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Deep Learning-Derived Myocardial Strain.
Kwan, Alan C; Chang, Ernest W; Jain, Ishan; Theurer, John; Tang, Xiu; Francisco, Nadia; Haddad, Francois; Liang, David; Fábián, Alexandra; Ferencz, Andrea; Yuan, Neal; Merkely, Béla; Siegel, Robert; Cheng, Susan; Kovács, Attila; Tokodi, Márton; Ouyang, David.
Affiliation
  • Kwan AC; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA. Electronic address: alan.kwan@cshs.org.
  • Chang EW; Leon H. Charney Division of Cardiology, Department of Medicine, New York University Grossman School of Medicine, New York, New York, USA.
  • Jain I; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Theurer J; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Tang X; Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Francisco N; Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Haddad F; Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Liang D; Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Fábián A; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Ferencz A; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Yuan N; Division of Cardiology, Department of Medicine, San Francisco VA, University of California-San Francisco, San Francisco, California, USA.
  • Merkely B; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Siegel R; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Cheng S; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Kovács A; Heart and Vascular Center, Semmelweis University, Budapest, Hungary; Department of Surgical Research and Techniques, Semmelweis University, Budapest, Hungary.
  • Tokodi M; Heart and Vascular Center, Semmelweis University, Budapest, Hungary; Department of Surgical Research and Techniques, Semmelweis University, Budapest, Hungary.
  • Ouyang D; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA. Electronic address: David.Ouyang@cshs.org.
JACC Cardiovasc Imaging ; 17(7): 715-725, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38551533
ABSTRACT

BACKGROUND:

Echocardiographic strain measurements require extensive operator experience and have significant intervendor variability. Creating an automated, open-source, vendor-agnostic method to retrospectively measure global longitudinal strain (GLS) from standard echocardiography B-mode images would greatly improve post hoc research applications and may streamline patient analyses.

OBJECTIVES:

This study was seeking to develop an automated deep learning strain (DLS) analysis pipeline and validate its performance across multiple applications and populations.

METHODS:

Interobserver/-vendor variation of traditional GLS, and simulated effects of variation in contour on speckle-tracking measurements were assessed. The DLS pipeline was designed to take semantic segmentation results from EchoNet-Dynamic and derive longitudinal strain by calculating change in the length of the left ventricular endocardial contour. DLS was evaluated for agreement with GLS on a large external dataset and applied across a range of conditions that result in cardiac hypertrophy.

RESULTS:

In patients scanned by 2 sonographers using 2 vendors, GLS had an intraclass correlation of 0.29 (95% CI -0.01 to 0.53, P = 0.03) between vendor measurements and 0.63 (95% CI 0.48-0.74, P < 0.001) between sonographers. With minor changes in initial input contour, step-wise pixel shifts resulted in a mean absolute error of 3.48% and proportional strain difference of 13.52% by a 6-pixel shift. In external validation, DLS maintained moderate agreement with 2-dimensional GLS (intraclass correlation coefficient [ICC] 0.56, P = 0.002) with a bias of -3.31% (limits of agreement -11.65% to 5.02%). The DLS method showed differences (P < 0.0001) between populations with cardiac hypertrophy and had moderate agreement in a patient population of advanced cardiac amyloidosis ICC was 0.64 (95% CI 0.53-0.72), P < 0.001, with a bias of 0.57%, limits of agreement of -4.87% to 6.01% vs 2-dimensional GLS.

CONCLUSIONS:

The open-source DLS provides lower variation than human measurements and similar quantitative results. The method is rapid, consistent, vendor-agnostic, publicly released, and applicable across a wide range of imaging qualities.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Echocardiography / Image Interpretation, Computer-Assisted / Observer Variation / Predictive Value of Tests / Ventricular Function, Left / Deep Learning Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JACC Cardiovasc Imaging Journal subject: ANGIOLOGIA / CARDIOLOGIA / DIAGNOSTICO POR IMAGEM Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Echocardiography / Image Interpretation, Computer-Assisted / Observer Variation / Predictive Value of Tests / Ventricular Function, Left / Deep Learning Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JACC Cardiovasc Imaging Journal subject: ANGIOLOGIA / CARDIOLOGIA / DIAGNOSTICO POR IMAGEM Year: 2024 Type: Article