Vis enkel innførsel

dc.contributor.authorWexels, Fredrik
dc.contributor.authorDahl, Ola Einar
dc.contributor.authorPripp, Are Hugo
dc.contributor.authorSeljeflot, Ingebjørg
dc.date.accessioned2018-05-30T14:22:19Z
dc.date.available2018-05-30T14:22:19Z
dc.date.created2017-08-23T11:38:10Z
dc.date.issued2017
dc.identifier.citationClinical and applied thrombosis/hemostasis. 2017, 23 (5), 416-421.nb_NO
dc.identifier.issn1076-0296
dc.identifier.urihttp://hdl.handle.net/11250/2499832
dc.description.abstractIncreasing number of patients with clinically suspected venous thromboembolism is referred to radiological departments for definitive diagnosis. A simple assay to exclude the diagnosis and avoid radiological examinations is needed. We have reported correlations between D-dimer and prothrombin fragment 1 + 2 measured in plasma and urine. To further develop an analysis based on urine, more understanding of thrombin generation in these patients is needed. The aim of this study was to compare ex vivo thrombin generation with in vivo markers in plasma and urine in patients with and without venous thromboembolism. Urine and blood samples were collected from patients with suspected venous thromboembolism. Commercially available enzyme-linked immunosorbent assay (ELISA) kits were used to analyze the samples for in vivo thrombin generation. The ex vivo thrombogram parameters were measured by the calibrated automated thrombogram assay. Venous thromboembolism was verified with compression ultrasound of the lower extremity deep veins or with computer tomography of the pulmonary arteries. Venous thromboembolism was diagnosed in 117 of 591 patients, and they had significantly higher levels of urine and plasma prothromin fragment 1 + 2, D-dimer, lag time, time to peak, and endogenous thrombin potential when adjusted for covariates. The pattern of ex vivo and in vivo thrombin generation in patients with suspected venous thromboembolism was comparable when adjusted for covariates. Prothrombin fragment 1 + 2 in plasma and urine reflects thrombin generation ex vivo in the same manner. This indicates that urine may be an alternative substrate to quantify a procoagulant state.nb_NO
dc.description.sponsorshipThe author(s) received no financial support for the research, authorship, and/or publication of this article.nb_NO
dc.language.isoengnb_NO
dc.relation.urihttp://journals.sagepub.com/doi/10.1177/1076029617700999
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectdeep venous thrombosisnb_NO
dc.subjectthrombosisnb_NO
dc.subjectvenous thromboembolismnb_NO
dc.subjectpulmonary embolismnb_NO
dc.titleThrombin Generation in Patients with Suspected Venous Thromboembolismnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber416-421nb_NO
dc.source.volume23nb_NO
dc.source.journalClinical and applied thrombosis/hemostasisnb_NO
dc.source.issue5nb_NO
dc.identifier.doi10.1177/1076029617700999
dc.identifier.cristin1488107
cristin.unitcode1991,1,2,0
cristin.unitnameAvd Forskning
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Navngivelse 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Navngivelse 4.0 Internasjonal