Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: A prospective study using single-dose challenges
Continuous subcutaneous (SC) infusion of the dopamine agonist apomorphine was shown in retrospective studies to improve drug‐induced dyskinesias in Parkinson's disease (PD). We prospectively assessed the antidyskinetic effect of continuous SC apomorphine therapy using subjective and objective m...
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Veröffentlicht in: | Movement disorders 2005-02, Vol.20 (2), p.151-157 |
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description | Continuous subcutaneous (SC) infusion of the dopamine agonist apomorphine was shown in retrospective studies to improve drug‐induced dyskinesias in Parkinson's disease (PD). We prospectively assessed the antidyskinetic effect of continuous SC apomorphine therapy using subjective and objective measures, and sought to determine whether any observed dyskinesia reduction could be corroborated using single‐dose dopaminergic challenges. Twelve PD patients with on–off fluctuations and disabling dyskinesias who were scheduled to start apomorphine pump treatment underwent acute levodopa and apomorphine challenges at baseline and 6 months later. Video recordings involving motor tasks were rated blindly by two independent raters using modified AIMS and Goetz dyskinesia scales. At 6 months, mean apomorphine dose was 75.2 mg per day and the mean l‐dopa dose had been reduced by 55%. Daily off time in patients' diaries was reduced by 38% (2.4 hours). The l‐dopa challenges showed a reduction of 44% in AIMS and 40% in Goetz scores (both P < 0.01). Apomorphine challenges showed a reduction of 39% in AIMS and 36% in Goetz scores (both P < 0.01). Patients' self‐assessment scores reflected these significant changes. Dyskinesia improvement correlated with reduction in oral medication and with the final apomorphine dose (P < 0.05). This prospective study confirms marked dyskinesia reduction on continuous subcutaneous apomorphine therapy, paralleled by reduced dyskinesias during dopaminergic challenge tests. Our findings support the concept that replacement of short‐acting oral antiparkinsonian medication with continuous dopamine receptor stimulation may reverse, at least partially, the sensitization process believed to mediate the development of drug‐induced dyskinesias in PD. © 2004 Movement Disorder Society |
doi_str_mv | 10.1002/mds.20276 |
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We prospectively assessed the antidyskinetic effect of continuous SC apomorphine therapy using subjective and objective measures, and sought to determine whether any observed dyskinesia reduction could be corroborated using single‐dose dopaminergic challenges. Twelve PD patients with on–off fluctuations and disabling dyskinesias who were scheduled to start apomorphine pump treatment underwent acute levodopa and apomorphine challenges at baseline and 6 months later. Video recordings involving motor tasks were rated blindly by two independent raters using modified AIMS and Goetz dyskinesia scales. At 6 months, mean apomorphine dose was 75.2 mg per day and the mean l‐dopa dose had been reduced by 55%. Daily off time in patients' diaries was reduced by 38% (2.4 hours). The l‐dopa challenges showed a reduction of 44% in AIMS and 40% in Goetz scores (both P < 0.01). Apomorphine challenges showed a reduction of 39% in AIMS and 36% in Goetz scores (both P < 0.01). Patients' self‐assessment scores reflected these significant changes. Dyskinesia improvement correlated with reduction in oral medication and with the final apomorphine dose (P < 0.05). This prospective study confirms marked dyskinesia reduction on continuous subcutaneous apomorphine therapy, paralleled by reduced dyskinesias during dopaminergic challenge tests. Our findings support the concept that replacement of short‐acting oral antiparkinsonian medication with continuous dopamine receptor stimulation may reverse, at least partially, the sensitization process believed to mediate the development of drug‐induced dyskinesias in PD. © 2004 Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.20276</identifier><identifier>PMID: 15390035</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Aged, 80 and over ; Antiparkinson Agents - therapeutic use ; apomorphine ; Apomorphine - therapeutic use ; Biological and medical sciences ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Drug toxicity and drugs side effects treatment ; dyskinesias ; Dyskinesias - drug therapy ; Dyskinesias - etiology ; Female ; Follow-Up Studies ; Humans ; Injections, Subcutaneous ; Levodopa - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Neurologic Examination ; Neurology ; Pain Measurement - methods ; Parkinson Disease - complications ; Parkinson's disease ; Pharmacology. Drug treatments ; Prospective Studies ; Self-Assessment ; Statistics, Nonparametric ; Toxicity: nervous system and muscle</subject><ispartof>Movement disorders, 2005-02, Vol.20 (2), p.151-157</ispartof><rights>Copyright © 2004 Movement Disorder Society</rights><rights>2005 INIST-CNRS</rights><rights>Copyright 2004 Movement Disorder Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4226-be6b1ab052fcf6d871f02edb09f68cbfb4e2774127ac9c93e2bab0fd9ade96e43</citedby><cites>FETCH-LOGICAL-c4226-be6b1ab052fcf6d871f02edb09f68cbfb4e2774127ac9c93e2bab0fd9ade96e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.20276$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.20276$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16569354$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15390035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katzenschlager, Regina</creatorcontrib><creatorcontrib>Hughes, Andrew</creatorcontrib><creatorcontrib>Evans, Andrew</creatorcontrib><creatorcontrib>Manson, Alice J.</creatorcontrib><creatorcontrib>Hoffman, Marion</creatorcontrib><creatorcontrib>Swinn, Lesley</creatorcontrib><creatorcontrib>Watt, Hilary</creatorcontrib><creatorcontrib>Bhatia, Kailash</creatorcontrib><creatorcontrib>Quinn, Niall</creatorcontrib><creatorcontrib>Lees, Andrew J.</creatorcontrib><title>Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: A prospective study using single-dose challenges</title><title>Movement disorders</title><addtitle>Mov. Disord</addtitle><description>Continuous subcutaneous (SC) infusion of the dopamine agonist apomorphine was shown in retrospective studies to improve drug‐induced dyskinesias in Parkinson's disease (PD). We prospectively assessed the antidyskinetic effect of continuous SC apomorphine therapy using subjective and objective measures, and sought to determine whether any observed dyskinesia reduction could be corroborated using single‐dose dopaminergic challenges. Twelve PD patients with on–off fluctuations and disabling dyskinesias who were scheduled to start apomorphine pump treatment underwent acute levodopa and apomorphine challenges at baseline and 6 months later. Video recordings involving motor tasks were rated blindly by two independent raters using modified AIMS and Goetz dyskinesia scales. At 6 months, mean apomorphine dose was 75.2 mg per day and the mean l‐dopa dose had been reduced by 55%. Daily off time in patients' diaries was reduced by 38% (2.4 hours). The l‐dopa challenges showed a reduction of 44% in AIMS and 40% in Goetz scores (both P < 0.01). Apomorphine challenges showed a reduction of 39% in AIMS and 36% in Goetz scores (both P < 0.01). Patients' self‐assessment scores reflected these significant changes. Dyskinesia improvement correlated with reduction in oral medication and with the final apomorphine dose (P < 0.05). This prospective study confirms marked dyskinesia reduction on continuous subcutaneous apomorphine therapy, paralleled by reduced dyskinesias during dopaminergic challenge tests. Our findings support the concept that replacement of short‐acting oral antiparkinsonian medication with continuous dopamine receptor stimulation may reverse, at least partially, the sensitization process believed to mediate the development of drug‐induced dyskinesias in PD. © 2004 Movement Disorder Society</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>apomorphine</subject><subject>Apomorphine - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>dyskinesias</subject><subject>Dyskinesias - drug therapy</subject><subject>Dyskinesias - etiology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Injections, Subcutaneous</subject><subject>Levodopa - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurologic Examination</subject><subject>Neurology</subject><subject>Pain Measurement - methods</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson's disease</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>Self-Assessment</subject><subject>Statistics, Nonparametric</subject><subject>Toxicity: nervous system and muscle</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1TAQhi0EoofCghdA3gBikdZ2YidhV51yCqJcxKVIbCxfJj2G3MgkhTwCb40POdAVYjOj0Xwz498_Ifc5O-KMiePG45FgIlc3yIrLlCeFkPlNsmJFIZOUF_KA3EH8whjnkqvb5CBCJWOpXJGf664dQzt1E1KcrJtG08KuMH3XdEO_DS3QcQuD6Wcamn7orgCpn_FrbGAwSENL35ohlti1j2MrIBiEp_SERhh7cGO4Aorj5Gc6YWgv6S7UkPgOgbqtqWtoLwHvkluVqRHu7fMh-bh59mH9PDl_c_ZifXKeuEwIlVhQlhvLpKhcpXyR84oJ8JaVlSqcrWwGIs8zLnLjSlemIGykK18aD6WCLD0kj5a98XnfJsBRNwEd1PUiXKs8y0qm1H9BEX9TilJG8MkCuigYB6h0P4TGDLPmTO8M0tEg_dugyD7YL51sA_6a3DsSgYd7wKAzdTWY1gW85pRUZSp3Mo4X7nuoYf73Rf3q9P2f08kyEXCEH38nondRc5pL_en1mVbvNi8vTj9v9EX6C4-Cu18</recordid><startdate>200502</startdate><enddate>200502</enddate><creator>Katzenschlager, Regina</creator><creator>Hughes, Andrew</creator><creator>Evans, Andrew</creator><creator>Manson, Alice J.</creator><creator>Hoffman, Marion</creator><creator>Swinn, Lesley</creator><creator>Watt, Hilary</creator><creator>Bhatia, Kailash</creator><creator>Quinn, Niall</creator><creator>Lees, Andrew J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>200502</creationdate><title>Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: A prospective study using single-dose challenges</title><author>Katzenschlager, Regina ; Hughes, Andrew ; Evans, Andrew ; Manson, Alice J. ; Hoffman, Marion ; Swinn, Lesley ; Watt, Hilary ; Bhatia, Kailash ; Quinn, Niall ; Lees, Andrew J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4226-be6b1ab052fcf6d871f02edb09f68cbfb4e2774127ac9c93e2bab0fd9ade96e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antiparkinson Agents - therapeutic use</topic><topic>apomorphine</topic><topic>Apomorphine - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>dyskinesias</topic><topic>Dyskinesias - drug therapy</topic><topic>Dyskinesias - etiology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Injections, Subcutaneous</topic><topic>Levodopa - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurologic Examination</topic><topic>Neurology</topic><topic>Pain Measurement - methods</topic><topic>Parkinson Disease - complications</topic><topic>Parkinson's disease</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Self-Assessment</topic><topic>Statistics, Nonparametric</topic><topic>Toxicity: nervous system and muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katzenschlager, Regina</creatorcontrib><creatorcontrib>Hughes, Andrew</creatorcontrib><creatorcontrib>Evans, Andrew</creatorcontrib><creatorcontrib>Manson, Alice J.</creatorcontrib><creatorcontrib>Hoffman, Marion</creatorcontrib><creatorcontrib>Swinn, Lesley</creatorcontrib><creatorcontrib>Watt, Hilary</creatorcontrib><creatorcontrib>Bhatia, Kailash</creatorcontrib><creatorcontrib>Quinn, Niall</creatorcontrib><creatorcontrib>Lees, Andrew J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katzenschlager, Regina</au><au>Hughes, Andrew</au><au>Evans, Andrew</au><au>Manson, Alice J.</au><au>Hoffman, Marion</au><au>Swinn, Lesley</au><au>Watt, Hilary</au><au>Bhatia, Kailash</au><au>Quinn, Niall</au><au>Lees, Andrew J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: A prospective study using single-dose challenges</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>2005-02</date><risdate>2005</risdate><volume>20</volume><issue>2</issue><spage>151</spage><epage>157</epage><pages>151-157</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>Continuous subcutaneous (SC) infusion of the dopamine agonist apomorphine was shown in retrospective studies to improve drug‐induced dyskinesias in Parkinson's disease (PD). We prospectively assessed the antidyskinetic effect of continuous SC apomorphine therapy using subjective and objective measures, and sought to determine whether any observed dyskinesia reduction could be corroborated using single‐dose dopaminergic challenges. Twelve PD patients with on–off fluctuations and disabling dyskinesias who were scheduled to start apomorphine pump treatment underwent acute levodopa and apomorphine challenges at baseline and 6 months later. Video recordings involving motor tasks were rated blindly by two independent raters using modified AIMS and Goetz dyskinesia scales. At 6 months, mean apomorphine dose was 75.2 mg per day and the mean l‐dopa dose had been reduced by 55%. Daily off time in patients' diaries was reduced by 38% (2.4 hours). The l‐dopa challenges showed a reduction of 44% in AIMS and 40% in Goetz scores (both P < 0.01). Apomorphine challenges showed a reduction of 39% in AIMS and 36% in Goetz scores (both P < 0.01). Patients' self‐assessment scores reflected these significant changes. Dyskinesia improvement correlated with reduction in oral medication and with the final apomorphine dose (P < 0.05). This prospective study confirms marked dyskinesia reduction on continuous subcutaneous apomorphine therapy, paralleled by reduced dyskinesias during dopaminergic challenge tests. Our findings support the concept that replacement of short‐acting oral antiparkinsonian medication with continuous dopamine receptor stimulation may reverse, at least partially, the sensitization process believed to mediate the development of drug‐induced dyskinesias in PD. © 2004 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15390035</pmid><doi>10.1002/mds.20276</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Antiparkinson Agents - therapeutic use apomorphine Apomorphine - therapeutic use Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dose-Response Relationship, Drug Drug Administration Schedule Drug toxicity and drugs side effects treatment dyskinesias Dyskinesias - drug therapy Dyskinesias - etiology Female Follow-Up Studies Humans Injections, Subcutaneous Levodopa - therapeutic use Male Medical sciences Middle Aged Neurologic Examination Neurology Pain Measurement - methods Parkinson Disease - complications Parkinson's disease Pharmacology. Drug treatments Prospective Studies Self-Assessment Statistics, Nonparametric Toxicity: nervous system and muscle |
title | Continuous subcutaneous apomorphine therapy improves dyskinesias in Parkinson's disease: A prospective study using single-dose challenges |
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