Fica C Alberto, Céspedes J Ignacio, Gompertz G Macarena, Jalón V Mauricio, Sakurada Z Andrea, Sáez L Enzo
Sección de Infectología, Hospital Clínico Universidad de Chile, Santiago, Chile.
Rev Chilena Infectol. 2007 Oct;24(5):360-7. doi: 10.4067/s0716-10182007000500002. Epub 2007 Oct 26.
Emergence of panresistant gram negative bacilli has lead to the progressive reintroduction of intravenous colistin.
To describe the clinical experience observed with this compound.
A retrospective analysis was performed for all treatments lasting >/= 48 hours. Medical records were analyzed to obtain clinical parameters and microbiological data, evaluate clinical response and evolution until discharge.
24 treatments lasting >/= 48 hours were applied between June 2005 and September 2006. Intravenous colistin was indicated to treat cases of ventilator-associated (VA) pneumonia (n = 10; 41.7%), abscess or collections (12.5%), bloodstream infections, non-VA pneumonia or urinary tract infections (4.2% each one, respectively). Treatment was initiated on average at 3.2 days (+/- 2.85) from diagnosis of infection. All courses were microbiologically-guided, and involved P. aeruginosa or A. baumannii isolates. Susceptibility was evaluated by E-test in 11 isolates (MIC90 3.6 nicrog/mL, range 0.38 to 4 microg/mL). One isolate was resistant to colistin (9%). A favorable response was observed in 12 treatments (50%) with a relapse in 5 cases (41.7%). Being treated for pneumonia was the only factor associated to failure, (p = 0.04) Eradication was documented in 8 cases (33.3%) and persistence in 11 (45.8%). In 5 cases a microbiological follow-up was not available. Survival at time of discharge was 45.5%. (n = 10) None of the treatment courses was associated with nefrotoxicity.
Intravenous colistin is a safe compound useful to treat various nosocomial infections due to pan-resistant gram negative bacilli. Nonetheless, its clinical efficacy is limited, especially among patients treated for nosocomial pneumonia.
泛耐药革兰氏阴性杆菌的出现导致静脉注射黏菌素的重新启用。
描述使用该药物的临床经验。
对所有持续时间≥48小时的治疗进行回顾性分析。分析病历以获取临床参数和微生物学数据,评估临床反应及直至出院的病情演变。
2005年6月至2006年9月间应用了24次持续时间≥48小时的治疗。静脉注射黏菌素用于治疗呼吸机相关性(VA)肺炎(n = 10;41.7%)、脓肿或积液(12.5%)、血流感染、非VA肺炎或尿路感染(各占4.2%)。治疗平均在感染诊断后3.2天(±2.85)开始。所有疗程均在微生物学指导下进行,涉及铜绿假单胞菌或鲍曼不动杆菌分离株。11株分离株通过E试验评估敏感性(MIC90为3.6微克/毫升,范围为0.38至4微克/毫升)。1株分离株对黏菌素耐药(9%)。12次治疗(50%)观察到良好反应,5例(41.7%)复发。接受肺炎治疗是与治疗失败相关的唯一因素(p = 0.04)。8例(33.3%)记录有根除,11例(45.8%)持续存在。5例未进行微生物学随访。出院时生存率为45.5%(n = 10)。没有一个治疗疗程与肾毒性相关。
静脉注射黏菌素是一种安全的药物,可用于治疗由泛耐药革兰氏阴性杆菌引起的各种医院感染。然而,其临床疗效有限,尤其是在接受医院获得性肺炎治疗的患者中。