Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease of unclear cause and poor prognosis (1 – 3). Advanced IPF is frequently associated with pulmonary hypertension (PH), characterized by an increase in mean pulmonary arterial pressure (mPAP) (4 – 6). The development of PH correlates with the prognosis of IPF patients (6 – 8).
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