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Recombinant Factor VIIa Improves Coagulopathy Caused by Liver Failure

 

作者: Jeffrey Brown,   Karan Emerick,   Deborah Brown,   Peter Whitington,   Estella Alonso,  

 

期刊: Journal of Pediatric Gastroenterology and Nutrition  (OVID Available online 2003)
卷期: Volume 37, issue 3  

页码: 268-272

 

ISSN:0277-2116

 

年代: 2003

 

出版商: OVID

 

关键词: Recombinant FVIIa;Coagulopathy;Liver failure

 

数据来源: OVID

 

摘要:

ObjectiveCoagulopathy is an important cause of morbidity and mortality in patients with liver failure. The benefit of traditional therapies to correct coagulation is often limited and short-lived. Our aim is to identify indications for rFVIIa use and the outcome of treatment in children with liver failure.MethodsA retrospective review from July 2000 to December 2001 was performed to identify consecutive patients with acute or chronic liver failure who received rFVIIa. Prothrombin times (PT) before and after therapy were compared by pairedttest.ResultsFifteen patients were treated with rFVIIa for coagulopathy caused by liver failure. All were receiving fresh frozen plasma (mean infusion rate, 39.7 mL/kg/day) when rFVIIa therapy was started. The mean PT before rFVIIa was 32.0 ± 7.0 seconds. One hour after infusion, the PT normalized to 13.7 ± 2.4 seconds (P< 0.0001) and remained significantly reduced at 6 hours (19.8 ± 5.3 seconds;P< 0.0001). A sustained improvement was maintained during the subsequent 3 days. Five of seven patients with bleeding complications improved clinically after rFVIIa treatment. Two of the bleeding patients also benefited from improved fluid balance as fresh frozen plasma support was reduced. No thrombotic events were attributed to rFVIIa therapy.ConclusionsIn patients with liver failure, rFVIIa therapy quickly normalizes the PT and maintains improved hemostasis, even when coagulopathy has been refractory to fresh frozen plasma. Therapy subjectively reduces clinical bleeding and can improve fluid balance, without complications.

 

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