Breau Rodney H, Lavallée Luke T, Cnossen Sonya, Witiuk Kelsey, Cagiannos Ilias, Momoli Franco, Bryson Gregory, Kanji Salmaan, Morash Christopher, Turgeon Alexis, Zarychanski Ryan, Mallick Ranjeeta, Knoll Greg, Fergusson Dean A
Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Division of Urology, Department of Surgery, The Ottawa Hospital, Ottawa, ON, Canada.
Trials. 2018 May 2;19(1):261. doi: 10.1186/s13063-018-2626-3.
Radical cystectomy for bladder cancer is associated with a high risk of needing red blood cell transfusion. Tranexamic acid reduces blood loss during cardiac and orthopedic surgery, but no study has yet evaluated tranexamic acid use during cystectomy.
A randomized, double-blind (surgeon-, anesthesiologist-, patient-, data-monitor-blinded), placebo-controlled trial of tranexamic acid during cystectomy was initiated in June 2013. Prior to incision, the intervention arm participants receive a 10 mg/kg loading dose of intravenously administered tranexamic acid, followed by a 5 mg/kg/h maintenance infusion. In the control arm, the patient receives an identical volume of normal saline that is indistinguishable from the intervention. The primary outcome is any blood transfusion from the start of surgery up to 30 days post operative. There are no strict criteria to mandate the transfusion of blood products. The decision to transfuse is entirely at the discretion of the treating physicians who are blinded to patient allocation. Physicians are allowed to utilize all resources to make transfusion decisions, including serum hemoglobin concentration and vital signs. To date, 147 patients of a planned 354 have been randomized to the study.
This protocol reviews pertinent data relating to blood transfusion during radical cystectomy, highlighting the need to identify methods for reducing blood loss and preventing transfusion in patients receiving radical cystectomy. It explains the clinical rationale for using tranexamic acid to reduce blood loss during cystectomy, and outlines the study methods of our ongoing randomized controlled trial.
Canadian Institute for Health Research (CIHR) Protocol: MOP-342559; ClinicalTrials.gov, ID: NCT01869413. Registered on 5 June 2013.
膀胱癌根治性膀胱切除术与需要输注红细胞的高风险相关。氨甲环酸可减少心脏和骨科手术中的失血,但尚无研究评估其在膀胱切除术中的应用。
2013年6月启动了一项关于氨甲环酸在膀胱切除术中应用的随机、双盲(外科医生、麻醉医生、患者、数据监测人员均不知情)、安慰剂对照试验。在切开前,干预组参与者静脉注射10mg/kg负荷剂量的氨甲环酸,随后以5mg/kg/h的速度持续输注。在对照组中,患者接受与干预组体积相同、难以区分的生理盐水。主要结局是从手术开始至术后30天内的任何输血情况。没有严格的标准来强制要求输注血液制品。输血的决定完全由对患者分组不知情的治疗医生自行决定。医生可以利用所有资源来做出输血决定,包括血清血红蛋白浓度和生命体征。迄今为止,计划纳入的354例患者中有147例已随机分组进入该研究。
本方案回顾了与根治性膀胱切除术期间输血相关的相关数据,强调了识别减少接受根治性膀胱切除术患者失血和预防输血方法的必要性。它解释了使用氨甲环酸减少膀胱切除术期间失血的临床原理,并概述了我们正在进行的随机对照试验的研究方法。
加拿大卫生研究院(CIHR)方案:MOP - 342559;ClinicalTrials.gov标识符:NCT01869413。于2013年6月5日注册。