Med Surg/ Pediatrics Exam 2 - Pedi GI Review, Study Guides, Projects, Research of Pediatrics

Med Surg/ Pediatrics Exam 2 - Pedi GI Review

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Med Surg/ Pediatrics Exam 2 - Pedi GI Review
1.Why are infants and children more at risk than adults for dehydration?:
The have more total body water (TBW)
-greater/more rapid fluid loss
-more insensible fluid loss
2.TBW of premies and infants: premie
90% infant 75%
3.TBW of late adolescents: 45%
4.What age does the total body water start equaling adults?: about 2 y/o
5.Examples of insensible fluid loss: -Fever
-Respiratory tract
-Heat & humidity
-Respiratory rate
-Skin
6.Examples of sensible fluid loss: -Urine
-Feces
-Emesis
7.Labs for dehydration: ‘H & H, specific gravity, BUN,
creatinine “serum sodium, potassium, chloride,
magnesium
8.How do you treat Mild to Moderate Dehydration?: -Pedialyte
-ORAL fluids
When rehydrated resume regular diet
9.How do you treat severe dehydration?: §Initial IV infusion of 20ml/kg of
NS or LR
§Reassess and may need 1 ½ fluid maintenance
10.If a patient is vomiting, what position would you put them in?: Side lying
to prevent aspiration
11.If a patient is vomiting, how will you reintroduce their regular diet?: start
w small amounts of water/ food
12.Acute diarrhea in infants most likely: Roatvirus!
13.If a patient is vomiting, what will you rehydrate them with?: Rehydrate
with glucose-electrolyte solution, IV fluid (D5NS?)
14.Patients with chronic diarrhea are at increased risk of what?: FLUID LOSS
15.Infectious gastroenteritis caused by: -Viral pathogens
-Bacterial pathogens
-Parasitic and helminthic pathogens
16.Viral pathogens of infectious gastroenteritis:
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Med Surg/ Pediatrics Exam 2 - Pedi GI Review

  1. Why are infants and children more at risk than adults for dehydration?: The have more total body water (TBW) -greater/more rapid fluid loss -more insensible fluid loss
  2. TBW of premies and infants: premie 90% infant 75%
  3. TBW of late adolescents: 45%
  4. What age does the total body water start equaling adults?: about 2 y/o
  5. Examples of insensible fluid loss: -Fever -Respiratory tract -Heat & humidity -Respiratory rate -Skin
  6. Examples of sensible fluid loss: -Urine -Feces -Emesis
  7. Labs for dehydration: ‘H & H, specific gravity, BUN, creatinine “serum sodium, potassium, chloride, magnesium
  8. How do you treat Mild to Moderate Dehydration?: -Pedialyte -ORAL fluids When rehydrated resume regular diet
  9. How do you treat severe dehydration?: §Initial IV infusion of 20ml/kg of NS or LR §Reassess and may need 1 ½ fluid maintenance
  10. If a patient is vomiting, what position would you put them in?: Side lying to prevent aspiration
  11. If a patient is vomiting, how will you reintroduce their regular diet?: start w small amounts of water/ food
  12. Acute diarrhea in infants most likely: Roatvirus!
  13. If a patient is vomiting, what will you rehydrate them with?: Rehydrate with glucose-electrolyte solution, IV fluid (D5NS?)
  14. Patients with chronic diarrhea are at increased risk of what?: FLUID LOSS
  15. Infectious gastroenteritis caused by: -Viral pathogens -Bacterial pathogens -Parasitic and helminthic pathogens
  16. Viral pathogens of infectious gastroenteritis:

Rotavirus Norwalk virus Cytomegalovirus (CMV)

acute diarrhea?: They can slow motility and prolong the illness

  1. Patient must do what before giving potassium?: VOID
  2. What kind of temperature should a nurse not do on a kid with chronic diarrhea: rectal temp
  3. What should the nurse do with the diapers of a baby with chronic diar- rhea?: Weigh all diapers and note the characteristic of stool
  4. How to prevent diarrhea?: fecal-oral route -Handwashing!!! -Clean water supply -Careful food prep -Rotavirus vaccine -dont go to school w diarrhea
  5. Hypertrophic Pyloric Stenosis (HPS): Circular muscle of the pylorus becomes hypertrophied causing thickness Occurs between 3-6 weeks of life
  6. Hypertrophic Pyloric Stenosis (HPS) what will the nurse palpate?: Olive when palpating the RUQ
  7. Hypertrophic Pyloric Stenosis (HPS) s/s: -Vomiting small amounts of milk -Progressively gets worse -No longer keep any milk/formula down -Forceful Projectile Vomiting -They will still be hungry! not in pain just cant keep anything down
  8. Severe dehydration symptoms: sunken fontenelles, dry mucus membranes, sunken eyes, poor skin turgor
  9. Nursing interventions for Hypertrophic Pyloric Stenosis: Fluid management Family anxiety Post Op: Oral feedings can slowly resume after 1-2 days
  10. Treatment of Hypertrophic Pyloric Stenosis: pyloromyotomy
  11. Oral Candidiasis (Thrush): Fungal infection of the oral mucosa
  12. Who is at risk for thrush?: -Common in infants -Immune disorder -Corticosteroid inhalers -Immune system suppression (chemo) -Antibiotic use -Can be transmitted during breastfeeding

-NO TUMMY TIME

  1. When is the cleft palate usually repaired?: 9-18 months
  2. Post Surgical Nursing Considerations for Cleft Palate: -Elbow restraints, encourage bonding -Monitor respiratory status -Assess for infection -May lie infant on abdomen or side -Monitor fever and pain -Soft food items -Avoid placing anything in mouth that can damage surgical repair -Suction, tongue depressors, spoons or straws
  3. Esophageal Atresia (EA) &Tracheoesophageal Fistula (TEF): Rare malfor- mations that results in a failed separation of the esophagus & trachea.
  4. Atresia (EA): closure of esophagus medical emergency
  5. Fistula (TEF): trachea/ esophagus connect
  6. 3 C's symptoms of EA and TEF: Coughing, Choking, Cyanosis
  7. s/s of EA and TEF: -Infant with excessive amount of frothy saliva from nose and mouth -3 C's = Coughing, Choking, Cyanosis -Apnea -Increased respiratory distress during feeds -Abdominal distention -The exact anomaly is diagnosed by x-ray -If polyhydraminous is seen on ultrasound it may be an indication of EA -Most are dx soon after birth via xray.
  8. Nursing care of EA/TEF: -Assess the newborn for S & S of EA or TEF with 1st feed = look for the 3 C's -Intermittent or continuous suction to blind pouch -NPO, IV fluid, ‘ HOB -Prophylactic broad spectrum antibiotics: prevent pneumonia -Ongoing resp. assessment, airway management, thermoregulation, fluid & elec- trolyte management & nutritional support
  9. What is Associated tracheomalacia of EA/TEF: A weakness in the tracheal wall that occurs early in fetal life.
  10. Omphalocele: -Congenital defect of the umbilical ring involving the anterior abdominal wall -Abdominal contents enter the external peritoneal sac -Organs in the sac are usually normal and malrotation is common

itself

  1. Diagnosis/ hallmark sign of Intussusception: -Air or barium enema -Hallmark sign: presence of a palpated SAUSAGE shaped mass in the upper midabdomen.
  2. Intussusception s/s: -Belly pain occurs often. -At first it may seem to be colic.

-Straining -Knees drawn up -Extreme irritability

  • Vomiting
  • Bloody stool
  • Red, jelly-like stool
  • Fever
  • Extreme tiredness or lethargy
  • Vomiting bile
  • Diarrhea
  • Sweating
  • Dehydration
  • Swollen belly
  1. Umbillical hernia usually goes away how?: On its own
  2. Intussusception treatment: Hydrostatic reduction... ...is a nonsurgical procedure. Either barium or a water soluble contrast with forced air pressure is used to reduce the Intussusception. -Successful in 80% of cases -Recurrence may occur
  3. Nursing considerations for Intussusception: -Prepare parents and child for procedure -IVF if dehydrated -If child passes brown stool it usually is an indication that Intussusception has reduced itself.
  4. Malrotation & Volvulus: -Congenital disorder -Intestine is abnormally attached and the mesentery narrows Volvulus occurs when the intestine twists on itself causing obstruction
  5. Malrotation & Volvulus s/s: -usually the 1st few weeks of life -Bilious vomiting, abdominal pain, distention, hypoactive bowels sounds, bloody stools, tachycardia, shock, necrosis.
  6. Malrotation & Volvulus management: A Ladd surgical procedure
  7. Appendicitis: ages: 10-12 y/o peak Dull, steady pain Rebound pain/tenderness in RLQ at mcburneys point
  8. Appendicitis sudden pain relief could mean what??: it could have ruptured!! sepsis OR STAT
  1. Management of GERD in infants: -HOB elevated 30 degrees for 45 minutes after feeds -Home apnea monitor for infants prone to ALTE -CPR education for parents & caregivers -Diet -Small frequent feeding -Thickened feeding with cereal
  2. Medications for GERD: Histamine2 receptor antagonists: ranitidine (Zantac), famotidine (Pepcid) Proton pump inhibitors: esoeprazole (Nexium,) lansoprazole (Prevacid), pantoprazole (Protonix), omepra- zole (Prilosec)
  3. Nursing Considerations for GER: -Identifying children with symptoms -Education -Feeding, positioning, medications -Reassure parents that most children outgrow GER
  4. Surgery for GERD in infants: Nissen Fundoplication
  5. complications of Nissen Fundoplication: -Breakdown of the wrap -Small bowel obstruction -Abdominal bloating -Infection -Retching -Dumping syndrome
  6. Constipation: An alteration in frequency, consistency, or ease of passage of stool.
  7. Encopresis: -Fecal impaction causing leakage of diarrhea around fecal mass. -Can have a psychosocial impact on child due to frequent soiling.
  8. functional cause of constipation: -Child holds stool due to painful experience during defecation -Sexual abuse
  9. secondary causes of constipation: -Strictures, failure to pass meconium by 24 hours after birth, Hirschsprung disease, hypothyroidism, chronic lead poisoning, spinal cord lesions or injury.
  10. drugs that cause constipation: Antacids, diuretics, antiepileptics, antihista- mines, opioids and iron supplementation.
  11. Treating constipation: -Change diet, add fiber & fluids, eliminate constipating foods

Bottle fed infant- increase carbohydrate (sugar or corn syrup) in formula

-Pain assessment and management

-Maintain hydration -S & S infection

  1. Malabsorption Syndromes: Characterized by chronic diarrhea and malab- sorption of nutrients that may result in failure to thrive (FTT) digestive, absorptive, and anatomic defects
  2. Digestive defects malabsorption syndromes: Cystic fibrosis, biliary or liver disease, or lactase deficiency
  3. Absorptive defects malabsorption syndromes: celiac disease or secondary to ulcerative colitis and Hirschsprung.
  4. Anatomic defects malabsorption syndromes: extensive resection of the bowel, known as short bowel syndrome.
  5. Celiac Disease: -Inappropriate immune response to ingested gluten proteins found in wheat, rye & barely. -Damage to the vili in the small intestines -Genetic predisposition, autoimmune disorders
  6. Four characteristics of Celiac Disease: -Steatorrhea -Fatty, foul, frothy, bulky stools -General malnutrition -Abdominal distention -Secondary vitamin deficiencies
  7. Nursing Considerations for Celiac Disease: -Encourage adherence to diet: diet high in calories and protein, with simple carbohydrates such as fruits & veggies and low in fat. -Celiac Support Association in America (celiac.com) that provide educational mate- rial, support and recipes.
  8. Gluten free foods: fruits/ veggies, beans/lentils, dairy, nuts/seeds, eggs, flax seeds, soy, red meat, fish, poultry, quinoa, black wheat, millet, corn, rice, potato flour
  9. Biliary Atresia: -Absence of some or all of the biliary ducts -Causes bile duct obstruction -Progressive fibrosis with end-stage cirrhosis of the liver
  10. Biliary Atresia s/s: -Jaundice (Most common early symptom) -Dark urine that stains diapers -White or tan stools -Foul-smelling stools -Abdominal distention: hepatomegaly -Poor weight gain, FTT

-Irritability -Difficult to console

  1. Therapeutic Management - Biliary Atresia: -Kasai procedure creates an artificial portal to allow the liver to drain into the intestines as it should normally function -Improves prognosis but is not a cure -Liver transplantation -If Kasai unsuccessful, done by age 2. If untreated, death by 2 y/o
  2. Nursing Considerations - Biliary Atresia: -Fat soluble vitamin (DEKA) -Special formula (Medium-chain) triglycerides -NGT feeds (High calorie) -Assess for infections (IV antibiotics as needed) -Diuretics and dietary restrictions (manage ascites) -Support family (high anxiety d/t prognosis)