Could a levodopa pump help reduce my dad’s ‘off’ periods?
He isn't sold on the idea, but I think it could help
Written by |
Levodopa was first used in clinical trials for Parkinson’s disease in 1961, and it eventually became the gold standard for treatment. Today, it’s still the most common medication available for managing symptoms like tremors and stiffness.
But “off” periods — when the medication wears off — still leave people with Parkinson’s, like my dad, feeling unable to commit to social activities and other events. As the disease progresses, those off periods seem to be occurring more frequently for Dad, which makes me wonder if there are things we can do to better manage them.
In October 2024, the U.S. Food and Drug Administration approved the first continuous 24-hour subcutaneous levodopa infusion. I heard about the pump from someone whose wife had recently begun using it. He said it had been a game changer for her, since she no longer had to worry about manually timing her medication by taking it orally.
On giving it a try
The pump’s delivery system makes it easier for some people with Parkinson’s to avoid those off periods. I suspect that my dad could benefit from it, too.
He doesn’t have it yet, though, and isn’t particularly keen on the idea of installing any kind of hardware into his body. But I know he struggles to maintain consistency with the timing of his medication. In the daytime hours, he functions on a pretty regular schedule. But when evening comes, he stops taking his medication, which has led to reduced mobility before bed and more nighttime symptoms.
For a disease that’s so unpredictable, the prospect of using a system that can help manage symptoms around the clock is alluring to me. What if maintaining a regular medication schedule would improve his sleep quality? How would his quality of life improve if we were able to remove even a fraction of the unpredictability that comes with Parkinson’s?
What I also find attractive about this system is that it bypasses the stomach. I know Dad notices differences in his medication absorption, particularly when he’s eating protein-heavy diets. So my guess is that entirely bypassing the stomach could help to eliminate this issue.
Of course, there are risks associated with installing anything into the body. But I wish he’d give it a try.
Note: Parkinson’s News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Parkinson’s News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to Parkinson’s disease.
Christine Scheer
Hi Mary Beth, a friend of mine has the Vyaleve (sp?) pump, and the difference with it is dramatic! Is there a forum discussion about this? Maybe if your dad heard a variety of perspectives, he’d consider it? Good luck!
Francisco Manuel Gonçalves
Boa tarde.
Fiz cirurgia dbs em 2024.
Gostava de saber,se é possível implementar a bomba que menciona
Tomo muito pouca levodopa.
Grato
Francisco
Kate Grant
Could your dad not have controlled release Sinemet/Madopar an hour before bedtime to see him through the night?
Janelle Montgomery
My mom had that. It was a nightmare to keep it working and to put it on. If you don’t have care for your dad to help, forget it. It also made my mom worse.
Robert Ruiz
My symptoms pushed me to have DBS surgery about 2 years ago...the off periods were getting longer. I couldn't drive...i noticed that sleeping was the only way to calm. So I started to wither away...im a combat veteran. The VA has been completely awesome...
I'm in Puerto Rico right now and just got back from a walk. I'm here by myself. I swam in the ocean yesterday....its truly amazing.....
I thank God every day. I am blessed.
Look into it DBS surgery deep brain stimulation.
Genia Mizelle
I’m fixing to start the vyleve pump. I hope it helps with my off times and not to difficult to manage.
KELLY STILLWELL
THANK YOU FOR THE NEWS LETTER
Toby Maddison
I feel that my experiences might be of assistance to others, who may be considering having a pump to replace oral levodopa. I have had a Produodopa pump for almost a year And I can honestly say it has changed my life for the better.
I was diagnosed with Parkinsons almost 20 years (47 years old) ago and by June 2025 I was finding life extremely difficult.
I was offered a Produodopa pump with a sub-cutaneous delivery system in July 2025. It is not entirely without problems, particularly in regard to infection of the injection sites but it has given me a completely new ’lease on life’ and I am again able to live a relatively normal life. The particular benefit for me is that I no longer suffer from both the Parkinson’s symptoms and the dreadful dyskinesia, the side effect of oral Levidopa.
I do not have any idea of how long the Produodopa pump will provide relief from the symptoms of Parkinson’s and the side effects of oral levodopa tablets but I have no hesitation in recommending the Produodopa pump system.
Joan Cannon
I was interested in the pump but for some reason the Parkinson’s nurse put me on Neupro patches instead. I haven’t got on well with them so I’d like to explore the pump further. I seem to remember that it needs to be replaced quite frequently and the process might be rather invasive!
Joan Cannon
I’m also interested in the pump dispenser but I’m not sure how long it lasts or how difficult it is to maintain!