Clinical Toxicology · 2020 · 21 citations · 19 references
MedicineHematologyInternal MedicineClinical PharmacologyHemostasisPharmacovigilanceAntivenom TherapyCoagulation AbnormalitiesCoagulation DisordersCoagulopathy Management In TraumaSnake EnvenomationThrombosisCoagulopathy In SnakebiteControl Group DesignHospital Stay DurationMatched Control GroupPolyvalent AntivenomProthrombin ActivationSnakebite Envenomation ManagementTissue Damage Mechanisms
Introduction In French Guiana, most snakebites are caused by crotalids, with the main signs being tissue damage and bleeding due to venom-induced coagulopathy. Since December 2014 the Western Guiana Hospital (WGH) has used Antivipmyn TriTM, a Mexican polyvalent antivenom. The aim of the study was to assess its benefit on the correction of snakebite-related coagulopathy.Methods This retrospective study included patients hospitalized at the WGH with snakebite and a coagulopathy defined by: a prothrombin rate (PR) lower than 45%, an activated partial thromboplastin time ratio (aPTTr) greater than 2 or a fibrinogen lower than 100 mg.dL−1. The antivenom group included patients receiving Antivipmyn TriTM from December 2014 to September 2017. The control group included patients admitted between January 2013 and November 2014 (when antivenom was unavailable) or admitted between December 2014 and September 2017 during times of antivenom shortage. We graphically compared the time courses of PR, aPTTr and fibrinogen between groups. Other endpoints were the length of hospital stay and the need for surgery or dialysis.Results 84 patients were included: 42 in the antivenom group, 42 in the control group. Both groups were similar for age, sex-ratio, proportion of bleedings, necrosis, and severity. Most patients in the antivenom group received 3 vials. There were no significant differences in recovery of PR, aPTTr and fibrinogen through the first 24 h. Fibrinogen declined again in the control group at 30 h and showed a slower rise to normal concentration. There were no significant differences in any secondary endpoint.Conclusion Antivipmyn TriTM as currently used did not show any benefit in recovery from coagulopathy.
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