Key result
Antithrombin supplementation fails to reduce heparin dose requirements during venovenous ECMO.
Why the study?
Antithrombin supplementation during extracorporeal membrane oxygenation might reduce heparin requirements to reach anticoagulation targets, but exogenous antithrombin may also increase bleeding risk, warranting evaluation of its effects on heparin dose, anticoagulation adequacy, and safety.
Does antithrombin concentrate supplementation to maintain plasmatic levels of 80-120% reduce the total amount of heparin required to maintain target aPTT in adult patients on venovenous ECMO for severe respiratory failure?
RCT (n=48)
Randomized 1:1
Yes
Does antithrombin concentrate supplementation to maintain plasmatic levels of 80-120% reduce the total amount of heparin required to maintain target aPTT in adult patients on venovenous ECMO for severe respiratory failure?
Routine antithrombin supplementation to maintain normal plasma levels during venovenous ECMO does not reduce unfractionated heparin requirements nor impact bleeding or thrombotic complications.
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.
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Panigada et al. (2020) conducted an RCT in Severe respiratory failure requiring venovenous extracorporeal membrane oxygenation (ECMO) (n=48). Antithrombin concentrate supplementation vs. No antithrombin supplementation (control) was evaluated on Total amount of heparin required to maintain activated partial thromboplastin time ratio 1.5-2 (IU/kg/hr) (p=0.33). Antithrombin supplementation during venovenous ECMO did not significantly reduce heparin dose requirements compared to control (13.5 vs 15.1 IU/kg/hr; p=0.33).
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