http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2358657-C2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_47ab7168b57b9095e02471b569c7e5a4
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61B10-00
filingDate 2007-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ce70a15d9892e807a6900cb2f1b1365
publicationDate 2009-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2358657-C2
titleOfInvention Hyperfibrinolysis prediction and diagnostic technique
abstract FIELD: medicine. n SUBSTANCE: invention refers to medicine, namely to haemostasis and fibrinolysis system analysis methods. Coagulation properties of two citrated blood samples are analysed simultaneously by re-calcification with kaolin added. One blood sample is added with plasmin in amount 1.5 times extending coagulation time as compared to the reference thus calculating the coagulation prolongation percentage by formula: where t with plasm is coagulation time with plasmin, t without plasm is coagulation time without plasmin. The coagulation prolongation percentage is compared to the reference results in hyperfibrinolysis prediction and diagnostics. n EFFECT: method provides improved quality of treatment ensured by higher diagnostic accuracy and possibility to predict thromboses and haemorrhages in surgical, therapeutic and neurologic patients. n 3 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2618402-C1
priorityDate 2007-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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