Malande Oliver Ombeva, Du Plessis Annerie, Rip Diane, Bamford Colleen, Eley Brian
Paediatric Infectious Diseases Unit, Red Cross War Memorial Children's Hospital, Cape Town, and Department of Paediatrics and Child Health, University of Cape Town, South Africa.
S Afr Med J. 2016 Aug 18;106(9):877-82. doi: 10.7196/SAMJ.2016.v106i9.11028.
There are no paediatric reports of invasive infection caused by carbapenem-resistant Enterobacteriaceae (CRE) from Africa.
To document a series of cases of CRE infections at a tertiary children's hospital in Cape Town, South Africa, describing the clinical and microbiological findings in these children.
A retrospective, descriptive study was completed using data from a series of children with invasive CRE infection between 2010 and 2015, sourced from their clinical notes and microbiology results.
The first of 10 invasive CRE infections during the study period occurred in November 2012. Nine CRE infections were caused by Klebsiella pneumoniae, and one by both K. pneumoniae and Escherichia coli. The median age was 25 months (interquartile range (IQR) 5 - 60). All 10 CRE infections were hospital acquired. The median length of hospitalisation before CRE infection was 28.5 days (IQR 20 - 44). Eight of the children were exposed to carbapenems during the 12-month period prior to invasive CRE infection. Six were treated with colistin and carbapenem combination therapy, of whom 2 died, including 1 of a non-CRE event. The other 4 children received colistin monotherapy. All these children died, including 2 from non-CRE events.
Children with invasive CRE infection and severe underlying disease must be treated with combination antibiotic therapy. Strict infection control practice and antibiotic stewardship are necessary to contain the spread of CRE and limit the number of new infections.
非洲尚无关于耐碳青霉烯类肠杆菌科细菌(CRE)引起侵袭性感染的儿科报告。
记录南非开普敦一家三级儿童医院的一系列CRE感染病例,描述这些儿童的临床和微生物学检查结果。
采用回顾性描述性研究方法,使用2010年至2015年间一系列侵袭性CRE感染儿童的数据,这些数据来源于他们的临床记录和微生物学检查结果。
研究期间10例侵袭性CRE感染中的首例发生于2012年11月。9例CRE感染由肺炎克雷伯菌引起,1例由肺炎克雷伯菌和大肠埃希菌共同引起。中位年龄为25个月(四分位间距[IQR]5 - 60)。所有10例CRE感染均为医院获得性感染。CRE感染前的中位住院时间为28.5天(IQR 20 - 44)。8名儿童在侵袭性CRE感染前12个月内接触过碳青霉烯类药物。6名儿童接受了黏菌素和碳青霉烯类联合治疗,其中2例死亡,包括1例死于非CRE事件。其他4名儿童接受了黏菌素单药治疗。所有这些儿童均死亡,包括2例死于非CRE事件。
侵袭性CRE感染且有严重基础疾病的儿童必须接受联合抗生素治疗。严格的感染控制措施和抗生素管理对于遏制CRE的传播和限制新感染病例数量是必要的。