Diagnostic and prognostic value of plasma volume status at emergency department admission in dyspneic patients: results from the PARADISE cohort.


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:
May 2019
Historique:
received: 26 05 2018
accepted: 18 10 2018
pubmed: 30 10 2018
medline: 29 8 2019
entrez: 30 10 2018
Statut: ppublish

Résumé

Systemic congestion, evaluated by estimated plasma volume status (ePVS), is associated with in-hospital mortality in acute heart failure (AHF). However, the diagnostic and prognostic value of ePVS in patients with acute dyspnea has been insufficiently studied. To assess the association between the first ePVS calculated from blood samples on admission in the emergency department (ED) and discharge diagnosis of AHF and in-hospital mortality in patients admitted for acute dyspnea. The study included 1369 patients admitted for dyspnea in the ED in 2015. ePVS was calculated from hematocrit and hemoglobin values at admission. Comparisons of baseline characteristics according to ePVS tertiles were carried out and then associations between ePVS and the two outcomes "AHF diagnosis" and "intra-hospital mortality" were assessed using a logistic regression model. 36.6% had a BNP > 400 pg/mL and median ePVS was 4.58 dL/g [3.96-5.55]. Overall in-hospital mortality was 11.1% (n = 149). In multivariable analysis, the third ePVS tertile (> 5.12 dL/g) had a significantly increased risk of having AHF (OR = 1.64 [1.16-2.33], p = 0.005). In-hospital mortality rose across ePVS tertiles (8.4-13.8% p < 0.01). ePVS greater than the first or second tertile threshold (respectively, 4.17 dL/g and 5.12 dL/g) were both significantly associated with a higher risk of in-hospital mortality (OR for 2nd/3rd tertile = 2.06 [1.25-3.38], p = 0.004 and OR for 3rd tertile = 1.54 [1.01-2.36], p = 0.04). Higher ePVS values determined from first blood sample at admission are associated with a higher probability of AHF and in-hospital mortality in patients admitted in the ED for acute dyspnea.

Sections du résumé

BACKGROUND BACKGROUND
Systemic congestion, evaluated by estimated plasma volume status (ePVS), is associated with in-hospital mortality in acute heart failure (AHF). However, the diagnostic and prognostic value of ePVS in patients with acute dyspnea has been insufficiently studied.
OBJECTIVES OBJECTIVE
To assess the association between the first ePVS calculated from blood samples on admission in the emergency department (ED) and discharge diagnosis of AHF and in-hospital mortality in patients admitted for acute dyspnea.
METHODS METHODS
The study included 1369 patients admitted for dyspnea in the ED in 2015. ePVS was calculated from hematocrit and hemoglobin values at admission. Comparisons of baseline characteristics according to ePVS tertiles were carried out and then associations between ePVS and the two outcomes "AHF diagnosis" and "intra-hospital mortality" were assessed using a logistic regression model.
RESULTS RESULTS
36.6% had a BNP > 400 pg/mL and median ePVS was 4.58 dL/g [3.96-5.55]. Overall in-hospital mortality was 11.1% (n = 149). In multivariable analysis, the third ePVS tertile (> 5.12 dL/g) had a significantly increased risk of having AHF (OR = 1.64 [1.16-2.33], p = 0.005). In-hospital mortality rose across ePVS tertiles (8.4-13.8% p < 0.01). ePVS greater than the first or second tertile threshold (respectively, 4.17 dL/g and 5.12 dL/g) were both significantly associated with a higher risk of in-hospital mortality (OR for 2nd/3rd tertile = 2.06 [1.25-3.38], p = 0.004 and OR for 3rd tertile = 1.54 [1.01-2.36], p = 0.04).
CONCLUSION CONCLUSIONS
Higher ePVS values determined from first blood sample at admission are associated with a higher probability of AHF and in-hospital mortality in patients admitted in the ED for acute dyspnea.

Identifiants

pubmed: 30370469
doi: 10.1007/s00392-018-1388-y
pii: 10.1007/s00392-018-1388-y
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

563-573

Subventions

Organisme : French National Research Agency Fighting Heart Failure
ID : ANR-15-RHU-0004

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Auteurs

Tahar Chouihed (T)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.
INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.
F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

Patrick Rossignol (P)

INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.
F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

Adrien Bassand (A)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.
INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.

Kévin Duarte (K)

INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.
Université de Lorraine, Institut Elie Cartan de Lorraine, Unité Mixte de Recherche 7502, Vandoeuvre-lès-Nancy, France.
Centre National de la Recherche Scientifique, Institut Elie Cartan de Lorraine, Unité Mixte de Recherche 7502, Vandoeuvre-lès-Nancy, France.
INRIA, Project-Team BIGS, Villers-lès-Nancy, France.

Masatake Kobayashi (M)

INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.
Department of Cardiology, Tokyo Medical University, Tokyo, Japan.

Déborah Jaeger (D)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.
INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.

Sonia Sadoune (S)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.

Aurélien Buessler (A)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.

Lionel Nace (L)

Réanimation Médicale, Hôpital Central, CHRU Nancy, Vandoeuvre les Nancy, France.

Gaetan Giacomin (G)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.

Thibaut Hutter (T)

Emergency Department, University Hospital of Nancy, Vandoeuvre les Nancy, France.

Françoise Barbé (F)

Biochimie, Biologie moléculaire, Nutrition, Métabolisme, Hôpital de Brabois, CHRU Nancy, Nancy, France.

Sylvain Salignac (S)

Hématologie, Hôpital de Brabois, CHRU Nancy, Vandoeuvre les Nancy, France.

Nicolas Jay (N)

Department of Medical Informatics, University Hospital, Vandoeuvre les Nancy, France.
Orpailleur, LORIA UMR 7503, Vandoeuvre les Nancy, France.

Faiez Zannad (F)

INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France.
F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.
Pôle de Cardiologie, Institut Lorrain du Coeur et des Vaisseaux, CHRU Nancy, Vandoeuvre les Nancy, France.

Nicolas Girerd (N)

INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Institut Lorrain du Coeur et des Vaisseaux, Vandoeuvre les Nancy, France. nicolas_girerd@yahoo.com.
Groupe choc, Faculté de Médecine, INSERM U1116, 54500, Vandoeuvre les Nancy, France. nicolas_girerd@yahoo.com.
F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France. nicolas_girerd@yahoo.com.
Pôle de Cardiologie, Institut Lorrain du Coeur et des Vaisseaux, CHRU Nancy, Vandoeuvre les Nancy, France. nicolas_girerd@yahoo.com.

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