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Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison

Summary Objective This mixed treatment comparison is used to compare the adverse effects of eleven different drugs used to treat Parkinson's disease (PD). The drugs that we compare include the following: ropinirole, rasagiline, rotigotine, entacapone, apomorphine, pramipexole, sumanirole, bromo...

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Published in:CNS neuroscience & therapeutics 2017-10, Vol.23 (10), p.827-842
Main Authors: Li, Bao‐Dong, Bi, Zhen‐Yun, Liu, Jing‐Feng, Si, Wei‐Jun, Shi, Qian‐Qian, Xue, Li‐Peng, Bai, Jing
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container_issue 10
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container_title CNS neuroscience & therapeutics
container_volume 23
creator Li, Bao‐Dong
Bi, Zhen‐Yun
Liu, Jing‐Feng
Si, Wei‐Jun
Shi, Qian‐Qian
Xue, Li‐Peng
Bai, Jing
description Summary Objective This mixed treatment comparison is used to compare the adverse effects of eleven different drugs used to treat Parkinson's disease (PD). The drugs that we compare include the following: ropinirole, rasagiline, rotigotine, entacapone, apomorphine, pramipexole, sumanirole, bromocriptine, piribedil, pergolide, and levodopa. Methods PubMed, EMBASE, and Cochrane Library were searched from the inception to December 2015. Our analysis combines the evidences of direct comparison and indirect comparison between various literatures. We evaluated the merging odds ratios (OR) value and surface under the cumulative ranking curves (SUCRA) of each of the drugs and used this as a mode of comparison. Results Twenty‐four randomized controlled trials (RCTs) were included in this study. Our results demonstrated that the incidence of adverse reactions of ropinirole, rotigotine, entacapone, and sumanirole were obviously higher in terms of nausea compared to the placebo. Ropinirole produced the highest incidence rates of dyskinesia side effects, whereas pramipexole was significantly higher in terms of patients’ hallucination. In addition, the SUCRA values of all the drugs showed that the incidence of adverse reaction of pergolide was relatively high (nausea: 83.5%; hallucination: 79.8%); for dyskinesia and somnolence, the incidence of ropinirole was higher (dyskinesia: 80.5%; somnolence: 69.4%); the incidence of adverse reaction of piribedil was higher on PD in terms of dizziness (67.0%); and the incidence of bromocriptine was relatively high in terms of constipation (62.3%). Conclusions This mixed treatment comparison showed that the drugs ropinirole, bromocriptine, and piribedil produced the highest incidence rates of nausea, dyskinesia, hallucination, dizziness, constipation, and somnolence symptoms. Thus, we conclude that as these three drugs produced the most frequent symptoms, they are not recommended for the treatment of patients with Parkinson's disease.
doi_str_mv 10.1111/cns.12727
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The drugs that we compare include the following: ropinirole, rasagiline, rotigotine, entacapone, apomorphine, pramipexole, sumanirole, bromocriptine, piribedil, pergolide, and levodopa. Methods PubMed, EMBASE, and Cochrane Library were searched from the inception to December 2015. Our analysis combines the evidences of direct comparison and indirect comparison between various literatures. We evaluated the merging odds ratios (OR) value and surface under the cumulative ranking curves (SUCRA) of each of the drugs and used this as a mode of comparison. Results Twenty‐four randomized controlled trials (RCTs) were included in this study. Our results demonstrated that the incidence of adverse reactions of ropinirole, rotigotine, entacapone, and sumanirole were obviously higher in terms of nausea compared to the placebo. Ropinirole produced the highest incidence rates of dyskinesia side effects, whereas pramipexole was significantly higher in terms of patients’ hallucination. In addition, the SUCRA values of all the drugs showed that the incidence of adverse reaction of pergolide was relatively high (nausea: 83.5%; hallucination: 79.8%); for dyskinesia and somnolence, the incidence of ropinirole was higher (dyskinesia: 80.5%; somnolence: 69.4%); the incidence of adverse reaction of piribedil was higher on PD in terms of dizziness (67.0%); and the incidence of bromocriptine was relatively high in terms of constipation (62.3%). Conclusions This mixed treatment comparison showed that the drugs ropinirole, bromocriptine, and piribedil produced the highest incidence rates of nausea, dyskinesia, hallucination, dizziness, constipation, and somnolence symptoms. Thus, we conclude that as these three drugs produced the most frequent symptoms, they are not recommended for the treatment of patients with Parkinson's disease.</description><identifier>ISSN: 1755-5930</identifier><identifier>EISSN: 1755-5949</identifier><identifier>DOI: 10.1111/cns.12727</identifier><identifier>PMID: 28872217</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>adverse events ; Antiparkinson Agents - adverse effects ; Antiparkinson Agents - therapeutic use ; Apomorphine ; bayesian network model ; Bromocriptine ; Clinical trials ; Constipation ; Drugs ; Dyskinesia ; Hallucinations ; Humans ; Levodopa ; Movement disorders ; Nausea ; Neurodegenerative diseases ; Original ; Parkinson Disease - drug therapy ; Parkinson's disease ; Pramipexole ; randomized controlled trials ; Randomized Controlled Trials as Topic ; Rasagiline ; Side effects ; surface under the cumulative ranking curves</subject><ispartof>CNS neuroscience &amp; therapeutics, 2017-10, Vol.23 (10), p.827-842</ispartof><rights>2017 John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4437-dcc3f3fd1a955d5beb32b7e1bb9a8ec42481ca4e51c90dacfce93f53648106e63</citedby><cites>FETCH-LOGICAL-c4437-dcc3f3fd1a955d5beb32b7e1bb9a8ec42481ca4e51c90dacfce93f53648106e63</cites><orcidid>0000-0002-2314-7406</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492757/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492757/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,11543,27905,27906,46033,46457,53772,53774</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcns.12727$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28872217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Bao‐Dong</creatorcontrib><creatorcontrib>Bi, Zhen‐Yun</creatorcontrib><creatorcontrib>Liu, Jing‐Feng</creatorcontrib><creatorcontrib>Si, Wei‐Jun</creatorcontrib><creatorcontrib>Shi, Qian‐Qian</creatorcontrib><creatorcontrib>Xue, Li‐Peng</creatorcontrib><creatorcontrib>Bai, Jing</creatorcontrib><title>Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison</title><title>CNS neuroscience &amp; therapeutics</title><addtitle>CNS Neurosci Ther</addtitle><description>Summary Objective This mixed treatment comparison is used to compare the adverse effects of eleven different drugs used to treat Parkinson's disease (PD). The drugs that we compare include the following: ropinirole, rasagiline, rotigotine, entacapone, apomorphine, pramipexole, sumanirole, bromocriptine, piribedil, pergolide, and levodopa. Methods PubMed, EMBASE, and Cochrane Library were searched from the inception to December 2015. Our analysis combines the evidences of direct comparison and indirect comparison between various literatures. We evaluated the merging odds ratios (OR) value and surface under the cumulative ranking curves (SUCRA) of each of the drugs and used this as a mode of comparison. Results Twenty‐four randomized controlled trials (RCTs) were included in this study. Our results demonstrated that the incidence of adverse reactions of ropinirole, rotigotine, entacapone, and sumanirole were obviously higher in terms of nausea compared to the placebo. Ropinirole produced the highest incidence rates of dyskinesia side effects, whereas pramipexole was significantly higher in terms of patients’ hallucination. In addition, the SUCRA values of all the drugs showed that the incidence of adverse reaction of pergolide was relatively high (nausea: 83.5%; hallucination: 79.8%); for dyskinesia and somnolence, the incidence of ropinirole was higher (dyskinesia: 80.5%; somnolence: 69.4%); the incidence of adverse reaction of piribedil was higher on PD in terms of dizziness (67.0%); and the incidence of bromocriptine was relatively high in terms of constipation (62.3%). Conclusions This mixed treatment comparison showed that the drugs ropinirole, bromocriptine, and piribedil produced the highest incidence rates of nausea, dyskinesia, hallucination, dizziness, constipation, and somnolence symptoms. Thus, we conclude that as these three drugs produced the most frequent symptoms, they are not recommended for the treatment of patients with Parkinson's disease.</description><subject>adverse events</subject><subject>Antiparkinson Agents - adverse effects</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>Apomorphine</subject><subject>bayesian network model</subject><subject>Bromocriptine</subject><subject>Clinical trials</subject><subject>Constipation</subject><subject>Drugs</subject><subject>Dyskinesia</subject><subject>Hallucinations</subject><subject>Humans</subject><subject>Levodopa</subject><subject>Movement disorders</subject><subject>Nausea</subject><subject>Neurodegenerative diseases</subject><subject>Original</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson's disease</subject><subject>Pramipexole</subject><subject>randomized controlled trials</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Rasagiline</subject><subject>Side effects</subject><subject>surface under the cumulative ranking curves</subject><issn>1755-5930</issn><issn>1755-5949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kU9PGzEQxa0KVELaQ79AZakHxCFh7V2v1z0gRRH_JNRWanu2vPY4OGTXwd4N5NvjNCHQA76M9eY3b0Z6CH0h2Zikd6bbOCaUU_4BDQhnbMREIQ72_zw7QscxzrOspJWoPqIjWlWcUsIHaDUxKwgRMFgLuot4GbzpNRhcr7FxSQzQdtiEfhZxH5PuWtzdAe4CqK7Z9LzFv1S4d2307UlMQxFUhO94ghv3lAZeSe2bpQoucZ_QoVWLCJ93dYj-Xl78mV6Pbn9e3UwntyNdFDkfGa1zm1tDlGDMsBrqnNYcSF0LVYEuaFERrQpgRIvMKG01iNyyvEx6VkKZD9H51nfZ1w0Yna4IaiGXwTUqrKVXTv7fad2dnPmVLAtBOePJ4NvOIPiHHmIn574PbbpZEpH2lBkjVaJOt5QOPsYAdr-BZHITkUwRyX8RJfbr25P25EsmCTjbAo9uAev3neT0x--t5TPYxZ6l</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Li, Bao‐Dong</creator><creator>Bi, Zhen‐Yun</creator><creator>Liu, Jing‐Feng</creator><creator>Si, Wei‐Jun</creator><creator>Shi, Qian‐Qian</creator><creator>Xue, Li‐Peng</creator><creator>Bai, Jing</creator><general>John Wiley &amp; 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Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CNS neuroscience &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Li, Bao‐Dong</au><au>Bi, Zhen‐Yun</au><au>Liu, Jing‐Feng</au><au>Si, Wei‐Jun</au><au>Shi, Qian‐Qian</au><au>Xue, Li‐Peng</au><au>Bai, Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison</atitle><jtitle>CNS neuroscience &amp; therapeutics</jtitle><addtitle>CNS Neurosci Ther</addtitle><date>2017-10</date><risdate>2017</risdate><volume>23</volume><issue>10</issue><spage>827</spage><epage>842</epage><pages>827-842</pages><issn>1755-5930</issn><eissn>1755-5949</eissn><abstract>Summary Objective This mixed treatment comparison is used to compare the adverse effects of eleven different drugs used to treat Parkinson's disease (PD). The drugs that we compare include the following: ropinirole, rasagiline, rotigotine, entacapone, apomorphine, pramipexole, sumanirole, bromocriptine, piribedil, pergolide, and levodopa. Methods PubMed, EMBASE, and Cochrane Library were searched from the inception to December 2015. Our analysis combines the evidences of direct comparison and indirect comparison between various literatures. We evaluated the merging odds ratios (OR) value and surface under the cumulative ranking curves (SUCRA) of each of the drugs and used this as a mode of comparison. Results Twenty‐four randomized controlled trials (RCTs) were included in this study. Our results demonstrated that the incidence of adverse reactions of ropinirole, rotigotine, entacapone, and sumanirole were obviously higher in terms of nausea compared to the placebo. Ropinirole produced the highest incidence rates of dyskinesia side effects, whereas pramipexole was significantly higher in terms of patients’ hallucination. In addition, the SUCRA values of all the drugs showed that the incidence of adverse reaction of pergolide was relatively high (nausea: 83.5%; hallucination: 79.8%); for dyskinesia and somnolence, the incidence of ropinirole was higher (dyskinesia: 80.5%; somnolence: 69.4%); the incidence of adverse reaction of piribedil was higher on PD in terms of dizziness (67.0%); and the incidence of bromocriptine was relatively high in terms of constipation (62.3%). Conclusions This mixed treatment comparison showed that the drugs ropinirole, bromocriptine, and piribedil produced the highest incidence rates of nausea, dyskinesia, hallucination, dizziness, constipation, and somnolence symptoms. Thus, we conclude that as these three drugs produced the most frequent symptoms, they are not recommended for the treatment of patients with Parkinson's disease.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>28872217</pmid><doi>10.1111/cns.12727</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-2314-7406</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Open Access
subjects adverse events
Antiparkinson Agents - adverse effects
Antiparkinson Agents - therapeutic use
Apomorphine
bayesian network model
Bromocriptine
Clinical trials
Constipation
Drugs
Dyskinesia
Hallucinations
Humans
Levodopa
Movement disorders
Nausea
Neurodegenerative diseases
Original
Parkinson Disease - drug therapy
Parkinson's disease
Pramipexole
randomized controlled trials
Randomized Controlled Trials as Topic
Rasagiline
Side effects
surface under the cumulative ranking curves
title Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison
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