TY - JOUR
T1 - Interaction of low molecular weight heparin with ketorolac
AU - Green, David
AU - Klement, Petr
AU - Liao, Peng
AU - Weitz, Jeffrey
N1 - Funding Information:
ow-molecular-weight heparins were recent ly li-censed for use in the prevention of thrombo-L embolism in patients having orthopedic surgery. In randomized, controlled, double-blind From the Department of Medicine, Northwestern University Medical School, Chicago; McMaster University and the Hamilton Civic Hospitals Research Centre, Henderson General Division. Supported by grants from Wyeth/Ayerst Research, the Heart and Stroke Foundation of Ontario, and the Medical Research Council of Canada. J.W. is a Career Investigator of The Hear1 and Stroke Foundation of Ontario. Submitted for publication Sept. 18, 1995; revision submitted Dec. 13, 1995; accepted Jan. 12, 1996. Reprint requests: David Green, MD, PhD, 345 E. Superior St., Room 1407, Chicago, IL 60611. Copyright © 1996 by Mosby-Year Book, Inc, 0022-2143/96 $5.00 + 0 5/1/71836 clinical trials these agents were found to be effective in this setting and to have a bleeding risk of approximately 5%. ~ In contrast, the risk of bleeding with low-dose unfractionated (standard) heparin (5000 U, two to three times daily) ranges from 5% to 9%. Ketorolac is a nonsteroidal antiinflammatory agent that is effective in the management of moderate to severe pain, particularly in postoperative patients. 2 Single intramuscular injections produce analgesic effects equivalent or superior to those of morphine, and ketorolac may be used as the sole agent for analgesia. 3 Ketorolac is a reversible inhibitor of platelet cyclooxygenase and produces a modest prolongation of the skin bleeding time 4'5 but has no effect on the partial thromboplastin time or the prothrombin time. 6 Although a study in healthy young volunteers has suggested that ketorolac does not interact with hep-
PY - 1996/6
Y1 - 1996/6
N2 - Postoperative patients may receive ketorolac, a nonsteroidal antiinflammatory drug that inhibits platelet function, for analgesia and may receive low-molecular-weight heparin (LMWH) for thrombosis prevention. We investigated whether the combination of these two agents increases blood loss in a rabbit model of hemostasis. In a randomized, blinded study, animals received either intramuscular ketorolac (0.5 mg/kg or 1.0 mg/kg) and subcutaneous saline solution, subcutaneous LMWH (100 U/kg) and intramuscular saline solution, ketorolac (0.5 mg/kg or 1.0 mg/kg) and subcutaneous LMWH (100 U/kg), or intramuscular and subcutaneous saline solution given 30 minutes before ear incision and measurement of blood loss. Collagen-induced platelet aggregation was examined and anti-Xa levels were determined by using a chromogenic substrate method. As compared with results in saline- treated controls, blood loss was significantly increased in animals receiving ketorolac in a dose of 1.0 mg/kg but not in those treated with 0.5 mg/kg. The addition of LMWH did not further increase blood loss above that observed with either dose of ketorolac alone. Platelet aggregation was inhibited by both doses of ketorolac. The anti-Xa levels in the LMWH- treated animals were comparable to those measured in patients receiving these agents for prophylaxis (0.09 to 0.13 U/ml). We conclude that in the rabbit model, LMWH does not augment ketorolac-associated bleeding when both agents are used in doses comparable to those given to human patients.
AB - Postoperative patients may receive ketorolac, a nonsteroidal antiinflammatory drug that inhibits platelet function, for analgesia and may receive low-molecular-weight heparin (LMWH) for thrombosis prevention. We investigated whether the combination of these two agents increases blood loss in a rabbit model of hemostasis. In a randomized, blinded study, animals received either intramuscular ketorolac (0.5 mg/kg or 1.0 mg/kg) and subcutaneous saline solution, subcutaneous LMWH (100 U/kg) and intramuscular saline solution, ketorolac (0.5 mg/kg or 1.0 mg/kg) and subcutaneous LMWH (100 U/kg), or intramuscular and subcutaneous saline solution given 30 minutes before ear incision and measurement of blood loss. Collagen-induced platelet aggregation was examined and anti-Xa levels were determined by using a chromogenic substrate method. As compared with results in saline- treated controls, blood loss was significantly increased in animals receiving ketorolac in a dose of 1.0 mg/kg but not in those treated with 0.5 mg/kg. The addition of LMWH did not further increase blood loss above that observed with either dose of ketorolac alone. Platelet aggregation was inhibited by both doses of ketorolac. The anti-Xa levels in the LMWH- treated animals were comparable to those measured in patients receiving these agents for prophylaxis (0.09 to 0.13 U/ml). We conclude that in the rabbit model, LMWH does not augment ketorolac-associated bleeding when both agents are used in doses comparable to those given to human patients.
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U2 - 10.1016/S0022-2143(96)90149-3
DO - 10.1016/S0022-2143(96)90149-3
M3 - Article
C2 - 8648263
AN - SCOPUS:0030174278
SN - 0022-2143
VL - 127
SP - 583
EP - 587
JO - Journal of Laboratory and Clinical Medicine
JF - Journal of Laboratory and Clinical Medicine
IS - 6
ER -