Calculating dangerous heartbeat

How ventricular fibrillation will behave in an individual patient can be accurately modelled and predicted using a single mathematical equation, according to Flinders University researchers.

Ventricular fibrillation (VF) is a life-threatening heart rhythm, or arrhythmia, that causes the heart to beat irregularly and is one of the leading causes of sudden death in Australia.

The findings, recently published in the journal Heart Rhythm, could be used to improve patient treatment, including identifying when to intervene or to develop individualised treatment plans that can work more effectively.

Dr Dhani Dharmaprani

Developed by Dr Dhani Dharmaprani from the Flinders Heart Rhythm Research Group in the College of Medicine and Public Health, led by Associate Professor Anand Ganesan, the research team studied the statistical properties of VF, identifying the unique patterns that consistently occurred in human patients, as well as animal and computer models of VF in the heart.

“The issue we have with VF is that because the rhythm is so chaotic it’s been very difficult to fully understand the mechanisms that are responsible for the disorder,” says Dr Dharmaprani, a Biomedical Engineer and Postdoctoral Research Associate in Cardiac Electrophysiology.

“This is further complicated by the fact that everyone’s heart is unique, so how the heart reacts during VF changes from patient to patient.

“However, by identifying the characteristics that consistently occurred, we were able to demonstrate for the first time that a single mathematical equation could be used to accurately model and then predict the behaviour of VF.”

The equation uses principles from a branch of mathematics known as renewal theory to predict the population dynamics of ‘rotors’ – mini tornadoes of electricity found in the heart during VF. These rotors are responsible for giving rise to VF’s chaotic heart rhythm, and therefore understanding their dynamics is central to treating the disorder.

The researchers say when applied, the equation could be used to improve patient care in two distinct ways.

Associate Professor Anand Ganesan

“Firstly, the equation seems to predict whether fibrillation will continue to persist, or whether it will stop on its own, this could be important as it could help us identify between patients that require treatment and those where no intervention is needed,” says senior author Associate Professor Anand Ganesan, a practising cardiologist and Matthew Flinders Fellow in Electrophysiology at Flinders University.

“Secondly, because the mathematical equation can model how an individual patient will react to VF, we can use it to potentially develop individualised treatments that work much more effectively.”

Previous research has also demonstrated the equation can be applied to atrial fibrillation (AF), another form of heart arrhythmia that is the most common in the world.

The next step for the research team is to translate these findings towards potential therapies, including using the equation to develop patient specific computer models that accurately replicate patient dynamics, and understanding how this equation relates to clinical characteristics.

The team, led by Associate Professor Ganesan, was last week awarded a $1.1 million dollar grant from the National Health and Medical Research Foundation to continue their research. The paper was recently accepted into one of the disciplines most competitive early career competitions: The Heart Rhythm Society Young Investigator Award, alongside finalists from John Hopkins, The Mayo Clinic and Harvard Medical School.

“A governing equation for rotor and wavelet number in human clinical ventricular fibrillation: Implications for sudden cardiac death” by Dhani Dharmaprani, Evan V. Jenkins, Jing X. Quah, Anandaroop Lahiri, Kathryn Tiver, Lewis Mitchell, Christopher P. Bradley, Martin Hayward, David J. Paterson, Peter Taggart, Richard H. Clayton, Martyn P. Nash and Anand N. Ganesan is published in the journal Heart Rhythm. DOI: 10.1016/j.hrthm.2021.10.008.

The work was supported by the National Health and Medical Research Council of Australia Project Grant (1063754) and National Heart Foundation of Australia (101188).

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