Abstract | BACKGROUND: METHODS: Forty-four healthy volunteers received a 2 ng/kg endotoxin infusion (to induce coagulation) together with clinically relevant doses of lepirudin or heparin in a prospective, placebo-controlled, randomised fashion. Measurements of CCP-partial thromboplastin time (aPTT) were compared to laboratory STA-aPTT. RESULTS: As expected, baseline values of CCP-aPTT were shorter than STA-aPTT. Lepirudin increased CCP-aPTT 3-fold, and STA-aPTT 2-fold 1 h after bolus infusion. During lepirudin infusion, the correlation between CCP-aPTT and STA-aPTT was excellent (r=0.86-0.92). Both methods were equally sensitive to over-anticoagulation with heparin. Acute systemic inflammation had little effects on CCP-aPTT. CONCLUSION: CCP-aPTT is suitable for longitudinal point of care monitoring of lepirudin therapy. As baseline values of CCP-aPTT are shorter than STA-aPTT, it is recommended not to indiscriminately change between methods in the follow-up of individual patients.
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Authors | Monika Homoncik, Thomas Pernerstorfer, Rosemarie Reiter, Maarten Knechtelsdorfer, Peter Quehenberger, Bernd Jilma |
Journal | Thrombosis research
(Thromb Res)
Vol. 108
Issue 1
Pg. 91-5
(Oct 01 2002)
ISSN: 0049-3848 [Print] United States |
PMID | 12586138
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anticoagulants
- Hirudins
- Lipopolysaccharides
- Recombinant Proteins
- Heparin
- lepirudin
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Topics |
- Adult
- Anticoagulants
(therapeutic use)
- Blood Coagulation
(drug effects)
- Blood Coagulation Tests
(methods, statistics & numerical data)
- Heparin
(therapeutic use)
- Hirudins
(analogs & derivatives)
- Humans
- Inflammation
(blood, drug therapy)
- Lipopolysaccharides
(administration & dosage)
- Male
- Partial Thromboplastin Time
- Point-of-Care Systems
(statistics & numerical data)
- Prospective Studies
- Recombinant Proteins
(therapeutic use)
- Sensitivity and Specificity
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