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Intraoperative use of tranexamic acid to reduce transfusion rate in patients undergoing radical retropubic prostatectomy: double blind randomised placebo controlled trial

机译:术中使用氨甲环酸降低接受根治性耻骨后前列腺切除术的患者的输血速度:双盲随机安慰剂对照试验

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摘要

>Objectives To determine the efficacy of intraoperative treatment with low dose tranexamic acid in reducing the rate of perioperative transfusions in patients undergoing radical retropubic prostatectomy.>Design Double blind, parallel group, randomised, placebo controlled trial.>Setting One university hospital in Milan, Italy.>Participants 200 patients older than 18 years and undergoing radical retropubic prostatectomy agreed to participate in the trial. Exclusion criteria were atrial fibrillation, coronary artery disease treated with drug eluting stent, severe chronic renal failure, congenital or acquired thrombophilia, and known or suspected allergy to tranexamic acid.>Interventions Intravenous infusion of tranexamic acid or equivalent volume of placebo (saline) according to the following protocol: loading dose of 500 mg tranexamic acid 20 minutes before surgery followed by continuous infusion of tranexamic acid at 250 mg/h during surgery.>Main outcome measures Primary outcome: number of patients receiving blood transfusions perioperatively. Secondary outcome: intraoperative blood loss. Six month follow-up to assess long term safety in terms of mortality and thromboembolic events.>Results All patients completed treatment and none was lost to follow-up. Patients transfused were 34 (34%) in the tranexamic acid group and 55 (55%) in the control group (absolute reduction in transfusion rate 21% (95% CI 7% to 34%); relative risk of receiving transfusions for patients treated with tranexamic acid 0.62 (0.45 to 0.85); number needed to treat 5 (3 to 14); P=0.004). At follow-up, no patients died and the occurrence of thromboembolic events did not differ between the two groups.>Conclusions Intraoperative treatment with low dose tranexamic acid is safe and effective in reducing the rate of perioperative blood transfusions in patients undergoing radical retropubic prostatectomy. >Trial registration ClinicalTrials.gov identifier .
机译:>目标:确定低剂量氨甲环酸的术中治疗降低行根治性耻骨后前列腺切除术患者围手术期输血率的功效。>设计双盲,平行分组,随机分组,安慰剂对照试验。>设置意大利米兰的一所大学医院。>参与者 200名年龄在18岁以上且接受根治性耻骨后前列腺切除术的患者同意参加该试验。排除标准为房颤,药物洗脱支架治疗的冠状动脉疾病,严重的慢性肾功能衰竭,先天性或获得性血栓形成性血友病,以及已知或怀疑对氨甲环酸过敏。>干预根据以下方案服用安慰剂(盐水):术前20分钟加注500毫克氨甲环酸的剂量,然后在手术过程中以250 mg / h的速度连续输注氨甲环酸。>主要疗效指标:主要疗效:围手术期接受输血的患者人数。次要结果:术中失血。六个月的随访,以评估死亡率和血栓栓塞事件的长期安全性。>结果所有患者均已完成治疗,但均未失去随访。氨甲环酸组的输血患者为34(34%),对照组为55(55%)(绝对输血率降低21%(95%CI为7%至34%);接受治疗的患者接受输血的相对风险用氨甲环酸0.62(0.45至0.85);治疗5所需的数字(3至14); P = 0.004)。随访时,两组均无患者死亡,血栓栓塞事件的发生率无差异。>结论术中低剂量氨甲环酸治疗对降低围手术期输血率是安全有效的。根治性耻骨后前列腺切除术的患者。 >试验注册 ClinicalTrials.gov标识符。

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