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Long‐term administration of intravenous inotropes in advanced heart failure

BACKGROUND: Patients in heart transplantation (HTx) waiting list for advanced heart failure (HF) are susceptible to acute deterioration refractory to standard HF medical therapies. Limited data are available on long‐term in‐hospital continuous intravenous (IV) inotropic therapy as bridge to definite...

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Autores principales: Gentile, Piero, Marini, Claudia, Ammirati, Enrico, Perna, Enrico, Saponara, Gianluigi, Garascia, Andrea, D'Angelo, Luciana, Verde, Alessandro, Foti, Grazia, Masciocco, Gabriella, Frigerio, Maria, Cipriani, Manlio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497373/
https://www.ncbi.nlm.nih.gov/pubmed/34191408
http://dx.doi.org/10.1002/ehf2.13394
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author Gentile, Piero
Marini, Claudia
Ammirati, Enrico
Perna, Enrico
Saponara, Gianluigi
Garascia, Andrea
D'Angelo, Luciana
Verde, Alessandro
Foti, Grazia
Masciocco, Gabriella
Frigerio, Maria
Cipriani, Manlio
author_facet Gentile, Piero
Marini, Claudia
Ammirati, Enrico
Perna, Enrico
Saponara, Gianluigi
Garascia, Andrea
D'Angelo, Luciana
Verde, Alessandro
Foti, Grazia
Masciocco, Gabriella
Frigerio, Maria
Cipriani, Manlio
author_sort Gentile, Piero
collection PubMed
description BACKGROUND: Patients in heart transplantation (HTx) waiting list for advanced heart failure (HF) are susceptible to acute deterioration refractory to standard HF medical therapies. Limited data are available on long‐term in‐hospital continuous intravenous (IV) inotropic therapy as bridge to definite therapies. METHODS AND RESULTS: We reviewed medical records of all heart transplant recipients treated in the pre‐HTx phase with in‐hospital continuous IV inotropes at our institution between 2012 and 2018. We analysed data before the beginning of continuous IV therapy and at the moment of HTx. We report data of 24 patients (mean age of 43.5 ± 15.7 years) treated with IV inotropes as bridge to HTx (median follow‐up of 28 months after HTx). The main length of IV inotropic therapy was 84 ± 66 days (min 22; max 264 days). At the beginning, the most frequently used inotrope was dopamine (median dosage of 3 mcg/kg/min, interquartile range 2.5–3.75), alone (n = 11, 46%) or in combination with other inotropes (n = 13, 54%). In 18 patients, the class of inotropes was changed during the hospitalization. We registered a progressive improvement of perfusion markers and neuro‐hormonal activation. CONCLUSION: In‐hospital continuous parenteral inotropic therapy may serve as a temporary pharmacological bridge to HTx in patients with advanced HF that are actively listed to HTx with good reply in terms of prognosis and perfusion markers.
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spelling pubmed-84973732021-10-12 Long‐term administration of intravenous inotropes in advanced heart failure Gentile, Piero Marini, Claudia Ammirati, Enrico Perna, Enrico Saponara, Gianluigi Garascia, Andrea D'Angelo, Luciana Verde, Alessandro Foti, Grazia Masciocco, Gabriella Frigerio, Maria Cipriani, Manlio ESC Heart Fail Short Communications BACKGROUND: Patients in heart transplantation (HTx) waiting list for advanced heart failure (HF) are susceptible to acute deterioration refractory to standard HF medical therapies. Limited data are available on long‐term in‐hospital continuous intravenous (IV) inotropic therapy as bridge to definite therapies. METHODS AND RESULTS: We reviewed medical records of all heart transplant recipients treated in the pre‐HTx phase with in‐hospital continuous IV inotropes at our institution between 2012 and 2018. We analysed data before the beginning of continuous IV therapy and at the moment of HTx. We report data of 24 patients (mean age of 43.5 ± 15.7 years) treated with IV inotropes as bridge to HTx (median follow‐up of 28 months after HTx). The main length of IV inotropic therapy was 84 ± 66 days (min 22; max 264 days). At the beginning, the most frequently used inotrope was dopamine (median dosage of 3 mcg/kg/min, interquartile range 2.5–3.75), alone (n = 11, 46%) or in combination with other inotropes (n = 13, 54%). In 18 patients, the class of inotropes was changed during the hospitalization. We registered a progressive improvement of perfusion markers and neuro‐hormonal activation. CONCLUSION: In‐hospital continuous parenteral inotropic therapy may serve as a temporary pharmacological bridge to HTx in patients with advanced HF that are actively listed to HTx with good reply in terms of prognosis and perfusion markers. John Wiley and Sons Inc. 2021-06-30 /pmc/articles/PMC8497373/ /pubmed/34191408 http://dx.doi.org/10.1002/ehf2.13394 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Short Communications
Gentile, Piero
Marini, Claudia
Ammirati, Enrico
Perna, Enrico
Saponara, Gianluigi
Garascia, Andrea
D'Angelo, Luciana
Verde, Alessandro
Foti, Grazia
Masciocco, Gabriella
Frigerio, Maria
Cipriani, Manlio
Long‐term administration of intravenous inotropes in advanced heart failure
title Long‐term administration of intravenous inotropes in advanced heart failure
title_full Long‐term administration of intravenous inotropes in advanced heart failure
title_fullStr Long‐term administration of intravenous inotropes in advanced heart failure
title_full_unstemmed Long‐term administration of intravenous inotropes in advanced heart failure
title_short Long‐term administration of intravenous inotropes in advanced heart failure
title_sort long‐term administration of intravenous inotropes in advanced heart failure
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497373/
https://www.ncbi.nlm.nih.gov/pubmed/34191408
http://dx.doi.org/10.1002/ehf2.13394
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