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ABDOMINAL WALL DEFECTS
OMPHALOCELE VS GASTROSCHISIS
Rusila Tikoitoga
MBBS 4
2016
OBJECTIVES
• Background
• Epidemiology
• Etiology
• Pathophysiology
• Clinical Features
• Diagnosis
• Management
• Prognosis
History
• 1634 - Ambroise Paré (French barber surgeon) first
described Omphalocele.
• Derived from Latin word “Omphalos” meaning
prominence or navel.
• 1733 – James Calder (Scottish neonatal surgeon) first
described Gastroschisis.
• Derived from the Greek word “Gaster”(Gastro)
meaning belly and “schisis” meaning to tear or split
from "
Epidemiology
 Gastroschisis
 Incidence - 4 per 10,000
 M:F is 1:1
• 10-15% association with
congenital anomalies such as
CHD(VSD), cleft palate and
intestinal atresia
• 40% are premature/SGA
 Omphalocele
 Incidence - 3 per 5,000
 M:F is 1.5:1
 >70% association with
congenital anomalies such
Bowel atresia, Imperforated
anus, Trisomies 13, 18, 21,
Beckwith-Wiedemann
Syndrome & Pentalogy of
Cantrell
Etiology
• Gastroschisis
o Congenital abdominal wall defect
towards the right side of the
umbilicus and protruded bowel is not
covered by a membrane.
o Failure of migration and fusion of the
lateral folds of the embryonic disc on
the 3rd-4th week of gestation.
o Disruption of the right
omphalomesenteric artery as midgut
returns to abdomen by the 10th week
causing ischemia of the abdominal
wall and weakness then herniation.
o Rupture of omphalocele
• Omphalocele
o Congenital abdominal wall defect with
protrusion of abdominal viscera
contained within a parietal peritoneum
and amniotic membranous sac with
Wharton’s jelly.
o Due to failure of the midgut to return
to abdomen by the 10th week of
gestation during midgut rotation.
Risk Factors
Omphalocele
• Increased maternal age
• Twins
• High gravida
• Consecutive children
Gastroschisis
• Young maternal age
• Low gravida
• Prematurity
• Low birth-weight
secondary to IUGR
OMPHALOCELE GASTROSCHISIS
OMPHALOCELE GASTROSCHISIS
Embryology of GIT
Clinical Features
OMPHALOCELE
• central defect of the abdominal wall beneath the
umbilical ring.
• Defect may be 2-12 cm (Small-<5cm)(Large>8cm)
• Always covered by sac
• Sac is made of amnion, Wharton’s jelly and
peritoneum
• The umbilical cord inserts directly into the sac in an apical
or lateral position.
• Small contains intestinal loops only. Large may
involve liver, spleen and bladder, testes/ovary
• >50% have associated anomalies
GASTROSCHISIS
• Defect to the right of an intact umbilical cord allowing
extrusion of abdominal content
• Umbilical cord arises from normal place in abdominal wall
• Opening <=5 cm
• No covering sac (never has a sac )
• Evisceration usually only contains intestinal loops
• Bowels often thickened, matted and edematous
• 10-15% have associated anomalies
• 40% are premature/SGA
Diagnosis
• Alpha-feto-protein-synthesized in fetal liver and
excreted by fetal kidneys and crosses placenta by 12
weeks.
• Elevated maternal AFP - neural tube defects,
abdominal wall defects, duodenal or esophageal
atresia
• 40% false positive rate
• Fetal ultrasound after 14 weeks gestation is the
confirmatory test.
Prenatal Ultrasound
• Normal umbilical cord
insertion site
• Small bowel loops seen in the
amniotic cavity
• No covering membrane over
the loops of bowel
• Can include stomach and large
bowel
• Majority occur to the right of
the umbilical cord
Gastroschisis
Prenatal Ultrasound
• Umbilical cord
insertion is typically
midline on the mass
• Located centrally
• Contents are intestinal
loops and maybe liver,
spleen and gonads.
Omphalocele
Management
Perinatal Management
• Maternal Screening
 Fetal Ultrasound = positive findings
 Alpha-feto-protein elevated = 90%
Omphalocele 10% Gastroschisis
• Prenatal counselling
 Pre-operative Management
• ABC
• Heat Management
– Sterile wrap or sterile bowel bag
– Radiant warmer
• Fluid Management
– IV bolus 20 ml/kg LR/NS
– D10¼NS 2-3 maintenance rate
• Nutrition
– TPN (central venous line )
• Abdominal Distention
– OG/NG tube
– urinary catheter
• Infection Control
Broad-spectrum antibiotics - Ampicillin and Gentamycin
• Closure of the Defect
Omphalocele
• Conservative
1. Large omphalocele (10-12cm)
apply topical application -
Betadine ointment or silver
sulfadiazine to the intact sac.
2. Secondary eschar formation and
granulation.
3. Healing lasts for 12 months then
repaired as ventral hernia.
o Primary Closure
 Small defects (<4cm)
 excision of the sac and closure
of the fascia and skin over the
abdominal contents
o Mesh patch
 Medium defects (6-8cm)
• Post operative care
o NICU
o Ventilation
o Feeding:
– Minimal volume
o 48 hrs Antibiotics
o Hernia dealt with at 1
yr old
Gastroschisis
• Primary closure
o If bowel easily reduced
• Staged closure
o Silo fashioning:
Sac excised
Silo sewn to rectus fascia/full thickness
• Post operative care
o NICU
o Feeding delayed for
weeks
o Oral stimulation/sucking
reflex
o Broad spectrum
antibiotics
Long Term Outcomes
Omphalocele
• Small - recover well
• Large:
– Gastro-oesophageal reflux - 43%
– Majority improve over time
– 20% pulmonary insufficiency
– Respiratory Infections
– Asthma
– Feeding difficulties;
• 60% with giant omphalocele
• May need gastrostomy for feeding
– Failure to thrive
Gastroschisis
• Generally excellent if no atresia
• NEC:
– 18.5% of neonates more with formula
– Bowel loss - short gut syndrome
• Cryptorchidism:
– 15-30%
– Due either being outside/prematurity
– Replacement and orchidopexy by 1 yr
• 60% have psychosocial stress if
umbilicus sacrificed
Summary
References:
• Up to Date
• Medscape
• O.P Ghai E.pediatrics
• Rudolph’s pediatrics

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Omphalocele vs gastroschisis

  • 1. ABDOMINAL WALL DEFECTS OMPHALOCELE VS GASTROSCHISIS Rusila Tikoitoga MBBS 4 2016
  • 2. OBJECTIVES • Background • Epidemiology • Etiology • Pathophysiology • Clinical Features • Diagnosis • Management • Prognosis
  • 3. History • 1634 - Ambroise Paré (French barber surgeon) first described Omphalocele. • Derived from Latin word “Omphalos” meaning prominence or navel. • 1733 – James Calder (Scottish neonatal surgeon) first described Gastroschisis. • Derived from the Greek word “Gaster”(Gastro) meaning belly and “schisis” meaning to tear or split from "
  • 4. Epidemiology  Gastroschisis  Incidence - 4 per 10,000  M:F is 1:1 • 10-15% association with congenital anomalies such as CHD(VSD), cleft palate and intestinal atresia • 40% are premature/SGA  Omphalocele  Incidence - 3 per 5,000  M:F is 1.5:1  >70% association with congenital anomalies such Bowel atresia, Imperforated anus, Trisomies 13, 18, 21, Beckwith-Wiedemann Syndrome & Pentalogy of Cantrell
  • 5. Etiology • Gastroschisis o Congenital abdominal wall defect towards the right side of the umbilicus and protruded bowel is not covered by a membrane. o Failure of migration and fusion of the lateral folds of the embryonic disc on the 3rd-4th week of gestation. o Disruption of the right omphalomesenteric artery as midgut returns to abdomen by the 10th week causing ischemia of the abdominal wall and weakness then herniation. o Rupture of omphalocele • Omphalocele o Congenital abdominal wall defect with protrusion of abdominal viscera contained within a parietal peritoneum and amniotic membranous sac with Wharton’s jelly. o Due to failure of the midgut to return to abdomen by the 10th week of gestation during midgut rotation.
  • 6. Risk Factors Omphalocele • Increased maternal age • Twins • High gravida • Consecutive children Gastroschisis • Young maternal age • Low gravida • Prematurity • Low birth-weight secondary to IUGR
  • 10.
  • 11. Clinical Features OMPHALOCELE • central defect of the abdominal wall beneath the umbilical ring. • Defect may be 2-12 cm (Small-<5cm)(Large>8cm) • Always covered by sac • Sac is made of amnion, Wharton’s jelly and peritoneum • The umbilical cord inserts directly into the sac in an apical or lateral position. • Small contains intestinal loops only. Large may involve liver, spleen and bladder, testes/ovary • >50% have associated anomalies GASTROSCHISIS • Defect to the right of an intact umbilical cord allowing extrusion of abdominal content • Umbilical cord arises from normal place in abdominal wall • Opening <=5 cm • No covering sac (never has a sac ) • Evisceration usually only contains intestinal loops • Bowels often thickened, matted and edematous • 10-15% have associated anomalies • 40% are premature/SGA
  • 12. Diagnosis • Alpha-feto-protein-synthesized in fetal liver and excreted by fetal kidneys and crosses placenta by 12 weeks. • Elevated maternal AFP - neural tube defects, abdominal wall defects, duodenal or esophageal atresia • 40% false positive rate • Fetal ultrasound after 14 weeks gestation is the confirmatory test.
  • 13. Prenatal Ultrasound • Normal umbilical cord insertion site • Small bowel loops seen in the amniotic cavity • No covering membrane over the loops of bowel • Can include stomach and large bowel • Majority occur to the right of the umbilical cord Gastroschisis
  • 14. Prenatal Ultrasound • Umbilical cord insertion is typically midline on the mass • Located centrally • Contents are intestinal loops and maybe liver, spleen and gonads. Omphalocele
  • 15. Management Perinatal Management • Maternal Screening  Fetal Ultrasound = positive findings  Alpha-feto-protein elevated = 90% Omphalocele 10% Gastroschisis • Prenatal counselling
  • 16.  Pre-operative Management • ABC • Heat Management – Sterile wrap or sterile bowel bag – Radiant warmer • Fluid Management – IV bolus 20 ml/kg LR/NS – D10¼NS 2-3 maintenance rate • Nutrition – TPN (central venous line ) • Abdominal Distention – OG/NG tube – urinary catheter • Infection Control Broad-spectrum antibiotics - Ampicillin and Gentamycin • Closure of the Defect
  • 17. Omphalocele • Conservative 1. Large omphalocele (10-12cm) apply topical application - Betadine ointment or silver sulfadiazine to the intact sac. 2. Secondary eschar formation and granulation. 3. Healing lasts for 12 months then repaired as ventral hernia. o Primary Closure  Small defects (<4cm)  excision of the sac and closure of the fascia and skin over the abdominal contents o Mesh patch  Medium defects (6-8cm)
  • 18. • Post operative care o NICU o Ventilation o Feeding: – Minimal volume o 48 hrs Antibiotics o Hernia dealt with at 1 yr old
  • 19. Gastroschisis • Primary closure o If bowel easily reduced • Staged closure o Silo fashioning: Sac excised Silo sewn to rectus fascia/full thickness
  • 20. • Post operative care o NICU o Feeding delayed for weeks o Oral stimulation/sucking reflex o Broad spectrum antibiotics
  • 21. Long Term Outcomes Omphalocele • Small - recover well • Large: – Gastro-oesophageal reflux - 43% – Majority improve over time – 20% pulmonary insufficiency – Respiratory Infections – Asthma – Feeding difficulties; • 60% with giant omphalocele • May need gastrostomy for feeding – Failure to thrive Gastroschisis • Generally excellent if no atresia • NEC: – 18.5% of neonates more with formula – Bowel loss - short gut syndrome • Cryptorchidism: – 15-30% – Due either being outside/prematurity – Replacement and orchidopexy by 1 yr • 60% have psychosocial stress if umbilicus sacrificed
  • 23. References: • Up to Date • Medscape • O.P Ghai E.pediatrics • Rudolph’s pediatrics