Buys Heloise, Muloiwa Rudzani, Bamford Colleen, Eley Brian
Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, Klipfontein Road, Cape Town, Rondebosch, 7700, South Africa.
University of Cape Town, Cape Town, South Africa.
BMC Infect Dis. 2016 Oct 17;16(1):570. doi: 10.1186/s12879-016-1919-y.
Klebsiella pneumoniae (KP) is a significant paediatric bloodstream pathogen in children. There is little data from Africa. In this study we describe the epidemiology of multi-drug resistant Klebsiella pneumoniae bloodstream infection (KPBSI) at Red Cross War Memorial Children's Hospital, Cape Town, South Africa.
We conducted a retrospective cross-sectional study of KPBSI from 1 January 2006 to 31 December 2011 using conventional descriptive and inferential statistical methods.
Of 410 hospitalised children with laboratory confirmed KPBSI, 339 (83 %) were caused by extended-spectrum β-lactamase (ESBL) producing isolates. The median age (IQR) was 5.0 (2-16) months, 212 (51.7 %) were male, 82 (20 %) were HIV-infected, and 241 (58.8 %) were moderately or severely underweight. The infection was hospital-acquired or healthcare-associated in 389 (95 %) children and community-acquired in 21 (5 %) children. Significant risk factors for ESBL-KPBSI included cephalosporin exposure in the 12 months prior to the KPBSI, adjusted risk ratio (aRR) 1.18 (95 % CI: 1.06-1.31); HIV infection, aRR 1.14 (1.04-1.25), and intravenous infusions for more than 3 days before the KPBSI, aRR 1.15 (95 % CI: 1.04-1.28). A total of 109 (26.6 %) children died within 30 days of the KPBSI, their median age was four (IQR 1-11) months. The median (IQR) time between KPBSI and death was three (1-9) days. HIV-infection, aRR 2.44(95 % CI: 1.59-3.74); skin erosions at the time of KPBSI, aRR 2.15 (95 % CI: 1.54-3.00); being in PICU at the time of the KPBSI, aRR 1.64 (95 % CI: 1.03-2.61) or needing PICU admission after developing KPBSI, aRR 1.72 (95 % CI: 1.10-2.70) were significant risk factors for death.
ESBL-producing KP is an important cause of laboratory confirmed bloodstream infection in hospitalised children and is associated with high mortality.
肺炎克雷伯菌(KP)是儿童重要的血流病原体。非洲的数据很少。在本研究中,我们描述了南非开普敦红十字会战争纪念儿童医院耐多药肺炎克雷伯菌血流感染(KPBSI)的流行病学情况。
我们采用传统的描述性和推断性统计方法,对2006年1月1日至2011年12月31日期间的KPBSI进行了回顾性横断面研究。
在410例实验室确诊为KPBSI的住院儿童中,339例(83%)由产超广谱β-内酰胺酶(ESBL)的菌株引起。中位年龄(四分位间距)为5.0(2 - 16)个月,212例(51.7%)为男性,82例(20%)感染了HIV,241例(58.8%)为中度或重度体重不足。389例(95%)儿童的感染为医院获得性或与医疗保健相关,21例(5%)儿童为社区获得性。ESBL-KPBSI的显著危险因素包括在KPBSI前12个月内使用头孢菌素,调整风险比(aRR)为1.18(95%可信区间:1.06 - 1.31);HIV感染,aRR为1.14(1.04 - 1.25),以及在KPBSI前静脉输液超过3天,aRR为1.15(95%可信区间:1.04 - 1.28)。共有109例(26.6%)儿童在KPBSI后30天内死亡,他们的中位年龄为4(四分位间距1 - 11)个月。KPBSI与死亡之间的中位(四分位间距)时间为3(1 - 9)天。HIV感染,aRR为2.44(95%可信区间:1.59 - 3.74);KPBSI时皮肤糜烂,aRR为2.15(95%可信区间:1.54 - 3.00);KPBSI时在儿科重症监护病房(PICU),aRR为1.64(95%可信区间:1.03 - 2.61)或在发生KPBSI后需要入住PICU,aRR为1.72(95%可信区间:1.10 - 2.70)是死亡的显著危险因素。
产ESBL的KP是住院儿童实验室确诊血流感染的重要原因,且与高死亡率相关。