TY - JOUR
T1 - Cost-effectiveness of anticoagulants for suspected heparin-induced thrombocytopenia in the United States
AU - Aljabri, Ahmed
AU - Huckleberry, Yvonne
AU - Karnes, Jason H.
AU - Gharaibeh, Mahdi
AU - Kutbi, Hussam I.
AU - Raz, Yuval
AU - Yun, Seongseok
AU - Abraham, Ivo
AU - Erstad, Brian
N1 - Funding Information:
The authors thank James Camamo for his efforts in calculating AWP. They also also thank anonymous reviewers for the suggestion to include additional analyses with different HIT incidence rates and durations of therapy, as well as sensitivity analyses on the efficacy side. The authors thank the members of the postdoctoral fellowship programs in (1) Clinical Research in Human Therapeutics and (2) Health Outcomes, Effectiveness, and Economics Research at the University of Arizona for their comments on this study; these programs funded the work reported here. J.H.K. is supported by a Futures Grant from the American College of Clinical Pharmacy Research Institute (Lenexa, KS).
Publisher Copyright:
© 2016 by The American Society of Hematology.
PY - 2016/12/29
Y1 - 2016/12/29
N2 - Despite the availability of multiple nonheparin anticoagulants for the treatment of heparin-induced thrombocytopenia (HIT), few data are available comparing the cost-effectiveness of these agents. This analysis is particularly important when considering differences in the risk of adverse effects, routes of administration, requirements for phlebotomy and laboratory monitoring, and overall drug costs. We conducted a cost-effectiveness analysis of argatroban, bivalirudin, and fondaparinux for the treatment of suspected HIT from the institutional perspective. A 3-arm decision-tree model was developed that employs standard practices for anticoagulation monitoring. We incorporated published data on drug efficacy and probability of HIT-related thromboembolism and major bleeding. We considered both institutional costs and average wholesale price (AWP) and performed probabilistic sensitivity analyses (PSA) to address any uncertainty in model parameters. Using institutional costs, fondaparinux prevailed over both argatroban and bivalirudin in terms of cost ($151 vs $1250 and $1466, respectively) and adverse events averted (0.9989 vs 0.9957 and 0.9947, respectively). Results were consistent when AWP was used, with fondaparinux being less expensive ($555 vs $3081 and $2187, respectively) and more effective in terms of adverse events averted (0.9989 vs 0.9957 and 0.9947, respectively). The PSA confirmed our findings using both institutional costs and AWP. In conclusion, fondaparinux subcutaneous injection afforded significant advantages in terms of cost savings and adverse events averted compared with IV argatroban or bivalirudin infusions. Our data strongly suggest potential cost savings with fondaparinux and underscore the critical need for larger clinical studies of fondaparinux in the treatment of suspected HIT.
AB - Despite the availability of multiple nonheparin anticoagulants for the treatment of heparin-induced thrombocytopenia (HIT), few data are available comparing the cost-effectiveness of these agents. This analysis is particularly important when considering differences in the risk of adverse effects, routes of administration, requirements for phlebotomy and laboratory monitoring, and overall drug costs. We conducted a cost-effectiveness analysis of argatroban, bivalirudin, and fondaparinux for the treatment of suspected HIT from the institutional perspective. A 3-arm decision-tree model was developed that employs standard practices for anticoagulation monitoring. We incorporated published data on drug efficacy and probability of HIT-related thromboembolism and major bleeding. We considered both institutional costs and average wholesale price (AWP) and performed probabilistic sensitivity analyses (PSA) to address any uncertainty in model parameters. Using institutional costs, fondaparinux prevailed over both argatroban and bivalirudin in terms of cost ($151 vs $1250 and $1466, respectively) and adverse events averted (0.9989 vs 0.9957 and 0.9947, respectively). Results were consistent when AWP was used, with fondaparinux being less expensive ($555 vs $3081 and $2187, respectively) and more effective in terms of adverse events averted (0.9989 vs 0.9957 and 0.9947, respectively). The PSA confirmed our findings using both institutional costs and AWP. In conclusion, fondaparinux subcutaneous injection afforded significant advantages in terms of cost savings and adverse events averted compared with IV argatroban or bivalirudin infusions. Our data strongly suggest potential cost savings with fondaparinux and underscore the critical need for larger clinical studies of fondaparinux in the treatment of suspected HIT.
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U2 - 10.1182/blood-2016-07-728030
DO - 10.1182/blood-2016-07-728030
M3 - Article
C2 - 27793877
AN - SCOPUS:85015007359
SN - 0006-4971
VL - 128
SP - 3043
EP - 3051
JO - Blood
JF - Blood
IS - 26
ER -