Introduction
Congenital aortic stenosis is accounting for approximately 2 to 6% of all CHDs. The optimal management must balance the need for effective relief of obstruction while minimising potential complications. Reference Xie, Wang, Zhao, Li, Zhang and Ouyang1 Advancements in interventional cardiology have introduced percutaneous transcatheter balloon valvuloplasty as a minimally invasive and effective alternative for the treatment. Studies have extensively documented the immediate outcomes of percutaneous transcatheter balloon valvuloplasty, with recurrent aortic stenosis and aortic regurgitation cited as the most common complications. Reference Chand, Shaikh and Kumar2 However, the potential for arrhythmogenic complications, including ventricular arrhythmias, remains underreported. Reference Tempio, Pruiti and Conti3 This knowledge gap is particularly concerning, as arrhythmias can have significant prognostic implications if left undetected. While such an occurrence is rare, its timely detection underscores the importance of vigilance in post-percutaneous transcatheter balloon valvuloplasty follow-up care.
Case report
A four-month-old female infant presented with increased sweating and respiratory distress for one week duration. Upon arrival at the emergency department, she was alert with good peripheral perfusion. However, she exhibited moderate respiratory distress. Cardiovascular examination identified a grade 4/6 ejection systolic murmur at the upper right sternal border. Abdominal examination revealed mild hepatomegaly. Other systemic evaluations were unremarkable. A chest radiograph revealed cardiomegaly with the evidence of pulmonary oedema. Transthoracic echocardiography demonstrated a bicuspid aortic valve with dysplastic leaflets. The z-score of the aortic annulus was −3 standard deviations. The peak systolic gradient across the aortic valve measured 79 mmHg. The left ventricle was hypertrophied with preserved systolic function. The findings of echocardiogram confirmed a diagnosis of severe aortic stenosis. Consequently, percutaneous transcatheter balloon valvuloplasty of the aortic valve was planned.
During the procedure, a 4 Fr introducer sheath was inserted via the right femoral artery, followed by the advancement of a 4 Fr right coronary catheter over a 0.035” × 180 cm hydrophilic guidewire to the ascending aorta. The hydrophilic guidewire was subsequently exchanged for a 0.014” × 182 cm intermediate support guidewire, which was manoeuvered across the aortic valve to the apical region of the left ventricle. After appropriate positioning, the 4 Fr right coronary catheter was withdrawn, and a Mini Tyshak 6 × 20 mm balloon (NuMED, New York, USA) was introduced and advanced to the aortic valve. The balloon was inflated to 4.5 ATM twice for 10 s using an insufflation syringe. During the intervention, the patient exhibited intermittent, non-sustained ventricular tachycardia, which was transient and spontaneously resolved. Post-procedure, the patient developed sinus bradycardia, with a heart rate of 50 beats per minute as observed on cardiac monitoring. She was initiated on a low-dose intravenous adrenaline infusion, which resulted in an increase in heart rate to 120 beats per minute. A repeated echocardiogram demonstrated residual aortic stenosis, with a peak gradient of 57 mmHg, but no evidence of aortic regurgitation. A 12-lead electrocardiogram revealed sinus rhythm with a heart rate of 110 beats per minute. The patient was discharged three days post-procedure with a scheduled follow-up in six weeks duration.
At the six-week follow-up, the infant remained clinically stable without any active complaints. A 12-lead electrocardiogram demonstrated bigeminy with a heart rate of 150 beats per minute (figure 1). Further analysis indicated that the premature ventricular contractions originated from the left mid-septal region and the left bundle of His, suggestive of inflammatory changes in the conductive pathway following percutaneous transcatheter balloon valvuloplasty for aortic stenosis. Echocardiographic assessment revealed residual aortic stenosis with a peak gradient of 50 mmHg, absence of aortic regurgitation, and normal left ventricle function. As the patient was asymptomatic, her caregivers were advised to closely monitor for any symptoms. Six weeks later, a 12-lead electrocardiogram demonstrated sinus rhythm with isolated premature ventricular contractions, indicating resolution of the inflammatory changes in the bundle of His (Figure 2). The patient continued to remain clinically stable, with adequate weight gain, reaching 6 kg at six months of age. Given the persistence of aortic valve pathology, she remains under cardiac surveillance and is anticipated to require aortic valve repair in the future.
Displays an ECG taken during the six-week follow-up after PTBV of the aortic valve, revealing ventricular bigeminy. The premature ventricular contractions (PVCs) are unifocal, originating from the left ventricle, as indicated by the dominant R wave in lead V1.

Presents an ECG recorded 12 weeks after PTBV of the aortic valve, demonstrating the occurrence of infrequent PVCs.

Discussion
Arrhythmias represent a significant clinical concern in the paediatric population, with an estimated overall incidence of 55.1 per 100,000 paediatric emergency room visits. Among these, ventricular arrhythmias including premature ventricular contractions, are of particular relevance in children undergoing cardiac interventions. Premature ventricular contractions result from premature depolarisation of the ventricles, leading to early and uncoordinated systolic contraction. Their occurrence post-cardiac intervention warrants closer evaluation due to potential implications for patient outcomes. Reference St. George-Hyslop, Morton and Daley4 Bigeminy, characterised by alternating normal sinus beats with premature ventricular contractions, is a specific subset of ventricular arrhythmias. In many cases, bigeminy presents immediately and transiently in response to exposure to anaesthetic agents, electrolyte disturbances, or procedural stress. Reference Dalal and Chaudhari5 However, in this case, it was detected six weeks after percutaneous transcatheter balloon valvuloplasty during routine follow-up, which was an atypical manifestation.
Several plausible explanations for the late-onset bigeminy observed in this case can be considered. The presence of left ventricle hypertrophy and dilation is a common sequelae of chronic pressure overload in aortic stenosis, which may predispose the myocardium to arrhythmogenic events. The elevation of systolic ventricular overload and reduced contractile function significantly increases the risk of ventricular arrhythmias. Furthermore, local tissue injury and oedema near the subaortic valve during the percutaneous transcatheter balloon valvuloplasty procedure could contribute to electrical instability. Reference Tempio, Pruiti and Conti3 While such triggers are often immediate, the delayed detection in this case could reflect asymptomatic occurrences that went unrecognised until the follow-up visit. The use of pharmacological agents such as propranolol and steroids appears justified. Reference St. George-Hyslop, Morton and Daley4 Both medications are supported by evidence for their efficacy in managing arrhythmias in high-risk paediatric cases, though further research is needed to establish standardised post-percutaneous transcatheter balloon valvuloplasty protocols.
The rarity of such presentation underscores the need for meticulous post-procedural monitoring and the development of risk stratification tools to identify patients susceptible to arrhythmias. Regular follow-up with electrocardiogram evaluation should be considered a standard component of care to facilitate early detection and management of complications. Large-scale studies evaluating the incidence, risk factors, and optimal management strategies for arrhythmias post-percutaneous transcatheter balloon valvuloplasty of aortic stenosis would provide valuable insights and improve outcomes for paediatric patients.
Conclusion
This case highlights the need for a holistic approach to managing congenital aortic stenosis, including attention to potential late-onset complications. By integrating vigilant post-procedural care with evidence-based interventions, the risk of adverse outcomes can be minimised, thereby ensuring improved quality of life for patients undergoing percutaneous transcatheter balloon valvuloplasty.
Acknowledgements
We express our gratitude to the director of HPUSM for permitting us to share the patient’s data.
Financial support
This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.
Competing interests
The authors declare none.
