PET – Cardiac Positron Emission Tomography
77 Wimpole Street brings another first for RB&HH – the ability to offer cutting edge PET-CT imaging.
A s one of the few PET-CT scanners in the country offering Rubidium Cardiac PET, and one of the first
in London, our Imaging Team offers complex cardiac diagnostics to our private and international patients.
Advanced Myocardial Perfusion Imaging with PET
PET is based on the detection of 2 identical ‘coincident’ photons emitted after injection of a specifically selected radiopharmaceutical which concentrates in the area of interest within the body.
Coincidence detection of photons creates distinct advantages for PET, including the ability to provide attenuation-corrected images in order to more accurately display information, thereby greatly increasing specificity. Coincidence detection also makes for high count sensitivity which increases reporter confidence.
Myocardial perfusion imaging (MPI) utilising the radiopharmaceutical Rubidium-82 is a highly sensitive method for mapping myocardial blood flow; this involves injection of 82Rb at rest and under pharmacological stress (hyperaemia).
82Rb is a PET tracer with very short halflife of 75 seconds which allows the full procedure to be completed in less than an hour (an imaging time of about 30 min), as opposed to 4+ hours for routine SPECT imaging. This also contributes to a significant reduction in the radiation burden to patients, cutting the dose by up to a quarter.
Due to the diagnostic capability of the multislice CT scanner, patients can have a calcium score and high definition coronary angiography scan in the same appointment thereby offering increased diagnostic certainty with greatly improved sensitivity and specificity.
Which patients benefit most from 82Rb PET imaging?
- Obese patients; where other imaging modalities may have reduced diagnostic accuracy, cardiac PET is a promising noninvasive modality offering good prognostic value.
- Where large breast attenuation is likely to degrade image quality.
- Advanced atherosclerosis; multivessel disease, haemodynamic significance of known disease.
- High risk demographics with early atherosclerosis.
- Suspected coronary disease in younger patients.
- Microvascular disease i.e. Syndrome X
Why quantify flow?
Interpretation of SPECT and PET images is visual or semi-quantitative and based on relative uptake. Areas of the myocardium with the highest uptake are presumed to be supplied by unobstructed coronary arteries while those with decreased uptake during stress are assumed to be supplied by obstructed e.g. atherosclerotic arteries. Nonetheless, stenoses with luminal diameters around 50% may be undetected by this visual interpretation alone.
Moreover, patients with subclinical coronary ischemia or microvascular diffuse disease may present with only mildly heterogeneous or even homogeneous myocardial uptake and similarly in the situation of threevessel coronary disease, a reduction of myocardial uptake may be balanced in all coronary arteries, resulting in a homogeneous left ventricle myocardium at stress. Each of these pathological variants could potentially lead to false negative results.
Measurements of absolute myocardial blood flow (MBF) in millilitre per gram per minute and myocardial flow reserve (MFR), which is the maximum increase in blood flow above the normal resting volume, help identify subclinical coronary ischemia by characterising extent and severity in multi-vessel disease. Furthermore, it has been clinically observed that the measurement of hyperaemic MBF and MFR with PET-CT may predict, better than other methods, the occurrence of hard cardiac events.
Myocardial hibernation imaging
Identification of viable myocardium is important when planning the strategy for revascularisation in patients with chronic ischaemic heart disease. Identifying and treating dysfunctional but vascularised, viable myocardium reduces patient morbidity and mortality.
18Flourine labelled Fleuro-deoxy– glucose (FDG) behaves as an analogue of glucose when in the body and concentrates in chronically ischaemic dysfunctional but viable myocardium. In conjunction with 82Rb perfusion imaging, such pathology can be identified to plan the revascularisation strategy.
Confidence in the FDG identification method has only further grown following a large meta-analysis of observational studies looking at predicting the recovery of cardiac function following imaging and subsequent advised therapy. Results showed that FDG PET was the most sensitive method for identifying hibernating myocardium and hence considered the ‘gold standard’.
Infection and Inflammation
PET-CT can also be used to identify areas within tissue which are affected by inflammatory and infectious processes; for example it is very valuable in the diagnosis, management and monitoring treatment response in cardiac sarcoidosis patients.
Sarcoidosis involving the cardiac tissue leads to arrhythmias which can potentially be fatal but FDG imaging can be used to identify these areas of inflammatory cardiac involvement so that they can be treated accordingly.
In fact, the recent Heart Rhythm Society consensus statement recommends screening for cardiac sarcoidosis using PET or MRI, for example in young patients with unexplained second degree heart block.
FDG imaging is also proving useful in other difficult to diagnose cardiovascular inflammatory conditions such as Giant cell vasculitis and Takayasu’s arteritis.
Similarly following device implantation where patients display signs of infection, PET-CT imaging is helpful in pinpointing areas of device related infections, e.g. with pacemakers, or in patients with pyrexia of unknown origin due to concentration of FDG at the site of infection.
|The key benefits of 82Rb PET:
1. Short 1 hour protocol in total (stress + rest)
Dr Kshama Wechalekar
Dr Wechalekar leads the Wimpole Street PET and RBH specialist radionuclide imaging services for heart and lung imaging and is expert in myocardial perfusion imaging.
If you would like to refer a patient for PET-CT or understand more about the benefits PET can offer to your practice email firstname.lastname@example.org or call 0207 351 8186.