DISC, Department of Surgical Sciences and Integrated Diagnostics, University of Genoa, Genoa, Italy; Unit of Microbiology, Ospedale Policlinico San Martino, Genoa, Italy.
DISC, Department of Surgical Sciences and Integrated Diagnostics, University of Genoa, Genoa, Italy.
J Hosp Infect. 2022 Nov;129:102-109. doi: 10.1016/j.jhin.2022.05.020. Epub 2022 Jun 8.
Surveillance of carbapenem-resistant Enterobacterales (CRE) carriers is the first measure of hospital infection control. Screening of CRE carriage can be assessed through culture and molecular techniques, each with specific properties of turnaround-times, sensitivity and specificity.
This was a prospective study in a 1200-bed university hospital in Genoa, Italy, where CRE screening is performed analysing cultures from rectal swabs. Our 18-months intervention was to extend the incubation time of the corresponding plates from 48 to 288 h, after reporting negative tests, to evaluate the possible impact on the cultures.
A total of 362 patients giving 19,278 swabs and corresponding plates were included. After baseline incubation, plate positivity was 3%, while after the overall lengthened times it was 3.7%. Extended incubation was associated with change in the relative frequency of the most represented species. In particular, we observed reduced presence of total and resistant Klebsiella pneumoniae strains (P<0.001) and increased presence of Enterobacter cloacae complex, total and sensitive (P<0.001). By extending incubation time, a reduced frequency of overall Enterobacterales strains with high resistance to ertapenem (MIC ≥4 mg/L) was also found (P=0.005), particularly that of K. pneumoniae (P<0.001), while the presence of E. cloacae complex increased among organisms with low resistance levels to ertapenem (P<0.001).
Extending the incubation time of the cultures increased the number of CREs grown, and expanded the bacterial scenario of rectal colonization through the recovery of poorly resistant strains and otherwise undetected species.
对耐碳青霉烯肠杆菌科(CRE)携带者的监测是医院感染控制的首要措施。通过培养和分子技术均可对 CRE 携带情况进行评估,两者各有其不同的检测时间、灵敏度和特异性。
这是意大利热那亚一家 1200 床位的大学医院的前瞻性研究,CRE 筛查通过分析直肠拭子培养物进行。我们的 18 个月干预措施是将相应平板的孵育时间从 48 小时延长至 288 小时,在报告阴性检测结果后,以评估其对培养物的可能影响。
共纳入 362 名患者,共提供 19278 个拭子和相应平板。在基线孵育后,平板阳性率为 3%,而在总体延长孵育时间后为 3.7%。延长孵育时间与最具代表性的物种相对频率变化相关。具体而言,我们观察到总耐药和耐药肺炎克雷伯菌菌株的存在减少(P<0.001),而肠杆菌科复杂、总敏感和敏感菌株的存在增加(P<0.001)。通过延长孵育时间,还发现对厄他培南高度耐药(MIC≥4mg/L)的肠杆菌科菌株总频率降低(P=0.005),特别是肺炎克雷伯菌(P<0.001),而对厄他培南低耐药水平的肠杆菌科复杂菌株的存在增加(P<0.001)。
延长培养物的孵育时间增加了生长的 CRE 数量,并通过恢复低耐药水平的菌株和其他未被发现的物种,扩大了直肠定植的细菌谱。