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抗生素对预防实验性脆弱拟杆菌心内膜炎的作用。

Effect of antibiotics on the prevention of experimental Bacteroides fragilis endocarditis.

作者信息

Goldman P L, Durack D T, Petersdorf R G

出版信息

Antimicrob Agents Chemother. 1978 Nov;14(5):755-60. doi: 10.1128/AAC.14.5.755.

Abstract

The relative efficacy of single doses of antibiotics in modifying the development of Bacteroides fragilis subsp. fragilis endocarditis was studied in an experimental model. Antibiotics were administered 0.5 h before intravenous injection of B. fragilis subsp. fragilis into rabbits prepared by insertion of a polyethylene catheter into the left side of the heart; 48 h later, intracardiac vegetations were excised and cultured anaerobically. B. fragilis was recovered from 92% of untreated animals. After a single dose of procaine penicillin G (250 mg/kg intramuscularly), 80% of the animals remained infected. Chloramphenicol (30 mg/kg), carbenicillin (50 mg/kg), and metronidazole (10 mg/kg) were also ineffective (76, 80, and 75% infected, respectively). Cefamandole (30 mg/kg), cefoxitin (30 mg/kg), and erythromycin (30 mg/kg) were significantly more active (50, 55, and 45% infected, respectively), as were higher doses of carbenicillin. Clindamycin (50 mg/kg) was the most effective regimen (11% infected). At present, the relevance of these results to the therapy of serious B. fragilis infections is not known, but this model may prove useful in the evaluation of the prevention of B. fragilis subsp. fragilis bacteremia.

摘要

在一个实验模型中研究了单剂量抗生素对脆弱拟杆菌脆弱亚种心内膜炎发展的影响。在通过将聚乙烯导管插入兔心脏左侧制备的动物模型中,于静脉注射脆弱拟杆菌脆弱亚种前0.5小时给予抗生素;48小时后,切除心内赘生物并进行厌氧培养。92%的未治疗动物中可分离出脆弱拟杆菌。单剂量普鲁卡因青霉素G(250mg/kg肌肉注射)后,80%的动物仍被感染。氯霉素(30mg/kg)、羧苄西林(50mg/kg)和甲硝唑(10mg/kg)也无效(分别有76%、80%和75%的动物被感染)。头孢孟多(30mg/kg)、头孢西丁(30mg/kg)和红霉素(30mg/kg)的活性显著更高(分别有50%、55%和45%的动物被感染),更高剂量的羧苄西林也是如此。克林霉素(50mg/kg)是最有效的方案(11%的动物被感染)。目前,这些结果与严重脆弱拟杆菌感染治疗的相关性尚不清楚,但该模型可能在评估脆弱拟杆菌脆弱亚种菌血症的预防方面证明有用。

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