Diastolic dyssynchrony assessment by gated myocardial perfusion-SPECT in subjects who underwent cardiac resynchronization therapy.


Journal

Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology
ISSN: 1532-6551
Titre abrégé: J Nucl Cardiol
Pays: United States
ID NLM: 9423534

Informations de publication

Date de publication:
08 2021
Historique:
received: 18 06 2019
accepted: 23 07 2019
pubmed: 15 8 2019
medline: 17 2 2022
entrez: 15 8 2019
Statut: ppublish

Résumé

Left ventricular diastolic dyssynchrony (LVDD) can be assessed by gated myocardial perfusion single-photon emission computed tomography (GMP-SPECT). LVDD is an area of interest in subjects who underwent cardiac resynchronization therapy (CRT). The aim of this post hoc analysis was to assess the role of LVDD in subjects with CRT who were followed up at 6-month period. Left ventricular diastolic dyssynchrony was assessed by GMP-SPECT at baseline and after CRT procedure in 160 subjects from 10 different cardiological centers. CRT procedure was performed as per current guidelines. Outcomes were defined as improvement in ≥1 New York Heart Association (NYHA) class, left ventricular ejection fraction (LVEF) by 5%, and reduction in end-systolic volume (ESV) by 15% and 5% points in Minnesota Living with Heart Failure Questionnaire. LVDD was defined as diastolic phase standard deviation ≥40 ± 14°. Improvement in NYHA functional class occurred in 105 (65.6%), LVEF in 74 (46.3%), decrease in ESV in 86 (53.8%), and Minnesota score in 85 (53.1%) cases. Baseline LV diastolic standard deviation was 53.53° ± 20.85 and at follow-up 40.44° ± 26.1283; (P < 0.001). LVDD was not associated with improvement in clinical outcomes at follow-up. CRT improves both systolic and diastolic dyssynchrony values at 6-month follow-up. LVDD at baseline is correlated with cardiac functionality at follow-up, but not with overall favorable clinical outcomes.

Sections du résumé

BACKGROUND
Left ventricular diastolic dyssynchrony (LVDD) can be assessed by gated myocardial perfusion single-photon emission computed tomography (GMP-SPECT). LVDD is an area of interest in subjects who underwent cardiac resynchronization therapy (CRT). The aim of this post hoc analysis was to assess the role of LVDD in subjects with CRT who were followed up at 6-month period.
MATERIAL & METHODS
Left ventricular diastolic dyssynchrony was assessed by GMP-SPECT at baseline and after CRT procedure in 160 subjects from 10 different cardiological centers. CRT procedure was performed as per current guidelines. Outcomes were defined as improvement in ≥1 New York Heart Association (NYHA) class, left ventricular ejection fraction (LVEF) by 5%, and reduction in end-systolic volume (ESV) by 15% and 5% points in Minnesota Living with Heart Failure Questionnaire. LVDD was defined as diastolic phase standard deviation ≥40 ± 14°.
RESULTS
Improvement in NYHA functional class occurred in 105 (65.6%), LVEF in 74 (46.3%), decrease in ESV in 86 (53.8%), and Minnesota score in 85 (53.1%) cases. Baseline LV diastolic standard deviation was 53.53° ± 20.85 and at follow-up 40.44° ± 26.1283; (P < 0.001). LVDD was not associated with improvement in clinical outcomes at follow-up.
CONCLUSION
CRT improves both systolic and diastolic dyssynchrony values at 6-month follow-up. LVDD at baseline is correlated with cardiac functionality at follow-up, but not with overall favorable clinical outcomes.

Identifiants

pubmed: 31410734
doi: 10.1007/s12350-019-01845-2
pii: 10.1007/s12350-019-01845-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1413-1421

Informations de copyright

© 2019. American Society of Nuclear Cardiology.

Références

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Auteurs

Erick Alexanderson-Rosas (E)

Department of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Juan Badiano Nº 1, Colonia Seccion XVI, Tlalpan, P.C. 14080, Mexico City, Mexico. alexandersonerick@gmail.com.
Department of Physiology, Faculty of Medicine, National Autonomous University of Mexico, Mexico City, Mexico. alexandersonerick@gmail.com.

Nilda Espinola-Zavaleta (N)

Department of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Juan Badiano Nº 1, Colonia Seccion XVI, Tlalpan, P.C. 14080, Mexico City, Mexico.

Ernest V Garcia (EV)

Emory University, Atlanta, GA, USA.

Amalia Peix (A)

Nuclear Medicine Department, Institute of Cardiology, La Habana, Cuba.

Teresa Massardo (T)

Hospital Clinico Universidad de Chile, Santiago, Chile.

Luz M Pabon (LM)

Fundacion Valle del Lili, Cali, Colombia.

Neftali Eduardo Antonio-Villa (NE)

Facultad de Medicina, Universidad Nacional Autonoma de Mexico, Mexico City, Mexico.

Isabel Carvajal-Juarez (I)

Department of Nuclear Cardiology, National Institute of Cardiology Ignacio Chavez, Juan Badiano Nº 1, Colonia Seccion XVI, Tlalpan, P.C. 14080, Mexico City, Mexico.

Claudio T Mesquita (CT)

Hospital Universitario Antonio Pedro, Niteroi, Brazil.

Amelia Jimenez-Heffernan (A)

Hospital Juan Ramon Jimenez, Huelva, Spain.

Chetan Patel (C)

All India Institute of Medical Sciences, New Delhi, India.

Ganesan Karthikeyan (G)

All India Institute of Medical Sciences, New Delhi, India.

Alka Kumar (A)

Dr. B L Kapur Memorial Hospital, New Delhi, India.

Sadaf Butt (S)

Oncology and Radiotherapy Institute (NORI), Islamabad, Pakistan.

Mani Kalaivani (M)

All India Institute of Medical Sciences, New Delhi, India.

Victor Marin (V)

Fundacion Cardioinfantil, Bogota, Colombia.

Olga Morozova (O)

Nuclear Medicine and Diagnostic Imaging Section, International Atomic Energy Agency, Vienna, Austria.

Diana Paez (D)

Nuclear Medicine and Diagnostic Imaging Section, International Atomic Energy Agency, Vienna, Austria.

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