Kernodle D S, Kaiser A B
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2605.
Antimicrob Agents Chemother. 1994 Jun;38(6):1325-30. doi: 10.1128/AAC.38.6.1325.
Recent shifts in the species and antibiotic resistance patterns of bacteria causing nosocomial infections present new challenges for providing effective prophylaxis in surgery. Traditional regimens lack activity against methicillin-resistant staphylococci and many gram-negative species causing nosocomial infections. The new fluoroquinolones exhibit in vitro activity against many emerging surgical wound pathogens. To determine the potential of this class of antimicrobial agents for use in surgery, we compared the prophylactic efficacies of ciprofloxacin and ofloxacin with those of cefazolin and vancomycin in a guinea pig model of abscess formation. Four Staphylococcus aureus strains, one Staphylococcus epidermidis strain, and one Staphylococcus haemolyticus strain were evaluated. Vancomycin was the most effective prophylactic agent, exhibiting in vivo activity against all strains which was superior or equivalent to those of all other agents tested. Cefazolin was the least effective agent and surpassed the two quinolones in prophylactic efficacy against only one organism, a quinolone- and methicillin-resistant strain of S. aureus. The two quinolones provided excellent protection against infection with all but the quinolone-resistant isolate. The in vivo emergence of quinolone resistance among quinolone-susceptible isolates was not detected. The methicillin-resistant, quinolone-susceptible S. epidermidis and S. haemolyticus isolates were extremely susceptible to prophylaxis, exhibiting 50% infective doses above 4 x 10(6) CFU for seven of the eight antibiotic-strain combinations. We conclude that ciprofloxacin and ofloxacin may be effective antistaphylococcal agents in surgery. The role of these agents remains to be defined, and the definition should include consideration of an adverse effect upon antibiotic resistance patterns of organisms causing nosocomial infections.
引起医院感染的细菌种类和抗生素耐药模式最近发生的变化,给手术中提供有效的预防措施带来了新的挑战。传统的用药方案对耐甲氧西林葡萄球菌和许多引起医院感染的革兰氏阴性菌缺乏活性。新型氟喹诺酮类药物在体外对许多新出现的手术伤口病原体具有活性。为了确定这类抗菌药物在手术中的应用潜力,我们在豚鼠脓肿形成模型中比较了环丙沙星和氧氟沙星与头孢唑林和万古霉素的预防效果。评估了4株金黄色葡萄球菌、1株表皮葡萄球菌和1株溶血葡萄球菌。万古霉素是最有效的预防药物,对所有菌株均表现出体内活性,优于或等同于所有其他受试药物。头孢唑林是最无效的药物,仅对一种菌株(一株对喹诺酮和甲氧西林耐药的金黄色葡萄球菌)的预防效果超过了两种喹诺酮类药物。除了对喹诺酮耐药的分离株外,这两种喹诺酮类药物对所有感染均提供了良好的保护。未检测到喹诺酮敏感分离株在体内出现喹诺酮耐药性。耐甲氧西林、喹诺酮敏感的表皮葡萄球菌和溶血葡萄球菌分离株对预防极为敏感,在8种抗生素-菌株组合中的7种中,其半数感染剂量高于4×10(6)CFU。我们得出结论,环丙沙星和氧氟沙星在手术中可能是有效的抗葡萄球菌药物。这些药物的作用仍有待确定,而且这种确定应包括考虑对引起医院感染的生物体抗生素耐药模式的不良影响。