Hypersensitivity Pneumonitis (Including Environmental Assessment): Diagnosis and Management

被引:1
|
作者
Tam, Wing Sun [1 ]
Islam, Tasnim [1 ]
Nambiar, Anoop M. [1 ,2 ]
机构
[1] Univ Texas Hlth San Antonio, Div Pulm & Crit Care, Dept Med, San Antonio, TX 78229 USA
[2] South Texas Hlth Care Syst, Audie L Murphy Vet Affairs Hosp, San Antonio, TX 78229 USA
关键词
Chronic hypersensitivity pneumonitis; Interstitial lung disease; Fibrotic hypersensitivity pneumonitis; Acute hypersensitivity pneumonitis; IDIOPATHIC PULMONARY-FIBROSIS; HIGH-RESOLUTION CT; INTERSTITIAL LUNG-DISEASE; CORTICOSTEROID TREATMENT; BRONCHOALVEOLAR LAVAGE; PREDICTS SURVIVAL; ANTIGEN; PATTERNS; CLASSIFICATION; IDENTIFICATION;
D O I
10.1007/s13665-019-00239-6
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of Review This article aims to provide an overview on the diagnosis and management of hypersensitivity pneumonitis (HP). We will focus on the issues surrounding the lack of an international consensus on the diagnosis of HP, and review the existing treatment options for HP. Recent Findings There is emerging international consensus that HP should be classified based on clinical, radiologic, and pathologic features and not solely on disease duration. Environmental assessment and antigen avoidance remains the most important step in managing HP. Antifibrotics may soon become a viable option for chronic HP in the near future. Well-designed prospective controlled studies are underway. Substantial gaps still remain in our understanding of the diagnosis and management of HP. Further research should focus on establishing internationally accepted diagnostic criteria and clinical practice guidelines to aid the clinician in the challenging treatment of patients with HP.
引用
收藏
页码:131 / 138
页数:8
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