Cost-effectiveness of Fibrinogen Concentrate vs Cryoprecipitate for Treating Acquired Hypofibrinogenemia in Bleeding Adult Cardiac Surgical Patients

被引:8
作者
Abrahamyan, Lusine [1 ,2 ,3 ,4 ]
Tomlinson, George [2 ,4 ,5 ]
Callum, Jeannie [6 ]
Carcone, Steven [2 ,3 ]
Grewal, Deep [7 ]
Bartoszko, Justyna [4 ,7 ,8 ,9 ]
Krahn, Murray [2 ,3 ,4 ]
Karkouti, Keyvan [2 ,4 ,7 ,8 ,9 ]
机构
[1] Toronto Gen Hosp, Res Inst, 10th Floor Eaton North,Room 237,200 Elizabeth St, Toronto, ON M5G 2C4, Canada
[2] Univ Hlth Network, Toronto Gen Hosp, Res Inst, Toronto, ON, Canada
[3] Univ Hlth Network, Toronto Hlth Econ & Technol Assessment THETA Colla, Toronto, ON, Canada
[4] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[5] Univ Hlth Network, Biostat Res Unit, Toronto, ON, Canada
[6] Queens Univ, Kingston Hlth Sci Ctr, Dept Pathol & Mol Med, Kingston, ON, Canada
[7] Univ Hlth Network, Sinai Hlth Syst, Womens Coll Hosp, Dept Anesthesia & Pain Management, Toronto, ON, Canada
[8] Univ Toronto, Dept Anesthesiol & Pain Med, Toronto, ON, Canada
[9] Univ Hlth Network, Peter Munk Cardiac Ctr, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
TRANSFUSION; SAFETY;
D O I
10.1001/jamasurg.2022.6818
中图分类号
R61 [外科手术学];
学科分类号
摘要
IMPORTANCE Excessive bleeding requiring fibrinogen replacement isa serious complication of cardiac surgery. However, the relative cost-effectiveness of the 2 available therapies & mdash;fibrinogen concentrate and cryoprecipitate & mdash;is unknown.OBJECTIVE To determine cost-effectiveness of fibrinogen concentrate vs cryoprecipitate for managing active bleeding in adult patients who underwent cardiac surgery.DESIGN, SETTING, AND PARTICIPANTS A within-trial economic evaluation of the Fibrinogen Replenishment in Surgery (FIBERS) randomized clinical trial (February 2017 to November 2018) that took place at 4 hospitals based in Ontario, Canada, hospitals examined all in-hospital resource utilization costs and allogeneic blood product (ABP) transfusion costs incurred within 28 days of surgery. Participants included a subset of 495 adult patients from the FIBERS trial who underwent cardiac surgery and developed active bleeding and acquired hypofibrinogenemia requiring fibrinogen replacement.INTERVENTIONS Fibrinogen concentrate (4 g per dose) or cryoprecipitate (10 units per dose) randomized (1:1) up to 24 hours postcardiopulmonary bypass.MAIN OUTCOMES AND MEASURES Effectiveness outcomes included number of ABPs administered within 24 hours and 7 days of cardiopulmonary bypass. ABP transfusion (7-day) and in-hospital resource utilization (28-day) costs were evaluated anda multivariable net benefit regression model built for the full sample and predefined subgroups.RESULTS Patient level costs for 495 patients were evaluated (mean [SD] age 59.2 [15.4] years and 69.3% male.) Consistent with FIBERS, ABP transfusions and adverse events were similar in both treatment groups. Median (IQR) total 7-day ABP cost was CAD $2280 (US dollars [USD] $1697) (CAD $930 [USD $692]-CAD $4970 [USD $3701]) in the fibrinogen concentrate group and CAD $2770 (USD $1690) (IQR, CAD $1140 [USD $849]-CAD $5000 [USD $3723]) in the cryoprecipitate group. Median (interquartile range) total 28-day cost was CAD $38180 (USD $28431) $(IQR, CAD $26 350 [USD $19 622]-CAD $65 080 [USD $48463]) in the fibrinogen concentrate group and CAD $38 790 (USD $28 886) (IQR, CAD $26180 [USD $19 495]-CAD $70 380 [USD $52 409]) in the cryoprecipitate group. After exclusion of patients who were critically ill before surgery (11%) due to substantial variability in costs, the incremental net benefit of fibrinogen concentrate vs cryoprecipitate was positive (probability of being cost-effective 86% and 97% at $0 and CAD $2000 (USD $1489) willingness-to-pay, respectively). Net benefit was highly uncertain for nonelective and patients with critical illness.CONCLUSIONS AND RELEVANCE Fibrinogen concentrate is cost-effective when compared with cryoprecipitate in most bleeding adult patients who underwent cardiac surgery with acquired hypofibrinogenemia requiring fibrinogen replacement. The generalizability of these findings outside the Canadian health system needs to be verified.
引用
收藏
页码:245 / 253
页数:9
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