Benjamin Richard J, McDonald Carl P
American Red Cross Biomedical Services, Medical Office, Rockville, MD.
National Bacteriology Laboratory, NHS Blood and Transplant, London, UK.
Transfus Med Rev. 2014 Apr;28(2):61-71. doi: 10.1016/j.tmrv.2014.01.001. Epub 2014 Feb 5.
The BacT/ALERT microbial detection system (bioMerieux, Inc, Durham, NC) is in routine use in many blood centers as a prerelease test for platelet collections. Published reports document wide variation in practices and outcomes. A systematic review of the English literature was performed to describe publications assessing the use of the BacT/ALERT culture system on platelet collections as a routine screen test of more than 10000 platelet components. Sixteen publications report the use of confirmatory testing to substantiate initial positive culture results but use varying nomenclature to classify the results. Preanalytical and analytical variables that may affect the outcomes differ widely between centers. Incomplete description of protocol details complicates comparison between sites. Initial positive culture results range from 539 to 10606 per million (0.054%-1.061%) and confirmed positive from 127 to 1035 per million (0.013%-0.104%) donations. False-negative results determined by outdate culture range from 662 to 2173 per million (0.066%-0.217%) and by septic reactions from 0 to 66 per million (0%-0.007%) collections. Current culture protocols represent pragmatic compromises between optimizing analytical sensitivity and ensuring the timely availability of platelets for clinical needs. Insights into the effect of protocol variations on outcomes are generally restricted to individual sites that implement limited changes to their protocols over time. Platelet manufacturers should reassess the adequacy of their BacT/ALERT screening protocols in light of the growing international experience and provide detailed documentation of all variables that may affect culture outcomes when reporting results. We propose a framework for a standardized nomenclature for reporting of the results of BacT/ALERT screening.
BacT/ALERT微生物检测系统(生物梅里埃公司,北卡罗来纳州达勒姆)在许多血液中心作为血小板采集的预放行检测被常规使用。已发表的报告记录了实践和结果的广泛差异。对英文文献进行了系统综述,以描述评估BacT/ALERT培养系统用于血小板采集作为超过10000个血小板成分常规筛查试验的出版物。16篇出版物报告了使用确证检测来证实初始阳性培养结果,但使用了不同的术语来对结果进行分类。可能影响结果的分析前和分析变量在各中心之间差异很大。方案细节描述不完整使各站点之间的比较变得复杂。初始阳性培养结果范围为每百万539至10606(0.054%-1.061%),确证阳性结果范围为每百万127至1035(0.013%-0.104%)次捐献。过时培养确定的假阴性结果范围为每百万662至2173(0.066%-0.217%),败血症反应导致的假阴性结果范围为每百万0至66(0%-0.007%)次采集。当前的培养方案是在优化分析灵敏度和确保血小板及时满足临床需求之间的务实折衷。对方案变化对结果影响的见解通常仅限于随着时间推移对其方案进行有限更改的个别站点。血小板制造商应根据不断增加的国际经验重新评估其BacT/ALERT筛查方案的充分性,并在报告结果时提供所有可能影响培养结果的变量的详细文件。我们提出了一个用于报告BacT/ALERT筛查结果的标准化术语框架。