Baltch A L, Smith R P
Am J Med. 1985 Jul 15;79(1A):8-16. doi: 10.1016/0002-9343(85)90185-8.
Pseudomonas aeruginosa continues to cause serious infections, especially bacteremias, in hospitalized and immunocompromised patients. During the past 10 years, bacteremia due to this organism has increased in frequency in many institutions, and mortality rates in patients with rapidly fatal disease remain as high as 85 percent despite antibiotic therapy. Available data do not allow firm conclusions regarding the in vivo predictive value of in vitro synergy testing for P. aeruginosa, but in vitro demonstration of synergy appears important in selecting therapy for patients with P. aeruginosa infections. Combinations of aminoglycosides (amikacin or tobramycin) with highly active antipseudomonal beta-lactam antibiotics are most likely to be associated with in vitro synergy. Experimental studies in animals models support the use of combination therapy for local and bacteremic infections. Similarly, the retrospective and prospective studies in humans suggest better survival with combinations of antimicrobials, usually including aminoglycosides and beta-lactams, in immunocompromised hosts. At present, the use of newer penicillins, piperacillin, azlocillin, or selected antipseudomonal cephalosporins, in combination with amikacin or tobramycin, appears to be the preferable antimicrobial therapy for serious P. aeruginosa infections.
铜绿假单胞菌继续在住院患者和免疫功能低下患者中引发严重感染,尤其是菌血症。在过去10年里,许多医疗机构中由该病原体引起的菌血症发生率有所上升,尽管进行了抗生素治疗,但病情迅速恶化的患者死亡率仍高达85%。现有数据无法就体外协同试验对铜绿假单胞菌的体内预测价值得出确凿结论,但体外协同试验结果在为铜绿假单胞菌感染患者选择治疗方案时似乎很重要。氨基糖苷类药物(阿米卡星或妥布霉素)与高活性抗假单胞菌β-内酰胺类抗生素联合使用最有可能产生体外协同作用。动物模型的实验研究支持联合治疗对局部感染和菌血症感染的应用。同样,针对人类的回顾性和前瞻性研究表明,在免疫功能低下宿主中,联合使用抗菌药物(通常包括氨基糖苷类和β-内酰胺类)可提高生存率。目前,使用新型青霉素(哌拉西林、阿洛西林)或特定的抗假单胞菌头孢菌素与阿米卡星或妥布霉素联合使用,似乎是治疗严重铜绿假单胞菌感染的首选抗菌治疗方法。