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A matched analysis of the use of high flow nasal cannula for pediatric severe acute asthma
被引:1
|作者:
Rogerson, Colin
[1
,2
]
AbuSultaneh, Samer
[1
]
Sanchez-Pinto, L. Nelson
[3
]
Gaston, Benjamin
[1
]
Wiehe, Sarah
[1
,4
]
Schleyer, Titus
[1
,2
]
Tu, Wanzhu
[5
]
Mendonca, Eneida
[1
,6
]
机构:
[1] Indiana Univ Sch Med, Dept Pediat, Div Crit Care, Indianapolis, IN USA
[2] Regenstrief Inst Ctr Biomed Informat, Indianapolis, IN USA
[3] Northwestern Univ, Anne & Robert H Lurie Childrens Hosp, Chicago, IL USA
[4] Regenstrief Inst Ctr Hlth Serv Res, Indianapolis, IN USA
[5] Indiana Univ, Dept Biostat, Indianapolis, IN USA
[6] Cincinnati Childrens Hosp & Med Ctr, Dept Pediat, Div Crit Care, Cincinnati, OH USA
关键词:
asthma;
clinical research;
informatics;
pediatrics;
OXYGEN-THERAPY;
EPIDEMIOLOGY;
CHILDREN;
D O I:
10.1002/ppul.27233
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
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.
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页码:3457 / 3466
页数:10
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