Is non-invasive ventilation effective in improving the exercise capacity in patients with cardiac heart failure?: a randomised crossover trial

UDC.coleccionInvestigación
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicas
UDC.grupoInvIntervención Psicosocial e Rehabilitación Funcional
UDC.issue7
UDC.journalTitlePLoS One
UDC.startPagee0327399.
UDC.volume20
dc.contributor.authorMazzucco, Guillermo
dc.contributor.authorTorres-Castro, Rodrigo
dc.contributor.authorIntelangelo, Leonardo
dc.contributor.authorLista-Paz, Ana
dc.contributor.authorEscalante, Juan Pablo
dc.contributor.authorZumeta-Olaskoaga, Lore
dc.contributor.authorVeiga, Gonzalo
dc.contributor.authorArbillaga-Etxarri, Ane
dc.date.accessioned2025-08-21T09:41:29Z
dc.date.available2025-08-21T09:41:29Z
dc.date.issued2025-07-07
dc.descriptionRandomized controlled trial
dc.description.abstract[Abstract] Introduction: Heart failure (HF) is a prevalent global health issue, characterized by the heart's inability to effectively pump or fill with blood, leading to inadequate cardiac output. Despite advances in medical treatments, exercise intolerance remains a significant challenge, impacting their quality of life and contributing to frequent hospitalizations. Recent studies suggest that non-invasive ventilation (NIV) may further enhance exercise performance by reducing ventilatory workload and fatigue. However, limited research has directly compared different ventilatory modes during exercise in patients with heart failure. This study aims to evaluate the effects of two NIV devices on exercise capacity. Methods: A randomised crossover trial was conducted in patients with HF, reduced ejection fraction (≤ 40%), New York Heart Association functional class I-III and clinically stable. All participants underwent an initial assessment followed by an incremental exercise test to determine maximum aerobic velocity. They were then randomized to perform three constant work rate tests on separate days under three conditions: (1) with Continuous Positive Airway Pressure (CPAP), (2) with pressure support (PS) and (3) without NIV. The primary outcome was time to exhaustion. Key physiological variables were recorded during each test. Participants were recruited and completed all testing between April 29 and July 18, 2022. ClinicalTrials.gov registration number: NCT05433610. Results: A total of 11 patients (mean age: 67 ± 9.6 years) completed the study. Exercise duration was significantly longer in the pressure support group (9.8 ± 6.2 minutes) compared to the CPAP group (8.9 ± 6.0 minutes) and the control group (7.3 ± 6.2 minutes) (p = 0.043). No significant differences were found in average heart rate (HR), final HR, or oxygen saturation (SpO₂) between the groups (p > 0.05). Similarly, dyspnea and leg fatigue (modified Borg scale) showed no statistically significant differences between conditions (p > 0.05). Conclusion: The use of NIV, particularly the PS mode, during exercise significantly improved exercise duration in patients with HF compared to CPAP or no ventilatory support.
dc.identifier.citationMazzucco G, Torres-Castro R, Intelangelo L, Lista-Paz A, Escalante JP, Zumeta-Olaskoaga L, Veiga G, Etxarri AA. Is non-invasive ventilation effective in improving the exercise capacity in patients with cardiac heart failure?: a randomised crossover trial. PLoS One. 2025 Jul 7;20(7):e0327399.
dc.identifier.doi10.1371/journal.pone.0327399
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/2183/45611
dc.language.isoeng
dc.publisherPLoS
dc.relation.urihttps://doi.org/10.1371/journal.pone.0327399
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectExercise tolerance
dc.subjectHeart failure
dc.subjectNoninvasive ventilation
dc.titleIs non-invasive ventilation effective in improving the exercise capacity in patients with cardiac heart failure?: a randomised crossover trial
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication7ba00e49-1005-4f9a-9cba-8ec17f9773fc
relation.isAuthorOfPublication.latestForDiscovery7ba00e49-1005-4f9a-9cba-8ec17f9773fc

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