[通过使用生物活性物质预防细菌种群中耐药性的形成]。

Antibiotiki Pub Date : 1984-06-01
G E Afinogenov, T V Kopylova, N I Vladimirov, L N Briantseva
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引用次数: 0

摘要

采用卡那霉素电泳联合双酚酸氯己定抗菌剂治疗四肢感染创面。与单用卡那霉素治疗的患者相比,该组患者创面缩小率高2倍。这些患者体内的微生物污染水平要低得多。需氧菌群污染水平低4.8倍,其中葡萄球菌污染水平低5.9倍。卡那霉素耐药菌的污染水平低了22倍。单独使用卡那霉素治疗导致伤口微生物种群中抗生素耐药变异数量增加2.6倍。在48.2%的患者中,这伴随着伤口的整个微生物种群对卡那霉素的耐药性的发展。18.1%的患者的葡萄球菌群体中卡那霉素耐药性的发展与初始菌株的敏感性变化有关,并且在81.9%的患者中与耐药菌株的重复感染有关。在治疗期间,未观察到初始革兰氏阴性菌对卡那霉素的敏感性发生变化。双光酸氯己定作为一种生物活性物质与卡那霉素联合使用,增强了抗生素的作用,防止了伤口微生物种群中抗生素耐药变异的发展和积累,以及这些种群中耐药性的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prevention of the formation of drug resistance in bacterial populations by using biologically active substances].

The patients with infected wounds of the extremities were treated with kanamycin electrophoresis in combination with chlorhexidine bigluconate, an antiseptic. As compared to the patients treated with kanamycin alone, the rate of the wound size decrease in such patients was 2 times higher. The levels of microbial contamination in these patients were much lower. The contamination level with the aerobic flora was 4.8 times lower, including staphylococci, the level of contamination with which was 5.9 times lower. The contamination level with the kanamycin-resistant bacteria was 22 times lower. The treatment with kanamycin alone resulted in a 2.6-fold increase in the number of the antibiotic-resistant variants in the microbial populations of the wounds. In 48.2 per cent of the patients, this was accompanied by development of resistance to kanamycin in the whole microbial population of the wound. The development of the kanamycin resistance in the staphylococcal populations of 18.1 per cent of the patients was associated with changed sensitivity of the initial strains and in 81.9 per cent of the patients, with superinfection by the resistant strains. No changes in the kanamycin sensitivity of the initial gram-negative organisms during the treatment were observed. The use of chlorhexidine bigluconate, as a biologically active substance in combination with kanamycin potentiated the action of the antibiotic, prevented development and accumulation of the antibiotic-resistant variants in the microbial populations of the wounds and development of the drug resistance in these populations.

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