A Randomized Controlled Trial of Antithrombin Supplementation During Extracorporeal Membrane Oxygenation

被引:46
作者
Panigada, Mauro [1 ]
Cucino, Alberto [2 ]
Spinelli, Elena [1 ]
Occhipinti, Giovanna [3 ]
Panarello, Giovanna [3 ]
Novembrino, Cristina [4 ]
Consonni, Dario [5 ]
Protti, Alessandro [6 ]
Lissoni, Alfredo [1 ]
Arcadipane, Antonio [3 ]
Pesenti, Antonio [1 ,2 ]
Grasselli, Giacomo [1 ,2 ]
机构
[1] Osped Maggiore Policlin, Dept Anaesthesia & Crit Care, Fdn IRCCS Ca Granda, Milan, Italy
[2] Univ Milan, Dept Pathophysiol & Transplantat, Milan, Italy
[3] UPMC, Ist Mediterraneo Trapianti Terapie & Alta Special, Dept Anesthesiol & Intens Care, ISMETT IRCCS, Palermo, Italy
[4] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Clin Lab, Milan, Italy
[5] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Epidemiol Unit, Milan, Italy
[6] IRCCS, Dept Anesthesia & Intens Care, Humanitas Clin & Res Ctr, Milan, Italy
关键词
acute respiratory distress syndrome; antithrombin; coagulation; extracorporeal membrane oxygenation; hemorrhage; thrombosis; CONCENTRATE USE; UNFRACTIONATED HEPARIN; III SUPPLEMENTATION; ANTICOAGULATION; COAGULATION; CHILDREN; RESISTANCE; INFANTS;
D O I
10.1097/CCM.0000000000004590
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: Supplementation of antithrombin might decrease the amount of heparin needed to achieve a given anticoagulation target during extracorporeal membrane oxygenation. However, exogenous antithrombin itself may increase the risk of bleeding. We conceived a study to evaluate the effect of antithrombin supplementation in adult patients requiring venovenous extracorporeal membrane oxygenation for respiratory failure on heparin dose, adequacy of anticoagulation, and safety. Design: Prospective randomized controlled trial. Setting: ICUs of two Italian referral extracorporeal membrane oxygenation centers. Patients: Adult patients requiring venovenous extracorporeal membrane oxygenation for severe respiratory failure and unfractionated heparin for systemic anticoagulation. Interventions: Before extracorporeal membrane oxygenation start, patients were randomized to either receive antithrombin concentrate to maintain a plasmatic level 80-120% (treatment) or not (control) during the extracorporeal membrane oxygenation course. Measurements and Main Results: The primary outcome was the total amount of heparin required to maintain activated partial thromboplastin time ratio 1.5-2. Secondary outcomes were anti-factor Xa, the incidence of hemorrhagic and thrombotic events, and the amount of blood products transfused. Twenty-four patients in the treatment group and 24 in the control group were included in the intention-to-treat analysis. Antithrombin was 109.5% (93.0-123.0%) in the treatment group and 84.0% (68.5-98.0%) in the control group (p= 0.001). Supplementation of antithrombin did not decrease heparin dose (13.5 international units/kg/hr [9.6-17.9 international units/kg/hr] vs 15.1 international units/kg/hr [10.7-18.3 international units/kg/hr] in the treatment and control group, respectively;p= 0.33) and anti-Factor Xa levels (0.4 international units/mL [0.3-0.5 international units/mL] vs 0.3 international units/mL [0.2-0.5 international units/mL] in the treatment group and control group respectively;p= 0.65). Bleeding, blood product transfusions, and thrombosis were not different in the two groups. Conclusions: Antithrombin supplementation may not decrease heparin requirement nor diminish the incidence of bleeding and/or thrombosis in adult patients on venovenous extracorporeal membrane oxygenation.
引用
收藏
页码:1636 / 1644
页数:9
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