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在Groupamatic设备上实现梅毒絮凝试验的自动化。

Automation of a flocculation test for syphilis on Groupamatic equipment.

作者信息

Garretta M, Paris-Hamelin A, Gener J, Muller A, Matte C, Vaisman A

出版信息

Br J Vener Dis. 1975 Aug;51(4):232-9. doi: 10.1136/sti.51.4.232.

Abstract

A flocculation reaction employing a cardiolipid antigen was used for syphilis screening on Groupamatic equipment in parallel with conventional screening reactions: Kolmer CF, RPCF, Kahn, Kline, and RPR. The positive samples were confirmed by FTA-200, FTA-ABS, TPI, and in some cases by TPHA. There were 5,212 known samples which had already been tested by all methods and of which 1,648 were positive, and 58,636 screened samples including 65 positives. Half of the samples in the first series were taken without anticoagulant; the remainder were collected in potassium EDTA. The percentage of false positives with the Groupamatic was about 1-4 per cent. The percentage of false negatives among positve (greater than or equal+) samples varied from 0-18 to 1-3 per cent.; on the other hand the sensitivity was less good for samples giving doubtful and/or dissociated reactions in conventional screening reactions. The specificity and sensitivity of this technique are acceptable for a blood transfusion centre. The reproducibility is excellent and the automatic reading of results accurate. Additional advantages are rapidity (340 samples processed per hour); simultaneous performance of eleven other immunohaematological reactions; no contamination between samples; automatic reading, interpretation, and print-out of results; and saving of time because samples are not filed sequentially and are automatically identified when the results are obtained. Although the importance of syphilis in blood transfusion seems small, estimates of the risk are difficult and further investigations are planned.

摘要

采用心磷脂抗原的絮凝反应在Groupamatic设备上用于梅毒筛查,同时进行传统的筛查反应:科尔默补体结合试验(Kolmer CF)、快速血浆补体结合试验(RPCF)、康氏反应(Kahn)、克莱恩反应(Kline)和快速血浆反应素环状卡片试验(RPR)。阳性样本通过荧光螺旋体抗体吸收试验(FTA-200)、荧光螺旋体抗体吸附试验(FTA-ABS)、梅毒螺旋体颗粒凝集试验(TPI)进行确认,部分样本通过梅毒螺旋体血凝试验(TPHA)进行确认。有5212份已知样本已通过所有方法检测,其中1648份为阳性,另有58636份筛查样本,包括65份阳性样本。第一批样本中有一半未加抗凝剂采集;其余样本采集于乙二胺四乙酸钾(EDTA钾)中。Groupamatic设备的假阳性率约为1%至4%。阳性(大于或等于阳性+)样本中的假阴性率在0.18%至1.3%之间;另一方面,对于在传统筛查反应中给出可疑和/或解离反应的样本,该技术的敏感性较差。该技术的特异性和敏感性对于输血中心来说是可以接受的。重复性极佳,结果自动读取准确。其他优点包括速度快(每小时处理340个样本);可同时进行其他十一项免疫血液学反应;样本之间无交叉污染;结果自动读取、判读和打印输出;由于样本不是按顺序存档,并且在获得结果时自动识别,因此节省了时间。尽管梅毒在输血中的重要性似乎较小,但风险评估困难,因此计划进行进一步调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02f8/1046556/0288a74f4902/brjvendis00058-0014-a.jpg

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