Santana Ruth N S, Santos Victor S, Ribeiro-Júnior Ruy F, Freire Marina S, Menezes Maria A S, Cipolotti Rosana, Gurgel Ricardo Q
Department of Medicine, Federal University of Sergipe, R. Cláudio Batista, s/n - Cidade Nova, Aracaju, 49060-108, Brazil.
Postgraduate Program in Health Sciences, Federal University of Sergipe, R. Cláudio Batista, s/n - Cidade Nova, Aracaju, 49060-108, Brazil.
BMC Infect Dis. 2017 May 30;17(1):375. doi: 10.1186/s12879-017-2482-x.
The inhibition of gastric acid secretion with ranitidine is frequently prescribed off-label to newborns admitted to neonatal intensive care units (NICU). Some studies show that the use of inhibitors of gastric acid secretion (IGAS) may predispose to infections and necrotising enterocolitis (NEC), but there are few data to confirm this association. This study aimed to compare the rates of neonatal infections and NEC among preterm infants (<37 weeks gestation) hospitalised in a NICU exposed or not to treatment with ranitidine.
A retrospective cohort study was conducted with all consecutive preterm newborns admitted to a NICU between August-2014 and October-2015. The rates of infection, NEC, and death of newborns exposed or not to ranitidine were recorded.
A total of 300 newborns were enrolled, of which 115 had received ranitidine and 185 had not. The two groups were similar with regard to the main demographic and clinical characteristics. Forty-eight (41.7%) of the 115 infants exposed to ranitidine and 49 (26.5%) of the 185 infants not exposed were infected (RR = 1.6, 95%CI 1.1-2.2, p = 0.006). The late onset (>48 h) blood culture positive infection rate was higher in the group exposed to ranitidine than in the untreated group (13.0% vs. 3.8%, p = 0.001). There was no significant association between the use of ranitidine and NEC (Bell stage >II) (p = 0.36). The mortality rate risk was 4-fold higher in infants receiving ranitidine (16.5% vs. 8.6%, p < 0.001).
Ranitidine use in neonates was associated with an increased risk of infections and mortality, but not with NEC.
雷尼替丁抑制胃酸分泌常用于新生儿重症监护病房(NICU)新生儿的非适应症用药。一些研究表明,使用胃酸分泌抑制剂(IGAS)可能易引发感染和坏死性小肠结肠炎(NEC),但鲜有数据证实这种关联。本研究旨在比较在NICU住院的早产(孕周<37周)婴儿中,接受或未接受雷尼替丁治疗的新生儿感染率和NEC发生率。
对2014年8月至2015年10月期间入住某NICU的所有连续早产新生儿进行回顾性队列研究。记录接受或未接受雷尼替丁治疗的新生儿的感染率、NEC发生率和死亡率。
共纳入300例新生儿,其中115例接受了雷尼替丁治疗,185例未接受。两组在主要人口统计学和临床特征方面相似。115例接受雷尼替丁治疗的婴儿中有48例(41.7%)感染,185例未接受治疗的婴儿中有49例(26.5%)感染(相对危险度=1.6,95%置信区间1.1 - 2.2,p = 0.006)。接受雷尼替丁治疗组的迟发性(>48小时)血培养阳性感染率高于未治疗组(13.0%对3.8%,p = 0.001)。雷尼替丁的使用与NEC(贝尔分期>II期)之间无显著关联(p = 0.36)。接受雷尼替丁治疗的婴儿死亡率风险高出4倍(16.5%对8.6%,p < 0.001)。
新生儿使用雷尼替丁与感染风险和死亡率增加相关,但与NEC无关。