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TACO-BEL-3:在十家医院中对接受输血的患者使用利尿剂的可行性研究和回顾性审计。

TACO-BEL-3: a feasibility study and a retrospective audit of diuretics for patients receiving blood transfusion at ten hospitals.

机构信息

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.

Laboratory Medicine Program, University Health Network, Toronto, ON, Canada.

出版信息

Vox Sang. 2021 Apr;116(4):434-439. doi: 10.1111/vox.12994. Epub 2020 Oct 26.

Abstract

BACKGROUND AND OBJECTIVES

Transfusion-associated circulatory overload (TACO) is the leading cause of transfusion-related morbidity and mortality. A recently completed pilot trial randomized patients to pre-transfusion furosemide versus placebo but had a slower than expected enrollment rate. We sought to determine whether the lack of recruitment was due to a paucity of eligible patients or excessively restrictive eligibility criteria.

MATERIALS AND METHODS

At 10 sites, eligible patients were retrospectively identified by first screening blood bank databases over one month for all transfusion episodes meeting trial inclusion criteria, defined as non-surgical patients receiving single RBC unit transfusions. The age threshold was decreased from 65 to 50 years. The first 10 patients meeting inclusion criteria then underwent detailed chart review for the exclusion criteria. The incidence of TACO and furosemide use was also recorded.

RESULTS

At the 10 sites, 11 969 red cell units were transfused over 1 month and 1356 met the inclusion criteria. Of the 100 charts reviewed, 60 (60%) had no exclusion criteria. Active bleeding was the most common reason for ineligibility. There were 813 eligible transfusion episodes. Of the eligible patients, 17 (28·3%) had evidence of congestive heart failure, and furosemide was prescribed in 24 (40%). Despite the use of a lower age threshold, three cases of TACO were detected with an incidence of 3%.

CONCLUSION

A large number of transfusion episodes met eligibility criteria. With a 3% incidence of TACO, 50% decrease through the use pre-transfusion furosemide and a target consent rate of 30%, a definitive trial of approximately 3000 patients could be completed within 1 year.

摘要

背景与目的

输血相关性循环超负荷(TACO)是输血相关发病率和死亡率的主要原因。最近完成的一项试点试验将患者随机分配至输血前呋塞米组与安慰剂组,但入组速度比预期慢。我们旨在确定招募不足是否是由于合格患者数量不足还是过于严格的入选标准。

材料与方法

在 10 个地点,通过首先在一个月内筛选血库数据库,对符合试验纳入标准的所有输血事件进行回顾性识别,定义为接受单个 RBC 单位输血的非手术患者。年龄阈值从 65 岁降低至 50 岁。符合纳入标准的前 10 名患者随后接受详细的图表审查以排除标准。还记录了 TACO 的发生率和呋塞米的使用情况。

结果

在 10 个地点,在 1 个月内输注了 11969 个红细胞单位,有 1356 个符合纳入标准。在审查的 100 份图表中,有 60 份(60%)没有排除标准。活动性出血是最常见的不合格原因。有 813 个符合输血条件的事件。在符合条件的患者中,有 17 例(28.3%)有充血性心力衰竭的证据,24 例(40%)开具了呋塞米。尽管使用了较低的年龄阈值,但仍检测到 3 例 TACO,发生率为 3%。

结论

大量输血事件符合入选标准。使用 TACO 的发生率为 3%,通过使用输血前呋塞米降低 50%,并设定 30%的目标同意率,可在 1 年内完成大约 3000 名患者的确定性试验。

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