Prognostic impact of plasma volume estimated from hemoglobin and hematocrit in heart failure with preserved ejection fraction.


Journal

Clinical research in cardiology : official journal of the German Cardiac Society
ISSN: 1861-0692
Titre abrégé: Clin Res Cardiol
Pays: Germany
ID NLM: 101264123

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 29 01 2020
accepted: 24 03 2020
pubmed: 8 4 2020
medline: 11 8 2021
entrez: 8 4 2020
Statut: ppublish

Résumé

Plasma volume (PV) estimated from Duarte's formula (based on hemoglobin/hematocrit) has been associated with poor prognosis in patients with heart failure (HF). There are, however, limited data regarding the association of estimated PV status (ePVS) derived from hemoglobin/hematocrit with clinical profiles and study outcomes in patients with HF and preserved ejection fraction (HFpEF). Patients from North and South America enrolled in the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist trial (TOPCAT) with available hemoglobin/hematocrit data were studied. The association between ePVS (Duarte formula and Hakim formula) and the composite of cardiovascular mortality, HF hospitalization, or aborted cardiac arrest was assessed. Among 1747 patients (age 71.6 years; males 50.1%), mean ePVS derived from Duarte formula was 4.9 ± 1.0 mL/g. Higher Duarte-derived ePVS was associated with prior HF admission, diabetes, more severe congestion, poor renal function, higher natriuretic peptide level, and E/e'. After adjustment for potential covariates including natriuretic peptide, higher Duarte-derived ePVS was associated with an increased rate of the primary outcome [highest vs. lowest ePVS quartile: adjusted-HR (95%CI) = 1.79 (1.28-2.50), p < 0.001]. Duarte-derived ePVS improved prognostic performance on top of clinical and routine variables (including natriuretic peptides) (NRI = 11, p < 0.001), whereas Hakim-derived ePVS did not (p = 0.59). The prognostic value of Duarte-derived ePVS was not modified by renal function (P interaction > 0.10 for all outcomes). ePVS from Duarte's formula was associated with congestion status and improved risk stratification regardless of renal function. Our findings suggest that Duarte-derived ePVS is a useful congestion variable in patients with HFpEF.

Sections du résumé

BACKGROUND BACKGROUND
Plasma volume (PV) estimated from Duarte's formula (based on hemoglobin/hematocrit) has been associated with poor prognosis in patients with heart failure (HF). There are, however, limited data regarding the association of estimated PV status (ePVS) derived from hemoglobin/hematocrit with clinical profiles and study outcomes in patients with HF and preserved ejection fraction (HFpEF).
METHODS AND RESULTS RESULTS
Patients from North and South America enrolled in the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist trial (TOPCAT) with available hemoglobin/hematocrit data were studied. The association between ePVS (Duarte formula and Hakim formula) and the composite of cardiovascular mortality, HF hospitalization, or aborted cardiac arrest was assessed. Among 1747 patients (age 71.6 years; males 50.1%), mean ePVS derived from Duarte formula was 4.9 ± 1.0 mL/g. Higher Duarte-derived ePVS was associated with prior HF admission, diabetes, more severe congestion, poor renal function, higher natriuretic peptide level, and E/e'. After adjustment for potential covariates including natriuretic peptide, higher Duarte-derived ePVS was associated with an increased rate of the primary outcome [highest vs. lowest ePVS quartile: adjusted-HR (95%CI) = 1.79 (1.28-2.50), p < 0.001]. Duarte-derived ePVS improved prognostic performance on top of clinical and routine variables (including natriuretic peptides) (NRI = 11, p < 0.001), whereas Hakim-derived ePVS did not (p = 0.59). The prognostic value of Duarte-derived ePVS was not modified by renal function (P interaction > 0.10 for all outcomes).
CONCLUSION CONCLUSIONS
ePVS from Duarte's formula was associated with congestion status and improved risk stratification regardless of renal function. Our findings suggest that Duarte-derived ePVS is a useful congestion variable in patients with HFpEF.

Identifiants

pubmed: 32253507
doi: 10.1007/s00392-020-01639-4
pii: 10.1007/s00392-020-01639-4
doi:

Substances chimiques

Biomarkers 0
Hemoglobins 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1392-1401

Subventions

Organisme : NHLBI NIH HHS
ID : HHSN268200425207C
Pays : United States
Organisme : Agence Nationale de la Recherche
ID : ANR-15-RHUS-0004
Organisme : Agence Nationale de la Recherche
ID : ANR-15-IDEX-04-LUE
Organisme : Agence Nationale de la Recherche
ID : ANR-15-CE14-0032-01
Organisme : Agence Nationale de la Recherche
ID : ANR-16-ECVD-0002-02
Organisme : NHLBI NIH HHS
ID : HHSN268200425207C
Pays : United States

Auteurs

Masatake Kobayashi (M)

Centre d'Investigations Cliniques 1433, Université de Lorraine, INSERM, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Institut Lorrain du cœur Et des, Vaisseaux Louis Mathieu, 4, rue du Morvan, 54500, Vandoeuvre-Les-Nancy, Nancy, France.

Nicolas Girerd (N)

Centre d'Investigations Cliniques 1433, Université de Lorraine, INSERM, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Institut Lorrain du cœur Et des, Vaisseaux Louis Mathieu, 4, rue du Morvan, 54500, Vandoeuvre-Les-Nancy, Nancy, France.

Kevin Duarte (K)

Centre d'Investigations Cliniques 1433, Université de Lorraine, INSERM, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Institut Lorrain du cœur Et des, Vaisseaux Louis Mathieu, 4, rue du Morvan, 54500, Vandoeuvre-Les-Nancy, Nancy, France.

Gregoire Preud'homme (G)

Centre d'Investigations Cliniques 1433, Université de Lorraine, INSERM, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Institut Lorrain du cœur Et des, Vaisseaux Louis Mathieu, 4, rue du Morvan, 54500, Vandoeuvre-Les-Nancy, Nancy, France.

Bertram Pitt (B)

Department of Medicine, University of Michigan School of Medicine, Ann Arbor, MI, USA.

Patrick Rossignol (P)

Centre d'Investigations Cliniques 1433, Université de Lorraine, INSERM, CHRU de Nancy, Inserm 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Institut Lorrain du cœur Et des, Vaisseaux Louis Mathieu, 4, rue du Morvan, 54500, Vandoeuvre-Les-Nancy, Nancy, France. p.rossignol@chru-nancy.fr.

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Classifications MeSH