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Pulmonary Hypertension Associated with Chronic Lung Diseases: Treatment Considerations

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Book cover Cardiac Considerations in Chronic Lung Disease

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Abstract

Pulmonary hypertension (PH) is an important complication of chronic parenchymal lung diseases. The current definition of PH requires an abnormal resting mean pulmonary arterial pressure >20 mmHg during right heart catheterization (RHC). The most common chronic lung conditions that cause PH are chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), but PH can occur in the context of other parenchymal lung diseases including combined pulmonary fibrosis and emphysema (CPFE), sarcoidosis, lymphangioleiomyomatosis (LAM), and pulmonary Langerhans cell histiocytosis (PLCH). PH that occurs due to chronic lung diseases or chronic hypoxia (high altitude or severe sleep-disordered breathing) comprises Group 3 PH, whereas conditions such as sarcoidosis, LAM, and PLCH have multiple or multifactorial mechanisms and are classified into Group 5 PH.

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Weatherald, J., Montani, D., Sitbon, O. (2020). Pulmonary Hypertension Associated with Chronic Lung Diseases: Treatment Considerations. In: Bhatt, S. (eds) Cardiac Considerations in Chronic Lung Disease. Respiratory Medicine. Humana, Cham. https://doi.org/10.1007/978-3-030-43435-9_6

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