The Research Institute at Nationwide Children's Hospital, 575 Children's Crossroads, Columbus, OH, 43215, USA.
Mallinckrodt Pharmaceuticals, Bedminster, NJ, USA.
BMC Pediatr. 2019 Jan 12;19(1):17. doi: 10.1186/s12887-018-1368-4.
Substantial numbers of neonates with hypoxic respiratory failure (HRF) do not immediately respond to inhaled nitric oxide (iNO) and are often labeled as non-responders. This retrospective data analysis assessed time to treatment response in the iNO key registration trial.
Treatment response was defined as a ≥10% increase in partial pressure of arterial oxygen (PaO) or a ≥10% decrease in oxygenation index (OI) after initiation of study gas without the need for extracorporeal membrane oxygenation (ECMO). The proportion of patients showing a response at 30 min, 1 h, 24 h, and >24 h after iNO or placebo initiation was calculated and stratified by baseline PaO and OI.
Data from 248 patients (iNO: n = 126; placebo: n = 122) were included; 66 patients receiving iNO showed improvement in oxygenation without needing ECMO versus 38 receiving placebo. Of the 66 iNO responders, 73% responded within ≤30 min, 9% within ≤1 h, 12% within ≤24 h, and 6% after 24 h. Of the 38 patients with improvement in oxygenation without needing ECMO while receiving placebo, 53% showed improvement within ≤30 min, 16% within ≤1 h, 29% within ≤24 h, and 3% after 24 h. Baseline disease severity was not predictive of time to response. Of the 48 patients in the iNO treatment group who were classified as non-responders due to eventual need for ECMO and not included in the analysis of responders, 40 (83%) had an initial improvement in oxygenation during iNO therapy.
Changes in PaO and OI after iNO initiation appear to be imprecise biomarkers of response to therapy in neonates with HRF. In some patients treated with iNO, it took up to 24 h to achieve improvement in oxygenation without need for ECMO, and a majority of those who eventually required ECMO did show an initial improvement in oxygenation during iNO treatment. Thus, reliable, objective, early criteria for iNO response still need to be established, and initial PaO/OI responses should be interpreted with caution, particularly when considering discontinuing iNO therapy.
大量患有低氧性呼吸衰竭(HRF)的新生儿对吸入性一氧化氮(iNO)没有立即反应,通常被标记为无反应者。这项回顾性数据分析评估了 iNO 关键注册试验中治疗反应的时间。
治疗反应定义为在开始研究气体后,动脉氧分压(PaO)增加≥10%或氧合指数(OI)降低≥10%,而无需体外膜氧合(ECMO)。计算了在 iNO 或安慰剂开始后 30 分钟、1 小时、24 小时和>24 小时时显示反应的患者比例,并按基线 PaO 和 OI 进行分层。
共纳入 248 名患者(iNO:n=126;安慰剂:n=122)的数据;与接受安慰剂的 38 名患者相比,66 名接受 iNO 的患者在不需要 ECMO 的情况下改善了氧合。在 66 名 iNO 反应者中,73%在≤30 分钟内有反应,9%在≤1 小时内有反应,12%在≤24 小时内有反应,6%在 24 小时后有反应。在接受安慰剂而不需要 ECMO 改善氧合的 38 名患者中,53%在≤30 分钟内有反应,16%在≤1 小时内有反应,29%在≤24 小时内有反应,3%在 24 小时后有反应。基线疾病严重程度不能预测反应时间。在 iNO 治疗组中,由于最终需要 ECMO 而未纳入反应者分析的 48 名非反应者中,40(83%)在 iNO 治疗期间初始氧合有改善。
在患有 HRF 的新生儿中,iNO 治疗后 PaO 和 OI 的变化似乎不是治疗反应的精确生物标志物。在接受 iNO 治疗的一些患者中,需要长达 24 小时才能改善氧合而无需 ECMO,而最终需要 ECMO 的大多数患者在 iNO 治疗期间确实表现出初始氧合改善。因此,仍需要建立可靠、客观的 iNO 反应早期标准,并且在考虑停止 iNO 治疗时,应谨慎解释初始 PaO/OI 反应,特别是当考虑停止 iNO 治疗时。