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影响哮喘一线治疗治疗依从性的药物不良反应:一项观察性研究。

Adverse drug reactions affecting treatment adherence in first-line treatment of asthma: An observational study.

机构信息

Izmir Bakırçay University, Çiğli Training and Research Hospital Pediatric Immunology and Allergy, Izmir, Turkey.

Department of Pediatric Allergy and Immunology, Istanbul Medipol University School of Medicine, Istanbul, Turkey;

出版信息

Allergol Immunopathol (Madr). 2023 Mar 1;51(2):11-16. doi: 10.15586/aei.v51i2.774. eCollection 2023.

Abstract

BACKGROUND

Asthma is the most common chronic lung disease among children. International guidelines recommend inhaled corticosteroids (ICS) as the first-line daily controller therapy for children with asthma and leukotriene receptor antagonists (LTRA) as the second alternative therapy. Adherence to treatment is the most significant component to optimize the benefits of therapy in asthma.

OBJECTIVE

This study aims to investigate the frequency of drug discontinuation due to adverse drug reactions (ADRs) that affect adherence to treatment in children with asthma or asthma and allergic rhinitis using LTRA or ICS as monotherapy.

METHODS

The subjects aged 4-18 years with asthma or asthma and allergic rhinitis and using montelukast or ICS as monotherapy were included in the study. They were evaluated in terms of ADRs affecting adherence to treatment in the first and third months of treatment.

RESULTS

A total of 468 cases, 356 of whom received montelukast monotherapy and 112 of whom received ICS treatment, with a mean age of 9.10 ± 3.08 (4-17) years, were included in the study. Males constituted 65.6% of the total cases (n = 307). In the first month of follow-up of the cases, it was observed that 4.8% (n = 17) of the patients in the montelukast group could not continue the treatment due to ADR. It was determined that the drug discontinuation rate in the montelukast group in the first month was significantly higher than in the ICS group (P = 0.016), and the risk of drug discontinuation due to ADR in the montelukast group was 1.333 (95% CI, 1.26-1.40) times higher.

CONCLUSIONS

As a result, it was observed that the drug was discontinued due to ADR at a higher rate in children with asthma who received montelukast monotherapy compared to those who received ICS monotherapy.

摘要

背景

哮喘是儿童中最常见的慢性肺部疾病。国际指南建议将吸入性皮质类固醇(ICS)作为哮喘患儿的一线每日控制治疗药物,将白三烯受体拮抗剂(LTRA)作为二线替代治疗药物。治疗的依从性是优化哮喘治疗获益的最重要组成部分。

目的

本研究旨在调查因不良反应(ADR)而停药的频率,这些不良反应会影响使用 LTRA 或 ICS 作为单一疗法治疗的哮喘儿童的治疗依从性。

方法

该研究纳入了年龄在 4-18 岁、使用孟鲁司特或 ICS 作为单一疗法的哮喘或哮喘合并变应性鼻炎患者。在治疗的第 1 个月和第 3 个月评估他们因治疗依从性而受影响的 ADR。

结果

共有 468 例患者入组,其中 356 例接受孟鲁司特单药治疗,112 例接受 ICS 治疗,平均年龄为 9.10 ± 3.08(4-17)岁,男性占总病例的 65.6%(n = 307)。在病例的第 1 个月随访中,发现孟鲁司特组有 4.8%(n = 17)的患者因 ADR 无法继续治疗。在第 1 个月,孟鲁司特组的停药率明显高于 ICS 组(P = 0.016),孟鲁司特组因 ADR 停药的风险是 ICS 组的 1.333 倍(95%CI,1.26-1.40)。

结论

因此,与接受 ICS 单药治疗的哮喘患儿相比,接受孟鲁司特单药治疗的患儿因 ADR 停药的比例更高。

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