Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado
Background: Pharmacological treatment improves survival in patients with heart failure with reduced ejection fraction. The use of sacubutril/valsartan and ivabradine has been recently approved and incorporated in the latest guidelines. Aim: To identify candidates eligible for these therapies among...
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Sociedad Médica de Santiago
2019
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oai:scielo:S0034-988720190003003302019-07-17Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializadoRossel,VíctorDuarte,ManuelMuñoz,PilarBravo,CatherineBobadilla,GustavoVerdugo,FernandoGuardamagna,Carmen Drug Therapy Heart Diseases Heart Failure Ivabradine Background: Pharmacological treatment improves survival in patients with heart failure with reduced ejection fraction. The use of sacubutril/valsartan and ivabradine has been recently approved and incorporated in the latest guidelines. Aim: To identify candidates eligible for these therapies among patients treated in a heart failure clinic, considering the inclusion criteria for the PARADIGM-HF and SHIFT trials. Material and Methods: Cross-sectional study on 158 patients aged 62 ± 11 years (67% male) with heart failure and reduced ejection fraction, with at least three months of follow-up and without decompensation. The percentage of patients complying for the inclusion criteria for the PARADIGM-HF y SHIFT trials was determined. Results: In 37%, the etiology of heart failure was ischemic, 49% were in functional class I, their ejection fraction was 33 ± 11% and their median Pro-brain natriuretic peptide was 800 pg/mL. Ninety five percent were treated with vasodilators, 97% with beta-blockers and 82% with aldosterone antagonists. Using PARADIGM-HF and SHIFT criteria, 11 patients (7%) were eligible for sacubitril / valsartan and 21 patients (13.3%) for ivabradine. Among the main causes of non-eligibility for sacubitril / valsartan were being functional class I (48.7%) and not achieving a stable dose of enalapril ≥ 20 mg / day or losartan ≥ 100 mg / day (24.7%). In the case of ivabradine, apart from those in functional class I, the absence of sinus rhythm and a heart rate < 70 / min when receiving a maximal tolerated dose of beta-blockers, were present in 22%. Conclusions: A low percentage of our patients were eligible for these therapies. Among the causes that explain these results were clinical stability, a high percentage of patients in functional class I and being in a disease modifying treatment.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.147 n.3 20192019-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300330es10.4067/S0034-98872019000300330 |
institution |
Scielo Chile |
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Scielo Chile |
language |
Spanish / Castilian |
topic |
Drug Therapy Heart Diseases Heart Failure Ivabradine |
spellingShingle |
Drug Therapy Heart Diseases Heart Failure Ivabradine Rossel,Víctor Duarte,Manuel Muñoz,Pilar Bravo,Catherine Bobadilla,Gustavo Verdugo,Fernando Guardamagna,Carmen Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
description |
Background: Pharmacological treatment improves survival in patients with heart failure with reduced ejection fraction. The use of sacubutril/valsartan and ivabradine has been recently approved and incorporated in the latest guidelines. Aim: To identify candidates eligible for these therapies among patients treated in a heart failure clinic, considering the inclusion criteria for the PARADIGM-HF and SHIFT trials. Material and Methods: Cross-sectional study on 158 patients aged 62 ± 11 years (67% male) with heart failure and reduced ejection fraction, with at least three months of follow-up and without decompensation. The percentage of patients complying for the inclusion criteria for the PARADIGM-HF y SHIFT trials was determined. Results: In 37%, the etiology of heart failure was ischemic, 49% were in functional class I, their ejection fraction was 33 ± 11% and their median Pro-brain natriuretic peptide was 800 pg/mL. Ninety five percent were treated with vasodilators, 97% with beta-blockers and 82% with aldosterone antagonists. Using PARADIGM-HF and SHIFT criteria, 11 patients (7%) were eligible for sacubitril / valsartan and 21 patients (13.3%) for ivabradine. Among the main causes of non-eligibility for sacubitril / valsartan were being functional class I (48.7%) and not achieving a stable dose of enalapril ≥ 20 mg / day or losartan ≥ 100 mg / day (24.7%). In the case of ivabradine, apart from those in functional class I, the absence of sinus rhythm and a heart rate < 70 / min when receiving a maximal tolerated dose of beta-blockers, were present in 22%. Conclusions: A low percentage of our patients were eligible for these therapies. Among the causes that explain these results were clinical stability, a high percentage of patients in functional class I and being in a disease modifying treatment. |
author |
Rossel,Víctor Duarte,Manuel Muñoz,Pilar Bravo,Catherine Bobadilla,Gustavo Verdugo,Fernando Guardamagna,Carmen |
author_facet |
Rossel,Víctor Duarte,Manuel Muñoz,Pilar Bravo,Catherine Bobadilla,Gustavo Verdugo,Fernando Guardamagna,Carmen |
author_sort |
Rossel,Víctor |
title |
Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
title_short |
Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
title_full |
Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
title_fullStr |
Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
title_full_unstemmed |
Pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
title_sort |
pacientes elegibles para las nuevas terapias de la insuficiencia cardíaca en un policlínico especializado |
publisher |
Sociedad Médica de Santiago |
publishDate |
2019 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300330 |
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