Supportive care of patients with fibrosing interstitial lung disease: answering a great clinical need.

Supportive care of patients with fibrosing interstitial lung disease: answering a great clinical need.
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DOI:
10.1183/20734735.0066-2020
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发表时间:
2020-09
期刊:
Breathe (Sheffield, England)
影响因子:
--
通讯作者:
Saini G
Saini G
中科院分区:
其他
文献类型:
--
作者:
Goodwin AT;Saini G

文献摘要

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纤维化间质性肺疾病(f - ild)是一个异质性的群体,包括特发性肺纤维化(IPF)、结缔组织病相关的间质性肺疾病、过敏性肺炎和石棉肺等。所有f - ild的共同特征是疤痕组织不可逆转地取代正常肺实质,导致气体交换受损,最终导致呼吸衰竭。纤维化间质性肺病(F-ILD)显著降低生活质量。F-ILD的护理包括症状管理,临终计划和支持措施,以及抗纤维化药物。患者和护理人员应该是所有护理决策的中心。https://bit.ly/2ZAE2Ks
The fibrosing interstitial lung diseases (F-ILDs) are a heterogeneous group, including idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated interstitial lung disease, hypersensitivity pneumonitis and asbestosis, among others. The common feature of all F-ILDs is the irreversible replacement of normal lung parenchyma with scar tissue, resulting in impaired gas exchange and culminating in respiratory failure. Fibrosing interstitial lung disease (F-ILD) significantly reduces quality of life. F-ILD care includes symptom management, end-of-life planning and supportive measures, as well as antifibrotics. Patients and carers should be central to all care decisions. https://bit.ly/2ZAE2Ks