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Cost Effectiveness of Pharmacotherapies in Early Parkinson’s Disease
Parkinson’s disease is one of the most common chronic neurodegenerative diseases. The progression of disease and the psychosocial consequences exert a major impact on patients’ health-related quality of life. Although levodopa provides the best symptomatic benefit with the fewest short-term adverse...
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Published in: | CNS drugs 2008-01, Vol.22 (10), p.841-860 |
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description | Parkinson’s disease is one of the most common chronic neurodegenerative diseases. The progression of disease and the psychosocial consequences exert a major impact on patients’ health-related quality of life. Although levodopa provides the best symptomatic benefit with the fewest short-term adverse effects, long-term treatment results in motor complications that are associated with both higher costs and considerable increase in patients’ discomfort. The introduction of dopamine agonists early in the treatment of Parkinson’s disease leads to a delay of these motor complications, but the treatment is associated with higher costs.
In this review we evaluate available cost-effectiveness analyses of the dopamine agonists pramipexole, pergolide, bromocriptine, ropinirole, cabergoline and levodopa in the treatment of early Parkinson’s disease. Considerable method-ological differences in the identified studies complicate a comparison and impede clear evidence as to which dopamine agonist treatment is the most cost effective in early Parkinson’s disease. Novel head-to-head comparisons considering the actual treatment guidelines are necessary to identify the most cost-effective alternative in treating
de novo
Parkinson’s disease patients. |
doi_str_mv | 10.2165/00023210-200822100-00005 |
format | article |
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In this review we evaluate available cost-effectiveness analyses of the dopamine agonists pramipexole, pergolide, bromocriptine, ropinirole, cabergoline and levodopa in the treatment of early Parkinson’s disease. Considerable method-ological differences in the identified studies complicate a comparison and impede clear evidence as to which dopamine agonist treatment is the most cost effective in early Parkinson’s disease. Novel head-to-head comparisons considering the actual treatment guidelines are necessary to identify the most cost-effective alternative in treating
de novo
Parkinson’s disease patients.</description><identifier>ISSN: 1172-7047</identifier><identifier>EISSN: 1179-1934</identifier><identifier>DOI: 10.2165/00023210-200822100-00005</identifier><identifier>PMID: 18788836</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult and adolescent clinical studies ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; Antiparkinson Agents - economics ; Antiparkinson Agents - therapeutic use ; Biological and medical sciences ; Cost-Benefit Analysis ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dopa ; Drug therapy ; Health aspects ; Humans ; Medical sciences ; Medicine ; Medicine & Public Health ; Nervous system (semeiology, syndromes) ; Nervous system as a whole ; Neurology ; Neuropharmacology ; Neurosciences ; Organic mental disorders. Neuropsychology ; Parkinson Disease - drug therapy ; Parkinson Disease - economics ; Parkinson's disease ; Patient outcomes ; Pharmacology. Drug treatments ; Pharmacotherapy ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychopharmacology ; Review Article</subject><ispartof>CNS drugs, 2008-01, Vol.22 (10), p.841-860</ispartof><rights>Adis Data Information BV 2008</rights><rights>2008 INIST-CNRS</rights><rights>COPYRIGHT 2008 Wolters Kluwer Health, Inc.</rights><rights>Copyright Wolters Kluwer Health Adis International 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-d91042cfef4c29e944d3f83af57efea466e39c8f1aed01d787c30a0a92652be73</citedby><cites>FETCH-LOGICAL-c518t-d91042cfef4c29e944d3f83af57efea466e39c8f1aed01d787c30a0a92652be73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20674745$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18788836$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eggert, Karla M.</creatorcontrib><creatorcontrib>Reese, Jens P.</creatorcontrib><creatorcontrib>Oertel, Wolfgang H.</creatorcontrib><creatorcontrib>Dodel, Richard</creatorcontrib><title>Cost Effectiveness of Pharmacotherapies in Early Parkinson’s Disease</title><title>CNS drugs</title><addtitle>CNS Drugs</addtitle><addtitle>CNS Drugs</addtitle><description>Parkinson’s disease is one of the most common chronic neurodegenerative diseases. The progression of disease and the psychosocial consequences exert a major impact on patients’ health-related quality of life. Although levodopa provides the best symptomatic benefit with the fewest short-term adverse effects, long-term treatment results in motor complications that are associated with both higher costs and considerable increase in patients’ discomfort. The introduction of dopamine agonists early in the treatment of Parkinson’s disease leads to a delay of these motor complications, but the treatment is associated with higher costs.
In this review we evaluate available cost-effectiveness analyses of the dopamine agonists pramipexole, pergolide, bromocriptine, ropinirole, cabergoline and levodopa in the treatment of early Parkinson’s disease. Considerable method-ological differences in the identified studies complicate a comparison and impede clear evidence as to which dopamine agonist treatment is the most cost effective in early Parkinson’s disease. Novel head-to-head comparisons considering the actual treatment guidelines are necessary to identify the most cost-effective alternative in treating
de novo
Parkinson’s disease patients.</description><subject>Adult and adolescent clinical studies</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>Antiparkinson Agents - economics</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cost-Benefit Analysis</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dopa</subject><subject>Drug therapy</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Nervous system as a whole</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Neurosciences</subject><subject>Organic mental disorders. Neuropsychology</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson Disease - economics</subject><subject>Parkinson's disease</subject><subject>Patient outcomes</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacotherapy</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. 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Antiepileptics. Antiparkinson agents</topic><topic>Antiparkinson Agents - economics</topic><topic>Antiparkinson Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cost-Benefit Analysis</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dopa</topic><topic>Drug therapy</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Nervous system as a whole</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Neurosciences</topic><topic>Organic mental disorders. Neuropsychology</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson Disease - economics</topic><topic>Parkinson's disease</topic><topic>Patient outcomes</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacotherapy</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Review Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eggert, Karla M.</creatorcontrib><creatorcontrib>Reese, Jens P.</creatorcontrib><creatorcontrib>Oertel, Wolfgang H.</creatorcontrib><creatorcontrib>Dodel, Richard</creatorcontrib><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>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>CNS drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eggert, Karla M.</au><au>Reese, Jens P.</au><au>Oertel, Wolfgang H.</au><au>Dodel, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cost Effectiveness of Pharmacotherapies in Early Parkinson’s Disease</atitle><jtitle>CNS drugs</jtitle><stitle>CNS Drugs</stitle><addtitle>CNS Drugs</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>22</volume><issue>10</issue><spage>841</spage><epage>860</epage><pages>841-860</pages><issn>1172-7047</issn><eissn>1179-1934</eissn><abstract>Parkinson’s disease is one of the most common chronic neurodegenerative diseases. The progression of disease and the psychosocial consequences exert a major impact on patients’ health-related quality of life. Although levodopa provides the best symptomatic benefit with the fewest short-term adverse effects, long-term treatment results in motor complications that are associated with both higher costs and considerable increase in patients’ discomfort. The introduction of dopamine agonists early in the treatment of Parkinson’s disease leads to a delay of these motor complications, but the treatment is associated with higher costs.
In this review we evaluate available cost-effectiveness analyses of the dopamine agonists pramipexole, pergolide, bromocriptine, ropinirole, cabergoline and levodopa in the treatment of early Parkinson’s disease. Considerable method-ological differences in the identified studies complicate a comparison and impede clear evidence as to which dopamine agonist treatment is the most cost effective in early Parkinson’s disease. Novel head-to-head comparisons considering the actual treatment guidelines are necessary to identify the most cost-effective alternative in treating
de novo
Parkinson’s disease patients.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>18788836</pmid><doi>10.2165/00023210-200822100-00005</doi><tpages>20</tpages></addata></record> |
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subjects | Adult and adolescent clinical studies Anticonvulsants. Antiepileptics. Antiparkinson agents Antiparkinson Agents - economics Antiparkinson Agents - therapeutic use Biological and medical sciences Cost-Benefit Analysis Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dopa Drug therapy Health aspects Humans Medical sciences Medicine Medicine & Public Health Nervous system (semeiology, syndromes) Nervous system as a whole Neurology Neuropharmacology Neurosciences Organic mental disorders. Neuropsychology Parkinson Disease - drug therapy Parkinson Disease - economics Parkinson's disease Patient outcomes Pharmacology. Drug treatments Pharmacotherapy Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychopharmacology Review Article |
title | Cost Effectiveness of Pharmacotherapies in Early Parkinson’s Disease |
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