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Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Clarifying the Cardiovascular Morphology and Associated Abnormalities in Patients with Double Inlet Right Ventricle
Niraj Nirmal Pandey1, Mansi Verma2, Sheetal Sharma2
1Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, 110029, India. nirajpandey2403@gmail.com.
Insights
Double inlet right ventricle (DIRV) is a complex congenital heart defect often accompanied by other cardiovascular anomalies. Multidetector CT angiography reveals common associated conditions like double outlet right ventricle and pulmonary outflow tract obstruction, crucial for surgical planning.
Area of Science:
- Cardiology
- Radiology
- Pediatric Congenital Heart Disease
Background:
- Double inlet right ventricle (DIRV) is a rare congenital heart defect characterized by both atria connecting to a single ventricle, typically the right ventricle.
- Understanding the spectrum of associated cardiovascular anomalies in DIRV is critical for effective clinical management and surgical planning.
Purpose of the Study:
- To evaluate the intracardiac morphology and associated cardiovascular anomalies in patients diagnosed with double inlet right ventricle (DIRV) using multidetector CT angiography.
- To identify the prevalence of specific anatomical variations and abnormalities in a cohort of DIRV patients.
Main Methods:
- Retrospective analysis of multidetector CT angiography data from January 2014 to January 2023.
- Systematic evaluation of intracardiac anatomy and associated cardiovascular abnormalities in 41 patients diagnosed with DIRV, excluding those with a common atrioventricular valve.
Main Results:
- DIRV was diagnosed in 41 patients, with hypoplastic left ventricle (95.1%), AV valve straddling (97.6%), and ventricular septal defects (100%) being highly prevalent.
- The most common ventriculo-arterial morphology was double outlet right ventricle (DORV) (61%), followed by pulmonary outflow tract obstruction (58.5%).
- Other anomalies included isomerism (21.5%), systemic venous anomalies (31.7%), pulmonary venous anomalies (14.6%), and coronary artery anomalies (19.5%).
Conclusions:
- Double inlet right ventricle (DIRV) is a complex single ventricle congenital heart disease frequently associated with other cardiovascular abnormalities, notably DORV and pulmonary outflow tract obstruction.
- Detailed anatomical assessment via CT angiography is essential for preoperative planning and can positively impact surgical outcomes in patients with DIRV.
Abstract:
We sought to evaluate the intracardiac morphology and associated cardiovascular anomalies in patients with double inlet right ventricle (DIRV) on multidetector CT angiography. A retrospective search of our departmental database was conducted from January 2014 to January 2023 to identify patients with a diagnosis of DIRV on CT angiography. The intracardiac anatomy and associated cardiovascular abnormalities were systematically evaluated. Patients with a common atrioventricular valve were excluded. DIRV was diagnosed in 41 patients (36 males, 5 females; mean age at imaging: 7.4 years [range: 4 months-30 years]). Mirror-imaged viscero-atrial arrangement was observed in 12/41 (29.3%) while right isomerism and left isomerism were seen in 6/41 (14.6%) and 2/41 (4.9%) patients respectively. Hypoplastic left ventricular cavity was seen in 39/41 (95.1%) patients. AV valve straddling was observed in 40/41 (97.6%) patients. Atrial septal defect was seen in 28/41 (68.3%) patients. All (100%) patients had presence of ventricular septal defect. Twisted atrioventricular connections were seen in 4/41 (9.8%) patients. The most common ventriculo-arterial morphology was presence of double outlet right ventricle (DORV) seen in 25/41 (61%) patients. Some degree of pulmonary outflow obstruction was seen in 24/41 (58.5%) patients. Systemic venous anomalies, pulmonary venous anomalies and coronary artery anomalies were observed in 13/41 (31.7%), 6/41 (14.6%) and 8/41 (19.5%) patients. DIRV is a type of single ventricle congenital heart disease associated with an array of cardiovascular abnormalities, most commonly DORV and pulmonary outflow tract obstruction. The knowledge of associated anomalies is imperative for preoperative planning. CT angiography allows for detailed anatomical evaluation of DIRV and associated cardiovascular anomalies which may positively impact surgical management in these patients.
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