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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1988-3-3
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pubmed:abstractText |
The study included 19 parkinsonian patients presenting with fluctuations in motor performance after L-dopa therapy (9.9 years on average, range 6 months to 17 years) and 2 other patients not pretreated with L-dopa. In all patients of the first group, after 3 months on stable 'optimal' dosage schedule, the previous L-dopa treatment was abruptly replaced, dose for dose, from one day to another by Madopar HBS, a new controlled-release form of Madopar. The first clinical assessment was performed just before the beginning of the HBS treatment. Then, 4-6 weeks were allowed to optimize the dosage schedule of Madopar HBS before performing a second assessment. Long-term therapeutic effects were systematically evaluated after 6 and 12 months. Catamnestic evaluation took place at the last check-up for patients treated for more than 1 year. Of the 19 patients with fluctuations 1 dropped out after 7 days due to lack of cooperation. Thus, 18 of these patients were evaluable. At the end of the dose adaptation phase 12 patients (2/3) were better controlled by the new dosage form and were eligible for a long-term follow-up aiming to evaluate the maintenance of the benefit. It was concluded that in most of the patients the initial benefit was maintained during 1 year and even up to 2 years and 7 months for some of them. The best results were obtained in patients with mild to moderate forms of fluctuations (early stage). Positive results in de novo cases need confirmation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Benserazide,
http://linkedlifedata.com/resource/pubmed/chemical/Delayed-Action Preparations,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Combinations,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrazines,
http://linkedlifedata.com/resource/pubmed/chemical/Levodopa,
http://linkedlifedata.com/resource/pubmed/chemical/benserazide, levodopa drug...
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pubmed:status |
MEDLINE
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pubmed:issn |
0014-3022
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
98-104
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pubmed:dateRevised |
2009-12-23
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pubmed:meshHeading |
pubmed-meshheading:3428311-Adult,
pubmed-meshheading:3428311-Aged,
pubmed-meshheading:3428311-Aged, 80 and over,
pubmed-meshheading:3428311-Benserazide,
pubmed-meshheading:3428311-Delayed-Action Preparations,
pubmed-meshheading:3428311-Dose-Response Relationship, Drug,
pubmed-meshheading:3428311-Drug Combinations,
pubmed-meshheading:3428311-Female,
pubmed-meshheading:3428311-Follow-Up Studies,
pubmed-meshheading:3428311-Humans,
pubmed-meshheading:3428311-Hydrazines,
pubmed-meshheading:3428311-Levodopa,
pubmed-meshheading:3428311-Male,
pubmed-meshheading:3428311-Middle Aged,
pubmed-meshheading:3428311-Movement Disorders,
pubmed-meshheading:3428311-Parkinson Disease
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pubmed:year |
1987
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pubmed:articleTitle |
Therapeutic value of Madopar HBS: judgment after 2 years experience.
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pubmed:affiliation |
Neurochirurgische Klinik, Universitätsspital, Zürich, Switzerland.
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pubmed:publicationType |
Journal Article
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