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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 |
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container_title | CNS neuroscience & therapeutics |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_24P</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6492757</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1936460518</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4437-dcc3f3fd1a955d5beb32b7e1bb9a8ec42481ca4e51c90dacfce93f53648106e63</originalsourceid><addsrcrecordid>eNp1kU9PGzEQxa0KVELaQ79AZakHxCFh7V2v1z0gRRH_JNRWanu2vPY4OGTXwd4N5NvjNCHQA76M9eY3b0Z6CH0h2Zikd6bbOCaUU_4BDQhnbMREIQ72_zw7QscxzrOspJWoPqIjWlWcUsIHaDUxKwgRMFgLuot4GbzpNRhcr7FxSQzQdtiEfhZxH5PuWtzdAe4CqK7Z9LzFv1S4d2307UlMQxFUhO94ghv3lAZeSe2bpQoucZ_QoVWLCJ93dYj-Xl78mV6Pbn9e3UwntyNdFDkfGa1zm1tDlGDMsBrqnNYcSF0LVYEuaFERrQpgRIvMKG01iNyyvEx6VkKZD9H51nfZ1w0Yna4IaiGXwTUqrKVXTv7fad2dnPmVLAtBOePJ4NvOIPiHHmIn574PbbpZEpH2lBkjVaJOt5QOPsYAdr-BZHITkUwRyX8RJfbr25P25EsmCTjbAo9uAev3neT0x--t5TPYxZ6l</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1936460518</pqid></control><display><type>article</type><title>Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison</title><source>Wiley Open Access</source><creator>Li, Bao‐Dong ; Bi, Zhen‐Yun ; Liu, Jing‐Feng ; Si, Wei‐Jun ; Shi, Qian‐Qian ; Xue, Li‐Peng ; Bai, Jing</creator><creatorcontrib>Li, Bao‐Dong ; Bi, Zhen‐Yun ; Liu, Jing‐Feng ; Si, Wei‐Jun ; Shi, Qian‐Qian ; Xue, Li‐Peng ; Bai, Jing</creatorcontrib><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><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 & 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 & therapeutics, 2017-10, Vol.23 (10), p.827-842</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & 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 & 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 & Sons, Inc</general><general>John Wiley and Sons Inc</general><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>K9.</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2314-7406</orcidid></search><sort><creationdate>201710</creationdate><title>Adverse effects produced by different drugs used in the treatment of Parkinson's disease: A mixed treatment comparison</title><author>Li, Bao‐Dong ; Bi, Zhen‐Yun ; Liu, Jing‐Feng ; Si, Wei‐Jun ; Shi, Qian‐Qian ; Xue, Li‐Peng ; Bai, Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4437-dcc3f3fd1a955d5beb32b7e1bb9a8ec42481ca4e51c90dacfce93f53648106e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>adverse events</topic><topic>Antiparkinson Agents - adverse effects</topic><topic>Antiparkinson Agents - therapeutic use</topic><topic>Apomorphine</topic><topic>bayesian network model</topic><topic>Bromocriptine</topic><topic>Clinical trials</topic><topic>Constipation</topic><topic>Drugs</topic><topic>Dyskinesia</topic><topic>Hallucinations</topic><topic>Humans</topic><topic>Levodopa</topic><topic>Movement disorders</topic><topic>Nausea</topic><topic>Neurodegenerative diseases</topic><topic>Original</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson's disease</topic><topic>Pramipexole</topic><topic>randomized controlled trials</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Rasagiline</topic><topic>Side effects</topic><topic>surface under the cumulative ranking curves</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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>ProQuest Health & Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>CNS neuroscience & 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 & 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 & 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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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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