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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorPedro Trujillo
dc.contributor.authorAzpiroz, Fernando
dc.contributor.authorDomingo Ribas, Enric
dc.contributor.authorBravo Masgoret, Carles
dc.contributor.authorCalabuig-Goena, Alvaro
dc.contributor.authorLópez Meseguer, Manuel
dc.contributor.authorGrignola, Juan
dc.date.accessioned2024-03-11T12:46:07Z
dc.date.available2024-03-11T12:46:07Z
dc.date.issued2024-03-06
dc.identifier.citationGrignola JC, Calabuig A, Trujillo P, Bravo C, Azpiroz F, López Messeguer M, et al. Pulmonary vascular pressure respiratory swings in COPD and ILD candidates for lung transplantation: Large but different. Pulm Circ. 2024 Mar 6;14(1):e12348.
dc.identifier.issn2045-8940
dc.identifier.urihttps://hdl.handle.net/11351/11175
dc.descriptionChronic lung disease; Esophageal pressure; Lung transplantation
dc.description.abstractWe analyzed the effect of respiratory swings on interpreting intravascular pulmonary vascular pressures (PVPs) in chronic obstructive pulmonary disease (COPD) and interstitial lung disease (ILD) candidates for lung transplantation (LTx) and the role of the alterations in pulmonary function tests on the dynamic respiratory variations. Twenty-eight consecutive patients were included. All patients underwent a complete hemodynamic study (right atrial, mean pulmonary arterial, and pulmonary arterial occlusion pressures [RAP, mPAP, and PAOP]-) and pulmonary function testing (force vital capacity [FVC], forced expiratory volume in the first second [FEV1], and residual volume [RV]). A subgroup of 10 patients underwent simultaneous esophageal pressure (PES). All hemodynamic parameters and PES were collected during apnea after an unforced expiration (ee) and during spontaneous breathing averaging five respiratory cycles (mrc). The respiratory swing (osc) was estimated as the difference between maximum–minimum values of pressures during the respiratory cycle. Intravascular RAPee, mPAPee, and PAOPee were higher than mrc values (p < 0.05), leading to 11% of pulmonary hypertension (PH) misdiagnosis and 37% of postcapillary PH misclassification. PAOPosc of COPD was higher than ILD patients and RAPosc (p < 0.05). Only PAOPosc correlated with FVC, FEV1, and RV (p < 0.05). ILD PESmrc was lower than COPD (p < 0.05), and it was associated with a significantly higher transmural than intravascular RAPmrc, mPAPmrc, and PAOPmrc. PESmrc was significantly correlated with FVC. Transmural mPAPmrc and PAOPmrc readings determined around 20% of reclassification of the patients compared to ee measurements. Candidates for LTx showed large respiratory swings in PVP, which were correlated with pulmonary function alterations. mrc PVP would be more closely approximated to the true transmural PVP leading to PH reclassification. Adjusting PVP for PES should be considered in COPD and ILD candidates of LTx with severe alterations in pulmonary functional tests and suspicion of a PESmrc far from 0. PES respiratory swings could be different in ILD to COPD patients.
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesPulmonary Circulation;14(1)
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectPulmons - Malalties obstructives
dc.subjectPulmons - Trasplantació
dc.subjectHipertensió pulmonar
dc.subject.meshPulmonary Disease, Chronic Obstructive
dc.subject.meshLung Diseases, Interstitial
dc.subject.meshLung Transplantation
dc.subject.meshHypertension, Pulmonary
dc.titlePulmonary vascular pressure respiratory swings in COPD and ILD candidates for lung transplantation: Large but different
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/pul2.12348
dc.subject.decsenfermedad pulmonar obstructiva crónica
dc.subject.decsenfermedades pulmonares intersticiales
dc.subject.decstrasplante de pulmón
dc.subject.decshipertensión pulmonar
dc.relation.publishversionhttps://doi.org/10.1002/pul2.12348
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Grignola JC] Departmento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. Unidad de Hipertensión Pulmonar, Hospital Maciel, Ministerio de Salud Pública, Montevideo, Uruguay. [Calabuig A] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Trujillo P] Unidad de Hipertensión Pulmonar, Hospital Maciel, Ministerio de Salud Pública, Montevideo, Uruguay. Departamento de Cardiología, Centro Cardiovascular Universitario, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. [Bravo C, López Messeguer M] Servei de Pneumologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Azpiroz F] Servei d’Aparell Digestiu, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (Ciberehd), Barcelona, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Domingo E] Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Fisiologia, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid38449519
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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