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吸入皮质类固醇治疗的儿童升级治疗方案的疗效比较:一项历史性队列研究。

Comparative Effectiveness of Step-up Therapies in Children with Asthma Prescribed Inhaled Corticosteroids: A Historical Cohort Study.

机构信息

Division of Infection, Immunity and Respiratory Medicine, Manchester Academic Health Science Centre, The University of Manchester, University Hospital of South Manchester, NHS Foundation Trust, Manchester; Royal Manchester Children's Hospital, Central Manchester University Hospitals, NHS Foundation Trust, Manchester, Manchester.

Primary Care and Population Sciences, University of Southampton, Southampton; NIHR Southampton Respiratory Biomedical Research Unit, Southampton.

出版信息

J Allergy Clin Immunol Pract. 2017 Jul-Aug;5(4):1082-1090.e7. doi: 10.1016/j.jaip.2016.12.028. Epub 2017 Mar 27.

Abstract

BACKGROUND

In children with uncontrolled asthma prescribed low-dose inhaled corticosteroids (ICSs), various step-up options are available: fixed-dose combination ICS/long-acting β-agonist (FDC), increasing ICS dose, or adding leukotriene receptor antagonist (LTRA). However, evidence of their relative effectiveness is limited.

OBJECTIVE

To compare the effectiveness of step-up treatment to FDC in children with asthma versus increased ICS dose, or LTRA.

METHODS

This matched cohort study used UK primary-care databases to study children prescribed their first step-up treatment to FDC, increased ICS dose, or LTRA. A year of baseline data was used for matching and identifying confounders. Outcomes over the following year were examined. The primary outcome was severe exacerbation rate; secondary outcomes included overall asthma control, derived from databases (no asthma-related admissions/hospital attendances/oral corticosteroids or antibiotics prescribed with a respiratory review, and average prescribed salbutamol ≤200 μg/day).

RESULTS

There were 971 matched pairs in the FDC and increased ICS dose cohorts (59% males; mean age, 9.4 years) and 785 in the FDC and LTRA cohorts (60% males; mean age, 9.0 years). Exacerbation rates in the outcome year were similar between FDC and increased ICS (adjusted incidence rate ratio [95% CI], 1.09 [0.75-1.59]) and FDC and LTRA (incidence rate ratio, 1.36 [0.93-2.01]). Increased ICS and LTRA significantly reduced the odds of achieving overall asthma control, compared with FDC (odds ratios [95% CI], 0.52 [0.42-0.64] and 0.53 [0.42-0.66], respectively)-this was driven by reduced short-acting beta-agonist use.

CONCLUSIONS

FDC is as effective as increased ICS or LTRA in reducing severe exacerbation rate, but more effective in achieving asthma control.

摘要

背景

在接受低剂量吸入皮质类固醇(ICS)治疗但哮喘仍未得到控制的儿童中,有多种升级治疗方案可供选择:固定剂量ICS/长效β激动剂(ICS/LABA)联合制剂、增加ICS 剂量或添加白三烯受体拮抗剂(LTRA)。然而,关于这些方案相对有效性的证据有限。

目的

比较哮喘儿童升级治疗为 ICS/LABA 联合制剂与增加 ICS 剂量或 LTRA 的有效性。

方法

本匹配队列研究使用英国初级保健数据库,研究了首次升级治疗为 ICS/LABA 联合制剂、增加 ICS 剂量或 LTRA 的患儿。在匹配和识别混杂因素时,使用了一年的基线数据。在接下来的一年中,观察了研究结果。主要结局为重度恶化发作率;次要结局包括数据库得出的总体哮喘控制情况(无哮喘相关住院、就诊或口服皮质激素治疗,或有呼吸道检查但未开具抗生素治疗,以及平均沙丁胺醇处方量≤200μg/天)。

结果

在 ICS/LABA 联合制剂与增加 ICS 剂量组中,有 971 对匹配的患者(59%为男性;平均年龄为 9.4 岁),在 ICS/LABA 联合制剂与 LTRA 组中,有 785 对匹配的患者(60%为男性;平均年龄为 9.0 岁)。在结局年度中,ICS/LABA 联合制剂与增加 ICS 剂量(校正发病率比[95%CI],1.09[0.75-1.59])和 ICS/LABA 联合制剂与 LTRA(发病率比,1.36[0.93-2.01])的重度恶化发作率相似。与 ICS/LABA 联合制剂相比,增加 ICS 剂量和 LTRA 显著降低了总体哮喘控制的可能性(比值比[95%CI],0.52[0.42-0.64]和 0.53[0.42-0.66]),这是由于短效β激动剂的使用减少所致。

结论

ICS/LABA 联合制剂在降低重度恶化发作率方面与增加 ICS 剂量或 LTRA 一样有效,但在实现哮喘控制方面更为有效。

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