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Effect of atrioventricular optimization on circulating N-terminal pro brain natriuretic peptide following cardiac resynchronization therapy.

Shanmugam, N; Campos, AG; Prada-Delgado, O; Bizrah, M; Valencia, O; Jones, S; Collinson, P; Anderson, L (2013) Effect of atrioventricular optimization on circulating N-terminal pro brain natriuretic peptide following cardiac resynchronization therapy. Eur J Heart Fail, 15 (5). pp. 534-542. ISSN 1879-0844 https://doi.org/10.1093/eurjhf/hft012
SGUL Authors: Anderson, Lisa Collinson, Paul

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Abstract

AIMS: Following CRT, atrioventricular (AV) optimization is not routinely practised. To evaluate its clinical utility, we examined the effect of AV delay optimization on the prognostic biomarker NT-proBNP. METHODS AND RESULTS: We prospectively studied 72 patients (mean age 73 ± 12.5 years, 70.8% male, 55.6% ischaemic) undergoing iterative AV optimization. Patients were divided into those whose nominal setting appeared ideal and not changed (Group 1, n = 22) and those whose AV delay was optimized (Group 2, n = 50). All patients underwent NT-proBNP assessment prior to CRT, and pre- and a median 5 days post-optimization. Compared with Group 1, NT-proBNP fell significantly in Group 2 patients (median 474 pg/mL) following optimization (P = 0.00001). A significant change in filling pattern (defined as a change in AV delay >50 ms) was required in 30% of patients, and it was this subgroup that derived the greater reduction in NT-proBNP levels [-1407 pg/mL, interquartile range (IQR) -3042 to -346 pg/mL] compared with those requiring <50 ms AV delay change (-125 pg/mL, IQR -1038 to 6 pg/mL), P = 0.0011. The benefit of AV optimization was principally observed in reverse remodelling non-responders (median -2167 pg/mL, IQR -3042 to -305 pg/mL) and in patients with a pseudonormal or restrictive filling pattern (median -1407 pg/mL, IQR -2809 to -342 pg/mL), compared with those with more benign diastolic filling (median - 264 pg/mL, IQR -1038 to -21 pg/mL), P = 0.033. CONCLUSIONS: In one-third of patients, major filling pattern changes are achieved with AV optimization, associated with subsequent rapid falls in NT-proBNP. The greater the AV delay change, the larger the NT-proBNP fall, and non-responders and those with restrictive or pseudonormal filling despite CRT are most likely to benefit.

Item Type: Article
Additional Information: This is the peer reviewed version of the following article: Shanmugam, N., Campos, A. G., Prada-Delgado, O., Bizrah, M., Valencia, O., Jones, S., Collinson, P. and Anderson, L. (2013), Effect of atrioventricular optimization on circulating N-terminal pro brain natriuretic peptide following cardiac resynchronization therapy. European Journal of Heart Failure, 15: 534–542, which has been published in final form at http://doi.org/10.1093/eurjhf/hft012. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Keywords: Aged, Aged, 80 and over, Biomarkers, Cardiac Resynchronization Therapy, Echocardiography, Female, Follow-Up Studies, Heart Failure, Humans, Male, Middle Aged, Natriuretic Peptide, Brain, Peptide Fragments, Prognosis, Prospective Studies, Ventricular Remodeling, Humans, Natriuretic Peptide, Brain, Peptide Fragments, Biological Markers, Echocardiography, Prognosis, Follow-Up Studies, Prospective Studies, Ventricular Remodeling, Aged, Aged, 80 and over, Middle Aged, Female, Male, Heart Failure, Cardiac Resynchronization Therapy, Heart failure, Cardiac resynchronization therapy, Optimization of cardiac resynchronization therapy, Atrioventricular delay, NT-proBNP, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, CARDIAC & CARDIOVASCULAR SYSTEMS, Heart failure, Cardiac resynchronization therapy, Optimization of cardiac resynchronization therapy, Atrioventricular delay, NT-proBNP, CHRONIC HEART-FAILURE, DILATED CARDIOMYOPATHY, SYSTOLIC FUNCTION, CONDUCTION DELAY, DOPPLER, CHAMBER, ECHOCARDIOGRAPHY, RECOMMENDATIONS, DEFIBRILLATOR, HEMODYNAMICS, Cardiovascular System & Hematology, 1102 Cardiovascular Medicine And Haematology
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cardiac (INCCCA)
Journal or Publication Title: Eur J Heart Fail
ISSN: 1879-0844
Language: eng
Dates:
DateEvent
27 January 2014Published Online
May 2013Published
14 December 2012Accepted
Publisher License: Publisher's own licence
PubMed ID: 23388091
Web of Science ID: WOS:000318552200009
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/109539
Publisher's version: https://doi.org/10.1093/eurjhf/hft012

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