Is linezolid a risk factor for Gram-negative bacillus infections in intensive care unit patients? A comparative study with vancomycin

被引:4
|
作者
Sterzik, Holger [2 ]
Soriano, Alejandro [1 ]
Mohamad, Al-Montaser [2 ]
Antonio Martinez, Jose [1 ]
Fernandez, Javier [3 ]
Cobos, Nazaret [1 ]
Morata, Laura [4 ]
Mensa, Josep [1 ]
机构
[1] Hosp Clin Barcelona, Nosocomial Infect Unit, Dept Infect Dis, Barcelona 08036, Spain
[2] Hosp Univ Insular Gran Canaria, Dept Internal Med, Las Palmas Gran Canaria, Spain
[3] Hosp Clin Barcelona, Hepatol Dept, Barcelona 08036, Spain
[4] Hosp Severo Ochoa Madrid, Madrid, Spain
关键词
Linezolid; vancomycin; Gram-negative; ICU; kidney failure; 2; DOUBLE-BLIND; COMPLICATED SKIN; RESISTANT; PNEUMONIA;
D O I
10.3109/00365548.2011.586368
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Linezolid is frequently used in critically ill patients with ventilator-associated pneumonia. Its potent activity against Gram-positive microorganisms and its high tissue penetration may favour Gram-negative colonization and infection. The aim of our study was to evaluate the risk for Gram-negative infections in critically ill patients treated with linezolid or vancomycin. Methods: The cases of all patients admitted over an 18-month period to a hepatic intensive care unit for >= 1 week, and treated with linezolid or vancomycin, were retrospectively reviewed. The main clinical characteristics and infections due to Gram-negative bacteria in the month after starting linezolid or vancomycin were obtained. Results: Seventy-one patients treated with linezolid and 68 treated with vancomycin fulfilled the inclusion criteria. Co-morbidities were similar in both groups. Patients on linezolid treatment had a longer stay in the ICU (mean +/- standard deviation 41 +/- 38 days vs 18.4 +/- 13 days), received this treatment later (14.3 +/- 15.1 days vs 6.3 +/- 6.5 days), had a higher mean serum creatinine concentration (1.71 +/- 1.18 mg/dl vs 1.04 +/- 1.04 mg/dl), more often required haemodiafiltration (29.6% vs 13.2%), and 30 day-mortality was higher (42.3% vs 20.6%) than in patients receiving vancomycin. More than 95% in both groups received a broad-spectrum beta-lactam in addition to linezolid or vancomycin. The rate of Gram-negative infection during the following month was 28.2% in the linezolid group and 26.5% in the vancomycin group (p > 0.5). Conclusions: Linezolid was more frequently used in critically ill patients with longer ICU stay and renal failure. The rate of infection due to Gram-negative microorganisms was similar in patients who received linezolid or vancomycin.
引用
收藏
页码:765 / 770
页数:6
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