Prospective Study of Lead-associated Tricuspid Regurgitation in Patients Undergoing New Transvalvular Lead Insertion

The prevalence of tricuspid regurgitation (TR) in patients with a pacemaker or ICD/CRT device varies widely, ranging from 5% to 45% across different study protocols. To date, only retrospective analyses have shown that implantation of a device with a transvalvular lead can cause or worsen TR, highlighting the importance of early diagnosis. The aim of this study is to prospectively evaluate patients indicated for cardiac electronic device implantation to document the incidence of newly developed regurgitation (greater than trace) or worsening of existing regurgitation (by at least one grade). Additionally, the study will investigate predictive factors for the development or progression of TR.

Inclusion criteria

• medically indicated for pacemaker, ICD- or CRT implantation
• No previous diagnosis of severe tricuspid regurgitation on enrollment
• No existing transvalvular device (must be first implantation)
• No other diagnosed severe valvular heart disease
• Not previous diagnosis with pre-capillary pulmonary hypertension
• No previous diagnosis of structural disease of the right ventricle (i.e. ACM, cardiac sarcoidosis, carcinoid...)

Exclusion criteria

• Patients unable to give consent
• Under the age of 18 years
• Relevant pre-capillary pulmonary hypertension according to decision of the heart-team (sPAP echo >70 mmHg)
• Severe tricuspid valve regurgitation (Grade 3 or worse) on enrollment
• Patients who have undergone Lead-explantation
• Exisiting valvular heart disease requiring treatment according to the decision of the heart-team. These patients may be enrolled in the study following treatment.
• Previous tricuspid valve surgery
• Patients with congenital heart disease (i.e. tetralogy of fallot, Ebstein's anomaly,...)
• Pregnant or breastfeeding women
• Life expectancy < 12 months