
The Centre acts as a hub for PAD experts spanning Sydney Local Health District’s Royal Prince Alfred and Concord Hospitals, The University of Sydney, and several research institutes. It will help identify gaps in PAD pathophysiology, treatment, and patient care.
“Unfortunately, PAD is the poor cousin of heart health and cardiovascular disease, and many people are unaware of the condition,” said Prof Andrew Coats in his opening address.
“And with the number of Australians living with the condition predicted to grow, due to an ageing population and the diabetes epidemic, the establishment of the Centre for PAD is absolutely critical.
“We will do all we can to help raise awareness, transform treatment and improve the lives of patients.”
The Centre for PAD Consumer Group will aim to meet regularly, either in person or online, throughout the year.
PAD affects almost one in every five Australians, with about 50 per cent of people with PAD showing no symptoms, leading to under-diagnosis.
The symptoms of PAD will depend on which body part is affected, and in some cases, there are only mild or no symptoms until the disease is advanced. Symptoms may include:
- intermittent or irregular pain during activity and rest
- numbness, coldness or pins and needles in the affected body part
- blue- or purple-tinged skin
- sores or ulcers in the affected body part that do not heal
- blackened areas of skin or loss of skin (gangrene).
If you have symptoms of PAD, it is important to see your doctor.
If you are interested in getting involved, please contact CentreForPAD@hri.org.au
