Abstract
Methods: This multicenter follow-up study included patients from the original PRO-VAD cohort who performed a cardiopulmonary exercise test (CPET) twice. Patients were categorized into 4 groups based on pVO2 levels at the 2 CPETs: low at both tests, low at the first and high at the second test, high at the first and low at the second test, and high at both tests. Low pVO2 was defined as ≤14 ml/kg/min (or ≤12 ml/kg/min if beta-blocker tolerant), while values above these thresholds were considered high. Survival outcomes were analyzed using the Kaplan-Meier method and cause-specific Cox analysis.
Results: The study included 152 patients with repeated CPETs at approximately 6 and 12 months following LVAD implantation. The cohort showed slight but significant pVO2 improvement (median change: 0.4 ml/kg/min, p = 0.04). Persistently high pVO2 (76 patients) was associated with a 5-fold reduction in mortality hazard (hazard ratio [HR] 0.20, p = 0.002), compared with persistently low pVO2 (46 patients). Improvement from low to high pVO2 (21 patients) displayed similar benefits (HR 0.21, p = 0.02).
Conclusions: pVO2 measurements remain predictive of mortality upon reiteration in patients with LVAD, with changes in pVO2 providing additional prognostic value in identifying patients with an excellent outcome on ongoing LVAD support and in identifying patients requiring further interventions.
| Original language | English |
|---|---|
| Pages (from-to) | 236-245 |
| Number of pages | 10 |
| Journal | Journal of Heart and Lung Transplantation |
| Volume | 44 |
| Issue number | 2 |
| Early online date | 18 Oct 2024 |
| DOIs | |
| Publication status | Published - Feb 2025 |
Bibliographical note
Publisher Copyright:© 2024 International Society for the Heart and Lung Transplantation
Funding
Nielsen received funding from the Novo Nordisk Foundation (grant no. 20OC0060561) and support for meeting attendance from Pharmacosmos. Szymanski received honoraria from Chiesi and AstraZeneca, paid to UMC Utrecht. Van Laake is supported by grants from Medtronic and Abbott to UMC Utrecht and has received honoraria from CVOI, Medcon, and Abbott via UMC Utrecht. Schmidt is involved with the German Society of Cardiology and the German Society of Prevention and Rehabilitation of Cardiovascular Diseases and received bicycle ergometers on a free loan from Ergoline GmbH. Brahmbhatt received post-doctoral fellowship funding from Transform HF (Ontario, Canada) and support for meeting attendance from Abbott. Billia received a physician-initiated research grant from Abbott. Hsu is funded by the U.S. National Institutes of Health (grant no. NIH K23HL146889). Jakovljevic is supported by grants from Horizon Europe (STRATIFYHF research project), Horizon2020 (SGABU and SILICOFCM research projects), and Cardinal Health (HRVDISPOSE research project). Agostoni received funding from the European Union \u2013 Next Generation (grant no. PNRR-MAD-2022-12375794), consulting fees from Schiller, honoraria from CPX International, advisory board payments from AstraZeneca, and support for meeting attendance from Societ\u00E0 Italiana di Cardiologica and CPX International. Trombara received travel expenses from EasyNet (Lombardy region). Jorde received consulting fees from Abbott and serves on the ISHLT Research Oversight Committee. Reiss is involved with the German Society of Prevention and Rehabilitation of Cardiovascular Diseases. Russell received consulting fees from Medtronic (ended Jan 2023) and advisory board payments from Abbott. Meyns has an institutional research agreement with Abiomed, Berlin Heart, and RealHeart and received honoraria from Abbott. Gustafsson received consulting fees from Abbott, FineHeart, AdjuCor, Bayer, AstraZeneca, and Pfizer; honoraria from Novartis; advisory board payments from AdjuCor; and serves as an unpaid board member of the Heart Failure Association of the ESC. Authors Mirza, MacGowan, Rochlani, and Vandersmissen have nothing to disclose.
| Funders | Funder number |
|---|---|
| Novo Nordisk Fonden | 20OC0060561 |
| Chiesi Farmaceutici | |
| AstraZeneca | |
| Medtronic | |
| Abbott Laboratories | |
| TRANSFORM HF | |
| National Institutes of Health | K23HL146889 |
| Horizon Europe | |
| European Union | |
| CPX International | |
| Schiller |
Keywords
- left ventricular assist devices
- peak oxygen uptake
- prognosis
- pVO2
- repeated cardiopulmonary exercise testing