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Interpretation of clinical trials comparing different drug regimens for Parkinson's disease (PD) is complicated by the different dose intensities used: higher doses of levodopa and, possibly, other drugs produce better symptomatic control but more late complications. To address this problem, conversion factors have been calculated for antiparkinsonian drugs that yield a total daily levodopa equivalent dose (LED). LED estimates vary, so we undertook a systematic review of studies reporting LEDs to provide standardized formulae. Electronic database and hand searching of references identified 56 primary reports of LED estimates. Data were extracted and the mean and modal LEDs calculated. This yielded a standardized LED for each drug, providing a useful tool to express dose intensity of different antiparkinsonian drug regimens on a single scale. Using these conversion formulae to report LEDs would improve the consistency of reporting and assist the interpretation of clinical trials comparing different PD medications.
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Claire L Tomlinson
University of Birmingham
Rebecca Stowe
Corning (United States)
Smitaa Patel
Cancer Research UK Clinical Trials Unit
Movement Disorders
University of Birmingham
Cancer Research UK Clinical Trials Unit
Sandwell & West Birmingham Hospitals NHS Trust
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Tomlinson et al. (Wed,) studied this question.
synapsesocial.com/papers/69b99ba99157e5b9decf3e95 — DOI: https://doi.org/10.1002/mds.23429