Calderaro Adriana, Buttrini Mirko, Martinelli Monica, Montecchini Sara, Covan Silvia, Ruggeri Alberto, Rodighiero Isabella, Di Maio Alan, Galullo Mariapia, Larini Sandra, Arcangeletti Maria Cristina, Chezzi Carlo, De Conto Flora
Department of Medicine and Surgery, University of Parma, Parma, Italy
Department of Medicine and Surgery, University of Parma, Parma, Italy.
BMJ Open. 2021 Apr 19;11(4):e042290. doi: 10.1136/bmjopen-2020-042290.
The distribution of carbapenemase-producing (CPKP) phenotypes and genotypes in samples collected during 2011-2018 was evaluated. The association between patients with CPKP-positive rectal swab and those with CPKP infection, as well as the overall analysis of CPKP-infected patients, was performed.
The study was performed in a tertiary-care hospital located in Northern Italy.
Two groups were considered: 22 939 'at-risk' patients submitted to active surveillance for CPKP detection in rectal swabs/stools and 1094 CPKP-infected patients in which CPKP was detected in samples other than rectal swabs.
CPKP-positive rectal swabs were detected in 5% (1150/22 939). A CPKP infection was revealed in 3.1% (719/22 939) of patients: 582 with CPKP-positive rectal swab (50.6% of the 1150 CPKP-positive rectal swabs) and 137 with CPKP-negative rectal swab. The 49.4% (568/1150) of the patients with CPKP-positive rectal swab were carriers. The overall frequency of CPKP-positive patients (carriers and infected) was almost constant from 2012 to 2016 (excluding the 2015 peak) and then increased in 2017-2018. KPC was predominant followed by VIM. No difference was observed in the frequency of CPKP-positive rectal swab patients among the different material groups. Among the targeted carbapenemase genes, VIM was more significantly detected from urine than from other samples.
The high prevalence of carriers without evidence of infection, representing a potential reservoir of CPKP, suggests to maintain the guard about this problem, emphasising the importance of active surveillance for timely detection and separation of carriers, activation of contact precautions and antibiotic treatment guidance on suspicion of infection.
评估2011 - 2018年期间收集样本中产碳青霉烯酶(CPKP)表型和基因型的分布情况。对CPKP阳性直肠拭子患者与CPKP感染患者之间的关联以及CPKP感染患者进行全面分析。
该研究在意大利北部的一家三级医院进行。
分为两组:22939名接受直肠拭子/粪便中CPKP检测主动监测的“高危”患者,以及1094名在直肠拭子以外的样本中检测到CPKP的CPKP感染患者。
在5%(1150/22939)的患者中检测到CPKP阳性直肠拭子。3.1%(719/22939)的患者出现CPKP感染:582例直肠拭子CPKP阳性(占1150例CPKP阳性直肠拭子的50.6%),137例直肠拭子CPKP阴性。直肠拭子CPKP阳性患者中有49.4%(568/1150)为携带者。2012年至2016年CPKP阳性患者(携带者和感染者)的总体频率几乎保持不变(不包括2015年的峰值),然后在2017 - 2018年有所增加。KPC为主,其次是VIM。不同物质组中CPKP阳性直肠拭子患者的频率未观察到差异。在目标碳青霉烯酶基因中,VIM在尿液中比在其他样本中更显著地被检测到。
无感染证据的携带者患病率高,这代表了CPKP的潜在储存库,提示对此问题保持警惕,强调主动监测对于及时检测和隔离携带者、启动接触预防措施以及怀疑感染时的抗生素治疗指导的重要性。