Surfactant Protein D Is Associated With Severe Pediatric ARDS, Prolonged Ventilation, and Death in Children With Acute Respiratory Failure

Surfactant Protein D Is Associated With Severe Pediatric ARDS, Prolonged Ventilation, and Death in Children With Acute Respiratory Failure
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DOI:
10.1016/j.chest.2020.03.041
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发表时间:
2020-09-01
期刊:
影响因子:
9.6
通讯作者:
Quasney, Michael W.
Quasney, Michael W.
中科院分区:
医学1区
文献类型:
--
作者:
Dahmer, Mary K.;Flori, Heidi;Quasney, Michael W.

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背景:表面活性剂蛋白D (SP-D)升高是肺损伤的一个相对特异性指标,与成人急性和慢性肺部疾病以及早产儿呼吸窘迫综合征有关。急性呼吸衰竭患儿血浆SP-D与肺损伤的关系尚不清楚。研究问题:血浆SP-D是否与急性呼吸衰竭患儿的肺损伤或预后相关?研究设计和方法:这是一项前瞻性队列研究,研究对象为参加BALI多中心研究的2周至17岁急性呼吸衰竭儿童。在插管当天或随后2天中的某一天,使用第一个样本的血浆中SP-D水平进行分析。酶联免疫吸附法测定SP-D水平。结果:350例患者的血浆样本被用于分析;233例患有小儿ARDS (PARDS)。SP-D水平在原发性诊断中存在差异(P < 0.001)。在调整了年龄、儿童死亡风险III (PRISM-III)和初次诊断后,SP-D水平升高与严重PARDS相关(OR = 1.02; CI = 1.01-1.04; P = 0.011)。多变量分析还表明,SP-D水平升高与死亡(OR = 1.02; CI = 1.01-1.04; P = 0.004)、机械通气时间(P = 0.012)、PICU住院时间(P = 0.019)和最高氧合指数(P = 0.040)相关。SP-D水平也与年龄相关(rs = 0.16, P = 0.002)。结论:血浆SP-D水平升高与急性呼吸衰竭患儿严重PARDS和预后不良相关。未来的研究将确定SP-D是否可以用于预测肺损伤程度或对治疗的反应,以及SP-D是否有助于识别PARDS内源性类型。
BACKGROUND: Elevated surfactant protein D (SP-D) is a relatively specific indicator of lung injury and is associated with both acute and chronic lung disease in adults and respiratory distress syndrome in premature infants. The relationship between plasma SP-D and lung injury in children with acute respiratory failure is unclear.RESEARCH QUESTION: Is plasma SP-D associated with lung injury or outcome in children with acute respiratory failure?STUDY DESIGN AND METHODS: This was a prospective cohort study in children 2 weeks to 17 years of age with acute respiratory failure who participated in the BALI multi-center study. Analyses were done using SP-D levels in plasma from the first sample taken on either the day of intubation or one of the following 2 days. SP-D level was measured by enzyme-linked immunosorbent assay.RESULTS: Plasma samples from 350 patients were used in the analysis; 233 had pediatric ARDS (PARDS). SP-D levels varied across primary diagnoses (P < .001). Elevated SP-D levels were associated with severe PARDS after adjusting for age, pediatric risk of mortality III (PRISM-III), and primary diagnosis (OR = 1.02; CI = 1.01-1.04; P = .011). Multi variable analyses also indicated that elevated SP-D levels were associated with death (OR = 1.02; CI = 1.01-1.04; P = .004), duration of mechanical ventilation (P = .012), PICU length of stay (P = .019), and highest oxygenation index (P = .040). SP-D levels also correlated with age (rs = 0.16, P = .002).INTERPRETATION: Elevated plasma SP-D levels are associated with severe PARDS and poor outcomes in children with acute respiratory failure. Future studies will determine whether SP-D can be used to predict the degree of lung injury or response to treatment and whether SP-D is useful in identifying PARDS endotypes.