Week 3 GI Flashcards
What causes cleft lip/cleft palate
Failure of the maxillary processes to fuse between 5 to 12 weeks gestation. Failure of the tongue to move down at the correct time prevents the palatine processes from fusing
Risk factors that increase likelihood of cleft palate & RX
Advanced maternal age
Poor maternal care (vitamins, nutrition, drugs taken by mother, genetically linked, linked to poor income → lack of access to care
Rx → FOLIC ACID
Nursing management to facilitate feeding in cleft lip/palate
Cannot create suction; now newborns and infants feed
Use palate shield and bottles with nozzle-type attachment
OG / NG tubes
Diagnosis of esophageal atresia and tracheoesphageal fistula
Sx: THREE Cs – cyanosis, choking, coughing à if you have secretions ending in a blind pouch, it will either come back up or go into the lungs
Soon after birth, placing NG / OG tube – continuous suctioning
Might see a distending abdomen - air trapping
Gastroschisis VS omphalocele
Gastroschisis – ABD is open, contents exposed
Omphalocele – muscle has not formed but membrane is containing contents but they are visible
RX for Gastroschisis
create silo à meshy prosthetic sack that covers ABD. Top of sack is a cinch string that is tightened over time to put contents back under cover.
RX for Gastroschisis, omphalocele
folic acid
Anal stenosis and anal atresia
Narrowing or complete covering of rectum
Anal stenosis
wall is thickened or constricted
Decreased normal stool passage
Reports of ribbon like stool
Umbilical hernia
a weakness in umbilical ring – stomach contents protruding into abd. Can resolve on its own, older children may need surgery.
Meckel’s diverticulum
Omphalomesenteric duct fails to atrophy. One of the most common congenital anomalies. Happens a lot in utero but don’t see sx until much much older (may have been plagued with GI sx for a while though)
S/S of Meckel’s Diverticulum
Inflammation
Rectal bleeding
Intestinal obstruction
Hirschsprung disease
adequate motility that causes mechanical obstruction – congenital link
Congenital absence of ganglion cells in the rectum and colon
Can cause mega colin
S/S in newborn
want to see that meconium
over time back in doctor’s office with really infrequent stooling
abd distension
bile stained emesis → bowel contents backing up
can get ostomies
going to see failure to thrive, dev. Delays, severe constipation/ diarrhea
chronic care over time → diet, stool modifications forever
prevent dehydration
rectal stimulation
Pyloric stenosis presentation
Child presents with massive vomiting (exorcist) within 20 minutes it’s coming back up; then they are hungry again
Increased peristalsis prior to vomiting
Hyperactive bowel sounds
Olive shaped mass
In pyloric stenosis, the hypertrophied pyloric muscle (feels like a small olive) causes symptoms of projectile vomiting and visible peristalsis.
Picked up on ultrasound based on clinical presentation
At SEVERE risk for dehydration and F/E imbalance – needs to be corrected prior to OR.
Quick OR visit