Abayneh Mengistu, Tesfaw Getnet, Abdissa Alemseged
School of Medical Laboratory Sciences, Mizan-Tepi University, Mizan Aman, Ethiopia.
School of Medical Laboratory Sciences, Institute of Health Sciences, Jimma University, P.O. Box 378, Jimma, Ethiopia.
Can J Infect Dis Med Microbiol. 2018 Dec 13;2018:4846159. doi: 10.1155/2018/4846159. eCollection 2018.
BACKGROUND: and are the major extended-spectrum -lactamase- (ESBL-) producing organisms increasingly isolated as causes of complicated urinary tract infections and remain an important cause of failure of therapy with cephalosporins and have serious infection control consequence. OBJECTIVE: To assess the prevalence and antibiotics resistance patterns of ESBL-producing and from community-onset urinary tract infections in Jimma University Specialized hospital, Southwest Ethiopia, 2016. METHODOLOGY: A hospital-based cross-sectional study was conducted, and a total of 342 urine samples were cultured on MacConkey agar for the detection of etiologic agents. Double-disk synergy (DDS) methods were used for detection of ESBL-producing strains. A disc of amoxicillin + clavulanic acid (20/10 g) was placed in the center of the Mueller-Hinton agar plate, and cefotaxime (30 g) and ceftazidime (30 g) were placed at a distance of 20 mm (center to center) from the amoxicillin + clavulanic acid disc. Enhanced inhibition zone of any of the cephalosporin discs on the side facing amoxicillin + clavulanic acid was considered as ESBL producer. RESULTS: In the current study, ESBL-producing phenotypes were detected in 23% ( = 17) of urinary isolates, of which accounts for 76.5% ( = 13) and for 23.5% ( = 4). ESBL-producing phenotypes showed high resistance to cefotaxime (100%), ceftriaxone (100%), and ceftazidime (70.6%), while both ESBL-producing and non-ESBL-producing isolates showed low resistance to amikacin (9.5%), and no resistance was seen with imipenem. In the risk factors analysis, previous antibiotic use more than two cycles in the previous year (odds ratio (OR), 6.238; 95% confidence interval (CI), 1.257-30.957; = 0.025) and recurrent UTI more than two cycles in the last 6 months or more than three cycles in the last year (OR, 7.356; 95% CI, 1.429-37.867; = 0.017) were found to be significantly associated with the ESBL-producing groups. CONCLUSION: Extended-spectrum -lactamases- (ESBL-)producing strain was detected in urinary tract isolates. The occurrence of multidrug resistance to the third-generation cephalosporins, aminoglycosides, fluoroquinolones, trimethoprim-sulfamethoxazole, and tetracyclines is more common among ESBL producers. Thus, detecting and reporting of ESBL-producing organisms have paramount importance in the clinical decision-making.
背景:大肠埃希菌和肺炎克雷伯菌是产超广谱β-内酰胺酶(ESBL)的主要病原菌,越来越多地作为复杂性尿路感染的病因被分离出来,并且仍然是头孢菌素治疗失败的重要原因,具有严重的感染控制后果。 目的:评估2016年埃塞俄比亚西南部吉马大学专科医院社区获得性尿路感染中产ESBL的大肠埃希菌和肺炎克雷伯菌的流行率及抗生素耐药模式。 方法:进行了一项基于医院的横断面研究,共342份尿液样本在麦康凯琼脂上培养以检测病原体。采用双纸片协同试验(DDS)检测产ESBL菌株。将阿莫西林+克拉维酸(20/10μg)纸片置于穆勒-欣顿琼脂平板中心,头孢噻肟(30μg)和头孢他啶(30μg)纸片置于距阿莫西林+克拉维酸纸片中心20mm(中心对中心)处。头孢菌素纸片在面对阿莫西林+克拉维酸一侧的抑菌圈增大被视为产ESBL菌。 结果:在本研究中,23%(n = 17)的尿液分离株检测出产ESBL表型,其中大肠埃希菌占76.5%(n = 13),肺炎克雷伯菌占23.5%(n = 4)。产ESBL表型对头孢噻肟(100%)、头孢曲松(100%)和头孢他啶(70.6%)表现出高耐药性,而产ESBL和非产ESBL分离株对阿米卡星均表现出低耐药性(9.5%),对亚胺培南无耐药性。在危险因素分析中,发现前一年使用抗生素超过两个疗程(比值比(OR),6.238;95%置信区间(CI),1.257 - 30.957;P = 0.025)以及过去6个月内复发性尿路感染超过两个疗程或过去一年内超过三个疗程(OR,7.356;95%CI,1.429 - 37.867;P = 0.017)与产ESBL组显著相关。 结论:在尿路分离株中检测到产超广谱β-内酰胺酶(ESBL)菌株。产ESBL菌对第三代头孢菌素、氨基糖苷类、氟喹诺酮类、甲氧苄啶-磺胺甲恶唑和四环素的多重耐药情况更为常见。因此,产ESBL菌的检测和报告在临床决策中至关重要。
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