Effect of Fibrinogen Concentrate vs Cryoprecipitate on Blood Component Transfusion After Cardiac Surgery: The FIBRES Randomized Clinical Trial

被引:128
作者
Callum, Jeannie [1 ,2 ,3 ]
Farkouh, Michael E. [4 ,5 ]
Scales, Damon C. [6 ,7 ]
Heddle, Nancy M. [8 ,9 ]
Crowther, Mark [9 ]
Rao, Vivek [4 ,10 ,11 ]
Hucke, Hans-Peter [12 ]
Carroll, Jo [4 ,11 ,13 ]
Grewal, Deep [4 ,11 ,13 ]
Brar, Sukhpal [14 ,15 ]
Bussieres, Jean [16 ]
Grocott, Hilary [17 ,18 ,19 ]
Harle, Christopher [20 ]
Pavenski, Katerina [21 ]
Rochon, Antoine [22 ]
Saha, Tarit [23 ]
Shepherd, Lois [24 ]
Syed, Summer [25 ]
Tran, Diem [26 ]
Wong, Daniel [27 ]
Zeller, Michelle [28 ]
Karkouti, Keyvan [4 ,6 ,13 ,29 ,30 ]
机构
[1] Sunnybrook Hlth Sci Ctr, Dept Lab Med & Mol Diagnost, Toronto, ON, Canada
[2] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] Univ Hlth Network, Peter Munk Cardiac Ctr, Toronto, ON, Canada
[5] Univ Toronto, Heart & Stroke Richard Lewar Ctr, Toronto, ON, Canada
[6] Univ Toronto, Dept Med, Interdept Div Crit Care, Toronto, ON, Canada
[7] Sunnybrook Hlth Sci Ctr, Dept Crit Care Med, Sunnybrook Res Inst, Toronto, ON, Canada
[8] McMaster Univ, Fac Hlth Sci, Hamilton, ON, Canada
[9] McMaster Univ, Dept Med, Hamilton, ON, Canada
[10] Toronto Gen Hosp, Univ Hlth Network, Div Cardiovasc Surg, Toronto, ON, Canada
[11] Univ Toronto, Toronto, ON, Canada
[12] ERGOMED CDS GmbH, Dept Biostat, Cologne, Germany
[13] Univ Hlth Network, Womens Coll Hosp, Sinai Hlth Syst, Dept Anesthesia & Pain Management, Toronto, ON, Canada
[14] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC, Canada
[15] Royal Columbian Hosp, Vancouver, BC, Canada
[16] Univ Laval, Inst Univ Cardiol & Pneumol Quebec, Dept Anesthesiol, Quebec City, PQ, Canada
[17] Univ Manitoba, Dept Anesthesiol, Winnipeg, MB, Canada
[18] Univ Manitoba, Dept Perioperat & Pain Med, Winnipeg, MB, Canada
[19] Univ Manitoba, Dept Surg, Winnipeg, MB, Canada
[20] Western Univ, Dept Anesthesia & Perioperat Med, London, ON, Canada
[21] Univ Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Div Transfus Med, Toronto, ON, Canada
[22] Univ Montreal, Montreal Heart Inst, Dept Anesthesiol, Montreal, PQ, Canada
[23] Queens Univ, Kingston Gen Hosp, Dept Anesthesiol & Perioperat Med, Kingston, ON, Canada
[24] Queens Univ, Kingston Hlth Sci Ctr, Dept Pathol & Mol Med, Kingston, ON, Canada
[25] McMaster Univ, Hamilton Hlth Sci Corp, Dept Anesthesiol, Hamilton, ON, Canada
[26] Univ Ottawa, Div Cardiac Anesthesiol & Crit Care, Dept Anesthesia & Pain Med, Sch Epidemiol & Publ Hlth,Heart Inst, Ottawa, ON, Canada
[27] Univ British Columbia, Royal Columbian Hosp, Cardiac Surg, Vancouver, BC, Canada
[28] McMaster Univ, McMaster Ctr Transfus Res, Dept Med, Hamilton, ON, Canada
[29] Univ Toronto, Dept Anesthesia, Toronto, ON, Canada
[30] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2019年 / 322卷 / 20期
关键词
MASSIVE TRANSFUSION; BLEEDING PATIENTS; CELL TRANSFUSION; RISK; REPLACEMENT; HEMORRHAGE; MORTALITY; CHILDREN; EFFICACY;
D O I
10.1001/jama.2019.17312
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Importance Excessive bleeding is a common complication of cardiac surgery. An important cause of bleeding is acquired hypofibrinogenemia (fibrinogen level <1.5-2.0 g/L), for which guidelines recommend fibrinogen replacement with cryoprecipitate or fibrinogen concentrate. The 2 products have important differences, but comparative clinical data are lacking. Objective To determine if fibrinogen concentrate is noninferior to cryoprecipitate for treatment of bleeding related to hypofibrinogenemia after cardiac surgery. Design, Setting, and Participants Randomized clinical trial at 11 Canadian hospitals enrolling adult patients experiencing clinically significant bleeding and hypofibrinogenemia after cardiac surgery (from February 10, 2017, to November 1, 2018). Final 28-day follow-up visit was completed on November 28, 2018. Interventions Fibrinogen concentrate (4 g; n=415) or cryoprecipitate (10 units; n=412) for each ordered dose within 24 hours after cardiopulmonary bypass. Main Outcomes and Measures Primary outcome was blood components (red blood cells, platelets, plasma) administered during 24 hours post bypass. A 2-sample, 1-sided test for the ratio of the mean number of units was conducted to evaluate noninferiority (threshold for noninferiority ratio, <1.2). Results Of 827 randomized patients, 735 (372 fibrinogen concentrate, 363 cryoprecipitate) were treated and included in the primary analysis (median age, 64 [interquartile range, 53-72] years; 30% women; 72% underwent complex operations; 95% moderate to severe bleeding; and pretreatment fibrinogen level, 1.6 [interquartile range, 1.3-1.9] g/L). The trial met the a priori stopping criterion for noninferiority at the interim analysis after 827 of planned 1200 patients were randomized. Mean 24-hour postbypass allogeneic transfusions were 16.3 (95% CI, 14.9 to 17.8) units in the fibrinogen concentrate group and 17.0 (95% CI, 15.6 to 18.6) units in the cryoprecipitate group (ratio, 0.96 [1-sided 97.5% CI, -infinity to 1.09; P<.001 for noninferiority] [2-sided 95% CI, 0.84 to 1.09; P=.50 for superiority]). Thromboembolic events occurred in 26 patients (7.0%) in the fibrinogen concentrate group and 35 patients (9.6%) in the cryoprecipitate group. Conclusions and Relevance In patients undergoing cardiac surgery who develop clinically significant bleeding and hypofibrinogenemia after cardiopulmonary bypass, fibrinogen concentrate is noninferior to cryoprecipitate with regard to number of blood components transfused in a 24-hour period post bypass. Use of fibrinogen concentrate may be considered for management of bleeding in patients with acquired hypofibrinogenemia in cardiac surgery.
引用
收藏
页码:1966 / 1976
页数:11
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