Suppr超能文献

[理想队列中的患者:法国重症哮喘概况]

[Patients in the IDEAL cohort: A snapshot of severe asthma in France].

作者信息

Taillé C, Pison C, Nocent C, Devouassoux G, Prud'homme A, Gruber A, Gunsoy N, Albers F

机构信息

Service de pneumologie, centre de référence constitutif des maladies pulmonaires rares, DHU FIRE, hôpital Bichat, AP-HP, 46, rue Henri-Huchard, 75877 Paris cedex 18, France; Inserm U1152, université Paris-Diderot, Labex Inflamex, 75018 Paris, France.

Service hospitalier universitaire pneumologie physiologie, pôle thorax et vaisseaux, université Grenoble Alpes, CHU Grenoble Alpes, 38043 Grenoble cedex, France.

出版信息

Rev Mal Respir. 2019 Feb;36(2):179-190. doi: 10.1016/j.rmr.2018.10.005. Epub 2018 Nov 11.

Abstract

INTRODUCTION

This paper reports the French data from a post-hoc analysis of the international IDEAL study, which aimed to describe a recent cohort of patients with severe asthma, the impact of the disease on quality of life, as well as the population of patients eligible for treatment with omalizumab, mepolizumab and reslizumab.

METHODS

Eligible patients were≥12 years of age, with severe asthma (GINA steps 4 and 5).

RESULTS

A total of 129 patients were included in this post-hoc analysis. Their mean age was 53 years, the majority were overweight, they were mainly women (64%) and had at least one medical comorbidity (85%). More than half had suffered from asthma for more than 25 years and were non-smokers. Lung function was moderately impaired. Blood eosinophil count was≥150 cells/μL in 66% of patients,≥300 cells/μL in 34% of patients, and≥500 cells/μL in 12% of patients. One out of three patients was currently treated with omalizumab and 24% had maintenance oral corticosteroids. Asthma was poorly controlled with a negative impact on quality of life (ACQ≥1.5) in 67% of patients. In this population 40% of patients were eligible for omalizumab, 27% for mepolizumab and 2% for reslizumab.

CONCLUSIONS

These findings show that a considerable proportion of patients with severe asthma remain uncontrolled and are not eligible for any of the available biological treatments. This underlines the need for therapeutic innovations in this disease.

摘要

引言

本文报告了国际IDEAL研究事后分析中的法国数据,该研究旨在描述近期一组重度哮喘患者、该疾病对生活质量的影响,以及适合接受奥马珠单抗、美泊利珠单抗和瑞利珠单抗治疗的患者群体。

方法

符合条件的患者年龄≥12岁,患有重度哮喘(全球哮喘防治创议第4和5级)。

结果

共有129名患者纳入了此次事后分析。他们的平均年龄为53岁,大多数人超重,主要为女性(64%),且至少有一种合并症(85%)。超过一半的患者哮喘病史超过25年,且不吸烟。肺功能有中度受损。66%的患者血液嗜酸性粒细胞计数≥150个/μL,34%的患者≥300个/μL,12%的患者≥500个/μL。三分之一的患者目前正在接受奥马珠单抗治疗,24%的患者正在使用口服糖皮质激素维持治疗。67%的患者哮喘控制不佳,对生活质量有负面影响(哮喘控制问卷评分≥1.5)。在这一群体中,40%的患者适合使用奥马珠单抗,27%适合使用美泊利珠单抗,2%适合使用瑞利珠单抗。

结论

这些研究结果表明,相当一部分重度哮喘患者仍未得到控制,且不符合任何现有生物治疗的条件。这凸显了该疾病治疗创新的必要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验