Management and support of patients with fibrosing interstitial lung diseases

被引：2
作者：
Barbera, Tyonn [1 ]
Davila, Lesley [2 ]
Patel, Nina M. [3 ]
机构：
[1] Univ Texas Southwestern Med Ctr Dallas, Div Pulm & Crit Care Med, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Div Rheumat Dis, Dallas, TX 75390 USA
[3] Columbia Univ Coll Phys & Surg, Div Pulm Allergy & Crit Care Med, New York Presbyterian Hosp, Med, 630 W 168th St, New York, NY 10032 USA
来源：
NURSE PRACTITIONER | 2021年 / 46卷 / 07期
关键词：
fibrosing lung diseases; idiopathic pulmonary fibrosis; interstitial lung disease; lung fibrosis; patient education; progressive fibrosing interstitial lung disease; progressive fibrosing phenotype; IDIOPATHIC PULMONARY-FIBROSIS; DOUBLE-BLIND; CYCLOPHOSPHAMIDE; PIRFENIDONE; PLACEBO; CLASSIFICATION; AZATHIOPRINE; NINTEDANIB; MORTALITY; EFFICACY;
D O I：
10.1097/01.NPR.0000743332.64602.aa
中图分类号：
R47 [护理学];
学科分类号：
1011 ;
摘要：
Fibrosing interstitial lung diseases have a variable clinical course. Regular monitoring is important to assess disease progression and inform patient care and counseling. NPs play a key role in helping patients understand their disease and its treatment and manage the adverse reactions of pharmacologic therapies.
引用
收藏
页码：39 / 44
页数：6
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