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数字化监测吸入疗法:管理严重哮喘的“智能”方法?

Digitally monitored inhaled therapy: a 'smart' way to manage severe asthma?

机构信息

Respiratory Research Group, Hull York Medical School, Heslington, UK.

Department of Respiratory Medicine, Hull University Teaching Hospitals NHS Trust, Cottingham, UK.

出版信息

J Asthma. 2024 Sep;61(9):970-975. doi: 10.1080/02770903.2024.2316726. Epub 2024 Feb 16.

Abstract

INTRODUCTION

One of the fundamental challenges of managing patients with severe asthma is treatment adherence, particularly with inhaled corticosteroids. Adherence is difficult to measure objectively and poor adherence is associated with worse outcomes. In this study, assess the ability of a 'smart' inhaler to record adherence in severe asthma patients and measure the impact of this on asthma control.

METHODS

Consecutive consenting patients meeting criteria for biologics had their existing high-dose ICS/LABA//LAMA combination inhaler/s switched to mometasone/indacaterol/glycopyrronium (114/46/136). Routine clinical data, including blood eosinophils, FeNO, and ACQ-6 scores were collected at baseline and at 4 wk. Adherence was then checked on the Propeller Health app, and good adherence was defined as >80% of prescribed usage. Participants were then followed-up at 12 months to record the proportion of patients who were initiated on biologics.

RESULTS

77 patients (mean [SD] age = 50.4 [15.7] years, 67.5% female [ = 52]) participated. 71 participants were able to use the device and 65% ( = 46) of these attained good asthma control and were not initiated on biologics at 12-month follow-up. Both groups demonstrated a significant reduction in ACQ6 score at follow-up (2.81 vs. 1.92, < 0.001 and 3.05 vs. 2.60, < 0.001, respectively), but there was no statistically significant difference in improvement between groups. Patients with optimal adherence also demonstrated a significant reduction in median FeNO at follow-up (47 ppb vs. 40 ppb, = 0.003).

CONCLUSIONS

In severe asthma patients, 'smart' inhalers may represent an effective management tool to improve adherence and asthma control, therefore avoiding the need for patients to commence biological therapies.

摘要

简介

管理重症哮喘患者的基本挑战之一是治疗依从性,特别是吸入皮质类固醇的依从性。依从性难以客观衡量,而依从性差与结局较差相关。在这项研究中,评估“智能”吸入器记录重症哮喘患者依从性的能力,并测量这对哮喘控制的影响。

方法

连续同意的符合生物制剂标准的患者将其现有的高剂量 ICS/LABA//LAMA 联合吸入器/切换为莫米松/茚达特罗/格隆溴铵(114/46/136)。在基线和 4 周时收集常规临床数据,包括血嗜酸性粒细胞、FeNO 和 ACQ-6 评分。然后在 Propeller Health 应用程序上检查依从性,将良好的依从性定义为> 80%的规定使用量。然后在 12 个月时对参与者进行随访,以记录开始使用生物制剂的患者比例。

结果

77 名患者(平均[SD]年龄= 50.4[15.7]岁,67.5%女性[= 52])参与。71 名参与者能够使用该设备,其中 65%(= 46)达到良好的哮喘控制,并且在 12 个月随访时未开始使用生物制剂。两组在随访时的 ACQ6 评分均显著降低(2.81 对 1.92,< 0.001 和 3.05 对 2.60,< 0.001),但组间改善无统计学差异。最佳依从性的患者在随访时的中位 FeNO 也显著降低(47 ppb 对 40 ppb,= 0.003)。

结论

在重症哮喘患者中,“智能”吸入器可能是一种有效的管理工具,可提高依从性和哮喘控制,从而避免患者开始使用生物疗法。

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