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四川大学华西医院针对预计需大量输注红细胞的非心脏手术的个体化急性等容血液稀释:一项随机对照试验的研究方案

Individualised acute normovolaemic haemodilution for non-cardiac surgery with anticipated high-dose red cell transfusion: study protocol for a randomised controlled trial in West China Hospital of Sichuan University.

作者信息

Liao Chenxi, Tan Jinzhe, An Jingjing, Zhong Jie, Lai Xingning, Tian Leilei, Liao Ren

机构信息

Department of Anesthesia and Operation Center, West China Hospital of Sichuan University, Chengdu, Sichuan, China.

Chinese Academy of Medical Sciences (2018RU012), Chengdu, Sichuan, China.

出版信息

BMJ Open. 2025 Jan 2;15(1):e088326. doi: 10.1136/bmjopen-2024-088326.

Abstract

INTRODUCTION

Acute normovolaemic haemodilution (ANH) is a perioperative blood management technique involving the removal of whole blood and simultaneous infusion of colloids or crystalloids to achieve haemodilution while maintaining normovolaemia. However, its efficacy in reducing the requirement for perioperative allogeneic blood transfusion remains controversial due to inconsistent findings in the literature. An individualised red cell transfusion strategy, guided by the West China Liu's Score, has demonstrated effectiveness in reducing the need for allogeneic red cell transfusion. Building on this evidence, we propose an individualised ANH approach and hypothesise that individualised ANH, guided by the West China Liu's Score, can reduce the requirement for allogeneic red cells during the perioperative period.

METHODS AND ANALYSIS

This is a single centre, prospective, randomised controlled trial designed to evaluate the superiority of the individualised ANH, based on the West China Liu's Score, in reducing perioperative red cell requirements compared with current clinical practice. Adult patients undergoing elective non-cardiac surgery with an anticipated red cell transfusion volume exceeding eight units (or 1600 mL) will be enrolled and randomly allocated to either the 'ANH group' or the 'Control group' in a 1:1 ratio. The primary outcome is the perioperative consumption of the allogeneic red blood cells. Data analysis will adhere to the intent-to-treat principle.

ETHICS AND DISSEMINATION

The study protocol (V.1.0) has been approved by the Biological Medical Ethical Committee of the West China Hospital of Sichuan University, with approval No. 2024(595) on 17 April 2024. The results of this trial will be disseminated by publication in peer-reviewed journals and academic conference presentations.

TRIAL REGISTRATION NUMBER

National Institutes of Health Clinical Trials Registry, NCT06399536. 2 May 2024.

摘要

引言

急性等容血液稀释(ANH)是一种围手术期血液管理技术,包括采集全血并同时输注胶体液或晶体液以实现血液稀释,同时维持血容量正常。然而,由于文献中的研究结果不一致,其在减少围手术期异体输血需求方面的疗效仍存在争议。以西华刘氏评分指导的个体化红细胞输血策略已证明在减少异体红细胞输血需求方面有效。基于这一证据,我们提出一种个体化ANH方法,并假设以西华刘氏评分为指导的个体化ANH可减少围手术期异体红细胞的需求。

方法与分析

这是一项单中心、前瞻性、随机对照试验,旨在评估以西华刘氏评分为基础的个体化ANH在减少围手术期红细胞需求方面优于当前临床实践。预计红细胞输血量超过8单位(或1600毫升)的择期非心脏手术成年患者将被纳入研究,并以1:1的比例随机分配至“ANH组”或“对照组”。主要结局是围手术期异体红细胞的消耗量。数据分析将遵循意向性分析原则。

伦理与传播

本研究方案(V.1.0)已获得四川大学华西医院生物医学伦理委员会批准,批准号为2024(595),批准日期为2024年4月17日。本试验结果将通过在同行评审期刊上发表及在学术会议上报告进行传播。

试验注册号

美国国立卫生研究院临床试验注册中心,NCT06399536。2024年5月2日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84e0/11749195/c57291f02a08/bmjopen-15-1-g001.jpg

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