医学
间质性肺病
混合性结缔组织病
特发性肺纤维化
结缔组织病
病理
疾病
结缔组织
肺
肺纤维化
纤维化
寻常性间质性肺炎
肺活检
肺功能测试
肺病
皮肌炎
CTD公司
全身性疾病
肺动脉高压
多发性肌炎
作者
Leticia Kawano-Dourado,Joyce S. Lee
标识
DOI:10.1016/j.ccm.2021.03.010
摘要
The presence of interstitial lung disease (ILD) negatively affects prognosis among patients with an underlying connective tissue disease (CTD). The initial approach to care should determine whether the CTD-ILD needs pharmacologic treatment or not. There is little direct evidence to guide who and how to treat. At present, any severe, active, and/or progressive ILD should be pharmacologically treated. Immunosuppressants and/or corticosteroids are the mainstay of pharmacologic therapy for all CTD-ILDs, whereas antifibrotics may be beneficial in some scenarios. A comprehensive and multidisciplinary approach to management is also an important aspect of patient care.
科研通智能强力驱动
Strongly Powered by AbleSci AI