Lung and heart-lung transplantation in pulmonary arterial hypertension
López-Meseguer, Manuel (Biomedical Research Networking Center on Respiratory Diseases)
Quezada, Carlos A. (Hospital Universitario 12 de Octubre (Madrid))
Ramon, Maria A. (Biomedical Research Networking Center on Respiratory Diseases)
Lázaro, María (Hospital Virgen de la Salud (Toledo))
Dos, Laura (Hospital Universitari Vall d'Hebron. Institut de Recerca)
Lara, Antonio (Hospital Universitario de Canarias (La Laguna))
López, Raquel (Hospital Universitari i Politècnic La Fe (València))
Blanco, Isabel (Universitat de Barcelona)
Escribano Subias, Pilar (Hospital Universitario 12 de Octubre (Madrid))
Roman, Antonio (Biomedical Research Networking Center on Respiratory Diseases)
Universitat Autònoma de Barcelona

Data:	2017
Resum:	Real use of lung (LT) and heart-lung (HLT) transplantation in pulmonary arterial hypertension (PAH) is unknown. The objectives were to describe the indication of these procedures on PAH treatment in a national cohort of PAH patients, and to analyze the potential improvement of its indication in severe patients. Eligibility for LT/HLT was assessed for each deceased patient. Incident patients from REHAP diagnosed between January 2007 and March 2015 and considered eligible for LT/HLT were grouped as follows: those who finally underwent transplantation (LTP) and those who died (D-Non-LT). Of 1391 patients included in REHAP, 36 (3%) were LTP and 375 (27%) died. Among those who died, 36 (3%) were D-Non-LT. LTP and D-Non-LT were equal in terms of age, gender, and clinical status. Ten percent of those who died were functional class I-II. Patients functional class IV were less likely to undergo LT (8. 3% LTP vs. 30. 6% D-Non-LT, p = 0. 017). Patients with idiopathic and drug/toxin-associated PAH were more likely to undergo LT (44. 4% LTP vs. 16. 7% D-Non-LT, p = 0. 011). The present results show that the use of LT/HLT could double for this indication. Relevant mortality in early functional class reflects the difficulties in establishing the risk of death in PAH.
Drets:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.
Llengua:	Anglès
Document:	Article ; recerca ; Versió publicada
Publicat a:	PloS one, Vol. 12 (november 2017) , ISSN 1932-6203

DOI: 10.1371/journal.pone.0187811
PMID: 29161284

12 p, 2.1 MB

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