Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy
Background: Cardiac resynchronization therapy (CRT) produces acute changes in electric resynchronization that can be measured noninvasively with electrocardiographic body surface mapping (ECGi). The relation between baseline acute electrophysiology metrics and their manipulation with CRT and reverse...
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2021-02-01
|
Series: | Heart Rhythm O2 |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2666501821000064 |
id |
doaj-b84897e7d6e04ab2bbe7ff49f0097af5 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas Jackson, MBBS Simon Claridge, PhD Jonathan Behar, PhD Cheng Yao, PhD Mark Elliott, MBBS Vishal Mehta, MBBS Justin Gould, PhD Baldeep Sidhu, MBBS Helder Pereira, MSc Steven Niederer, PhD Gerald Carr-White, PhD Christopher A. Rinaldi, MD, FHRS |
spellingShingle |
Thomas Jackson, MBBS Simon Claridge, PhD Jonathan Behar, PhD Cheng Yao, PhD Mark Elliott, MBBS Vishal Mehta, MBBS Justin Gould, PhD Baldeep Sidhu, MBBS Helder Pereira, MSc Steven Niederer, PhD Gerald Carr-White, PhD Christopher A. Rinaldi, MD, FHRS Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy Heart Rhythm O2 Body surface mapping Cardiac resynchronization therapy ECG imaging Heart failure LV activation mapping |
author_facet |
Thomas Jackson, MBBS Simon Claridge, PhD Jonathan Behar, PhD Cheng Yao, PhD Mark Elliott, MBBS Vishal Mehta, MBBS Justin Gould, PhD Baldeep Sidhu, MBBS Helder Pereira, MSc Steven Niederer, PhD Gerald Carr-White, PhD Christopher A. Rinaldi, MD, FHRS |
author_sort |
Thomas Jackson, MBBS |
title |
Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
title_short |
Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
title_full |
Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
title_fullStr |
Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
title_full_unstemmed |
Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
title_sort |
noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapy |
publisher |
Elsevier |
series |
Heart Rhythm O2 |
issn |
2666-5018 |
publishDate |
2021-02-01 |
description |
Background: Cardiac resynchronization therapy (CRT) produces acute changes in electric resynchronization that can be measured noninvasively with electrocardiographic body surface mapping (ECGi). The relation between baseline acute electrophysiology metrics and their manipulation with CRT and reverse remodeling is unclear. Objective: To test (ECGi) derived parameters of electrical activation as predictors of volumetric response to CRT. Methods: ECGi was performed in 21 patients directly following CRT implant. Activation parameters (left ventricular total activation time [LVtat], global biventricular total activation time [VVtat], global left/right ventricular electrical synchrony [VVsync], and global left ventricular dispersion of activation times [LVdisp]) were measured at baseline and following echocardiographically optimized CRT. Remodeling response (>15% reduction left ventricular end-systolic volume) was assessed 6 months post CRT. Results: Patients were aged 68.9 ± 12.1 years, 81% were male, and 57% were ischemic. Baseline measures of dyssynchrony were more pronounced in left bundle branch block (LBBB) vs non-LBBB. ECGi demonstrated a trend of greater interventricular dyssynchrony between responders and nonresponders that did not reach statistical significance (VVsync: -45.7 ± 22.4 ms vs -25.1 ± 29.3 ms, P = .227). Remaining activation parameters were similar between responders and nonresponders (VVtat 101 ± 22.0 ms vs 98.9 ± 23.4 ms, P = .838; LVtat 86.4 ± 17.1 ms vs 85.1 ± 27.7 ms, P = .904; LVdisp 28.2 ± 6.3 ms vs 27.0 ± 8.7 ms, P = .726). In volumetric responders activation parameters were significantly improved with CRT compared to nonresponders: VV sync (-45.67 ± 22.41 ms vs 2.33±18.87 ms, P = .001), VVtat (101 ± 22.04 ms vs 71 ± 14.01 ms, P = .002), LVtat (86.44 ± 17.15 ms vs 67.67 ± 11.31 ms, P = .006), and LVdisp (28.22 ± 6.3 ms vs 21.56 ± 4.45 ms, P = .008). Conclusion: Baseline ECGi activation times did not predict CRT volumetric response. Volumetric responders exhibited significant improvements in ECGi-derived metrics with CRT. ECGi does not select CRT candidates but may be a useful adjunct to guide left ventricle lead implants and to perform postimplant CRT optimization. |
topic |
Body surface mapping Cardiac resynchronization therapy ECG imaging Heart failure LV activation mapping |
url |
http://www.sciencedirect.com/science/article/pii/S2666501821000064 |
work_keys_str_mv |
AT thomasjacksonmbbs noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT simonclaridgephd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT jonathanbeharphd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT chengyaophd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT markelliottmbbs noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT vishalmehtambbs noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT justingouldphd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT baldeepsidhumbbs noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT helderpereiramsc noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT stevenniedererphd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT geraldcarrwhitephd noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy AT christopherarinaldimdfhrs noninvasiveelectrocardiographicassessmentofventricularactivationandremodelingresponsetocardiacresynchronizationtherapy |
_version_ |
1717817879202627584 |
spelling |
doaj-b84897e7d6e04ab2bbe7ff49f0097af52021-09-03T04:47:31ZengElsevierHeart Rhythm O22666-50182021-02-01211218Noninvasive electrocardiographic assessment of ventricular activation and remodeling response to cardiac resynchronization therapyThomas Jackson, MBBS0Simon Claridge, PhD1Jonathan Behar, PhD2Cheng Yao, PhD3Mark Elliott, MBBS4Vishal Mehta, MBBS5Justin Gould, PhD6Baldeep Sidhu, MBBS7Helder Pereira, MSc8Steven Niederer, PhD9Gerald Carr-White, PhD10Christopher A. Rinaldi, MD, FHRS11School of Biomedical Engineering and Imaging Sciences, King’s College London, London, United Kingdom; Address reprint requests and correspondence: Dr Thomas Jackson, Department of Cardiology, Salisbury NHS Foundation Trust, Salisbury, Wiltshire SP2 8BJ, UK.School of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomMedtronic Ltd./CardioInsight, Cleveland, OhioSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United KingdomMedtronic Ltd./CardioInsight, Cleveland, OhioSchool of Biomedical Engineering and Imaging Sciences, King’s College London, London, United Kingdom; Guy’s and St Thomas’ NHS Trust, London, United KingdomBackground: Cardiac resynchronization therapy (CRT) produces acute changes in electric resynchronization that can be measured noninvasively with electrocardiographic body surface mapping (ECGi). The relation between baseline acute electrophysiology metrics and their manipulation with CRT and reverse remodeling is unclear. Objective: To test (ECGi) derived parameters of electrical activation as predictors of volumetric response to CRT. Methods: ECGi was performed in 21 patients directly following CRT implant. Activation parameters (left ventricular total activation time [LVtat], global biventricular total activation time [VVtat], global left/right ventricular electrical synchrony [VVsync], and global left ventricular dispersion of activation times [LVdisp]) were measured at baseline and following echocardiographically optimized CRT. Remodeling response (>15% reduction left ventricular end-systolic volume) was assessed 6 months post CRT. Results: Patients were aged 68.9 ± 12.1 years, 81% were male, and 57% were ischemic. Baseline measures of dyssynchrony were more pronounced in left bundle branch block (LBBB) vs non-LBBB. ECGi demonstrated a trend of greater interventricular dyssynchrony between responders and nonresponders that did not reach statistical significance (VVsync: -45.7 ± 22.4 ms vs -25.1 ± 29.3 ms, P = .227). Remaining activation parameters were similar between responders and nonresponders (VVtat 101 ± 22.0 ms vs 98.9 ± 23.4 ms, P = .838; LVtat 86.4 ± 17.1 ms vs 85.1 ± 27.7 ms, P = .904; LVdisp 28.2 ± 6.3 ms vs 27.0 ± 8.7 ms, P = .726). In volumetric responders activation parameters were significantly improved with CRT compared to nonresponders: VV sync (-45.67 ± 22.41 ms vs 2.33±18.87 ms, P = .001), VVtat (101 ± 22.04 ms vs 71 ± 14.01 ms, P = .002), LVtat (86.44 ± 17.15 ms vs 67.67 ± 11.31 ms, P = .006), and LVdisp (28.22 ± 6.3 ms vs 21.56 ± 4.45 ms, P = .008). Conclusion: Baseline ECGi activation times did not predict CRT volumetric response. Volumetric responders exhibited significant improvements in ECGi-derived metrics with CRT. ECGi does not select CRT candidates but may be a useful adjunct to guide left ventricle lead implants and to perform postimplant CRT optimization.http://www.sciencedirect.com/science/article/pii/S2666501821000064Body surface mappingCardiac resynchronization therapyECG imagingHeart failureLV activation mapping |