PN / LVN Focused

Pediatric GI Disorders

The gastrointestinal conditions of infancy and childhood — cleft lip and palate, pyloric stenosis, intussusception, Hirschsprung disease, and gastroenteritis with dehydration. High-yield pediatric content where fluid balance is everything, for the LPN/LVN exit exam and NCLEX-PN.

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01

Pediatric GI Overview

In children, fluid balance is the recurring theme.

Children — especially infants — have a higher percentage of body water and a faster metabolic rate than adults, so vomiting and diarrhea can cause dehydration and electrolyte imbalances very quickly. Across nearly every pediatric GI disorder, the nurse's job is to watch fluid status closely.

The Pediatric GI Theme

Whether the problem is projectile vomiting (pyloric stenosis), bloody stools (intussusception), or simple gastroenteritis, the common thread is fluid and electrolyte loss. Daily weights and strict intake/output are your best tools, and dehydration is the danger to catch early.

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02

Cleft Lip & Palate

A congenital opening in the lip and/or the roof of the mouth.

Cleft lip and cleft palate are congenital defects where the lip and/or palate don't fuse. The big challenges are feeding (the infant can't form suction) and, after surgery, protecting the repair.

  • Feeding: use special wide-based or squeezable nipples, hold the infant upright, and burp frequently (they swallow air).
  • After cleft LIP repair: protect the suture line — position on the back or side (not prone/face down), use soft elbow restraints, and keep the baby from crying hard.
  • After cleft PALATE repair: nothing hard in the mouth — no straws, pacifiers, hard utensils, or suction near the suture line; soft elbow restraints; soft/liquid diet.
Protect That Suture Line

The post-op priority for cleft repairs is keeping fingers and objects away from the incision. Elbow restraints stop the child from touching the repair, and avoiding straws, pacifiers, and hard foods prevents disrupting a palate repair. Always watch the airway too — swelling can compromise breathing.

03

Pyloric Stenosis

A tight stomach outlet → projectile vomiting.

In pyloric stenosis, the pylorus (the muscle at the stomach outlet) thickens and blocks the stomach from emptying, usually showing up around 3–6 weeks of age.

Classic Signs

  • Projectile, non-bilious vomiting (no bile — the blockage is before the bile duct)
  • The infant is hungry and eager to eat again right after vomiting
  • A small, firm olive-shaped mass in the right upper quadrant
  • Dehydration and metabolic alkalosis (from vomiting away stomach acid/HCl)

Treatment: surgical pyloromyotomy after correcting fluid and electrolyte imbalances.

Why Alkalosis, Not Acidosis?

Projectile vomiting loses hydrochloric acid from the stomach, so the blood becomes alkalotic (metabolic alkalosis) — the opposite of what you might expect. Correcting fluids and electrolytes comes before surgery.

04

Intussusception

One part of the bowel telescopes into another.

Intussusception is when a segment of intestine slides into the segment ahead of it (like a collapsing telescope), cutting off blood flow.

Classic Signs

  • Sudden, severe, colicky abdominal pain — the infant suddenly draws the knees up and cries, then calms between episodes
  • "Currant jelly" stools — stool mixed with blood and mucus
  • A sausage-shaped mass in the abdomen; vomiting

Treatment: an air or contrast enema can push the bowel back into place; surgery is done if that fails or the bowel is damaged.

A Sudden Normal Stool Can Be a Warning

If a child with intussusception suddenly passes a normal brown stool, it may mean the intussusception has spontaneously reduced — but report it, because the picture can change quickly. "Currant jelly" stool plus colicky pain and a sausage-shaped mass is the classic triad to recognize.

05

Hirschsprung Disease

A section of colon with no nerves can't move stool.

In Hirschsprung disease (congenital aganglionic megacolon), part of the colon is missing the nerve cells needed to push stool along, so stool backs up behind it.

Signs

  • No meconium passed within 24–48 hours of birth (a key newborn clue)
  • Abdominal distension; ribbon-like, foul-smelling stools
  • Poor feeding, vomiting, and failure to thrive

Treatment: surgery to remove the affected (aganglionic) segment, sometimes with a temporary colostomy.

The Newborn Clue

A newborn who hasn't passed meconium in the first day or two should raise suspicion for Hirschsprung disease. Pair that with a distended abdomen and ribbon-like stools, and the diagnosis fits.

06

Gastroenteritis & Dehydration

The most common — and the most important to assess.

Gastroenteritis (often viral, such as rotavirus) causes vomiting and diarrhea. In young children the main danger is dehydration.

Signs of Dehydration in a Child

  • Sunken anterior fontanel (in infants), sunken eyes
  • Fewer wet diapers / decreased urine output
  • Dry mucous membranes, no tears when crying
  • Poor skin turgor (tenting), fast heart rate, lethargy or irritability

Treatment: oral rehydration solution (ORS) for mild–moderate dehydration; IV fluids for severe dehydration or persistent vomiting. Avoid plain water, juice, and soda (they don't replace electrolytes).

Daily Weight = Best Indicator

A child's daily weight is the most sensitive measure of fluid status — a drop in weight reflects fluid loss. Combine it with strict intake/output, counting wet diapers, and checking the fontanel and turgor.

? An infant with gastroenteritis is irritable, has a sunken fontanel, and hasn't had a wet diaper in 6 hours. What is the priority intervention?
The priority is rehydration. Signs of dehydration (sunken fontanel, decreased wet diapers, irritability) indicate significant fluid loss. Start with oral rehydration solution for mild-to-moderate dehydration; if the infant is severely dehydrated or cannot tolerate oral fluids, IV access and IV fluids are needed. Daily weight is the best ongoing indicator of fluid status.
07

Infant GERD & Tracheoesophageal Fistula

Reflux is common; a fistula is an emergency.

Infant GERD

  • Frequent spitting up/regurgitation; usually improves with age.
  • Care: keep the infant upright after feeds, give smaller more frequent feeds, and thicken feeds if prescribed.

Tracheoesophageal Fistula (TEF) / Esophageal Atresia

  • A congenital abnormal connection between the esophagus and trachea.
  • Watch for the "3 C's" with feeding: Coughing, Choking, and Cyanosis, plus excessive drooling — a surgical emergency.
The 3 C's of TEF

A newborn who coughs, chokes, and turns blue (cyanosis) with feeding, and drools excessively, may have a tracheoesophageal fistula. Stop the feeding, keep the airway clear, and notify the provider — milk can enter the lungs.

08

Nursing Care & Hydration

The shared priorities across pediatric GI problems.

  • Monitor fluid status — daily weights, strict intake/output, wet-diaper counts, fontanel and skin turgor.
  • Rehydrate — ORS for mild–moderate; IV fluids for severe.
  • Feeding teaching — positioning, special techniques (cleft, GERD), and what foods/fluids to use.
  • Post-op care — protect suture lines (cleft), elbow restraints, pain control, and airway monitoring.
  • Family support — teach parents the signs of dehydration and when to seek care.
The Big Picture for the Exam

Match the hallmark to the disorder: projectile vomiting + olive mass = pyloric stenosis; currant-jelly stool + colicky pain = intussusception; no meconium + ribbon stools = Hirschsprung; 3 C's with feeding = TEF. And in every case, watch for dehydration.

09

Frequently Asked Questions

Common student questions on this topic.

What are the signs of pyloric stenosis?
Projectile, non-bilious vomiting (around 3–6 weeks), an infant hungry right after vomiting, an olive-shaped mass in the RUQ, and dehydration with metabolic alkalosis. Treated with a pyloromyotomy after correcting fluids/electrolytes.
What is the classic sign of intussusception?
"Currant jelly" stools (blood + mucus), plus sudden colicky pain (knees drawn up) and a sausage-shaped mass. Often reduced with an air/contrast enema; surgery if that fails.
What is Hirschsprung disease?
A congenital lack of nerve cells in part of the colon, so stool backs up. Clue: no meconium within 24–48 hours, plus distension and ribbon-like stools. Corrected surgically.
How do you recognize dehydration in an infant?
Sunken fontanel, fewer wet diapers, dry mucous membranes, no tears, poor skin turgor, sunken eyes, tachycardia, and lethargy. Daily weight is the most sensitive indicator.
What is the priority after cleft palate repair?
Protect the suture line: no straws, pacifiers, hard utensils, or suction near it, use soft elbow restraints, keep the child calm, and watch the airway.
Why is oral rehydration preferred for pediatric gastroenteritis?
ORS safely replaces fluids and electrolytes, is less invasive than IV, and can be done at home. Plain water/juice/soda are avoided. IV fluids are reserved for severe dehydration or persistent vomiting.
10

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Pediatric GI Disorders Cheatsheet

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