Neutrophil gelatinase-associated lipocalin, cystatin C and eGFR indicate acute kidney injury and predict prognosis of patients with acute pulmonary embolism

ObjectiveRisk stratification in acute pulmonary embolism (APE) includes the assessment of clinical status, right ventricular dysfunction and troponin concentrations. Since acute renal impairment is one of the important predictors of mortality in cardiovascular diseases, the authors hypothesised that...

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Veröffentlicht in:Heart (British Cardiac Society) 2012-08, Vol.98 (16), p.1221-1228
Hauptverfasser: Kostrubiec, Maciej, Łabyk, Andrzej, Pedowska-Włoszek, Justyna, Dzikowska-Diduch, Olga, Wojciechowski, Artur, Garlińska, Marzena, Ciurzyński, Michał, Pruszczyk, Piotr
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container_end_page 1228
container_issue 16
container_start_page 1221
container_title Heart (British Cardiac Society)
container_volume 98
creator Kostrubiec, Maciej
Łabyk, Andrzej
Pedowska-Włoszek, Justyna
Dzikowska-Diduch, Olga
Wojciechowski, Artur
Garlińska, Marzena
Ciurzyński, Michał
Pruszczyk, Piotr
description ObjectiveRisk stratification in acute pulmonary embolism (APE) includes the assessment of clinical status, right ventricular dysfunction and troponin concentrations. Since acute renal impairment is one of the important predictors of mortality in cardiovascular diseases, the authors hypothesised that it is an independent mortality marker in APE.Material and methodsThe authors observed 142 consecutive patients (52 M/90 F, 64±18 years) with APE diagnosed with contrast enhanced multislice CT. On admission, blood samples were collected for neutrophil gelatinase-associated lipocalin (N-GAL), cystatin C and creatinine assays. Estimated glomerular filtration rate (eGFR) was calculated using MDRD formula.ResultsFourteen (10%) of 142 patients died by the 30th day of observation. eGFR≤60 ml/min was noted in 68 (48%) patients and eGFR≤30 ml/min in 11 (8%) patients. eGFR was higher in survivors than in non-survivors (66 (17–169) vs 46 (10–119) ml/min, respectively, p=0.02). In 80 (56%) patients, N-GAL was >50 ng/ml indicating acute kidney injury. N-GAL was higher in non-survivors than in survivors (88.8 (28.4–200.0) vs 53.0 (7.1–200.0) ng/ml, p50 ng/ml was found in 11 (79%) patients with fatal outcome. Area under the curve of N-GAL for all-cause mortality in ROC analysis was 0.715. N-GAL>75 ng/ml was present in 44 (31%) patients, while cystatin C >1900 ng/ml in 14 (10%) subjects. They showed sensitivity, specificity, positive predictive value and negative predictive value for prediction of all-cause death ((64%, 73%, 21%, 95%) and (36%, 91%, 30% 93%), respectively). N-GAL>75 ng/ml and cystatin C>1900 ng/ml increased the risk of death (HR 4.4 (95% CI 1.48 to 13.2, p
doi_str_mv 10.1136/heartjnl-2012-301884
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Since acute renal impairment is one of the important predictors of mortality in cardiovascular diseases, the authors hypothesised that it is an independent mortality marker in APE.Material and methodsThe authors observed 142 consecutive patients (52 M/90 F, 64±18 years) with APE diagnosed with contrast enhanced multislice CT. On admission, blood samples were collected for neutrophil gelatinase-associated lipocalin (N-GAL), cystatin C and creatinine assays. Estimated glomerular filtration rate (eGFR) was calculated using MDRD formula.ResultsFourteen (10%) of 142 patients died by the 30th day of observation. eGFR≤60 ml/min was noted in 68 (48%) patients and eGFR≤30 ml/min in 11 (8%) patients. eGFR was higher in survivors than in non-survivors (66 (17–169) vs 46 (10–119) ml/min, respectively, p=0.02). In 80 (56%) patients, N-GAL was &gt;50 ng/ml indicating acute kidney injury. N-GAL was higher in non-survivors than in survivors (88.8 (28.4–200.0) vs 53.0 (7.1–200.0) ng/ml, p&lt;0.01). N-GAL level &gt;50 ng/ml was found in 11 (79%) patients with fatal outcome. Area under the curve of N-GAL for all-cause mortality in ROC analysis was 0.715. N-GAL&gt;75 ng/ml was present in 44 (31%) patients, while cystatin C &gt;1900 ng/ml in 14 (10%) subjects. They showed sensitivity, specificity, positive predictive value and negative predictive value for prediction of all-cause death ((64%, 73%, 21%, 95%) and (36%, 91%, 30% 93%), respectively). N-GAL&gt;75 ng/ml and cystatin C&gt;1900 ng/ml increased the risk of death (HR 4.4 (95% CI 1.48 to 13.2, p&lt;0.01) and 4.7 (95% CI 1.56 to 13.9, p=0.01), respectively).ConclusionsAcute kidney injury assessed by N-GAL occurs in 30% of APE and may contribute to the impairment of renal function present in half of them. Moreover, N-GAL, cystatin C elevation and low eGFR are associated with a poor 30-day prognosis in APE.</description><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/heartjnl-2012-301884</identifier><identifier>PMID: 22705926</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><subject>Acute coronary syndromes ; Acute Disease ; Acute Kidney Injury - blood ; Acute Kidney Injury - diagnosis ; Acute Kidney Injury - mortality ; Acute Kidney Injury - physiopathology ; Acute-Phase Proteins ; Aged ; Aged, 80 and over ; allied specialities ; aorta ; aortic valve disease ; Biological and medical sciences ; Biomarkers ; Biomarkers - blood ; Blood platelets ; Cardiology ; Cardiology. Vascular system ; cardiorenal syndrome ; Chi-Square Distribution ; Creatinine - blood ; cystatin C ; Cystatin C - blood ; eGFR ; Embolisms ; Emergency medical care ; emergency medicine ; endothelial function ; endothelium ; Female ; Glomerular Filtration Rate ; great vessels and trauma ; haematology ; Heart failure ; Humans ; Immunoassay ; Kaplan-Meier Estimate ; Kidney - physiopathology ; Kidney diseases ; Kidneys ; Lipocalin-2 ; Lipocalins - blood ; Male ; Medical prognosis ; Medical sciences ; Middle Aged ; mitral stenosis ; Mortality ; Multidetector Computed Tomography ; Multivariate Analysis ; N-GAL ; Nephrology. Urinary tract diseases ; Neutrophils ; Plasma ; Pneumology ; Poland ; Predictive Value of Tests ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Proto-Oncogene Proteins - blood ; pulmonary embolism ; Pulmonary Embolism - diagnosis ; Pulmonary Embolism - diagnostic imaging ; Pulmonary Embolism - mortality ; Pulmonary Embolism - physiopathology ; Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases ; quality of care and outcomes ; renal disease ; Renal failure ; renovascular disease ; Risk Assessment ; Risk Factors ; ROC Curve ; Sensitivity and Specificity ; Time Factors ; Urinary system involvement in other diseases. Miscellaneous ; Urine ; valvular disease ; venous thromboembolism ; Ventricular Function, Right</subject><ispartof>Heart (British Cardiac Society), 2012-08, Vol.98 (16), p.1221-1228</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2012 (c) 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b443t-9fc9b4a1a23aa5be2df34a775972eb1b0ea6e30b66f387057d7b321aec647d143</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://heart.bmj.com/content/98/16/1221.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://heart.bmj.com/content/98/16/1221.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26196493$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22705926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kostrubiec, Maciej</creatorcontrib><creatorcontrib>Łabyk, Andrzej</creatorcontrib><creatorcontrib>Pedowska-Włoszek, Justyna</creatorcontrib><creatorcontrib>Dzikowska-Diduch, Olga</creatorcontrib><creatorcontrib>Wojciechowski, Artur</creatorcontrib><creatorcontrib>Garlińska, Marzena</creatorcontrib><creatorcontrib>Ciurzyński, Michał</creatorcontrib><creatorcontrib>Pruszczyk, Piotr</creatorcontrib><title>Neutrophil gelatinase-associated lipocalin, cystatin C and eGFR indicate acute kidney injury and predict prognosis of patients with acute pulmonary embolism</title><title>Heart (British Cardiac Society)</title><addtitle>Heart</addtitle><description>ObjectiveRisk stratification in acute pulmonary embolism (APE) includes the assessment of clinical status, right ventricular dysfunction and troponin concentrations. Since acute renal impairment is one of the important predictors of mortality in cardiovascular diseases, the authors hypothesised that it is an independent mortality marker in APE.Material and methodsThe authors observed 142 consecutive patients (52 M/90 F, 64±18 years) with APE diagnosed with contrast enhanced multislice CT. On admission, blood samples were collected for neutrophil gelatinase-associated lipocalin (N-GAL), cystatin C and creatinine assays. Estimated glomerular filtration rate (eGFR) was calculated using MDRD formula.ResultsFourteen (10%) of 142 patients died by the 30th day of observation. eGFR≤60 ml/min was noted in 68 (48%) patients and eGFR≤30 ml/min in 11 (8%) patients. eGFR was higher in survivors than in non-survivors (66 (17–169) vs 46 (10–119) ml/min, respectively, p=0.02). In 80 (56%) patients, N-GAL was &gt;50 ng/ml indicating acute kidney injury. N-GAL was higher in non-survivors than in survivors (88.8 (28.4–200.0) vs 53.0 (7.1–200.0) ng/ml, p&lt;0.01). N-GAL level &gt;50 ng/ml was found in 11 (79%) patients with fatal outcome. Area under the curve of N-GAL for all-cause mortality in ROC analysis was 0.715. N-GAL&gt;75 ng/ml was present in 44 (31%) patients, while cystatin C &gt;1900 ng/ml in 14 (10%) subjects. They showed sensitivity, specificity, positive predictive value and negative predictive value for prediction of all-cause death ((64%, 73%, 21%, 95%) and (36%, 91%, 30% 93%), respectively). N-GAL&gt;75 ng/ml and cystatin C&gt;1900 ng/ml increased the risk of death (HR 4.4 (95% CI 1.48 to 13.2, p&lt;0.01) and 4.7 (95% CI 1.56 to 13.9, p=0.01), respectively).ConclusionsAcute kidney injury assessed by N-GAL occurs in 30% of APE and may contribute to the impairment of renal function present in half of them. Moreover, N-GAL, cystatin C elevation and low eGFR are associated with a poor 30-day prognosis in APE.</description><subject>Acute coronary syndromes</subject><subject>Acute Disease</subject><subject>Acute Kidney Injury - blood</subject><subject>Acute Kidney Injury - diagnosis</subject><subject>Acute Kidney Injury - mortality</subject><subject>Acute Kidney Injury - physiopathology</subject><subject>Acute-Phase Proteins</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>allied specialities</subject><subject>aorta</subject><subject>aortic valve disease</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Blood platelets</subject><subject>Cardiology</subject><subject>Cardiology. Vascular system</subject><subject>cardiorenal syndrome</subject><subject>Chi-Square Distribution</subject><subject>Creatinine - blood</subject><subject>cystatin C</subject><subject>Cystatin C - blood</subject><subject>eGFR</subject><subject>Embolisms</subject><subject>Emergency medical care</subject><subject>emergency medicine</subject><subject>endothelial function</subject><subject>endothelium</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>great vessels and trauma</subject><subject>haematology</subject><subject>Heart failure</subject><subject>Humans</subject><subject>Immunoassay</subject><subject>Kaplan-Meier Estimate</subject><subject>Kidney - physiopathology</subject><subject>Kidney diseases</subject><subject>Kidneys</subject><subject>Lipocalin-2</subject><subject>Lipocalins - blood</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>mitral stenosis</subject><subject>Mortality</subject><subject>Multidetector Computed Tomography</subject><subject>Multivariate Analysis</subject><subject>N-GAL</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Neutrophils</subject><subject>Plasma</subject><subject>Pneumology</subject><subject>Poland</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Proto-Oncogene Proteins - blood</subject><subject>pulmonary embolism</subject><subject>Pulmonary Embolism - diagnosis</subject><subject>Pulmonary Embolism - diagnostic imaging</subject><subject>Pulmonary Embolism - mortality</subject><subject>Pulmonary Embolism - physiopathology</subject><subject>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</subject><subject>quality of care and outcomes</subject><subject>renal disease</subject><subject>Renal failure</subject><subject>renovascular disease</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><subject>Time Factors</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urine</subject><subject>valvular disease</subject><subject>venous thromboembolism</subject><subject>Ventricular Function, Right</subject><issn>1355-6037</issn><issn>1468-201X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkd1u1DAQhSMEoqXwBghZQkhcEOq_2MklBFqQqgXxJ8SNNUkmXW8TO8SOYN-Fh8XLbovEFTcea-Y7RzM6WfaQ0eeMCXW6Rpjjxg05p4zngrKylLeyYyZVuWt9vZ3-oihyRYU-yu6FsKGUyqpUd7MjzjUtKq6Os18rXOLsp7UdyCUOEK2DgDmE4FsLETsy2Mm3MFj3jLTbEHcEqQm4juD52QdiXWfbBBJol_Re2c7hNnU3y7z9Q00zJiKm6i-dDzYQ35Mp2aCLgfywcX2QTsswegdJhmPjBxvG-9mdHoaADw71JPt89vpT_Sa_eHf-tn5xkTdSiphXfVs1EhhwAVA0yLteSNC6qDTHhjUUQaGgjVK9KNPhutON4AywVVJ3TIqT7OneN-34fcEQzWhDi8MADv0SDKNcl0LKQif08T_oxi-zS9sZpkuqOauYSpTcU-3sQ5ixN9Nsx3RasjK79Mx1emaXntmnl2SPDuZLM2J3I7qOKwFPDgCElEk_g2tt-MspVilZicTle86GiD9v5jBfGaWFLszqS20-1u-FWn17ZV4m_nTPN-Pm_1b9DRtCxk8</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Kostrubiec, Maciej</creator><creator>Łabyk, Andrzej</creator><creator>Pedowska-Włoszek, Justyna</creator><creator>Dzikowska-Diduch, Olga</creator><creator>Wojciechowski, Artur</creator><creator>Garlińska, Marzena</creator><creator>Ciurzyński, Michał</creator><creator>Pruszczyk, Piotr</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ Publishing Group</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20120801</creationdate><title>Neutrophil gelatinase-associated lipocalin, cystatin C and eGFR indicate acute kidney injury and predict prognosis of patients with acute pulmonary embolism</title><author>Kostrubiec, Maciej ; Łabyk, Andrzej ; Pedowska-Włoszek, Justyna ; Dzikowska-Diduch, Olga ; Wojciechowski, Artur ; Garlińska, Marzena ; Ciurzyński, Michał ; Pruszczyk, Piotr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b443t-9fc9b4a1a23aa5be2df34a775972eb1b0ea6e30b66f387057d7b321aec647d143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acute coronary syndromes</topic><topic>Acute Disease</topic><topic>Acute Kidney Injury - blood</topic><topic>Acute Kidney Injury - diagnosis</topic><topic>Acute Kidney Injury - mortality</topic><topic>Acute Kidney Injury - physiopathology</topic><topic>Acute-Phase Proteins</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>allied specialities</topic><topic>aorta</topic><topic>aortic valve disease</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Blood platelets</topic><topic>Cardiology</topic><topic>Cardiology. Vascular system</topic><topic>cardiorenal syndrome</topic><topic>Chi-Square Distribution</topic><topic>Creatinine - blood</topic><topic>cystatin C</topic><topic>Cystatin C - blood</topic><topic>eGFR</topic><topic>Embolisms</topic><topic>Emergency medical care</topic><topic>emergency medicine</topic><topic>endothelial function</topic><topic>endothelium</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>great vessels and trauma</topic><topic>haematology</topic><topic>Heart failure</topic><topic>Humans</topic><topic>Immunoassay</topic><topic>Kaplan-Meier Estimate</topic><topic>Kidney - physiopathology</topic><topic>Kidney diseases</topic><topic>Kidneys</topic><topic>Lipocalin-2</topic><topic>Lipocalins - blood</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>mitral stenosis</topic><topic>Mortality</topic><topic>Multidetector Computed Tomography</topic><topic>Multivariate Analysis</topic><topic>N-GAL</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Neutrophils</topic><topic>Plasma</topic><topic>Pneumology</topic><topic>Poland</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Proto-Oncogene Proteins - blood</topic><topic>pulmonary embolism</topic><topic>Pulmonary Embolism - diagnosis</topic><topic>Pulmonary Embolism - diagnostic imaging</topic><topic>Pulmonary Embolism - mortality</topic><topic>Pulmonary Embolism - physiopathology</topic><topic>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</topic><topic>quality of care and outcomes</topic><topic>renal disease</topic><topic>Renal failure</topic><topic>renovascular disease</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>ROC Curve</topic><topic>Sensitivity and Specificity</topic><topic>Time Factors</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urine</topic><topic>valvular disease</topic><topic>venous thromboembolism</topic><topic>Ventricular Function, Right</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kostrubiec, Maciej</creatorcontrib><creatorcontrib>Łabyk, Andrzej</creatorcontrib><creatorcontrib>Pedowska-Włoszek, Justyna</creatorcontrib><creatorcontrib>Dzikowska-Diduch, Olga</creatorcontrib><creatorcontrib>Wojciechowski, Artur</creatorcontrib><creatorcontrib>Garlińska, Marzena</creatorcontrib><creatorcontrib>Ciurzyński, Michał</creatorcontrib><creatorcontrib>Pruszczyk, Piotr</creatorcontrib><collection>Istex</collection><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 Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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 Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science 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 Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Heart (British Cardiac Society)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kostrubiec, Maciej</au><au>Łabyk, Andrzej</au><au>Pedowska-Włoszek, Justyna</au><au>Dzikowska-Diduch, Olga</au><au>Wojciechowski, Artur</au><au>Garlińska, Marzena</au><au>Ciurzyński, Michał</au><au>Pruszczyk, Piotr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neutrophil gelatinase-associated lipocalin, cystatin C and eGFR indicate acute kidney injury and predict prognosis of patients with acute pulmonary embolism</atitle><jtitle>Heart (British Cardiac Society)</jtitle><addtitle>Heart</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>98</volume><issue>16</issue><spage>1221</spage><epage>1228</epage><pages>1221-1228</pages><issn>1355-6037</issn><eissn>1468-201X</eissn><abstract>ObjectiveRisk stratification in acute pulmonary embolism (APE) includes the assessment of clinical status, right ventricular dysfunction and troponin concentrations. Since acute renal impairment is one of the important predictors of mortality in cardiovascular diseases, the authors hypothesised that it is an independent mortality marker in APE.Material and methodsThe authors observed 142 consecutive patients (52 M/90 F, 64±18 years) with APE diagnosed with contrast enhanced multislice CT. On admission, blood samples were collected for neutrophil gelatinase-associated lipocalin (N-GAL), cystatin C and creatinine assays. Estimated glomerular filtration rate (eGFR) was calculated using MDRD formula.ResultsFourteen (10%) of 142 patients died by the 30th day of observation. eGFR≤60 ml/min was noted in 68 (48%) patients and eGFR≤30 ml/min in 11 (8%) patients. eGFR was higher in survivors than in non-survivors (66 (17–169) vs 46 (10–119) ml/min, respectively, p=0.02). In 80 (56%) patients, N-GAL was &gt;50 ng/ml indicating acute kidney injury. N-GAL was higher in non-survivors than in survivors (88.8 (28.4–200.0) vs 53.0 (7.1–200.0) ng/ml, p&lt;0.01). N-GAL level &gt;50 ng/ml was found in 11 (79%) patients with fatal outcome. Area under the curve of N-GAL for all-cause mortality in ROC analysis was 0.715. N-GAL&gt;75 ng/ml was present in 44 (31%) patients, while cystatin C &gt;1900 ng/ml in 14 (10%) subjects. They showed sensitivity, specificity, positive predictive value and negative predictive value for prediction of all-cause death ((64%, 73%, 21%, 95%) and (36%, 91%, 30% 93%), respectively). N-GAL&gt;75 ng/ml and cystatin C&gt;1900 ng/ml increased the risk of death (HR 4.4 (95% CI 1.48 to 13.2, p&lt;0.01) and 4.7 (95% CI 1.56 to 13.9, p=0.01), respectively).ConclusionsAcute kidney injury assessed by N-GAL occurs in 30% of APE and may contribute to the impairment of renal function present in half of them. Moreover, N-GAL, cystatin C elevation and low eGFR are associated with a poor 30-day prognosis in APE.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>22705926</pmid><doi>10.1136/heartjnl-2012-301884</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 1355-6037
ispartof Heart (British Cardiac Society), 2012-08, Vol.98 (16), p.1221-1228
issn 1355-6037
1468-201X
language eng
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source MEDLINE; BMJ Journals - NESLi2; PubMed Central
subjects Acute coronary syndromes
Acute Disease
Acute Kidney Injury - blood
Acute Kidney Injury - diagnosis
Acute Kidney Injury - mortality
Acute Kidney Injury - physiopathology
Acute-Phase Proteins
Aged
Aged, 80 and over
allied specialities
aorta
aortic valve disease
Biological and medical sciences
Biomarkers
Biomarkers - blood
Blood platelets
Cardiology
Cardiology. Vascular system
cardiorenal syndrome
Chi-Square Distribution
Creatinine - blood
cystatin C
Cystatin C - blood
eGFR
Embolisms
Emergency medical care
emergency medicine
endothelial function
endothelium
Female
Glomerular Filtration Rate
great vessels and trauma
haematology
Heart failure
Humans
Immunoassay
Kaplan-Meier Estimate
Kidney - physiopathology
Kidney diseases
Kidneys
Lipocalin-2
Lipocalins - blood
Male
Medical prognosis
Medical sciences
Middle Aged
mitral stenosis
Mortality
Multidetector Computed Tomography
Multivariate Analysis
N-GAL
Nephrology. Urinary tract diseases
Neutrophils
Plasma
Pneumology
Poland
Predictive Value of Tests
Prognosis
Proportional Hazards Models
Prospective Studies
Proto-Oncogene Proteins - blood
pulmonary embolism
Pulmonary Embolism - diagnosis
Pulmonary Embolism - diagnostic imaging
Pulmonary Embolism - mortality
Pulmonary Embolism - physiopathology
Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases
quality of care and outcomes
renal disease
Renal failure
renovascular disease
Risk Assessment
Risk Factors
ROC Curve
Sensitivity and Specificity
Time Factors
Urinary system involvement in other diseases. Miscellaneous
Urine
valvular disease
venous thromboembolism
Ventricular Function, Right
title Neutrophil gelatinase-associated lipocalin, cystatin C and eGFR indicate acute kidney injury and predict prognosis of patients with acute pulmonary embolism
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