What are the characteristics and complications of Gastroschisis (a congenital defect where the intestines protrude through a hole in the abdominal wall)?

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Gastroschisis: Characteristics and Complications

Gastroschisis is characterized by prolonged postoperative ileus following surgical repair, and is not typically associated with other anomalies or chromosomal disorders. 1

Definition and Key Features

  • Gastroschisis is a congenital abdominal wall defect where intestines and sometimes other abdominal contents herniate through an opening in the abdominal wall, typically located to the right side of a normally inserted umbilical cord 1
  • Unlike omphalocele, gastroschisis has no membrane covering the herniated abdominal contents, which is a key distinguishing feature 2, 1
  • The prevalence has been increasing worldwide from approximately 0.1 per 10,000 births in the 1970s to over 5 per 10,000 in the early 2000s 1

Associated Conditions and Anomalies

  • Gastroschisis is rarely associated with chromosomal abnormalities or other non-bowel defects, making it distinct from omphalocele 1, 3
  • Omphalocele, in contrast, is frequently associated with other structural anomalies (39.4% have cardiovascular defects) and chromosomal abnormalities (15.5% have conditions such as trisomies 13,18, and 21) 2
  • Gastroschisis is located to the right of the umbilical cord insertion, not on the left 1

Complications and Postoperative Course

  • Prolonged postoperative ileus is a hallmark complication following gastroschisis repair 1
  • Neonatal morbidity depends on significant complicating factors such as bowel atresia, necrosis, and the prolonged ileus 1
  • Complex gastroschisis (complicated by intestinal atresia, stenosis, perforation, volvulus and/or necrosis) requires multiple surgeries and has higher morbidity and mortality than simple gastroschisis 4
  • Fetuses with gastroschisis are more likely to be born premature and with intrauterine growth restriction (IUGR), with approximately 48% of affected fetuses showing growth retardation 5

Management and Outcomes

  • Gastroschisis requires early surgical intervention after birth, often followed by prolonged neonatal care 1
  • Despite the challenging neonatal course, advances in surgical and post-operative care have improved survival rates to approximately 90% 1, 3
  • Elective delivery at 37 weeks' gestation in a tertiary pediatric center is recommended based on compelling evidence 3
  • Cesarean section should be reserved for routine obstetrical indications rather than being performed solely due to the presence of gastroschisis 3

Risk Factors

  • Young maternal age is strongly associated with gastroschisis 1, 6
  • Other potential risk factors include maternal smoking and recreational drug use 1, 6
  • The etiology remains unknown, though both genetic and non-genetic factors appear to play roles in its development 6

In conclusion, gastroschisis is a congenital abdominal wall defect that is not typically associated with other anomalies or chromosomal disorders, is located to the right of the umbilical cord, and is characterized by prolonged postoperative ileus following surgical repair.

References

Guideline

Congenital Abdominal Wall Defects

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Gastroschisis--what should be told to parents?

Prenatal diagnosis, 2014

Research

Complex gastroschisis: a new indication for fetal surgery?

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2021

Research

Growth retardation in prenatally diagnosed cases of gastroschisis.

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine, 1993

Research

Non-genetic risk factors for gastroschisis.

American journal of medical genetics. Part C, Seminars in medical genetics, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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