Pulmonary Hypertension in Interstitial Lung Disease: Management Options to Move Beyond Supportive Care
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://link.springer.com/content/pdf/10.1007/s13665-023-00311-2.pdf
Reference55 articles.
1. •• Humbert M, Kovacs G, Hoeper MM, Badagliacca R, Berger RMF, Brida M, et al. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension. Eur Heart J. 2022;43(38):3618–731. https://doi.org/10.1093/eurheartj/ehac237.
2. Wijeratne DT, Lajkosz K, Brogly SB, Lougheed MD, Jiang L, Housin A, et al. Increasing incidence and prevalence of world health organization groups 1 to 4 pulmonary hypertension: a population-based cohort study in Ontario, Canada. Circ Cardiovasc Qual Outcomes. 2018;11(2):e003973. https://doi.org/10.1161/circoutcomes.117.003973.
3. Prins KW, Rose L, Archer SL, Pritzker M, Weir EK, Kazmirczak F, et al. Disproportionate right ventricular dysfunction and poor survival in group 3 pulmonary hypertension. Am J Respir Crit Care Med. 2018;197(11):1496–9. https://doi.org/10.1164/rccm.201712-2405LE.
4. Mejía M, Carrillo G, Rojas-Serrano J, Estrada A, Suárez T, Alonso D, et al. Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension. Chest. 2009;136(1):10–5. https://doi.org/10.1378/chest.08-2306.
5. Takahashi K, Taniguchi H, Ando M, Sakamoto K, Kondoh Y, Watanabe N, et al. Mean pulmonary arterial pressure as a prognostic indicator in connective tissue disease associated with interstitial lung disease: a retrospective cohort study. BMC Pulm Med. 2016;16(1):55. https://doi.org/10.1186/s12890-016-0207-3.
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