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单采血小板供者筛查细菌污染:PASSPORT 研究结果。

Screening of single-donor apheresis platelets for bacterial contamination: the PASSPORT study results.

机构信息

Department of Pathology, Dartmouth Medical School, Lebanon, New Hampshire 03756, USA.

出版信息

Transfusion. 2010 Mar;50(3):589-99. doi: 10.1111/j.1537-2995.2009.02460.x. Epub 2009 Nov 19.

Abstract

BACKGROUND

The PASSPORT study was an FDA-mandated surveillance of outdated 7-day apheresis platelets (APs) to assess the bacterial culture release test (RT) performance and the chance of transfusing APs containing viable bacteria compared to untested 5-day APs.

STUDY DESIGN AND METHODS

Aerobic and anaerobic culture bottles were inoculated with 4 to 5 mL from APs 24 to 36 hours postcollection. APs were released after 24 hours if no growth was observed. Released APs were recalled for RT positives, and clinical services were notified. Day 8 APs were recultured (surveillance test [ST]). Initially positive RTs and STs were confirmed by AP reculture.

RESULTS

A total of 388,903 RTs were accrued September 2005 through January 2008 from 52 regional blood centers: RT-positive APs interdicted before transfusion, 76 true positive (TP; 195/million; 95% confidence interval [CI], 154-244/million) and 57 indeterminate (IN); and RT-positive APs transfused, 14 TP and 242 IN. There were 14 reported septic transfusion reactions (STRs) from 13 AP collections (23 units) transfused on Days 3 through 7; three STRs were from Day 6 or 7 APs. There were two false-negative RTs causing STRs in three patients. No deaths were reported. STs had four TPs of 6039 tested (662/million; 95% CI, 180-1695/million).

CONCLUSIONS

RT culturing prevents issuance of some bacterially contaminated APs. ST culture data and clinical reports suggest that this screening fails to detect all contaminated units. No fatalities were reported related to AP transfusion. Additional actions or testing may be required to further reduce the residual STR risk of RT APs, even with a 5-day storage limitation.

摘要

背景

PASSPORT 研究是一项由 FDA 授权的针对过时的 7 天单采血小板(AP)的监测研究,旨在评估细菌培养释放试验(RT)的性能,以及与未经测试的 5 天 AP 相比,输注含有存活细菌的 AP 的可能性。

研究设计和方法

在采集后 24 至 36 小时,将需氧和厌氧培养瓶接种 4 至 5 毫升 AP。如果未观察到生长,则在 24 小时后释放 AP。如果 RT 阳性,召回 AP 进行 RT,并通知临床服务部门。第 8 天的 AP 进行再次培养(监测试验 [ST])。最初的阳性 RT 和 ST 通过 AP 再次培养得到确认。

结果

2005 年 9 月至 2008 年 1 月,从 52 个地区血库共获得 388903 次 RT:在输血前被拦截的 RT 阳性 AP,76 次为真阳性(TP;195/百万;95%置信区间 [CI],154-244/百万)和 57 次为不确定(IN);以及输注的 RT 阳性 AP,14 次 TP 和 242 次 IN。在输注第 3 至 7 天的 13 个 AP 采集物(23 个单位)中,有 14 例报告了败血症输血反应(STR);其中 3 例来自第 6 或 7 天的 AP。有 2 次 RT 假阴性导致 3 名患者发生 STR。无死亡报告。ST 检测了 6039 个样本,其中有 4 个 TP(662/百万;95%CI,180-1695/百万)。

结论

RT 培养可防止一些细菌污染的 AP 的发放。ST 培养数据和临床报告表明,这种筛选未能检测到所有污染的单位。与 AP 输血相关,无死亡报告。即使有 5 天的储存限制,可能还需要采取额外的措施或测试,以进一步降低 RT AP 的残留 STR 风险。

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