Bivalirudin for Alternative Anticoagulation in Extracorporeal Membrane Oxygenation: A Systematic Review

被引:106
作者
Sanfilippo, Filippo [1 ,2 ]
Asmussen, Sven [3 ,4 ,5 ]
Maybauer, Dirk M. [4 ,5 ,6 ]
Santonocito, Cristina [1 ]
Fraser, John F. [4 ,5 ]
Erdoes, Gabor [7 ]
Maybauer, Marc O. [4 ,5 ,6 ,8 ]
机构
[1] ISMETT Ist Mediterraneo Trapianti & Terapie Ad Al, Dept Anesthesia & Intens Care, IRCCS, Via Tricomi 5, I-90127 Palermo, Italy
[2] Univ Catania, Sch Anaesthesia & Intens Care, Catania, Italy
[3] Ruhr Univ Bochum, Univ Hosp Knappschaftskrankenhaus, Dept Anaesthesiol, Bochum, Germany
[4] Prince Charles Hosp, Crit Care Res Grp, Brisbane, Qld, Australia
[5] Univ Queensland, Brisbane, Qld, Australia
[6] Philipps Univ, Dept Anaesthesiol & Intens Care Med, Marburg, Germany
[7] Univ Hosp Bern, Dept Anaesthesiol & Pain Therapy, Inselspital, Bern, Switzerland
[8] Univ Manchester, Manchester Royal Infirm, Cent Manchester Univ Hosp NHS Fdn Trust, Cardiothorac Anaesthesia & Intens Care,Manchester, Manchester, Lancs, England
关键词
cardiopulmonary bypass; ECMO; heparin-induced thrombocytopenia; HIT; direct thrombin inhibitor; HEPARIN-INDUCED THROMBOCYTOPENIA; RECOMBINANT FACTOR VIIA; CARDIOPULMONARY BYPASS; CARDIAC-SURGERY; AMERICAN-COLLEGE; RENAL-FUNCTION; PATIENT; ECMO; FONDAPARINUX; PREVENTION;
D O I
10.1177/0885066616656333
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Extracorporeal membrane oxygenation (ECMO) offers therapeutic options in refractory respiratory and/or cardiac failure. Systemic anticoagulation with heparin is routinely administered. However, in patients with heparin-induced thrombocytopenia or heparin resistance, the direct thrombin inhibitor bivalirudin is a valid option and has been increasingly used for ECMO anticoagulation. We aimed at evaluating its safety and its optimal dosing for ECMO. Methods: Systematic web-based literature search of PubMed and EMBASE performed via National Health Service Library Evidence and manually, updated until January 30, 2016. Results: The search revealed 8 publications relevant to the topic (5 case reports). In total, 58 patients (24 pediatrics) were reported (18 received heparin as control groups). Bivalirudin was used with or without loading dose, followed by infusion at different ranges (lowest 0.1-0.2 mg/kg/h without loading dose; highest 0.5 mg/kg/h after loading dose). The strategies for monitoring anticoagulation and optimal targets were dissimilar (activated partial thromboplastin time 45-60 seconds to 42-88 seconds; activated clotting time 180-200 seconds to 200-220 seconds; thromboelastography in 1 study). Conclusion: Bivalirudin loading dose was not always used; infusion range and anticoagulation targets were different. In this systematic review, we discuss the reasons for this variability. Larger studies are needed to establish the optimal approach with the use of bivalirudin for ECMO.
引用
收藏
页码:312 / 319
页数:8
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