When can bone growth stimulation not be used?

Bone growth stimulation should not be used:

- In patients who are pregnant or planning to become pregnant, as the vibrations from the device may potentially harm the foetus.

- In patients who have skin or bone infections in the area where the device is to be implanted. This can increase the risk of infection and further complications.

- In patients with a history of malignant bone tumours or those with active bone tumours. The device may interfere with the diagnosis and treatment of bone cancer.

- In patients with any electrical devices already implanted, such as pacemakers, defibrillators, deep brain electrodes. The electromagnetic field generated by the device can interfere with the function or effectiveness of these devices.

- In patients with metal hardware or joint replacements in the area where the device is to be placed, as the device may interfere with the function of these implants.

- In patients with a history of keloid formation, hypertrophic scarring or other skin conditions that impair skin integrity. The device's implantation can exacerbate these conditions, leading to excessive scar tissue and potential complications.

It's important to have a thorough consultation and evaluation by a qualified medical professional before considering bone growth stimulation to determine if it is suitable for your specific circumstances.