A novel sublingual apomorphine treatment for patients with fluctuating Parkinson's disease
Identifieur interne : 004E25 ( Main/Exploration ); précédent : 004E24; suivant : 004E26A novel sublingual apomorphine treatment for patients with fluctuating Parkinson's disease
Auteurs : William Ondo [États-Unis] ; Christine Hunter [États-Unis] ; Michael Almaguer [États-Unis] ; Joseph Jankovic [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1999-07.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Administration, Sublingual, Agonist, Antiparkinson Agents (administration & dosage), Antiparkinson Agents (therapeutic use), Apomorphine, Apomorphine (administration & dosage), Apomorphine (therapeutic use), Chemotherapy, Disease Progression, Dopamine agonists, Dopamine receptor, Drug Administration Schedule, Female, Human, Humans, Male, Middle Aged, Parkinson Disease (classification), Parkinson Disease (drug therapy), Parkinson disease, Parkinson's disease, Sublingual administration, Time Factors, Treatment, Treatment Outcome.
- MESH :
- chemical , administration & dosage : Antiparkinson Agents, Apomorphine.
- chemical , therapeutic use : Antiparkinson Agents, Apomorphine.
- classification : Parkinson Disease.
- drug therapy : Parkinson Disease.
- Administration, Sublingual, Disease Progression, Drug Administration Schedule, Female, Humans, Male, Middle Aged, Time Factors, Treatment Outcome.
Abstract
We tested a novel preparation of a sublingual apomorphine hydrochloride tablet (APO) in 10 patients with advanced Parkinson's disease complicated by motor fluctuations. After a dose titration, patients took either 40 mg APO three times per day alternating with levodopa doses (eight patients) or six doses of 20 mg APO taken concurrently with levodopa doses (two patients) for 3 months. Assessments included timed tapping and ambulation tests, Unified Parkinson's Disease Rating Scale (UPDRS), and patient diaries. Tapping speed while taking only APO (12 hours after stopping levodopa) was faster than while taking only levodopa (p <0.05). The daily levodopa dose decreased by 32.1% (p <0.01), yet the total “on” time increased from 73.5% ± 10.2% to 81.5% ± 7.5% of the day (p <0.01) after starting APO. “On” UPDRS part II scores (p <0.05) and “on” UPDRS part III (motor examination) scores (p <0.05) also improved. Adverse events such as nausea, orthostatic hypotension, and disagreeable taste did not limit the dose of APO in any case. The short‐term benefit and tolerability demonstrated in this study warrant further study of this new APO preparation.
Url:
DOI: 10.1002/1531-8257(199907)14:4<664::AID-MDS1017>3.0.CO;2-5
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">We tested a novel preparation of a sublingual apomorphine hydrochloride tablet (APO) in 10 patients with advanced Parkinson's disease complicated by motor fluctuations. After a dose titration, patients took either 40 mg APO three times per day alternating with levodopa doses (eight patients) or six doses of 20 mg APO taken concurrently with levodopa doses (two patients) for 3 months. Assessments included timed tapping and ambulation tests, Unified Parkinson's Disease Rating Scale (UPDRS), and patient diaries. Tapping speed while taking only APO (12 hours after stopping levodopa) was faster than while taking only levodopa (p <0.05). The daily levodopa dose decreased by 32.1% (p <0.01), yet the total “on” time increased from 73.5% ± 10.2% to 81.5% ± 7.5% of the day (p <0.01) after starting APO. “On” UPDRS part II scores (p <0.05) and “on” UPDRS part III (motor examination) scores (p <0.05) also improved. Adverse events such as nausea, orthostatic hypotension, and disagreeable taste did not limit the dose of APO in any case. The short‐term benefit and tolerability demonstrated in this study warrant further study of this new APO preparation.</div>
</front>
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<name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
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