ABDOMINAL WALL
DEFECTS
Introduction
Abdominal wall defects are a type of congenital
defects that allows the stomach , the intestines ,
or other organs to protrude through an unusual
opening that forms on the abdomen . During the
development of the fetus , many unexpected
changes occur inside the womb .
Definition
Abdominal wall defects are birth defects that
allows the stomach or intestines to protrude
Types
The two main abdominal wall defects are;
Omphalocele
Gastroschisis
OMPHALOCELE
Definition
It is a defect in abdominal wall musculature
and skin with protrusion of abdominal viscera
contained within a membranous sac.
Incidence
Small omphalocele 1:5,000
Large omphalocele 1:10,000
Male to female ratio 1:1
Pacific Islanders have low risk for omphalocele
70% associated with congenital anomalies
such as Bowel atresia , Imperforated anus ,
Trisomes 13, 18, 21, Beckwith – Wiedman
Syndrome
Etiology
Due to failure of midgut to return to abdomen by
the 10th week of gestation during midgut
rotation
Pathophysiology
o Failure of the midgut to return to abdomen by
the 10th week of gestation
Risk Factors
 Increased maternal age more than 40 years
 Twins
 High gravida
 Consecutive births
Clinical Features
Covered clinical defects of the umbilical ring
Defects may vary from 2-10cm
Sac is composed of amnion, Wharton’s jelly
& peritoneum
The umbilical cord insert directly into the sac
in an apical or lateral position
Small one contains intestinal loops only
Large one contains liver , spleen , bladder ,
testes/ovary
Diagnosis
o About 90% of Omphalocele & Gastroschisis
diagnosed prenatally
o Alpha – feto – protein synthesised in fetal liver &
excreted by fetal kidney & crosses placenta by 12th
weeks.
o Prenatal ultrasound after 14th week gestation is the
confirmatory test
Prenatal Ultrasound
Findings are
Abdominal organs herniated outside the
abdominal cavity with an abnormal insertion
of umbilical cord into the membrane rather
than into abdominal wall
The mass contents are intestinal loops , liver ,
spleen , gonads etc
Management
Evaluation for associated anomalies &
monitoring of fetal growth
Echocardiography: high risk for CHD
Prenatal monitoring of fetal growth : high risk
of IUGR
Other specific evaluation for associated
pulmonary hypoplasia
Prenatal counseling about the expected
hospital course & the long term prognosis
After Delivery
The initial evaluation & resuscitation to a babies
with an omphalocele is
Follow same protocol & sequence of all
newborns
Should be handled carefully to prevent the
omphalocele membrane from tearing
After initial stabilization for the newborn should
be inspected to confirm that it is intact & then
covered with a non adherent dressing to protect
the sac
Primary closure
Small defects (<4cm) excision of the sac and
closure of the fascia and skin over the
abdominal contents
Mesh patch
o Medium defects(6-8cm)
Consecutive
o Large defects (1o-12cm)apply topical application –
Beta-dine ointment or silver sulfadiazine to make
intact sac till the baby is bigger & more able to
tolerate major operations
Long Term Outcomes
Small will recovery well
The outcomes determine by the severity of
associated anomalies , so babies with giant
omphalocele have increased morality &
morbidity
GERD
Hernias
Respiratory infection
Failure to thrive
GASTROSCHISIS
Definition
• It is the defect in the abdominal wall was
displaced to the right of the umbilicus and
eviscerated bowel was not covered by a
membrane
Incidence
o 1:20,000-30,000
o Sex ratio 1:1
o 10-15% have associated anomalies
o 40% are premature /SGA
Etiology
Failure of migration and fusion of the lateral folds
of the embryonic disc on the 3rd – 4th week of
gestation
Disruption of the right omphalomesenteric artery
as midgut returns to abdomen by 10th week of
gestation causing ischemia of the abdominal wall
and weakness then herniation
Rupture of omphalocele
Folic acid deficiency
Pathophysiology
Abnormal involution of right umbilical vein
Rupture of a small omphalocele
Failure of migration and fusion of the lateral
folds of the embryonic disc on 3rd -4th week of
gestation
Risk Factors
Young maternal age
Low gravida
Prematurity
Low birth –weight secondary to IUGR
Clinical Features
o Defect to the right of intact umbilical cord
allowing extrution of abdominal content
o No covering sac
o Bowels often thickened, matted, and edematous
o Evisceration of the bowel leads to malrotation
o Constriction of the base may cause intestinal
stenosis , atresia , and volvulus
o Undecended testicles
Diagnosis
 About 90% of Gastroschisis & Omphalocele
diagnosed prenatally
 Polyhydramnios
 MSAFP
 Amniocentesis
Prenatal Ultrasound
• The diagnostic prenatal ultrasound findings of
Gastroschisis are extra abdominal loops of
bowel without covering sac
Management
After Delivery
• The perfusion of the herniated contents should
be carefully evaluated . If bowel ischemia or
infarction suspected immediate surgical
consultation is indicated .
• If the viscera are well perfused, it is important
to next place a clear plastic bag over the
exposed bowel as a temporary covering to
minimize evaporative heat and fluid loss .
Pre-operative Management
• Heat management
-sterile wrap or sterile bowel bag
-radiant warmer
• Fluid management
-IV bolus 20ml/kg LR/NS
-D10 ¼ NS 2-3 maintenance rate
• Nutrition
-TPN(central venous line)
• Abdominal Distention
-OG/NG tube
-urinary catheter
• Infection control
-Broad spectrum antibiotics
• Closure of the defect
• ABC
Surgical Management
Skin flabs
Primary closure : Use of own baby umbilical
stump as biological dressing to seal
gastrochisis defect without attempting a
primary fascial closure
Staged closure : In 1969 ,Allen and Wrenn
adapted Schuster’s technique to treat
gastroschisis
Long Term Outcomes
• Almost always with intestinal malformation
• Hernias at the site of repair
• Intestinal atresia
• Short bowel syndrome
Conclusion
Abdominal wall defects are type of congenital
defect that allows the stomach , the intestines ,or
other organs to protrude through an unusual
opening that forms on the abdomen.
Abdominal  wall defect

Abdominal wall defect

  • 1.
  • 2.
    Introduction Abdominal wall defectsare a type of congenital defects that allows the stomach , the intestines , or other organs to protrude through an unusual opening that forms on the abdomen . During the development of the fetus , many unexpected changes occur inside the womb .
  • 3.
    Definition Abdominal wall defectsare birth defects that allows the stomach or intestines to protrude
  • 4.
    Types The two mainabdominal wall defects are; Omphalocele Gastroschisis
  • 5.
    OMPHALOCELE Definition It is adefect in abdominal wall musculature and skin with protrusion of abdominal viscera contained within a membranous sac.
  • 6.
    Incidence Small omphalocele 1:5,000 Largeomphalocele 1:10,000 Male to female ratio 1:1 Pacific Islanders have low risk for omphalocele 70% associated with congenital anomalies such as Bowel atresia , Imperforated anus , Trisomes 13, 18, 21, Beckwith – Wiedman Syndrome
  • 7.
    Etiology Due to failureof midgut to return to abdomen by the 10th week of gestation during midgut rotation
  • 8.
    Pathophysiology o Failure ofthe midgut to return to abdomen by the 10th week of gestation
  • 9.
    Risk Factors  Increasedmaternal age more than 40 years  Twins  High gravida  Consecutive births
  • 10.
    Clinical Features Covered clinicaldefects of the umbilical ring Defects may vary from 2-10cm Sac is composed of amnion, Wharton’s jelly & peritoneum The umbilical cord insert directly into the sac in an apical or lateral position Small one contains intestinal loops only Large one contains liver , spleen , bladder , testes/ovary
  • 11.
    Diagnosis o About 90%of Omphalocele & Gastroschisis diagnosed prenatally o Alpha – feto – protein synthesised in fetal liver & excreted by fetal kidney & crosses placenta by 12th weeks. o Prenatal ultrasound after 14th week gestation is the confirmatory test
  • 12.
    Prenatal Ultrasound Findings are Abdominalorgans herniated outside the abdominal cavity with an abnormal insertion of umbilical cord into the membrane rather than into abdominal wall The mass contents are intestinal loops , liver , spleen , gonads etc
  • 13.
    Management Evaluation for associatedanomalies & monitoring of fetal growth Echocardiography: high risk for CHD Prenatal monitoring of fetal growth : high risk of IUGR Other specific evaluation for associated pulmonary hypoplasia Prenatal counseling about the expected hospital course & the long term prognosis
  • 14.
    After Delivery The initialevaluation & resuscitation to a babies with an omphalocele is Follow same protocol & sequence of all newborns Should be handled carefully to prevent the omphalocele membrane from tearing After initial stabilization for the newborn should be inspected to confirm that it is intact & then covered with a non adherent dressing to protect the sac
  • 15.
    Primary closure Small defects(<4cm) excision of the sac and closure of the fascia and skin over the abdominal contents
  • 16.
    Mesh patch o Mediumdefects(6-8cm) Consecutive o Large defects (1o-12cm)apply topical application – Beta-dine ointment or silver sulfadiazine to make intact sac till the baby is bigger & more able to tolerate major operations
  • 17.
    Long Term Outcomes Smallwill recovery well The outcomes determine by the severity of associated anomalies , so babies with giant omphalocele have increased morality & morbidity GERD Hernias Respiratory infection Failure to thrive
  • 18.
    GASTROSCHISIS Definition • It isthe defect in the abdominal wall was displaced to the right of the umbilicus and eviscerated bowel was not covered by a membrane
  • 19.
    Incidence o 1:20,000-30,000 o Sexratio 1:1 o 10-15% have associated anomalies o 40% are premature /SGA
  • 20.
    Etiology Failure of migrationand fusion of the lateral folds of the embryonic disc on the 3rd – 4th week of gestation Disruption of the right omphalomesenteric artery as midgut returns to abdomen by 10th week of gestation causing ischemia of the abdominal wall and weakness then herniation Rupture of omphalocele Folic acid deficiency
  • 21.
    Pathophysiology Abnormal involution ofright umbilical vein Rupture of a small omphalocele Failure of migration and fusion of the lateral folds of the embryonic disc on 3rd -4th week of gestation
  • 22.
    Risk Factors Young maternalage Low gravida Prematurity Low birth –weight secondary to IUGR
  • 23.
    Clinical Features o Defectto the right of intact umbilical cord allowing extrution of abdominal content o No covering sac o Bowels often thickened, matted, and edematous o Evisceration of the bowel leads to malrotation o Constriction of the base may cause intestinal stenosis , atresia , and volvulus o Undecended testicles
  • 24.
    Diagnosis  About 90%of Gastroschisis & Omphalocele diagnosed prenatally  Polyhydramnios  MSAFP  Amniocentesis
  • 25.
    Prenatal Ultrasound • Thediagnostic prenatal ultrasound findings of Gastroschisis are extra abdominal loops of bowel without covering sac
  • 26.
    Management After Delivery • Theperfusion of the herniated contents should be carefully evaluated . If bowel ischemia or infarction suspected immediate surgical consultation is indicated . • If the viscera are well perfused, it is important to next place a clear plastic bag over the exposed bowel as a temporary covering to minimize evaporative heat and fluid loss .
  • 27.
    Pre-operative Management • Heatmanagement -sterile wrap or sterile bowel bag -radiant warmer • Fluid management -IV bolus 20ml/kg LR/NS -D10 ¼ NS 2-3 maintenance rate
  • 28.
    • Nutrition -TPN(central venousline) • Abdominal Distention -OG/NG tube -urinary catheter • Infection control -Broad spectrum antibiotics • Closure of the defect • ABC
  • 29.
    Surgical Management Skin flabs Primaryclosure : Use of own baby umbilical stump as biological dressing to seal gastrochisis defect without attempting a primary fascial closure Staged closure : In 1969 ,Allen and Wrenn adapted Schuster’s technique to treat gastroschisis
  • 30.
    Long Term Outcomes •Almost always with intestinal malformation • Hernias at the site of repair • Intestinal atresia • Short bowel syndrome
  • 31.
    Conclusion Abdominal wall defectsare type of congenital defect that allows the stomach , the intestines ,or other organs to protrude through an unusual opening that forms on the abdomen.