Fortaleza Carlos Magno C B, Freire Maristela P, Filho Djalma de C Moreira, de Carvalho Ramos Marcelo
Universidade Estadual de Campinas, Campinas, Sao Paulo, Brazil.
Infect Control Hosp Epidemiol. 2006 Sep;27(9):901-6. doi: 10.1086/507288. Epub 2006 Aug 21.
The prevalence of resistance to imipenem and ceftazidime among Pseudomonas aeruginosa isolates is increasing worldwide.
Risk factors for nosocomial recovery (defined as the finding of culture-positive isolates after hospital admission) of imipenem-resistant P. aeruginosa (IRPA) and ceftazidime-resistant P. aeruginosa (CRPA) were determined.
Two separate case-control studies were conducted. Control subjects were matched to case patients (ratio, 2:1) on the basis of admission to the same ward at the same time as the case patient. Variables investigated included demographic characteristics, comorbid conditions, and the classes of antimicrobials used.
The study was conducted in a 400-bed general teaching hospital in Campinas, Brazil that has 14,500 admissions per year. Case patients and control subjects were selected from persons who were admitted to the hospital during 1992-2002.
IRPA and CRPA isolates were obtained from 108 and 55 patients, respectively. Statistically significant risk factors for acquisition of IRPA were previous admission to another hospital (odds ratio [OR], 4.21 [95% confidence interval {CI}, 1.40-12.66]; P=.01), hemodialysis (OR, 7.79 [95% CI, 1.59-38.16]; P=.01), and therapy with imipenem (OR, 18.51 [95% CI, 6.30-54.43]; P<.001), amikacin (OR, 3.22 [95% CI, 1.40-7.41]; P=.005), and/or vancomycin (OR, 2.48 [95% CI, 1.08-5.64]; P=.03). Risk factors for recovery of CRPA were previous admission to another hospital (OR, 18.69 [95% CI, 2.00-174.28]; P=.01) and amikacin use (OR, 3.69 [95% CI, 1.32-10.35]; P=.01).
Our study suggests a definite role for several classes of antimicrobials as risk factors for recovery of IRPA but not for recovery of CRPA. Limiting the use of only imipenem and ceftazidime may not be a wise strategy to contain the spread of resistant P. aeruginosa strains.
在全球范围内,铜绿假单胞菌分离株对亚胺培南和头孢他啶的耐药率正在上升。
确定耐亚胺培南铜绿假单胞菌(IRPA)和耐头孢他啶铜绿假单胞菌(CRPA)医院内感染(定义为入院后培养阳性分离株的检出)的危险因素。
进行了两项独立的病例对照研究。对照对象与病例患者按2:1的比例匹配,匹配条件为与病例患者同时入住同一病房。研究的变量包括人口统计学特征、合并症以及使用的抗菌药物类别。
该研究在巴西坎皮纳斯一家拥有400张床位的综合性教学医院进行,该医院每年有14500例住院患者。病例患者和对照对象选自1992年至2002年期间入院的患者。
分别从108例和55例患者中分离出IRPA和CRPA。获得IRPA的统计学显著危险因素包括既往曾入住其他医院(比值比[OR],4.21[95%置信区间{CI},1.40 - 12.66];P = 0.01)、血液透析(OR,7.79[95% CI,1.59 - 38.16];P = 0.01)以及使用亚胺培南治疗(OR,18.51[95% CI,6.30 - 54.43];P < 0.001)、阿米卡星(OR,3.22[95% CI,1.40 - 7.41];P = 0.005)和/或万古霉素(OR,2.48[95% CI,1.08 - 5.64];P = 0.03)。CRPA感染的危险因素包括既往曾入住其他医院(OR,18.69[95% CI,2.00 - 174.28];P = 0.01)和使用阿米卡星(OR,3.69[95% CI,1.32 - 10.35];P = 0.01)。
我们的研究表明几类抗菌药物作为IRPA感染的危险因素具有明确作用,但对CRPA感染并非如此。仅限制亚胺培南和头孢他啶的使用可能不是控制耐药铜绿假单胞菌菌株传播的明智策略。