Impact and Modifiers of Ventricular Pacing in Patients With Single Ventricle Circulation
Palliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPMv) may be associated with additional adverse long-term outcomes. The goal of this study was to quant...
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Published in | Journal of the American College of Cardiology Vol. 80; no. 9; pp. 902 - 914 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
30.08.2022
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Online Access | Get full text |
ISSN | 0735-1097 1558-3597 1558-3597 |
DOI | 10.1016/j.jacc.2022.05.053 |
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Abstract | Palliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPMv) may be associated with additional adverse long-term outcomes.
The goal of this study was to quantify the attributable risk of PPMv in patients with SV, and to identify modifiable risk factors.
This international study was sponsored by the Pediatric and Congenital Electrophysiology Society. Centers contributed baseline and longitudinal data for functionally SV patients with PPMv. Enrollment was at implantation. Controls were matched 1:1 to PPMv subjects by ventricular morphology and sex, identified within center, and enrolled at matched age. Primary outcome was transplantation or death.
In total, 236 PPMv subjects and 213 matched controls were identified (22 centers, 9 countries). Median age at enrollment was 5.3 years (quartiles: 1.5-13.2 years), follow-up 6.9 years (3.4-11.6 years). Median percent ventricular pacing (Vp) was 90.8% (25th-75th percentile: 4.3%-100%) in the PPMv cohort. Across 213 matched pairs, multivariable HR for death/transplant associated with PPMv was 3.8 (95% CI 1.9-7.6; P < 0.001). Within the PPMv population, higher Vp (HR: 1.009 per %; P = 0.009), higher QRS z-score (HR: 1.19; P = 0.009) and nonapical lead position (HR: 2.17; P = 0.042) were all associated with death/transplantation.
PPMv in patients with SV is associated with increased risk of heart transplantation and death, despite controlling for increased associated morbidity of the PPMv cohort. Increased Vp, higher QRS z-score, and nonapical ventricular lead position are all associated with higher risk of adverse outcome and may be modifiable risk factors.
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AbstractList | Palliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPMv) may be associated with additional adverse long-term outcomes.BACKGROUNDPalliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPMv) may be associated with additional adverse long-term outcomes.The goal of this study was to quantify the attributable risk of PPMv in patients with SV, and to identify modifiable risk factors.OBJECTIVESThe goal of this study was to quantify the attributable risk of PPMv in patients with SV, and to identify modifiable risk factors.This international study was sponsored by the Pediatric and Congenital Electrophysiology Society. Centers contributed baseline and longitudinal data for functionally SV patients with PPMv. Enrollment was at implantation. Controls were matched 1:1 to PPMv subjects by ventricular morphology and sex, identified within center, and enrolled at matched age. Primary outcome was transplantation or death.METHODSThis international study was sponsored by the Pediatric and Congenital Electrophysiology Society. Centers contributed baseline and longitudinal data for functionally SV patients with PPMv. Enrollment was at implantation. Controls were matched 1:1 to PPMv subjects by ventricular morphology and sex, identified within center, and enrolled at matched age. Primary outcome was transplantation or death.In total, 236 PPMv subjects and 213 matched controls were identified (22 centers, 9 countries). Median age at enrollment was 5.3 years (quartiles: 1.5-13.2 years), follow-up 6.9 years (3.4-11.6 years). Median percent ventricular pacing (Vp) was 90.8% (25th-75th percentile: 4.3%-100%) in the PPMv cohort. Across 213 matched pairs, multivariable HR for death/transplant associated with PPMv was 3.8 (95% CI 1.9-7.6; P < 0.001). Within the PPMv population, higher Vp (HR: 1.009 per %; P = 0.009), higher QRS z-score (HR: 1.19; P = 0.009) and nonapical lead position (HR: 2.17; P = 0.042) were all associated with death/transplantation.RESULTSIn total, 236 PPMv subjects and 213 matched controls were identified (22 centers, 9 countries). Median age at enrollment was 5.3 years (quartiles: 1.5-13.2 years), follow-up 6.9 years (3.4-11.6 years). Median percent ventricular pacing (Vp) was 90.8% (25th-75th percentile: 4.3%-100%) in the PPMv cohort. Across 213 matched pairs, multivariable HR for death/transplant associated with PPMv was 3.8 (95% CI 1.9-7.6; P < 0.001). Within the PPMv population, higher Vp (HR: 1.009 per %; P = 0.009), higher QRS z-score (HR: 1.19; P = 0.009) and nonapical lead position (HR: 2.17; P = 0.042) were all associated with death/transplantation.PPMv in patients with SV is associated with increased risk of heart transplantation and death, despite controlling for increased associated morbidity of the PPMv cohort. Increased Vp, higher QRS z-score, and nonapical ventricular lead position are all associated with higher risk of adverse outcome and may be modifiable risk factors.CONCLUSIONSPPMv in patients with SV is associated with increased risk of heart transplantation and death, despite controlling for increased associated morbidity of the PPMv cohort. Increased Vp, higher QRS z-score, and nonapical ventricular lead position are all associated with higher risk of adverse outcome and may be modifiable risk factors. AbstractBackgroundPalliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPM v) may be associated with additional adverse long-term outcomes. ObjectivesThe goal of this study was to quantify the attributable risk of PPM v in patients with SV, and to identify modifiable risk factors. MethodsThis international study was sponsored by the Pediatric and Congenital Electrophysiology Society. Centers contributed baseline and longitudinal data for functionally SV patients with PPM v. Enrollment was at implantation. Controls were matched 1:1 to PPM v subjects by ventricular morphology and sex, identified within center, and enrolled at matched age. Primary outcome was transplantation or death. ResultsIn total, 236 PPM v subjects and 213 matched controls were identified (22 centers, 9 countries). Median age at enrollment was 5.3 years (quartiles: 1.5-13.2 years), follow-up 6.9 years (3.4-11.6 years). Median percent ventricular pacing (Vp) was 90.8% (25th-75th percentile: 4.3%-100%) in the PPM v cohort. Across 213 matched pairs, multivariable HR for death/transplant associated with PPM v was 3.8 (95% CI 1.9-7.6; P < 0.001). Within the PPM v population, higher Vp (HR: 1.009 per %; P = 0.009), higher QRS z-score (HR: 1.19; P = 0.009) and nonapical lead position (HR: 2.17; P = 0.042) were all associated with death/transplantation. ConclusionsPPM v in patients with SV is associated with increased risk of heart transplantation and death, despite controlling for increased associated morbidity of the PPM v cohort. Increased Vp, higher QRS z-score, and nonapical ventricular lead position are all associated with higher risk of adverse outcome and may be modifiable risk factors. Palliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a permanent ventricular pacing system (PPMv) may be associated with additional adverse long-term outcomes. The goal of this study was to quantify the attributable risk of PPMv in patients with SV, and to identify modifiable risk factors. This international study was sponsored by the Pediatric and Congenital Electrophysiology Society. Centers contributed baseline and longitudinal data for functionally SV patients with PPMv. Enrollment was at implantation. Controls were matched 1:1 to PPMv subjects by ventricular morphology and sex, identified within center, and enrolled at matched age. Primary outcome was transplantation or death. In total, 236 PPMv subjects and 213 matched controls were identified (22 centers, 9 countries). Median age at enrollment was 5.3 years (quartiles: 1.5-13.2 years), follow-up 6.9 years (3.4-11.6 years). Median percent ventricular pacing (Vp) was 90.8% (25th-75th percentile: 4.3%-100%) in the PPMv cohort. Across 213 matched pairs, multivariable HR for death/transplant associated with PPMv was 3.8 (95% CI 1.9-7.6; P < 0.001). Within the PPMv population, higher Vp (HR: 1.009 per %; P = 0.009), higher QRS z-score (HR: 1.19; P = 0.009) and nonapical lead position (HR: 2.17; P = 0.042) were all associated with death/transplantation. PPMv in patients with SV is associated with increased risk of heart transplantation and death, despite controlling for increased associated morbidity of the PPMv cohort. Increased Vp, higher QRS z-score, and nonapical ventricular lead position are all associated with higher risk of adverse outcome and may be modifiable risk factors. [Display omitted] |
Author | Mangat, Jasveer Chubb, Henry Kwok, Sit Yee Horndasch, Michaela Tanel, Ronn Janousek, Jan Young, Ming-Lon Escudero, Carolina Regan, William Dubin, Anne M. Hill, Allison C. Balaji, Seshadri Pflaumer, Andreas Asakai, Hiroko Bradley, David J. Ochoa Nunez, Luis A. Paul, Thomas Mah, Douglas Czosek, Richard J. Malloy-Walton, Lindsey McElhinney, Doff B. Fischbach, Peter Asaki, S. Yukiko Rosenthal, Eric Bulic, Anica Moore, Jeremy P. Fumanelli, Jennifer |
Author_xml | – sequence: 1 givenname: Henry surname: Chubb fullname: Chubb, Henry email: mhchubb@stanford.edu organization: Division of Pediatric Cardiology, Department of Pediatrics, Stanford University, Stanford, California, USA – sequence: 2 givenname: Anica surname: Bulic fullname: Bulic, Anica organization: Labatt Family Heart Centre, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada – sequence: 3 givenname: Douglas surname: Mah fullname: Mah, Douglas organization: Department of Cardiology, Boston Children’s Hospital, Boston, Massachusetts, USA – sequence: 4 givenname: Jeremy P. surname: Moore fullname: Moore, Jeremy P. organization: Division of Cardiology, Department of Pediatrics, UCLA Health System, Los Angeles, California, USA – sequence: 5 givenname: Jan surname: Janousek fullname: Janousek, Jan organization: Children's Heart Centre, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic – sequence: 6 givenname: Jennifer surname: Fumanelli fullname: Fumanelli, Jennifer organization: Children's Heart Centre, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic – sequence: 7 givenname: S. Yukiko surname: Asaki fullname: Asaki, S. Yukiko organization: Primary Children’s Hospital, University of Utah, Salt Lake City, Utah, USA – sequence: 8 givenname: Andreas orcidid: 0000-0002-3830-3643 surname: Pflaumer fullname: Pflaumer, Andreas organization: The Royal Children’s Hospital, MCRI and University of Melbourne, Melbourne, Victoria, Australia – sequence: 9 givenname: Allison C. surname: Hill fullname: Hill, Allison C. organization: Division of Cardiology, Children’s Hospital Los Angeles, Los Angeles, California, USA – sequence: 10 givenname: Carolina surname: Escudero fullname: Escudero, Carolina organization: Department of Pediatrics, Division of Pediatric Cardiology, University of Alberta, Stollery Children’s Hospital, Edmonton, Alberta, Canada – sequence: 11 givenname: Sit Yee surname: Kwok fullname: Kwok, Sit Yee organization: Cardiology Centre, Department of Paediatrics and Adolescent Medicine, Hong Kong Children’s Hospital, Hong Kong SAR, China – sequence: 12 givenname: Jasveer surname: Mangat fullname: Mangat, Jasveer organization: Paediatric Cardiology, Great Ormond Street, London, United Kingdom – sequence: 13 givenname: Luis A. surname: Ochoa Nunez fullname: Ochoa Nunez, Luis A. organization: University of Iowa Healthcare, Iowa City, Iowa, USA – sequence: 14 givenname: Seshadri surname: Balaji fullname: Balaji, Seshadri organization: Department of Pediatrics, Division of Cardiology, Oregon Health & Science University, Portland, Oregon, USA – sequence: 15 givenname: Eric surname: Rosenthal fullname: Rosenthal, Eric organization: Paediatric Cardiology, Evelina London Children’s Hospital, London, United Kingdom – sequence: 16 givenname: William surname: Regan fullname: Regan, William organization: Paediatric Cardiology, Evelina London Children’s Hospital, London, United Kingdom – sequence: 17 givenname: Michaela surname: Horndasch fullname: Horndasch, Michaela organization: Department of Congenital Heart Diseases and Pediatric Cardiology, German Heart Center Munich, Munich, Germany – sequence: 18 givenname: Hiroko surname: Asakai fullname: Asakai, Hiroko organization: Department of Paediatrics, University of Tokyo Hospital, Tokyo, Japan – sequence: 19 givenname: Ronn surname: Tanel fullname: Tanel, Ronn organization: Division of Pediatric Cardiology, Department of Pediatrics, UCSF School of Medicine, San Francisco, California, USA – sequence: 20 givenname: Richard J. surname: Czosek fullname: Czosek, Richard J. organization: The Heart Institute, Cincinnati Children’s Hospital Medical Center, Ohio, USA – sequence: 21 givenname: Ming-Lon surname: Young fullname: Young, Ming-Lon organization: Joe DiMaggio Children’s Hospital, Hollywood, Florida, USA – sequence: 22 givenname: David J. surname: Bradley fullname: Bradley, David J. organization: University of Michigan, CS Mott Children’s Hospital, Ann Arbor, Michigan, USA – sequence: 23 givenname: Thomas surname: Paul fullname: Paul, Thomas organization: Department of Pediatric Cardiology, Georg-August-University Medical Center, Göttingen, Germany – sequence: 24 givenname: Peter surname: Fischbach fullname: Fischbach, Peter organization: Sibley Heart Center, Atlanta, Georgia, USA – sequence: 25 givenname: Lindsey surname: Malloy-Walton fullname: Malloy-Walton, Lindsey organization: Children’s Mercy Hospital, University of Missouri, Kansas City, Missouri, USA – sequence: 26 givenname: Doff B. surname: McElhinney fullname: McElhinney, Doff B. organization: Division of Pediatric Cardiology, Department of Pediatrics, Stanford University, Stanford, California, USA – sequence: 27 givenname: Anne M. surname: Dubin fullname: Dubin, Anne M. organization: Division of Pediatric Cardiology, Department of Pediatrics, Stanford University, Stanford, California, USA |
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Keywords | heart failure SV CRT cardiac resynchronization therapy single ventricle ECG PLE PPMv pediatric AVVR congenital heart disease VAD cardiac transplant Vp Glenn electrical dyssynchrony Fontan ventricular pacing protein losing enteropathy PPM v ventricular assist device electrocardiogram permanent pacemaker with ventricular lead atrioventricular valve regurgitation |
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Snippet | Palliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified that the need for a... AbstractBackgroundPalliation of the single ventricle (SV) circulation is associated with a burden of lifelong complications. Previous studies have identified... |
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SubjectTerms | cardiac resynchronization therapy cardiac transplant Cardiovascular congenital heart disease electrical dyssynchrony Fontan Glenn heart failure pediatric single ventricle |
Title | Impact and Modifiers of Ventricular Pacing in Patients With Single Ventricle Circulation |
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