【细菌诊断新培养方法】。

Medizinische Klinik (Klinik-Ausg.) Pub Date : 1982-01-01
M Bacharach, F C Sitzmann, M A Abdou, H B Kastert
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引用次数: 0

摘要

本研究的目的是检查一种新的培养方法检测尿路感染的临床意义,特别是在含有抗菌药物残留的尿液样本中。新程序涉及尿液收集和培养杯(UCCC Biotest Serum研究所),其中含有含有化疗药物拮抗剂的回收琼脂(RA5)。将UCCC的效率与常见的半胱氨酸乳糖电解质缺乏琼脂(cystein lactose electrolyte deficient, ced)和MacConkey琼脂包被的浸渍载玻片进行了比较。本研究以305名儿童为研究对象。调查分别在化疗开始前、开始后3 - 5天和停止化疗后3 - 5天进行。尿样中微生物计数与整个临床诊断之间的相关性最高的是RA5。与麦康基琼脂的相关性最低。在开始治疗前确定了良好的相关性,在治疗期间确定了适度的相关性,在停止治疗后确定了非常好的相关性。对于复发和再感染,RA5组治疗期间相关细菌的检出率为90%,ccledagar组为62%,MacConkey组为34.5%。事实证明,RA5对随访非常有用,特别是在使用抗菌药物治疗期间,可以考虑作为体内药敏试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[New culture method for the diagnosis of bacteriurias].

The aim of this study is to check the clinical relevance of a new cultural method for the detection of urinary tract infection especially in urine samples containing residue of antimicrobial agents. The new procedure concerns a urine collecting and cultivating cup (UCCC Biotest Serum Institute), containing a recovery agar (RA5) with incorporated chemotherapeutica antagonists. The efficiency of the UCCC is compared with the familiar dip slide coated with cystein lactose electrolyte deficient (CLED) agar and MacConkey agar. A collective of 305 children is considered in this study. The investigation was carried out before starting, three to five days after starting and three to five days after stopping the chemotherapy. The highest correlation between the microbial count in urine samples and the whole clinical diagnosis was achieved with RA5. The lowest correlation was attained with MacConkey agar. With CLED agar a good correlation was determined before starting therapy, a modest correlation during therapy and very good correlation after stopping therapy. Regarding relapses and reinfections the detection quote of relevant bacteriuria during therapy amounted to 90% as RA5 was used, 62% with CLED agar and 34,5% with MacConkey. RA5 proved very useful for follow-up purposes, especially during treatment with antimicrobial agents and may be considered as a susceptibility testing in vivo.

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