Al-Mouqdad Mountasser Mohammad, Egunsola Oluwaseun, Ali Sheraz, Asfour Suzan Suahil
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.
Pediatr Qual Saf. 2019 Dec 9;4(6):e239. doi: 10.1097/pq9.0000000000000239. eCollection 2019 Nov-Dec.
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.
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.
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).
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.
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。
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。
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)。
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。