2001
DOI: 10.1097/00005344-200108000-00003
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Prohemorrhagic Potential of Dipyrone, Ibuprofen, Ketorolac, and Aspirin: Mechanisms Associated with Blood Flow and Erythrocyte Deformability

Abstract: Dipyrone, ibuprofen, ketorolac, and aspirin were tested in a well-defined perfusion system (shear rates: 300/s, 800/s, and 1,800/s). Whole blood samples were treated with the drugs at analgesic doses and platelet interaction with damaged subendothelium was measured. All the drugs fully inhibited platelet cyclooxygenase, as assessed by classic aggregometry. Perfusion studies showed that there was a general tendency to reduce the percentage of large aggregates (thrombus; %T), to increase the percentage of adhere… Show more

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Cited by 35 publications
(15 citation statements)
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“…A study by O'Neal 57 showed a peak plasma concentration 15 minutes after administration, compared with greater than 45 minutes with oral administration. 51 The risk of hospitalization for gastrointestinal bleeding is also higher with ketorolac. They also have the advantage of more predictable and precise therapeutic dosing.…”
Section: Nsaids and Acetaminophenmentioning
confidence: 99%
“…A study by O'Neal 57 showed a peak plasma concentration 15 minutes after administration, compared with greater than 45 minutes with oral administration. 51 The risk of hospitalization for gastrointestinal bleeding is also higher with ketorolac. They also have the advantage of more predictable and precise therapeutic dosing.…”
Section: Nsaids and Acetaminophenmentioning
confidence: 99%
“…Apart from a minor central effect metamizol and its metabolites act mainly via both COX 1 and COX 2 inhibition [3] [4]. In vitro studies showed that the prohaemorrhagic effect of metamizol was comparable with the one of aspirin [5]. In contrast to classical COX inhibitors metamizol is a stronger inhibitor of platelet aggregation [5], but has no anti-inflammatory effect and low gastrointestinal toxicity, indicating a different mode of action [2].…”
Section: Introductionmentioning
confidence: 99%
“…In contrast to classical COX inhibitors, metamizol is a stronger inhibitor of platelet aggregation [5], but has no anti-inflammatory effect and low gastrointestinal toxicity, indicating a different mode of action [2]. The classical NSAIDs act by competing with arachidonic acid for binding to the cyclooxygenase active site.…”
mentioning
confidence: 99%
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