# Clinical Evaluation of Neonatal Arrhythmias: Experience from a Specialized Pediatric Cardiac Center

**Authors:** Halise Zeynep Genc, Elnur Karimov, Seyma Yakut, Dilek Yavuzcan Ozturk, Demet Oguz, Merih Cetinkaya, Gulhan Tunca Sahin, Erkut Ozturk

PMC · DOI: 10.3390/jcdd13020065 · Journal of Cardiovascular Development and Disease · 2026-01-27

## TL;DR

This study examines the types, treatment, and outcomes of neonatal arrhythmias at a specialized pediatric hospital, finding that most are non-benign but manageable with early intervention.

## Contribution

The study provides a detailed clinical evaluation of neonatal arrhythmias in a specialized center, highlighting management strategies and outcomes.

## Key findings

- Non-benign arrhythmias were more common (77%) than benign ones (23%).
- Supraventricular tachycardia was the most frequent non-benign arrhythmia (35%).
- No mortality was observed during a median follow-up of 12.8 months.

## Abstract

Neonatal arrhythmias, though relatively uncommon, can range from benign self-limiting conditions to life-threatening disorders requiring intensive management. Data on their clinical spectrum, management, and outcomes remain limited. This study aimed to evaluate the types, frequency, clinical characteristics, treatment strategies, and prognosis of neonatal arrhythmias in a tertiary pediatric cardiac center. We retrospectively reviewed neonates diagnosed with arrhythmia within the first 28 days of life at Basaksehir Cam and Sakura City Hospital between 1 January 2021 and 1 May 2025. Demographic data, electrocardiographic and echocardiographic findings, treatment modalities, recurrence, morbidity, and mortality were analyzed. Patients were categorized as having benign or non-benign arrhythmias. A total of 65 neonates (57% male, mean weight 3.2 kg) were included. Non-benign arrhythmias were more frequent (77%) compared to benign arrhythmias (23%). Supraventricular tachycardia (35%) was the most common non-benign arrhythmia, followed by long QT syndrome (10.7%) and complete atrioventricular block (9.2%). Antiarrhythmic therapy was required in 55% of patients. Pacemaker implantation was performed in seven infants with conduction disorders. Recurrence occurred in 3% of cases, exclusively among patients with supraventricular tachycardia. During a median follow-up of 12.8 months, no mortality was observed. Prenatal diagnosis and early management contribute to favorable outcomes, as reflected in the absence of mortality in this cohort. Larger, prospective studies are warranted to define optimal management strategies and treatment durations for neonatal arrhythmias.

## Linked entities

- **Diseases:** long QT syndrome (MONDO:0002442), complete atrioventricular block (MONDO:0000468)

## Full-text entities

- **Genes:** KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757] {aka ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1}, KCNQ1 (potassium voltage-gated channel subfamily Q member 1) [NCBI Gene 3784] {aka ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1}, TRPM4 (transient receptor potential cation channel subfamily M member 4) [NCBI Gene 54795] {aka EKVP6, LTrpC4, PFHB1B, TRPM4B, hTRPM4}, SCN5A (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 6331] {aka CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD}
- **Diseases:** PJRT (MESH:D054139), channelopathy (MESH:D053447), electrolyte (MESH:D014883), cardiogenic shock (MESH:D012770), RBBB (MESH:D002037), Sjogren's syndrome (MESH:D012859), sinus arrhythmia (MESH:D001146), injury to (MESH:D014947), AVSD (MESH:C562831), congenital defects (MESH:D000013), conduction disorders (MESH:D019955), systemic lupus erythematosus (MESH:D008180), Bradyarrhythmia (MESH:D001919), junctional rhythms (MESH:D021081), PVC (MESH:D018879), respiratory distress (MESH:D012128), PACs (MESH:D018880), cardiomyopathy (MESH:D009202), Benign arrhythmias (MESH:D001145), structural (MESH:D020914), long QT syndrome type 2 (MESH:C563614), RT (MESH:C563738), Tachyarrhythmia (MESH:D013610), Congenital Heart Disease (MESH:D006330), rheumatologic disorders (MESH:D012216), tachypnea (MESH:D059246), AV block (MESH:D054537), dilated cardiomyopathy (MESH:D002311), ventricular ectopy (MESH:D050030), SVT (MESH:D013617), C (OMIM:211750), deaths (MESH:D003643), ectopia (MESH:C563268), long QT syndrome type 3 (MESH:C537034), C-TGA (MESH:D014188), AF (MESH:D001282), WPW (MESH:D014927), total anomalous pulmonary venous drainage (MESH:D012587), long QT syndrome (MESH:D000094024), long QT syndrome type 1 (MESH:D029597), ventricular fibrillation (MESH:D014693), VT (MESH:D017180), long QT syndrome (MESH:D008133), transposition (MESH:C536650), PAC (MESH:C537560), cardiac conduction disease (MESH:D006331), congestive heart failure (MESH:D006333), congenital complete atrioventricular block (MESH:C535758)
- **Chemicals:** sotalol (MESH:D013015), propranolol (MESH:D011433), propafenone (MESH:D011405), flecainide (MESH:D005424), amiodarone (MESH:D000638)
- **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/PMC12941173/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941173/full.md

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Source: https://tomesphere.com/paper/PMC12941173