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Bicarotid trunk: how much is "not uncommon"?
Lisa Reinshagen1, Janez Vodiskar1, Eberhard Mühler2
1Department of Pediatric Cardiac Surgery, Rheinisch-Westfaelische Technische Hochschule Aachen University, Aachen, Germany.
Insights
The bicarotid trunk, a common aortic arch variation, occurs in 15.2% of pediatric patients with congenital heart defects. This anatomical finding is associated with aortic coarctation and requires careful surgical planning.
Area of Science:
- Cardiovascular anatomy and congenital heart disease research.
- Pediatric cardiology and surgical risk assessment.
Background:
- The bicarotid trunk is the most frequent aortic arch branching variation.
- This anatomical variation can significantly impact surgical strategies for congenital heart defects.
Purpose of the Study:
- To determine the prevalence of the bicarotid trunk in pediatric patients with congenital heart defects.
- To investigate the association between the bicarotid trunk and aortic coarctation.
Main Methods:
- Analysis of 2,033 pediatric cardiac catheterization reports from 1979-2010.
- Evaluation of aortic arch branching patterns, prevalence of aortic coarctation, associated defects, vascular anomalies, and genetic syndromes.
Main Results:
- A bicarotid trunk was present in 15.2% of the studied pediatric population.
- Ventricular septal defects, valvular pulmonary stenosis, and atrial septal defect were common in patients with a bicarotid trunk.
- Aberrant right subclavian artery and trisomy 21 were frequent associated findings.
Conclusions:
- The bicarotid trunk is not rare, with a prevalence of 15.2% in this cohort and 17.6% in patients with aortic coarctation.
- Clear depiction of aortic arch anatomy is crucial due to potential surgical risks associated with the bicarotid trunk.
- Advanced imaging like MRI or angiography may be needed if ultrasonography is inconclusive.
Background:
Bicarotid trunk is the most common variation of aortic arch branching patterns. Bicarotid trunk can be a decisive factor in the surgical management of congenital heart defects. Our objective was to determine the prevalence of the bicarotid trunk among pediatric patients with congenital heart defects and to identify whether there is an association between bicarotid trunk and aortic coarctation.
Methods:
From a total of 4,371 pediatric cardiac catheterizations between the years 1979 and 2010, a group of 2,033 patients were selected. Prevalence of the aortic coarctation in patients with bicarotid trunk and with a normal branching pattern was determined by evaluating the catheterization reports. In addition, associated congenital defects, vascular anomalies, and genetic syndromes were also assessed.
Results:
Of 2,033 patients in our database, 84.8% of patients had a normal branching pattern of the aortic arch and 15.2% had a bicarotid trunk. The most frequent congenital heart defects in patients with a bicarotid trunk were ventricular septal defects, valvular pulmonary stenosis, and atrial septal defect. The most common associated vascular anomaly was the aberrant right subclavian artery. Most frequent genetic syndromes were trisomy 21, Williams syndrome, and CHARGE syndrome.
Conclusions:
The prevalence of bicarotid trunk of 17.6% among patients with aortic coarctation and 15.2% among the entire population studied made it not at all a rare phenomenon. Because bicarotid trunk can be a risk factor for surgery, the anatomy of the aortic arch needs to be clearly depicted and described. If ultrasonography examination cannot exclude bicarotid trunk, enhanced magnetic resonance imaging or aortic arch angiography may be necessary.
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