欧洲胸科协会/美国胸科协会将重度哮喘定义为未来使用生物制剂/支气管热成形术的决定因素

IF 1.6 Q3 ALLERGY
H. Nishiyama, Y. Kanemitsu, Kensuke Fukumitsu, N. Takeda, Ryota Kurokawa, T. Tajiri, K. Ito, Jenifer Maries Go Yap, S. Fukuda, T. Uemura, H. Ohkubo, K. Maeno, Y. Ito, T. Oguri, M. Takemura, A. Niimi
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Patients were assessed using the European Thoracic Society/American Thoracic Society (ERS/ATS) severe uncontrolled asthma guideline as defined by these 4 characteristics: poor control (ACT < 20), frequent exacerbations (≥2/yr), admissions (≥1/yr), and airflow limitation (forced expiratory volume in 1 second < 80% of predicted), along with comorbidities, and biomarkers, including blood granulocytes, fractional nitric oxide, and capsaicin cough reflex sensitivity (C-CS). These indices were compared between patients with and without Bio/BT introduction, and multivariate logistic regression analysis was performed to determine the association of the 4 definitions with treatment needs for Bio/BT. Results Patients who were introduced to Bio/BT had heightened C-CS, heavier smoking history, and a greater prevalence of diabetes mellitus than those without (p < 0.05). 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引用次数: 2

摘要

国际指南定义了严重不受控制的哮喘。对于此类患者,建议使用生物制剂或支气管热成形术(Bio/BT)。目的:确定哪些严重不受控制哮喘定义与严重不受控制哮喘患者额外的生物/BT治疗相关。方法连续107例哮喘患者(包括15例在检查后3个月内引入生物/BT的患者),根据全球哮喘倡议2015指南分类为治疗步骤4,符合本分析的条件。采用欧洲胸科学会/美国胸科学会(ERS/ATS)严重不受控制哮喘指南对患者进行评估,该指南由以下4个特征定义:控制不良(ACT < 20)、频繁发作(≥2次/年)、入院(≥1次/年)和气流受限(1秒用力呼气量<预测的80%),以及合共病和生物标志物,包括血液粒细胞、分数一氧化氮和辣椒素咳嗽反射敏感性(C-CS)。将这些指标在引入和未引入生物/BT的患者之间进行比较,并进行多因素logistic回归分析,以确定4种定义与生物/BT治疗需求的相关性。结果引入Bio/BT的患者C-CS升高,吸烟史加重,糖尿病患病率高于未引入Bio/BT的患者(p < 0.05)。在多因素回归分析中,哮喘控制不良(ACT < 20)、频繁发作(≥2次/年)和入院(≥1次/年)与未来使用Bio/BT相关。2型相关生物标志物,包括绝对嗜酸性粒细胞计数,生物引入组患者高于BT引入组患者。同时,生物组患者与BT组患者严重未控制哮喘定义的4个特征无显著差异。结论虽然治疗费用和哮喘表型等多种因素影响治疗决策,但哮喘控制不良的定义、频繁加重和根据ERS/ATS指南入院是对严重未控制哮喘进行额外强化治疗的重要因素。临床试验注册:UMIN000024734
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of the European Thoracic Society/American Thoracic Society severe asthma definition as a determinant of future use of biologics/bronchial thermoplasty
Background International guidelines define severe uncontrolled asthma. Biologics or bronchial thermoplasty (Bio/BT) are recommended for such patients. Objectives To determine which definitions of severe uncontrolled asthma are associated with an additional Bio/BT treatment in patients with severe uncontrolled asthma. Methods Consecutive 107 asthmatics (including 15 patients for whom Bio/BT was introduced within 3 months after examination), classified as treatment step 4 according to the Global Initiative for Asthma 2015 guideline, were eligible for this analysis. Patients were assessed using the European Thoracic Society/American Thoracic Society (ERS/ATS) severe uncontrolled asthma guideline as defined by these 4 characteristics: poor control (ACT < 20), frequent exacerbations (≥2/yr), admissions (≥1/yr), and airflow limitation (forced expiratory volume in 1 second < 80% of predicted), along with comorbidities, and biomarkers, including blood granulocytes, fractional nitric oxide, and capsaicin cough reflex sensitivity (C-CS). These indices were compared between patients with and without Bio/BT introduction, and multivariate logistic regression analysis was performed to determine the association of the 4 definitions with treatment needs for Bio/BT. Results Patients who were introduced to Bio/BT had heightened C-CS, heavier smoking history, and a greater prevalence of diabetes mellitus than those without (p < 0.05). Poor asthma control (ACT < 20), frequent exacerbations (≥2/yr), and admissions (≥1/yr) were relevant to the future use of Bio/BT in the multivariate regression analysis. Type 2-related biomarkers including absolute eosinophil counts were higher in patients in the Bio introduction group than in the BT introduction group. Meanwhile, there was no significant difference of the 4 characteristics of severe uncontrolled asthma definition between patients in the Bio and those in the BT groups. Conclusion Although multiple factors such as treatment cost and asthma phenotypes affect treatment decision-making, the definition of poor asthma control, frequent exacerbations and admission by the ERS/ATS guidelines were important factors for an additional intensive treatment for severe uncontrolled asthma. Trial Registration UMIN Clinical Trials Registry: UMIN000024734
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来源期刊
CiteScore
2.50
自引率
5.90%
发文量
33
期刊介绍: Asia Pacific Allergy (AP Allergy) is the official journal of the Asia Pacific Association of Allergy, Asthma and Clinical Immunology (APAAACI). Although the primary aim of the journal is to promote communication between Asia Pacific scientists who are interested in allergy, asthma, and clinical immunology including immunodeficiency, the journal is intended to be available worldwide. To enable scientists and clinicians from emerging societies appreciate the scope and intent of the journal, early issues will contain more educational review material. For better communication and understanding, it will include rational concepts related to the diagnosis and management of asthma and other immunological conditions. Over time, the journal will increase the number of original research papers to become the foremost citation journal for allergy and clinical immunology information of the Asia Pacific in the future.
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