Zeng Yali, Huang Zhifeng, Wang Yanqiong, Lin Binchun, Zhao Depeng, Yang Chuanzhong, Chen Xueyu
Department of Neonatology, Shenzhen Maternity and Child Healthcare Hospital, the First School of Medicine, Southern Medical University, Shenzhen, China.
Department of Reproductive Medicine, Shenzhen maternity and child healthcare hospital, the First School of Medicine, Southern Medical University, Shenzhen, China.
Pediatr Pulmonol. 2025 Jan;60(1):e27384. doi: 10.1002/ppul.27384. Epub 2024 Nov 6.
To test the effect of azithromycin in reducing bronchopulmonary dysplasia (BPD) risk in extremely preterm infants (EPI) without pulmonary infection.
A retrospective cohort study was performed in EPI in a tertiary unit from September 2018 to September 2022. Since only Ureaplasma species positive infants were treated with azithromycin, we included infants without Ureaplasma species (no azithromycin treatment) and those diagnosed with Ureaplasma species colonization (azithromycin treatment) in the study, while infants with Ureaplasma species pneumonia were excluded. The primary outcome was grade II BPD, defined as BPD of grade II or higher according to the updated NICHD criteria (2018). Multiple logistic regression analysis was used to identify the independent association between grade II BPD and azithromycin treatment.
A total of 237 EPIs were included in the current study, of which 202 infants were classified as no azithromycin treatment (Ureaplasma species negative) and 35 infants were classified as azithromycin treatment (Ureaplasma species colonization). Clinical characteristics were similar between groups. Infants treated with azithromycin had a significantly lower rate of grade II BPD (8.6% vs. 31.2%, p = 0.006), and shorter duration of invasive ventilation (0 vs. 3 days, p = 0.045) compared to untreated ones. After adjusting for confounders, azithromycin treatment was significantly associated with reduced risk of grade II BPD in the whole cohort (odd ratio [OR] 0.211, 95% CI: 0.056, 0.786, p = 0.020], and infants absent of other pulmonary infection (OR 0.115, 95% CI: 0.014, 0.979, p = 0.048).
Azithromycin is associated with a reduced risk of grade II BPD in EPIs, likely due to its anti-inflammatory effect.
测试阿奇霉素对降低无肺部感染的极早产儿(EPI)发生支气管肺发育不良(BPD)风险的作用。
2018年9月至2022年9月在一家三级医疗单位对极早产儿进行了一项回顾性队列研究。由于仅对解脲脲原体阳性的婴儿使用阿奇霉素治疗,因此本研究纳入了解脲脲原体阴性(未接受阿奇霉素治疗)的婴儿和诊断为解脲脲原体定植(接受阿奇霉素治疗)的婴儿,而解脲脲原体肺炎婴儿被排除。主要结局为II级BPD,根据更新的美国国立儿童健康与人类发展研究所(NICHD)标准(2018年)定义为II级或更高等级的BPD。采用多因素logistic回归分析确定II级BPD与阿奇霉素治疗之间的独立关联。
本研究共纳入237例极早产儿,其中202例婴儿被归类为未接受阿奇霉素治疗(解脲脲原体阴性),35例婴儿被归类为接受阿奇霉素治疗(解脲脲原体定植)。两组间临床特征相似。与未治疗的婴儿相比,接受阿奇霉素治疗的婴儿II级BPD发生率显著更低(8.6%对31.2%,p = 0.006),有创通气持续时间更短(0天对3天,p = 0.045)。在对混杂因素进行校正后,阿奇霉素治疗与整个队列中II级BPD风险降低显著相关(比值比[OR] 0.211,95%置信区间:0.056,0.786,p = 0.020),在无其他肺部感染的婴儿中也是如此(OR 0.115,95%置信区间:0.014,0.979,p = 0.048)。
阿奇霉素与极早产儿II级BPD风险降低相关,可能归因于其抗炎作用。