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Intermittent levosimendan infusions in advanced heart failure: a real world experience
OBJECTIVE: To analyse the effects of levosimendan infusions in advanced heart failure. METHODS: Patients with advanced heart failure treated with repeated levosimendan infusions were retrospectively compared with controls. Clinical, blood and echocardiographic parameters were obtained at baseline an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536589/ https://www.ncbi.nlm.nih.gov/pubmed/28222634 http://dx.doi.org/10.1177/0300060516655244 |
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author | Ortis, Benedetta Villani, Alessandra Oldani, Matteo Giglio, Alessia Ciambellotti, Francesca Facchini, Mario Parati, Gianfranco Malfatto, Gabriella |
author_facet | Ortis, Benedetta Villani, Alessandra Oldani, Matteo Giglio, Alessia Ciambellotti, Francesca Facchini, Mario Parati, Gianfranco Malfatto, Gabriella |
author_sort | Ortis, Benedetta |
collection | PubMed |
description | OBJECTIVE: To analyse the effects of levosimendan infusions in advanced heart failure. METHODS: Patients with advanced heart failure treated with repeated levosimendan infusions were retrospectively compared with controls. Clinical, blood and echocardiographic parameters were obtained at baseline and after 12 months, and before and after each levosimendan infusion. Hospitalizations for heart failure and in-hospital length of stay in the 6 months before enrolment and after 6 and 12 months were recorded, along with 1-year mortality. RESULTS: Twenty-five patients treated with levosimendan and 25 controls were studied. After each levosimendan infusion, ventricular function and various clinical and metabolic parameters were improved. After 12 months, left ventricular ejection fraction (LVEF) had improved compared with baseline in the levosimendan group. The 1-year mortality rate was similar in both groups. During the 6 months before enrolment, hospitalizations were fewer in controls compared with the levosimendan group; after 6 and 12 months they increased in controls and decreased in the levosimendan group. Seven patients were super-responders to levosimendan, with LVEF improving more than 20% and hospitalizations being reduced at 12 months compared with the rest of the levosimendan group. CONCLUSION: Intermittent levosimendan improved LVEF and decreased hospitalizations in advanced heart failure and represents a therapeutic option for patients whose disease is worsening. |
format | Online Article Text |
id | pubmed-5536589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55365892017-10-03 Intermittent levosimendan infusions in advanced heart failure: a real world experience Ortis, Benedetta Villani, Alessandra Oldani, Matteo Giglio, Alessia Ciambellotti, Francesca Facchini, Mario Parati, Gianfranco Malfatto, Gabriella J Int Med Res Clinical Note OBJECTIVE: To analyse the effects of levosimendan infusions in advanced heart failure. METHODS: Patients with advanced heart failure treated with repeated levosimendan infusions were retrospectively compared with controls. Clinical, blood and echocardiographic parameters were obtained at baseline and after 12 months, and before and after each levosimendan infusion. Hospitalizations for heart failure and in-hospital length of stay in the 6 months before enrolment and after 6 and 12 months were recorded, along with 1-year mortality. RESULTS: Twenty-five patients treated with levosimendan and 25 controls were studied. After each levosimendan infusion, ventricular function and various clinical and metabolic parameters were improved. After 12 months, left ventricular ejection fraction (LVEF) had improved compared with baseline in the levosimendan group. The 1-year mortality rate was similar in both groups. During the 6 months before enrolment, hospitalizations were fewer in controls compared with the levosimendan group; after 6 and 12 months they increased in controls and decreased in the levosimendan group. Seven patients were super-responders to levosimendan, with LVEF improving more than 20% and hospitalizations being reduced at 12 months compared with the rest of the levosimendan group. CONCLUSION: Intermittent levosimendan improved LVEF and decreased hospitalizations in advanced heart failure and represents a therapeutic option for patients whose disease is worsening. SAGE Publications 2017-01-17 2017-02 /pmc/articles/PMC5536589/ /pubmed/28222634 http://dx.doi.org/10.1177/0300060516655244 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Note Ortis, Benedetta Villani, Alessandra Oldani, Matteo Giglio, Alessia Ciambellotti, Francesca Facchini, Mario Parati, Gianfranco Malfatto, Gabriella Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title | Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title_full | Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title_fullStr | Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title_full_unstemmed | Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title_short | Intermittent levosimendan infusions in advanced heart failure: a real world experience |
title_sort | intermittent levosimendan infusions in advanced heart failure: a real world experience |
topic | Clinical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536589/ https://www.ncbi.nlm.nih.gov/pubmed/28222634 http://dx.doi.org/10.1177/0300060516655244 |
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