Atmaca Ozgür, Zarakolu Pınar, Karahan Ceren, Cakır Banu, Unal Serhat
Hacettepe University Faculty of Medicine, Department of Internal Medicine, Ankara, Turkey.
Mikrobiyol Bul. 2014 Oct;48(4):523-37. doi: 10.5578/mb.8280.
The aim of this study was to evaluate methicillin-resistant Staphylococcus aureus (MRSA) bacteremia cases who were followed at the Infectious Diseases Unit of Internal Medicine Department, at Hacettepe University Adult and Oncology Hospitals between January 2004-December 2011. A total of 198 patients, of them 99 had positive MRSA blood cultures (case group), and 99 without MRSA bacteremia (control group) who were selected randomly among patients at the same wards during the same time period, were included in the study. Demographic data, risk factors for MRSA bacteremia and antibiotic use of case (60 male, 39 female; mean age: 59.37 ± 16.96 yrs) and control (60 male, 39 female; mean age: 59.11 ± 17.60 yrs) groups were obtained from the patient files and the hospital data system and were compared. Methicillin susceptibility was determined by the cefoxitin (30 µg, BD, USA) disc diffusion method and confirmed by mecA PCR test. Antimicrobial susceptibilities were also determined by disc diffusion and Etest (BioMerieux, France) methods according to CLSI guidelines. There was no statistically significant difference between the two groups according to age, gender, presence of an underlying chronic disease, burn, hemodialysis, malignancy or immunosupression (p> 0.05). The results of the univariate analysis revealed that antibiotic use and parameters most likely to be associated with MRSA bacteremia (obesity, cerebrovascular event, hospitalization history, central/arterial catheter, presence of tracheostomy, invasive/non-invasive mechanical ventilation, use of proton pump inhibitors, H2 receptor blockers, sucralfate, nasogastric or urinary tubes, gastrostomia, total parenteral nutrition, acute organ failure and surgical operation) were found to be statistically higher in the case group (p< 0.05). Median length of hospital stay was also higher in the case group (59 days versus 8 days; p< 0.001). Multivariate regression analysis indicated that obesity (OR= 7.98; p= 0.013), central venous catheterization (OR= 6.65; p= 0.005), nasogastric tube (OR= 16.58; p< 0.001) and use of H2 receptor blockers (OR= 4.41; p= 0.010) were independent risk factors. The number of patient given at least one antibiotic (92 in case group, 51 in control group) was statistically higher than those who were not (48 in case group, 7 in control group) (OR= 14.86; p< 0.001). Use of antibiotics [ampicillin-sulbactam and/or amoxicillin-clavulanate, fluoroquinolones, aminoglycosides, piperacillin-tazobactam (TZP), meropenem (MEM), imipenem (IPM), vancomycin (VAN), cephalosporins and teicoplanin (TEC)] were found to be statistically significantly higher in the case group by univariate analysis (p< 0.05). In multivariate analysis, it was determined that TZP (OR= 6.82; p< 0.001), IPM (OR= 3.97; p= 0.023) and VAN (OR= 8.46; p= 0.001) use were independent risk factors in MRSA bacteremia. The duration of MEM (p= 0.037) and cephalosporin use (p< 0.001) were significantly longer in the case group, however there was no statistically significant difference between the duration of use of other antibiotics (p> 0.05). All MRSA isolates were mecA gene positive (n= 99), the resistance rates for ciprofloxacin, rifampin, gentamicin, tetracyclin, cefoxitin, erythromycin and clindamycin were 95%, 95%, 94%, 96%, 98%, 71% and 36%, respectively. All of the isolates were found to be susceptible to trimethoprim-sulfamethoxazole, VAN, TEC, tigecycline, linezolid and daptomycin. Mortality rates in patients who were infected with MRSA strains exhibiting vancomycin MIC value of ≤ 1.0 µg/ml (n= 49) and with MRSA strains exhibiting MIC > 1.0 µg/ml (n= 50) were 34.6% (17/49) and 60% (30/50), respectively. This difference was found to be statistically significant (p= 0.012). Thus it was concluded that the mortality rate increased in patients infected with MRSA with high (> 1.0 µg/ml) vancomycin MIC value. The results of this study indicated that obesity, presence of central venous catheter and nasogastric tube, and the use of H2 receptor blockers, IPM, TZP and VAN were independent risk factors for MRSA bacteremia. This was the first study showing the relationship between increasing mortality and high vancomycin MIC values in MRSA bacteremia in Turkey.
本研究旨在评估2004年1月至2011年12月期间在哈杰泰佩大学成人及肿瘤医院内科传染病科接受随访的耐甲氧西林金黄色葡萄球菌(MRSA)菌血症病例。本研究纳入了198例患者,其中99例血培养MRSA阳性(病例组),99例无MRSA菌血症(对照组),对照组为同期在同一病房随机选取的患者。从患者病历和医院数据系统中获取病例组(60例男性,39例女性;平均年龄:59.37±16.96岁)和对照组(60例男性,39例女性;平均年龄:59.11±17.60岁)的人口统计学数据、MRSA菌血症的危险因素及抗生素使用情况,并进行比较。采用头孢西丁(30μg,美国BD公司)纸片扩散法测定甲氧西林敏感性,并通过mecA PCR试验进行确认。根据CLSI指南,还采用纸片扩散法和Etest(法国生物梅里埃公司)方法测定抗菌药物敏感性。两组在年龄、性别、潜在慢性病、烧伤、血液透析、恶性肿瘤或免疫抑制方面无统计学显著差异(p>0.05)。单因素分析结果显示,病例组抗生素使用情况以及最可能与MRSA菌血症相关的参数(肥胖、脑血管事件、住院史、中心/动脉导管、气管切开、有创/无创机械通气、使用质子泵抑制剂、H2受体阻滞剂、硫糖铝、鼻胃管或尿管、胃造口术、全胃肠外营养、急性器官衰竭和外科手术)在统计学上更高(p<0.05)。病例组的中位住院时间也更长(59天对8天;p<0.001)。多因素回归分析表明,肥胖(OR=7.98;p=0.013)、中心静脉置管(OR=6.65;p=0.005)、鼻胃管(OR=16.58;p<0.001)和使用H2受体阻滞剂(OR=4.41;p=0.010)是独立危险因素。接受至少一种抗生素治疗的患者数量(病例组92例,对照组51例)在统计学上高于未接受治疗的患者(病例组48例,对照组7例)(OR=14.86;p<0.001)。单因素分析发现,病例组抗生素[氨苄西林-舒巴坦和/或阿莫西林-克拉维酸、氟喹诺酮类、氨基糖苷类、哌拉西林-他唑巴坦(TZP)、美罗培南(MEM)、亚胺培南(IPM)、万古霉素(VAN)、头孢菌素类和替考拉宁(TEC)]的使用在统计学上显著更高(p<0.05)。多因素分析确定,TZP(OR=6.82;p<0.001)、IPM(OR=3.97;p=0.023)和VAN(OR=8.46;p=0.001)的使用是MRSA菌血症的独立危险因素。病例组MEM(p=0.037)和头孢菌素类使用时间(p<0.001)显著更长,然而其他抗生素的使用时间无统计学显著差异(p>0.05)。所有MRSA分离株mecA基因均为阳性(n=99),对环丙沙星、利福平、庆大霉素、四环素、头孢西丁、红霉素和克林霉素的耐药率分别为95%、95%、94%、96%、98%、71%和36%。所有分离株对复方磺胺甲恶唑、VAN、TEC、替加环素、利奈唑胺和达托霉素敏感。万古霉素MIC值≤1.0μg/ml的MRSA菌株感染患者(n=49)和MIC>1.0μg/ml的MRSA菌株感染患者(n=50)的死亡率分别为34.6%(17/49)和60%(30/50)。发现这种差异具有统计学显著性(p=0.012)。因此得出结论,万古霉素MIC值高(>1.0μg/ml)的MRSA感染患者死亡率增加。本研究结果表明,肥胖、中心静脉导管和鼻胃管的存在以及H2受体阻滞剂、IPM、TZP和VAN的使用是MRSA菌血症的独立危险因素。这是土耳其第一项显示MRSA菌血症中死亡率增加与高万古霉素MIC值之间关系的研究。