Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2001-7-3
pubmed:abstractText
Heparin-induced thrombocytopenia (HIT) is a hypercoagulable syndrome strongly associated with thrombosis that is usually treated with drugs that inhibit factor Xa (danaparoid) or thrombin (lepirudin). In the present study the outcome of HIT-patients treated with danaparoid or lepirudin was compared using the single or combined endpoints of new thromboembolic complications (new TECs), amputations and/or death, and major bleeding. HIT-patients treated with lepirudin were enrolled in two prospective trials and patients, who were identified in the same two laboratories during the same time period, who were not enrolled into these studies but treated with danaparoid, were assessed retrospectively according to a standardized questionnaire. 126 danaparoid (60.3% female) and 175 lepirudin treated patients (58.3% female) fulfilled the same inclusion and exclusion criteria. In a time-to-event-analysis the cumulative risk of combined endpoint was higher in HIT-patients without thromboembolic complication at baseline treated with danaparoid (usually in prophylactic dose 750 anti-factor Xa units b.i.d. or t.i.d.s.c.) as compared to lepirudin (aPTT adjusted) (P = 0.020). Whereas HIT-patients with TEC at baseline who were usually treated with therapeutic dose had a similar outcome in both treatment groups (P = 0.913). Major bleeding occurred in 2.5% (95% CI 0.5-7.0%) of danaparoid treated patients as compared to 10.4% (95% CI 6.3-15.9%) of lepirudin treated patients until day 42 (P = 0.009). This indicates that the efficacies of therapeutic doses of danaparoid or lepirudin in preventing death, amputation or new TEC in HIT-patients do not differ largely, but the risk of bleeding seems to be higher in lepirudin treated patients. The prophylactic dose of danaparoid approved in the European Union for HIT without TEC at baseline seems suboptimal. A prospective comparative trial is required to verify these preliminary conclusions.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0340-6245
pubmed:author
pubmed:issnType
Print
pubmed:volume
85
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
950-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11434701-Age Factors, pubmed-meshheading:11434701-Aged, pubmed-meshheading:11434701-Amputation, pubmed-meshheading:11434701-Anticoagulants, pubmed-meshheading:11434701-Chondroitin Sulfates, pubmed-meshheading:11434701-Dermatan Sulfate, pubmed-meshheading:11434701-Drug Combinations, pubmed-meshheading:11434701-Drug Evaluation, pubmed-meshheading:11434701-Female, pubmed-meshheading:11434701-Hemorrhage, pubmed-meshheading:11434701-Heparin, pubmed-meshheading:11434701-Heparitin Sulfate, pubmed-meshheading:11434701-Hirudins, pubmed-meshheading:11434701-Humans, pubmed-meshheading:11434701-Incidence, pubmed-meshheading:11434701-Male, pubmed-meshheading:11434701-Middle Aged, pubmed-meshheading:11434701-Questionnaires, pubmed-meshheading:11434701-Recombinant Proteins, pubmed-meshheading:11434701-Retrospective Studies, pubmed-meshheading:11434701-Thrombocytopenia, pubmed-meshheading:11434701-Thromboembolism, pubmed-meshheading:11434701-Treatment Outcome
pubmed:year
2001
pubmed:articleTitle
A comparison of danaparoid and lepirudin in heparin-induced thrombocytopenia.
pubmed:affiliation
Institute for Immunology and Transfusion Medicine, Ernst-Moritz-Arndt-University, Greifswald, Germany.
pubmed:publicationType
Journal Article, Clinical Trial, Comparative Study, Research Support, Non-U.S. Gov't