Effect of Levosimendan on Estimated Glomerular Filtration Rate in Hospitalized Patients with Decompensated Heart Failure and Renal Dysfunction

Summary Background Only limited data of the long‐term effect of levosimendan on renal dysfunction in patients with decompensated heart failure (DHF) have been published previously. To date, there has been no similar study carried out in a Chinese population. Design and Methods A prospective, randomi...

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Veröffentlicht in:Cardiovascular therapeutics 2013-04, Vol.31 (2), p.108-114
Hauptverfasser: Hou, Zhi‐Qiang, Sun, Zhao‐Xia, Su, Chong‐Yi, Tan, Hui, Zhong, Xia, Hu, Bo, Zhou, Yi, Shang, De‐Ya
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container_end_page 114
container_issue 2
container_start_page 108
container_title Cardiovascular therapeutics
container_volume 31
creator Hou, Zhi‐Qiang
Sun, Zhao‐Xia
Su, Chong‐Yi
Tan, Hui
Zhong, Xia
Hu, Bo
Zhou, Yi
Shang, De‐Ya
description Summary Background Only limited data of the long‐term effect of levosimendan on renal dysfunction in patients with decompensated heart failure (DHF) have been published previously. To date, there has been no similar study carried out in a Chinese population. Design and Methods A prospective, randomized, placebo‐controlled, and double‐blind study was performed to investigate the effect of levosimendan on estimated glomerular filtration rate (eGFR) in DHF patients with renal dysfunction during a 30‐day period. Sixty‐six patients with left ventricular ejection fraction (LVEF) ≤40% and eGFR 15–89 mL/min/1.73 m2 were randomized in a 1:1 ratio to receive a 24‐h infusion with levosimendan or placebo. The B‐type natriuretic peptide (BNP) and eGFR were determined at baseline and day 1, 3, 7, 14, 30 after the start of treatment. Results The eGFR levels were obviously enhanced following levosimendan, peaked at 3 days, sustained for at least 14 days, and returned to baseline by day 30 after starting infusion. In contrast, placebo did not induce any significant changes in eGFR levels during the follow‐up. In addition, levosimendan resulted in a distinct decrease in BNP levels in comparison with placebo, and the beneficial effect returned to baseline by day 14 and remained so at day 30 postinfusion. Conclusions A 24‐h infusion with levosimendan transiently improved the renal dysfunction compared with placebo in patients with DHF, and its beneficial effects persisted for at least 14 days after the initiation of treatment.
doi_str_mv 10.1111/1755-5922.12001
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To date, there has been no similar study carried out in a Chinese population. Design and Methods A prospective, randomized, placebo‐controlled, and double‐blind study was performed to investigate the effect of levosimendan on estimated glomerular filtration rate (eGFR) in DHF patients with renal dysfunction during a 30‐day period. Sixty‐six patients with left ventricular ejection fraction (LVEF) ≤40% and eGFR 15–89 mL/min/1.73 m2 were randomized in a 1:1 ratio to receive a 24‐h infusion with levosimendan or placebo. The B‐type natriuretic peptide (BNP) and eGFR were determined at baseline and day 1, 3, 7, 14, 30 after the start of treatment. Results The eGFR levels were obviously enhanced following levosimendan, peaked at 3 days, sustained for at least 14 days, and returned to baseline by day 30 after starting infusion. In contrast, placebo did not induce any significant changes in eGFR levels during the follow‐up. In addition, levosimendan resulted in a distinct decrease in BNP levels in comparison with placebo, and the beneficial effect returned to baseline by day 14 and remained so at day 30 postinfusion. Conclusions A 24‐h infusion with levosimendan transiently improved the renal dysfunction compared with placebo in patients with DHF, and its beneficial effects persisted for at least 14 days after the initiation of treatment.</description><identifier>ISSN: 1755-5914</identifier><identifier>EISSN: 1755-5922</identifier><identifier>DOI: 10.1111/1755-5922.12001</identifier><identifier>PMID: 23490237</identifier><language>eng</language><publisher>Oxford: Blackwell</publisher><subject>Aged ; Aged, 80 and over ; Analysis of Variance ; Biological and medical sciences ; Biomarkers - blood ; Blood Pressure - drug effects ; B‐type Natriuretic peptide ; Cardiology. Vascular system ; Cardiotonic Agents - administration &amp; dosage ; Cardiotonic Agents - therapeutic use ; Cardiovascular system ; Chi-Square Distribution ; China ; Decompensated heart failure ; Double-Blind Method ; Drug therapy ; Estimated glomerular filtration rate ; Female ; Glomerular Filtration Rate - drug effects ; Heart ; Heart failure ; Heart Failure - blood ; Heart Failure - complications ; Heart Failure - diagnosis ; Heart Failure - drug therapy ; Heart Failure - physiopathology ; Heart failure, cardiogenic pulmonary edema, cardiac enlargement ; Heart Rate - drug effects ; Hospitalization ; Humans ; Hydrazones - administration &amp; dosage ; Hydrazones - therapeutic use ; Infusions, Intravenous ; Kidney Diseases - blood ; Kidney Diseases - complications ; Kidney Diseases - physiopathology ; Levosimendan ; Linear Models ; Male ; Medical sciences ; Middle Aged ; Natriuretic Peptide, Brain - blood ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Pharmacology. Drug treatments ; Placebo ; Prospective Studies ; Pyridazines - administration &amp; dosage ; Pyridazines - therapeutic use ; Renal dysfunction ; Renal failure ; Stroke Volume ; Time Factors ; Treatment Outcome ; Urination - drug effects ; Ventricular Function, Left - drug effects</subject><ispartof>Cardiovascular therapeutics, 2013-04, Vol.31 (2), p.108-114</ispartof><rights>2012 Blackwell Publishing Ltd</rights><rights>2014 INIST-CNRS</rights><rights>2012 Blackwell Publishing Ltd.</rights><rights>2013 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4011-b38b7ffbcd8768aa9fd1f80c4e26045af91ed7ea736ffc96509bf52d9cb04d543</citedby><cites>FETCH-LOGICAL-c4011-b38b7ffbcd8768aa9fd1f80c4e26045af91ed7ea736ffc96509bf52d9cb04d543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1755-5922.12001$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1755-5922.12001$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1427,11541,27901,27902,46027,46384,46451,46808</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2F1755-5922.12001$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27145348$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23490237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hou, Zhi‐Qiang</creatorcontrib><creatorcontrib>Sun, Zhao‐Xia</creatorcontrib><creatorcontrib>Su, Chong‐Yi</creatorcontrib><creatorcontrib>Tan, Hui</creatorcontrib><creatorcontrib>Zhong, Xia</creatorcontrib><creatorcontrib>Hu, Bo</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Shang, De‐Ya</creatorcontrib><title>Effect of Levosimendan on Estimated Glomerular Filtration Rate in Hospitalized Patients with Decompensated Heart Failure and Renal Dysfunction</title><title>Cardiovascular therapeutics</title><addtitle>Cardiovasc Ther</addtitle><description>Summary Background Only limited data of the long‐term effect of levosimendan on renal dysfunction in patients with decompensated heart failure (DHF) have been published previously. To date, there has been no similar study carried out in a Chinese population. Design and Methods A prospective, randomized, placebo‐controlled, and double‐blind study was performed to investigate the effect of levosimendan on estimated glomerular filtration rate (eGFR) in DHF patients with renal dysfunction during a 30‐day period. Sixty‐six patients with left ventricular ejection fraction (LVEF) ≤40% and eGFR 15–89 mL/min/1.73 m2 were randomized in a 1:1 ratio to receive a 24‐h infusion with levosimendan or placebo. The B‐type natriuretic peptide (BNP) and eGFR were determined at baseline and day 1, 3, 7, 14, 30 after the start of treatment. Results The eGFR levels were obviously enhanced following levosimendan, peaked at 3 days, sustained for at least 14 days, and returned to baseline by day 30 after starting infusion. In contrast, placebo did not induce any significant changes in eGFR levels during the follow‐up. In addition, levosimendan resulted in a distinct decrease in BNP levels in comparison with placebo, and the beneficial effect returned to baseline by day 14 and remained so at day 30 postinfusion. Conclusions A 24‐h infusion with levosimendan transiently improved the renal dysfunction compared with placebo in patients with DHF, and its beneficial effects persisted for at least 14 days after the initiation of treatment.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Blood Pressure - drug effects</subject><subject>B‐type Natriuretic peptide</subject><subject>Cardiology. Vascular system</subject><subject>Cardiotonic Agents - administration &amp; dosage</subject><subject>Cardiotonic Agents - therapeutic use</subject><subject>Cardiovascular system</subject><subject>Chi-Square Distribution</subject><subject>China</subject><subject>Decompensated heart failure</subject><subject>Double-Blind Method</subject><subject>Drug therapy</subject><subject>Estimated glomerular filtration rate</subject><subject>Female</subject><subject>Glomerular Filtration Rate - drug effects</subject><subject>Heart</subject><subject>Heart failure</subject><subject>Heart Failure - blood</subject><subject>Heart Failure - complications</subject><subject>Heart Failure - diagnosis</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - physiopathology</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Heart Rate - drug effects</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Hydrazones - administration &amp; dosage</subject><subject>Hydrazones - therapeutic use</subject><subject>Infusions, Intravenous</subject><subject>Kidney Diseases - blood</subject><subject>Kidney Diseases - complications</subject><subject>Kidney Diseases - physiopathology</subject><subject>Levosimendan</subject><subject>Linear Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Natriuretic Peptide, Brain - blood</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Pharmacology. Drug treatments</subject><subject>Placebo</subject><subject>Prospective Studies</subject><subject>Pyridazines - administration &amp; dosage</subject><subject>Pyridazines - therapeutic use</subject><subject>Renal dysfunction</subject><subject>Renal failure</subject><subject>Stroke Volume</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Urination - drug effects</subject><subject>Ventricular Function, Left - drug effects</subject><issn>1755-5914</issn><issn>1755-5922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9r3DAQxU1padK0596KoBRy2USyJcs6lv2TLSw0LOnZyPKIKsjSVpIbNh8inznaeLuFXqrLCL3fvBn0iuIjwVckn2vCGZsxUZZXpMSYvCrOTy-vT3dCz4p3Md5jXGNRk7fFWVlRgcuKnxdPS61BJeQ12sBvH80ArpcOeYeWMZlBJujRjfUDhNHKgFbGpiCTyfo2a8g4tPZxZ5K05jGjt1kDlyJ6MOknWoDyww5cfLFZgwwJraSxYwAkXY-24KRFi33Uo1MH0_fFGy1thA_HelH8WC3v5uvZ5vvNt_nXzUxRTMisq5qOa92pvuF1I6XQPdENVhTKGlMmtSDQc5C8qrVWomZYdJqVvVAdpj2j1UVxOfnugv81QkztYKICa6UDP8aWVIQ3tGlYmdHP_6D3fgx574miouGMZ-p6olTwMQbQ7S7k3wv7luD2EFV7CKM9BNO-RJU7Ph19x26A_sT_ySYDX46AjEpaHaRTJv7lOKGsok3m2MQ9GAv7_81t54vttMAzeoGsbA</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Hou, Zhi‐Qiang</creator><creator>Sun, Zhao‐Xia</creator><creator>Su, Chong‐Yi</creator><creator>Tan, Hui</creator><creator>Zhong, Xia</creator><creator>Hu, Bo</creator><creator>Zhou, Yi</creator><creator>Shang, De‐Ya</creator><general>Blackwell</general><general>Hindawi Limited</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>201304</creationdate><title>Effect of Levosimendan on Estimated Glomerular Filtration Rate in Hospitalized Patients with Decompensated Heart Failure and Renal Dysfunction</title><author>Hou, Zhi‐Qiang ; Sun, Zhao‐Xia ; Su, Chong‐Yi ; Tan, Hui ; Zhong, Xia ; Hu, Bo ; Zhou, Yi ; Shang, De‐Ya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4011-b38b7ffbcd8768aa9fd1f80c4e26045af91ed7ea736ffc96509bf52d9cb04d543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Blood Pressure - drug effects</topic><topic>B‐type Natriuretic peptide</topic><topic>Cardiology. Vascular system</topic><topic>Cardiotonic Agents - administration &amp; dosage</topic><topic>Cardiotonic Agents - therapeutic use</topic><topic>Cardiovascular system</topic><topic>Chi-Square Distribution</topic><topic>China</topic><topic>Decompensated heart failure</topic><topic>Double-Blind Method</topic><topic>Drug therapy</topic><topic>Estimated glomerular filtration rate</topic><topic>Female</topic><topic>Glomerular Filtration Rate - drug effects</topic><topic>Heart</topic><topic>Heart failure</topic><topic>Heart Failure - blood</topic><topic>Heart Failure - complications</topic><topic>Heart Failure - diagnosis</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - physiopathology</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Heart Rate - drug effects</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Hydrazones - administration &amp; dosage</topic><topic>Hydrazones - therapeutic use</topic><topic>Infusions, Intravenous</topic><topic>Kidney Diseases - blood</topic><topic>Kidney Diseases - complications</topic><topic>Kidney Diseases - physiopathology</topic><topic>Levosimendan</topic><topic>Linear Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Natriuretic Peptide, Brain - blood</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Pharmacology. Drug treatments</topic><topic>Placebo</topic><topic>Prospective Studies</topic><topic>Pyridazines - administration &amp; dosage</topic><topic>Pyridazines - therapeutic use</topic><topic>Renal dysfunction</topic><topic>Renal failure</topic><topic>Stroke Volume</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Urination - drug effects</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hou, Zhi‐Qiang</creatorcontrib><creatorcontrib>Sun, Zhao‐Xia</creatorcontrib><creatorcontrib>Su, Chong‐Yi</creatorcontrib><creatorcontrib>Tan, Hui</creatorcontrib><creatorcontrib>Zhong, Xia</creatorcontrib><creatorcontrib>Hu, Bo</creatorcontrib><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Shang, De‐Ya</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 Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Cardiovascular therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Hou, Zhi‐Qiang</au><au>Sun, Zhao‐Xia</au><au>Su, Chong‐Yi</au><au>Tan, Hui</au><au>Zhong, Xia</au><au>Hu, Bo</au><au>Zhou, Yi</au><au>Shang, De‐Ya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Levosimendan on Estimated Glomerular Filtration Rate in Hospitalized Patients with Decompensated Heart Failure and Renal Dysfunction</atitle><jtitle>Cardiovascular therapeutics</jtitle><addtitle>Cardiovasc Ther</addtitle><date>2013-04</date><risdate>2013</risdate><volume>31</volume><issue>2</issue><spage>108</spage><epage>114</epage><pages>108-114</pages><issn>1755-5914</issn><eissn>1755-5922</eissn><abstract>Summary Background Only limited data of the long‐term effect of levosimendan on renal dysfunction in patients with decompensated heart failure (DHF) have been published previously. To date, there has been no similar study carried out in a Chinese population. Design and Methods A prospective, randomized, placebo‐controlled, and double‐blind study was performed to investigate the effect of levosimendan on estimated glomerular filtration rate (eGFR) in DHF patients with renal dysfunction during a 30‐day period. Sixty‐six patients with left ventricular ejection fraction (LVEF) ≤40% and eGFR 15–89 mL/min/1.73 m2 were randomized in a 1:1 ratio to receive a 24‐h infusion with levosimendan or placebo. The B‐type natriuretic peptide (BNP) and eGFR were determined at baseline and day 1, 3, 7, 14, 30 after the start of treatment. Results The eGFR levels were obviously enhanced following levosimendan, peaked at 3 days, sustained for at least 14 days, and returned to baseline by day 30 after starting infusion. In contrast, placebo did not induce any significant changes in eGFR levels during the follow‐up. In addition, levosimendan resulted in a distinct decrease in BNP levels in comparison with placebo, and the beneficial effect returned to baseline by day 14 and remained so at day 30 postinfusion. Conclusions A 24‐h infusion with levosimendan transiently improved the renal dysfunction compared with placebo in patients with DHF, and its beneficial effects persisted for at least 14 days after the initiation of treatment.</abstract><cop>Oxford</cop><pub>Blackwell</pub><pmid>23490237</pmid><doi>10.1111/1755-5922.12001</doi><tpages>7</tpages></addata></record>
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source Wiley-Blackwell Open Access Titles
subjects Aged
Aged, 80 and over
Analysis of Variance
Biological and medical sciences
Biomarkers - blood
Blood Pressure - drug effects
B‐type Natriuretic peptide
Cardiology. Vascular system
Cardiotonic Agents - administration & dosage
Cardiotonic Agents - therapeutic use
Cardiovascular system
Chi-Square Distribution
China
Decompensated heart failure
Double-Blind Method
Drug therapy
Estimated glomerular filtration rate
Female
Glomerular Filtration Rate - drug effects
Heart
Heart failure
Heart Failure - blood
Heart Failure - complications
Heart Failure - diagnosis
Heart Failure - drug therapy
Heart Failure - physiopathology
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
Heart Rate - drug effects
Hospitalization
Humans
Hydrazones - administration & dosage
Hydrazones - therapeutic use
Infusions, Intravenous
Kidney Diseases - blood
Kidney Diseases - complications
Kidney Diseases - physiopathology
Levosimendan
Linear Models
Male
Medical sciences
Middle Aged
Natriuretic Peptide, Brain - blood
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
Pharmacology. Drug treatments
Placebo
Prospective Studies
Pyridazines - administration & dosage
Pyridazines - therapeutic use
Renal dysfunction
Renal failure
Stroke Volume
Time Factors
Treatment Outcome
Urination - drug effects
Ventricular Function, Left - drug effects
title Effect of Levosimendan on Estimated Glomerular Filtration Rate in Hospitalized Patients with Decompensated Heart Failure and Renal Dysfunction
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