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高流量鼻导管在儿科重症急性哮喘中的应用的匹配分析。

A matched analysis of the use of high flow nasal cannula for pediatric severe acute asthma.

机构信息

Department of Pediatrics, Division of Critical Care, Indiana University School of Medicine, Indiana, USA.

Regenstrief Institute Center for Biomedical Informatics, Indiana, USA.

出版信息

Pediatr Pulmonol. 2024 Dec;59(12):3457-3466. doi: 10.1002/ppul.27233. Epub 2024 Aug 30.

Abstract

RATIONALE

The high-flow nasal cannula (HFNC) device is commonly used to treat pediatric severe acute asthma. However, there is little evidence regarding its effectiveness in real-world practice.

OBJECTIVES

We sought to compare the physiologic effects and clinical outcomes for children treated for severe acute asthma with HFNC versus matched controls.

METHODS

This was a single-center retrospective matched cohort study at a quaternary care children's hospital. Children ages 2-18 hospitalized for severe acute asthma from 2015 to 2022 were included. Encounters receiving treatment with HFNC within the first 24 h of hospitalization were included as cases. Controls were primarily treated with oxygen facemask. Logistic regression 1:1 propensity score matching was done using demographics, initial vital signs, and medications. The primary outcome was an improvement in clinical asthma symptoms in the first 24 h of hospitalization measured as percent change from initial.

MEASUREMENTS AND MAIN RESULTS

Of 693 eligible cases, 443 were matched to eligible controls. Propensity scores were closely aligned between the cohorts, with the only significant difference in clinical characteristics being a higher percentage of patients of Black race in the control group (54.3% vs. 46.6%; p = 0.02). Compared to the matched controls, the HFNC cohort had smaller improvements in heart rate (-11.5% [-20.9; -0.9] vs. -14.7% [-22.6;-5.7]; p < 0.01), respiratory rate (-14.3% [-27.9;5.4] vs. -16.7% [-31.5;0.0]; p = 0.03), and pediatric asthma severity score (-14.3% [-28.6;0.0] vs. -20.0% [-33.3;0.0]; p < 0.01) after 24 h of hospitalization. The HFNC cohort also had longer pediatric intensive care unit (PICU) length of stay (LOS) (1.5 days [1.1;2.1] vs. 1.2 days [0.9;1.8]; p < 0.01) and hospital LOS (2.8 days [2.1;3.8] vs. 2.5 days [1.9;3.4]; p < 0.01). When subgrouping to younger patients (2-3 years old), or those with the highest severity scores (PASS > 9), those treated with HFNC had no difference in clinical symptom improvements but maintained a longer PICU LOS.

CONCLUSIONS

Encounters using HFNC for severe acute pediatric asthma had decreased clinical improvement in 24 h of hospitalization compared to matched controls and increased LOS. Specific subgroups of younger patients and those with the highest severity scores showed no differences in clinical symptom improvement suggesting differential effects in specific patient populations.

摘要

背景

高流量鼻导管(HFNC)装置常用于治疗儿科严重急性哮喘。然而,关于其在实际实践中的有效性的证据很少。

目的

我们旨在比较 HFNC 治疗与匹配对照的儿科严重急性哮喘患儿的生理效果和临床结局。

方法

这是一家四级儿童保健医院的单中心回顾性匹配队列研究。纳入 2015 年至 2022 年因严重急性哮喘住院的 2-18 岁儿童。入院后 24 小时内接受 HFNC 治疗的患者被纳入病例组。对照组主要接受氧面罩治疗。使用人口统计学、初始生命体征和药物进行逻辑回归 1:1 倾向评分匹配。主要结局为住院 24 小时内临床哮喘症状的改善,以初始值的百分比变化来衡量。

测量和主要结果

在 693 例符合条件的病例中,443 例与符合条件的对照组相匹配。队列之间的倾向评分非常一致,唯一显著的临床特征差异是对照组中黑人患者的比例较高(54.3%对 46.6%;p=0.02)。与匹配的对照组相比,HFNC 组的心率改善较小(-11.5%[-20.9;-0.9]对-14.7%[-22.6;-5.7];p<0.01)、呼吸率改善较小(-14.3%[-27.9;5.4]对-16.7%[-31.5;0.0];p=0.03)和儿科哮喘严重程度评分改善较小(-14.3%[-28.6;0.0]对-20.0%[-33.3;0.0];p<0.01)。HFNC 组患儿的儿科重症监护病房(PICU)住院时间(1.5 天[1.1;2.1]对 1.2 天[0.9;1.8];p<0.01)和总住院时间(2.8 天[2.1;3.8]对 2.5 天[1.9;3.4];p<0.01)也更长。当亚组为年龄较小的患者(2-3 岁)或严重程度评分最高的患者(PASS>9)时,HFNC 治疗的患者在临床症状改善方面无差异,但 PICU 住院时间延长。

结论

与匹配对照组相比,HFNC 治疗严重急性儿科哮喘患儿的住院 24 小时临床改善程度降低,住院时间延长。年龄较小和严重程度评分最高的特定亚组患者的临床症状改善无差异,提示特定患者人群的治疗效果存在差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f948/11601001/be79f3a381be/PPUL-59-3457-g001.jpg

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