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Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European Collaboration.
Bonthrone, Alexandra F; Stegeman, Raymond; Feldmann, Maria; Claessens, Nathalie H P; Nijman, Maaike; Jansen, Nicolaas J G; Nijman, Joppe; Groenendaal, Floris; de Vries, Linda S; Benders, Manon J N L; Haas, Felix; Bekker, Mirielle N; Logeswaran, Thushiha; Reich, Bettina; Kottke, Raimund; Hagmann, Cornelia; Latal, Beatrice; Dave, Hitendu; Simpson, John; Pushparajah, Kuberan; Austin, Conal; Kelly, Christopher J; Arulkumaran, Sophie; Rutherford, Mary A; Counsell, Serena J; Knirsch, Walter; Breur, Johannes M P J.
Affiliation
  • Bonthrone AF; 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.).
  • Stegeman R; 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.
  • Feldmann M; 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.
  • Claessens NHP; Child Development Center (M.F., B.L.), University Children's Hospital Zurich, Switzerland.
  • Nijman M; 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.
  • Jansen NJG; 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.
  • Nijman J; Department of Pediatric Cardiology (N.H.P.C., M.N., J.M.P.J.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.
  • Groenendaal F; 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.
  • de Vries LS; 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.
  • Benders MJNL; 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.
  • Haas F; Department of Pediatric Cardiology (N.H.P.C., M.N., J.M.P.J.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.
  • Bekker MN; 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.
  • Logeswaran T; 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.
  • Reich B; Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, the Netherlands (N.J.G.J.).
  • Kottke R; 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.
  • Hagmann C; 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.
  • Latal B; 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.
  • Dave H; 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.
  • Simpson J; 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.
  • Pushparajah K; Congenital Cardiothoracic Surgery (F.H.), University Medical Center Utrecht, Utrecht University, the Netherlands.
  • Austin C; Department of Obstetrics (M.N.B.), University Medical Center Utrecht, Utrecht University, the Netherlands.
  • Kelly CJ; Pediatric Heart Center, University Hospital Giessen, Justus-Liebig-University Giessen, Germany (T.L.).
  • Arulkumaran S; Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technical University of Munich, Germany (B.R.).
  • Rutherford MA; Department of Diagnostic Imaging (R.K.), University Children's Hospital Zurich, Switzerland.
  • Counsell SJ; Department of Neonatology and Pediatric Intensive Care (C.H.), University Children's Hospital Zurich, Switzerland.
  • Knirsch W; Child Development Center (M.F., B.L.), University Children's Hospital Zurich, Switzerland.
  • Breur JMPJ; 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.
Stroke ; 53(12): 3652-3661, 2022 12.
Article in En | MEDLINE | ID: mdl-36300371
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.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Transposition of Great Vessels / Brain Injuries / Venous Thrombosis / Ischemic Stroke / Heart Defects, Congenital Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Infant / Newborn Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Transposition of Great Vessels / Brain Injuries / Venous Thrombosis / Ischemic Stroke / Heart Defects, Congenital Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Infant / Newborn Language: En Year: 2022 Type: Article