医学
重症监护医学
特发性肺纤维化
缓和医疗
社会心理的
肺康复
生活质量(医疗保健)
多学科方法
心理干预
疾病
康复
物理疗法
肺
内科学
护理部
社会科学
精神科
社会学
作者
Onofre Morán-Mendoza,Rebecca E. Colman,Meena Kalluri,Czerysh Cabalteja,Ingrid Harle
标识
DOI:10.1080/17476348.2019.1627204
摘要
Introduction: Idiopathic pulmonary fibrosis (IPF) is a debilitating, progressive, and fatal fibrotic pulmonary disease with a prognosis comparable to that of lung cancer. IPF management is a complex process that involves pharmacological and nonpharmacological interventions, extensive patient education, and addressing patient needs that change through the course of the illness.Areas covered: This review summarizes the key aspects of a multifaceted, multidisciplinary, individualized approach to IPF care that incorporates available treatment options, strategies to improve compliance with antifibrotic therapies, pulmonary rehabilitation, and the integration of palliative care for symptom management. Aspects of care discussed include the use of antifibrotic therapy and nonpharmacological treatments, targeted education and psychosocial support, evaluation and management of comorbidities, and early integration of palliative care.Expert opinion: By incorporating this comprehensive approach to disease management, physicians can address most aspects of care for a patient with IPF to optimize survival and quality of life.
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