
High-risk heart failure patients should receive lifesaving implantable defibrillators sooner

Lifesaving implantable defibrillators should be given to heart failure patients at highest risk of heart rhythm problems at an earlier stage in their treatment, according to research we’ve funded published in Circulation.
The team behind the multi-centre clinical trial, led by Professor Divaka Perera at King’s College London, say their results provide new evidence which could influence heart failure guidelines in the UK, Europe and internationally.
There are 2.3 million people living with coronary heart disease in the UK, and it is a leading cause of heart failure. It develops when the blood vessels supplying the heart become narrowed by a build-up of a fatty substance in their walls, stopping blood which carries vital oxygen and nutrients getting to the heart muscle.
This can lead to damage of the left chamber of the heart – which is responsible for pumping blood around the rest of the body – and a higher risk of dangerously abnormal heart rhythms and sudden death.
90 day wait
For people who have severe heart failure due to coronary heart disease, as well as prescribing medication, doctors may insert stents to open any blocked arteries in the first instance. They then wait for at least 90 days to see if the pumping action of the heart has improved based on these treatments.
It’s only after this wait that patients are re-evaluated to see if they are still at high risk of a life-threatening heart rhythm disturbance and would benefit from having an implantable cardioverter defibrillator device (ICD). These defibrillators shock and kickstart the heart if it goes into a life-threatening rhythm or cardiac arrest.
Multi-centre trial
Researchers recruited a total of 700 patients from 40 hospitals across the UK who had coronary heart disease and severely weakened function of the left ventricle of their heart. All patients received ‘optimal medical therapy’ which included heart failure medication, and, in many cases, pacemakers designed to improve heart function and ICDs. Half of the patients were randomly assigned to also have stents fitted to open-up their narrowed arteries that supply the heart with blood. Patients were followed-up closely for at least two, and up to eight, years.
They found that stents did not reliably improve the heart’s ability to pump, nor did they reduce the risk of life-threatening heart rhythm disturbances, or number of cardiac arrests and deaths. As a result, the team say that patients who are at risk should not have to wait until after stent insertion before they are fitted with a potentially lifesaving ICD.
While stents were shown not to improve heart function in patients with severe heart failure, the researchers stress that they are still an effective treatment for heart attack patients or people with angina (chest pain due to reduced blood flow to the heart).
'Wait and see approach isn't always best'
Dr Holly Morgan, BHF Clinical Research Fellow at King’s College London BHF Centre of Research Excellence, who was involved in the research said: “Our findings have revealed that many patients with high risk of heart failure could benefit from receiving an ICD straight away, rather than facing a 90-day wait.
“By showing that coronary stents had limited benefit for this group of heart patients, we have exposed a clear window of missed opportunity to reduce chances of dying from an abnormal heart rhythm. We hope our findings will influence existing guidance, so patients can be spared unnecessary waits to receive a potentially lifesaving defibrillator.”
Dr Sonya Babu-Narayan, our Associate Medical Director, said: “The results from this large UK-wide trial could lead to re-evaluation of how best to treat people living with severe heart failure due to coronary heart disease. The findings suggest that the current ‘wait and see’ approach to find out whether a patients’ heart function improves with medication and stents isn’t always best, and that an unnecessary wait could even be the difference between life and death.”