The efficacy and safety of adjunct bromocriptine therapy for levodopa-induced motor complications: A systematic review
OBJECTIVES To assess the efficacy and safety of adjunct bromocriptine (BR) compared with placebo in the treatment of patients with Parkinson's disease (PD) who have motor complications. DESIGN A systematic review of the literature from 1966–1999 on randomized, controlled trials. Outcome measure...
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Veröffentlicht in: | Movement disorders 2000-01, Vol.15 (1), p.56-64 |
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creator | Ramaker, Claudia van de Beek, Willem Johan T. Finken, Martijn J. J. van Hilten, Bob J. J. |
description | OBJECTIVES
To assess the efficacy and safety of adjunct bromocriptine (BR) compared with placebo in the treatment of patients with Parkinson's disease (PD) who have motor complications.
DESIGN
A systematic review of the literature from 1966–1999 on randomized, controlled trials. Outcome measures were occurrence and severity of motor complications, scores on impairment and disability, and the occurrence of side effects.
RESULTS
We included eight trials of which the methodologic quality of seven showed important shortcomings. All studies failed to adequately describe randomization procedures and seven studies failed to report sample size calculations. Only one trial was analyzed according to the intention‐to‐treat principle. It frequently remained unclear if patients with PD actually had motor complications. Differences between studies concerning the baseline characteristics, the BR titration phase, and the applied outcomes were found. The various methods used to evaluate the occurrence and/or severity of motor complications lacked a sound clinimetric basis. A great diversity of impairment and disability scales were applied. For those studies that reported the incidence of side effects, no clear pattern of BR‐related side effects emerged. A trend was found for orthostatic hypotension, which more frequently resulted in withdrawal of patients in the BR group.
CONCLUSIONS
Major methodologic problems and sources of heterogeneity not only hamper the comparability of trials, but also preclude a conclusion on the efficacy and safety of BR in the adjunct treatment of patients with PD who have motor complications. |
doi_str_mv | 10.1002/1531-8257(200001)15:1<56::AID-MDS1010>3.0.CO;2-2 |
format | Article |
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To assess the efficacy and safety of adjunct bromocriptine (BR) compared with placebo in the treatment of patients with Parkinson's disease (PD) who have motor complications.
DESIGN
A systematic review of the literature from 1966–1999 on randomized, controlled trials. Outcome measures were occurrence and severity of motor complications, scores on impairment and disability, and the occurrence of side effects.
RESULTS
We included eight trials of which the methodologic quality of seven showed important shortcomings. All studies failed to adequately describe randomization procedures and seven studies failed to report sample size calculations. Only one trial was analyzed according to the intention‐to‐treat principle. It frequently remained unclear if patients with PD actually had motor complications. Differences between studies concerning the baseline characteristics, the BR titration phase, and the applied outcomes were found. The various methods used to evaluate the occurrence and/or severity of motor complications lacked a sound clinimetric basis. A great diversity of impairment and disability scales were applied. For those studies that reported the incidence of side effects, no clear pattern of BR‐related side effects emerged. A trend was found for orthostatic hypotension, which more frequently resulted in withdrawal of patients in the BR group.
CONCLUSIONS
Major methodologic problems and sources of heterogeneity not only hamper the comparability of trials, but also preclude a conclusion on the efficacy and safety of BR in the adjunct treatment of patients with PD who have motor complications.</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/1531-8257(200001)15:1<56::AID-MDS1010>3.0.CO;2-2</identifier><identifier>PMID: 10634242</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Antiparkinson Agents - adverse effects ; Antiparkinson Agents - therapeutic use ; Biological and medical sciences ; Bromocriptine ; Bromocriptine - adverse effects ; Bromocriptine - therapeutic use ; Dopamine Agonists - adverse effects ; Dopamine Agonists - therapeutic use ; Double-Blind Method ; Drug toxicity and drugs side effects treatment ; Dyskinesia, Drug-Induced - diagnosis ; Dyskinesia, Drug-Induced - drug therapy ; Humans ; Levodopa - adverse effects ; Levodopa - therapeutic use ; Medical sciences ; Motor complications ; Neurologic Examination - drug effects ; Parkinson Disease - diagnosis ; Parkinson Disease - drug therapy ; Parkinson's disease ; Pharmacology. Drug treatments ; Randomized Controlled Trials as Topic ; Systematic review ; Toxicity: nervous system and muscle ; Treatment Outcome</subject><ispartof>Movement disorders, 2000-01, Vol.15 (1), p.56-64</ispartof><rights>Copyright © 2000 Movement Disorder Society</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4550-a7536a268fff300dac35898636ab7723d535fc333607483b1702cc6145f90de03</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%2F1531-8257%28200001%2915%3A1%3C56%3A%3AAID-MDS1010%3E3.0.CO%3B2-2$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1531-8257%28200001%2915%3A1%3C56%3A%3AAID-MDS1010%3E3.0.CO%3B2-2$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,1416,4040,4041,23921,23922,25131,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1227699$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10634242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramaker, Claudia</creatorcontrib><creatorcontrib>van de Beek, Willem Johan T.</creatorcontrib><creatorcontrib>Finken, Martijn J. J.</creatorcontrib><creatorcontrib>van Hilten, Bob J. J.</creatorcontrib><title>The efficacy and safety of adjunct bromocriptine therapy for levodopa-induced motor complications: A systematic review</title><title>Movement disorders</title><addtitle>Mov. Disord</addtitle><description>OBJECTIVES
To assess the efficacy and safety of adjunct bromocriptine (BR) compared with placebo in the treatment of patients with Parkinson's disease (PD) who have motor complications.
DESIGN
A systematic review of the literature from 1966–1999 on randomized, controlled trials. Outcome measures were occurrence and severity of motor complications, scores on impairment and disability, and the occurrence of side effects.
RESULTS
We included eight trials of which the methodologic quality of seven showed important shortcomings. All studies failed to adequately describe randomization procedures and seven studies failed to report sample size calculations. Only one trial was analyzed according to the intention‐to‐treat principle. It frequently remained unclear if patients with PD actually had motor complications. Differences between studies concerning the baseline characteristics, the BR titration phase, and the applied outcomes were found. The various methods used to evaluate the occurrence and/or severity of motor complications lacked a sound clinimetric basis. A great diversity of impairment and disability scales were applied. For those studies that reported the incidence of side effects, no clear pattern of BR‐related side effects emerged. A trend was found for orthostatic hypotension, which more frequently resulted in withdrawal of patients in the BR group.
CONCLUSIONS
Major methodologic problems and sources of heterogeneity not only hamper the comparability of trials, but also preclude a conclusion on the efficacy and safety of BR in the adjunct treatment of patients with PD who have motor complications.</description><subject>Antiparkinson Agents - adverse effects</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bromocriptine</subject><subject>Bromocriptine - adverse effects</subject><subject>Bromocriptine - therapeutic use</subject><subject>Dopamine Agonists - adverse effects</subject><subject>Dopamine Agonists - therapeutic use</subject><subject>Double-Blind Method</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Dyskinesia, Drug-Induced - diagnosis</subject><subject>Dyskinesia, Drug-Induced - drug therapy</subject><subject>Humans</subject><subject>Levodopa - adverse effects</subject><subject>Levodopa - therapeutic use</subject><subject>Medical sciences</subject><subject>Motor complications</subject><subject>Neurologic Examination - drug effects</subject><subject>Parkinson Disease - diagnosis</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson's disease</subject><subject>Pharmacology. Drug treatments</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Systematic review</subject><subject>Toxicity: nervous system and muscle</subject><subject>Treatment Outcome</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUuP0zAUhSMEYsrAX0BeIASLFD9iJy0IqcpAGTRQBOWxu3IdW-MhiYOddMi_x1XKwIIF3lg-Ovfz0T1JUhA8JxjTZ4QzkhaU508ojoc8JXxJXnCxXK7Oz9J3Z58IJvglm-N5uXlOU3ormd2M3E5muCh4ykjBT5J7IVxFAOFE3E1OCBYsoxmdJfvtpUbaGKukGpFsKxSk0f2InEGyuhpa1aOdd41T3na9bTXqL7WX3YiM86jWe1e5Tqa2rQalK9S4PsrKNV0dib11bViiFQpj6HUT3wp5vbf6-n5yx8g66AfH-zT5_PrVtnyTXmzW5-XqIlUZ5ziVOWdCUlEYYxjGlVSMF4tCRHGX55RVnHGjGGMC51nBdiTHVClBMm4WuNKYnSaPJ27n3Y9Bhx4aG5Sua9lqNwSgJI4QsojGD5NReReC1wY6bxvpRyAYDl3AYbFwWCxMXUQBCHABELuAYxfAAEO5AQo0Ih8e_x52ja7-Ak7Lj4ZHR4MMStbGy1bZ8MdHaS4Wh2jbyXZtaz3-f65_x_otRWw6YW3s5ucNVvrvIHKWc_j6fg1vv6z5ulx8g4_sFwMwvgo</recordid><startdate>200001</startdate><enddate>200001</enddate><creator>Ramaker, Claudia</creator><creator>van de Beek, Willem Johan T.</creator><creator>Finken, Martijn J. J.</creator><creator>van Hilten, Bob J. J.</creator><general>John Wiley & Sons, Inc</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></search><sort><creationdate>200001</creationdate><title>The efficacy and safety of adjunct bromocriptine therapy for levodopa-induced motor complications: A systematic review</title><author>Ramaker, Claudia ; van de Beek, Willem Johan T. ; Finken, Martijn J. J. ; van Hilten, Bob J. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4550-a7536a268fff300dac35898636ab7723d535fc333607483b1702cc6145f90de03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Antiparkinson Agents - adverse effects</topic><topic>Antiparkinson Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bromocriptine</topic><topic>Bromocriptine - adverse effects</topic><topic>Bromocriptine - therapeutic use</topic><topic>Dopamine Agonists - adverse effects</topic><topic>Dopamine Agonists - therapeutic use</topic><topic>Double-Blind Method</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Dyskinesia, Drug-Induced - diagnosis</topic><topic>Dyskinesia, Drug-Induced - drug therapy</topic><topic>Humans</topic><topic>Levodopa - adverse effects</topic><topic>Levodopa - therapeutic use</topic><topic>Medical sciences</topic><topic>Motor complications</topic><topic>Neurologic Examination - drug effects</topic><topic>Parkinson Disease - diagnosis</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson's disease</topic><topic>Pharmacology. Drug treatments</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Systematic review</topic><topic>Toxicity: nervous system and muscle</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramaker, Claudia</creatorcontrib><creatorcontrib>van de Beek, Willem Johan T.</creatorcontrib><creatorcontrib>Finken, Martijn J. J.</creatorcontrib><creatorcontrib>van Hilten, Bob J. 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><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramaker, Claudia</au><au>van de Beek, Willem Johan T.</au><au>Finken, Martijn J. J.</au><au>van Hilten, Bob J. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The efficacy and safety of adjunct bromocriptine therapy for levodopa-induced motor complications: A systematic review</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>2000-01</date><risdate>2000</risdate><volume>15</volume><issue>1</issue><spage>56</spage><epage>64</epage><pages>56-64</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>OBJECTIVES
To assess the efficacy and safety of adjunct bromocriptine (BR) compared with placebo in the treatment of patients with Parkinson's disease (PD) who have motor complications.
DESIGN
A systematic review of the literature from 1966–1999 on randomized, controlled trials. Outcome measures were occurrence and severity of motor complications, scores on impairment and disability, and the occurrence of side effects.
RESULTS
We included eight trials of which the methodologic quality of seven showed important shortcomings. All studies failed to adequately describe randomization procedures and seven studies failed to report sample size calculations. Only one trial was analyzed according to the intention‐to‐treat principle. It frequently remained unclear if patients with PD actually had motor complications. Differences between studies concerning the baseline characteristics, the BR titration phase, and the applied outcomes were found. The various methods used to evaluate the occurrence and/or severity of motor complications lacked a sound clinimetric basis. A great diversity of impairment and disability scales were applied. For those studies that reported the incidence of side effects, no clear pattern of BR‐related side effects emerged. A trend was found for orthostatic hypotension, which more frequently resulted in withdrawal of patients in the BR group.
CONCLUSIONS
Major methodologic problems and sources of heterogeneity not only hamper the comparability of trials, but also preclude a conclusion on the efficacy and safety of BR in the adjunct treatment of patients with PD who have motor complications.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10634242</pmid><doi>10.1002/1531-8257(200001)15:1<56::AID-MDS1010>3.0.CO;2-2</doi><tpages>9</tpages></addata></record> |
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subjects | Antiparkinson Agents - adverse effects Antiparkinson Agents - therapeutic use Biological and medical sciences Bromocriptine Bromocriptine - adverse effects Bromocriptine - therapeutic use Dopamine Agonists - adverse effects Dopamine Agonists - therapeutic use Double-Blind Method Drug toxicity and drugs side effects treatment Dyskinesia, Drug-Induced - diagnosis Dyskinesia, Drug-Induced - drug therapy Humans Levodopa - adverse effects Levodopa - therapeutic use Medical sciences Motor complications Neurologic Examination - drug effects Parkinson Disease - diagnosis Parkinson Disease - drug therapy Parkinson's disease Pharmacology. Drug treatments Randomized Controlled Trials as Topic Systematic review Toxicity: nervous system and muscle Treatment Outcome |
title | The efficacy and safety of adjunct bromocriptine therapy for levodopa-induced motor complications: A systematic review |
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