Pathogen aetiology and risk factors for death among neonates with bloodstream infections at lower-tier South African hospitals: a cross-sectional study.

IF 20.9 1区 生物学 Q1 INFECTIOUS DISEASES
Susan Meiring, Vanessa Quan, Rudzani Mashau, Olga Perovic, Rindidzani Magobo, Marshagne Smith, Ruth Mpembe, Anne von Gottberg, Linda de Gouveia, Sibongile Walaza, Cheryl Cohen, Constance Kapongo, Cheryl Mackay, Mphekwa Thomas Mailula, Omphile Mekgoe, Lerato Motjale, Rose Phayane, Angela Dramowski, Nelesh P Govender
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引用次数: 0

Abstract

Background: Infections are among the top causes of neonatal mortality, particularly in low-income and middle-income countries. We aimed to describe the clinical characteristics of neonates diagnosed with culture-confirmed bloodstream infections at six lower-tier hospitals in South Africa.

Methods: We did a cross-sectional study of culture-confirmed bloodstream infections among neonates (aged 0-27 days) at six lower-tier hospitals in South Africa. Clinical, demographic, and pathogen data from sick, hospitalised neonates were analysed and bloodstream infections were categorised as early-onset sepsis (EOS; 0-2 days of life) or late-onset sepsis (LOS; 3-27 days of life). Incidence of bloodstream infection and crude in-hospital mortality in neonates with bloodstream infection were calculated and factors associated with death were analysed using multivariable logistic regression models.

Findings: From Oct 1, 2019 to Sept 30, 2020, we identified 907 neonatal bloodstream infection episodes. Incidence was 6·4 cases per 1000 patient-days. Most neonates were preterm (median gestation 33 weeks [IQR 29-37]), with 30·5% (n=277) of bloodstream infections classified as EOS and 69·5% (n=630) as LOS. Gram-negative pathogens dominated (63·2% [n=573]), including Klebsiella pneumoniae (25·7% [n=233]) and Acinetobacter baumannii (19·2% [n=174]). Crude in-hospital mortality in neonates with bloodstream infection was 25·5% (n=231), accounting for 21·4% (231 of 1078 cases) of all in-hospital neonatal deaths. Increased all-cause mortality was associated with Gram-negative bloodstream infection (vs Gram-positive pathogens, adjusted odds ratio 3·70 [95% CI 1·46-9·39]; p=0·0059), inborn LOS (vs EOS, 2·42 [1·11-5·29];  p=0·027), preterm birth (5·00 [2·16-11·59]; p=0·0002), and neonatal intensive care unit admission (3·26 [1·51-7·03]; p=0·0026).

Interpretation: Hospitalised, preterm neonates who developed Gram-negative bloodstream infections had high in-hospital mortality. Many small vulnerable newborns require prolonged stays in lower-tier hospitals and acquire life-threatening bloodstream infection; appropriate resources are needed at this level of care to prevent infections and save lives.

Funding: Bill & Melinda Gates Foundation.

南非低级别医院血液感染新生儿的病原体病原学和死亡危险因素:一项横断面研究。
背景:感染是新生儿死亡的主要原因之一,特别是在低收入和中等收入国家。我们的目的是描述在南非六家低级别医院中被诊断为培养证实的血流感染的新生儿的临床特征。方法:我们在南非六家低级别医院对培养证实的新生儿(0-27天)血液感染进行了横断面研究。对住院新生儿的临床、人口统计学和病原体数据进行了分析,并将血液感染归类为早发性败血症(EOS;0-2天的生命)或晚发性败血症(LOS;3-27天的生命)。计算血液感染新生儿的血液感染发生率和院内粗死亡率,并使用多变量logistic回归模型分析与死亡相关的因素。结果:从2019年10月1日至2020年9月30日,我们确定了907例新生儿血液感染事件。发病率为6.4例/ 1000患者日。大多数新生儿为早产儿(中位妊娠期33周[IQR 29-37]),其中30.5% (n=277)的血流感染为EOS, 69.5% (n=630)为LOS。革兰氏阴性病原菌占多数(63.2% [n=573]),包括肺炎克雷伯菌(25.7% [n=233])和鲍曼不动杆菌(19.2% [n=174])。血液感染新生儿的粗院内死亡率为25.5% (n=231),占所有院内新生儿死亡的21.4%(1078例中的231例)。增加的全因死亡率与革兰氏阴性血流感染相关(与革兰氏阳性病原体相比,校正优势比为3.70 [95% CI 1.46 - 9.39];p= 0.0059),先天性LOS (vs EOS, 2.42 [1.11 - 5.29]; p= 0.027),早产(5.00 [2.16 - 11.59];P = 0.0002),新生儿重症监护病房住院率(3.26 [1.51 ~ 7.03];p = 0·0026)。解释:住院的革兰氏阴性血流感染的早产儿有很高的住院死亡率。许多脆弱的小新生儿需要在较低级别医院长时间住院,并获得危及生命的血液感染;在这一级护理中需要适当的资源来预防感染和挽救生命。资助:比尔及梅琳达·盖茨基金会。
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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
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