Comparison of mechanical circulatory support with venoarterial extracorporeal membrane oxygenation or Impella for patients with cardiogenic shock: a propensity-matched analysis

Background Percutaneous mechanical circulatory devices are increasingly used in patients with cardiogenic shock (CS). As evidence from randomized studies comparing these devices are lacking, optimal choice of the device type is unclear. Here we aim to compare outcomes of patients with CS supported w...

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Veröffentlicht in:Clinical research in cardiology 2021-09, Vol.110 (9), p.1404-1411
Hauptverfasser: Karatolios, Konstantinos, Chatzis, Georgios, Markus, Birgit, Luesebrink, Ulrich, Ahrens, Holger, Divchev, Dimitar, Syntila, Styliani, Jerrentrup, Andreas, Schieffer, Bernhard
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container_end_page 1411
container_issue 9
container_start_page 1404
container_title Clinical research in cardiology
container_volume 110
creator Karatolios, Konstantinos
Chatzis, Georgios
Markus, Birgit
Luesebrink, Ulrich
Ahrens, Holger
Divchev, Dimitar
Syntila, Styliani
Jerrentrup, Andreas
Schieffer, Bernhard
description Background Percutaneous mechanical circulatory devices are increasingly used in patients with cardiogenic shock (CS). As evidence from randomized studies comparing these devices are lacking, optimal choice of the device type is unclear. Here we aim to compare outcomes of patients with CS supported with either Impella or vaECMO. Methods Retrospective single-center analysis of patients with CS, from September 2014 to September 2019. Patients were assisted with either Impella 2.5/CP or vaECMO. Patients supported ultimately with both devices were analyzed according to the first device implanted. Primary outcomes were hospital and 6-month survival. Secondary endpoints were complications. Survival outcomes were compared using propensity-matched analysis to account for differences in baseline characteristics between both groups. Results A total of 423 patients were included (Impella, n  = 300 and vaECMO, n  = 123). Survival rates were similar in both groups (hospital survival: Impella 47.7% and vaECMO 37.3%, p  = 0.07; 6-month survival Impella 45.7% and vaECMO 35.8%, p  = 0.07). There was no significant difference in survival rates, even after adjustment for baseline differences (hospital survival: Impella 50.6% and vaECMO 38.6%, p  = 0.16; 6-month survival Impella 45.8% and vaECMO 38.6%, p  = 0.43). Access-site bleeding and leg ischemia occurred more frequently in patients with vaECMO (17% versus 7.3%, p  = 0.004; 17% versus 7.7%, p  = 0.008). Conclusions In this retrospective analysis of patients with CS, treatment with Impella 2.5/CP or vaECMO was associated with similar hospital and 6-month survival rates. Device-related access-site vascular complications occurred more frequently in the vaECMO group. A randomized trial is warranted to examine the effects of these devices on outcomes and to determine the optimal device choice in patients with CS.
doi_str_mv 10.1007/s00392-020-01777-9
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As evidence from randomized studies comparing these devices are lacking, optimal choice of the device type is unclear. Here we aim to compare outcomes of patients with CS supported with either Impella or vaECMO. Methods Retrospective single-center analysis of patients with CS, from September 2014 to September 2019. Patients were assisted with either Impella 2.5/CP or vaECMO. Patients supported ultimately with both devices were analyzed according to the first device implanted. Primary outcomes were hospital and 6-month survival. Secondary endpoints were complications. Survival outcomes were compared using propensity-matched analysis to account for differences in baseline characteristics between both groups. Results A total of 423 patients were included (Impella, n  = 300 and vaECMO, n  = 123). Survival rates were similar in both groups (hospital survival: Impella 47.7% and vaECMO 37.3%, p  = 0.07; 6-month survival Impella 45.7% and vaECMO 35.8%, p  = 0.07). There was no significant difference in survival rates, even after adjustment for baseline differences (hospital survival: Impella 50.6% and vaECMO 38.6%, p  = 0.16; 6-month survival Impella 45.8% and vaECMO 38.6%, p  = 0.43). Access-site bleeding and leg ischemia occurred more frequently in patients with vaECMO (17% versus 7.3%, p  = 0.004; 17% versus 7.7%, p  = 0.008). Conclusions In this retrospective analysis of patients with CS, treatment with Impella 2.5/CP or vaECMO was associated with similar hospital and 6-month survival rates. Device-related access-site vascular complications occurred more frequently in the vaECMO group. A randomized trial is warranted to examine the effects of these devices on outcomes and to determine the optimal device choice in patients with CS.</description><identifier>ISSN: 1861-0684</identifier><identifier>EISSN: 1861-0692</identifier><identifier>DOI: 10.1007/s00392-020-01777-9</identifier><identifier>PMID: 33185749</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aged ; Aged, 80 and over ; Cardiology ; Complications ; Extracorporeal membrane oxygenation ; Extracorporeal Membrane Oxygenation - adverse effects ; Extracorporeal Membrane Oxygenation - methods ; Female ; Heart-Assist Devices - adverse effects ; Hemorrhage - epidemiology ; Hemorrhage - etiology ; Humans ; Ischemia ; Ischemia - epidemiology ; Ischemia - etiology ; Life support systems ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Original Paper ; Oxygenation ; Patients ; Propensity Score ; Retrospective Studies ; Shock (Circulatory) ; Shock, Cardiogenic - mortality ; Shock, Cardiogenic - therapy ; Survival ; Survival Rate ; Treatment Outcome</subject><ispartof>Clinical research in cardiology, 2021-09, Vol.110 (9), p.1404-1411</ispartof><rights>The Author(s) 2020</rights><rights>2020. The Author(s).</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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As evidence from randomized studies comparing these devices are lacking, optimal choice of the device type is unclear. Here we aim to compare outcomes of patients with CS supported with either Impella or vaECMO. Methods Retrospective single-center analysis of patients with CS, from September 2014 to September 2019. Patients were assisted with either Impella 2.5/CP or vaECMO. Patients supported ultimately with both devices were analyzed according to the first device implanted. Primary outcomes were hospital and 6-month survival. Secondary endpoints were complications. Survival outcomes were compared using propensity-matched analysis to account for differences in baseline characteristics between both groups. Results A total of 423 patients were included (Impella, n  = 300 and vaECMO, n  = 123). Survival rates were similar in both groups (hospital survival: Impella 47.7% and vaECMO 37.3%, p  = 0.07; 6-month survival Impella 45.7% and vaECMO 35.8%, p  = 0.07). There was no significant difference in survival rates, even after adjustment for baseline differences (hospital survival: Impella 50.6% and vaECMO 38.6%, p  = 0.16; 6-month survival Impella 45.8% and vaECMO 38.6%, p  = 0.43). Access-site bleeding and leg ischemia occurred more frequently in patients with vaECMO (17% versus 7.3%, p  = 0.004; 17% versus 7.7%, p  = 0.008). Conclusions In this retrospective analysis of patients with CS, treatment with Impella 2.5/CP or vaECMO was associated with similar hospital and 6-month survival rates. Device-related access-site vascular complications occurred more frequently in the vaECMO group. A randomized trial is warranted to examine the effects of these devices on outcomes and to determine the optimal device choice in patients with CS.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cardiology</subject><subject>Complications</subject><subject>Extracorporeal membrane oxygenation</subject><subject>Extracorporeal Membrane Oxygenation - adverse effects</subject><subject>Extracorporeal Membrane Oxygenation - methods</subject><subject>Female</subject><subject>Heart-Assist Devices - adverse effects</subject><subject>Hemorrhage - epidemiology</subject><subject>Hemorrhage - etiology</subject><subject>Humans</subject><subject>Ischemia</subject><subject>Ischemia - epidemiology</subject><subject>Ischemia - etiology</subject><subject>Life support systems</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Original Paper</subject><subject>Oxygenation</subject><subject>Patients</subject><subject>Propensity Score</subject><subject>Retrospective Studies</subject><subject>Shock (Circulatory)</subject><subject>Shock, Cardiogenic - mortality</subject><subject>Shock, Cardiogenic - therapy</subject><subject>Survival</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><issn>1861-0684</issn><issn>1861-0692</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9ks1u1TAQhSMEoqXwAiyQJTZsAuOf2AkLpOqKQqVKbGBtOY5z45LYwXZK81Y8Yn1JufwsWHns8_l4xjpF8RzDawwg3kQA2pASCJSAhRBl86A4xTXHJfCGPDzWNTspnsR4DVBhoOxxcUIprivBmtPix85Pswo2eod8jyajB-WsViPSNuhlVMmHFcVlnn1I6LtNA7oxzquQTLCZMrcpKO1Dlk3eTmZqg3IG-dt1b5xK9uAb0OU0m3FUqM_1nE-NS3Fz0yp01mfWahQHr7--RQrNwc_GRZvWclJJD6ZDyqlxjTY-LR71aozm2f16Vny5eP9597G8-vThcnd-VWomWCoZ1JiIpmoraPsOCMVV1-AeWKUFV1y3gGtBiWEaWtW3mPMaV6wGUlNNmrahZ8W7zXde2sl0Oncc1CjnYCcVVumVlX8rzg5y729kzaCqcJ0NXt0bBP9tMTHJyUZ9-AVn_BIlYRwEbxoBGX35D3rtl5AHzlTFOWacUp4pslE6-BiD6Y_NYJCHQMgtEDIHQv4MhDyM8eLPMY5XfiUgA3QDYpbc3oTfb__H9g5qCsaa</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Karatolios, Konstantinos</creator><creator>Chatzis, Georgios</creator><creator>Markus, Birgit</creator><creator>Luesebrink, Ulrich</creator><creator>Ahrens, Holger</creator><creator>Divchev, Dimitar</creator><creator>Syntila, Styliani</creator><creator>Jerrentrup, Andreas</creator><creator>Schieffer, Bernhard</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</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>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7996-7019</orcidid></search><sort><creationdate>20210901</creationdate><title>Comparison of mechanical circulatory support with venoarterial extracorporeal membrane oxygenation or Impella for patients with cardiogenic shock: a propensity-matched analysis</title><author>Karatolios, Konstantinos ; Chatzis, Georgios ; Markus, Birgit ; Luesebrink, Ulrich ; Ahrens, Holger ; Divchev, Dimitar ; Syntila, Styliani ; Jerrentrup, Andreas ; Schieffer, Bernhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-40812795b50bfd02315d91f045c76a6cb018732e4c0bafb166815480283c29b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cardiology</topic><topic>Complications</topic><topic>Extracorporeal membrane oxygenation</topic><topic>Extracorporeal Membrane Oxygenation - adverse effects</topic><topic>Extracorporeal Membrane Oxygenation - methods</topic><topic>Female</topic><topic>Heart-Assist Devices - adverse effects</topic><topic>Hemorrhage - epidemiology</topic><topic>Hemorrhage - etiology</topic><topic>Humans</topic><topic>Ischemia</topic><topic>Ischemia - epidemiology</topic><topic>Ischemia - etiology</topic><topic>Life support systems</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Original Paper</topic><topic>Oxygenation</topic><topic>Patients</topic><topic>Propensity Score</topic><topic>Retrospective Studies</topic><topic>Shock (Circulatory)</topic><topic>Shock, Cardiogenic - mortality</topic><topic>Shock, Cardiogenic - therapy</topic><topic>Survival</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karatolios, Konstantinos</creatorcontrib><creatorcontrib>Chatzis, Georgios</creatorcontrib><creatorcontrib>Markus, Birgit</creatorcontrib><creatorcontrib>Luesebrink, Ulrich</creatorcontrib><creatorcontrib>Ahrens, Holger</creatorcontrib><creatorcontrib>Divchev, Dimitar</creatorcontrib><creatorcontrib>Syntila, Styliani</creatorcontrib><creatorcontrib>Jerrentrup, Andreas</creatorcontrib><creatorcontrib>Schieffer, Bernhard</creatorcontrib><collection>Springer Nature OA Free Journals</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; 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As evidence from randomized studies comparing these devices are lacking, optimal choice of the device type is unclear. Here we aim to compare outcomes of patients with CS supported with either Impella or vaECMO. Methods Retrospective single-center analysis of patients with CS, from September 2014 to September 2019. Patients were assisted with either Impella 2.5/CP or vaECMO. Patients supported ultimately with both devices were analyzed according to the first device implanted. Primary outcomes were hospital and 6-month survival. Secondary endpoints were complications. Survival outcomes were compared using propensity-matched analysis to account for differences in baseline characteristics between both groups. Results A total of 423 patients were included (Impella, n  = 300 and vaECMO, n  = 123). Survival rates were similar in both groups (hospital survival: Impella 47.7% and vaECMO 37.3%, p  = 0.07; 6-month survival Impella 45.7% and vaECMO 35.8%, p  = 0.07). There was no significant difference in survival rates, even after adjustment for baseline differences (hospital survival: Impella 50.6% and vaECMO 38.6%, p  = 0.16; 6-month survival Impella 45.8% and vaECMO 38.6%, p  = 0.43). Access-site bleeding and leg ischemia occurred more frequently in patients with vaECMO (17% versus 7.3%, p  = 0.004; 17% versus 7.7%, p  = 0.008). Conclusions In this retrospective analysis of patients with CS, treatment with Impella 2.5/CP or vaECMO was associated with similar hospital and 6-month survival rates. Device-related access-site vascular complications occurred more frequently in the vaECMO group. A randomized trial is warranted to examine the effects of these devices on outcomes and to determine the optimal device choice in patients with CS.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33185749</pmid><doi>10.1007/s00392-020-01777-9</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7996-7019</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Cardiology
Complications
Extracorporeal membrane oxygenation
Extracorporeal Membrane Oxygenation - adverse effects
Extracorporeal Membrane Oxygenation - methods
Female
Heart-Assist Devices - adverse effects
Hemorrhage - epidemiology
Hemorrhage - etiology
Humans
Ischemia
Ischemia - epidemiology
Ischemia - etiology
Life support systems
Male
Medicine
Medicine & Public Health
Middle Aged
Original Paper
Oxygenation
Patients
Propensity Score
Retrospective Studies
Shock (Circulatory)
Shock, Cardiogenic - mortality
Shock, Cardiogenic - therapy
Survival
Survival Rate
Treatment Outcome
title Comparison of mechanical circulatory support with venoarterial extracorporeal membrane oxygenation or Impella for patients with cardiogenic shock: a propensity-matched analysis
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