The place of instrumental methods in making diagnosis of different types of congenitally corrected transposition of the great arteries and in determining indications for certain surgical operations of the congenital heart disease

Authors

  • O. Stohova Center for Pediatric Cardiology and Cardiac Surgery, Ukraine
  • N. Rudenko Center for Pediatric Cardiology and Cardiac Surgery; Shupyk National Medical Academy of Postgraduate Education, Ukraine
  • Т. Yalynska Center for Pediatric Cardiology and Cardiac Surgery, Ukraine
  • О. Motrechko Center for Pediatric Cardiology and Cardiac Surgery, Ukraine

Keywords:

congenital heart disease, congenitally corrected transposition of the great arteries, echocardiography, magnetic resonance imaging, computed tomography

Abstract

The goal of the research. To evaluate the ability of instrumental methods to determine indications for certain operations of congenitally corrected transposition of the great arteries (ccTGA).

Materials and Methods. Methods of the research were data of patients with ccTGA which were examinated or underwent surgery at UCCC from 1993 to December 2018. Transthoracic echocardiography (TTE), transesophageal echocardiography (TEE), diagnostic heart catheterization, computed tomography (CT), magnetic resonance imaging (MRI) were used for diagnostics.

Results. From 1993 to December 2018 124 children with ccTGA were examinated or underwent surgery at UCCC. Heart catheterization, CT and MRI were used in 69 (55.6%) patients. The isolated form was revealed in 27 (21.8%) patients, 97 (78.2%) patients were diagnosed with concomitant heart anomalies, 103 (83.0%) patients had situs solitus. The associated defects, diagnosed in 97 patients were as follows: ventricular septum defect (VSD) in 79 (81.4%) patients, pulmonary artery stenosis (PS) — 35 (36.1%), pulmonary artery atresia (PA) — in 18 (18.6%), coarctation of the aorta (CoA) — in 10 (10.3%), Ebsteinlike tricuspid valve dysplasia — in 19 (19.6%), severe tricuspid valve insufficiency — in 12 (12.4%), one patient had a total anomalous pulmonary vein drainage (TAPVC), supracardiac form, and two patients had large aorto-pulmonary collateral arteries (MAPCA's). Additional instrumental diagnostic methods were used in 69 (55.6%) patients with ccTGA. Heart catheterization was performed in 61 (49.2%) patients, CT in 33 (26.6%) patients, and MRI in 24 (19.4%) patients. TEE was used in 18 patients.

Conclusions. Congenitally corrected transposition of the great arteries is a complex heart defect which is combined in majority of cases with other intracardiac abnormalities. The variety of anatomical variants of the disease require a comprehensive approach in diagnosis with engagement of a wide range of instrumental methods, which allow to evaluate the anatomy of the heart and great vessels, other organs and to determine the treatment course and results of operations.

The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee or National Bioethics Committee of all participating institution. The informed consent of the patient was obtained for conducting the studies.

References

Yalinskaya TA, Raad Tammo, Rokitskaya NV et al. (2013). Modern methods of diagnosis of congenital heart diseases. Sovremennaya Pediatriya. 7(55): 161–164.

Cardell LS. (1956). Corrected transposition of the great vessels. Br Heart J. 18: 186. https://doi.org/10.1136/hrt.18.2.186; PMid:13315848 PMCid:PMC479577

Catherine L. Webb. (1999). Congenitally corrected transposition of the great arteries: clinical features, diagnosis and prognosis. Progress in Pediatric Cardiology.10: 17–30. https://doi.org/10.1016/S1058-9813(99)00011-9

Connelly MS, Liu PP, Williams WG, Webb GD et al. (1996). Congenitally corrected transposition of the great arteries in the adult: functional status and complications. J Am Coll Cardiol. 27: 1238–43. https://doi.org/10.1016/0735-1097(95)00567-6

Friedberg DZ, Nadas AS. (1970). Clinical profile of patients with congenitally corrected transposition of the great arteries. a study of 16 cases. N Engl J Med. 282: 1053. https://doi.org/10.1056/NEJM197005072821901; PMid:5438426

Goitein O, Salem Y, Jacobson J, Goitein D et al. (2014). The role of cardiac computed tomography in infants with congenital heart disease. Isr Med Assoc J. 16(3): 147–52.

Gonzalo A Wallis, Diane Debich-Spicer, Robert H Anderson et al. (2011). Congenitally corrected transposition. Orphanet Journal of Rare Diseases. 6: 22. https://doi.org/10.1186/1750-1172-6-22; PMid:21569592 PMCid:PMC3116458

Graham TP Jr, Bernard YD, Mellen BG et al. (2000). Long-term outcome in congenitally corrected transposition of the great arteries: a multi-institutional study. J Am Coll Cardiol. 36: 255–61.

Huhta JC, Maloney JD, Ritter DG et al. (1983). Complete atrioventricular block in patients with atrioventricular discordance. Circulation. 183: 1374. https://doi.org/10.1161/01.CIR.67.6.1374; PMid:6851033

Schiebler GL, Edwards JE, Burchell HB et al. (1961). Congenitally corrected transposition of the great vessels: a study of 33 patients. Pediatrics. 27:II 849.

Valsangiacomo Buechel ER, Grosse-Wortmann L, Fratz S et al. (2015). Indications for cardiovascular magnetic resonance in children with congenital and acquired heart disease: an expert consensus paper of the Imaging Working Group of the AEPC and the Cardiovascular Magnetic Resonance Section of the EACVI. European Heart Journal — Cardiovascular Imaging.16(3): 281—297. https://doi.org/10.1093/ehjci/jeu129; PMid:25712078

Published

2020-03-28

Issue

Section

Original articles