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地塞米松对实验性耐青霉素和头孢菌素肺炎球菌脑膜炎治疗的影响。

Effect of dexamethasone on therapy of experimental penicillin- and cephalosporin-resistant pneumococcal meningitis.

作者信息

París M M, Hickey S M, Uscher M I, Shelton S, Olsen K D, McCracken G H

机构信息

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235-9063.

出版信息

Antimicrob Agents Chemother. 1994 Jun;38(6):1320-4. doi: 10.1128/AAC.38.6.1320.

Abstract

Treatment of pneumococcal meningitis has become problematic because of the emergence of penicillin- and cephalosporin-resistant strains and because of the concern that dexamethasone therapy might reduce penetration of antibiotics into the cerebrospinal fluid (CSF). We addressed these issues with our rabbit meningitis model by studying two pneumococcal isolates that were resistant to penicillin and ceftriaxone and susceptible to vancomycin and rifampin. Ceftriaxone, vancomycin, and rifampin were given alone or in combination, with or without coadministration of dexamethasone. Treatment was started 12 to 14 h after intracisternal inoculation of approximately 10(4) CFU of one of the organisms. Rifampin concentrations in serum and CSF were similar, regardless of whether dexamethasone was given, whereas those of ceftriaxone were somewhat lower at each time point in animals given dexamethasone. The penetration of vancomycin into CSF was consistently and substantially reduced with dexamethasone treatment, which resulted in a delay in CSF sterilization not observed in non-dexamethasone-treated animals. When rifampin was used with ceftriaxone for treatment of meningitis caused by the more resistant strain, bacteriologic cure occurred promptly, with or without dexamethasone therapy. In areas with high rates of occurrence of resistant pneumococcal strains, we believe initial empiric therapy of bacterial meningitis should include two antibiotics: ceftriaxone and either rifampin or vancomycin. When dexamethasone is used, the combination of ceftriaxone and rifampin is preferred for therapy.

摘要

由于对青霉素和头孢菌素耐药菌株的出现,以及担心地塞米松治疗可能会降低抗生素进入脑脊液(CSF)的渗透率,肺炎球菌脑膜炎的治疗已成为一个难题。我们通过研究两种对青霉素和头孢曲松耐药但对万古霉素和利福平敏感的肺炎球菌分离株,利用我们的兔脑膜炎模型解决了这些问题。头孢曲松、万古霉素和利福平单独或联合给药,同时给予或不给予地塞米松。在脑池内接种约10⁴CFU的其中一种细菌后12至14小时开始治疗。无论是否给予地塞米松,血清和脑脊液中的利福平浓度相似,而在给予地塞米松的动物中,每个时间点的头孢曲松浓度略低。地塞米松治疗使万古霉素进入脑脊液的渗透率持续且大幅降低,这导致脑脊液灭菌延迟,而在未用地塞米松治疗的动物中未观察到这种情况。当利福平与头孢曲松联合用于治疗由耐药性更强的菌株引起的脑膜炎时,无论是否进行地塞米松治疗,细菌学治愈均迅速出现。在耐药肺炎球菌菌株发生率高的地区,我们认为细菌性脑膜炎的初始经验性治疗应包括两种抗生素:头孢曲松和利福平或万古霉素。当地塞米松使用时,头孢曲松和利福平联合治疗是首选。

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