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Efficacy and safety of colistin in the treatment of infections caused by multidrug-resistant Pseudomonas aeruginosa in patients with hematologic malignancy: a matched pair analysis.

机译:粘菌素治疗恶性血液病患者多重耐药铜绿假单胞菌感染的疗效和安全性:匹配对分析。

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摘要

OBJECTIVE: ududA rise in infections with multidrug-resistant Pseudomonas aeruginosa (MDR-PA) is a significant contributor to increased morbidity and mortality of patients with hematologic malignancies. The aim of this study was to determine the efficacy and safety of colistin (colistimethate sodium) in the treatment of serious infections caused by MDR-PA in these patients.udud----- PATIENTS AND METHODS: ududA matched pair analysis of renal function, toxicities, and outcome of 26 patients receiving colistin and control subjects was done. All patients had clinical signs of sepsis; P. aeruginosa was isolated from blood in 69% of patients in colistin group and 84% in control group. Patients treated with colistin received 3 million units every 8 hours for a median duration of 13 days. Additionally, patients received at least two additional antimicrobial or antifungal drugs.udud----- RESULTS: ududResolution of infection was achieved in twenty patients (76.9%) receiving colistin and in 17 (65.4%) control subjects. Mortality rate was 11% in both groups. There was no statistically significant difference in the level of serum creatinine, creatinine clearance, or potassium levels before and after treatment between groups. Only one patient receiving colistin developed de novo renal failure and one displayed transient neurologic toxicity.udud----- CONCLUSION: ududOur results suggest that in patients with hematologic malignancies, colistin is effective in treating severe infections caused by MDR-PA while maintaining an acceptable toxicity profile. Prospective randomized studies comparing efficacy and safety of colistin with those of other antipseudomonal drugs are needed.
机译:目的:多药耐药铜绿假单胞菌(MDR-PA)感染的增加是血液系统恶性肿瘤患者发病率和死亡率增加的重要原因。这项研究的目的是确定大肠粘菌素(colistimethate sodium)在这些患者中治疗由MDR-PA引起的严重感染的疗效和安全性。 ud ud -----患者和方法: ud udA对26名接受粘菌素和对照组的患者的肾功能,毒性和预后进行配对分析。所有患者都有败血症的临床体征。粘菌素组69%的患者和对照组中84%的患者从血液中分离出铜绿假单胞菌。用粘菌素治疗的患者每8小时收到300万单位,中位持续时间为13天。此外,患者还接受了至少两种其他的抗微生物或抗真菌药物。 ud ud -----结果: ud ud感染的解决方案在接受大肠杆菌素的20名患者(76.9%)和17名(65.4%)的对照受试者中得以实现。两组的死亡率均为11%。两组之间治疗前后的血清肌酐水平,肌酐清除率或钾水平无统计学差异。结论: ud ud结论: ud ud我们的结果表明,在血液系统恶性肿瘤患者中,粘菌素可有效治疗由重度肾病引起的严重感染MDR-PA,同时保持可接受的毒性。需要进行前瞻性随机研究,以比较大肠菌素与其他抗假性伪狂犬病药物的功效和安全性。

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