Carlton Erin F, Weeks Heidi M, Dahmer Mary K, Quasney Michael W, Sapru Anil, Curley Martha A Q, Flori Heidi R
Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Michigan, Ann Arbor, MI.
Susan B. Meister Child Health Evaluation and Research Center, Department of Pediatrics, University of Michigan, Ann Arbor, MI.
Crit Care Explor. 2021 Jul 13;3(7):e0467. doi: 10.1097/CCE.0000000000000467. eCollection 2021 Jul.
To evaluate the link between early acute respiratory failure and functional morbidity in survivors using the plasma biomarkers interleukin-8, interleukin-1 receptor antagonist, thrombomodulin, and plasminogen activator inhibitor-1. We hypothesized that children with acute respiratory failure with higher levels of inflammation would have worse functional outcomes at discharge, as measured by Pediatric Overall Performance Category.
Secondary analysis of the Genetic Variation and Biomarkers in Children with Acute Lung Injury (R01HL095410) study.
Twenty-two PICUs participating in the multisite clinical trial, Randomized Evaluation of Sedation Titration for Respiratory Failure (U01 HL086622) and the ancillary study (Biomarkers in Children with Acute Lung Injury).
Children 2 weeks to 17 years requiring invasive mechanical ventilation for acute airways and/or parenchymal lung disease. Patients with an admission Pediatric Overall Performance Category greater than 3 (severe disability, coma, or brain death) were excluded.
None.
Among survivors, 387 patients had no worsening of Pediatric Overall Performance Category at discharge while 40 had worsening functional status, defined as any increase in Pediatric Overall Performance Category from baseline. There was no significant relationship between worsening of Pediatric Overall Performance Category and interleukin-8 or plasminogen activator inhibitor-1 on any day. There was no significant relationship between interleukin-1 receptor antagonist, or thrombomodulin, and worsening Pediatric Overall Performance Category on day 1. Plasma interleukin-1 receptor antagonist and thrombomodulin were significantly elevated on days 2 and 3 in those with worse functional status at discharge compared with those without. In multivariable analysis, interleukin-1 receptor antagonist and thrombomodulin were associated with a decline in functional status on days 2 and 3 after adjustment for age and highest oxygenation index. However, after adjusting for age and cardiovascular failure, only day 2 thrombomodulin levels were associated with a worsening in Pediatric Overall Performance Category.
Higher levels of interleukin-1 receptor antagonist or thrombomodulin following intubation were associated with worse Pediatric Overall Performance Category scores at hospital discharge in children who survive acute respiratory failure. These data suggest that persistent inflammation may be related to functional decline.
使用血浆生物标志物白细胞介素-8、白细胞介素-1受体拮抗剂、血栓调节蛋白和纤溶酶原激活物抑制剂-1来评估幸存者早期急性呼吸衰竭与功能障碍之间的联系。我们假设,炎症水平较高的急性呼吸衰竭患儿出院时的功能结局会更差,这通过儿科总体表现分类来衡量。
对急性肺损伤儿童的基因变异与生物标志物(R01HL095410)研究进行二次分析。
22个儿科重症监护病房参与了多中心临床试验“呼吸衰竭镇静滴定的随机评估”(U01 HL086622)及辅助研究(急性肺损伤儿童的生物标志物)。
因急性气道和/或实质性肺部疾病需要有创机械通气的2周龄至17岁儿童患者。入院时儿科总体表现分类大于3(严重残疾、昏迷或脑死亡)的患者被排除。
无。
在幸存者中,387例患者出院时儿科总体表现分类未恶化,而40例患者功能状态恶化,定义为儿科总体表现分类较基线有任何增加。儿科总体表现分类恶化与白细胞介素-8或纤溶酶原激活物抑制剂-1在任何一天之间均无显著关系。白细胞介素-1受体拮抗剂或血栓调节蛋白与第1天儿科总体表现分类恶化之间无显著关系。与出院时功能状态未恶化的患者相比,出院时功能状态较差的患者血浆白细胞介素-1受体拮抗剂和血栓调节蛋白在第2天和第3天显著升高。在多变量分析中,调整年龄和最高氧合指数后,白细胞介素-1受体拮抗剂和血栓调节蛋白与第2天和第3天的功能状态下降有关。然而,在调整年龄和心血管衰竭后,仅第2天的血栓调节蛋白水平与儿科总体表现分类恶化有关。
插管后白细胞介素-1受体拮抗剂或血栓调节蛋白水平较高与急性呼吸衰竭存活儿童出院时较差的儿科总体表现分类评分有关。这些数据表明持续炎症可能与功能下降有关。