Invasive versus non-invasive paediatric home mechanical ventilation: review of the international evolution over the past 24 years.

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM
Thorax Pub Date : 2024-05-20 DOI:10.1136/thorax-2023-220888
Michel Toussaint, Olivier van Hove, Dimitri Leduc, Lise Ansay, Nicolas Deconinck, Brigitte Fauroux, Sonia Khirani
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引用次数: 0

Abstract

Background: Home mechanical ventilation (HMV) is the treatment for chronic hypercapnic alveolar hypoventilation. The proportion and evolution of paediatric invasive (IMV) and non-invasive (NIV) HMV across the world is unknown, as well as the disorders and age of children using HMV.

Methods: Search of Medline/PubMed for publications of paediatric surveys on HMV from 2000 to 2023.

Results: Data from 32 international reports, representing 8815 children (59% boys) using HMV, were analysed. A substantial number of children had neuromuscular disorders (NMD; 37%), followed by cardiorespiratory (Cardio-Resp; 16%), central nervous system (CNS; 16%), upper airway (UA; 13%), other disorders (Others; 10%), central hypoventilation (4%), thoracic (3%) and genetic/congenital disorders (Gen/Cong; 1%). Mean age±SD (range) at HMV initiation was 6.7±3.7 (0.5-14.7) years. Age distribution was bimodal, with two peaks around 1-2 and 14-15 years. The number and proportion of children using NIV was significantly greater than that of children using IMV (n=6362 vs 2453, p=0.03; 72% vs 28%, p=0.048), with wide variations among countries, studies and disorders. NIV was used preferentially in the preponderance of children affected by UA, Gen/Cong, Thoracic, NMD and Cardio-Resp disorders. Children with NMD still receiving primary invasive HMV were mainly type I spinal muscular atrophy (SMA). Mean age±SD at initiation of IMV and NIV was 3.3±3.3 and 8.2±4.4 years (p<0.01), respectively. The rate of children receiving additional daytime HMV was higher with IMV as compared with NIV (69% vs 10%, p<0.001). The evolution of paediatric HMV over the last two decades consists of a growing number of children using HMV, in parallel to an increasing use of NIV in recent years (2020-2023). There is no clear trend in the profile of children over time (age at HMV). However, an increasing number of patients requiring HMV were observed in the Gen/Cong, CNS and Others groups. Finally, the estimated prevalence of paediatric HMV was calculated at 7.4/100 000 children.

Conclusions: Patients with NMD represent the largest group of children using HMV. NIV is increasingly favoured in recent years, but IMV is still a prevalent intervention in young children, particularly in countries indicating less experience with NIV.

有创与无创儿科家庭机械通气:回顾过去 24 年的国际演变。
背景:家庭机械通气(HMV)是治疗慢性高碳酸血症肺泡通气不足的方法。全世界儿科有创(IMV)和无创(NIV)家用机械通气的比例和演变情况,以及使用家用机械通气的儿童的疾病和年龄均不清楚:方法:在 Medline/PubMed 上搜索 2000 年至 2023 年有关 HMV 儿科调查的出版物:分析了 32 份国际报告中的数据,这些报告代表了 8815 名使用 HMV 的儿童(59% 为男孩)。大量儿童患有神经肌肉疾病(NMD;37%),其次是心肺疾病(Cardio-Resp;16%)、中枢神经系统(CNS;16%)、上气道疾病(UA;13%)、其他疾病(Others;10%)、中枢通气不足(4%)、胸腔疾病(3%)和遗传/先天性疾病(Gen/Cong;1%)。开始使用 HMV 时的平均年龄为 6.7±3.7 (0.5-14.7)岁。年龄分布呈双峰型,1-2 岁和 14-15 岁为两个高峰。使用 NIV 的儿童人数和比例明显高于使用 IMV 的儿童人数和比例(n=6362 vs 2453,p=0.03;72% vs 28%,p=0.048),不同国家、不同研究和不同疾病之间的差异很大。在 UA、Gen/Cong、胸腔、NMD 和 Cardio-Resp 疾病患儿中,NIV 被优先使用。仍在接受原发性侵入性 HMV 的 NMD 患儿主要是 I 型脊髓性肌萎缩症(SMA)患儿。开始接受 IMV 和 NIV 治疗时的平均年龄为(3.3±3.3)岁和(8.2±4.4)岁(p 结论:NMD 患者是最大的群体:NMD 患者是使用 HMV 的最大儿童群体。近年来,NIV 越来越受到青睐,但 IMV 仍是幼儿常用的干预方法,尤其是在 NIV 经验较少的国家。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Thorax
Thorax 医学-呼吸系统
CiteScore
16.10
自引率
2.00%
发文量
197
审稿时长
1 months
期刊介绍: Thorax stands as one of the premier respiratory medicine journals globally, featuring clinical and experimental research articles spanning respiratory medicine, pediatrics, immunology, pharmacology, pathology, and surgery. The journal's mission is to publish noteworthy advancements in scientific understanding that are poised to influence clinical practice significantly. This encompasses articles delving into basic and translational mechanisms applicable to clinical material, covering areas such as cell and molecular biology, genetics, epidemiology, and immunology.
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