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Duopa

Duopa

My husbands PD Doctor would like him try Duopa but I would like to talk with people that are actually on that program and ask, is it better than the pills, how is it working for you ?

A MyParkinsonsTeam Member said:

Thanks for the info on Duopa. I really didn't know much about it before, but doesn't sound like something we would try either.

edited, originally posted over 4 years ago
A MyParkinsonsTeam Member said:

Here is an interesting note by MJF

https://www.michaeljfox.org/foundation/news-det...-duopa-levodopa-carbidopa-intestinal-gel-delivery-method-new-to-market

FDA Approves Duopa — Carbidopa/Levodopa Enteral Suspension Method New to U.S. Market

Posted by Holly Teichholtz, January 12, 2015

Less than a week after the U.S. Food and Drug Administration (FDA) approved an extended-release oral formulation of levodopa/carbidopa, government regulators have delivered another positive ruling for Parkinson’s therapy. Today pharmaceutical company AbbVie announced it has obtained approval for Duopa, its gel formulation of carbidopa/levodopa enteral suspension infused directly into the small intestine. This treatment has been approved in Europe under the name Duodopa since 2004.

In the advanced stages of Parkinson’s disease, patients may begin to experience “off” time, or periods of poor mobility, slowness and stiffness. Additionally, in Parkinson’s disease patients, the spontaneous emptying of the stomach becomes delayed and unpredictable, which can affect the timing of when orally administered medicines leave the stomach and are absorbed in the small intestine. Duopa is delivered directly into the small intestine through a tube — a type of administration intended to bypass the stomach. A small infusion pump administers the drug continuously over 16 hours. In clinical trials, use of Duopa led to two fewer hours of “off time” than treatment with immediate-release, oral levodopa/carbidopa pills.

Duopa represents a promising new option especially for those in later stages of the disease. With that said, no treatment is perfect. Duopa requires that patients wear a large, external “box” in the belt region. Patients require help from caregivers to manage the device, tend to the skin where the tube enters the body and facilitate medication refills. In early studies, people experienced device-related problems with the intestinal tube, which can clog, bend or move out of position.

FYI.....
One month's supply of Duopa costs $6,054.00 / month; PEG-J tube insertion and administration-related expenses will significantly increase the cost of treatment

edited, originally posted over 4 years ago
A MyParkinsonsTeam Member said:

I would also be interested in that also. My husband is having a terrible time swallowing his pills. I usually push them far back on his tongue and then he can get them down with liquid or Apple sauce. I don't especially like putting my fingers in his mouth but do what I have to to get his meds in him.

posted over 4 years ago
A MyParkinsonsTeam Member said:

I agree totally @A MyParkinsonsTeam Member... the expense is out rageous just for the medication. let alone the potential for serious infection at the PEG-J Tube port site and all the additional care that requires.. Taking pills just seem so much easier to me...

posted over 4 years ago
A MyParkinsonsTeam Member said:

I admit I read about Duopa and I didn't like the sounds of that at all.

edited, originally posted over 4 years ago
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