Impact of Loop Diuretic Use on Outcomes Following Transcatheter Aortic Valve Implantation
•Severe AS is characterized by chronic pressure overload and impairment in left ventricular remodeling.•Loop-diuretic therapy prior to TAVI is a marker of higher-risk patients with more medical co-morbidities and echocardiographic evidence of advanced left ventricular remodeling.•Loop-diuretic thera...
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Veröffentlicht in: | The American journal of cardiology 2020-09, Vol.131, p.67-73 |
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creator | Cantey, Eric P. Chang, Kevin Y. Blair, John E.A. Brummel, Kent Sweis, Ranya N. Pham, Duc T. Adi, Adin-Christian Churyla, Andrei Ricciardi, Mark J. Malaisrie, S. Chris Davidson, Charles J. Flaherty, James D. |
description | •Severe AS is characterized by chronic pressure overload and impairment in left ventricular remodeling.•Loop-diuretic therapy prior to TAVI is a marker of higher-risk patients with more medical co-morbidities and echocardiographic evidence of advanced left ventricular remodeling.•Loop-diuretic therapy was associated with a trend towards 1-year mortality on propensity-matched analysis.
The use of LDT may signify significant hemodynamic changes and left ventricular remodeling in severe aortic stenosis (AS). Therefore, we sought to determine whether loop diuretic therapy (LDT) is associated with adverse outcomes following transcatheter aortic valve implantation (TAVI) in patients with severe symptomatic AS. Subjects undergoing TAVI at a single institution from June 2008 to December 2017 were analyzed. LDT doses were normalized to oral furosemide daily equivalents. All outcomes were adjudicated using VARC2 criteria. Descriptive statistics, multivariate logistic regression, and propensity score matching were used. Of the 804 subjects studied, 48.3% were on pre-TAVI LDT with a mean dose of 51.1 mg furosemide dose-equivalents. Subjects on LDT were higher risk, frail patients with more co-morbidities including chronic kidney disease, coronary artery disease requiring prior bypass grafting, peripheral arterial disease, atrial fibrillation or flutter, and diabetes with more severe heart failure symptoms. Those on LDT also had worse left ventricular systolic function, lower transvalvular gradients, and markers of adverse left ventricular remodeling, including increased left ventricular mass index and higher rates of concentric and eccentric hypertrophy. On propensity-score matching, death within one year post-TAVI was borderline significantly higher in the pre-LDT as compared with no-LDT group (16.9% vs 10.4 %, p = 0.068). In conclusion, use of pre-TAVI LDT for severe symptomatic AS is associated with a trend towards worse 1-year mortality and is a marker of high-risk, frail individuals with advanced left ventricular remodeling. |
doi_str_mv | 10.1016/j.amjcard.2020.06.033 |
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The use of LDT may signify significant hemodynamic changes and left ventricular remodeling in severe aortic stenosis (AS). Therefore, we sought to determine whether loop diuretic therapy (LDT) is associated with adverse outcomes following transcatheter aortic valve implantation (TAVI) in patients with severe symptomatic AS. Subjects undergoing TAVI at a single institution from June 2008 to December 2017 were analyzed. LDT doses were normalized to oral furosemide daily equivalents. All outcomes were adjudicated using VARC2 criteria. Descriptive statistics, multivariate logistic regression, and propensity score matching were used. Of the 804 subjects studied, 48.3% were on pre-TAVI LDT with a mean dose of 51.1 mg furosemide dose-equivalents. Subjects on LDT were higher risk, frail patients with more co-morbidities including chronic kidney disease, coronary artery disease requiring prior bypass grafting, peripheral arterial disease, atrial fibrillation or flutter, and diabetes with more severe heart failure symptoms. Those on LDT also had worse left ventricular systolic function, lower transvalvular gradients, and markers of adverse left ventricular remodeling, including increased left ventricular mass index and higher rates of concentric and eccentric hypertrophy. On propensity-score matching, death within one year post-TAVI was borderline significantly higher in the pre-LDT as compared with no-LDT group (16.9% vs 10.4 %, p = 0.068). In conclusion, use of pre-TAVI LDT for severe symptomatic AS is associated with a trend towards worse 1-year mortality and is a marker of high-risk, frail individuals with advanced left ventricular remodeling.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2020.06.033</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>Aorta ; Aortic stenosis ; Aortic valve ; Cardiovascular disease ; Congestive heart failure ; Coronary artery ; Coronary artery disease ; Coronary vessels ; Creatinine ; Diabetes mellitus ; Diuretics ; Equivalence ; Fibrillation ; Flutter ; Frailty ; Furosemide ; Heart failure ; Heart valves ; Hemodynamics ; Hospitalization ; Hypertrophy ; Implantation ; Kidney diseases ; Markers ; Matching ; Medical prognosis ; Mortality ; Multivariate analysis ; Peptides ; Pulmonary arteries ; Regression analysis ; Rheumatic heart disease ; Signs and symptoms ; Stenosis ; Transplants & implants ; Ventricle</subject><ispartof>The American journal of cardiology, 2020-09, Vol.131, p.67-73</ispartof><rights>2020 Elsevier Inc.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-a61838f6f0e2db3f35efb8b9d4dd9bcf94754daad0d4121471346eeacbfc425c3</citedby><cites>FETCH-LOGICAL-c370t-a61838f6f0e2db3f35efb8b9d4dd9bcf94754daad0d4121471346eeacbfc425c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S000291492030610X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Cantey, Eric P.</creatorcontrib><creatorcontrib>Chang, Kevin Y.</creatorcontrib><creatorcontrib>Blair, John E.A.</creatorcontrib><creatorcontrib>Brummel, Kent</creatorcontrib><creatorcontrib>Sweis, Ranya N.</creatorcontrib><creatorcontrib>Pham, Duc T.</creatorcontrib><creatorcontrib>Adi, Adin-Christian</creatorcontrib><creatorcontrib>Churyla, Andrei</creatorcontrib><creatorcontrib>Ricciardi, Mark J.</creatorcontrib><creatorcontrib>Malaisrie, S. Chris</creatorcontrib><creatorcontrib>Davidson, Charles J.</creatorcontrib><creatorcontrib>Flaherty, James D.</creatorcontrib><title>Impact of Loop Diuretic Use on Outcomes Following Transcatheter Aortic Valve Implantation</title><title>The American journal of cardiology</title><description>•Severe AS is characterized by chronic pressure overload and impairment in left ventricular remodeling.•Loop-diuretic therapy prior to TAVI is a marker of higher-risk patients with more medical co-morbidities and echocardiographic evidence of advanced left ventricular remodeling.•Loop-diuretic therapy was associated with a trend towards 1-year mortality on propensity-matched analysis.
The use of LDT may signify significant hemodynamic changes and left ventricular remodeling in severe aortic stenosis (AS). Therefore, we sought to determine whether loop diuretic therapy (LDT) is associated with adverse outcomes following transcatheter aortic valve implantation (TAVI) in patients with severe symptomatic AS. Subjects undergoing TAVI at a single institution from June 2008 to December 2017 were analyzed. LDT doses were normalized to oral furosemide daily equivalents. All outcomes were adjudicated using VARC2 criteria. Descriptive statistics, multivariate logistic regression, and propensity score matching were used. Of the 804 subjects studied, 48.3% were on pre-TAVI LDT with a mean dose of 51.1 mg furosemide dose-equivalents. Subjects on LDT were higher risk, frail patients with more co-morbidities including chronic kidney disease, coronary artery disease requiring prior bypass grafting, peripheral arterial disease, atrial fibrillation or flutter, and diabetes with more severe heart failure symptoms. Those on LDT also had worse left ventricular systolic function, lower transvalvular gradients, and markers of adverse left ventricular remodeling, including increased left ventricular mass index and higher rates of concentric and eccentric hypertrophy. On propensity-score matching, death within one year post-TAVI was borderline significantly higher in the pre-LDT as compared with no-LDT group (16.9% vs 10.4 %, p = 0.068). In conclusion, use of pre-TAVI LDT for severe symptomatic AS is associated with a trend towards worse 1-year mortality and is a marker of high-risk, frail individuals with advanced left ventricular remodeling.</description><subject>Aorta</subject><subject>Aortic stenosis</subject><subject>Aortic valve</subject><subject>Cardiovascular disease</subject><subject>Congestive heart failure</subject><subject>Coronary artery</subject><subject>Coronary artery disease</subject><subject>Coronary vessels</subject><subject>Creatinine</subject><subject>Diabetes mellitus</subject><subject>Diuretics</subject><subject>Equivalence</subject><subject>Fibrillation</subject><subject>Flutter</subject><subject>Frailty</subject><subject>Furosemide</subject><subject>Heart failure</subject><subject>Heart valves</subject><subject>Hemodynamics</subject><subject>Hospitalization</subject><subject>Hypertrophy</subject><subject>Implantation</subject><subject>Kidney diseases</subject><subject>Markers</subject><subject>Matching</subject><subject>Medical prognosis</subject><subject>Mortality</subject><subject>Multivariate analysis</subject><subject>Peptides</subject><subject>Pulmonary arteries</subject><subject>Regression analysis</subject><subject>Rheumatic heart disease</subject><subject>Signs and symptoms</subject><subject>Stenosis</subject><subject>Transplants & implants</subject><subject>Ventricle</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkMtqHDEQRUWwIeNJPiEgyCabbuvVD62MceIHDHhjG7ISaqmUqOlujSW1Q_7eGsYrb7wqCs49VF2EvlFSU0Lb87HW82h0tDUjjNSkrQnnn9CG9p2sqKT8BG0IIaySVMjP6CylsayUNu0G_b6b99pkHBzehbDHP_0aIXuDHxPgsOD7NZswQ8LXYZrCP7_8wQ9RL8no_BcyRHwZ4gF_0tML4CKb9JJ19mH5gk6dnhJ8fZtb9Hj96-Hqttrd39xdXe4qwzuSK93SnveudQSYHbjjDbihH6QV1srBOCm6RlitLbGCMio6ykULoM3gjGCN4Vv04-jdx_C8Qspq9snAVA6BsCbFBOsFbWTDCvr9HTqGNS7lukLxjktGi36LmiNlYkgpglP76Gcd_ytK1KFwNaq3wtWhcEVaVQovuYtjDsq3Lx6iSsbDYsD6CCYrG_wHhlegzoyK</recordid><startdate>20200915</startdate><enddate>20200915</enddate><creator>Cantey, Eric P.</creator><creator>Chang, Kevin Y.</creator><creator>Blair, John E.A.</creator><creator>Brummel, Kent</creator><creator>Sweis, Ranya N.</creator><creator>Pham, Duc T.</creator><creator>Adi, Adin-Christian</creator><creator>Churyla, Andrei</creator><creator>Ricciardi, Mark J.</creator><creator>Malaisrie, S. Chris</creator><creator>Davidson, Charles J.</creator><creator>Flaherty, James D.</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7Z</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20200915</creationdate><title>Impact of Loop Diuretic Use on Outcomes Following Transcatheter Aortic Valve Implantation</title><author>Cantey, Eric P. ; Chang, Kevin Y. ; Blair, John E.A. ; Brummel, Kent ; Sweis, Ranya N. ; Pham, Duc T. ; Adi, Adin-Christian ; Churyla, Andrei ; Ricciardi, Mark J. ; Malaisrie, S. Chris ; Davidson, Charles J. ; Flaherty, James D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-a61838f6f0e2db3f35efb8b9d4dd9bcf94754daad0d4121471346eeacbfc425c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aorta</topic><topic>Aortic stenosis</topic><topic>Aortic valve</topic><topic>Cardiovascular disease</topic><topic>Congestive heart failure</topic><topic>Coronary artery</topic><topic>Coronary artery disease</topic><topic>Coronary vessels</topic><topic>Creatinine</topic><topic>Diabetes mellitus</topic><topic>Diuretics</topic><topic>Equivalence</topic><topic>Fibrillation</topic><topic>Flutter</topic><topic>Frailty</topic><topic>Furosemide</topic><topic>Heart failure</topic><topic>Heart valves</topic><topic>Hemodynamics</topic><topic>Hospitalization</topic><topic>Hypertrophy</topic><topic>Implantation</topic><topic>Kidney diseases</topic><topic>Markers</topic><topic>Matching</topic><topic>Medical prognosis</topic><topic>Mortality</topic><topic>Multivariate analysis</topic><topic>Peptides</topic><topic>Pulmonary arteries</topic><topic>Regression analysis</topic><topic>Rheumatic heart disease</topic><topic>Signs and symptoms</topic><topic>Stenosis</topic><topic>Transplants & implants</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cantey, Eric P.</creatorcontrib><creatorcontrib>Chang, Kevin Y.</creatorcontrib><creatorcontrib>Blair, John E.A.</creatorcontrib><creatorcontrib>Brummel, Kent</creatorcontrib><creatorcontrib>Sweis, Ranya N.</creatorcontrib><creatorcontrib>Pham, Duc T.</creatorcontrib><creatorcontrib>Adi, Adin-Christian</creatorcontrib><creatorcontrib>Churyla, Andrei</creatorcontrib><creatorcontrib>Ricciardi, Mark J.</creatorcontrib><creatorcontrib>Malaisrie, S. 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Chris</au><au>Davidson, Charles J.</au><au>Flaherty, James D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Loop Diuretic Use on Outcomes Following Transcatheter Aortic Valve Implantation</atitle><jtitle>The American journal of cardiology</jtitle><date>2020-09-15</date><risdate>2020</risdate><volume>131</volume><spage>67</spage><epage>73</epage><pages>67-73</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><abstract>•Severe AS is characterized by chronic pressure overload and impairment in left ventricular remodeling.•Loop-diuretic therapy prior to TAVI is a marker of higher-risk patients with more medical co-morbidities and echocardiographic evidence of advanced left ventricular remodeling.•Loop-diuretic therapy was associated with a trend towards 1-year mortality on propensity-matched analysis.
The use of LDT may signify significant hemodynamic changes and left ventricular remodeling in severe aortic stenosis (AS). Therefore, we sought to determine whether loop diuretic therapy (LDT) is associated with adverse outcomes following transcatheter aortic valve implantation (TAVI) in patients with severe symptomatic AS. Subjects undergoing TAVI at a single institution from June 2008 to December 2017 were analyzed. LDT doses were normalized to oral furosemide daily equivalents. All outcomes were adjudicated using VARC2 criteria. Descriptive statistics, multivariate logistic regression, and propensity score matching were used. Of the 804 subjects studied, 48.3% were on pre-TAVI LDT with a mean dose of 51.1 mg furosemide dose-equivalents. Subjects on LDT were higher risk, frail patients with more co-morbidities including chronic kidney disease, coronary artery disease requiring prior bypass grafting, peripheral arterial disease, atrial fibrillation or flutter, and diabetes with more severe heart failure symptoms. Those on LDT also had worse left ventricular systolic function, lower transvalvular gradients, and markers of adverse left ventricular remodeling, including increased left ventricular mass index and higher rates of concentric and eccentric hypertrophy. On propensity-score matching, death within one year post-TAVI was borderline significantly higher in the pre-LDT as compared with no-LDT group (16.9% vs 10.4 %, p = 0.068). In conclusion, use of pre-TAVI LDT for severe symptomatic AS is associated with a trend towards worse 1-year mortality and is a marker of high-risk, frail individuals with advanced left ventricular remodeling.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><doi>10.1016/j.amjcard.2020.06.033</doi><tpages>7</tpages></addata></record> |
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subjects | Aorta Aortic stenosis Aortic valve Cardiovascular disease Congestive heart failure Coronary artery Coronary artery disease Coronary vessels Creatinine Diabetes mellitus Diuretics Equivalence Fibrillation Flutter Frailty Furosemide Heart failure Heart valves Hemodynamics Hospitalization Hypertrophy Implantation Kidney diseases Markers Matching Medical prognosis Mortality Multivariate analysis Peptides Pulmonary arteries Regression analysis Rheumatic heart disease Signs and symptoms Stenosis Transplants & implants Ventricle |
title | Impact of Loop Diuretic Use on Outcomes Following Transcatheter Aortic Valve Implantation |
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