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环丙沙星和头孢唑肟诱导的革兰氏阴性杆菌耐药的治疗。

Treatment of ciprofloxacin- and ceftizoxime-induced resistant gram-negative bacilli.

作者信息

Fasching C E, Gerding D N, Peterson L R

出版信息

Am J Med. 1987 Apr 27;82(4A):80-6.

PMID:3472465
Abstract

Gram-negative bacilli that had been selected for resistance to either ciprofloxacin or ceftizoxime as a result of previous exposure to these agents were inoculated into semipermeable subcutaneous chambers in rabbits, modeling a locally neutropenic closed-space infection. Five resistant organisms, one Serratia marcescens (157) and four Pseudomonas aeruginosa (864, 876, 913, and 915) strains, were selected by previous therapy with ciprofloxacin, and six Pseudomonas strains (833, 845, 864, 876, 913, and 915) were selected by previous therapy with ceftizoxime. Animals were treated with either single antibiotics or combinations of antibiotics for four days, and the response was determined by quantitative bacterial count measurements. The selected (induced) resistance was stable for at least four days, both in vivo and in vitro, but was limited to the antibiotic class of the agent used for induction. Four of five isolates for which resistance had been induced by ciprofloxacin returned to preinduction susceptibility by the eight day of subculture. Organisms that were selected for resistance to ciprofloxacin were successfully treated by a combination of azlocillin and amikacin, and were as sensitive to that regimen as were the parent, uninduced strains. Organisms selected for resistance by pretreatment with ceftizoxime were successfully treated by the combination of ciprofloxacin plus azlocillin, and this regimen was also equally active against the selected strains as it was against the parental isolates. Although selection or induction of resistance is a potential problem with all new potent antimicrobial agents, it appears that infections due to these isolates can still be treated successfully through the use of appropriate combination chemotherapy.

摘要

因先前接触环丙沙星或头孢唑肟而被选择具有对这些药物耐药性的革兰氏阴性杆菌,被接种到兔的半透性皮下腔室中,模拟局部中性粒细胞减少的封闭空间感染。通过先前用环丙沙星治疗选择了5种耐药菌,1株粘质沙雷氏菌(157)和4株铜绿假单胞菌(864、876、913和915)菌株,通过先前用头孢唑肟治疗选择了6株铜绿假单胞菌菌株(833、845、864、876、913和915)。动物用单一抗生素或抗生素组合治疗4天,并通过定量细菌计数测量来确定反应。所选(诱导)的耐药性在体内和体外至少4天内是稳定的,但仅限于用于诱导的药物的抗生素类别。环丙沙星诱导耐药的5株分离株中有4株在传代培养的第8天恢复到诱导前的敏感性。对环丙沙星耐药的菌株通过阿洛西林和阿米卡星联合成功治疗,并且对该方案的敏感性与未诱导的亲本菌株相同。通过头孢唑肟预处理选择耐药的菌株通过环丙沙星加阿洛西林联合成功治疗,并且该方案对所选菌株的活性与对亲本分离株的活性相同。尽管耐药性的选择或诱导是所有新型强效抗菌药物的一个潜在问题,但似乎由这些分离株引起的感染仍可通过使用适当的联合化疗成功治疗。

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