Pergolide compared with bromocriptine in Parkinson's disease: A multicenter, crossover, controlled study
Identifieur interne : 008D05 ( Main/Merge ); précédent : 008D04; suivant : 008D06Pergolide compared with bromocriptine in Parkinson's disease: A multicenter, crossover, controlled study
Auteurs : Pezzoli [Italie] ; E. Martignoni [Italie] ; C. Pacchetti [Italie] ; V. A. Angeleri [Italie] ; P. Lamberti [Italie] ; A. Muratorio [Italie] ; U. Bonuccelli [Italie] ; M. De Mari [Italie] ; N. Foschi [Italie] ; E. Cossutta [Italie] ; F. Nicoletti [Italie] ; F. Giammona [Italie] ; M. Canesi [Italie] ; G. Scarlato [Italie] ; T. Caraceni [Italie] ; E. Moscarelli [Italie]Source :
- Movement Disorders [ 0885-3185 ] ; 1994.
English descriptors
- KwdEn :
- Aged, Bromocriptine, Bromocriptine (adverse effects), Bromocriptine (therapeutic use), Cross-Over Studies, Disability Evaluation, Dose-Response Relationship, Drug, Drug Therapy, Combination, Humans, Infant, Levodopa, Levodopa (adverse effects), Levodopa (therapeutic use), Male, Middle Aged, Neurologic Examination (drug effects), Parkinson Disease (drug therapy), Parkinson's disease, Pergolide, Pergolide (adverse effects), Pergolide (therapeutic use), Single-Blind Method, Treatment Outcome.
- MESH :
- chemical , adverse effects : Bromocriptine, Levodopa, Pergolide.
- chemical , therapeutic use : Bromocriptine, Levodopa, Pergolide.
- drug effects : Neurologic Examination.
- drug therapy : Parkinson Disease.
- Aged, Cross-Over Studies, Disability Evaluation, Dose-Response Relationship, Drug, Drug Therapy, Combination, Humans, Infant, Male, Middle Aged, Single-Blind Method, Treatment Outcome.
Abstract
We compared the efficacy and safety of pergolide and bromocriptine in 57 patients with Parkinson's disease (PD) with a declining response to levodopa therapy in a single‐blind, crossover study. Patients were placed randomly on the sequence bromocriptine‐pergolide (12 + 12 weeks) or vice versa. Regular evaluations using the New York University Parkinson's Disease Scale were performed by a clinician blinded to treatment assignment. Patients' and clinicians' impressions also were recorded. The average daily dose of pergolide was 2.3 ± 0.8 mg, and that of bromocriptine was 24.2 ± 8.4 mg. Significantly greater efficacy was demonstrated by both drugs as adjunctive therapy to levodopa compared with previous treatment of levodopa alone (pergolide, p = 0.0001; bromocriptine, p = 0.0005; Wilcoxon t test). Pergolide was more effective than bromocriptine in daily living scores (p = 0.020) and motor scores (p = 0.038). No difference in dyskinesias, dystonias, and psychosis was observed. Adverse events were more frequent in bromocriptine‐treated patients. Most patients and physicians preferred pergolide to bromocriptine. Pergolide as adjunctive therapy to levodopa was more effective than bromocriptine in this short‐term trial.
Url:
DOI: 10.1002/mds.870090409
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ISTEX:59255A37FA939BB771C3B14940E03285C7A77CBCLe document en format XML
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<term>Bromocriptine (therapeutic use)</term>
<term>Cross-Over Studies</term>
<term>Disability Evaluation</term>
<term>Dose-Response Relationship, Drug</term>
<term>Drug Therapy, Combination</term>
<term>Humans</term>
<term>Infant</term>
<term>Levodopa</term>
<term>Levodopa (adverse effects)</term>
<term>Levodopa (therapeutic use)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination (drug effects)</term>
<term>Parkinson Disease (drug therapy)</term>
<term>Parkinson's disease</term>
<term>Pergolide</term>
<term>Pergolide (adverse effects)</term>
<term>Pergolide (therapeutic use)</term>
<term>Single-Blind Method</term>
<term>Treatment Outcome</term>
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<term>Levodopa</term>
<term>Pergolide</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Bromocriptine</term>
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<front><div type="abstract" xml:lang="en">We compared the efficacy and safety of pergolide and bromocriptine in 57 patients with Parkinson's disease (PD) with a declining response to levodopa therapy in a single‐blind, crossover study. Patients were placed randomly on the sequence bromocriptine‐pergolide (12 + 12 weeks) or vice versa. Regular evaluations using the New York University Parkinson's Disease Scale were performed by a clinician blinded to treatment assignment. Patients' and clinicians' impressions also were recorded. The average daily dose of pergolide was 2.3 ± 0.8 mg, and that of bromocriptine was 24.2 ± 8.4 mg. Significantly greater efficacy was demonstrated by both drugs as adjunctive therapy to levodopa compared with previous treatment of levodopa alone (pergolide, p = 0.0001; bromocriptine, p = 0.0005; Wilcoxon t test). Pergolide was more effective than bromocriptine in daily living scores (p = 0.020) and motor scores (p = 0.038). No difference in dyskinesias, dystonias, and psychosis was observed. Adverse events were more frequent in bromocriptine‐treated patients. Most patients and physicians preferred pergolide to bromocriptine. Pergolide as adjunctive therapy to levodopa was more effective than bromocriptine in this short‐term trial.</div>
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<wicri:regionArea>Institute of Neurology, University of Bari, Bari</wicri:regionArea>
<wicri:noRegion>Bari</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Muratorio, A" sort="Muratorio, A" uniqKey="Muratorio A" first="A." last="Muratorio">A. Muratorio</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Clinical Neurology, University of Pisa, Pisa</wicri:regionArea>
<wicri:noRegion>Pisa</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bonuccelli, U" sort="Bonuccelli, U" uniqKey="Bonuccelli U" first="U." last="Bonuccelli">U. Bonuccelli</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Clinical Neurology, University of Pisa, Pisa</wicri:regionArea>
<wicri:noRegion>Pisa</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="De Mari, M" sort="De Mari, M" uniqKey="De Mari M" first="M." last="De Mari">M. De Mari</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Neurology, University of Bari, Bari</wicri:regionArea>
<wicri:noRegion>Bari</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Foschi, N" sort="Foschi, N" uniqKey="Foschi N" first="N." last="Foschi">N. Foschi</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Neurology, University of Ancona, Ancona</wicri:regionArea>
<wicri:noRegion>Ancona</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Cossutta, E" sort="Cossutta, E" uniqKey="Cossutta E" first="E." last="Cossutta">E. Cossutta</name>
<affiliation wicri:level="3"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Neurology, Neurological Institute C. Besta, Milan, Milan</wicri:regionArea>
<placeName><settlement type="city">Milan</settlement>
<region nuts="2">Lombardie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Nicoletti, F" sort="Nicoletti, F" uniqKey="Nicoletti F" first="F." last="Nicoletti">F. Nicoletti</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Pharmacology, University of Catania, Catania</wicri:regionArea>
<wicri:noRegion>Catania</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Giammona, F" sort="Giammona, F" uniqKey="Giammona F" first="F." last="Giammona">F. Giammona</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Pharmacology, University of Catania, Catania</wicri:regionArea>
<wicri:noRegion>Catania</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Canesi, M" sort="Canesi, M" uniqKey="Canesi M" first="M." last="Canesi">M. Canesi</name>
<affiliation wicri:level="3"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Clinical Neurology, University of Milan, Milan</wicri:regionArea>
<placeName><settlement type="city">Milan</settlement>
<region nuts="2">Lombardie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Scarlato, G" sort="Scarlato, G" uniqKey="Scarlato G" first="G." last="Scarlato">G. Scarlato</name>
<affiliation wicri:level="3"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Institute of Clinical Neurology, University of Milan, Milan</wicri:regionArea>
<placeName><settlement type="city">Milan</settlement>
<region nuts="2">Lombardie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Caraceni, T" sort="Caraceni, T" uniqKey="Caraceni T" first="T." last="Caraceni">T. Caraceni</name>
<affiliation wicri:level="3"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Neurology, Neurological Institute C. Besta, Milan, Milan</wicri:regionArea>
<placeName><settlement type="city">Milan</settlement>
<region nuts="2">Lombardie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Moscarelli, E" sort="Moscarelli, E" uniqKey="Moscarelli E" first="E." last="Moscarelli">E. Moscarelli</name>
<affiliation wicri:level="1"><country xml:lang="fr">Italie</country>
<wicri:regionArea>Eli Lilly Italia, Sesto Fiorentio</wicri:regionArea>
<wicri:noRegion>Sesto Fiorentio</wicri:noRegion>
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</author>
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<series><title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="1994">1994</date>
<biblScope unit="vol">9</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="431">431</biblScope>
<biblScope unit="page" to="436">436</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
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<idno type="DOI">10.1002/mds.870090409</idno>
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<term>Pergolide</term>
</keywords>
</textClass>
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<front><div type="abstract" xml:lang="en">We compared the efficacy and safety of pergolide and bromocriptine in 57 patients with Parkinson's disease (PD) with a declining response to levodopa therapy in a single‐blind, crossover study. Patients were placed randomly on the sequence bromocriptine‐pergolide (12 + 12 weeks) or vice versa. Regular evaluations using the New York University Parkinson's Disease Scale were performed by a clinician blinded to treatment assignment. Patients' and clinicians' impressions also were recorded. The average daily dose of pergolide was 2.3 ± 0.8 mg, and that of bromocriptine was 24.2 ± 8.4 mg. Significantly greater efficacy was demonstrated by both drugs as adjunctive therapy to levodopa compared with previous treatment of levodopa alone (pergolide, p = 0.0001; bromocriptine, p = 0.0005; Wilcoxon t test). Pergolide was more effective than bromocriptine in daily living scores (p = 0.020) and motor scores (p = 0.038). No difference in dyskinesias, dystonias, and psychosis was observed. Adverse events were more frequent in bromocriptine‐treated patients. Most patients and physicians preferred pergolide to bromocriptine. Pergolide as adjunctive therapy to levodopa was more effective than bromocriptine in this short‐term trial.</div>
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<country xml:lang="fr">Italie</country>
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<author><name sortKey="Angeleri, V A" sort="Angeleri, V A" uniqKey="Angeleri V" first="V A" last="Angeleri">V A Angeleri</name>
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<author><name sortKey="Lamberti, P" sort="Lamberti, P" uniqKey="Lamberti P" first="P" last="Lamberti">P. Lamberti</name>
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<author><name sortKey="Muratorio, A" sort="Muratorio, A" uniqKey="Muratorio A" first="A" last="Muratorio">A. Muratorio</name>
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<author><name sortKey="Bonuccelli, U" sort="Bonuccelli, U" uniqKey="Bonuccelli U" first="U" last="Bonuccelli">U. Bonuccelli</name>
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<author><name sortKey="De Mari, M" sort="De Mari, M" uniqKey="De Mari M" first="M" last="De Mari">M. De Mari</name>
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<author><name sortKey="Foschi, N" sort="Foschi, N" uniqKey="Foschi N" first="N" last="Foschi">N. Foschi</name>
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<author><name sortKey="Cossutta, E" sort="Cossutta, E" uniqKey="Cossutta E" first="E" last="Cossutta">E. Cossutta</name>
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<author><name sortKey="Martignoni, E" sort="Martignoni, E" uniqKey="Martignoni E" first="E" last="Martignoni">E. Martignoni</name>
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<author><name sortKey="Angeleri, V A" sort="Angeleri, V A" uniqKey="Angeleri V" first="V A" last="Angeleri">V A Angeleri</name>
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<author><name sortKey="Lamberti, P" sort="Lamberti, P" uniqKey="Lamberti P" first="P" last="Lamberti">P. Lamberti</name>
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<author><name sortKey="Muratorio, A" sort="Muratorio, A" uniqKey="Muratorio A" first="A" last="Muratorio">A. Muratorio</name>
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<author><name sortKey="Bonuccelli, U" sort="Bonuccelli, U" uniqKey="Bonuccelli U" first="U" last="Bonuccelli">U. Bonuccelli</name>
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<author><name sortKey="De Mari, M" sort="De Mari, M" uniqKey="De Mari M" first="M" last="De Mari">M. De Mari</name>
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<author><name sortKey="Foschi, N" sort="Foschi, N" uniqKey="Foschi N" first="N" last="Foschi">N. Foschi</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Bromocriptine (adverse effects)</term>
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<term>Cross-Over Studies</term>
<term>Disability Evaluation</term>
<term>Dose-Response Relationship, Drug</term>
<term>Drug Therapy, Combination</term>
<term>Humans</term>
<term>Infant</term>
<term>Levodopa (adverse effects)</term>
<term>Levodopa (therapeutic use)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination (drug effects)</term>
<term>Parkinson Disease (drug therapy)</term>
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<term>Pergolide (therapeutic use)</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Neurologic Examination</term>
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</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
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<term>Disability Evaluation</term>
<term>Dose-Response Relationship, Drug</term>
<term>Drug Therapy, Combination</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
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<term>Single-Blind Method</term>
<term>Treatment Outcome</term>
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<front><div type="abstract" xml:lang="en">We compared the efficacy and safety of pergolide and bromocriptine in 57 patients with Parkinson's disease (PD) with a declining response to levodopa therapy in a single-blind, crossover study. Patients were placed randomly on the sequence bromocriptine-pergolide (12 + 12 weeks) or vice versa. Regular evaluations using the New York University Parkinson's Disease Scale were performed by a clinician blinded to treatment assignment. Patients' and clinicians' impressions also were recorded. The average daily dose of pergolide was 2.3 +/0- 0.8 mg, and that of bromocriptine was 24.2 +/- 8.4 mg. Significantly greater efficacy was demonstrated by both drugs as adjunctive therapy to levodopa compared with previous treatment of levodopa alone (pergolide, p = 0.0001; bromocriptine, p = 0.0005; Wilcoxon t test). Pergolide was more effective than bromocriptine in daily living scores (p = 0.020) and motor scores (p = 0.038). No difference in dyskinesias, dystonias, and psychosis was observed. Adverse events were more frequent in bromocriptine-treated patients. Most patients and physicians preferred pergolide to bromocriptine. Pergolide as adjunctive therapy to levodopa was more effective than bromocriptine in this short-term trial.</div>
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