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Preoperative nutritional optimization and physical exercise for patients scheduled for elective implantation for a left-ventricular assist device — The PROPER-LVAD study

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-288317
  • Background: Prehabilitation is gaining increasing interest and shows promising effects on short- and long-term outcomes among patients undergoing major surgery. The effect of multimodal, interdisciplinary prehabilitation has not yet been studied in patients with severe heart failure scheduled for the implantation of a left-ventricular assist device (LVAD). Methods: This randomized controlled multi-center study evaluates the effect of preoperative combined optimization of nutritional and functional status. Patients in the intervention group areBackground: Prehabilitation is gaining increasing interest and shows promising effects on short- and long-term outcomes among patients undergoing major surgery. The effect of multimodal, interdisciplinary prehabilitation has not yet been studied in patients with severe heart failure scheduled for the implantation of a left-ventricular assist device (LVAD). Methods: This randomized controlled multi-center study evaluates the effect of preoperative combined optimization of nutritional and functional status. Patients in the intervention group are prescribed daily in-bed cycling and oral nutrition supplements (ONS) from study inclusion until the day before LVAD-implantation. Patients in the control group receive standard of care treatment. The primary outcomes for the pilot study that involves 48 patients are safety (occurrence of adverse events), efficacy (group separation regarding the intake of macronutrients), feasibility of the trial protocol (compliance (percentage of received interventions) and confirmation of recruitment rates. Secondary outcomes include longitudinal measurements of muscle mass, muscle strength, physical function and quality of life, next to traditional clinical outcomes (30-day mortality, hospital and ICU length of stay, duration of mechanical ventilation and number of complications and infections). If the pilot study is successful, a larger confirmatory, international multicenter study is warranted.zeige mehrzeige weniger

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Metadaten
Autor(en): Aileen Hill, Vera von Dossow, Daren K. Heyland, Rolf Rossaint, Patrick MeybohmORCiD, Henrik Fox, Michiel Morshuis, Gunnar Elke, Bernd Panholzer, Assad Haneya, Andreas Böning, Bernd Niemann, Rashad Zayat, Ajay Moza, Christian Stoppe
URN:urn:nbn:de:bvb:20-opus-288317
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Klinik und Poliklinik für Anästhesiologie (ab 2004)
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Surgeries
ISSN:2673-4095
Erscheinungsjahr:2022
Band / Jahrgang:3
Heft / Ausgabe:4
Erste Seite:284
Letzte Seite:296
Originalveröffentlichung / Quelle:Surgeries (2022) 3:4, 284-296. https://doi.org/10.3390/surgeries3040031
DOI:https://doi.org/10.3390/surgeries3040031
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):clinical trial; in-bed cycling; left-ventricular assist device; medical nutrition therapy; oral nutrition supplements; prehabilitation; trial protocol
Datum der Freischaltung:22.09.2023
Datum der Erstveröffentlichung:30.09.2022
Anmerkungen:
Funding: This investigator-initiated trial is supported by a grant from Fresenius Kabi Deutschland (Fresenius Kabi Deutschland GmbH, Else-Kröner-Straße 1, 61352 Bad Homburg). The oral nutrition supplements (Fresubin PRO®) are provided by Fresenius Kabi Germany.
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International