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赖特蛋白补体结合法的多项实验室评估

MULTIPLE LABORATORY EVALUATION OF THE REITER PROTEIN COMPLEMENT FIXATION METHOD.

作者信息

Miller J N, Carpenter C M, Boak R A, Peterson E T, Pait C F, Lawrence C A, Heidbreder G A, Linscott W D, Fazzan F P

出版信息

Calif Med. 1961 Apr;94(4):203-8.

Abstract

Duplicate Reiter protein complement fixation tests were carried out on different days at the UCLA laboratory on 636 specimens entailing diagnostic problems. Results were in agreement in 94.2 per cent of cases.A comparison of the results obtained with the first RPCF test carried out on 639 diagnostic problem specimens submitted to four Los Angeles laboratories showed disagreement ranging from 10 to 13 per cent.Agreement between RPCF and TPI results in each of the four laboratories ranged from 81.2 to 82.7 per cent.A greater correlation was obtained between RPCF and TPI results than between TPI and STS or RPCF and STS. In the presence of nonreactive RPCF tests, from 5.6 to 7.1 per cent of the specimens tested in each laboratory were reactive to VDRL and TPI tests. Nonreactive VDRL and reactive TPI results ranged from 7.2 to 8.3 per cent of the specimens tested. In the presence of reactive TPI and RPCF results, 5.5 to 6.4 per cent of the specimens tested in each laboratory showed nonreactive VDRL tests.Twenty-nine or 4.6 per cent of 625 specimens tested showed nonreactive VDRL, reactive cardiolipin Kolmer and reactive TPI tests.Of the weakly reactive RPCF, VDRL or cardiolipin Kolmer tests, a higher percentage of the RPCF results gave reactive TPI tests than did either the VDRL or cardiolipin Kolmer procedures. The number of specimens showing discrepant RPCF results upon being retested in the four laboratories ranged from 33 to 68. Reactive TPI tests on those specimens ranged from 30.3 per cent to 54.4 per cent.

摘要

在加州大学洛杉矶分校实验室,对636份存在诊断问题的标本在不同日期进行了重复的赖特蛋白补体结合试验。94.2%的病例结果一致。对提交给四个洛杉矶实验室的639份存在诊断问题的标本进行首次赖特蛋白补体结合试验后,所得结果的不一致率在10%至13%之间。四个实验室中每个实验室的赖特蛋白补体结合试验(RPCF)和梅毒螺旋体免疫试验(TPI)结果之间的一致率在81.2%至82.7%之间。赖特蛋白补体结合试验和梅毒螺旋体免疫试验结果之间的相关性高于梅毒螺旋体免疫试验与性病研究实验室试验(STS)或赖特蛋白补体结合试验与性病研究实验室试验之间的相关性。在赖特蛋白补体结合试验无反应的情况下,每个实验室检测的标本中有5.6%至7.1%对性病研究实验室试验(VDRL)和梅毒螺旋体免疫试验呈阳性反应。性病研究实验室试验无反应而梅毒螺旋体免疫试验呈阳性反应的标本占检测标本的7.2%至8.3%。在梅毒螺旋体免疫试验和赖特蛋白补体结合试验呈阳性反应的情况下,每个实验室检测的标本中有5.5%至6.4%的性病研究实验室试验无反应。在625份检测标本中,29份(占4.6%)的性病研究实验室试验无反应、心磷脂科尔默试验呈阳性反应且梅毒螺旋体免疫试验呈阳性反应。在赖特蛋白补体结合试验、性病研究实验室试验或心磷脂科尔默试验弱阳性的情况下,与性病研究实验室试验或心磷脂科尔默试验相比,更高比例的赖特蛋白补体结合试验结果使梅毒螺旋体免疫试验呈阳性反应。在四个实验室对这些标本重新检测时,出现不一致赖特蛋白补体结合试验结果的标本数量在33至68份之间。这些标本中梅毒螺旋体免疫试验呈阳性反应的比例在30.3%至54.4%之间。

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