Wei Jienan, Lu Yan, Han Fang, Zhang Jing, Liu Lan, Chen Qingqing
Department of Pediatrics, Shengli Oilfield Central Hospital, Dongying, China.
Department of Hematology, Shengli Oilfield Central Hospital, Dongying, China.
Front Pediatr. 2019 Dec 13;7:503. doi: 10.3389/fped.2019.00503. eCollection 2019.
This systematic review and meta-analysis was conducted to compare relapse rates and adverse effects with oral dexamethasone vs. oral prednisone for acute asthma exacerbations in pediatric patients. A computerized literature search of PubMed, Embase, Scopus, CENTRAL (Cochrane Central Register of Controlled Trials) and Google scholar databases was carried out till 1st August 2019. Six Randomized controlled trials (RCTs) and 1 quasi-RCT were included. Dosage of dexamethasone and prednisone varied across studies. Studies were grouped based on the follow-up period and duration of dexamethasone administration. There was no significant difference in the relapse rate between dexamethasone and prednisone at 1-5 days (RR 1.46, 95%CI 0.69-3.7, = 0.32; = 0%) and 10-15 days of follow up (RR 1.16, 95%CI 0.80-1.68, = 0.44; = 0%). Pooled analysis found no significant difference in relapse rates with 1-day (RR 1.15, 95%CI 0.68-1.95, = 0.60; = 0%) and 2-day dosage of dexamethasone (RR 1.25, 95%CI 0.82-1.92, = 0.30; = 0%) compared to prednisone. Hospital readmission rates after initial discharge were not significantly different between the two drugs (RR 1.49, 95%CI 0.56-4.01, = 0.43; = 0%). Frequency of vomiting at ED (RR 0.21, 95%CI 0.05-0.96, = 0.04; = 50%) and at home (RR 0.42, 95%CI 0.25-0.69, = 0.0007; = 0%) was significantly higher with prednisone as compared to dexamethasone. While our results indicate that both dexamethasone and prednisone have similar relapse rates when used for acute asthmatic exacerbations, strong conclusions cannot be drawn due to paucity of large scale RCTs and limited quality of evidence. Dexamethasone is however associated with lower incidence of vomiting as compared to prednisone. Further homogenous RCTs are needed to provide robust evidence on this topic.
本系统评价和荟萃分析旨在比较口服地塞米松与口服泼尼松用于小儿急性哮喘加重期的复发率和不良反应。截至2019年8月1日,对PubMed、Embase、Scopus、CENTRAL(Cochrane对照试验中心注册库)和谷歌学术数据库进行了计算机文献检索。纳入了6项随机对照试验(RCT)和1项半随机对照试验。各研究中地塞米松和泼尼松的剂量不同。根据随访期和地塞米松给药持续时间对研究进行分组。在随访1 - 5天(RR 1.46,95%CI 0.69 - 3.7,P = 0.32;I² = 0%)和10 - 15天(RR 1.16,95%CI 0.80 - 1.68,P = 0.44;I² = 0%)时,地塞米松和泼尼松的复发率无显著差异。汇总分析发现,与泼尼松相比,地塞米松使用1天(RR 1.15,95%CI 0.68 - 1.95,P = 0.60;I² = 0%)和2天(RR 1.25,95%CI 0.82 - 1.92,P = 0.30;I² = 0%)时的复发率无显著差异。两种药物初始出院后的再入院率无显著差异(RR 1.49,95%CI 0.56 - 4.01,P = 0.43;I² = 0%)。与地塞米松相比,泼尼松在急诊科(RR 0.21,95%CI 0.05 - 0.96,P = 0.04;I² = 50%)和家中(RR 0.42,95%CI 0.