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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Prevalence and Short-Term Outcomes of Postprocedural Complete Heart Block in Congenital Heart Disease Correction in
Chehreh Mahdavi1, Mohammad Reza Sabri1, Alireza Ahmadi1
1Pediatric Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.
Insights
Complete heart block (CHB) occurred in 2.6% of pediatric patients after congenital heart defect (CHD) correction. Younger patients and surgical procedures were linked to higher CHB risk, necessitating vigilant post-procedure monitoring.
Area of Science:
- Pediatric Cardiology
- Cardiac Surgery
- Congenital Heart Defects
Background:
- Complete heart block (CHB) is a recognized complication following congenital heart disease (CHD) correction in children.
- Limited data exists on the incidence and short-term outcomes of postprocedural CHB in this pediatric population.
Purpose of the Study:
- To determine the prevalence of postprocedural CHB in pediatric patients undergoing surgical or transcatheter CHD correction.
- To analyze the risk factors and short-term outcomes associated with postprocedural CHB.
Main Methods:
- Retrospective cohort study of 840 pediatric patients (<18 years) undergoing CHD correction.
- Exclusion of patients with pre-existing arrhythmias or heart block.
- Analysis of medical records for postprocedural CHB incidence, risk factors, and outcomes.
Main Results:
- CHB was identified in 2.6% of patients (0.6% transcatheter, 4.7% surgical).
- Younger age, surgical procedures, and ventricular septal defects (VSD) were associated with increased CHB risk.
- CHB patients had longer pediatric cardiac critical care unit stays; in-hospital mortality was 5.2% without CHB correlation.
Conclusions:
- Postprocedural CHB monitoring is crucial, especially in younger pediatric patients, for timely intervention.
- Further research is needed on long-term complications and risk factors of CHB post-CHD correction.
Background:
Complete heart block (CHB) is a known complication of congenital heart disease (CHD) corrections in children. However, data on the prevalence and short-term outcomes of postprocedural CHB in this population are scarce.
Objectives:
This study aimed to investigate the prevalence and short-term outcomes of postprocedural CHB in pediatric patients undergoing surgical or transcatheter procedures to correct CHD.
Method:
A retrospective cohort study was conducted on pediatric patients under 18 years old who underwent CHD corrections between March 2019 and April 2020 at a tertiary cardiac center in Isfahan, Iran. Patients with a history of arrhythmia or heart block before surgery were excluded. The medical records of these patients were reviewed to identify cases of postprocedural CHB. The prevalence, risk factors, and short-term outcomes of postprocedural CHB were analyzed.
Result:
This study involved 840 patients with a mean age of 3.4 ± 4.3 years, with 47.8% being male. CHB was identified in 22 patients (2.6%) during the postprocedural period, with a prevalence of 0.6% in the transcatheter group and 4.7% in the surgical group. Patients with postprocedural CHB were younger than non-CHB patients. The most common CHDs were patent ductus arteriosus and ventricular septal defect (VSD). Univariate and multivariate regression analyses showed that the type of procedure (surgical method) and the type of CHD (VSD) correlated with postprocedural CHB. Patients who developed postprocedural CHB had a longer mean stay in the pediatric cardiac critical care unit than non-CHB patients. The postoperative in-hospital mortality rate was 5.2%, with no correlation between CHB occurrence and in-hospital mortality.
Conclusion:
The findings highlight the importance of attentive monitoring for postprocedural CHB, particularly in younger patients, to facilitate timely intervention and improve outcomes. Further research is warranted to explore the long-term complications and risk factors associated with postprocedural CHB in this patient population.
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