Efficacy of aminocaproic, tranexamic acids in the control of bleeding during total knee replacement: a randomized clinical trial

Risks and costs of allogeneic blood transfusions mandate strategies to reduce blood loss in surgery. The objective of this study was to assess the efficacy of antifibrinolytic treatment in reducing perioperative blood loss during total knee replacement. A double-blind, randomized and placebo-control...

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Veröffentlicht in:British journal of anaesthesia : BJA 2006-05, Vol.96 (5), p.576-582
Hauptverfasser: Camarasa, M.A., Ollé, G., Serra-Prat, M., Martín, A., Sánchez, M., Ricós, P., Pérez, A., Opisso, L.
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container_issue 5
container_start_page 576
container_title British journal of anaesthesia : BJA
container_volume 96
creator Camarasa, M.A.
Ollé, G.
Serra-Prat, M.
Martín, A.
Sánchez, M.
Ricós, P.
Pérez, A.
Opisso, L.
description Risks and costs of allogeneic blood transfusions mandate strategies to reduce blood loss in surgery. The objective of this study was to assess the efficacy of antifibrinolytic treatment in reducing perioperative blood loss during total knee replacement. A double-blind, randomized and placebo-controlled clinical trial was carried out on 127 patients undergoing total knee replacement. Patients in the study group received tranexamic acid 10 mg kg−1 i.v. just before the tourniquet was deflated and 3 h later, or epsilon-aminocaproic acid 100 mg kg−1 before tourniquet deflation followed by continuous perfusion (1 g h−1) during 3 h. External perioperative blood loss was measured and total blood loss was calculated. The number of patients transfused and number of packed red cell (PRC) units transfused was recorded and possible postoperative thromboembolic complications were investigated. Total blood loss [mean (sd)] was 1099 ml (535) in the group that received antifibrinolytic agents and 1784 ml (660) in the control group (P
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The objective of this study was to assess the efficacy of antifibrinolytic treatment in reducing perioperative blood loss during total knee replacement. A double-blind, randomized and placebo-controlled clinical trial was carried out on 127 patients undergoing total knee replacement. Patients in the study group received tranexamic acid 10 mg kg−1 i.v. just before the tourniquet was deflated and 3 h later, or epsilon-aminocaproic acid 100 mg kg−1 before tourniquet deflation followed by continuous perfusion (1 g h−1) during 3 h. External perioperative blood loss was measured and total blood loss was calculated. The number of patients transfused and number of packed red cell (PRC) units transfused was recorded and possible postoperative thromboembolic complications were investigated. Total blood loss [mean (sd)] was 1099 ml (535) in the group that received antifibrinolytic agents and 1784 ml (660) in the control group (P&lt;0.001). Five patients (7.5%) in the study group and 23 (38.3%) in the control group (P&lt;0.001) received blood transfusions; the first group received a mean of 0.10 PRC unit per patient and the second, 0.58 (P&lt;0.001). Mean reduction in haemoglobin levels (g dl−1) between preoperative and fifth day postoperative readings was 2.5 (0.9) in the study group and 3.4 (1.2) in the control group (P&lt;0.001). Clinical assessment did not reveal any thromboembolic complications. 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The objective of this study was to assess the efficacy of antifibrinolytic treatment in reducing perioperative blood loss during total knee replacement. A double-blind, randomized and placebo-controlled clinical trial was carried out on 127 patients undergoing total knee replacement. Patients in the study group received tranexamic acid 10 mg kg−1 i.v. just before the tourniquet was deflated and 3 h later, or epsilon-aminocaproic acid 100 mg kg−1 before tourniquet deflation followed by continuous perfusion (1 g h−1) during 3 h. External perioperative blood loss was measured and total blood loss was calculated. The number of patients transfused and number of packed red cell (PRC) units transfused was recorded and possible postoperative thromboembolic complications were investigated. Total blood loss [mean (sd)] was 1099 ml (535) in the group that received antifibrinolytic agents and 1784 ml (660) in the control group (P&lt;0.001). Five patients (7.5%) in the study group and 23 (38.3%) in the control group (P&lt;0.001) received blood transfusions; the first group received a mean of 0.10 PRC unit per patient and the second, 0.58 (P&lt;0.001). Mean reduction in haemoglobin levels (g dl−1) between preoperative and fifth day postoperative readings was 2.5 (0.9) in the study group and 3.4 (1.2) in the control group (P&lt;0.001). Clinical assessment did not reveal any thromboembolic complications. 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subjects 6-aminocaproic acid
Aged
Aged, 80 and over
agents
agents, antifibrinolytic, 6-aminocaproic acid
agents, antifibrinolytic, tranexamic acid
Aminocaproic Acid - therapeutic use
Anesthesia
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
antifibrinolytic
Antifibrinolytic Agents - therapeutic use
arthroplasty
Arthroplasty, Replacement, Knee
Biological and medical sciences
blood
Blood Loss, Surgical - prevention & control
Blood Transfusion
blood, loss, surgical
Double-Blind Method
Female
Hemoglobins - metabolism
Hemostasis, Surgical - methods
Humans
knee replacement
loss
Male
Medical sciences
Middle Aged
surgery
surgery, arthroplasty, knee replacement
surgical
tranexamic acid
Tranexamic Acid - therapeutic use
Treatment Outcome
title Efficacy of aminocaproic, tranexamic acids in the control of bleeding during total knee replacement: a randomized clinical trial
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