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儿童重症监护病房毛细支气管炎的呼吸支持实践。

Respiratory Support Practices for Bronchiolitis in the Pediatric Intensive Care Unit.

机构信息

Division of Critical Care Medicine, Department of Pediatrics, Akron Children's Hospital, Akron, Ohio.

Department of Pediatrics, Northeast Ohio Medical University College of Medicine, Rootstown, Ohio.

出版信息

JAMA Netw Open. 2024 May 1;7(5):e2410746. doi: 10.1001/jamanetworkopen.2024.10746.

DOI:10.1001/jamanetworkopen.2024.10746
PMID:38728028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11087830/
Abstract

IMPORTANCE

Admissions to the pediatric intensive care unit (PICU) due to bronchiolitis are increasing. Whether this increase is associated with changes in noninvasive respiratory support practices is unknown.

OBJECTIVE

To assess whether the number of PICU admissions for bronchiolitis between 2013 and 2022 was associated with changes in the use of high-flow nasal cannula (HFNC), noninvasive ventilation (NIV), and invasive mechanical ventilation (IMV) and to identify factors associated with HFNC and NIV success and failure.

DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study examined encounter data from the Virtual Pediatric Systems database on annual PICU admissions for bronchiolitis and ventilation practices among patients aged younger than 2 years admitted to 27 PICUs between January 1, 2013, and December 31, 2022. Use of HFNC and NIV was defined as successful if patients were weaned to less invasive support (room air or low-flow nasal cannula for HFNC; room air, low-flow nasal cannula, or HFNC for NIV).

MAIN OUTCOMES AND MEASURES

The main outcome was the number of PICU admissions for bronchiolitis requiring the use of HFNC, NIV, or IMV. Linear regression was used to analyze the association between admission year and absolute numbers of encounters stratified by the maximum level of respiratory support required. Multivariable logistic regression was used to analyze factors associated with HFNC and NIV success and failure (defined as not meeting the criteria for success).

RESULTS

Included in the analysis were 33 816 encounters for patients with bronchiolitis (20 186 males [59.7%]; 1910 patients [5.6%] aged ≤28 days and 31 906 patients [94.4%] aged 29 days to <2 years) treated at 27 PICUs from 2013 to 2022. A total of 7615 of 15 518 patients (49.1%) had respiratory syncytial virus infection and 1522 of 33 816 (4.5%) had preexisting cardiac disease. Admissions to the PICU increased by 350 (95% CI, 170-531) encounters annually. When data were grouped by the maximum level of respiratory support required, HFNC use increased by 242 (95% CI, 139-345) encounters per year and NIV use increased by 126 (95% CI, 64-189) encounters per year. The use of IMV did not significantly change (10 [95% CI, -11 to 31] encounters per year). In all, 22 381 patients (81.8%) were successfully weaned from HFNC to low-flow oxygen therapy or room air, 431 (1.6%) were restarted on HFNC, 3057 (11.2%) were escalated to NIV, and 1476 (5.4%) were escalated to IMV or extracorporeal membrane oxygenation (ECMO). Successful use of HFNC increased from 820 of 1027 encounters (79.8%) in 2013 to 3693 of 4399 encounters (84.0%) in 2022 (P = .002). In all, 8476 patients (81.5%) were successfully weaned from NIV, 787 (7.6%) were restarted on NIV, and 1135 (10.9%) were escalated to IMV or ECMO. Success with NIV increased from 224 of 306 encounters (73.2%) in 2013 to 1335 of 1589 encounters (84.0%) in 2022 (P < .001). In multivariable logistic regression, lower weight, higher Pediatric Risk of Mortality III score, cardiac disease, and PICU admission from outside the emergency department were associated with greater odds of HFNC and NIV failure.

CONCLUSIONS AND RELEVANCE

Findings of this cross-sectional study of patients aged younger than 2 years admitted for bronchiolitis suggest there was a 3-fold increase in PICU admissions between 2013 and 2022 associated with a 4.8-fold increase in HFNC use and a 5.8-fold increase in NIV use. Further research is needed to standardize approaches to HFNC and NIV support in bronchiolitis to reduce resource strain.

摘要

重要性

因细支气管炎而入住儿科重症监护病房 (PICU) 的人数正在增加。这种增加是否与无创呼吸支持治疗的变化有关尚不清楚。

目的

评估 2013 年至 2022 年期间,因细支气管炎而入住 PICU 的人数与高频鼻导管 (HFNC)、无创通气 (NIV) 和有创机械通气 (IMV) 的使用变化是否相关,并确定与 HFNC 和 NIV 成功和失败相关的因素。

设计、设置和参与者:这项横断面研究分析了 2013 年 1 月 1 日至 2022 年 12 月 31 日期间,27 家儿科重症监护病房收治的 2 岁以下因细支气管炎接受通气治疗的患者的年度 PICU 住院数据和通气实践。HFNC 和 NIV 的使用被定义为如果患者成功地被撤机到侵入性较小的支持(HFNC 下的空气或低流量鼻导管;NIV 下的空气、低流量鼻导管或 HFNC)。

主要结局和测量指标

主要结局是需要使用 HFNC、NIV 或 IMV 的因细支气管炎而入住 PICU 的人数。线性回归用于分析按所需的最大呼吸支持水平分层的入院年份与接触人数之间的关联。多变量逻辑回归用于分析与 HFNC 和 NIV 成功和失败相关的因素(定义为不符合成功标准)。

结果

分析纳入了 2013 年至 2022 年期间因细支气管炎在 27 家儿科重症监护病房接受治疗的 33816 例患者(男性 20186 例[59.7%];28 天以下患者 1910 例[5.6%];29 天至<2 岁患者 31906 例[94.4%])。15518 例患者中共有 7615 例(49.1%)感染了呼吸道合胞病毒,33816 例患者中共有 1522 例(4.5%)患有先心病。PICU 的入院人数每年增加 350 人(95%CI,170-531)。当按所需的最大呼吸支持水平分组时,HFNC 的使用每年增加 242 人(95%CI,139-345),NIV 的使用每年增加 126 人(95%CI,64-189)。IMV 的使用没有显著变化(每年增加 10 人[95%CI,-11 至 31])。共有 22381 例(81.8%)患者成功地从 HFNC 转为低流量吸氧或空气,431 例(1.6%)患者重新开始使用 HFNC,3057 例(11.2%)患者升级为 NIV,1476 例(5.4%)患者升级为 IMV 或体外膜氧合 (ECMO)。HFNC 的成功使用从 2013 年的 1027 次接触中的 798 次(79.8%)增加到 2022 年的 4399 次接触中的 3693 次(84.0%)(P=0.002)。共有 8476 例(81.5%)患者成功地从 NIV 中撤机,787 例(7.6%)患者重新开始使用 NIV,1135 例(10.9%)患者升级为 IMV 或 ECMO。NIV 的成功率从 2013 年的 306 次接触中的 224 次(73.2%)增加到 2022 年的 1589 次接触中的 1335 次(84.0%)(P<0.001)。多变量逻辑回归显示,体重较轻、儿科死亡风险评分较高、心脏病和从急诊部门以外的地方入院与 HFNC 和 NIV 失败的可能性更大相关。

结论和相关性

这项对 2 岁以下因细支气管炎入院的患者的横断面研究发现,2013 年至 2022 年期间 PICU 入院人数增加了 3 倍,与 HFNC 使用增加了 4.8 倍和 NIV 使用增加了 5.8 倍有关。需要进一步研究以标准化细支气管炎中 HFNC 和 NIV 的支持方法,以减轻资源压力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/4ee027bf5b4c/jamanetwopen-e2410746-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/330c0de4e437/jamanetwopen-e2410746-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/7e5d1ae61eca/jamanetwopen-e2410746-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/4ee027bf5b4c/jamanetwopen-e2410746-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/330c0de4e437/jamanetwopen-e2410746-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/7e5d1ae61eca/jamanetwopen-e2410746-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0534/11087830/4ee027bf5b4c/jamanetwopen-e2410746-g003.jpg

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