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Research ArticleOriginal Research

Artificial Intelligence Tools for Preconception Cardiomyopathy Screening Among Women of Reproductive Age

Anja Kinaszczuk, Andrea Carolina Morales-Lara, Wendy Tatiana Garzon-Siatoya, Sara El-Attar, Adrianna D. Clapp, Ifeloluwa A. Olutola, Ryan Moerer, Patrick Johnson, Mikolaj A. Wieczorek, Zachi I. Attia, Francisco Lopez-Jimenez, Paul A. Friedman, Rickey E. Carter, Peter A. Noseworthy and Demilade Adedinsewo
The Annals of Family Medicine May 2025, 23 (3) 246-254; DOI: https://doi.org/10.1370/afm.230627
Anja Kinaszczuk
Department of Family Medicine, Mayo Clinic, Jacksonville, Florida (Kinaszczuk, Clapp, Olutola)
DO
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Andrea Carolina Morales-Lara
Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, Florida (Morales-Lara, Garzon-Siatoya, El-Attar, Adedinsewo)
MD
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Wendy Tatiana Garzon-Siatoya
Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, Florida (Morales-Lara, Garzon-Siatoya, El-Attar, Adedinsewo)
MD
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Sara El-Attar
Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, Florida (Morales-Lara, Garzon-Siatoya, El-Attar, Adedinsewo)
MD
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Adrianna D. Clapp
Department of Family Medicine, Mayo Clinic, Jacksonville, Florida (Kinaszczuk, Clapp, Olutola)
MD
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Ifeloluwa A. Olutola
Department of Family Medicine, Mayo Clinic, Jacksonville, Florida (Kinaszczuk, Clapp, Olutola)
MD
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Ryan Moerer
Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida (Moerer, Johnson, Wieczorek, Carter)
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Patrick Johnson
Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida (Moerer, Johnson, Wieczorek, Carter)
MS
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Mikolaj A. Wieczorek
Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida (Moerer, Johnson, Wieczorek, Carter)
MS
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Zachi I. Attia
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota (Attia, Lopez-Jimenez, Friedman, Noseworthy)
PhD
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Francisco Lopez-Jimenez
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota (Attia, Lopez-Jimenez, Friedman, Noseworthy)
MS, MD
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Paul A. Friedman
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota (Attia, Lopez-Jimenez, Friedman, Noseworthy)
MD
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Rickey E. Carter
Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida (Moerer, Johnson, Wieczorek, Carter)
PhD
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Peter A. Noseworthy
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota (Attia, Lopez-Jimenez, Friedman, Noseworthy)
MD, MBA
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Demilade Adedinsewo
Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, Florida (Morales-Lara, Garzon-Siatoya, El-Attar, Adedinsewo)
MD, MPH
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  • For correspondence: adedinsewo.demilade@mayo.edu
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    Figure 1.

    Digital Stethoscope Recording Positions

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    Figure 2.

    Study Flow Diagram

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    Figure 3.

    Receiver Operating Characteristic Curve and Confusion Matrix for 12-Lead ECG

    AI = artificial intelligence; AUC = area under the curve; ECG = electrocardiography; ROC = receiver operating characteristic curve.

    Note: The panel on the left shows the ROC curve and diagnostic performance metrics of the AI-ECG model based on 12-lead ECGs. Data are presented as % (95% CI). The panel on the right shows the associated confusion matrix comparing dichotomous AI prediction results with the ground truth (ECG results).

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    Figure 4.

    Receiver Operating Characteristic Curve and Confusion Matrix for Digital Stethoscope (Maximum Prediction)

    AI = artificial intelligence; AUC = area under the curve; ECG = electrocardiography; ROC = receiver operating characteristic curve.

    Note: The panel on the left shows the ROC curve and diagnostic performance metrics of the AI-stethoscope model (maximum prediction). Data are presented as % (95% CI). The panel on the right shows the associated confusion matrix comparing dichotomous AI-stethoscope prediction results with the ground truth (ECG results).

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    Table 1.

    Demographic and Clinical Characteristics of Study Sample

    CharacteristicCohort 1 n = 100Cohort 2 n = 100Total N = 200P Valuea
    Age at ECG, median (Q1, Q3)40.535.638.6.041
    (32.5, 45.7)(28.5, 44.0)(30.3, 45.5)
    Gender, no. (%)1.00
        Female99 (99.0)100 (100.0)199 (99.5)
        Transgender1 (1.0)0 (0)1 (0.5)
    Race/ethnicity, no. (%).044
        Hispanic/Latino9 (9.0)14 (14.0)23 (11.5)
        Non-Hispanic Black17 (17.0)9 (9.0)26 (13.0)
        Non-Hispanic White73 (73.0)70 (70.0)143 (71.5)
        Other/multiracial1 (1.0)7 (7.0)8 (4.0)
    Pregnancy status, no. (%).76
        Not pregnant95 (95.0)97 (97.0)192 (96.0)
        Pregnant3 (3.0)2 (2.0)5 (2.5)
        Postpartum (≤12 mo)2 (2.0)1 (1.0)3 (1.5)
    Clinical comorbid conditions, no. (%)
        Cancer6 (6.0)2 (2.0)8 (4.0).28
        Cerebrovascular disease5 (5.0)1 (1.0)6 (3.0).21
        Chronic pulmonary disease17 (17.0)15 (15.0)32 (16.0).85
        Congestive heart failure18 (18.0)0 (0)18 (9.0)<.001
        Diabetes7 (7.0)2 (2.0)9 (4.5).17
        Diabetes with organ damage3 (3.0)0 (0)3 (1.5).25
        Hypertension20 (20.0)12 (12.0)32 (16.0).18
        Moderate to severe liver disease4 (4.0)0 (0)4 (2.0).12
        Moderate to severe renal disease19 (19.0)1 (1.0)20 (10.0)<.001
        Myocardial infarction4 (4.0)1 (1.0)5 (2.5).37
        Peripheral vascular disease4 (4.0)2 (2.0)6 (3.0).68
        Rheumatologic disease5 (5.0)3 (3.0)8 (4.0).72
        Ulcer2 (2.0)3 (3.0)5 (2.5)1.00
    • ECG = electrocardiography; Q = quartile.

    • ↵a Fisher exact test.

    • Note: Cohort 1 participants were consecutive primary care clinic patients already scheduled/referred for echocardiography as part of their ongoing medical care, and cohort 2 participants were recruited consecutively at an outpatient primary care clinic.

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    Table 2.

    Echocardiographic Parameters Stratified by Left Ventricular Ejection Fraction Among Participants in Cohort 1

    Echocardiographic parameterLVEF ≥50%LVEF <50%TotalP Value
    nMedian (Q1, Q3)nMedian (Q1, Q3)NMedian (Q1, Q3)
    BMI (kg/m2)9527.2 (23.0, 31.8)534.3 (23.4, 38.9)10027.2 (23.0, 32.7).35
    Heart rate9576.0 (67.0, 84.0)582.0 (64.0, 85.0)10076.0 (66.8, 84.0)1.00
    LV end-diastolic diameter (mm)9544.0 (42.0, 48.0)559.0 (58.0, 65.0)10045.0 (42.0, 49.0)< .001
    LV end-systolic diameter (mm)9529.0 (26.5, 32.0)552.0 (47.0, 53.0)10029.5 (27.0, 32.0)< .001
    Mitral valve E/e` ratioa948.5 (6.7, 10.0)420.0 (12.3, 26.2)988.6 (6.7, 10.7).032
    Cardiac output (L/min)885.5 (4.7, 6.3)55.2 (4.1, 5.3)935.5 (4.6, 6.3).31
    Cardiac index (L/min/m2)882.9 (2.6, 3.5)52.6 (2.5, 2.9)932.9 (2.6, 3.4).12
    LV geometry95No. (%)5No. (%)100No. (%)< .001
        Concentric hypertrophy10.0 (10.5)0 (0)10.0 (10.0)
        Concentric remodeling30.0 (31.6)0 (0)30.0 (30.0)
        Eccentric hypertrophy3.0 (3.2)4.0 (80.0)7.0 (7.0)
        Normal geometry52.0 (54.7)1.0 (20.0)53.0 (53.0)
    • BMI = body mass index; LV = left ventricular; LVEF = left ventricular ejection fraction; Q = quartile.

    • ↵a Mitral valve E/e` ratio was calculated as mitral valve early diastolic filling velocity E (meters/second) divided by medial mitral annulus early diastolic velocity by tissue Doppler e’ (meters/second).

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    Table 3.

    Measures of Diagnostic Accuracy for AI Models for Cardiomyopathy Detection Based on Standard 12-Lead ECG and Digital Stethoscope Recordings

    naAUC (95% CI)Sensitivity, % (95% CI)Specificity, % (95% CI)Accuracy, % (95% CI)F1 scoreNegative predictive value, % (95% CI)Odds ratioPositive predictive value, % (95% CI)
    12-lead ECG (LVEF <50%)
        AI-ECG1000.939
    (0.883-0.995)
    40.0
    (5.3-85.3)
    95.8
    (89.6-98.8)
    93.0
    (86.1-97.1)
    36.496.8
    (91.0-99.3)
    15.2
    (2.0-117.9)
    33.3
    (4.3-77.7)
    Digital stethoscope ECG + PCG (LVEF < 50%)
        Angled990.983
    (0.955-1.000)
    80.0
    (28.4-99.5)
    93.6
    (86.6-97.6)
    92.9
    (86.0-97.1)
    53.398.9
    (93.9-100.0)
    58.7
    (5.6-610.4)
    40.0
    (12.2-73.8)
        Subclavicular960.857
    (0.672-1.000)
    60.0
    (14.7-94.7)
    90.1
    (82.1-95.4)
    88.5
    (80.4-94.1)
    35.397.6
    (91.7-99.7)
    13.7
    (2.0-92.9)
    25.0
    (5.5-57.2)
        V21000.949
    (0.871-1.000)
    80.0
    (28.4-99.5)
    91.6
    (84.1-96.3)
    91.0
    (83.6-95.8)
    47.198.9
    (93.8-100.0)
    43.5
    (4.3-437.3)
    33.3
    (9.9-65.1)
    Mean prediction1000.971
    (0.929-1.000)
    60.0
    (14.7-94.7)
    93.7
    (86.8-97.6)
    92.0
    (84.8-96.5)
    42.997.8
    (92.3-99.7)
    22.2
    (3.1-159.7)
    33.3
    (7.5-70.1)
    Maximum prediction1000.979
    (0.950-1.000)
    100.0
    (47.8-100.0)
    82.1
    (72.9-89.2)
    83.0
    (74.2-89.8)
    37.0100.0
    (95.4-100.0)
    49.3
    (2.6-934.3)
    22.7
    (7.8-45.4)
    • AI = artificial intelligence; AUC = area under the curve; ECG = electrocardiography; LVEF = left ventricular ejection fraction; PCG = phonocardiogram.

    • ↵a Results shown represent available AI prediction results based on diagnostic-quality ECG/phonocardiography. Missing or recorded ECG/phonocardiography data deemed to be of poor quality were excluded from analysis, resulting in a sample size <100 for some of the digital stethoscope recording locations.

Additional Files

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  • VISUAL ABSTRACT IN PDF FILE BELOW

    • Adedinsewo_VA_23_3_Final_v2.pdf -

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  • PLAIN-LANGUAGE SUMMARY

    Original Research

    AI-Enabled Tools for Cardiovascular Screening Show Promise in Identifying Heart Dysfunction in Women of Reproductive Age

    Background and Goal:Cardiomyopathy, a disease that weakens the heart muscle and makes it harder to pump blood, is a major health threat during pregnancy and accounts for 40% to 60% of late maternal deaths. This study evaluated the performance of an artificial intelligence–enabled electrocardiogram (AI-ECG) and an AI-powered digital stethoscope to see how well they could detect early signs of heart dysfunction in women of reproductive age.

    Study Approach: In this cross-sectional pilot study, researchers examined two groups of women aged 18 to 49 who were considering pregnancy. Women who were currently pregnant or within one year postpartum were also included. The first group included 100 women who were already scheduled for an echocardiogram. The second group of women had no indication for an echocardiogram and were seen at a primary care appointment for routine care. All participants received two tests: a standard 10-second 12-lead electrocardiogram (ECG) and a digital stethoscope recording that captured a 15-second, single-lead ECG and phonocardiogram (heart sounds) from up to three locations on the chest. AI models analyzed the ECG and stethoscope recordings to estimate each participant’s risk of having left ventricular systolic dysfunction (LVSD), a type of heart dysfunction. In the second group, patients flagged with LVSD by the 12-lead ECG were then referred to an echocardiogram. 

    Main Results: 

    Group 1 (diagnostic cohort, women scheduled for echocardiograms):

    • 5% of women had LVSD.

    • Negative results were highly reliable, with the AI-ECG showing a negative predictive value of 96.8% and the AI-stethoscope achieving 100%.

    • Among women who screened positive using the AI tools, 33.3% (using the AI-ECG) and 22.7% (using the AI-stethoscope) truly had LVSD.

    Group 2 (screening cohort, women seen during routine primary care visits):

    • Using the AI-ECG, only 1% of women in this low-risk sample screened positive. A follow-up echocardiogram in that patient showed a normal ventricular ejection fraction. With the AI-stethoscope, 3.2% of the sample had a positive screen.    

    Why It Matters:Many women of reproductive age do not receive routine heart screening before pregnancy. The findings from this study highlight the potential of quick, low-cost AI tools to help detect early signs of heart dysfunction during regular primary care visits.     

    Artificial Intelligence Tools for Preconception Cardiomyopathy Screening Among Women of Reproductive Age 

    Demilade Adedinsewo, MD, MPH, et al
    Department of Cardiovascular Diseases, Mayo Clinic, Jacksonville, Florida

    Visual Abstract:

  • SUPPLEMENTAL MATERIALS IN PDF FILE BELOW

    • Adedinsewo-Appendix_Tables_Figures.pdf -

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The Annals of Family Medicine: 23 (3)
The Annals of Family Medicine: 23 (3)
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Artificial Intelligence Tools for Preconception Cardiomyopathy Screening Among Women of Reproductive Age
Anja Kinaszczuk, Andrea Carolina Morales-Lara, Wendy Tatiana Garzon-Siatoya, Sara El-Attar, Adrianna D. Clapp, Ifeloluwa A. Olutola, Ryan Moerer, Patrick Johnson, Mikolaj A. Wieczorek, Zachi I. Attia, Francisco Lopez-Jimenez, Paul A. Friedman, Rickey E. Carter, Peter A. Noseworthy, Demilade Adedinsewo
The Annals of Family Medicine May 2025, 23 (3) 246-254; DOI: 10.1370/afm.230627

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Artificial Intelligence Tools for Preconception Cardiomyopathy Screening Among Women of Reproductive Age
Anja Kinaszczuk, Andrea Carolina Morales-Lara, Wendy Tatiana Garzon-Siatoya, Sara El-Attar, Adrianna D. Clapp, Ifeloluwa A. Olutola, Ryan Moerer, Patrick Johnson, Mikolaj A. Wieczorek, Zachi I. Attia, Francisco Lopez-Jimenez, Paul A. Friedman, Rickey E. Carter, Peter A. Noseworthy, Demilade Adedinsewo
The Annals of Family Medicine May 2025, 23 (3) 246-254; DOI: 10.1370/afm.230627
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Keywords

  • artificial intelligence
  • cardiomyopathy
  • electrocardiography
  • preconception care
  • primary health care

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