Brain Natriuretic Peptide for Prevention of Contrast-Induced Nephropathy After Percutaneous Coronary Intervention or Coronary Angiography

Abstract Background Many methods reportedly prevent contrast-induced nephropathy (CIN), but the effect of brain natriuretic peptide (BNP) on CIN is unknown. In this study we investigated recombinant BNP use before coronary angiography (CA) or nonemergent percutaneous coronary intervention (PCI) in p...

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Veröffentlicht in:Canadian journal of cardiology 2014-12, Vol.30 (12), p.1607-1612
Hauptverfasser: Liu, Jin-Ming, MS, Xie, Ya-Nan, MS, Gao, Zi-Han, MS, Zu, Xiu-Guang, MS, Li, Yong-Jun, MD, Hao, Yu-Ming, MD, Chang, Liang, MD
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container_end_page 1612
container_issue 12
container_start_page 1607
container_title Canadian journal of cardiology
container_volume 30
creator Liu, Jin-Ming, MS
Xie, Ya-Nan, MS
Gao, Zi-Han, MS
Zu, Xiu-Guang, MS
Li, Yong-Jun, MD
Hao, Yu-Ming, MD
Chang, Liang, MD
description Abstract Background Many methods reportedly prevent contrast-induced nephropathy (CIN), but the effect of brain natriuretic peptide (BNP) on CIN is unknown. In this study we investigated recombinant BNP use before coronary angiography (CA) or nonemergent percutaneous coronary intervention (PCI) in patients with unstable angina. Methods One thousand patients with unstable angina were prospectively evaluated. The patients were randomly assigned to: group A, isotonic normal saline (NaCl 0.9%, 1 mL/kg/h) for 24 hours before CA or PCI; and group B, human recombinant BNP (rhBNP; 0.005 μg/kg/min). Serum creatinine (Scr) levels and estimated glomerular filtration rate were measured before and 24, 48, and 72 hours, and 7 days after the procedure. The primary outcome was CIN incidence defined according to a relative (≥ 25%) or absolute (≥ 0.5 mg/dL and 44 μmol/L, respectively) increase in Scr from baseline within 48 hours. The secondary end points were the changes in the Scr and estimated glomerular filtration rate, before and after the procedure. Results Contrast volume, a history of diabetes mellitus, and BNP administration independently predicted CIN. The incidence of CIN was significantly greater in group A than in group B (14.8% vs 5.6%; P < 0.01). Renal function was less compromised in patients who received rhBNP. The Scr of all patients with CIN remained increased for 24 hours, but it was lower and recovered faster in patients who received rhBNP. Conclusions rhBNP administration before CA or PCI protects renal function and can significantly decrease CIN incidence.
doi_str_mv 10.1016/j.cjca.2014.08.012
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In this study we investigated recombinant BNP use before coronary angiography (CA) or nonemergent percutaneous coronary intervention (PCI) in patients with unstable angina. Methods One thousand patients with unstable angina were prospectively evaluated. The patients were randomly assigned to: group A, isotonic normal saline (NaCl 0.9%, 1 mL/kg/h) for 24 hours before CA or PCI; and group B, human recombinant BNP (rhBNP; 0.005 μg/kg/min). Serum creatinine (Scr) levels and estimated glomerular filtration rate were measured before and 24, 48, and 72 hours, and 7 days after the procedure. The primary outcome was CIN incidence defined according to a relative (≥ 25%) or absolute (≥ 0.5 mg/dL and 44 μmol/L, respectively) increase in Scr from baseline within 48 hours. The secondary end points were the changes in the Scr and estimated glomerular filtration rate, before and after the procedure. Results Contrast volume, a history of diabetes mellitus, and BNP administration independently predicted CIN. The incidence of CIN was significantly greater in group A than in group B (14.8% vs 5.6%; P &lt; 0.01). Renal function was less compromised in patients who received rhBNP. The Scr of all patients with CIN remained increased for 24 hours, but it was lower and recovered faster in patients who received rhBNP. Conclusions rhBNP administration before CA or PCI protects renal function and can significantly decrease CIN incidence.</description><identifier>ISSN: 0828-282X</identifier><identifier>EISSN: 1916-7075</identifier><identifier>DOI: 10.1016/j.cjca.2014.08.012</identifier><identifier>PMID: 25418218</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Aged ; Angina, Unstable - blood ; Angina, Unstable - diagnostic imaging ; Angina, Unstable - surgery ; Biomarkers - blood ; Cardiovascular ; Contrast Media - adverse effects ; Coronary Angiography - adverse effects ; Creatinine - blood ; Female ; Follow-Up Studies ; Glomerular Filtration Rate ; Humans ; Kidney Diseases - blood ; Kidney Diseases - chemically induced ; Kidney Diseases - prevention &amp; control ; Kidney Function Tests ; Male ; Natriuretic Agents - therapeutic use ; Natriuretic Peptide, Brain - therapeutic use ; Percutaneous Coronary Intervention ; Prospective Studies ; Treatment Outcome</subject><ispartof>Canadian journal of cardiology, 2014-12, Vol.30 (12), p.1607-1612</ispartof><rights>Canadian Cardiovascular Society</rights><rights>2014 Canadian Cardiovascular Society</rights><rights>Copyright © 2014 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-979221a2c91905f0cc7ea04524ce822b3c186def099b021902a713978901103b3</citedby><cites>FETCH-LOGICAL-c477t-979221a2c91905f0cc7ea04524ce822b3c186def099b021902a713978901103b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cjca.2014.08.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25418218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Jin-Ming, MS</creatorcontrib><creatorcontrib>Xie, Ya-Nan, MS</creatorcontrib><creatorcontrib>Gao, Zi-Han, MS</creatorcontrib><creatorcontrib>Zu, Xiu-Guang, MS</creatorcontrib><creatorcontrib>Li, Yong-Jun, MD</creatorcontrib><creatorcontrib>Hao, Yu-Ming, MD</creatorcontrib><creatorcontrib>Chang, Liang, MD</creatorcontrib><title>Brain Natriuretic Peptide for Prevention of Contrast-Induced Nephropathy After Percutaneous Coronary Intervention or Coronary Angiography</title><title>Canadian journal of cardiology</title><addtitle>Can J Cardiol</addtitle><description>Abstract Background Many methods reportedly prevent contrast-induced nephropathy (CIN), but the effect of brain natriuretic peptide (BNP) on CIN is unknown. In this study we investigated recombinant BNP use before coronary angiography (CA) or nonemergent percutaneous coronary intervention (PCI) in patients with unstable angina. Methods One thousand patients with unstable angina were prospectively evaluated. The patients were randomly assigned to: group A, isotonic normal saline (NaCl 0.9%, 1 mL/kg/h) for 24 hours before CA or PCI; and group B, human recombinant BNP (rhBNP; 0.005 μg/kg/min). Serum creatinine (Scr) levels and estimated glomerular filtration rate were measured before and 24, 48, and 72 hours, and 7 days after the procedure. The primary outcome was CIN incidence defined according to a relative (≥ 25%) or absolute (≥ 0.5 mg/dL and 44 μmol/L, respectively) increase in Scr from baseline within 48 hours. The secondary end points were the changes in the Scr and estimated glomerular filtration rate, before and after the procedure. Results Contrast volume, a history of diabetes mellitus, and BNP administration independently predicted CIN. The incidence of CIN was significantly greater in group A than in group B (14.8% vs 5.6%; P &lt; 0.01). Renal function was less compromised in patients who received rhBNP. The Scr of all patients with CIN remained increased for 24 hours, but it was lower and recovered faster in patients who received rhBNP. Conclusions rhBNP administration before CA or PCI protects renal function and can significantly decrease CIN incidence.</description><subject>Aged</subject><subject>Angina, Unstable - blood</subject><subject>Angina, Unstable - diagnostic imaging</subject><subject>Angina, Unstable - surgery</subject><subject>Biomarkers - blood</subject><subject>Cardiovascular</subject><subject>Contrast Media - adverse effects</subject><subject>Coronary Angiography - adverse effects</subject><subject>Creatinine - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glomerular Filtration Rate</subject><subject>Humans</subject><subject>Kidney Diseases - blood</subject><subject>Kidney Diseases - chemically induced</subject><subject>Kidney Diseases - prevention &amp; control</subject><subject>Kidney Function Tests</subject><subject>Male</subject><subject>Natriuretic Agents - therapeutic use</subject><subject>Natriuretic Peptide, Brain - therapeutic use</subject><subject>Percutaneous Coronary Intervention</subject><subject>Prospective Studies</subject><subject>Treatment Outcome</subject><issn>0828-282X</issn><issn>1916-7075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ks1u1DAUhS0EotPCC7BAWbJJuHZ-7EgIaRhRGKkqlQCpO8vj3HQcMnawnUrzCLw1jqYUiQUrL-53jq7PuYS8olBQoM3bodCDVgUDWhUgCqDsCVnRljY5B14_JSsQTORMsNszch7CAFBRzpvn5IzVFRWMihX59cErY7NrFb2ZPUajsxucoukw653Pbjzeo43G2cz12cbZ6FWI-dZ2s8Yuu8Zp792k4v6YrfuISYBez1FZdHNIvHdW-WO2tWn2aOT_Dtb2zrg7r6b98QV51qsx4MuH94J8v_z4bfM5v_ryabtZX-W64jzmLW8Zo4rplrZQ96A1RwVVzSqNgrFdqaloOuyhbXfAEsMUp2XLRQuUQrkrL8ibk-_k3c8ZQ5QHEzSO42lpSZuyYpw1UCeUnVDtXQgeezl5c0h7SwpyqUAOcqlALhVIEDJVkESvH_zn3QG7R8mfzBPw7gRg-uW9QS-DNmhTnsajjrJz5v_-7_-R69FYo9X4A48YBjd7m_KTVAYmQX5djmC5AVoltYDb8jdyRa5S</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Liu, Jin-Ming, MS</creator><creator>Xie, Ya-Nan, MS</creator><creator>Gao, Zi-Han, MS</creator><creator>Zu, Xiu-Guang, MS</creator><creator>Li, Yong-Jun, MD</creator><creator>Hao, Yu-Ming, MD</creator><creator>Chang, Liang, MD</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Brain Natriuretic Peptide for Prevention of Contrast-Induced Nephropathy After Percutaneous Coronary Intervention or Coronary Angiography</title><author>Liu, Jin-Ming, MS ; Xie, Ya-Nan, MS ; Gao, Zi-Han, MS ; Zu, Xiu-Guang, MS ; Li, Yong-Jun, MD ; Hao, Yu-Ming, MD ; Chang, Liang, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-979221a2c91905f0cc7ea04524ce822b3c186def099b021902a713978901103b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Angina, Unstable - blood</topic><topic>Angina, Unstable - diagnostic imaging</topic><topic>Angina, Unstable - surgery</topic><topic>Biomarkers - blood</topic><topic>Cardiovascular</topic><topic>Contrast Media - adverse effects</topic><topic>Coronary Angiography - adverse effects</topic><topic>Creatinine - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glomerular Filtration Rate</topic><topic>Humans</topic><topic>Kidney Diseases - blood</topic><topic>Kidney Diseases - chemically induced</topic><topic>Kidney Diseases - prevention &amp; control</topic><topic>Kidney Function Tests</topic><topic>Male</topic><topic>Natriuretic Agents - therapeutic use</topic><topic>Natriuretic Peptide, Brain - therapeutic use</topic><topic>Percutaneous Coronary Intervention</topic><topic>Prospective Studies</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jin-Ming, MS</creatorcontrib><creatorcontrib>Xie, Ya-Nan, MS</creatorcontrib><creatorcontrib>Gao, Zi-Han, MS</creatorcontrib><creatorcontrib>Zu, Xiu-Guang, MS</creatorcontrib><creatorcontrib>Li, Yong-Jun, MD</creatorcontrib><creatorcontrib>Hao, Yu-Ming, MD</creatorcontrib><creatorcontrib>Chang, Liang, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Canadian journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jin-Ming, MS</au><au>Xie, Ya-Nan, MS</au><au>Gao, Zi-Han, MS</au><au>Zu, Xiu-Guang, MS</au><au>Li, Yong-Jun, MD</au><au>Hao, Yu-Ming, MD</au><au>Chang, Liang, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain Natriuretic Peptide for Prevention of Contrast-Induced Nephropathy After Percutaneous Coronary Intervention or Coronary Angiography</atitle><jtitle>Canadian journal of cardiology</jtitle><addtitle>Can J Cardiol</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>30</volume><issue>12</issue><spage>1607</spage><epage>1612</epage><pages>1607-1612</pages><issn>0828-282X</issn><eissn>1916-7075</eissn><abstract>Abstract Background Many methods reportedly prevent contrast-induced nephropathy (CIN), but the effect of brain natriuretic peptide (BNP) on CIN is unknown. In this study we investigated recombinant BNP use before coronary angiography (CA) or nonemergent percutaneous coronary intervention (PCI) in patients with unstable angina. Methods One thousand patients with unstable angina were prospectively evaluated. The patients were randomly assigned to: group A, isotonic normal saline (NaCl 0.9%, 1 mL/kg/h) for 24 hours before CA or PCI; and group B, human recombinant BNP (rhBNP; 0.005 μg/kg/min). Serum creatinine (Scr) levels and estimated glomerular filtration rate were measured before and 24, 48, and 72 hours, and 7 days after the procedure. The primary outcome was CIN incidence defined according to a relative (≥ 25%) or absolute (≥ 0.5 mg/dL and 44 μmol/L, respectively) increase in Scr from baseline within 48 hours. The secondary end points were the changes in the Scr and estimated glomerular filtration rate, before and after the procedure. Results Contrast volume, a history of diabetes mellitus, and BNP administration independently predicted CIN. The incidence of CIN was significantly greater in group A than in group B (14.8% vs 5.6%; P &lt; 0.01). Renal function was less compromised in patients who received rhBNP. The Scr of all patients with CIN remained increased for 24 hours, but it was lower and recovered faster in patients who received rhBNP. Conclusions rhBNP administration before CA or PCI protects renal function and can significantly decrease CIN incidence.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>25418218</pmid><doi>10.1016/j.cjca.2014.08.012</doi><tpages>6</tpages></addata></record>
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subjects Aged
Angina, Unstable - blood
Angina, Unstable - diagnostic imaging
Angina, Unstable - surgery
Biomarkers - blood
Cardiovascular
Contrast Media - adverse effects
Coronary Angiography - adverse effects
Creatinine - blood
Female
Follow-Up Studies
Glomerular Filtration Rate
Humans
Kidney Diseases - blood
Kidney Diseases - chemically induced
Kidney Diseases - prevention & control
Kidney Function Tests
Male
Natriuretic Agents - therapeutic use
Natriuretic Peptide, Brain - therapeutic use
Percutaneous Coronary Intervention
Prospective Studies
Treatment Outcome
title Brain Natriuretic Peptide for Prevention of Contrast-Induced Nephropathy After Percutaneous Coronary Intervention or Coronary Angiography
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