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   Venom concentrations and clotting factor levels in a prospective cohort of russell’s viper bites with coagulopathy  
   
نویسنده isbister g.k. ,maduwage k. ,scorgie f.e. ,shahmy s. ,mohamed f. ,abeysinghe c. ,karunathilake h. ,o'leary m.a. ,gnanathasan c.a. ,lincz l.f.
منبع plos neglected tropical diseases - 2015 - دوره : 9 - شماره : 8
چکیده    Background russell’s viper envenoming is a major problem in south asia and causes venom induced consumption coagulopathy. this study aimed to investigate the kinetics and dynamics of venom and clotting function in russell’s viper envenoming. methodology/principal findings in a prospective cohort of 146 patients with russell’s viper envenoming,we measured venom concentrations,international normalised ratio [inr],prothrombin time (pt),activated partial thromboplastin time (aptt),coagulation factors i,ii,v,vii,viii,ix and x,and von willebrand factor antigen. the median age was 39y (16–82y) and 111 were male. the median peak inr was 6.8 (interquartile range[iqr]:3.7 to >13),associated with low fibrinogen [median,<0.01g/l;iqr:<0.01–0.9g/l),low factor v levels [median,<5%;iqr:<5–4%],low factor viii levels [median,40%;iqr:12–79%] and low factor x levels [median,48%; iqr:29–67%]. there were smaller reductions in factors ii,ix and vii over time. all factors recovered over 48h post-antivenom. the median inr remained >3 at 6h post-antivenom but had reduced to <2,by 24h. the aptt had also returned to close to normal (<50sec) at 24h. factor vii,viii and ix levels were unusually high pre-antivenom,median peak concentrations of 393%,307% and 468% respectively. pre-antivenom venom concentrations and the inr (r = 0.20,p = 0.02) and aptt (r = 0.19,p = 0.03) were correlated (non-parametric spearman analysis). conclusions russell’s viper coagulopathy results in prolonged aptt,inr,low fibrinogen,factors v,viii and x which recover over 48h. severity of clotting abnormalities was associated with venom concentrations. © 2015 isbister et al.
آدرس school of medicine and public health,university of newcastle,callaghan,nsw,australia,department of clinical toxicology and pharmacology,calvary mater newcastle,newcastle,nsw,australia,south asian clinical toxicology research collaboration (sactrc),university of peradeniya,peradeniya, Sri Lanka, school of medicine and public health,university of newcastle,callaghan,nsw,australia,south asian clinical toxicology research collaboration (sactrc),university of peradeniya,peradeniya,sri lanka,department of biochemistry,university of peradeniya,peradeniya, Sri Lanka, hunter haematology research group,calvary mater newcastle,newcastle,nsw, Australia, south asian clinical toxicology research collaboration (sactrc),university of peradeniya,peradeniya, Sri Lanka, south asian clinical toxicology research collaboration (sactrc),university of peradeniya,peradeniya, Sri Lanka, district hospital hingurakgoda,hingurakgoda, Sri Lanka, general hospital matara,matara, Sri Lanka, school of medicine and public health,university of newcastle,callaghan,nsw,australia,department of clinical toxicology and pharmacology,calvary mater newcastle,newcastle,nsw, Australia, department of clinical medicine,university of colombo,colombo, Sri Lanka, school of medicine and public health,university of newcastle,callaghan,nsw,australia,hunter haematology research group,calvary mater newcastle,newcastle,nsw, Australia
 
     
   
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