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Parkinson’s Disease Treatment

Treatment and supportive care aimed at managing movement symptoms and maintaining independence

What is parkinson’s disease treatment?

Parkinson's disease is the slow loss of the dopamine-producing cells in a small structure deep in the brain called the substantia nigra. By the time the first changes are noticeable, a large share of those cells has already gone, and the loss carries on quietly for years afterwards.

Medication replaces the missing dopamine and works well at the start. After some years the window of benefit from each dose narrows, and the day splits into stretches when the medicine is working and stretches when it is not. Adding doses shortens the gaps but brings involuntary movement of its own, so the two problems trade against each other.

Surgery does not slow the underlying loss of cells and does not treat the illness. What it does is steady that fluctuating day, by delivering continuous stimulation to the same circuits the drug acts on, so that a lower dose covers more hours.

What you might notice

  • Shaking that appears when you use your hands
  • A tremor in the hand when it is resting
  • Movements that have become slow and small

How it is diagnosed

The diagnosis is clinical. A neurologist makes it by examining you: how you rise from a chair, how you walk and turn, how your handwriting has changed, and how one side compares with the other. A DaTscan can support an uncertain examination, though a normal scan is more useful for ruling the diagnosis out than an abnormal one is for confirming it.

The assessment before an operation asks a different question. It measures how much of what you have left still responds to levodopa, because that response is the best available predictor of the response to stimulation. You are examined formally after a night off medication and again after a dose, and the two scores compared.

An MRI, a cognitive assessment and a psychiatric review complete it. Significant memory impairment or untreated depression changes what an operation is worth, and both are looked for deliberately.

Recovery

You spend a few days in hospital and go home with the system switched off. The first settings are dialled in a few weeks later, and finding the right combination of settings and medication takes several appointments across three to six months. Nothing about the first month is a fair test of the result.

There is usually a temporary improvement in the days after surgery, from the swelling around the electrodes, and it wears off. Expect that, so you do not read the fade as a failure.

The battery is checked at every visit. A non-rechargeable one is changed under a short anaesthetic every few years; a rechargeable one is topped up at home and lasts far longer.

If it is left untreated

Continuing on medication alone as the fluctuations worsen means the predictable part of the day keeps shrinking. Falls become more frequent as balance fails and the feet start to freeze in doorways, and a fall with a fracture is the commonest single reason a person with Parkinson's disease loses their independence.

Later in the illness swallowing weakens, and food or saliva entering the lungs is the usual cause of death. Neither medication nor stimulation prevents that, though both preserve mobility for longer along the way.

Waiting is reasonable, and correct, while the medication still covers most of the day. There is no advantage in operating early. Waiting stops being reasonable once the good hours have become unpredictable and adjusting the doses has stopped buying any more of them.

Questions about parkinson’s disease treatment

Does deep brain stimulation mean I can stop my tablets?

It usually means fewer of them, not none. Most people reduce their levodopa substantially after the settings have been optimised, and that reduction is part of the point, since it is what eases the involuntary movements that high doses cause. Stopping altogether is uncommon and stopping suddenly is dangerous. The reduction is made gradually by the team, in step with the programming, over the first several months.

Am I too old for it?

Age on its own is not the deciding factor; the deciding factors are how well you still respond to levodopa, whether your memory is intact, and whether you are fit for a general anaesthetic. Results are less predictable past the mid-seventies and memory problems weigh heavily against an implant, because stimulation does not help thinking and the anaesthetic and hospital stay can unsettle it. A formal assessment answers this properly for you, and it is worth asking for even if you expect the answer to be no.

Is it permanent, and what if I do not like it?

The stimulation can be turned down or switched off at any visit and the effect reverses within minutes to hours, so the treatment itself is adjustable in a way a lesion is not. The hardware is what is permanent while it stays in, and it can be removed if it is no longer wanted, although the electrode tracks in the brain remain. The reversibility is the main reason stimulation is chosen over a lesion in someone who is young, or who needs both sides treated.

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Talk to a care coordinator about parkinson’s disease treatment

Leave a number and a care coordinator calls you back with what the treatment involves and which hospital it would be at. They book a consult only if you want one

Talk to a care coordinator