Emicizumab prophylaxis for people with hemophilia A: Waste estimation and the Brazilian perspective

Costs of hemophilia A treatment are increasing. Waste of clotting products should be avoided. To estimate the first-year waste of emicizumab prophylaxis for people with hemophilia A and inhibitors (PwHAi) who failed immune tolerance induction (ITI), in Brazil. We evaluated the manufacturer and the B...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Ricardo Mesquita Camelo (Συγγραφέας), Mariana Michel Barbosa (Συγγραφέας), Luila Clicia Moura Henriques (Συγγραφέας), Antony Paul Martin (Συγγραφέας), Brian Godman (Συγγραφέας), Augusto Afonso Guerra Júnior (Συγγραφέας), Francisco de Assis Acurcio (Συγγραφέας), Juliana Alvares-Teodoro (Συγγραφέας)
Μορφή: Βιβλίο
Έκδοση: Elsevier, 2023-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ricardo Mesquita Camelo  |e author 
700 1 0 |a Mariana Michel Barbosa  |e author 
700 1 0 |a Luila Clicia Moura Henriques  |e author 
700 1 0 |a Antony Paul Martin  |e author 
700 1 0 |a Brian Godman  |e author 
700 1 0 |a Augusto Afonso Guerra Júnior  |e author 
700 1 0 |a Francisco de Assis Acurcio  |e author 
700 1 0 |a Juliana Alvares-Teodoro  |e author 
245 0 0 |a Emicizumab prophylaxis for people with hemophilia A: Waste estimation and the Brazilian perspective 
260 |b Elsevier,   |c 2023-12-01T00:00:00Z. 
500 |a 1319-0164 
500 |a 10.1016/j.jsps.2023.101867 
520 |a Costs of hemophilia A treatment are increasing. Waste of clotting products should be avoided. To estimate the first-year waste of emicizumab prophylaxis for people with hemophilia A and inhibitors (PwHAi) who failed immune tolerance induction (ITI), in Brazil. We evaluated the manufacturer and the Brazilian Ministry of Health (MoH) protocol-recommended regimens in a budget impact model. The loading dose consisted of 3.0 mg/kg/Q1W for 4 weeks, for both recommendations. The manufacturer maintenance regimens comprised 1.5 mg/kg/Q1W, 3.0 mg/kg/Q2W, and 6.0 mg/kg/Q4W. The MoH protocol maintenance regimen encompassed a hybrid Q1W/Q2W administration, depending on the body weight. The Q4W regimen was not recommended by the MoH protocol. Analyses were performed to estimate waste given its expense based on the World Health Organization body weight range (percentiles [P] 15, 50, and 85). The first-year emicizumab waste was estimated individually and for the disclosed PwHAi who failed ITI (n = 114). The highest emicizumab waste was estimated for the lowest body weights and the Q1W regimen. The Q4W regimen resulted in the lowest emicizumab waste, followed by the MoH protocol regimen. The total reconstituted costs estimated for the PwHAi who failed ITI according to the hybrid MoH protocol ranged from US$32,858,777 (P15) to US$47,186,858 (P85), with emicizumab waste ranging from 7.9 % (US$2,594,515) to 3.7 % (US$1,738,750), respectively. Lost resources due to current protocols for emicizumab prophylaxis for PwHAi who failed ITI in Brazil are considerable. Waste was more pronounced due to lower body weight and shorter administration intervals. 
546 |a EN 
690 |a hemophilia A 
690 |a emicizumab 
690 |a prophylaxis 
690 |a waste 
690 |a budget impact 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Saudi Pharmaceutical Journal, Vol 31, Iss 12, Pp 101867- (2023) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1319016423003626 
787 0 |n https://doaj.org/toc/1319-0164 
856 4 1 |u https://doaj.org/article/3ae9e39a606a43fda775ea83a08d2ba9  |z Connect to this object online.