Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European Collaboration

Author:

Bonthrone Alexandra F.1ORCID,Stegeman Raymond23ORCID,Feldmann Maria4ORCID,Claessens Nathalie H.P.2563ORCID,Nijman Maaike2563ORCID,Jansen Nicolaas J.G.57ORCID,Nijman Joppe5ORCID,Groenendaal Floris23,de Vries Linda S.2ORCID,Benders Manon J.N.L.2ORCID,Haas Felix8,Bekker Mirielle N.9ORCID,Logeswaran Thushiha10,Reich Bettina11,Kottke Raimund12ORCID,Hagmann Cornelia13,Latal Beatrice4,Dave Hitendu14,Simpson John15ORCID,Pushparajah Kuberan115ORCID,Austin Conal15,Kelly Christopher J.1ORCID,Arulkumaran Sophie1ORCID,Rutherford Mary A.1,Counsell Serena J.1ORCID,Knirsch Walter16ORCID,Breur Johannes M.P.J.6ORCID

Affiliation:

1. Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King’s College London, United Kingdom (A.F.B., K.P., C.J.K., S.A., M.A.R., S.J.C.).

2. Department of Neonatology (R.S., N.H.P.C., M.N., F.G., L.S.d.V., M.J.N.L.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.

3. Wilhelmina Children’s Hospital and Utrecht Brain Center (R.S., N.H.P.C., M.N., F.G.), University Medical Center Utrecht, Utrecht University, the Netherlands.

4. Child Development Center (M.F., B.L.), University Children’s Hospital Zurich, Switzerland.

5. Department of Pediatric Intensive Care (N.H.P.C., M.N., N.J.G.J., J.N.), University Medical Center Utrecht, Utrecht University, the Netherlands.

6. Department of Pediatric Cardiology (N.H.P.C., M.N., J.M.P.J.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.

7. Department of Pediatrics, Beatrix Children’s Hospital, University Medical Center Groningen, the Netherlands (N.J.G.J.).

8. Congenital Cardiothoracic Surgery (F.H.), University Medical Center Utrecht, Utrecht University, the Netherlands.

9. Department of Obstetrics (M.N.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.

10. Pediatric Heart Center, University Hospital Giessen, Justus-Liebig-University Giessen, Germany (T.L.).

11. Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technical University of Munich, Germany (B.R.).

12. Department of Diagnostic Imaging (R.K.), University Children’s Hospital Zurich, Switzerland.

13. Department of Neonatology and Pediatric Intensive Care (C.H.), University Children’s Hospital Zurich, Switzerland.

14. Division of Congenital Cardiovascular Surgery (H.D.), Pediatric Heart Center, Department of Surgery, Children’s Research Center, University Children’s Hospital Zurich, University of Zurich, Switzerland.

15. Pediatric Cardiology Department, Evelina Children’s Hospital London, United Kingdom (J.S., K.P., C.A.).

16. Pediatric Cardiology (W.K.), Pediatric Heart Center, Department of Surgery, Children’s Research Center, University Children’s Hospital Zurich, University of Zurich, Switzerland.

Abstract

Background: Infants with congenital heart disease are at risk of brain injury and impaired neurodevelopment. The aim was to investigate risk factors for perioperative brain lesions in infants with congenital heart disease. Methods: Infants with transposition of the great arteries, single ventricle physiology, and left ventricular outflow tract and/or aortic arch obstruction undergoing cardiac surgery <6 weeks after birth from 3 European cohorts (Utrecht, Zurich, and London) were combined. Brain lesions were scored on preoperative (transposition of the great arteries N=104; single ventricle physiology N=35; and left ventricular outflow tract and/or aortic arch obstruction N=41) and postoperative (transposition of the great arteries N=88; single ventricle physiology N=28; and left ventricular outflow tract and/or aortic arch obstruction N=30) magnetic resonance imaging for risk factor analysis of arterial ischemic stroke, cerebral sinus venous thrombosis, and white matter injury. Results: Preoperatively, induced vaginal delivery (odds ratio [OR], 2.23 [95% CI, 1.06–4.70]) was associated with white matter injury and balloon atrial septostomy increased the risk of white matter injury (OR, 2.51 [95% CI, 1.23–5.20]) and arterial ischemic stroke (OR, 4.49 [95% CI, 1.20–21.49]). Postoperatively, younger postnatal age at surgery (OR, 1.18 [95% CI, 1.05–1.33]) and selective cerebral perfusion, particularly at ≤20 °C (OR, 13.46 [95% CI, 3.58–67.10]), were associated with new arterial ischemic stroke. Single ventricle physiology was associated with new white matter injury (OR, 2.88 [95% CI, 1.20–6.95]) and transposition of the great arteries with new cerebral sinus venous thrombosis (OR, 13.47 [95% CI, 2.28–95.66]). Delayed sternal closure (OR, 3.47 [95% CI, 1.08–13.06]) and lower intraoperative temperatures (OR, 1.22 [95% CI, 1.07–1.36]) also increased the risk of new cerebral sinus venous thrombosis. Conclusions: Delivery planning and surgery timing may be modifiable risk factors that allow personalized treatment to minimize the risk of perioperative brain injury in severe congenital heart disease. Further research is needed to optimize cerebral perfusion techniques for neonatal surgery and to confirm the relationship between cerebral sinus venous thrombosis and perioperative risk factors.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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