Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients

Background Peripheral artery disease (PAD) is a common complication in patients receiving hemodialysis (HD). Cilostazol is used for the treatment of ischemic symptoms in patients with PAD, based on its antiplatelet and vasodilating effects. In addition to these beneficial effects on clinical symptom...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical and experimental nephrology 2011-12, Vol.15 (6), p.893-899
Hauptverfasser: Shiohira, Shunji, Yoshida, Takumi, Sugiura, Hidekazu, Yoshida, Satsuki, Mitobe, Michihiro, Shimada, Katsunori, Ohba, Takashi, Tsuchiya, Ken, Kabaya, Takashi, Nitta, Kosaku
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 899
container_issue 6
container_start_page 893
container_title Clinical and experimental nephrology
container_volume 15
creator Shiohira, Shunji
Yoshida, Takumi
Sugiura, Hidekazu
Yoshida, Satsuki
Mitobe, Michihiro
Shimada, Katsunori
Ohba, Takashi
Tsuchiya, Ken
Kabaya, Takashi
Nitta, Kosaku
description Background Peripheral artery disease (PAD) is a common complication in patients receiving hemodialysis (HD). Cilostazol is used for the treatment of ischemic symptoms in patients with PAD, based on its antiplatelet and vasodilating effects. In addition to these beneficial effects on clinical symptoms in PAD patients, cilostazol has been proposed to have additional effects on clinical symptoms in patients with restless legs syndrome (RLS) via the upregulation of dopamine. We performed an observational, prospective study to evaluate the effect of cilostazol on several clinical and biochemical parameters in HD patients with PAD and RLS. Methods All the study patients received cilostazol treatment for 12 months. During the study period, several biochemical parameters, such as high-sensitivity CRP, von Willebrand antigen (VW-Ag), triglyceride (TG), high-density lipoprotein (HDL) and malondialdehyde-modified low-density lipoprotein, were monitored. A questionnaire on the physical status of PAD and RLS was also completed. 45 HD patients who received cilostazol were compared with a control group of 22 patients. Results The patients who continued cilostazol treatment exhibited a improvement in their serum inflammatory and biochemical parameters (VW-Ag, TG, HDL). Although PAD and RLS scores were not improved by multivariate analysis, several patients showed improvement of signs and symptoms which were included in the PAD or RLS scores. Conclusion The treatment of HD patients with cilostazol improved some of the lipid-related and endovascular inflammatory biochemical parameters associated with PAD, and relieved the clinical symptoms and physical status of PAD in some cases.
doi_str_mv 10.1007/s10157-011-0485-2
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_908491236</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2527319451</sourcerecordid><originalsourceid>FETCH-LOGICAL-c544t-767d2984b8375c1bd0070da041d32dc68bd502095e1a0744404872228305e3463</originalsourceid><addsrcrecordid>eNp1kc1u1DAUhSNURH_gAdggi32K_zJOlqhqoVIlNrC2HPtmxpUdB18PUnhEngrPTKGrrmz5nnO-K5-mec_oNaNUfUJGWadaylhLZd-1_FVzwaRQrVLDcFbvQvKWqY6dN5eIj5TSfuiGN805Z0qJzcAumj-30wS2kDSRsgNi5uKXYAoEKMRsYS7E-pCwmN8pkDQTmF36ZdDug8nEz1MwMZqS8kpGn-wOorcmkMVkE6FAxprojsk2-Pk4wzUuJUU8IBfIftlBrs8mV_lKnEcwCEdbBiwBEEmALVbf7HKKUKmkcpLzJqzoscKKr4vi2-b1ZALCu6fzqvlxd_v95mv78O3L_c3nh9Z2UpZWbZTjQy_HXqjOstHVn6TOUMmc4M5u-tF1lNOhA2aoklLWr1Wc817QDoTciKvm4yl3yennvu6oH9M-zxWpB9rLgXFxELGTyOaEmGHSS_bR5FUzqg_l6VN5upanD-VpXj0fnoL3YwT33_GvrSrgJwHW0byF_Ex-OfUv6C2pmw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>908491236</pqid></control><display><type>article</type><title>Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Shiohira, Shunji ; Yoshida, Takumi ; Sugiura, Hidekazu ; Yoshida, Satsuki ; Mitobe, Michihiro ; Shimada, Katsunori ; Ohba, Takashi ; Tsuchiya, Ken ; Kabaya, Takashi ; Nitta, Kosaku</creator><creatorcontrib>Shiohira, Shunji ; Yoshida, Takumi ; Sugiura, Hidekazu ; Yoshida, Satsuki ; Mitobe, Michihiro ; Shimada, Katsunori ; Ohba, Takashi ; Tsuchiya, Ken ; Kabaya, Takashi ; Nitta, Kosaku</creatorcontrib><description>Background Peripheral artery disease (PAD) is a common complication in patients receiving hemodialysis (HD). Cilostazol is used for the treatment of ischemic symptoms in patients with PAD, based on its antiplatelet and vasodilating effects. In addition to these beneficial effects on clinical symptoms in PAD patients, cilostazol has been proposed to have additional effects on clinical symptoms in patients with restless legs syndrome (RLS) via the upregulation of dopamine. We performed an observational, prospective study to evaluate the effect of cilostazol on several clinical and biochemical parameters in HD patients with PAD and RLS. Methods All the study patients received cilostazol treatment for 12 months. During the study period, several biochemical parameters, such as high-sensitivity CRP, von Willebrand antigen (VW-Ag), triglyceride (TG), high-density lipoprotein (HDL) and malondialdehyde-modified low-density lipoprotein, were monitored. A questionnaire on the physical status of PAD and RLS was also completed. 45 HD patients who received cilostazol were compared with a control group of 22 patients. Results The patients who continued cilostazol treatment exhibited a improvement in their serum inflammatory and biochemical parameters (VW-Ag, TG, HDL). Although PAD and RLS scores were not improved by multivariate analysis, several patients showed improvement of signs and symptoms which were included in the PAD or RLS scores. Conclusion The treatment of HD patients with cilostazol improved some of the lipid-related and endovascular inflammatory biochemical parameters associated with PAD, and relieved the clinical symptoms and physical status of PAD in some cases.</description><identifier>ISSN: 1342-1751</identifier><identifier>EISSN: 1437-7799</identifier><identifier>DOI: 10.1007/s10157-011-0485-2</identifier><identifier>PMID: 21773691</identifier><identifier>CODEN: CENPFV</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Aged ; Biomarkers - blood ; Case-Control Studies ; Female ; Humans ; Inflammation Mediators - blood ; Japan ; Lipids - blood ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Multivariate Analysis ; Nephrology ; Original Article ; Peripheral Vascular Diseases - drug therapy ; Peripheral Vascular Diseases - etiology ; Peripheral Vascular Diseases - immunology ; Platelet Aggregation Inhibitors - adverse effects ; Platelet Aggregation Inhibitors - therapeutic use ; Prospective Studies ; Renal Dialysis - adverse effects ; Restless Legs Syndrome - drug therapy ; Restless Legs Syndrome - etiology ; Restless Legs Syndrome - immunology ; Surveys and Questionnaires ; Tetrazoles - adverse effects ; Tetrazoles - therapeutic use ; Time Factors ; Treatment Outcome ; Urology</subject><ispartof>Clinical and experimental nephrology, 2011-12, Vol.15 (6), p.893-899</ispartof><rights>Japanese Society of Nephrology 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c544t-767d2984b8375c1bd0070da041d32dc68bd502095e1a0744404872228305e3463</citedby><cites>FETCH-LOGICAL-c544t-767d2984b8375c1bd0070da041d32dc68bd502095e1a0744404872228305e3463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10157-011-0485-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10157-011-0485-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27928,27929,41492,42561,51323</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21773691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shiohira, Shunji</creatorcontrib><creatorcontrib>Yoshida, Takumi</creatorcontrib><creatorcontrib>Sugiura, Hidekazu</creatorcontrib><creatorcontrib>Yoshida, Satsuki</creatorcontrib><creatorcontrib>Mitobe, Michihiro</creatorcontrib><creatorcontrib>Shimada, Katsunori</creatorcontrib><creatorcontrib>Ohba, Takashi</creatorcontrib><creatorcontrib>Tsuchiya, Ken</creatorcontrib><creatorcontrib>Kabaya, Takashi</creatorcontrib><creatorcontrib>Nitta, Kosaku</creatorcontrib><title>Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients</title><title>Clinical and experimental nephrology</title><addtitle>Clin Exp Nephrol</addtitle><addtitle>Clin Exp Nephrol</addtitle><description>Background Peripheral artery disease (PAD) is a common complication in patients receiving hemodialysis (HD). Cilostazol is used for the treatment of ischemic symptoms in patients with PAD, based on its antiplatelet and vasodilating effects. In addition to these beneficial effects on clinical symptoms in PAD patients, cilostazol has been proposed to have additional effects on clinical symptoms in patients with restless legs syndrome (RLS) via the upregulation of dopamine. We performed an observational, prospective study to evaluate the effect of cilostazol on several clinical and biochemical parameters in HD patients with PAD and RLS. Methods All the study patients received cilostazol treatment for 12 months. During the study period, several biochemical parameters, such as high-sensitivity CRP, von Willebrand antigen (VW-Ag), triglyceride (TG), high-density lipoprotein (HDL) and malondialdehyde-modified low-density lipoprotein, were monitored. A questionnaire on the physical status of PAD and RLS was also completed. 45 HD patients who received cilostazol were compared with a control group of 22 patients. Results The patients who continued cilostazol treatment exhibited a improvement in their serum inflammatory and biochemical parameters (VW-Ag, TG, HDL). Although PAD and RLS scores were not improved by multivariate analysis, several patients showed improvement of signs and symptoms which were included in the PAD or RLS scores. Conclusion The treatment of HD patients with cilostazol improved some of the lipid-related and endovascular inflammatory biochemical parameters associated with PAD, and relieved the clinical symptoms and physical status of PAD in some cases.</description><subject>Aged</subject><subject>Biomarkers - blood</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammation Mediators - blood</subject><subject>Japan</subject><subject>Lipids - blood</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Nephrology</subject><subject>Original Article</subject><subject>Peripheral Vascular Diseases - drug therapy</subject><subject>Peripheral Vascular Diseases - etiology</subject><subject>Peripheral Vascular Diseases - immunology</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Prospective Studies</subject><subject>Renal Dialysis - adverse effects</subject><subject>Restless Legs Syndrome - drug therapy</subject><subject>Restless Legs Syndrome - etiology</subject><subject>Restless Legs Syndrome - immunology</subject><subject>Surveys and Questionnaires</subject><subject>Tetrazoles - adverse effects</subject><subject>Tetrazoles - therapeutic use</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Urology</subject><issn>1342-1751</issn><issn>1437-7799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kc1u1DAUhSNURH_gAdggi32K_zJOlqhqoVIlNrC2HPtmxpUdB18PUnhEngrPTKGrrmz5nnO-K5-mec_oNaNUfUJGWadaylhLZd-1_FVzwaRQrVLDcFbvQvKWqY6dN5eIj5TSfuiGN805Z0qJzcAumj-30wS2kDSRsgNi5uKXYAoEKMRsYS7E-pCwmN8pkDQTmF36ZdDug8nEz1MwMZqS8kpGn-wOorcmkMVkE6FAxprojsk2-Pk4wzUuJUU8IBfIftlBrs8mV_lKnEcwCEdbBiwBEEmALVbf7HKKUKmkcpLzJqzoscKKr4vi2-b1ZALCu6fzqvlxd_v95mv78O3L_c3nh9Z2UpZWbZTjQy_HXqjOstHVn6TOUMmc4M5u-tF1lNOhA2aoklLWr1Wc817QDoTciKvm4yl3yennvu6oH9M-zxWpB9rLgXFxELGTyOaEmGHSS_bR5FUzqg_l6VN5upanD-VpXj0fnoL3YwT33_GvrSrgJwHW0byF_Ex-OfUv6C2pmw</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Shiohira, Shunji</creator><creator>Yoshida, Takumi</creator><creator>Sugiura, Hidekazu</creator><creator>Yoshida, Satsuki</creator><creator>Mitobe, Michihiro</creator><creator>Shimada, Katsunori</creator><creator>Ohba, Takashi</creator><creator>Tsuchiya, Ken</creator><creator>Kabaya, Takashi</creator><creator>Nitta, Kosaku</creator><general>Springer Japan</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20111201</creationdate><title>Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients</title><author>Shiohira, Shunji ; Yoshida, Takumi ; Sugiura, Hidekazu ; Yoshida, Satsuki ; Mitobe, Michihiro ; Shimada, Katsunori ; Ohba, Takashi ; Tsuchiya, Ken ; Kabaya, Takashi ; Nitta, Kosaku</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c544t-767d2984b8375c1bd0070da041d32dc68bd502095e1a0744404872228305e3463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Biomarkers - blood</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammation Mediators - blood</topic><topic>Japan</topic><topic>Lipids - blood</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Nephrology</topic><topic>Original Article</topic><topic>Peripheral Vascular Diseases - drug therapy</topic><topic>Peripheral Vascular Diseases - etiology</topic><topic>Peripheral Vascular Diseases - immunology</topic><topic>Platelet Aggregation Inhibitors - adverse effects</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Prospective Studies</topic><topic>Renal Dialysis - adverse effects</topic><topic>Restless Legs Syndrome - drug therapy</topic><topic>Restless Legs Syndrome - etiology</topic><topic>Restless Legs Syndrome - immunology</topic><topic>Surveys and Questionnaires</topic><topic>Tetrazoles - adverse effects</topic><topic>Tetrazoles - therapeutic use</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shiohira, Shunji</creatorcontrib><creatorcontrib>Yoshida, Takumi</creatorcontrib><creatorcontrib>Sugiura, Hidekazu</creatorcontrib><creatorcontrib>Yoshida, Satsuki</creatorcontrib><creatorcontrib>Mitobe, Michihiro</creatorcontrib><creatorcontrib>Shimada, Katsunori</creatorcontrib><creatorcontrib>Ohba, Takashi</creatorcontrib><creatorcontrib>Tsuchiya, Ken</creatorcontrib><creatorcontrib>Kabaya, Takashi</creatorcontrib><creatorcontrib>Nitta, Kosaku</creatorcontrib><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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</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><jtitle>Clinical and experimental nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shiohira, Shunji</au><au>Yoshida, Takumi</au><au>Sugiura, Hidekazu</au><au>Yoshida, Satsuki</au><au>Mitobe, Michihiro</au><au>Shimada, Katsunori</au><au>Ohba, Takashi</au><au>Tsuchiya, Ken</au><au>Kabaya, Takashi</au><au>Nitta, Kosaku</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients</atitle><jtitle>Clinical and experimental nephrology</jtitle><stitle>Clin Exp Nephrol</stitle><addtitle>Clin Exp Nephrol</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>15</volume><issue>6</issue><spage>893</spage><epage>899</epage><pages>893-899</pages><issn>1342-1751</issn><eissn>1437-7799</eissn><coden>CENPFV</coden><abstract>Background Peripheral artery disease (PAD) is a common complication in patients receiving hemodialysis (HD). Cilostazol is used for the treatment of ischemic symptoms in patients with PAD, based on its antiplatelet and vasodilating effects. In addition to these beneficial effects on clinical symptoms in PAD patients, cilostazol has been proposed to have additional effects on clinical symptoms in patients with restless legs syndrome (RLS) via the upregulation of dopamine. We performed an observational, prospective study to evaluate the effect of cilostazol on several clinical and biochemical parameters in HD patients with PAD and RLS. Methods All the study patients received cilostazol treatment for 12 months. During the study period, several biochemical parameters, such as high-sensitivity CRP, von Willebrand antigen (VW-Ag), triglyceride (TG), high-density lipoprotein (HDL) and malondialdehyde-modified low-density lipoprotein, were monitored. A questionnaire on the physical status of PAD and RLS was also completed. 45 HD patients who received cilostazol were compared with a control group of 22 patients. Results The patients who continued cilostazol treatment exhibited a improvement in their serum inflammatory and biochemical parameters (VW-Ag, TG, HDL). Although PAD and RLS scores were not improved by multivariate analysis, several patients showed improvement of signs and symptoms which were included in the PAD or RLS scores. Conclusion The treatment of HD patients with cilostazol improved some of the lipid-related and endovascular inflammatory biochemical parameters associated with PAD, and relieved the clinical symptoms and physical status of PAD in some cases.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>21773691</pmid><doi>10.1007/s10157-011-0485-2</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1342-1751
ispartof Clinical and experimental nephrology, 2011-12, Vol.15 (6), p.893-899
issn 1342-1751
1437-7799
language eng
recordid cdi_proquest_journals_908491236
source MEDLINE; SpringerNature Journals
subjects Aged
Biomarkers - blood
Case-Control Studies
Female
Humans
Inflammation Mediators - blood
Japan
Lipids - blood
Male
Medicine
Medicine & Public Health
Middle Aged
Multivariate Analysis
Nephrology
Original Article
Peripheral Vascular Diseases - drug therapy
Peripheral Vascular Diseases - etiology
Peripheral Vascular Diseases - immunology
Platelet Aggregation Inhibitors - adverse effects
Platelet Aggregation Inhibitors - therapeutic use
Prospective Studies
Renal Dialysis - adverse effects
Restless Legs Syndrome - drug therapy
Restless Legs Syndrome - etiology
Restless Legs Syndrome - immunology
Surveys and Questionnaires
Tetrazoles - adverse effects
Tetrazoles - therapeutic use
Time Factors
Treatment Outcome
Urology
title Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T00%3A31%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20the%20antiplatelet%20agent%20cilostazol%20on%20endovascular%20inflammatory%20biochemical%20parameters%20and%20the%20clinical%20symptoms%20of%20peripheral%20artery%20disease%20and%20restless%20legs%20syndrome%20in%20hemodialysis%20patients&rft.jtitle=Clinical%20and%20experimental%20nephrology&rft.au=Shiohira,%20Shunji&rft.date=2011-12-01&rft.volume=15&rft.issue=6&rft.spage=893&rft.epage=899&rft.pages=893-899&rft.issn=1342-1751&rft.eissn=1437-7799&rft.coden=CENPFV&rft_id=info:doi/10.1007/s10157-011-0485-2&rft_dat=%3Cproquest_cross%3E2527319451%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=908491236&rft_id=info:pmid/21773691&rfr_iscdi=true