Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy

Detalhes bibliográficos
Autor(a) principal: Valentim Gonçalves, A
Data de Publicação: 2020
Outros Autores: Pereira-da-Silva, T, Galrinho, A, Rio, P, Soares, RM, Feliciano, J, Ilhão Moreira, R, Silva, S, Alves, S, Capilé, E, Cruz Ferreira, R
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/3533
Resumo: Background: Sacubitril/valsartan had its prognosis benefit confirmed in the PARADIGM-HF trial. However, data on cardiopulmonary exercise testing (CPET) changes with sacubitril-valsartan therapy are scarce. Objective: This study aimed to compare CPET parameters before and after sacubitril-valsartan therapy. Methods: Prospective evaluation of chronic heart failure (HF) patients with left ventricular ejection fraction ≤40% despite optimized standard of care therapy, who started sacubitril-valsartan therapy, expecting no additional HF treatment. CPET data were gathered in the week before and 6 months after sacubitril-valsartan therapy. Statistical differences with a p-value <0.05 were considered significant. Results: Out of 42 patients, 35 (83.3%) completed the 6-month follow-up, since 2 (4.8%) patients died and 5 (11.9%) discontinued treatment for adverse events. Mean age was 58.6±11.1 years. New York Heart Association class improved in 26 (74.3%) patients. Maximal oxygen uptake (VO2max) (14.4 vs. 18.3 ml/kg/min, p<0.001), VE/VCO2slope (36.7 vs. 31.1, p<0.001), and exercise duration (487.8 vs. 640.3 sec, p<0.001) also improved with sacubitril-valsartan. Benefit was maintained even with the 24/26 mg dose (13.5 vs. 19.2 ml/kg/min, p=0.018) of sacubitril-valsartan, as long as this was the highest tolerated dose. Conclusions: Sacubitril-valsartan therapy is associated with marked CPET improvement in VO2max, VE/VCO2slope, and exercise duration.
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spelling Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan TherapyMelhora no Consumo Máximo de Oxigênio e na Ventilação após Tratamento com Sacubitril-ValsartanaHSM CARAminobutyratesAgedAngiotensin Receptor AntagonistsDrug CombinationsHeart Failure / drug therapyHumansMiddle AgedProspective StudiesOxygenStroke VolumeTetrazolesTreatment OutcomeVentricular Function, LeftBackground: Sacubitril/valsartan had its prognosis benefit confirmed in the PARADIGM-HF trial. However, data on cardiopulmonary exercise testing (CPET) changes with sacubitril-valsartan therapy are scarce. Objective: This study aimed to compare CPET parameters before and after sacubitril-valsartan therapy. Methods: Prospective evaluation of chronic heart failure (HF) patients with left ventricular ejection fraction ≤40% despite optimized standard of care therapy, who started sacubitril-valsartan therapy, expecting no additional HF treatment. CPET data were gathered in the week before and 6 months after sacubitril-valsartan therapy. Statistical differences with a p-value <0.05 were considered significant. Results: Out of 42 patients, 35 (83.3%) completed the 6-month follow-up, since 2 (4.8%) patients died and 5 (11.9%) discontinued treatment for adverse events. Mean age was 58.6±11.1 years. New York Heart Association class improved in 26 (74.3%) patients. Maximal oxygen uptake (VO2max) (14.4 vs. 18.3 ml/kg/min, p<0.001), VE/VCO2slope (36.7 vs. 31.1, p<0.001), and exercise duration (487.8 vs. 640.3 sec, p<0.001) also improved with sacubitril-valsartan. Benefit was maintained even with the 24/26 mg dose (13.5 vs. 19.2 ml/kg/min, p=0.018) of sacubitril-valsartan, as long as this was the highest tolerated dose. Conclusions: Sacubitril-valsartan therapy is associated with marked CPET improvement in VO2max, VE/VCO2slope, and exercise duration.Sociedade Brasileira de CardiologiaRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEValentim Gonçalves, APereira-da-Silva, TGalrinho, ARio, PSoares, RMFeliciano, JIlhão Moreira, RSilva, SAlves, SCapilé, ECruz Ferreira, R2020-12-15T15:59:55Z2020-112020-11-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3533engArq Bras Cardiol. 2020 Nov;115(5):821-827.10.36660/abc.20190443info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:43:27Zoai:repositorio.chlc.min-saude.pt:10400.17/3533Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:20:50.662207Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
Melhora no Consumo Máximo de Oxigênio e na Ventilação após Tratamento com Sacubitril-Valsartana
title Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
spellingShingle Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
Valentim Gonçalves, A
HSM CAR
Aminobutyrates
Aged
Angiotensin Receptor Antagonists
Drug Combinations
Heart Failure / drug therapy
Humans
Middle Aged
Prospective Studies
Oxygen
Stroke Volume
Tetrazoles
Treatment Outcome
Ventricular Function, Left
title_short Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
title_full Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
title_fullStr Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
title_full_unstemmed Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
title_sort Maximal Oxygen Uptake and Ventilation Improvement Following Sacubitril-Valsartan Therapy
author Valentim Gonçalves, A
author_facet Valentim Gonçalves, A
Pereira-da-Silva, T
Galrinho, A
Rio, P
Soares, RM
Feliciano, J
Ilhão Moreira, R
Silva, S
Alves, S
Capilé, E
Cruz Ferreira, R
author_role author
author2 Pereira-da-Silva, T
Galrinho, A
Rio, P
Soares, RM
Feliciano, J
Ilhão Moreira, R
Silva, S
Alves, S
Capilé, E
Cruz Ferreira, R
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Valentim Gonçalves, A
Pereira-da-Silva, T
Galrinho, A
Rio, P
Soares, RM
Feliciano, J
Ilhão Moreira, R
Silva, S
Alves, S
Capilé, E
Cruz Ferreira, R
dc.subject.por.fl_str_mv HSM CAR
Aminobutyrates
Aged
Angiotensin Receptor Antagonists
Drug Combinations
Heart Failure / drug therapy
Humans
Middle Aged
Prospective Studies
Oxygen
Stroke Volume
Tetrazoles
Treatment Outcome
Ventricular Function, Left
topic HSM CAR
Aminobutyrates
Aged
Angiotensin Receptor Antagonists
Drug Combinations
Heart Failure / drug therapy
Humans
Middle Aged
Prospective Studies
Oxygen
Stroke Volume
Tetrazoles
Treatment Outcome
Ventricular Function, Left
description Background: Sacubitril/valsartan had its prognosis benefit confirmed in the PARADIGM-HF trial. However, data on cardiopulmonary exercise testing (CPET) changes with sacubitril-valsartan therapy are scarce. Objective: This study aimed to compare CPET parameters before and after sacubitril-valsartan therapy. Methods: Prospective evaluation of chronic heart failure (HF) patients with left ventricular ejection fraction ≤40% despite optimized standard of care therapy, who started sacubitril-valsartan therapy, expecting no additional HF treatment. CPET data were gathered in the week before and 6 months after sacubitril-valsartan therapy. Statistical differences with a p-value <0.05 were considered significant. Results: Out of 42 patients, 35 (83.3%) completed the 6-month follow-up, since 2 (4.8%) patients died and 5 (11.9%) discontinued treatment for adverse events. Mean age was 58.6±11.1 years. New York Heart Association class improved in 26 (74.3%) patients. Maximal oxygen uptake (VO2max) (14.4 vs. 18.3 ml/kg/min, p<0.001), VE/VCO2slope (36.7 vs. 31.1, p<0.001), and exercise duration (487.8 vs. 640.3 sec, p<0.001) also improved with sacubitril-valsartan. Benefit was maintained even with the 24/26 mg dose (13.5 vs. 19.2 ml/kg/min, p=0.018) of sacubitril-valsartan, as long as this was the highest tolerated dose. Conclusions: Sacubitril-valsartan therapy is associated with marked CPET improvement in VO2max, VE/VCO2slope, and exercise duration.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-15T15:59:55Z
2020-11
2020-11-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/3533
url http://hdl.handle.net/10400.17/3533
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Arq Bras Cardiol. 2020 Nov;115(5):821-827.
10.36660/abc.20190443
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia
publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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