Source:http://linkedlifedata.com/resource/pubmed/id/10830413
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2000-10-2
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pubmed:abstractText |
Putative neuroprotective agents for Parkinson's disease can be assessed in untreated patients using progression of clinical disability as an index of disease progression. To avoid the confound associated with symptomatic therapy, progression of the underlying disease can be assessed by evaluating the progression of clinical disability from an untreated baseline to a final visit following wash-out of symptomatic medication. In this type of analysis it is critical to use a washout of sufficient duration to ensure elimination of symptomatic effects. To assess the time course of resolution of symptomatic effects, we evaluated 31 patients at days 1, 8, and 15 following discontinuation of levodopa/carbidopa and bromocriptine. Mean total Unified Parkinson's Disease Rating Scale scores (+/- standard error) increased (worsened) by 7.4+/-1.5 from day 1 to day 15 (p <0.0001), 4.5+/-1.2 from day 1 to day 8 (p = 0.0009), and 2.9+/-1.0 from day 8 to day 15 (p = 0.01). We conclude that a wash-out of at least 2 weeks is required to eliminate the symptomatic effects of levodopa/carbidopa and bromocriptine in patients with early Parkinson's disease.
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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/Antiparkinson Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Bromocriptine,
http://linkedlifedata.com/resource/pubmed/chemical/Carbidopa,
http://linkedlifedata.com/resource/pubmed/chemical/Levodopa,
http://linkedlifedata.com/resource/pubmed/chemical/Selegiline
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0885-3185
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
485-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10830413-Aged,
pubmed-meshheading:10830413-Antiparkinson Agents,
pubmed-meshheading:10830413-Bromocriptine,
pubmed-meshheading:10830413-Carbidopa,
pubmed-meshheading:10830413-Disability Evaluation,
pubmed-meshheading:10830413-Disease Progression,
pubmed-meshheading:10830413-Double-Blind Method,
pubmed-meshheading:10830413-Female,
pubmed-meshheading:10830413-Humans,
pubmed-meshheading:10830413-Levodopa,
pubmed-meshheading:10830413-Male,
pubmed-meshheading:10830413-Middle Aged,
pubmed-meshheading:10830413-Neurologic Examination,
pubmed-meshheading:10830413-Parkinson Disease,
pubmed-meshheading:10830413-Prospective Studies,
pubmed-meshheading:10830413-Selegiline,
pubmed-meshheading:10830413-Substance Withdrawal Syndrome
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pubmed:year |
2000
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pubmed:articleTitle |
Time course of loss of clinical benefit following withdrawal of levodopa/carbidopa and bromocriptine in early Parkinson' s disease.
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pubmed:affiliation |
Parkinson's Disease and Movement Disorders Center, University of South Florida, Tampa 33606, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
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