GastroIntestinal Flashcards
Absorption in small intestine
Osmosis
Carrier mediated diffusion
Active energy driven transport “pump”
Absorption in large inestine
water, sodium, colonic bacteria working
Biliary Atresia
aka
EHBA
extrahepatic biliary atresia
Biliary Atresia is..
a progressive inflammatory process that causes bile duct fibrosis, resulting in ductal obstruction
Biliary Atresia
associated malformations
polysplenia, intestinal atresia, malrotation of intestine
Biliary Atresia
Patho
cause is unknown
develops after birth
Biliary Atresia
manifestations
infants are full term & healthy @ birth. If jaundice persists beyond 2 weeks of age
serum bilirubin is elevated
urine may be dark
stool become acholic or gray (indicating lack of bile pigment)
Hepatomegaly & firm on palpation.
Biliary Atresia
Diagnostic
- Hx, physical,
- Labs: CBC, serum bili, liver function, TORCH titers, antitrypsin level, cytomegalovirus, hepatitis serology
- ultrasound, nuclear scintiscan, liver biopsy
Biliary Atresia
Prognosis
surgically treated before 2 months of age…survive, but may need liver transplant: cirrhosis, malabsorption growth failure, pruritus, ascites,jaundice
Untreated: dead by 2 years old
Biliary Atresia
Treatment
Kasai portoenterostomy
Biliary Atresia
Nursing care
stoma care, nutritional therapy, supplements, gastrostomy feedings, growth failure, pruritus
Omphalocele
Omphalocele—herniation of abdominal contents through umbilical ring, usually with an INTACT PERITONEAL SAC
Gastroschisis
Gastroschisis—herniation is lateral to the umbilical ring (usually to the right), and peritoneal sac NOT present
Omphalocele associated with
many other anomalies: brain, heart, GU, skeletal, imperforate anus, trisomies 13, 18, 21
Prognosis for Omphalocele & Gastroschisis
Gastroschisis survivial w/ surgery: 90-95%
Omphalocele, less positive D/T associated anomilies