2015
DOI: 10.1002/ccr3.312
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A case of antithrombin replacement using recombinant human antithrombin in an adult patient supported with extracorporeal membrane oxygenation

Abstract: Key Clinical MessageIn the critically ill patient on extracorporeal life support, antithrombin production and activity can be decreased and may require replacement to therapeutic levels in order to maintain appropriate anticoagulation and prevent thrombosis.

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Cited by 5 publications
(3 citation statements)
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“…72,73 On the other side, in an adult patient with V-V ECMO support for respiratory failure, the AT activity level was 47%, and the heparin dosage to reach an ACT 160-180 was 15 U/kg/h. 74 Moreover, in patients on ECMO, the definition of heparin resistance lacks consensus, but Northrop et al set it at 60 U/kg/h, so while 15 U/kg/h is a value that we can consider normal, the target ACT value in this study was lower.…”
Section: Effects On Anticoagulationmentioning
confidence: 69%
“…72,73 On the other side, in an adult patient with V-V ECMO support for respiratory failure, the AT activity level was 47%, and the heparin dosage to reach an ACT 160-180 was 15 U/kg/h. 74 Moreover, in patients on ECMO, the definition of heparin resistance lacks consensus, but Northrop et al set it at 60 U/kg/h, so while 15 U/kg/h is a value that we can consider normal, the target ACT value in this study was lower.…”
Section: Effects On Anticoagulationmentioning
confidence: 69%
“…As plasma transfusions only marginally increase AT levels, some authors have evaluated the effect of AT concentrates. They have shown that AT concentrates can efficiently increase AT levels as they cause less hemodilution . This has mostly been evaluated in extracorporeal membrane oxygenation (ECMO), another clinical situation with a potential imbalance between pro‐ and anticoagulant factors, in which there is possibly some value in correcting low AT levels .…”
Section: Discussionmentioning
confidence: 99%
“…[101] Attention has focused on singlenucleotide polymorphisms (SNPs) of genes that encode two proteins: the cytochrome P450 2C9 enzyme and vitamin K epoxide reductase complex (VKORC1). [102] Studies suggest that CYP 2C9 influences warfarin metabolism and affects warfarin half-life, whereas VKORC1 plays a role in the pharmacodynamic response in expression of the enzymatic target of warfarin. For instance, patients who carry CYP 2C9*2 and CYP 2C9*3 alleles tend to require lower warfarin maintenance doses because of their slowed metabolism compared with patients who carry the "wild-type" allele.…”
Section: Current State Of Systemic Anticoagulation Usagementioning
confidence: 99%