DOI: 10.25881/20728255_2024_19_2_11

Authors

Khubulava G.G.1, 4, Naumov A.B.2, Marchenko S.P.1, Chupaeva О.Yu.1, 3, Kulemin E.S.3, Sazonov A.B.4

1 Pavlov First Saint Petersburg State Medical University, Saint-Petersburg

2 North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg

3 Saint-Petersburg State Pediatric Medical University, Saint-Petersburg

4 Military Medical Academy named after S.M. Kirov, Saint-Peterburg

Abstract

Objective: To identify risk factors for unfavorable outcome in newborns operated on for congenital pathology of the aortic arch.

Materials and methods of research: Data from the results of treatment of 79 patients with congenital pathology of the aortic arch were analyzed and the effectiveness of the therapy was assessed. All patients underwent an examination with the study of obstetric and gynecological history, life history and illness, with an assessment of existing complaints after birth and their changes over time. The obtained clinical, echocardiographic and laboratory parameters were analyzed and compared. The following surgical methods were used for surgical correction of congenital pathology of the aortic arch: resectionof coarctation with plastic surgery of the aortic arch with native tissues, resection of aortic coarctation with the imposition of an extended end-to-end anastomosis, hybrid version. The results of the performed operations and complications were evaluated.

Results: Factors such as the development of small ejection syndrome before surgery, the emergency nature of the intervention, and reduced left ventricular ejection fraction (less than 35%), increased heart rate, had a significant association with an unfavorable outcome. Signs of moderate significance that were associated with an unfavorable outcome of surgical treatment were the following clinical and hemodynamic preoperative parameters: increased respiratory rate, reduction of diastolic pressure in the lower extremities and reduction LV EDC. Anthropometric data and reduction of systolic pressure in the lower extremities had a weak connection with mortality.

Conclusions: The most significant factors of unfavorable outcome before surgery in newborns with congenital pathology of the aortic arch, those operated with the use of artificial blood circulation are: increased heart rate, decreased LV EF. Low anthropometric indicators of the child (weight, height, body surface area) are also have an impact on the outcome. Index of the end-diastolic size of the left ventricle as a factor reflecting his anatomically determined ability to produce a systemic blood flow it is important when choosing an option for surgical.

Keywords: newborns, congenital heart disease, coarctation of the aorta, hypoplasia of the aortic arch.

References

1. Bockeria LA, Stupakov IN, Samorodskaya IV, Botnar YuM. Cardiovascular diseases in the Russian Federation at the turn of the century: mortality, prevalence, risk factors. Serdechno-sosudistye zabolevaniya. Byulleten’ NTs SSKh im. A.N. Bakuleva RAMN. 2007; 5: 5-11 (In Russ.)

2. Bockeria LA, Tumanyan MR, Filaretova OV, Abramyan MA, Trunina II. Cardiac surgery of newborns. New approaches to the analysis of results and risk factors (current state of the problem). Serdechno-sosudistye zabolevaniya. Byulleten’ NTs SSKh im. A.N. Bakuleva RAMN. 2010; 6: 4-17. (In Russ.)

3. Szaflik K, Goreczny S. Predictors of Left Ventricular Outflow Tract Obstruction After Conventional Repair for Patients with interrupted aortic arch or coarctetion of the aorta,combined with ventricular septal defect: a single-center experience.Pediatr Cardiol. 2022; 3: 525-531.

4. Boyd, et al. Improving diagnostic accuracy in neonates with left heart obstruction in a transport setting. J. Paediatr. ChildHealth. 2021; 57(1): 26-32.

5. Soynov IA, Rzaeva KA, Gorbatykh YuN, et al. Fifteen years of experience in the treatment of aortic coarctation. Children’s heart and vascular diseases. 2023; 20(2): 126-140. (In Russ.) doi: 10.24022/1810-0686-2023-20-2-126-140.

6. Bockeria LA, et al. Cardiovascular surgery 2020. Diseases and congenital anomalies of the circulatory system. National Medical Research Center for Cardiovascular Surgery named after. A.N. Bakulev of the Ministry of Health of Russia. 2021: 294. (In Russ.)

7. Li X, Li J, et al. Surgical repair of persistent fifth aortic arch coarctation and interrupted fourth aortic arch without cardiopulmonary bypass: a case report. Transl Pediatr. 2022; 2: 306-310. doi: 10.21037/tp-21-350.

8. Trunina II. Hypotrophy, intrauterine infections and syndromic pathology as risk factors for neonatal cardiac surgery. Detskiye bolezni serdtsa i sosudov. 2012; 3: 23-30. (In Russ.)

9. Trunina II, Tumanyan MR, Sharykin AS, Filaretova OV. Risk factors affecting the survival of newborns after surgical correction of congenital heart defects. Pediatriya. 2017; 96 (1): 37-43. (In Russ.)

10. Derios L. Prenatal diagnosis of aortic coarctation: Prediction algorinm according to gestation age. Fetal Diagn Ther. 2021; 48: 819-828.

11. Jadczak A, Respondek-Liberska M, Sokolowski L. Hypoplastic left heart syndrome with prenatally diagnosed foramen ovale restriction: diagnosis,management and outcome. J Matern Fetal Neonatal Med. 2022; 2: 291-298. doi: 10.1080\14767058.2020.1716717.

12. Steiner I, Pisa M. Immediate results of percutaneous management of coarctation of the aorta: a 7-year single-centre experience. Int J Cardiol. 2021; 1: 103-106.

13. Lloyd D, van Poppel M, All E. Analysis of 3-Dimensional Arch Anatomy, Vascular Flow, and Postnatal Outcome in Cases of Suspected Coarctation of the aorta using fetal cardiac magnetic resonance imaging .Circ Cardiovasc Imaging. 2021; 7: 131-140.

14. Coarctation of the aorta. Federal clinical recommendations. 2019: 27. (In Russ.)

15. Marchenko SP, Khubulava GG, Naumov AB, et al. Pathophysiological principles and approaches to assessing hemodynamics. Pediatr. 2014; 5(4): 110-115. (In Russ.)

16. Colguit J, Loar R. Left heart hypoplasia in the fetus: Echocardiographic predictors of outcome. Prenat Diagn. 2022; 4: 447-460. doi: 10.1002/pd.6101.

17. Bedin AV, Abrahamyan MA, Shamrin YuN, et al. Results of surgical correction of aortic coarctation in combination with hypoplasia of the aortic arch using left-sided thoracotomy access. Children’s heart and vascular diseases. 2023; 20(1): 5-16. (In Russ.) doi: 10.24022\1810-0686-2023-20-1-5-16.

18. Grigoryants TR, Kim AI, Grigoryan AM. Two-stage elimination of aortic coarctation in critically ill newborns. Children’s diseases of the heart and blood vessels. 2021; 18(2): 147-152. (In Russ.) doi: 10.24022/1810-0686-2021-18-2-147-152.

19. Rzaeva KA, Soynov IA, Gorbatykh AV. Critical coarctation of the aorta. Possibilities of diagnosis and surgical correction of aortic coarctation in newborns // Pathology of blood circulation and cardiac surgery. 2020; 24(2): 46-62. (In Russ.) doi: 10.21688/1681-3472-2020-2-46-62.

20. Ungureanu TN, Grzhibovsky AM. Brief recommendations for description, statistical analysis and presentation of data in scientific publications. Human Ecology. 2011; 55: 55-60. (In Russ.)

21.Unal I. Defining an optimal cut-point value in ROC analysis: An alternative approach. Comput.Math. Methods Med. 2017; 1: 1-14. doi: 10.1155.2017.3762651.

For citation

Khubulava G.G., Naumov A.B., Marchenko S.P., Chupaeva О.Yu., Kulemin E.S., Sazonov A.B. Risk factors for unfavorable outcome in newborns operated on for congenital aortic arch pathology. Bulletin of Pirogov National Medical & Surgical Center. 2024;19(2):11-18. (In Russ.) https://doi.org/10.25881/20728255_2024_19_2_11