Idiopathic pulmonary fibrosis (IPF) is a progressive, chronic disease of the lungs which is characterized by heavy symptom burden, especially in the last year of life. Despite recently established anti-fibrotic treatment IPF prognosis is one of the worst among interstitial lung diseases. In this review available evidence regarding pharmacological and non-pharmacological management of the main IPF symptoms, dyspnea and cough, is presented.
Keywords: ambulatory oxygen therapy (AOT); breathlessness; cough; dyspnea; high flow nasal cannula (HFNC); idiopathic pulmonary fibrosis (IPF); non-invasive positive pressure ventilation (NIPPV); non-invasive ventilation (NIV).
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