NCT04554160

Arrhythmias in Pulmonary Hypertension Assessed by Continuous Long-term Cardiac Monitoring

ArrhythmiaS in Pulmonary arterIal hypeRtEnsion and Right Heart Failure Assessed by Continuous Long-term Cardiac Monitoring

• Status: Unknown
• Phase: —
• Study type: Observational
• Enrollment: 40 (estimated)
• Sponsor: Rigshospitalet, Denmark · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: —

Summary

Arrhythmias are considered a prominent phenomenon in pulmonary hypertension (PH) as the disease progresses. According primarily to retrospective studies with up to 24 hours of monitoring, supraventricular tachycardias (SVT) can be found in 8-35% of patients, with significant impact on survival. Furthermore, a few prospective studies to date deploying short-term monitoring (10 minutes-24 hours) have revealed lower heart rate variability (HRV) in patients with pulmonary arterial hypertension (PAH). In ASPIRE arrhythmias and heart rate variability is being assessed via long term monitoring. Currently the the loop-recorder is considered the gold standard for long-term continuous cardiac montoring. A non-invasive continuous monitoring could be of a great benefit for the patients, and could potentially contribute to treatment optimization. The study will assess apple watches as a non-invasive tool compared to to the loop recorder, which is considered as the current gold standard. Additionally, the study seeks to assess apple watches for monitoring as an independent wearable for risk assessment in PH.

Detailed description

In general there is a lack of evidence of the arrhythmic burden in PH. The present study is the first to apply continuous long-term cardiac monitoring in patients with PH to describe the prevalence of arrhythmias in PH by continuous long-term cardiac monitoring. Furthermore, the correlation between heart rate variability and risk assessment parameters including WHO functional class (FC), NT-proBNP, 6MWT, cardiac parameters and cardiac function will be studies. A few prospective studies have demonstrated lower HRV in PH than in healthy individuals, however only based on short-term monitoring (20 minutes to 24 hour) and only in a few patients. In retrospective studies, a higher mortality in children with PAH and low HRV has been shown with 24 hour Holter monitoring. Consequently, there is a lack of evidence regarding right heart failure and the prognostic value of HRV. Risk assessment in PH is essential in the selection of treatment in PH and for prognosis in the study ASPIRE the investigators will assess the use of heart rate variability in pulmonary hypertension. In conclusion the ASPIRE study will: 1. Assess the incidence and prevalence of arrhythmias using long term cardiac monitoring via a reveal LINQ loop recorder (Medtronic). Furthermore, the investigators will assess; Change in cardiac index, right atrial size, RV size, fibrosis and stroke volume. 2. The investigators will assess the arrhythmic burden in relation to: * Change in 6 MWT * Hemodynamic changes with RHC * Hemodynamic changes in echocardiography * The number of patients progressing one FC (Modified NYHA class) * Changes in NT-proBNP. * Hospital admission for any reason * Death or transplantation 3. Monitor heart rate variability and address a comparison to known risk markers and CMR and echocardiography. The study specifically seeks to investigate following: * The incidence and type of supraventricular and ventricular arrhythmias in PH by continuous long-term monitoring * The predictive value of both right and left ventricular cardiac magnetic resonance (CMR) imaging parameters for arrhythmogenesis in PAH, heart rate variability, and heart rate. * Optimization of specific therapy in PAH using continuous long-term arrhythmia monitoring 4. Monitor patients using smart watches (apple watches) to evaluate the applicability of long-term monitoring via apple watches in patients with pulmonary hypertension for irsk asessment.

Conditions

• Pulmonary Hypertension
• Arrhythmias, Cardiac
• Heart Rate Variability
• Risk Assessment

Interventions

Type	Name	Description
DEVICE	Loop recorder implantation	A loop recorder is implanted in the start of the study after informed consent is signed and enables continuous cardiac monitoring.
DEVICE	A smartwatch	A subgroup of the patients will be given an apple watch after informed consent to enables continuous monitoring via this non-invasive modality.

Timeline

• Start date: 2018-09-24
• Primary completion: 2024-11-01
• Completion: 2024-11-01
• First posted: 2020-09-18
• Last updated: 2024-04-10

Locations

1 site across 1 country: Denmark

Regulatory

• FDA-regulated device study