Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients: A Randomized Crossover Pilot Trial

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Standard

Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients : A Randomized Crossover Pilot Trial. / Ghotbi, Adam Ali; Sander, Mikael; Køber, Lars; Philbert, Berit Thornvig; Gustafsson, Finn; Hagemann, Christoffer; Kjær, Andreas; Jacobsen, Peter K.

I: P L o S One, Bind 10, Nr. 9, e0138124, 2015, s. 1-17.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ghotbi, AA, Sander, M, Køber, L, Philbert, BT, Gustafsson, F, Hagemann, C, Kjær, A & Jacobsen, PK 2015, 'Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients: A Randomized Crossover Pilot Trial', P L o S One, bind 10, nr. 9, e0138124, s. 1-17. https://doi.org/10.1371/journal.pone.0138124

APA

Ghotbi, A. A., Sander, M., Køber, L., Philbert, B. T., Gustafsson, F., Hagemann, C., Kjær, A., & Jacobsen, P. K. (2015). Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients: A Randomized Crossover Pilot Trial. P L o S One, 10(9), 1-17. [e0138124]. https://doi.org/10.1371/journal.pone.0138124

Vancouver

Ghotbi AA, Sander M, Køber L, Philbert BT, Gustafsson F, Hagemann C o.a. Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients: A Randomized Crossover Pilot Trial. P L o S One. 2015;10(9):1-17. e0138124. https://doi.org/10.1371/journal.pone.0138124

Author

Ghotbi, Adam Ali ; Sander, Mikael ; Køber, Lars ; Philbert, Berit Thornvig ; Gustafsson, Finn ; Hagemann, Christoffer ; Kjær, Andreas ; Jacobsen, Peter K. / Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients : A Randomized Crossover Pilot Trial. I: P L o S One. 2015 ; Bind 10, Nr. 9. s. 1-17.

Bibtex

@article{04c3084c51bd4856851f83c9412241ce,
title = "Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients: A Randomized Crossover Pilot Trial",
abstract = "BACKGROUND: The optimal pacing rate during cardiac resynchronization therapy (CRT) is unknown. Therefore, we investigated the impact of changing basal pacing frequencies on autonomic nerve function, cardiopulmonary exercise capacity and self-perceived quality of life (QoL).METHODS: Twelve CRT patients with non-ischemic heart failure (NYHA class II-III) were enrolled in a randomized, double-blind, crossover trial, in which the basal pacing rate was set at DDD-60 and DDD-80 for 3 months (DDD-R for 2 patients). At baseline, 3 months and 6 months, we assessed sympathetic nerve activity by microneurography (MSNA), peak oxygen consumption (pVO2), N-terminal pro-brain natriuretic peptide (p-NT-proBNP), echocardiography and QoL.RESULTS: DDD-80 pacing for 3 months increased the mean heart rate from 77.3 to 86.1 (p = 0.001) and reduced sympathetic activity compared to DDD-60 (51±14 bursts/100 cardiac cycles vs. 64±14 bursts/100 cardiac cycles, p<0.05). The mean pVO2 increased non-significantly from 15.6±6 mL/min/kg during DDD-60 to 16.7±6 mL/min/kg during DDD-80, and p-NT-proBNP remained unchanged. The QoL score indicated that DDD-60 was better tolerated.CONCLUSION: In CRT patients with non-ischemic heart failure, 3 months of DDD-80 pacing decreased sympathetic outflow (burst incidence only) compared to DDD-60 pacing. However, Qol scores were better during the lower pacing rate. Further and larger scale investigations are indicated.TRIAL REGISTRATION: ClinicalTrials.gov NCT02258061.",
keywords = "Aged, Calibration, Cardiac Resynchronization Therapy, Cross-Over Studies, Double-Blind Method, Exercise Tolerance, Female, Heart Failure, Heart Rate, Humans, Male, Middle Aged, Natriuretic Peptide, Brain, Oxygen Consumption, Peptide Fragments, Pilot Projects, Quality of Life",
author = "Ghotbi, {Adam Ali} and Mikael Sander and Lars K{\o}ber and Philbert, {Berit Thornvig} and Finn Gustafsson and Christoffer Hagemann and Andreas Kj{\ae}r and Jacobsen, {Peter K}",
year = "2015",
doi = "10.1371/journal.pone.0138124",
language = "English",
volume = "10",
pages = "1--17",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "9",

}

RIS

TY - JOUR

T1 - Optimal Cardiac Resynchronization Therapy Pacing Rate in Non-Ischemic Heart Failure Patients

T2 - A Randomized Crossover Pilot Trial

AU - Ghotbi, Adam Ali

AU - Sander, Mikael

AU - Køber, Lars

AU - Philbert, Berit Thornvig

AU - Gustafsson, Finn

AU - Hagemann, Christoffer

AU - Kjær, Andreas

AU - Jacobsen, Peter K

PY - 2015

Y1 - 2015

N2 - BACKGROUND: The optimal pacing rate during cardiac resynchronization therapy (CRT) is unknown. Therefore, we investigated the impact of changing basal pacing frequencies on autonomic nerve function, cardiopulmonary exercise capacity and self-perceived quality of life (QoL).METHODS: Twelve CRT patients with non-ischemic heart failure (NYHA class II-III) were enrolled in a randomized, double-blind, crossover trial, in which the basal pacing rate was set at DDD-60 and DDD-80 for 3 months (DDD-R for 2 patients). At baseline, 3 months and 6 months, we assessed sympathetic nerve activity by microneurography (MSNA), peak oxygen consumption (pVO2), N-terminal pro-brain natriuretic peptide (p-NT-proBNP), echocardiography and QoL.RESULTS: DDD-80 pacing for 3 months increased the mean heart rate from 77.3 to 86.1 (p = 0.001) and reduced sympathetic activity compared to DDD-60 (51±14 bursts/100 cardiac cycles vs. 64±14 bursts/100 cardiac cycles, p<0.05). The mean pVO2 increased non-significantly from 15.6±6 mL/min/kg during DDD-60 to 16.7±6 mL/min/kg during DDD-80, and p-NT-proBNP remained unchanged. The QoL score indicated that DDD-60 was better tolerated.CONCLUSION: In CRT patients with non-ischemic heart failure, 3 months of DDD-80 pacing decreased sympathetic outflow (burst incidence only) compared to DDD-60 pacing. However, Qol scores were better during the lower pacing rate. Further and larger scale investigations are indicated.TRIAL REGISTRATION: ClinicalTrials.gov NCT02258061.

AB - BACKGROUND: The optimal pacing rate during cardiac resynchronization therapy (CRT) is unknown. Therefore, we investigated the impact of changing basal pacing frequencies on autonomic nerve function, cardiopulmonary exercise capacity and self-perceived quality of life (QoL).METHODS: Twelve CRT patients with non-ischemic heart failure (NYHA class II-III) were enrolled in a randomized, double-blind, crossover trial, in which the basal pacing rate was set at DDD-60 and DDD-80 for 3 months (DDD-R for 2 patients). At baseline, 3 months and 6 months, we assessed sympathetic nerve activity by microneurography (MSNA), peak oxygen consumption (pVO2), N-terminal pro-brain natriuretic peptide (p-NT-proBNP), echocardiography and QoL.RESULTS: DDD-80 pacing for 3 months increased the mean heart rate from 77.3 to 86.1 (p = 0.001) and reduced sympathetic activity compared to DDD-60 (51±14 bursts/100 cardiac cycles vs. 64±14 bursts/100 cardiac cycles, p<0.05). The mean pVO2 increased non-significantly from 15.6±6 mL/min/kg during DDD-60 to 16.7±6 mL/min/kg during DDD-80, and p-NT-proBNP remained unchanged. The QoL score indicated that DDD-60 was better tolerated.CONCLUSION: In CRT patients with non-ischemic heart failure, 3 months of DDD-80 pacing decreased sympathetic outflow (burst incidence only) compared to DDD-60 pacing. However, Qol scores were better during the lower pacing rate. Further and larger scale investigations are indicated.TRIAL REGISTRATION: ClinicalTrials.gov NCT02258061.

KW - Aged

KW - Calibration

KW - Cardiac Resynchronization Therapy

KW - Cross-Over Studies

KW - Double-Blind Method

KW - Exercise Tolerance

KW - Female

KW - Heart Failure

KW - Heart Rate

KW - Humans

KW - Male

KW - Middle Aged

KW - Natriuretic Peptide, Brain

KW - Oxygen Consumption

KW - Peptide Fragments

KW - Pilot Projects

KW - Quality of Life

U2 - 10.1371/journal.pone.0138124

DO - 10.1371/journal.pone.0138124

M3 - Journal article

C2 - 26382243

VL - 10

SP - 1

EP - 17

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 9

M1 - e0138124

ER -

ID: 162453019