Journals / Çocuk Dergisi / 2026 / Cilt: 24 Sayı: 2

Ventricular Septal Defect Repair in a Patient with Hydrocephalus

Hande İştar(Muğla Sıtkı Koçman University Faculty of Medicine, Department of Cardiovascular Surgery)0000-0002-7150-0171
Utkan Sevük(Üsküdar University Medical Faculty, Department of Cardiovascular Surgery)0000-0001-7429-5997
Pages
132–134
Publication Date
2024-08-15
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The case reported here is a 10-month-old infant with ventricular septal defect repair diagnosed with hydrocephalus and postoperative early follow-up findings.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Congenital heart diseases may be associated with different syndromes or anomalies.
📊
Key Findings & Data:Congenital hydrocephalus is a rare disease that leads to increased intracranial pressure due to fluid accumulation through obstruction of intracranial aqueduct flow, Arnold Chiari and Dandy–Walker malformations, or abnormally increased fluid production into intracerebral ventricles.
💡
Conclusion & Impact:The case reported here is a 10-month-old infant with ventricular septal defect repair diagnosed with hydrocephalus and postoperative early follow-up findings.
🔬Design:Olgu Sunumu
📍Scope:Comprehensive Sample
⚙️Variables:Ventricular septal defect · hydrocephalus · congenital heart disease

Abstract

Congenital heart diseases may be associated with different syndromes or anomalies. Congenital hydrocephalus is a rare disease that leads to increased intracranial pressure due to fluid accumulation through obstruction of intracranial aqueduct flow, Arnold Chiari and Dandy–Walker malformations, or abnormally increased fluid production into intracerebral ventricles. Increased intracranial pressure may produce many problems during the anaesthesia for any operation. Moreover, the postoperative period may be complicated by hydrocephalus. In severe cases, shunt replacement may be necessary. The case reported here is a 10-month-old infant with ventricular septal defect repair diagnosed with hydrocephalus and postoperative early follow-up findings.

🔖

Cite This Article

İştar, H., Sevük, U. (2024). Ventricular Septal Defect Repair in a Patient with Hydrocephalus. Çocuk Dergisi, Cilt: 24 Sayı: 2, 132–134. https://doi.org/10.26650/jchild.2024.1285990

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Garne E, Loane M, Addor MC, Boyd PA, Barisic I, Dolk H. Congenital hydrocephalus prevalence, prenatal diagnosis and outcome of pregnancy in four European regions. European Journal of Paediatric Neurology. 2010;14(2):150–5. google scholar
  2. Mai CT, Isenburg JL, Canfield MA, Meyer RE, Correa A, Alverson CJ, et al. National population-based estimates for major birth defects, 2010–2014. Birth Defects Res. 2019;111(18):1420–35. google scholar
  3. Crawford TS, Olivero WC, Hanigan WC. The prognosis of children with hydrocephalus and congenital heart disease. Pediatr Neurosurg. 2000;33(1):12-5. google scholar
  4. Koo H; Chi J G. Congenital hydrocephalus. J Koreen Med Sci. 1991;6(9):287-98. google scholar
  5. Kohli J, Gupta A, Kerai S, Mosalpuria Y. Ventriculoperitonial shunt surgery in a neonate with atrial septal defect, ventricular septal defect, patent ductus arteriosus, MILD PS, and bicuspid aortic valve. Karnataka Anaesth J. 2015;1(3):146. google scholar
  6. Kumar R, Kumar K, Devendra B, Chhabra K. Occurrence of Split Cord Malformation in Meningomyelocele: Complex Spina bifida. Pediatr Neurosurg. 2002;36(3):119-27 google scholar
  7. Henningfeld J, Loomba RS, Encalada S, Magner K, Pfister J, Matthews A, et al. Pleural effusion in a child with a ventriculoperitoneal shunt and congenital heart disease. Springerplus. 2016 Jan 27;5(1):90. google scholar
  8. Singh M, Bindra A, Rath G P, Malik V, Prabhakar H. Ventriculoperitoneal shunt surgery in an infant with double aortic arch, patent ductus arteriosus and atrial septal defect. MEJ Anesth. 2009;20(2):309-12. google scholar
  9. Martínez-Lage JF, López-Guerrero AL, Piqueras C, Almagro MJ, Gilabert A. Intracranial hemorrhage following surgery for occult spinal dysraphism: a case-based update. Child’s Nervous System. 2015;31(6):837–42. google scholar