Choi S, Hahn T W, Osterhout G, O'Brien T P
Ocular Microbiology Laboratory, Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Arch Ophthalmol. 1996 Jan;114(1):61-5. doi: 10.1001/archopht.1996.01100130057009.
To evaluate the most effective intravitreal antibiotic treatment of vancomycin-sensitive and -resistant Enterococcus faecalis endophthalmitis.
Animal experiment.
Seventy-eight New Zealand white rabbits received an intravitreal injection of 10(5) vancomycin-sensitive or -resistant E faecalis organisms in one eye. Infections were allowed to proceed 3 hours before dividing animals randomly into the following treatment groups (n = 6, each): the vancomycin-sensitive E faecalis model--(1) vancomycin (1 mg/0.1 mL), (2) combined vancomycin (1 mg/0.1 mL) and amikacin (0.4 mg/0.1 mL), (3) combined vancomycin (1 mg/0.1 mL) and gentamicin (0.1 mg/0.1 mL), (4) combined vancomycin (1 mg/0.1 mL) and ceftazidime (2 mg/0.1 mL), (5) combined ampicillin (5 mg/0.1 mL) and gentamicin (0.1 mg/0.1 mL), and (6) pristinamycin (1 mg/0.1 mL); and the vancomycin-resistant E faecalis model--(1)same as above, excluding group 4. Control groups received sterile balanced salt solution. Twenty-four hours following intravitreal treatment, vitreous humor was collected for quantitative bacteriological studies.
Intravitreal therapy with combined vancomycin and amikacin provided the most effective reduction of vancomycin-sensitive E faecalis organisms compared with combined vancomycin and gentamicin therapy (P =.10, Wilcoxon's rank sum test) or any other treatment group (P < .01, Wilcoxon's rank sum test). For vancomycin-resistant E faecalis endophthalmitis model, the combined ampicillin and gentamicin therapy was the most effective, followed by the combined vancomycin and amikacin therapy (P < .01, Wilcoxon's rank sum test).
Treatment with intravitreal vancomycin plus amikacin and with intravitreal ampicillin plus gentamicin provide an effective bactericidal therapy for severe experimental vancomycin-sensitive and -resistant E faecalis endophthalmitis, respectively.
评估对万古霉素敏感和耐药的粪肠球菌性眼内炎最有效的玻璃体内抗生素治疗方法。
动物实验。
78只新西兰白兔,一只眼接受玻璃体内注射10⁵个万古霉素敏感或耐药的粪肠球菌菌株。感染3小时后,将动物随机分为以下治疗组(每组n = 6):万古霉素敏感粪肠球菌模型组——(1)万古霉素(1mg/0.1mL),(2)万古霉素(1mg/0.1mL)联合阿米卡星(0.4mg/0.1mL),(3)万古霉素(1mg/0.1mL)联合庆大霉素(0.1mg/0.1mL),(4)万古霉素(1mg/0.1mL)联合头孢他啶(2mg/0.1mL),(5)氨苄西林(5mg/0.1mL)联合庆大霉素(0.1mg/0.1mL),以及(6)利奈唑胺(1mg/0.1mL);万古霉素耐药粪肠球菌模型组——(1)与上述相同,但不包括第4组。对照组接受无菌平衡盐溶液。玻璃体内治疗24小时后,收集玻璃体液进行定量细菌学研究。
与万古霉素联合庆大霉素治疗(Wilcoxon秩和检验,P = 0.10)或任何其他治疗组(Wilcoxon秩和检验,P < 0.01)相比,万古霉素联合阿米卡星进行玻璃体内治疗能最有效地减少万古霉素敏感粪肠球菌菌株。对于万古霉素耐药粪肠球菌性眼内炎模型,氨苄西林联合庆大霉素治疗最有效,其次是万古霉素联合阿米卡星治疗(Wilcoxon秩和检验,P < 0.01)。
玻璃体内注射万古霉素加阿米卡星以及玻璃体内注射氨苄西林加庆大霉素分别为严重的实验性万古霉素敏感和耐药粪肠球菌性眼内炎提供了有效的杀菌治疗方法。