Ten years of experience with total perfusion for cerebral and end-organ protection during aortic arch reconstruction in neonates
Published 2026-04-14
Keywords
- aortic coarctation; congenital heart defect; fullflow perfusion; neurological dysfunction; renal dysfunction
How to Cite
Copyright (c) 2026 Velukhanov et al.

This work is licensed under a Creative Commons Attribution 4.0 International License.
Abstract
Introduction. Whole-body perfusion represents a promising alternative to traditional methods, such as deep hypothermic circulatory arrest and antegrade cerebral perfusion, potentially reducing the risks of both neurological complications and acute kidney injury. However, the experience with its application, especially in the most vulnerable group of neonates, remains insufficiently studied and requires systematic analysis of intraoperative and longterm outcomes.
Objective. To evaluate intraoperative and early postoperative outcomes in neonates undergoing aortic arch reconstruction with whole-body perfusion.
Methods. This prospective cohort study evaluated the efficacy and safety of surgical treatment in neonates undergoing aortic arch reconstruction with total perfusion (n = 43). The median patient age was 8 (IQR 5–28) days, and median body weight was 3.4 (IQR 2.9–4) kg. Male patients predominated 25 (58.2 %).
Results. The primary endpoint was acute kidney injury assessed using the pediatric KDIGO criteria. Acute kidney injury was observed in 9 (21 %) of patients. The only significant factor for acute kidney injury was the inotropic index on postoperative day 1 (OR = 1.08; 95 % CI (1.01; 1.17)). Neurological complications occurred in 4 (9.3 %) of patients. Hospital mortality was 1 (2.3 %).
Conclusion. Whole-body perfusion represents a straightforward, efficacious, and safe organ protection strategy for neonatal aortic arch reconstruction, demonstrating a low rate of acute kidney injury.
Received 25 August 2025. Revised 21 November 2025. Accepted 17 December 2025.
Informed consent
The patient’s official representative has provided informed consent for the use of the recordings for medical purposes.
Funding
The research was carried out within the framework of the state assignment of the Ministry of Health of the Russian Federation (No. 124022500251-0).
Conflict of interest
The authors declare no conflict of interest.
Сontribution of the authors
Conception and study design: I.A. Velukhanov, I.V. Bondarenko, O.S. Anikina, A.N. Arkhipov, I.A. Soynov
Data collection and analysis: I.A. Velukhanov, I.V. Bondarenko, O.S. Anikina
Statistical analysis: I.V. Bondarenko, Yu.Yu. Kulyabin, V.Y. Martynenkov, V.A. Nepomnyashchy
Drafting the article: I.A. Velukhanov, E.N. Amansakhatova, A.V. Voitov, I.A. Soynov
Critical revision of the article: E.N. Amansakhatova, O.S. Anikina, A.N. Arkhipov, I.A. Kornilov, I.A. Soynov
Final approval of the version to be published: all authors
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