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Haemodynamic Consequences of Targeted Single- and Dual-site Right Ventricular Pacing in Adults with Congenital Heart Disease Undergoing Surgical Pulmonary Valve Replacement

Overview
Journal Europace
Date 2014 Nov 6
PMID 25371427
Citations 6
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Abstract

Aims: The purpose of this study was to create an epicardial electroanatomic map of the right ventricle (RV) and then apply post-operative-targeted single- and dual-site RV temporary pacing with measurement of haemodynamic parameters. Cardiac resynchronization therapy is an established treatment for symptomatic left ventricular (LV) dysfunction. In congenital heart disease, RV dysfunction is a common cause of morbidity-little is known regarding the potential benefits of CRT in this setting.

Methods And Results: Sixteen adults (age = 32 ± 8 years; 6 M, 10 F) with right bundle branch block (RBBB) and repaired tetralogy of Fallot (n = 8) or corrected congenital pulmonary stenosis (n = 8) undergoing surgical pulmonary valve replacement (PVR) for pulmonary regurgitation underwent epicardial RV mapping and haemodynamic assessment of random pacing configurations including the site of latest RV activation. The pre-operative pulmonary regurgitant fraction was 49 ± 10%; mean LV end-diastolic volume (EDV) 85 ± 19 mL/min/m(2) and RVEDV 183 ± 89 mL/min/m(2) on cardiac magnetic resonance imaging. The mean pre-operative QRS duration is 136 ± 26 ms. The commonest site of latest activation was the RV free wall and DDD pacing here alone or combined with RV apical pacing resulted in significant increases in cardiac output (CO) vs. AAI pacing (P < 0.01 all measures). DDDRV alternative site pacing significantly improved CO by 16% vs. AAI (P = 0.018), and 8.5% vs. DDDRV apical pacing (P = 0.02).

Conclusion: Single-site RV pacing targeted to the region of latest activation in patients with RBBB undergoing PVR induces acute improvements in haemodynamics and supports the concept of 'RV CRT'. Targeted pacing in such patients has therapeutic potential both post-operatively and in the long term.

Citing Articles

Tetralogy of Fallot Across the Lifespan: A Focus on the Right Ventricle.

Ganni E, Ho S, Reddy S, Therrien J, Kearney K, Roche S CJC Pediatr Congenit Heart Dis. 2024; 2(6Part A):283-300.

PMID: 38161676 PMC: 10755834. DOI: 10.1016/j.cjcpc.2023.10.009.


Advancing the science of management of arrhythmic disease in children and adult congenital heart disease patients within the last 25 years.

Paul T, Krause U, Sanatani S, Etheridge S Europace. 2023; 25(8).

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Right ventricular dilatation in patients with pulmonary regurgitation after repair of tetralogy of Fallot: How fast does it progress?.

Hoelscher M, Bonassin F, Oxenius A, Seifert B, Leonardi B, Kellenberger C Ann Pediatr Cardiol. 2020; 13(4):294-300.

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The impact of right bundle branch block on right ventricular size and function assessed by three-dimensional speckle-tracking echocardiography.

Nakazawa N, Ishizu T, Seo Y, Kawamatsu N, Sato K, Yamamoto M Heart Vessels. 2019; 35(4):576-585.

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Resynchronization Therapy for Patients with Congenital Heart Disease: Are We Ready for Prime Time?.

Anjewierden S, Aziz P Curr Cardiol Rep. 2018; 20(9):75.

PMID: 30022366 DOI: 10.1007/s11886-018-1015-6.


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