支气管扩张
重症监护医学
疾病
粘液纤毛清除率
临床试验
生活质量(医疗保健)
气道
哮喘
医学
免疫学
外科
内科学
肺
护理部
作者
Hayoung Choi,Pamela J. McShane,Stefano Aliberti,James D. Chalmers
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2024-05-23
卷期号:: 2400518-2400518
标识
DOI:10.1183/13993003.00518-2024
摘要
Formerly regarded as a rare disease, bronchiectasis is increasingly recognised. A renewed interest in this disease has led to significant progress in bronchiectasis research. Randomised clinical trials have demonstrated the benefits of airway clearance techniques, inhaled antibiotics and long-term macrolide therapy in bronchiectasis patients. However, the heterogeneity of bronchiectasis remains one of the most challenging aspects of management. Phenotypes and endotypes of bronchiectasis have been identified to help find “treatable traits” and partially overcome disease complexity. The goals of therapy for bronchiectasis are to reduce the symptom burden, improve quality of life, reduce exacerbations and prevent disease progression. We review the pharmacological and non-pharmacological treatments that can improve mucociliary clearance, reduce airway inflammation and tackle airway infection, the key pathophysiological features of bronchiectasis. There are also promising treatments in development for the management of bronchiectasis, including novel anti-inflammatory therapies. This review provides a critical update on the management of bronchiectasis focusing on treatable traits and recent randomised clinical trials.
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