Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nutt, J. G.
Right arrow Articles by Carter, J. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nutt, J. G.
Right arrow Articles by Carter, J. H.
NEUROLOGY 1986;36:1206
© 1986 American Academy of Neurology

Clinical and biochemical studies with controlled-release levodopa/carbidopa

John G. Nutt, MD, William R. Woodward, PhD and Julie H. Carter, MN

Oregon Health Sciences University, Portland, OR.

In five patients with parkinsonism, the optimal dosage of a controlled-release levodopa/carbidopa preparation (CR-3) was three times higher than the dosage of Sinemet and produced higher plasma levodopa concentrations, but did not reduce the fluctuations in plasma levodopa or clinical response. Plasma levodopa concentrations were higher and clinical responses better before the first dose of the day with CR-3. CR-3 treatment benefited two patients, reducing the severity of off periods and off dystonia. Two patients were worse on CR-3 despite higher plasma levodopa levels than those adequate for clinical response to Sinemet or levodopa infusions. CR-3 could benefit a few severely affected patients, but it is necessary to understand the factors that affect absorption of levodopa from sustained-release preparations, as well as the consequences of prolonged elevation of plasma levodopa levels.

Address correspondence and reprint requests to Dr. Nutt, Oregon Health Sciences University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97201.

Supported in part by NINCDS 1 RO1 NS 21062–01, Clinical Centers Grant RR00334, and Merck Sharp & Dohme Laboratories.

Accepted for publication December 28, 1985.




This article has been cited by other articles:


Home page
Arch NeurolHome page
J. G. Nutt, J. H. Carter, and N. E. Carlson
Effects of Methylphenidate on Response to Oral Levodopa: A Double-blind Clinical Trial
Arch Neurol, March 1, 2007; 64(3): 319 - 323.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
S. Dethy, M. A. Laute, N. Van Blercom, P. Damhaut, S. Goldman, and J. Hildebrand
Microdialysis-HPLC for plasma levodopa and metabolites monitoring in parkinsonian patients
Clin. Chem., May 1, 1997; 43(5): 740 - 744.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
P. J. Karstaedt, J. H. Pincus, and S. S. Coughlin
Standard and Controlled-Release Levodopa/Carbidopa in Patients With Fluctuating Parkinson's Disease on a Protein Redistribution Diet: A Preliminary Report
Arch Neurol, April 1, 1991; 48(4): 402 - 405.
[Abstract] [PDF]


Home page
Arch NeurolHome page
J. T. Hutton, J. L. Morris, G. C. Roman, S. C. Imke, and J. W. Elias
Treatment of Chronic Parkinson's Disease With Controlled-Release Carbidopa/Levodopa
Arch Neurol, August 1, 1988; 45(8): 861 - 864.
[Abstract] [PDF]


Home page
Arch NeurolHome page
J. L. Juncos, G. Fabbrini, M. M. Mouradian, and T. N. Chase
Controlled Release Levodopa-Carbidopa (CR-5) in the Management of Parkinsonian Motor Fluctuations
Arch Neurol, October 1, 1987; 44(10): 1010 - 1012.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1986 by AAN Enterprises, Inc.