Department of Neonatology, Children's Hospital of Chongqing Medical University.
Ministry of Education Key Laboratory of Child Development and Disorders.
Am J Perinatol. 2024 Jun;41(8):1019-1026. doi: 10.1055/a-1788-5121. Epub 2022 Mar 4.
The aim of the study is to analyze the risk factors for neonatal acute respiratory distress syndrome (NARDS) development based on the Montreux definition among near- and full-term neonates with sepsis and received meropenem.
This was a single-center, case-control, retrospective trial from January 2019 to June 2020. Newborns of gestational ages (GAs) ≥35 weeks, diagnosed with sepsis and received meropenem were included. Patients who developed NARDS subsequently were defined as the study group (NARDS group), while the others without NARDS were enrolled in the control group (non-NARDS group).
Out of 213 eligible neonates, NARDS occurred in 52 (24.4%) cases. In univariate analysis, infants with NARDS had a lower GA and birth weight, but a higher rate of premature birth ( <0.05). The median onset times of sepsis were earlier among neonates with NARDS compared with those without NARDS (1 [1,1] vs. 6 [1,15] days, <0.001). Neonates with NARDS were more likely to suffer from early-onset sepsis (EOS), persistent pulmonary hypertension of newborns, pulmonary hemorrhage, septic shock, and patent ductus arteriosus ( <0.05). During labor, women whose neonates experienced NARDS were more likely to have a cesarean delivery (67.3 vs. 46.6%, = 0.009) and likely to receive at least one dose of corticosteroids (21.2 vs. 5.0%, = 0.001). In multivariable analyses, factors remaining independently associated with NARDS were premature birth, cesarean delivery, EOS, and septic shock. Compared with conventional inflammatory markers for NARDS, procalcitonin (PCT) was correlated with septic neonates who developed NARDS ( = 0.012) but had a low diagnostic value (area under the curve [AUC] = 0.609). C-reactive protein, white blood cells, and PLT did not correlate with morbidity of NARDS (AUC <0.05 and >0.05).
Premature birth, cesarean delivery, EOS, and septic shock were independently associated with NARDS among near- and full-term septic neonates. PCT showed limited predictive value for NARDS.
· NARDS is serious and sepsis is proved as a cause for it.. · But rare study suggests the risk factors of NARDS based on the Montreux definition.. · This study may first found the independent risk factors associated with NARDS in septic neonates..
根据蒙特勒定义,分析胎龄≥35 周、诊断为败血症且接受美罗培南治疗的近足月和足月新生儿发生新生儿急性呼吸窘迫综合征(NARDS)的危险因素。
这是一项单中心、病例对照、回顾性试验,于 2019 年 1 月至 2020 年 6 月进行。纳入胎龄(GA)≥35 周、诊断为败血症且接受美罗培南治疗的新生儿。随后发生 NARDS 的患者被定义为研究组(NARDS 组),而无 NARDS 的患者被纳入对照组(非 NARDS 组)。
在 213 例符合条件的新生儿中,52 例(24.4%)发生 NARDS。单因素分析显示,NARDS 组新生儿的 GA 和出生体重较低,但早产率较高(<0.05)。与无 NARDS 的新生儿相比,NARDS 组新生儿的败血症发病时间更早(1[1,1]vs.6[1,15]天,<0.001)。NARDS 组新生儿更易发生早发性败血症(EOS)、新生儿持续性肺动脉高压、肺出血、败血症性休克和动脉导管未闭(<0.05)。分娩时,NARDS 新生儿的母亲更有可能行剖宫产术(67.3%vs.46.6%,=0.009),更有可能接受至少一剂皮质类固醇(21.2%vs.5.0%,=0.001)。多变量分析显示,与 NARDS 相关的独立因素仍为早产、剖宫产术、EOS 和败血症性休克。与 NARDS 的常规炎症标志物相比,降钙素原(PCT)与发生 NARDS 的败血症新生儿相关(=0.012),但诊断价值较低(曲线下面积[AUC] =0.609)。C 反应蛋白、白细胞和血小板与 NARDS 发病率无关(AUC<0.05 和>0.05)。
早产、剖宫产术、EOS 和败血症性休克是近足月和足月败血症新生儿发生 NARDS 的独立危险因素。PCT 对 NARDS 的预测价值有限。
·NARDS 很严重,败血症被证实是其病因。·但鲜有研究根据蒙特勒定义探讨 NARDS 的危险因素。·本研究可能首次发现与败血症新生儿 NARDS 相关的独立危险因素。