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地塞米松预防儿童拔管后上呼吸道梗阻的网状 Meta 分析

A Network Meta-analysis of Dexamethasone for Preventing Postextubation Upper Airway Obstruction in Children.

机构信息

Fetal and Neonatal Institute, Division of Neonatology, and.

Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, California.

出版信息

Ann Am Thorac Soc. 2023 Jan;20(1):118-130. doi: 10.1513/AnnalsATS.202203-212OC.

DOI:10.1513/AnnalsATS.202203-212OC
PMID:35976878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9819263/
Abstract

Periextubation corticosteroids are commonly used in children to prevent upper airway obstruction (UAO). However, the best timing and dose combination of corticosteroids is unknown. To compare effectiveness of different corticosteroid regimens in preventing UAO and reintubation. MEDLINE, CINAHL, and Embase search identified randomized trials in children using corticosteroids to prevent UAO. All studies used dexamethasone. The studies were categorized based on timing of initiation of dexamethasone (early use: >12 h before extubation) and the dose (high dose: ⩾0.5 mg/kg/dose). We performed Bayesian network meta-analysis with studies grouped into four regimens: high dose, early use (HE); low dose, early use (LE); high dose, late use (HL); and low dose, late use. Eight trials ( = 903) were included in the analysis. For preventing UAO (odds ratio; 95% credible interval), HE (0.13; 0.04-0.36), HL (0.39; 0.19-0.74), and LE (0.15; 0.04-0.58) regimens appear to be more effective than no dexamethasone (low certainty). HE and LE had the highest probability of being the top-ranked regimens for preventing UAO (surface under the cumulative ranking curve 0.901 and 0.808, respectively). For preventing reintubation, the effect estimate was imprecise for all four dexamethasone regimens compared with no dexamethasone (very low certainty). HE and LE were the top-ranked regimens (surface under the cumulative ranking curve 0.803 and 0.720, respectively) for preventing reintubation. Sensitivity analysis showed that regimens that started >12 hours before extubation were likely more effective than regimens started >6 hours before extubation. Periextubation dexamethasone can prevent postextubation UAO in children, but effectiveness is highly dependent on timing and dosing regimen. Early initiation (ideally >12 h before extubation) appears to be more important than the dose of dexamethasone. Ultimately, the specific steroid strategy should be personalized, considering the potential for adverse events associated with dexamethasone and the individual risk of UAO and reintubation.

摘要

拔管后皮质类固醇常用于预防儿童上呼吸道阻塞 (UAO)。然而,皮质类固醇的最佳给药时机和剂量组合尚不清楚。为了比较不同皮质类固醇方案预防 UAO 和再插管的效果。

使用 MEDLINE、CINAHL 和 Embase 搜索确定了使用皮质类固醇预防 UAO 的儿童随机试验。所有研究均使用地塞米松。根据地塞米松开始给药的时间(早期使用:拔管前 >12 小时)和剂量(高剂量:≥0.5mg/kg/剂量)对研究进行分类。我们对研究进行了贝叶斯网络荟萃分析,将研究分为四种方案:高剂量,早期使用(HE);低剂量,早期使用(LE);高剂量,晚期使用(HL);和低剂量,晚期使用。

共纳入 8 项试验(n=903)。预防 UAO(比值比;95%可信区间)方面,HE(0.13;0.04-0.36)、HL(0.39;0.19-0.74)和 LE(0.15;0.04-0.58)方案似乎比不使用地塞米松更有效(低确定性)。HE 和 LE 最有可能成为预防 UAO 的最佳方案(累积排序曲线下面积分别为 0.901 和 0.808)。预防再插管方面,与不使用地塞米松相比,所有四种地塞米松方案的效果估计均不精确(极低确定性)。HE 和 LE 是预防再插管的最佳方案(累积排序曲线下面积分别为 0.803 和 0.720)。敏感性分析表明,拔管前 >12 小时开始给药的方案比拔管前 >6 小时开始给药的方案更有效。

儿童拔管后使用地塞米松可以预防拔管后 UAO,但效果高度依赖于给药时机和剂量方案。早期给药(理想情况下在拔管前 >12 小时)似乎比地塞米松的剂量更重要。最终,应根据与地塞米松相关的不良反应风险以及 UAO 和再插管的个体风险,个体化制定具体的类固醇治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/f02a3586157a/AnnalsATS.202203-212OCf5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/afd630cba38a/AnnalsATS.202203-212OCf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/33fac327d245/AnnalsATS.202203-212OCf2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/cb047d9594d5/AnnalsATS.202203-212OCf3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/f40ea4929658/AnnalsATS.202203-212OCf4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/f02a3586157a/AnnalsATS.202203-212OCf5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/afd630cba38a/AnnalsATS.202203-212OCf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/33fac327d245/AnnalsATS.202203-212OCf2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/cb047d9594d5/AnnalsATS.202203-212OCf3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/f40ea4929658/AnnalsATS.202203-212OCf4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7991/9819263/f02a3586157a/AnnalsATS.202203-212OCf5.jpg

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