Suppr超能文献

原发性纤毛运动障碍疾病的当前治疗方法。

Current treatment for primary ciliary dyskinesia conditions.

作者信息

Yoo Young, Koh Young Yull

机构信息

Departmet of Pediatrics, Seoul National University Hospital, Seoul, Korea.

出版信息

Expert Opin Pharmacother. 2004 Feb;5(2):369-77. doi: 10.1517/14656566.5.2.369.

Abstract

Primary ciliary dyskinesia (PCD) is a heterogeneous group of conditions characterised by ultrastructural defects of the cilia, which result in impaired mucociliary clearance. Although the incidence of PCD is low, early recognition and prompt management are important in order to prevent unnecessary morbidity, the progression of bronchiectasis and the deterioration of lung function. As the underlying defect in PCD cannot be corrected, the mainstay of therapy remains effective clearance of airway secretions and antibiotic therapy of respiratory tract infections. This paper highlights new developments in the field that have implications for the future management of PCD. These include beta-adrenergic agonists, arginine, uridine-5'-triphosphate, hypertonic saline and recombinant human DNase. It is to be hoped that these treatment modalities will have a therapeutic role in PCD.

摘要

原发性纤毛运动障碍(PCD)是一组异质性疾病,其特征为纤毛的超微结构缺陷,这会导致黏液纤毛清除功能受损。尽管PCD的发病率较低,但早期识别和及时治疗对于预防不必要的发病、支气管扩张的进展以及肺功能恶化至关重要。由于PCD的潜在缺陷无法纠正,治疗的主要手段仍然是有效清除气道分泌物以及对呼吸道感染进行抗生素治疗。本文重点介绍了该领域的新进展,这些进展对PCD的未来治疗具有重要意义。这些进展包括β-肾上腺素能激动剂、精氨酸、尿苷-5'-三磷酸、高渗盐水和重组人脱氧核糖核酸酶。希望这些治疗方式能在PCD治疗中发挥作用。

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