Institute of Clinical Medicine and Department of Pediatrics, University of Eastern Finland, Kuopio, Finland.
Department of Pediatrics, Kuopio University Hospital, Kuopio, Finland.
Acta Paediatr. 2024 Sep;113(9):2003-2010. doi: 10.1111/apa.17261. Epub 2024 May 4.
To analyse the evidence of non-invasive neurally adjusted ventilatory assist (NIV-NAVA) in preterm neonates compared to nasal continuous positive airway pressure (nCPAP) or nasal intermittent positive pressure ventilation (NIPPV).
We performed a systematic review and meta-analysis of randomised controlled trials and included studies where NIV-NAVA was analysed in preterm (<37 gestational weeks) born neonates. Our main outcomes were the need for endotracheal intubation, the need for surfactant therapy, and reintubation rates. Risk ratios (RRs) with 95% confidence intervals (CIs) were calculated.
A total of five studies were included. The endotracheal intubation rate was 25% in the NIV-NAVA group and 26% in the nCPAP group (RR 0.91, CI: 0.56-1.48). The respective rates for surfactant therapy were 30% and 35% (RR 0.85, CI: 0.56-1.29). The reintubation rate in neonates previously invasively ventilated was 8% in the NIV-NAVA group and 29% in the nCPAP/NIPPV group (RR 0.29, 95%CI: 0.10-0.81). Evidence certainty was rated as low for all outcomes.
NIV-NAVA as the primary respiratory support did not reduce the need for endotracheal intubation or surfactant therapy. NIV-NAVA seemed to reduce the reintubation rate after extubation in pre-term neonates.
分析与鼻塞持续气道正压通气(nCPAP)或经鼻间歇正压通气(NIPPV)相比,无创神经调节通气辅助(NIV-NAVA)在早产儿中的应用证据。
我们对随机对照试验进行了系统评价和荟萃分析,并纳入了分析早产儿(<37 孕周)应用 NIV-NAVA 的研究。我们的主要结局是需要气管内插管、需要表面活性剂治疗以及再插管率。计算了风险比(RR)及其 95%置信区间(CI)。
共纳入 5 项研究。NIV-NAVA 组气管内插管率为 25%,nCPAP 组为 26%(RR 0.91,95%CI:0.56-1.48)。相应的表面活性剂治疗率分别为 30%和 35%(RR 0.85,95%CI:0.56-1.29)。先前有创通气的新生儿再插管率在 NIV-NAVA 组为 8%,在 nCPAP/NIPPV 组为 29%(RR 0.29,95%CI:0.10-0.81)。所有结局的证据确定性均评为低。
作为主要呼吸支持手段,NIV-NAVA 并未降低气管内插管或表面活性剂治疗的需求。NIV-NAVA 似乎可降低早产儿拔管后的再插管率。