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生物发光尿液筛查在三级医疗机构中的应用。

Application of bioluminescent urine screens in a tertiary care facility.

作者信息

Males B M, Bartholomew W R, Amsterdam D

出版信息

Diagn Microbiol Infect Dis. 1986 Jan;4(1):1-10. doi: 10.1016/0732-8893(86)90050-7.

Abstract

Two adenosine triphosphate (ATP)-detection systems for quantitating bacteriuria, the LUMAC (noncentrifugation method) and MONOLIGHT (centrifugation method) urine screens, were separately evaluated for their capacity to detect bacteriuria in specimens from patients at a tertiary care teaching hospital. Results of each study were compared with the findings of conventional culture. Indices of test efficacy, sensitivity/predictive value for a negative test, were as follows: at greater than or equal to 10(4) CFU/ml--LUMAC 88%/93% and MONOLIGHT 82%/88%; and at greater than or equal to 10(5) CFU/ml--LUMAC 99%/99% and MONOLIGHT 97%/99%. Both systems were satisfactory urine screens for catheterized and midstream urine specimens when used at the traditional level of significance (greater than or equal to 10(5) CFU/ml). An assessment of the MONOLIGHT noncentrifugation protocol demonstrated efficacy of the system to detect significant bacteriuria at greater than or equal to 10(5) CFU/ml. Decreased numbers of false-positive results compared to the centrifugation method were obtained with this assay. False-positive and false-negative results were attributable to threshold sensitivity of the instruments. The presence of somatic cells and yeasts were associated with false-positive results. False-positive results might stem from the inability of conventional culture to recover selected microorganisms. Time and cost analyses of the LUMAC system indicated that significant savings over conventional methodology were not effected.

摘要

两种用于定量检测菌尿的三磷酸腺苷(ATP)检测系统,即LUMAC(非离心法)和MONOLIGHT(离心法)尿液筛查,在一家三级护理教学医院对其检测患者标本中菌尿的能力进行了单独评估。每项研究的结果都与传统培养的结果进行了比较。检测效能指标,即阴性检测的灵敏度/预测值如下:在菌落形成单位(CFU)/毫升大于或等于10⁴时,LUMAC为88%/93%,MONOLIGHT为82%/88%;在CFU/毫升大于或等于10⁵时,LUMAC为99%/99%,MONOLIGHT为97%/99%。当按照传统的显著水平(CFU/毫升大于或等于10⁵)使用时,这两种系统对于导尿和中段尿标本都是令人满意的尿液筛查方法。对MONOLIGHT非离心方案的评估表明,该系统在CFU/毫升大于或等于10⁵时检测显著菌尿的效能。与离心法相比,该检测方法获得的假阳性结果数量减少。假阳性和假阴性结果归因于仪器的阈值灵敏度。体细胞和酵母的存在与假阳性结果相关。假阳性结果可能源于传统培养无法回收某些微生物。对LUMAC系统的时间和成本分析表明,与传统方法相比并没有实现显著的节省。

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