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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Colistin is effective in treatment of infections caused by multidrug-resistant Pseudomonas aeruginosa in cancer patients.
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Colistin is effective in treatment of infections caused by multidrug-resistant Pseudomonas aeruginosa in cancer patients.

机译:Colistin可有效治疗由多药耐药的铜绿假单胞菌引起的感染。

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The increasing incidence of infections caused by multidrug-resistant Pseudomonas aeruginosa is a worldwide health problem. Because no new antipseudomonal agents are expected to be available in the near future, we evaluated the safety and efficacy of colistin, an old drug with bactericidal activity against this organism. We collected clinical and demographic data on 95 cancer patients diagnosed with infections caused by multidrug-resistant P. aeruginosa between January 2001 and January 2004 and treated with either colistin (colistin group) or at least one active antipseudomonal agent (a beta-lactam antibiotic or a quinolone) (control group). We compared the results obtained for both groups. Thirty-one patients had been treated with colistin and 64 had been treated with an antipseudomonal non-colistin-containing regimen. Compared with the control group, patients in the colistin group had a lower median age (52 and 62 years, respectively; P = 0.012) but were more likely to have had nosocomial infections (87% and 64%, respectively; P = 0.02). Twenty-five patients (81%) in the colistin group and 40 patients (63%) in the control group had an APACHE II score of >15 (P = 0.074). The overall clinical response rates were 52% in the colistin group and 31% in the control group (P = 0.055). Multiple logistic regression analysis showed that those patients treated with colistin were 2.9 times (95% confidence interval, 1.1 to 7.6 times) more likely than those in the control group to experience a clinical response to therapy (P = 0.026). Colistin therapy was at least as effective and as safe a beta-lactam antibiotic or a quinolone in the treatment of infections caused by multidrug-resistant P. aeruginosa and, hence, may be a useful or preferred alternative therapy for this infection in cancer patients.
机译:由多药耐药的铜绿假单胞菌引起的感染发生率增加是一个全球性的健康问题。因为预计在不久的将来将不会有新的抗假单胞菌药物,所以我们评估了粘菌素的安全性和有效性,粘菌素是一种对这种生物体具有杀菌活性的老药。我们收集了2001年1月至2004年1月间被确诊为多药耐药性铜绿假单胞菌感染的95例癌症患者的临床和人口统计学数据,并用大肠菌素(colistin组)或至少一种活性抗假性伪狂犬病药物(β-内酰胺抗生素或喹诺酮)(对照组)。我们比较了两组的结果。 31名患者接受了大肠粘菌素治疗,64名患者接受了抗假性非含colistin疗法。与对照组相比,大肠杆菌素组患者的中位年龄较低(分别为52岁和62岁; P = 0.012),但更有可能发生医院感染(分别为87%和64%; P = 0.02)。 。大肠菌素组中有25名患者(81%),对照组中有40名患者(63%)的APACHE II评分> 15(P = 0.074)。大肠菌素组的总体临床反应率为52%,对照组为31%(P = 0.055)。多元逻辑回归分析显示,用粘菌素治疗的患者发生临床反应的可能性是对照组的2.9倍(95%置信区间为1.1至7.6倍)(P = 0.026)。共利斯汀疗法在治疗由多药耐药的铜绿假单胞菌引起的感染方面至少与β-内酰胺抗生素或喹诺酮一样有效和安全,因此对于癌症患者的这种感染可能是有用的或首选的替代疗法。

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