,9 ]
Kuebler, Peter [5 ]
Howard, Monet [6 ]
Xu, Tao [7 ]
Flores, Carlos [8 ]
Chang, Tiffany [5 ,10 ]
Nissen, Francis [4 ]
机构
[1] Univ Calif Irvine, Div Pediat Hematol, Irvine, CA 92868 USA
[2] Univ Calif Irvine, Div Oncol, Irvine, CA 92868 USA
[3] CHOC Childrens Specialists, Irvine, CA 92868 USA
[4] F Hoffmann La Roche Ltd, Dept Real World Data Oncol Hematol, CH-4070 Basel, Switzerland
[5] Genentech Inc, Dept Personalized Healthcare Safety Interface, San Francisco, CA 94080 USA
[6] F Hoffmann La Roche Ltd, Dept Clin Safety, Mississauga, ON L5N 5M8, Canada
[7] F Hoffmann La Roche Ltd, Dept Personalized Healthcare Prod Dev, CH-4070 Basel, Switzerland
[8] Genesis Res, Dept Evidence Strategy, Hoboken, NJ 07030 USA
[9] Univ Maastricht, Fac Hlth Med & Life Sci, P Debyeplein15,DEB15, NL-6229 HA Maastricht, Netherlands
[10] Spark Therapeut, Dept Hematol, Philadelphia, PA 19104 USA
关键词
channeling; claims data; coagulation factor VIII; comorbidity; emicizumab; healthcare systems; hemophilia A; pharmacovigilance; safety; PROPHYLAXIS; REPLACEMENT; INHIBITORS; SAFETY;
D O I
10.2217/cer-2021-0278
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Aim: To determine if emicizumab was channeled to clinically complex people with hemophilia A upon approval. Methods: Claims data (16 November 2017, through 31 December 2019) from US-based insurance databases were analyzed to compare the clinical complexity of people with hemophilia A initiating emicizumab with matched individuals receiving factor VIII (FVIII) episodically or prophylactically. People with hemophilia A with evidence of previous bypassing agent use (indicating FVIII inhibitors) were excluded. Outcomes included bleeding events, arthropathy, pain, comorbidities and healthcare costs. Results: A larger proportion of emicizumab users had bleeding events, comorbidities and arthropathy and greater healthcare costs in the year prior to starting emicizumab compared with FVIII users. Conclusion: Claims-based data limitations prevent an absolute conclusion. Nevertheless, emicizumab users appear more clinically complex than FVIII users, suggesting post-approval channeling.
引用
收藏
页码:717 / 728
页数:12
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