RAM套管在儿童无创鼻通气中的门诊应用。

IF 1.7 Q2 PEDIATRICS
Brittany A Truitt, Erin F Kallam, Eric W Price, Amit S Shah, Dawn M Simon, Ajay S Kasi
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引用次数: 1

摘要

背景:RAM插管®由鼻尖组成,可用于给氧、持续和双水平气道正压治疗。研究报告了RAM套管在需要无创通气(NIV)的住院患者中的疗效和实用性;然而,关于在门诊使用RAM套管提供无创通气的文献有限。目的:本研究旨在描述门诊通过RAM插管使用NIV的儿童的临床特征和结果。设计:回顾性审查。方法:我们对2010年1月至2023年3月在我院门诊通过RAM套管治疗NIV的儿童进行回顾性分析。分析的数据包括年龄、诊断、NIV指征、RAM插管使用时间、并发症和6个月时的结果。结果:我们确定了20例在研究期间通过RAM插管使用门诊NIV的患者。通过RAM插管开始NIV的中位年龄为5.8个月(IQR 2.4-9.9个月)。NIV的适应症包括睡眠相关通气不足(15%)、限制性肺部疾病(25%)、阻塞性睡眠呼吸暂停(45%)和慢性呼吸衰竭(50%),有6名患者的NIV适应症大于或等于2。RAM插管用于无法耐受传统NIV接口(80%),缓解呼吸困难(60%),避免气管切开术(55%)。患者通过RAM插管使用NIV的中位持续时间为7.7个月(IQR 3.7-20.6个月)。患者结果包括持续使用RAM套管(55%),改用传统NIV接口(15%)或吸氧(10%),脱离呼吸支持(5%)和死亡(15%)。使用RAM插管没有并发症。结论:我们的研究表明,在临床改善或对常规接口耐受之前,门诊通过RAM插管的NIV对各种诊断的儿童都是有用的,并且避免了气管切开术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Outpatient Utilization of the RAM Cannula for Nasal Noninvasive Ventilation in Children.

Outpatient Utilization of the RAM Cannula for Nasal Noninvasive Ventilation in Children.

Outpatient Utilization of the RAM Cannula for Nasal Noninvasive Ventilation in Children.

Outpatient Utilization of the RAM Cannula for Nasal Noninvasive Ventilation in Children.

Background: The RAM cannula® consists of nasal prongs that can be used to administer oxygen, continuous, and bilevel positive airway pressure therapies. Studies have reported the efficacy and utility of the RAM cannula in inpatients requiring noninvasive ventilation (NIV); however, there is limited literature on the use of the RAM cannula to provide NIV in the outpatient setting.

Objectives: This study aimed to describe the clinical features and outcomes of children who used NIV via RAM cannula in the outpatient setting.

Design: Retrospective review.

Methods: We conducted a retrospective review of children treated with outpatient NIV via RAM cannula at our institution between January 2010 and March 2023. The analyzed data included age, diagnoses, indications for NIV, duration of RAM cannula use, complications, and outcomes at 6 months.

Results: We identified 20 patients who used outpatient NIV via RAM cannula during the study period. The median age at initiation of NIV via RAM cannula was 5.8 months (IQR 2.4-9.9 months). Indications for NIV included sleep-related hypoventilation (15%), restrictive lung disease (25%), obstructive sleep apnea (45%), and chronic respiratory failure (50%), with 6 patients having ⩾2 indications for NIV. RAM cannula was utilized for inability to tolerate conventional NIV interfaces (80%), to alleviate dyspnea (60%), and to avoid tracheostomy (55%). Patients used NIV via RAM cannula for a median duration of 7.7 months (IQR 3.7-20.6 months). Patient outcomes included ongoing usage of RAM cannula (55%), changing to conventional NIV interfaces (15%) or oxygen (10%), weaning off respiratory support (5%), and death (15%). There were no complications related to using the RAM cannula.

Conclusion: Our study demonstrates the utility of outpatient NIV via RAM cannula in children with a variety of diagnoses until clinical improvement or tolerance of conventional interfaces, and for avoidance of tracheostomy.

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