AI Based CMR Assessment of Biventricular Function: Clinical Significance of Intervendor Variability and Measurement Errors.


Journal

JACC. Cardiovascular imaging
ISSN: 1876-7591
Titre abrégé: JACC Cardiovasc Imaging
Pays: United States
ID NLM: 101467978

Informations de publication

Date de publication:
03 2022
Historique:
received: 17 12 2020
revised: 09 08 2021
accepted: 17 08 2021
pubmed: 18 10 2021
medline: 28 4 2022
entrez: 17 10 2021
Statut: ppublish

Résumé

The aim of this study was to determine whether left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) and left ventricular mass (LVM) measurements made using 3 fully automated deep learning (DL) algorithms are accurate and interchangeable and can be used to classify ventricular function and risk-stratify patients as accurately as an expert. Artificial intelligence is increasingly used to assess cardiac function and LVM from cardiac magnetic resonance images. Two hundred patients were identified from a registry of individuals who underwent vasodilator stress cardiac magnetic resonance. LVEF, LVM, and RVEF were determined using 3 fully automated commercial DL algorithms and by a clinical expert (CLIN) using conventional methodology. Additionally, LVEF values were classified according to clinically important ranges: <35%, 35% to 50%, and ≥50%. Both ejection fraction values and classifications made by the DL ejection fraction approaches were compared against CLIN ejection fraction reference. Receiver-operating characteristic curve analysis was performed to evaluate the ability of CLIN and each of the DL classifications to predict major adverse cardiovascular events. Excellent correlations were seen for each DL-LVEF compared with CLIN-LVEF (r = 0.83-0.93). Good correlations were present between DL-LVM and CLIN-LVM (r = 0.75-0.85). Modest correlations were observed between DL-RVEF and CLIN-RVEF (r = 0.59-0.68). A >10% error between CLIN and DL ejection fraction was present in 5% to 18% of cases for the left ventricle and 23% to 43% for the right ventricle. LVEF classification agreed with CLIN-LVEF classification in 86%, 80%, and 85% cases for the 3 DL-LVEF approaches. There were no differences among the 4 approaches in associations with major adverse cardiovascular events for LVEF, LVM, and RVEF. This study revealed good agreement between automated and expert-derived LVEF and similarly strong associations with outcomes, compared with an expert. However, the ability of these automated measurements to accurately classify left ventricular function for treatment decision remains limited. DL-LVM showed good agreement with CLIN-LVM. DL-RVEF approaches need further refinements.

Sections du résumé

OBJECTIVES
The aim of this study was to determine whether left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) and left ventricular mass (LVM) measurements made using 3 fully automated deep learning (DL) algorithms are accurate and interchangeable and can be used to classify ventricular function and risk-stratify patients as accurately as an expert.
BACKGROUND
Artificial intelligence is increasingly used to assess cardiac function and LVM from cardiac magnetic resonance images.
METHODS
Two hundred patients were identified from a registry of individuals who underwent vasodilator stress cardiac magnetic resonance. LVEF, LVM, and RVEF were determined using 3 fully automated commercial DL algorithms and by a clinical expert (CLIN) using conventional methodology. Additionally, LVEF values were classified according to clinically important ranges: <35%, 35% to 50%, and ≥50%. Both ejection fraction values and classifications made by the DL ejection fraction approaches were compared against CLIN ejection fraction reference. Receiver-operating characteristic curve analysis was performed to evaluate the ability of CLIN and each of the DL classifications to predict major adverse cardiovascular events.
RESULTS
Excellent correlations were seen for each DL-LVEF compared with CLIN-LVEF (r = 0.83-0.93). Good correlations were present between DL-LVM and CLIN-LVM (r = 0.75-0.85). Modest correlations were observed between DL-RVEF and CLIN-RVEF (r = 0.59-0.68). A >10% error between CLIN and DL ejection fraction was present in 5% to 18% of cases for the left ventricle and 23% to 43% for the right ventricle. LVEF classification agreed with CLIN-LVEF classification in 86%, 80%, and 85% cases for the 3 DL-LVEF approaches. There were no differences among the 4 approaches in associations with major adverse cardiovascular events for LVEF, LVM, and RVEF.
CONCLUSIONS
This study revealed good agreement between automated and expert-derived LVEF and similarly strong associations with outcomes, compared with an expert. However, the ability of these automated measurements to accurately classify left ventricular function for treatment decision remains limited. DL-LVM showed good agreement with CLIN-LVM. DL-RVEF approaches need further refinements.

Identifiants

pubmed: 34656471
pii: S1936-878X(21)00638-0
doi: 10.1016/j.jcmg.2021.08.011
pmc: PMC8917993
mid: NIHMS1737073
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

413-427

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL007381
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002389
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures This project was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health through grant 5UL1TR002389-02, which funds the Institute for Translational Medicine. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Dr A.R. Patel has received research support from Philips, Arterys, CircleCVI, and Neosoft. Dr H. Patel was funded by a T32 Cardiovascular Sciences Training Grant (5T32HL7381). All authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Références

Med Image Anal. 2020 Jan;59:101591
pubmed: 31704452
Circ Cardiovasc Imaging. 2015 Apr;8(4):
pubmed: 25852129
J Magn Reson Imaging. 2013 May;37(5):1213-22
pubmed: 23124767
Neth Heart J. 2019 Sep;27(9):403-413
pubmed: 31399886
Eur Heart J Cardiovasc Imaging. 2018 Jul 1;19(7):730-738
pubmed: 29538684
AJR Am J Roentgenol. 2020 Mar;214(3):529-535
pubmed: 31670597
J Cardiovasc Magn Reson. 2017 Feb 3;19(1):18
pubmed: 28178995
Echocardiography. 2014;31(1):87-100
pubmed: 24786629
J Cardiovasc Magn Reson. 2019 Feb 21;21(1):12
pubmed: 30786898
Radiology. 2017 May;283(2):381-390
pubmed: 28092203
MAGMA. 2016 Apr;29(2):155-95
pubmed: 26811173
Eur Heart J. 2004 Nov;25(21):1940-65
pubmed: 15522474
Front Cardiovasc Med. 2020 Mar 05;7:25
pubmed: 32195270
Clin Imaging. 2016 Jul-Aug;40(4):617-23
pubmed: 27317206
JACC Cardiovasc Imaging. 2018 Mar;11(3):423-433
pubmed: 28734928
J Cardiovasc Magn Reson. 2020 Mar 12;22(1):19
pubmed: 32160925
J Magn Reson Imaging. 2018 Jul;48(1):140-152
pubmed: 29316024
J Cardiovasc Magn Reson. 2019 Apr 25;21(1):24
pubmed: 31023305
J Cardiovasc Magn Reson. 2015 Jul 28;17:63
pubmed: 26215273
Annu Int Conf IEEE Eng Med Biol Soc. 2019 Jul;2019:4020-4023
pubmed: 31946753
J Cardiovasc Magn Reson. 2019 Oct 7;21(1):61
pubmed: 31590664
Circulation. 2013 Oct 15;128(16):e240-327
pubmed: 23741058
J Am Coll Cardiol. 2014 Jun 10;63(22):e57-185
pubmed: 24603191
Int J Cardiovasc Imaging. 2018 Feb;34(2):281-291
pubmed: 28836039
Med Image Anal. 2011 Apr;15(2):169-84
pubmed: 21216179
Br J Radiol. 2018 Apr;91(1084):20170717
pubmed: 29271236
Prog Cardiovasc Dis. 2020 May - Jun;63(3):367-376
pubmed: 32201286
Magn Reson Med. 2017 Dec;78(6):2439-2448
pubmed: 28205298
Circ Cardiovasc Imaging. 2019 Oct;12(10):e009214
pubmed: 31547689
J Am Soc Echocardiogr. 2014 Mar;27(3):292-301
pubmed: 24440110
IEEE Trans Med Imaging. 2018 Nov;37(11):2514-2525
pubmed: 29994302
Eur Heart J. 2012 Jul;33(14):1787-847
pubmed: 22611136
J Card Fail. 2016 Sep;22(9):659-69
pubmed: 27394189
Eur Heart J. 2000 Aug;21(16):1387-96
pubmed: 10952828
J Am Coll Cardiol. 2018 Nov 6;72(19):2360-2379
pubmed: 30384893
J Cardiovasc Magn Reson. 2018 Sep 14;20(1):65
pubmed: 30217194

Auteurs

Shuo Wang (S)

University of Chicago, Chicago, Illinois, USA; Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Hena Patel (H)

University of Chicago, Chicago, Illinois, USA.

Tamari Miller (T)

University of Chicago, Chicago, Illinois, USA.

Keith Ameyaw (K)

University of Chicago, Chicago, Illinois, USA.

Akhil Narang (A)

University of Chicago, Chicago, Illinois, USA.

Daksh Chauhan (D)

University of Chicago, Chicago, Illinois, USA.

Simran Anand (S)

University of Chicago, Chicago, Illinois, USA.

Emeka Anyanwu (E)

University of Chicago, Chicago, Illinois, USA.

Stephanie A Besser (SA)

University of Chicago, Chicago, Illinois, USA.

Keigo Kawaji (K)

University of Chicago, Chicago, Illinois, USA; Illinois Institute of Technology, Chicago, Illinois, USA.

Xing-Peng Liu (XP)

Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Roberto M Lang (RM)

University of Chicago, Chicago, Illinois, USA.

Victor Mor-Avi (V)

University of Chicago, Chicago, Illinois, USA.

Amit R Patel (AR)

University of Chicago, Chicago, Illinois, USA. Electronic address: amitpatel@uchicago.edu.

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