1999
DOI: 10.1016/s0041-1345(99)00378-4
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Comparative study of antifibrinolytic drugs in orthotopic liver transplantation

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Cited by 18 publications
(6 citation statements)
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“…Epsilon-aminocaproic acid (EACA) and placebo were delivered to the operating room in numbered, but otherwise identical vials labelled “study drug”Participants40 patients undergoing first-time coronary artery bypass grafting without prior sternotomy were randomised to one of two groups: Epsilon aminocaproic acid group: n = 21, M/F 14/7, mean (sd) age = 63 (9) yearsControl group (Placebo): n = 19, M/F = 18/1, mean (sd) age = 67 (10) years Interventions Epsilon aminocaproic acid group (EACA) received 10g of EACA in 40ml of saline solution given after induction of anaesthesia but before the skin incision. Another 40ml was given after heparin administration in the pump, and a third 40ml dose was given after the administration of protamine.Control group (Placebo) received equivalent volumes of saline solution. NB: Both groups were exposed to cell salvage.Outcomes Outcomes reported: Number of patients exposed to allogeneic blood, blood loss (12/24hrs), myocardial infarction, stroke (cerebrovascular accident), use of shed mediastinal bloodNotesQuality assessment score (Schulz criteria): 6/7Transfusion protocol used Risk of bias Item Authors’ judgement Description Adequate sequence generation?UnclearUnclearAllocation concealment?YesAdequateBlinding?All outcomesYesDouble blind Dalmau 1999…”
Section: Characteristics Of Included Studies [Ordered By Study Id]mentioning
confidence: 99%
“…Epsilon-aminocaproic acid (EACA) and placebo were delivered to the operating room in numbered, but otherwise identical vials labelled “study drug”Participants40 patients undergoing first-time coronary artery bypass grafting without prior sternotomy were randomised to one of two groups: Epsilon aminocaproic acid group: n = 21, M/F 14/7, mean (sd) age = 63 (9) yearsControl group (Placebo): n = 19, M/F = 18/1, mean (sd) age = 67 (10) years Interventions Epsilon aminocaproic acid group (EACA) received 10g of EACA in 40ml of saline solution given after induction of anaesthesia but before the skin incision. Another 40ml was given after heparin administration in the pump, and a third 40ml dose was given after the administration of protamine.Control group (Placebo) received equivalent volumes of saline solution. NB: Both groups were exposed to cell salvage.Outcomes Outcomes reported: Number of patients exposed to allogeneic blood, blood loss (12/24hrs), myocardial infarction, stroke (cerebrovascular accident), use of shed mediastinal bloodNotesQuality assessment score (Schulz criteria): 6/7Transfusion protocol used Risk of bias Item Authors’ judgement Description Adequate sequence generation?UnclearUnclearAllocation concealment?YesAdequateBlinding?All outcomesYesDouble blind Dalmau 1999…”
Section: Characteristics Of Included Studies [Ordered By Study Id]mentioning
confidence: 99%
“…In this report, 42 liver transplant patients received EACA (6 mg/hr), and 40 did not. EACA reduced transfusion requirements but not significantly 6. Taken together, EACA has been formally studied in very few liver transplant patients, and the published endpoints of analysis in these studies are difficult to interpret.…”
Section: Discussionmentioning
confidence: 94%
“…Epsilon‐aminocaprioic acid (EACA) has a long history of use during liver transplantation, and its empiric use has been generally safe and well tolerated. Dosing regimens for EACA are based on observational studies that were not blinded or controlled, or in which intraoperative transfusion was used as the primary endpoint for analysis 5, 6. Furthermore, dosing regimens adapted for use during liver transplantation are based on those established for patients without liver disease, and do not account for markedly altered volume of distribution in patients with ESLD 7…”
mentioning
confidence: 99%
“…No apparent benefit from the administration of epsilon‐aminocaproic acid administration on the requirements for ABT was found in three small randomized placebo‐controlled studies 31,38,39 . Similarly, a retrospective study including 36 patients did not show a reduction in the ABT rate 40…”
Section: Module I Pharmacological Alternatives To Reduce Blood Lossmentioning
confidence: 94%