Diagnostic Technique Assesses Structural Changes in Cardiac Arrhythmia to Enable Personalized Treatment

Atrial fibrillation, one of the most common types of cardiac arrhythmia, is characterized by irregular and rapid heartbeats that can lead to the formation of blood clots in the heart. This increases the risk of stroke, heart failure, and other related complications. Currently, atrial fibrillation is classified based on the duration of the arrhythmia, but this temporal classification does not provide information about the extent of structural and electrophysiological changes, known as atrial remodeling, that occur in the hearts of patients with atrial fibrillation. Atrial remodeling is a crucial parameter, especially in the initial months of the condition, as the underlying disease processes can progress at different rates. Now, a new diagnostic method allows for the simultaneous assessment of both electrical and mechanical (contractile) activity in the heart atria during atrial fibrillation, enabling timely intervention and better management of the condition.

Over the past 10 years, a team of national and international experts led by scientists at the Centro Nacional de Investigaciones Cardiovasculares (CNIC, Madrid, Spain) has been collaborating to integrate electrical and mechanical cardiac data in order to enable personalized characterization of the pathological changes associated with the progression of atrial fibrillation. The researchers were successful in achieving this through a multidisciplinary approach. Engineers and physicists worked together in the initial phase to devise the most suitable strategy for integrating the electrical and mechanical data. They found a solution to measure mechanical activity by using Doppler imaging, which offers a noninvasive method of providing information on atrial tissue movements, and to measure electrical activity by utilizing surface electrocardiography.

Both approaches are easy to implement in a clinical setting since they are noninvasive and can be performed during a transthoracic ultrasound examination, a routine study of the heart's shape and function along with some internal structures. The second phase involved experts in biology, biotechnology, biochemistry, and biomedical engineering working in collaboration with the CNIC Proteomics Unit and clinical cardiologists. Experimental studies in this phase correlated the information obtained through the new approach with underlying pathological changes in atrial tissue. This led to the development of advanced mapping techniques and computer simulations that shed light on the mechanisms underlying electrical and mechanical remodeling during the progression of atrial fibrillation.

In the final phase, a multicenter prospective study involving 83 patients in the early stages of atrial fibrillation was conducted to determine the prognostic value of simultaneously assessing electrical and mechanical activity in the atria of these patients. The experimental and clinical findings revealed an imbalance between electrical and mechanical activation in the atria during the early stages of the disease. This causes dissociation between the two parameters, termed "atrial electromechanical dissociation," where the contractile activation cannot keep up with the electrical activation. This phenomenon is specific to each individual patient and is usually observed within the first 2-3 months after an uninterrupted atrial fibrillation episode. A key advantage of this new approach is that it identifies atrial electromechanical dissociation before overt clinical signs of structural atrial remodeling appear. This early detection could be crucial for timely intervention and better management of the condition.

“The use of this new diagnostic approach allows early characterization of the underlying remodeling in patients with atrial fibrillation,” said study leader David Filgueiras. “The study shows that it is possible to integrate electrical and mechanical data from the atria of patients with atrial fibrillation to obtain personalized prognostic information about the clinical progression of the disease.”

Related Links:
CNIC

Visit expo >

Platinum Member

Real-Time Diagnostics Onscreen Viewer

GEMweb Live

Gold Member

12-Channel ECG

CM1200B

Xenon Light Source

CLV-S400

Silver Member

ECG Management System

NEMS Web