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The effect on peritoneal dialysis pathogens of changing topical antibiotic prophylaxis

机译:改变局部抗生素预防措施对腹膜透析病原体的影响

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Background: Prophylactic gentamicin 0.1% cream has demonstrated efficacy in preventing both exit-site infection (ESI) and peritonitis attributable to gram-positive and gram-negative organisms; however, the effect of this practice on the gentamicin susceptibility patterns of bacterial pathogens isolated from such infections is unknown. We therefore examined the effect of a change in our prophylactic topical antibiotic exit-site protocol (from mupirocin 2% cream to gentamicin 0.1% cream) on infection rates and susceptibility patterns. Methods: This retrospective observational cohort study examined two periods of time: before and after the change in exit-site protocol. Each period was 30 months in duration, with a 2-month implementation period between, during which patient data were excluded. Demographic, clinical, and microbiology data were collected for each patient and episode of infection. Results: Overall, 377 patients were evaluated. In the mupirocin period (MUP), 145 infections occurred in 79 patients, and in the gentamicin period, 145 infections occurred in 93 patients. No significant effect was found either in overall episodes of infection (0.53 per year) or in episodes of peritonitis (0.429 vs 0.375 per year), but episodes of ESI increased significantly (0.098 vs 0.153 per year; p = 0.024; odds ratio: 1.55; 95% confidence interval: 1.05 to 2.28). Episodes of Staphylococcus aureus peritonitis increased by 38% (0.018 vs 0.025 per year), and episodes of S. aureus ESI increased significantly by 150% (0.022 vs 0.055 per year; p = 0.03; hazard ratio: 3.00; 95% confidence interval: 1.09 to 8.26). Episodes of pseudomonal peritonitis declined by 68% (0.022 vs 0.007 per year), and episodes of pseudomonal ESI increased by 150% (0.007 vs 0.018 per year). The gentamicin susceptibility for gram-positive isolates demonstrated no significant change; however, the gentamicin susceptibility for Enterobacteriaceae decreased by 12% and for Pseudomonas, by 14%. Conclusions: The significant increase in episodes of ESI and the decrease in susceptibility for both Enterobacteriaceae and Pseudomonas isolates represent a concerning trend. Centers should examine trends in infection rates and in bacterial susceptibilities to determine the most appropriate agent for ESI prophylaxis.
机译:背景:0.1%庆大霉素预防霜已被证明可有效预防革兰氏阳性和革兰氏阴性菌引起的出口部位感染(ESI)和腹膜炎。然而,这种做法对从这种感染中分离出的细菌病原体的庆大霉素敏感性模式的影响尚不清楚。因此,我们研究了预防性局部用药抗生素退出现场方案的变化(从莫匹罗星2%乳膏变为庆大霉素0.1%乳膏)对感染率和药敏模式的影响。方法:这项回顾性观察队列研究研究了两个时间段:出口现场方案变更前后。每个时期为30个月,在2个月的实施期间,其中排除了患者数据。收集每位患者和感染发作的人口统计学,临床和微生物学数据。结果:总共评估了377例患者。在莫匹罗星期(MUP)中,有79例患者发生了145例感染,而在庆大霉素时期,93例患者中发生了145例感染。在总感染次数(每年0.53)或腹膜炎发作(每年0.429比0.375)中均未发现明显影响,但ESI发作明显增加(每年0.098比0.153; p = 0.024;优势比:1.55 ; 95%置信区间:1.05至2.28)。金黄色葡萄球菌腹膜炎发作增加38%(0.018 vs每年0.025),金黄色葡萄球菌ESI发作显着增加150%(每年0.022 vs 0.055; p = 0.03;危险比:3.00; 95%置信区间: 1.09至8.26)。假性腹膜炎发作减少了68%(每年0.022比0.007),假性ESI发作增加了150%(每年0.007比0.018)。庆大霉素对革兰氏阳性菌的敏感性无明显变化。然而,庆大霉素对肠杆菌科的敏感性降低了12%,对假单胞菌的敏感性降低了14%。结论:肠杆菌科和假单胞菌分离株的ESI发作显着增加和易感性下降是一个令人关注的趋势。中心应检查感染率和细菌敏感性的趋势,以确定最合适的ESI预防药物。

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