# Speckle Tracking Echocardiography in Pediatric and Congenital Heart Disease Patients with the Micra™ Leadless Pacemaker

**Authors:** Natalia Betancourt-Guzman, Jeremy Markowitz, Erick Jimenez, Daniel Cortez, Brenda Dugas, Daniel Peck, Matthew Ambrose, Bradley C. Clark

PMC · DOI: 10.19102/icrm.2025.16103 · The Journal of Innovations in Cardiac Rhythm Management · 2025-10-15

## TL;DR

This study explores using speckle tracking echocardiography to detect early signs of heart dysfunction in young patients with a specific type of pacemaker.

## Contribution

The study introduces the use of GLS for early detection of PICM in pediatric and congenital heart disease patients with leadless pacemakers.

## Key findings

- GLS values correlated with pacing percentages, suggesting potential for detecting myocardial dyssynchrony.
- Higher EF showed a mild correlation with more-negative GLS values.
- The study highlights the need for larger cohorts and longer follow-up to validate findings.

## Abstract

Right ventricular pacing can cause electrical and mechanical dyssynchrony, potentially leading to pacemaker-induced cardiomyopathy (PICM). This pilot study evaluates speckle tracking echocardiography for the early detection of subclinical left ventricular dysfunction in pediatric and congenital heart disease patients with Micra™ leadless pacemakers (Medtronic, Minneapolis, MN, USA). We analyzed echocardiograms of eight patients (mean age, 15 years; 63% women) with Micra™ pacemakers at implant and 1 month and 1 year post-implant. Data of interest included demographics, pacemaker position, ejection fraction (EF), shortening fraction, and global longitudinal strain (GLS). The pacing percentages varied from <0.1% to 100%, with three patients having burdens of >20%. The mean GLS was −17.99, and the mean EF was 59.6%. A higher EF correlated mildly with more-negative GLS values (r = 0.288; P = .218), and greater pacing percentages correlated with poorer GLS values (r = −0.381; P = .097). In summary, GLS has the potential to identify myocardial dyssynchrony, which may have the potential to support the early detection of PICM. Further research with larger cohorts and longer follow-up is needed to validate these findings.

## Linked entities

- **Diseases:** cardiomyopathy (MONDO:0004994), congenital heart disease (MONDO:0005453)

## Full-text entities

- **Diseases:** PICM (MESH:D009202), left ventricular dysfunction (MESH:D018487), Congenital Heart Disease (MESH:D006330)
- **Chemicals:** Micra (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12588584/full.md

## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588584/full.md

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Source: https://tomesphere.com/paper/PMC12588584