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本文引用的文献

1
Economic burden of neonatal sepsis in sub-Saharan Africa.撒哈拉以南非洲地区新生儿败血症的经济负担。
BMJ Glob Health. 2018 Jan 12;3(1):e000347. doi: 10.1136/bmjgh-2017-000347. eCollection 2018.
2
Global, regional, and national causes of under-5 mortality in 2000-15: an updated systematic analysis with implications for the Sustainable Development Goals.2000 - 2015年全球、区域和国家五岁以下儿童死亡原因:一项最新的系统分析及其对可持续发展目标的启示
Lancet. 2016 Dec 17;388(10063):3027-3035. doi: 10.1016/S0140-6736(16)31593-8. Epub 2016 Nov 11.
3
Defining neonatal sepsis.定义新生儿败血症。
Curr Opin Pediatr. 2016 Apr;28(2):135-40. doi: 10.1097/MOP.0000000000000315.
4
Prevalence of fecal carriage of extended-spectrum- and metallo-β-lactamase-producing gram-negative bacteria among neonates born in a hospital setting in central Saudi Arabia.沙特阿拉伯中部一家医院出生的新生儿中产超广谱β-内酰胺酶和金属β-内酰胺酶革兰氏阴性菌的粪便携带率。
Ann Saudi Med. 2015 May-Jun;35(3):240-7. doi: 10.5144/0256-4947.2015.240.
5
Late-onset neonatal sepsis: recent developments.迟发性新生儿败血症:最新进展
Arch Dis Child Fetal Neonatal Ed. 2015 May;100(3):F257-63. doi: 10.1136/archdischild-2014-306213. Epub 2014 Nov 25.
6
Changes in the incidence of candidiasis in neonatal intensive care units.新生儿重症监护病房念珠菌病发病率的变化。
Pediatrics. 2014 Feb;133(2):236-42. doi: 10.1542/peds.2013-0671. Epub 2014 Jan 20.
7
Neonatal severe bacterial infection impairment estimates in South Asia, sub-Saharan Africa, and Latin America for 2010.2010 年南亚、撒哈拉以南非洲和拉丁美洲新生儿严重细菌感染损害估计。
Pediatr Res. 2013 Dec;74 Suppl 1(Suppl 1):73-85. doi: 10.1038/pr.2013.207.
8
Group B streptococcus late-onset disease: 2003-2010.B 型链球菌晚发型疾病:2003-2010 年。
Pediatrics. 2013 Feb;131(2):e361-8. doi: 10.1542/peds.2012-1231. Epub 2013 Jan 6.
9
Risk factors and clinical analysis for invasive fungal infection in neonatal intensive care unit patients.新生儿重症监护病房患者侵袭性真菌感染的危险因素及临床分析。
Am J Perinatol. 2013 Aug;30(7):589-94. doi: 10.1055/s-0032-1329688. Epub 2012 Dec 31.
10
Use and misuse of antibiotics in the neonatal intensive care unit.新生儿重症监护病房中抗生素的使用与滥用
J Matern Fetal Neonatal Med. 2012 Oct;25 Suppl 4:35-7. doi: 10.3109/14767058.2012.714987.

新生儿病房使用经验性抗生素治疗晚发性新生儿败血症的回顾性研究

A Neonatal Unit Experience with Empiric Antibiotics for Late-onset Neonatal Sepsis: A Retrospective Study.

作者信息

Al-Mouqdad Mountasser Mohammad, Egunsola Oluwaseun, Ali Sheraz, Asfour Suzan Suahil

机构信息

King Saud Medical City, Ministry of Health, Riyadh, Saudi Arabia.

Clinical Pharmacology and Toxicology Research Group, Discipline of Pharmacology, School of Medical Sciences, Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.

出版信息

Pediatr Qual Saf. 2019 Dec 9;4(6):e239. doi: 10.1097/pq9.0000000000000239. eCollection 2019 Nov-Dec.

DOI:10.1097/pq9.0000000000000239
PMID:32010865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6946227/
Abstract

UNLABELLED

Neonatal sepsis remains a major cause of morbidity and mortality and warrants the immediate start of appropriate empiric treatment. Thus, this study compared the effectiveness of the 2 antibiotic regimens (cloxacillin-amikacin or cefotaxime-ampicillin) among neonates with late-onset neonatal sepsis.

METHODS

We conducted a retrospective cohort study comparing mortality between 2 treatment cohorts of very low birth weight neonates with late-onset sepsis, who had received amikacin-cloxacillin or cefotaxime-ampicillin between January 2014 and December 2017. There were 27 neonates in each treatment arm after 1:1 propensity score matching. Univariate analyses (Chi-square and independent tests, where appropriate) were performed to determine the association between variables. We determined the hazard ratio for all-cause mortality using the Cox regression model.

RESULTS

We identified a total of 132 neonates from the hospital's record. We included 27 neonates each in the amikacin-cloxacillin and cefotaxime-ampicillin groups. Intraventricular hemorrhage, necrotizing enterocolitis, birth weight, and gestational age were significantly associated with mortality ( < 0.05). The risk of mortality was significantly higher in neonates receiving empiric cefotaxime and ampicillin than those receiving amikacin and cloxacillin (hazard ratio: 2.91, 95% confidence interval: 1.17-7.30, = 0.023).

CONCLUSIONS

In our center, amikacin-cloxacillin combination therapy was associated with lower mortality in very low birth weight neonates with late-onset sepsis compared with cefotaxime-ampicillin therapy.

摘要

未标注

新生儿败血症仍然是发病和死亡的主要原因,需要立即开始适当的经验性治疗。因此,本研究比较了两种抗生素方案(氯唑西林-阿米卡星或头孢噻肟-氨苄西林)在晚发型新生儿败血症患儿中的疗效。

方法

我们进行了一项回顾性队列研究,比较2014年1月至2017年12月期间接受阿米卡星-氯唑西林或头孢噻肟-氨苄西林治疗的极低出生体重晚发型败血症新生儿两个治疗队列的死亡率。1:1倾向评分匹配后,每个治疗组有27例新生儿。进行单因素分析(卡方检验和独立检验,酌情使用)以确定变量之间的关联。我们使用Cox回归模型确定全因死亡率的风险比。

结果

我们从医院记录中总共识别出132例新生儿。阿米卡星-氯唑西林组和头孢噻肟-氨苄西林组各纳入27例新生儿。脑室内出血、坏死性小肠结肠炎、出生体重和胎龄与死亡率显著相关(P<0.05)。接受经验性头孢噻肟和氨苄西林治疗的新生儿的死亡风险显著高于接受阿米卡星和氯唑西林治疗的新生儿(风险比:2.91,95%置信区间:1.17-7.30,P=0.023)。

结论

在我们中心,与头孢噻肟-氨苄西林治疗相比,阿米卡星-氯唑西林联合治疗在极低出生体重晚发型败血症新生儿中的死亡率更低。