Cargando…
Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure
AIMS: Clinical outcomes for patients suspected of having heart failure (HF) who do not meet the diagnostic criteria of any type of HF by echocardiography remain unknown. The aim of this study was to investigate the clinical predictors of all‐cause mortality in patients with suspected HF, a raised N‐...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373941/ https://www.ncbi.nlm.nih.gov/pubmed/32496010 http://dx.doi.org/10.1002/ehf2.12742 |
_version_ | 1783561593987006464 |
---|---|
author | Garg, Pankaj Wood, Steven Swift, Andrew J. Fent, Graham Lewis, Nigel Rogers, Dominic Rothman, Alexander Charalampopoulos, Athanasios Al‐Mohammad, Abdallah |
author_facet | Garg, Pankaj Wood, Steven Swift, Andrew J. Fent, Graham Lewis, Nigel Rogers, Dominic Rothman, Alexander Charalampopoulos, Athanasios Al‐Mohammad, Abdallah |
author_sort | Garg, Pankaj |
collection | PubMed |
description | AIMS: Clinical outcomes for patients suspected of having heart failure (HF) who do not meet the diagnostic criteria of any type of HF by echocardiography remain unknown. The aim of this study was to investigate the clinical predictors of all‐cause mortality in patients with suspected HF, a raised N‐terminal pro‐b‐type natriuretic peptide (NTproBNP) and who do not meet the diagnostic criteria of any type of HF by echocardiography. METHODS AND RESULTS: Relevant data were taken from the Sheffield HEArt Failure (SHEAF) registry (222349P4). The inclusion criteria were presence of symptoms raising suspicion of HF, NTproBNP > 400 pg/mL, and preserved left ventricular function. Exclusion criteria were any type of HF by echocardiography. The outcome was defined as all‐cause mortality. Cox proportional‐hazards regression model was used to investigate the association between the survival time of patients and clinical variables; 1031 patients were identified with NTproBNP > 400 pg/mL but who did not have echocardiographic evidence of HF. All‐cause mortality was 21.5% (222 deaths) over the mean follow‐up (FU) period of 6 ± 2 years. NTproBNP was similar in patients who were alive or dead (P = 0.96). However, age (HR 1, P < 0.01), chronic kidney disease (CKD, HR 1.2, P < 0.01), chronic pulmonary obstructive disease (COPD, HR 1.6, P < 0.01), dementia (HR 5.9, P < 0.01), male gender (HR 1.4, P < 0.01), first‐degree atrioventricular block (HR 2.1, P < 0.01), left axis deviation (HR 1.6, P = 0.04), and diabetes (HR 1.4, P = 0.03) were associated with all‐cause mortality. In multivariate regression, age, gender, CKD stage, COPD, and dementia were independently associated with mortality. In patients with NTproBNP > 627 pg/mL, NYHA class predicted death (II, 19.6%; III, 27.4%; IV, 66.7%; P < 0.01). CONCLUSIONS: Patients with no HF on echocardiography but raised NTproBNP suffer excess mortality particularly in the presence of certain clinical variables. Age, male gender, worsening CKD stage, presence of COPD, and dementia are independently associated with all‐cause mortality in these patients. An NTproBNP > 627 pg/mL coupled with NYHA class could identify patients at greatest risk of death. |
format | Online Article Text |
id | pubmed-7373941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73739412020-07-22 Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure Garg, Pankaj Wood, Steven Swift, Andrew J. Fent, Graham Lewis, Nigel Rogers, Dominic Rothman, Alexander Charalampopoulos, Athanasios Al‐Mohammad, Abdallah ESC Heart Fail Original Research Articles AIMS: Clinical outcomes for patients suspected of having heart failure (HF) who do not meet the diagnostic criteria of any type of HF by echocardiography remain unknown. The aim of this study was to investigate the clinical predictors of all‐cause mortality in patients with suspected HF, a raised N‐terminal pro‐b‐type natriuretic peptide (NTproBNP) and who do not meet the diagnostic criteria of any type of HF by echocardiography. METHODS AND RESULTS: Relevant data were taken from the Sheffield HEArt Failure (SHEAF) registry (222349P4). The inclusion criteria were presence of symptoms raising suspicion of HF, NTproBNP > 400 pg/mL, and preserved left ventricular function. Exclusion criteria were any type of HF by echocardiography. The outcome was defined as all‐cause mortality. Cox proportional‐hazards regression model was used to investigate the association between the survival time of patients and clinical variables; 1031 patients were identified with NTproBNP > 400 pg/mL but who did not have echocardiographic evidence of HF. All‐cause mortality was 21.5% (222 deaths) over the mean follow‐up (FU) period of 6 ± 2 years. NTproBNP was similar in patients who were alive or dead (P = 0.96). However, age (HR 1, P < 0.01), chronic kidney disease (CKD, HR 1.2, P < 0.01), chronic pulmonary obstructive disease (COPD, HR 1.6, P < 0.01), dementia (HR 5.9, P < 0.01), male gender (HR 1.4, P < 0.01), first‐degree atrioventricular block (HR 2.1, P < 0.01), left axis deviation (HR 1.6, P = 0.04), and diabetes (HR 1.4, P = 0.03) were associated with all‐cause mortality. In multivariate regression, age, gender, CKD stage, COPD, and dementia were independently associated with mortality. In patients with NTproBNP > 627 pg/mL, NYHA class predicted death (II, 19.6%; III, 27.4%; IV, 66.7%; P < 0.01). CONCLUSIONS: Patients with no HF on echocardiography but raised NTproBNP suffer excess mortality particularly in the presence of certain clinical variables. Age, male gender, worsening CKD stage, presence of COPD, and dementia are independently associated with all‐cause mortality in these patients. An NTproBNP > 627 pg/mL coupled with NYHA class could identify patients at greatest risk of death. John Wiley and Sons Inc. 2020-06-04 /pmc/articles/PMC7373941/ /pubmed/32496010 http://dx.doi.org/10.1002/ehf2.12742 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Articles Garg, Pankaj Wood, Steven Swift, Andrew J. Fent, Graham Lewis, Nigel Rogers, Dominic Rothman, Alexander Charalampopoulos, Athanasios Al‐Mohammad, Abdallah Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title | Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title_full | Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title_fullStr | Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title_full_unstemmed | Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title_short | Clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised NT‐proBNP and no heart failure |
title_sort | clinical predictors of all‐cause mortality in patients presenting to specialist heart failure clinic with raised nt‐probnp and no heart failure |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373941/ https://www.ncbi.nlm.nih.gov/pubmed/32496010 http://dx.doi.org/10.1002/ehf2.12742 |
work_keys_str_mv | AT gargpankaj clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT woodsteven clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT swiftandrewj clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT fentgraham clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT lewisnigel clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT rogersdominic clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT rothmanalexander clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT charalampopoulosathanasios clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure AT almohammadabdallah clinicalpredictorsofallcausemortalityinpatientspresentingtospecialistheartfailureclinicwithraisedntprobnpandnoheartfailure |