Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The goal of this observational study is to learn about the factors which determine how well ventricular tachycardia (VT) is tolerated. The main questions it aims to answer are:
Participants who are undergoing a clinically indicated coronary angiogram or coronary angioplasty procedure will have measurements of blood pressure, coronary pressure and coronary flow made during pacing at a range of heart rates.
Ventricular tachycardia (VT) is a common and life-threatening arrhythmia that occurs in people with heart problems. Some patients who develop this arrhythmia remain very stable with very little symptoms while others become unstable with low blood pressure or even sudden death. It is not known why some people tolerate the arrhythmia well and others do not.
If VT is not tolerated then current practice is to offer an implantable cardioverter defibrillator (ICD) which can deliver a shock to the heart if dangerous heart rhythms are detected. While shocks can be life-saving, they are also harmful, including causing psychological distress. ICDs also frequently deliver shocks when they are not needed.
If research could identify which factors predispose a person to be stable or unstable in VT, this would allow doctors to help them in a range of ways. One way would be to treat patients to improve the tolerance of VT, so avoiding the need for an ICD. Another would be to assess the the risk of instability and so allow a patient-centred decision on whether an ICD is needed.
In this study the investigators plan to recruit patients who are referred for a coronary angiogram. During the angiogram, the investigators will stimulate the heart at a range of fast heart rates and measure their blood pressure and flow in their coronary arteries. In patients who undergo stenting for a coronary stenosis, the investigators will also make these measurements after stenting so they can see if there is any difference. By recruiting a range of different cardiology patients, the investigators will be able to assess which factors contribute to stability during VT.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Controls | 10 patients with unobstructed coronary arteries, normal microvascular function and normal LV function. |
| |
| Coronary artery disease | 25 patients with severe, single-vessel coronary artery disease of the proximal LAD or proximal other dominant vessel awaiting PCI. |
| |
| Microvascular dysfunction | 15 patients with without severe disease in any coronary artery, impaired microvascular function and normal LV function. |
| |
| Heart failure | 20 patients with LV systolic dysfunction (LVEF<40%). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pressure and flow measurement during simulated VT | Diagnostic Test | Participants undergoing coronary angiography will have measurements of blood pressure, coronary pressure and coronary flow during simulated VT. VT will be simulated using pacing at a range of heart rates. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in coronary flow in participants with different levels of coronary microvascular function. | At baseline and during simulated VT | |
| Change in coronary flow in participants immediately before and after PCI | At baseline and during simulated VT, immediately before PCI and after PCI | |
| Change in blood pressure in participants with different levels of coronary microvascular function. | At baseline and during simulated VT | |
| Change in blood pressure in participants before and after PCI | At baseline and during simulated VT, immediately before PCI and after PCI |
| Measure | Description | Time Frame |
|---|---|---|
| Change in coronary flow in participants with different levels of left ventricular function | At baseline and during simulated VT | |
| Change in blood pressure in participants with different levels of left ventricular function | At baseline and during simulated VT |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Adults referred for coronary angiography or coronary angioplasty.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Rahul Bahl | Contact | +44 20 7594 1093 | r.bahl@imperial.ac.uk | |
| Ricardo Petraco | Contact | +44 20 7594 1093 | r.petraco@imperial.ac.uk |
| Name | Affiliation | Role |
|---|---|---|
| Ricardo Petraco | Senior Clinical Research Fellow | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Imperial College NHS Foundation Trust | Recruiting | London | W12 0HS | United Kingdom |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D017180 | Tachycardia, Ventricular |
| D003324 | Coronary Artery Disease |
| D006333 | Heart Failure |
| D017566 | Microvascular Angina |
| ID | Term |
|---|---|
| D013610 | Tachycardia |
| D001145 | Arrhythmias, Cardiac |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D011312 | Pressure |
| ID | Term |
|---|---|
| D055595 | Mechanical Phenomena |
| D055585 | Physical Phenomena |
Not provided
Not provided
Not provided
Not provided
Not provided
| D000075224 |
| Cardiac Conduction System Disease |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D003327 | Coronary Disease |
| D017202 | Myocardial Ischemia |
| D001161 | Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |
| D000787 | Angina Pectoris |