Movement Disorders (revue)

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Apomorphine : An underutilized therapy for Parkinson's disease

Identifieur interne : 002B34 ( PascalFrancis/Corpus ); précédent : 002B33; suivant : 002B35

Apomorphine : An underutilized therapy for Parkinson's disease

Auteurs : Werner Poewe ; Gregor K. Wenning

Source :

RBID : Pascal:00-0481439

Descripteurs français

English descriptors

Abstract

Apomorphine was the first dopaminergic drug ever used to treat symptoms of Parkinson's disease. While powerful antiparkinsonian effects had been observed as early as 1951, the potential of treating fluctuating Parkinson's disease by subcutaneous administration of apomorphine has only recently become the subject of systematic study. A number of small scale clinical trials have unequivocally shown that intermittent subcutaneous apomorphine injections produce antiparkinsonian benefit close if not identical to that seen with levodopa and that apomorphine rescue injections can reliably revert off-periods even in patients with complex on-off motor swings. Continuous subcutaneous apomorphine infusions can reduce daily off-time by more than 50% in this group of patients, which appears to be a stronger effect than that generally seen with add-on therapy with oral dopamine agonists or COMT inhibitors. Extended follow-up studies of up to 8 years have demonstrated long-term persistence of apomorphine efficacy. In addition, there is convincing clinical evidence that monotherapy with continuous subcutaneous apomorphine infusions is associated with marked reductions of preexisting levodopainduced dyskinesias. The main side effects of subcutaneous apomorphine treatment are related to cutaneous tolerability problems, whereas sedation and psychiatric complications play a lesser role. Given the marked degree of efficacy of subcutaneous apomorphine treatment in fluctuating Parkinson's disease, this approach seems to deserve more widespread clinical use.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08 01  1  ENG  @1 Apomorphine : An underutilized therapy for Parkinson's disease
A11 01  1    @1 POEWE (Werner)
A11 02  1    @1 WENNING (Gregor K.)
A14 01      @1 Department of Neurology, University Hospital Innsbruck @2 Innsbruck @3 AUT @Z 1 aut. @Z 2 aut.
A20       @1 789-794
A21       @1 2000
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000091356830040
A44       @0 0000 @1 © 2000 INIST-CNRS. All rights reserved.
A45       @0 58 ref.
A47 01  1    @0 00-0481439
A60       @1 P
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C01 01    ENG  @0 Apomorphine was the first dopaminergic drug ever used to treat symptoms of Parkinson's disease. While powerful antiparkinsonian effects had been observed as early as 1951, the potential of treating fluctuating Parkinson's disease by subcutaneous administration of apomorphine has only recently become the subject of systematic study. A number of small scale clinical trials have unequivocally shown that intermittent subcutaneous apomorphine injections produce antiparkinsonian benefit close if not identical to that seen with levodopa and that apomorphine rescue injections can reliably revert off-periods even in patients with complex on-off motor swings. Continuous subcutaneous apomorphine infusions can reduce daily off-time by more than 50% in this group of patients, which appears to be a stronger effect than that generally seen with add-on therapy with oral dopamine agonists or COMT inhibitors. Extended follow-up studies of up to 8 years have demonstrated long-term persistence of apomorphine efficacy. In addition, there is convincing clinical evidence that monotherapy with continuous subcutaneous apomorphine infusions is associated with marked reductions of preexisting levodopainduced dyskinesias. The main side effects of subcutaneous apomorphine treatment are related to cutaneous tolerability problems, whereas sedation and psychiatric complications play a lesser role. Given the marked degree of efficacy of subcutaneous apomorphine treatment in fluctuating Parkinson's disease, this approach seems to deserve more widespread clinical use.
C02 01  X    @0 002B02B06
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C03 02  X  FRE  @0 Apomorphine @2 NK @2 FR @5 04
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C03 14  X  FRE  @0 Homme @5 20
C03 14  X  ENG  @0 Human @5 20
C03 14  X  SPA  @0 Hombre @5 20
C03 15  X  FRE  @0 Fluctuation motrice @4 INC @5 86
C07 01  X  FRE  @0 Système nerveux pathologie @5 37
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C07 03  X  SPA  @0 Encéfalo patología @5 39
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C07 04  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 05  X  FRE  @0 Maladie dégénérative @5 41
C07 05  X  ENG  @0 Degenerative disease @5 41
C07 05  X  SPA  @0 Enfermedad degenerativa @5 41
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C07 06  X  ENG  @0 Neurological disorder @5 62
C07 06  X  SPA  @0 Trastorno neurológico @5 62
C07 07  X  FRE  @0 Mouvement involontaire @5 63
C07 07  X  ENG  @0 Involuntary movement @5 63
C07 07  X  SPA  @0 Movimiento involuntario @5 63
N21       @1 318

Format Inist (serveur)

NO : PASCAL 00-0481439 INIST
ET : Apomorphine : An underutilized therapy for Parkinson's disease
AU : POEWE (Werner); WENNING (Gregor K.)
AF : Department of Neurology, University Hospital Innsbruck/Innsbruck/Autriche (1 aut., 2 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2000; Vol. 15; No. 5; Pp. 789-794; Bibl. 58 ref.
LA : Anglais
EA : Apomorphine was the first dopaminergic drug ever used to treat symptoms of Parkinson's disease. While powerful antiparkinsonian effects had been observed as early as 1951, the potential of treating fluctuating Parkinson's disease by subcutaneous administration of apomorphine has only recently become the subject of systematic study. A number of small scale clinical trials have unequivocally shown that intermittent subcutaneous apomorphine injections produce antiparkinsonian benefit close if not identical to that seen with levodopa and that apomorphine rescue injections can reliably revert off-periods even in patients with complex on-off motor swings. Continuous subcutaneous apomorphine infusions can reduce daily off-time by more than 50% in this group of patients, which appears to be a stronger effect than that generally seen with add-on therapy with oral dopamine agonists or COMT inhibitors. Extended follow-up studies of up to 8 years have demonstrated long-term persistence of apomorphine efficacy. In addition, there is convincing clinical evidence that monotherapy with continuous subcutaneous apomorphine infusions is associated with marked reductions of preexisting levodopainduced dyskinesias. The main side effects of subcutaneous apomorphine treatment are related to cutaneous tolerability problems, whereas sedation and psychiatric complications play a lesser role. Given the marked degree of efficacy of subcutaneous apomorphine treatment in fluctuating Parkinson's disease, this approach seems to deserve more widespread clinical use.
CC : 002B02B06
FD : Parkinson maladie; Apomorphine; Chimiothérapie; Agoniste; Récepteur dopaminergique; Stimulant dopaminergique; Voie souscutanée; Dyskinésie; Antiparkinsonien; Toxicité; Traitement; Indication; Complication; Homme; Fluctuation motrice
FG : Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Trouble neurologique; Mouvement involontaire
ED : Parkinson disease; Chemotherapy; Agonist; Dopamine receptor; Dopamine agonist; Subcutaneous administration; Dyskinesia; Antiparkinson agent; Toxicity; Treatment; Indication; Complication; Human
EG : Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Neurological disorder; Involuntary movement
SD : Parkinson enfermedad; Quimioterapia; Agonista; Receptor dopaminérgico; Estimulante dopaminérgico; Vía subcutánea; Disquinesia; Antiparkinsoniano; Toxicidad; Tratamiento; Indicación; Complicación; Hombre
LO : INIST-20953.354000091356830040
ID : 00-0481439

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Pascal:00-0481439

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<s5>19</s5>
</fC03>
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<s0>Complication</s0>
<s5>19</s5>
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<s5>19</s5>
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<s5>20</s5>
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<fC03 i1="14" i2="X" l="ENG">
<s0>Human</s0>
<s5>20</s5>
</fC03>
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<s0>Hombre</s0>
<s5>20</s5>
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<s5>86</s5>
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<s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
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<s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
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<s0>Système nerveux central pathologie</s0>
<s5>38</s5>
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<s0>Central nervous system disease</s0>
<s5>38</s5>
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<s0>Sistema nervosio central patología</s0>
<s5>38</s5>
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<s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>62</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>62</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>62</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>63</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>63</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>63</s5>
</fC07>
<fN21>
<s1>318</s1>
</fN21>
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<NO>PASCAL 00-0481439 INIST</NO>
<ET>Apomorphine : An underutilized therapy for Parkinson's disease</ET>
<AU>POEWE (Werner); WENNING (Gregor K.)</AU>
<AF>Department of Neurology, University Hospital Innsbruck/Innsbruck/Autriche (1 aut., 2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2000; Vol. 15; No. 5; Pp. 789-794; Bibl. 58 ref.</SO>
<LA>Anglais</LA>
<EA>Apomorphine was the first dopaminergic drug ever used to treat symptoms of Parkinson's disease. While powerful antiparkinsonian effects had been observed as early as 1951, the potential of treating fluctuating Parkinson's disease by subcutaneous administration of apomorphine has only recently become the subject of systematic study. A number of small scale clinical trials have unequivocally shown that intermittent subcutaneous apomorphine injections produce antiparkinsonian benefit close if not identical to that seen with levodopa and that apomorphine rescue injections can reliably revert off-periods even in patients with complex on-off motor swings. Continuous subcutaneous apomorphine infusions can reduce daily off-time by more than 50% in this group of patients, which appears to be a stronger effect than that generally seen with add-on therapy with oral dopamine agonists or COMT inhibitors. Extended follow-up studies of up to 8 years have demonstrated long-term persistence of apomorphine efficacy. In addition, there is convincing clinical evidence that monotherapy with continuous subcutaneous apomorphine infusions is associated with marked reductions of preexisting levodopainduced dyskinesias. The main side effects of subcutaneous apomorphine treatment are related to cutaneous tolerability problems, whereas sedation and psychiatric complications play a lesser role. Given the marked degree of efficacy of subcutaneous apomorphine treatment in fluctuating Parkinson's disease, this approach seems to deserve more widespread clinical use.</EA>
<CC>002B02B06</CC>
<FD>Parkinson maladie; Apomorphine; Chimiothérapie; Agoniste; Récepteur dopaminergique; Stimulant dopaminergique; Voie souscutanée; Dyskinésie; Antiparkinsonien; Toxicité; Traitement; Indication; Complication; Homme; Fluctuation motrice</FD>
<FG>Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Trouble neurologique; Mouvement involontaire</FG>
<ED>Parkinson disease; Chemotherapy; Agonist; Dopamine receptor; Dopamine agonist; Subcutaneous administration; Dyskinesia; Antiparkinson agent; Toxicity; Treatment; Indication; Complication; Human</ED>
<EG>Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Neurological disorder; Involuntary movement</EG>
<SD>Parkinson enfermedad; Quimioterapia; Agonista; Receptor dopaminérgico; Estimulante dopaminérgico; Vía subcutánea; Disquinesia; Antiparkinsoniano; Toxicidad; Tratamiento; Indicación; Complicación; Hombre</SD>
<LO>INIST-20953.354000091356830040</LO>
<ID>00-0481439</ID>
</server>
</inist>
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