GI Disorders MCN Notes
The Child with a Gastrointestinal Disorder
Objectives
Anatomy and Physiology Comparison
Identify differences between pediatric and adult gastrointestinal (GI) anatomy and physiology.
Medications and Treatments
Discuss common medications and treatments for managing pediatric GI disorders.
Nursing Assessments and Interventions
Identify assessments and interventions for children with GI illnesses.
Common GI Illnesses
Distinguish between cleft lip and palate, dehydration, hypertrophic pyloric stenosis, intussusception, gastroesophageal reflux, appendicitis, Hirschsprung disease, and celiac disease.
Variations in Pediatric Anatomy & Physiology
Mouth
Lower Esophageal Sphincter
Esophagus
Stomach
Intestines
Nursing Assessment
Health History
Evaluate growth patterns.
Address dietary concerns.
Review toilet training and bowel patterns.
Collect patient history and family history.
Diagnostic Testing
Esophageal pH probe
Ultrasound (abdominal)
KUB
Barium studies
Stool studies
Nursing Assessment Physical Exam
Inspection & Observation
Assess abdominal size and shape.
Auscultation
Percussion
Palpation
Dehydration
Occurs more readily in infants and young children due to:
Greater proportion of body water (up to 2 years of age).
Infants have higher insensible fluid losses and a higher body surface area (BSA) to body mass ratio.
The renal system of infants does not concentrate urine like adults.
Goal: Restore fluid volume and prevent hypovolemia.
Signs and Symptoms of Dehydration
Physical Signs
Sunken eyes.
Reduced level of consciousness.
Dry mucous membranes and tissue turgor.
Tachypnea and tachycardia.
Oliguria and hypotension.
Sudden weight loss.
Reduced capillary refill time.
Fluid Replacement
Mild to Moderate Dehydration:
Oral rehydration: 50-100 mL/kg with solutions like Pedialyte.
Severe Dehydration:
IV fluid management: 20 mL/kg with Lactated Ringer or Normal Saline.
Cleft Lip and Palate
Nursing Assessment
Risk Factors
Health history and physical exam.
Family education.
Post-Op Nursing Care for Cleft Lip
C: Calming techniques
L: Lie on back
E: Evaluate airway
F: Feeding techniques
T: Teaching
L: Lip protection (Logan bow)
I: Infection
P: Parent bonding
Post-Op Nursing Care for Cleft Palate
P: Pain management
A: Airway management
L: Liquid diet
A: Avoid hard foods and objects in the mouth
T: Avoid hot, spicy, and citrusy foods.
E: Educate parents on infection signs, use of arm restraints, and diet advancement.
Hypertrophic Pyloric Stenosis
Pathophysiology
Pylorus becomes hypertrophied leading to obstruction.
Nursing Assessment
Health History & Symptoms
Non-bilious emesis 30-60 minutes after feeding.
Signs of hunger despite feeding.
Physical Exam:
“Olive shaped” mass in the upper abdomen.
Progressive dehydration.
Nursing Management
Manage fluid and electrolyte levels.
Provide parental education.
Administer pre and post-operative care.
Resume feedings post-op.
Intussusception
Pathophysiology
Bowel telescopes into a distal segment, leading to edema, impaired blood circulation, and obstruction.
Nursing Assessment
Health History & Symptoms
Sudden onset of intermittent abdominal pain.
Bilious emesis and “currant jelly” stools.
Physical Exam:
Lethargy and “sausage”-shaped abdominal mass.
Nursing Management
Barium or air enema.
Surgical repair if necessary.
Pre and post-operative care.
Appendicitis
Pathophysiology
Obstruction leads to increased appendix pressure, edema, bacterial overgrowth, and potential perforation.
Nursing Assessment
Health History
Right lower quadrant pain, nausea, vomiting, fever.
Assessment Techniques
McBurney’s Point and rebound tenderness.
Labs:
CT scan or ultrasound.
Management for Appendicitis
Perforated (Complicated):
Appendectomy, peritoneal drainage, IV antibiotics.
Non-Perforated (Uncomplicated):
Appendectomy with pre-op antibiotics and fluids.
Alternative Options
Studied: Antibiotics only (provider preference).
Gastroesophageal Reflux Disease (GERD)
Health History and Symptoms
Failure to thrive, respiratory problems, irritability, “wet burps” or vomiting
Specific symptoms in infants and older children.
Nursing Management
Alter feeding techniques:
Small, frequent feedings; upright positioning; thickened formula.
Medications:
Histamine 2 blockers, proton pump inhibitors, prokinetics.
Consider Nissen fundoplication.
Hirschsprung Disease
Pathophysiology
Lack of ganglionic cells in the bowel resulting in inadequate motility.
Risk Factors
Not passing meconium within the first 24 hours, male.
Symptoms
Abdominal distension, pain, constipation, vomiting, slow growth.
Treatment
Surgical resection of bowel with reanastomosis; "pull-through" procedure.
Celiac Disease
Pathophysiology
Autoimmune disorder impairing the ability to digest gluten, leading to villous damage in the small intestine.
Medical Management
Implement a strict gluten-free diet.
Nursing Assessment
Health history and symptoms indicating malnutrition: anemia, steatorrhea, poor weight gain.
Diagnosis of Celiac Disease
Screening:
Blood test for Tissue Transglutaminase Antibodies (tTG-IgA) yields positive results in most cases.
Definitive Diagnosis:
Small bowel biopsy showing villi atrophy.
Genetic Testing:
Testing for HLA-DQ2 and HLA-DQ8 genes.