Digital Repository

A Randomized controlled trial of fresh frozen plasma for coagulopathy in Russell's viper (Daboia russelii) envenoming

Show simple item record

dc.contributor.author Isbister, G.K.
dc.contributor.author Jayamanne, S.
dc.contributor.author Mohamed, F.
dc.contributor.author Dawson, A.H.
dc.contributor.author Maduwage, K.
dc.contributor.author Gawarammana, I.
dc.contributor.author Lalloo, D.G.
dc.contributor.author de Silva, H.J.
dc.contributor.author Scorgie, F.E.
dc.contributor.author Lincz, L.F.
dc.contributor.author Buckley, N.A.
dc.date.accessioned 2017-01-23T06:44:22Z
dc.date.available 2017-01-23T06:44:22Z
dc.date.issued 2017
dc.identifier.citation Journal of Thrombosis and Haemostasis. 2017; 15(4): 645-654 en_US
dc.identifier.issn 1538-7933 (Print)
dc.identifier.issn 1538-7836 (Electronic)
dc.identifier.issn 1538-7836 (Linking)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/16015
dc.description Indexed in MEDLINE en_US
dc.description.abstract BACKGROUND: Russell's viper (Daboia russelii) envenoming is a major health issue in South Asia and causes venom induced consumption coagulopathy (VICC). OBJECTIVES: We investigated the effect of fresh frozen plasma (FFP) and two antivenom doses in correcting VICC. METHODS: We undertook an open-label randomized controlled trial in patients with VICC at two Sri Lankan hospitals. Patients with suspected Russell's viper bites and coagulopathy were randomly allocated (1:1) high-dose antivenom (20 vials) or low-dose antivenom (10 vials) plus 4U FFP. The primary outcome was the proportion of patients with an international normalized ratio (INR)<2, 6h post-antivenom. Secondary outcomes included anaphylaxis, major haemorrhage, death and clotting factor recovery. RESULTS: From 214 eligible patients, 141 were randomized; 71 to high-dose antivenom, 70 to low-dose antivenom/FFP; five had no post-antivenom bloods. The groups were similar except for a delay of 1h in antivenom administration for FFP patients. 6h post-antivenom 23/69 (33%) patients allocated high-dose antivenom had an INR<2 compared with 28/67 (42%) allocated low-dose antivenom/FFP [absolute difference 8%;95%Confidence Interval:-8% to 25%]. 15 patients allocated FFP did not receive it. Severe anaphylaxis occurred equally frequently in each group. One patient given FFP developed transfusion related acute lung injury. Three deaths occurred in low-dose/FFP patients including one intracranial haemorrhage. There was no difference in recovery rates of INR or fibrinogen, but more rapid initial recovery of factor V and X in FFP patients. CONCLUSION: FFP post-antivenom in Russell's viper bites didn't hasten recovery of coagulopathy. Low-dose antivenom/FFP did not worsen VICC, suggesting low-dose antivenom is sufficient. This article is protected by copyright. All rights reserved. en_US
dc.language.iso en_US en_US
dc.publisher Wiley-Blackwell en_US
dc.subject Snake Bites en_US
dc.subject Snake Bites-therapy en
dc.subject Russell's Viper en
dc.subject Snake Venoms en
dc.subject Antivenins en
dc.subject Antivenins-therapeutic use en
dc.subject Blood Coagulation en
dc.subject Disseminated Intravascular Coagulation en
dc.subject Plasma en
dc.subject Viper Venoms en
dc.subject Sri Lanka en
dc.subject Randomized Controlled Trial en
dc.subject Prospective Studies en
dc.title A Randomized controlled trial of fresh frozen plasma for coagulopathy in Russell's viper (Daboia russelii) envenoming en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search Digital Repository


Browse

My Account