Abstract | BACKGROUND: STUDY DESIGN AND METHODS: This crossover study tested the additive effects of PLT concentrates (PCs) after desmopressin ( DDAVP) infusion in antagonizing the anti-PLT effects of GPIIb/IIIa inhibitors and aspirin. After eptifibatide and aspirin infusion (at standard dosages), 10 healthy volunteers received DDAVP or placebo. Thereafter, increasing amounts of PLTs from fresh single-donor apheresis concentrates were added in vitro to blood samples of all volunteers to increase PLT counts by 30 x 10(9), 60 x 10(9), or 120 x 10(9) per L. RESULTS: Adding platelets in vitro further improved PLT function after DDAVP: it shortened collagen- adenosine diphosphate closure times (p < 0.01), to normal ranges as measured by the PLT function analyzer (PFA-100). In contrast, normal PLT function could not be restored even when PLT counts were increased by 50 percent (120 x 10(9)/L) in the placebo group. CONCLUSION: Combined use of PLTs from fresh apheresis PC and DDAVP additively enhances recovery of normal PLT function after eptifibatide infusion. Such a strategy may help to avoid excessive transfusion of PC.
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Authors | Rosemarie Reiter, Petra Jilma-Stohlawetz, Michaela Horvath, Bernd Jilma |
Journal | Transfusion
(Transfusion)
Vol. 45
Issue 3
Pg. 420-6
(Mar 2005)
ISSN: 0041-1132 [Print] United States |
PMID | 15752161
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anticoagulants
- Hemostatics
- Hirudins
- Peptides
- Platelet Aggregation Inhibitors
- Platelet Glycoprotein GPIIb-IIIa Complex
- Recombinant Proteins
- Deamino Arginine Vasopressin
- Eptifibatide
- Aspirin
- lepirudin
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Topics |
- Adult
- Anticoagulants
- Aspirin
(administration & dosage)
- Blood Component Removal
- Blood Platelets
(drug effects)
- Cross-Over Studies
- Deamino Arginine Vasopressin
(administration & dosage)
- Drug Synergism
- Eptifibatide
- Hemostatics
(administration & dosage)
- Hirudins
(analogs & derivatives)
- Humans
- Male
- Peptides
(administration & dosage)
- Platelet Aggregation Inhibitors
(administration & dosage)
- Platelet Glycoprotein GPIIb-IIIa Complex
(antagonists & inhibitors)
- Platelet Transfusion
- Recombinant Proteins
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