The electrical device is composed of two parts.
The first part is the implanted part, which includes a battery and an electrode made up of a tiny electrical wire; both are inserted under the skin of the lower back.
The second part is a hand-held controller, which allows the patient to turn the electrode on or off, as well as control the strength and frequency of the electrical stimulation.
When the electrode is turned on, they may feel a light or gentle pulling, tingling or buzzing sensation around their genitals and back passage.
Implanting the device takes place in two phases: a test phase and a permanent implantation phase.
The test phase involves a minor surgery to insert a temporary device under anaesthetic; it does not usually involve an overnight hospital stay, but this may occasionally be required according to individual circumstances.
The surgeon will review the patient one to three weeks after the temporary device has been inserted.
They will be taught how to control the frequency and strength of stimulation, and to monitor how their symptoms improve during that period.
At the follow-up review appointment, the specialist will remove the temporary device and assess whether there was a benefit from the treatment.
If appropriate, a permanent device will then be discussed and offered.
The main difference with the permanent device is that the battery is inserted under the skin just above the buttock, whereas the temporary device has an external battery.
Inserting the permanent device involves a minor surgery under anaesthetic. The battery will usually last four to five years.
The battery’s status will be checked regularly at follow-up appointments; it can also be viewed on the handset.
If the battery runs down it will need to be replaced, which involves a further minor surgery under anaesthetic.