The association of hematological indices with the response to cardiac resynchronization therapy: a single-center study.

Cardiac resynchronization therapy heart failure hematological indices predictors responders

Journal

Hippokratia
ISSN: 1108-4189
Titre abrégé: Hippokratia
Pays: Greece
ID NLM: 101296613

Informations de publication

Date de publication:
Historique:
entrez: 26 6 2020
pubmed: 26 6 2020
medline: 26 6 2020
Statut: ppublish

Résumé

Cardiac resynchronization therapy (CRT) is an established therapeutic option for patients with heart failure (HF) and left ventricular ejection fraction (LVEF) ≤35 % who meet specific criteria according to current guidelines. However, up to 40 % of patients have no response to CRT. Our study aimed to investigate the association between different hematological and biochemical indices and response to CRT. Patients with HF due to ischemic or dilated cardiomyopathy referred to our hospital for CRT implantation from January 2013 to November 2017 were included in the study. Response to CRT was defined as an increase in LVEF ≥10 % or a decrease in left ventricular end-systolic volume (LVESV) ≥15 % at six months of follow-up. A total of 48 patients (mean age: 66.2 ± 9.5 years, 81.3 % males) were included in the study. Of these HF patients, 29 (60.4 %) had ischemic cardiomyopathy, and 19 (39.6 %) had dilated cardiomyopathy. At six months of follow-up, 37 patients (77.1 %) had responded to CRT. Ten patients (20.8 %) had ventricular tachycardia (VT), 24 (50 %) patients were hospitalized, and two patients (4.2 %) died during the follow-up period. Multivariate analysis demonstrated that age (p =0.03) and creatinine levels (p =0.02) were independent predictors of the response to CRT. No significant associations between hematological markers (white blood cells, neutrophils, lymphocytes, platelets, neutrophil to lymphocyte ratio, red blood cells distribution width) and CRT response were observed. A smaller increase in LVEF and a smaller decrease in LVESV were predictive for VT occurrence and hospitalizations in patients receiving CRT. No significant association between hematological markers and response to CRT was found. HIPPOKRATIA 2019, 23(3): 118-125.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac resynchronization therapy (CRT) is an established therapeutic option for patients with heart failure (HF) and left ventricular ejection fraction (LVEF) ≤35 % who meet specific criteria according to current guidelines. However, up to 40 % of patients have no response to CRT. Our study aimed to investigate the association between different hematological and biochemical indices and response to CRT.
METHODS METHODS
Patients with HF due to ischemic or dilated cardiomyopathy referred to our hospital for CRT implantation from January 2013 to November 2017 were included in the study. Response to CRT was defined as an increase in LVEF ≥10 % or a decrease in left ventricular end-systolic volume (LVESV) ≥15 % at six months of follow-up.
RESULTS RESULTS
A total of 48 patients (mean age: 66.2 ± 9.5 years, 81.3 % males) were included in the study. Of these HF patients, 29 (60.4 %) had ischemic cardiomyopathy, and 19 (39.6 %) had dilated cardiomyopathy. At six months of follow-up, 37 patients (77.1 %) had responded to CRT. Ten patients (20.8 %) had ventricular tachycardia (VT), 24 (50 %) patients were hospitalized, and two patients (4.2 %) died during the follow-up period. Multivariate analysis demonstrated that age (p =0.03) and creatinine levels (p =0.02) were independent predictors of the response to CRT. No significant associations between hematological markers (white blood cells, neutrophils, lymphocytes, platelets, neutrophil to lymphocyte ratio, red blood cells distribution width) and CRT response were observed.
CONCLUSIONS CONCLUSIONS
A smaller increase in LVEF and a smaller decrease in LVESV were predictive for VT occurrence and hospitalizations in patients receiving CRT. No significant association between hematological markers and response to CRT was found. HIPPOKRATIA 2019, 23(3): 118-125.

Identifiants

pubmed: 32581497
pii: 111540327
pmc: PMC7307505

Types de publication

Journal Article

Langues

eng

Pagination

118-125

Informations de copyright

Copyright 2019, Hippokratio General Hospital of Thessaloniki.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest regarding this manuscript.

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Auteurs

G Bazoukis (G)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

A Saplaouras (A)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

K P Letsas (KP)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

C Yeung (C)

Department of Cardiology, Queen's University, Kingston, Ontario K7L 2V7, Canada.

S Xydonas (S)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

N Karamichalakis (N)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

C Thomopoulos (C)

Department of Cardiology, Helena Venizelou Hospital, Athens, Greece.

D Manolatos (D)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

G Papathanakos (G)

Intensive Care Unit, University Hospital of Ioannina, Ioannina, Greece.

K Vlachos (K)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

G Tse (G)

Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, Second Hospital of Tianjin Medical University, Tianjin, China.

P Korantzopoulos (P)

First Department of Cardiology, Medical School, University of Ioannina, Ioannina, Greece.

M Efremidis (M)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

A Sideris (A)

Second Department of Cardiology, General Hospital of Athens "Evangelismos", Athens, Greece.

K K Naka (KK)

Second Department of Cardiology; Michaelidion Cardiac Center, University of Ioannina, Ioannina, Greece.

Classifications MeSH