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富血小板血浆置换术用于减少围手术期异体输血

Platelet-rich-plasmapheresis for minimising peri-operative allogeneic blood transfusion.

作者信息

Carless P A, Rubens F D, Anthony D M, O'Connell D, Henry D A

机构信息

Discipline of Clinical Pharmacology, Faculty of Health, University of Newcastle, Level 5, Clinical Sciences Building, Newcastle Mater Hospital, Edith Street, Waratah, Newcastle, New South Wales, Australia.

出版信息

Cochrane Database Syst Rev. 2003(2):CD004172. doi: 10.1002/14651858.CD004172.

Abstract

BACKGROUND

Concerns regarding the safety of transfused blood have generated considerable enthusiasm for the use of technologies intended to reduce the use of allogeneic blood (blood from an unrelated donor). Platelet-rich plasmapheresis (PRP) offers an alternative approach to blood conservation.

OBJECTIVES

To examine the evidence for the efficacy of PRP in reducing peri-operative allogeneic red blood cell (RBC) transfusion, and the evidence for any effect on clinical outcomes such as mortality and re-operation rates.

SEARCH STRATEGY

Studies were identified by: computer searches of MEDLINE, EMBASE, Current Contents, and the Cochrane Library (to June 2001). These searches were supplemented by checking the reference lists of published articles, reports, and reviews.

SELECTION CRITERIA

Controlled parallel group trials in which adult patients, scheduled for non-urgent surgery, were randomised to PRP, or to a control group who did not receive the intervention.

DATA COLLECTION AND ANALYSIS

Main outcomes measured were: the number of patients receiving an allogeneic RBC transfusion, and the amount of RBC transfused. Trial quality was assessed using criteria proposed by Schulz et al. (Schulz 1995) and Jadad et al. (Jadad 1996).

MAIN RESULTS

Nineteen trials of PRP were identified that reported data for the number of patients exposed to allogeneic RBC transfusion. These trials evaluated a total of 1452 patients. The pooled relative risk (RR) of exposure to allogeneic blood transfusion in those patients randomised to PRP was 0.71 (95%CI: 0.56, 0.90), equating to a relative risk reduction (RRR) of 29%; the average absolute risk reduction (ARR) was 19% (RD = -0.19: 95%CI: -0.29, -0.09). On average, PRP did not significantly reduce the total volume of RBC transfused (weighted mean difference [WMD] = -0.69: 95%CI: -1.93, 0.56 units). Substantial statistical heterogeneity was observed (p < 0.001). Trials provided inadequate data regarding the impact of PRP on morbidity, mortality, and hospital length of stay. The majority of trials were small and of poor methodological quality.

REVIEWER'S CONCLUSIONS: Although the results suggest that PRP is effective in reducing allogeneic RBC transfusion in adult patients undergoing elective surgery, there was considerable heterogeneity in treatment effects and the trials were of poor methodological quality. As the majority of trials were unblinded, transfusion practices may have been influenced by knowledge of the patient's allocation status, potentially exaggerating the true magnitude of the beneficial effect of PRP. The available studies provided inadequate data for firm conclusions to be drawn regarding the impact of PRP on clinically important endpoints.

摘要

背景

对输血安全性的担忧引发了人们对使用旨在减少异体血(来自非亲属供体的血液)使用技术的极大热情。富血小板血浆置换术(PRP)提供了一种血液保护的替代方法。

目的

研究PRP在减少围手术期异体红细胞(RBC)输血方面的疗效证据,以及对诸如死亡率和再次手术率等临床结局的任何影响的证据。

检索策略

通过以下方式识别研究:对MEDLINE、EMBASE、《现刊目次》和Cochrane图书馆进行计算机检索(至2001年6月)。通过查阅已发表文章、报告和综述的参考文献列表对这些检索进行补充。

选择标准

对照平行组试验,其中计划进行非紧急手术的成年患者被随机分为PRP组或未接受干预的对照组。

数据收集与分析

主要测量结局为:接受异体RBC输血的患者数量以及输注的RBC量。使用Schulz等人(Schulz 1995年)和Jadad等人(Jadad 1996年)提出的标准评估试验质量。

主要结果

确定了19项PRP试验,这些试验报告了接受异体RBC输血患者数量的数据。这些试验共评估了1452例患者。随机分组至PRP组的患者接受异体输血的合并相对风险(RR)为0.71(95%CI:0.56,0.90),相当于相对风险降低(RRR)29%;平均绝对风险降低(ARR)为19%(RD = -0.19:95%CI:-0.29,-0.09)。平均而言,PRP并未显著减少输注的RBC总量(加权平均差[WMD] = -0.69:95%CI:-|.93,0.56单位)。观察到显著的统计学异质性(p < 0.001)。试验提供的关于PRP对发病率、死亡率和住院时间影响的数据不足。大多数试验规模较小且方法学质量较差。

综述作者结论

尽管结果表明PRP在减少接受择期手术的成年患者异体RBC输血方面有效,但治疗效果存在相当大的异质性,且试验方法学质量较差。由于大多数试验未设盲,输血操作可能受到患者分组状态知识的影响,这可能夸大了PRP有益效果的真实程度。现有研究提供的数据不足,无法就PRP对临床重要终点的影响得出确凿结论。

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