Lecture 04 GI Dysfunction Flashcards

1
Q

What are 5 different ways that a child’s GI is different from an adult’s?

A
  1. Increased peristalsis/ smaller capacity; stomach empties faster
  2. Decreased gastric aciditiy
  3. Immature GI system (affects digestion of some food)
  4. Infants have no bowel control and increased sensitivity to taste
  5. Immature liver function
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2
Q

Read and state 5 signs of GI dysfunction in children

A
  1. }Growth Failure
  2. }Spitting
  3. }Vomiting
  4. }Nausea
  5. }Constipation
  6. }Encopresis
  7. }Diarrhea
  8. }Hypo, hyper, absent bowel sounds
  9. }Abdominal distension
  10. }Abdominal pain
  11. }GI bleeding
  12. }Jaundice
  13. }Dysphagia
  14. }Dysfunctional swallowing
  15. }Fever
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3
Q

What is Hirschsprung’s Congenital Aganglionic Megacolon?

A
  • Ganglion cells are absent in portion of bowel, which results in lack of peristalsis, causing enlargement proximal to defect
  • Most common area affected is anorectum, but can occur at any part
  • Colon can become very distended, with build up fecal material
  • May be asymptomatic several weeks after birth.
  • Diagnosis by rectal biopsy
  • It’s difficult to pass stool
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4
Q

Hirschsprung’s Assessments (6)

A
  1. •Cardinal Sign delayed passage off meconium for 24-48 hours after birth
  2. •Meconium ileus
  3. •Signs of obstruction; lack bowel sounds, abdominal distention
  4. •Food refusal or vomiting
  5. •Ribbon-like, foul smelling explosive stool with digital exam
  6. •Extreme (older children) or intermittent recurring constipation
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5
Q

How would you treat Hirschsprung?

A

Surgical Correction

  • }Treatment with enema regime. Repair may be primary take down or two stage with surgical repair with temporary colostomy followed by later re-anastomosis. Both with removal of aganglionic bowel

Post-operatively

  • }Pain control
  • }IV antibiotics 48 to 72 hours post-op
  • }NOTHING per rectum
  • }NPO until return of bowel function
  • }NG Tube to prevent abdominal distension (primary); monitor losses
  • }Teaching includes ostomy care for children with two stage repair
  • }What is a priority assessment post-op for any patient? ALWAYS assess for airway, don’t get distracted by post op part
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6
Q

What is GER?

Common in what type of people?

A

Ger is transfer of gastric contents back into the esophagus, though to occur from transient relaxation of lower esophageal sphincter.

It’s common in preemie babies. About 1.2 of babies less than 2 months old have this, and it’s resolved by 1 year of age.

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7
Q

What are some GER complications?

A

Frequency and persistence make this problematic

Complications include: FTT, bleeding, respiratory symptoms. Asthma is an issue. Can lead to GERD.

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8
Q

Assessment of Reflux?

A
  1. excessive spitting/forceful vomiting
  2. FTT, weight loss
  3. Aspiration, may lead to apnea and respiratory infection
  4. arching and irritability
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9
Q

What are the general intervention steps for GER?

A

At first none, symptoms typically diminish between 8 weeks to 6 months and resolve by year 1.

Muscale develops and becomes stronger.

If symptomatic with weight loss or aspiration, first medical management attempted, then surgical intervention.

Surgical interventions would invovle suture in muscle to tighten it.

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10
Q

What are some anti reflux precatuions?

A

Initiate anti reflux precautions

  • ◦Small, more frequent feeds
  • ◦Frequent burping/bubbling after every ounce
  • ◦Thickened formula: stays in stomach
  • –1 tsp - 1 Tbs rice cereal/oz formula
  • –may need larger hole in nipple
  • ◦Breast fed less likely to have GER: Ó transit time
  • ◦Positional therapy: upright 30 degrees after meals to Ô vomiting; may offer pacifier
  • ◦Prone positioning only in severe cases (AAP Safe Sleep 2011)

May require NG feeds if reflux severe and poor weight gain

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11
Q

What are aspiration risk factors for NG Feeds? (5)

A
  1. Sedation
  2. Coughing
  3. Artificial Airway
  4. Nasotracheal suctioning
  5. Decrease LOC
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12
Q

What occurs during the surgical treatment of GERD? (2)

A
  1. Nissen Fundoplication, 360 degree wrap of stomach fundus around esophagus.
  2. Gastrostomy tube is placed at the same time and feeding resumes through the G tube

PO feeds occur when post op swelling goes down, signs would be pt drooling less, tolerating secretions

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13
Q

Severe GER prognosis?

A

If it can’t be medically manged, it’ll elad to esophageal strictures and scarring, respiratory distress, aspiration pneumonia, and FTT

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14
Q

What is Acute Appendicitis?

Caused by?

Common when?

A

Acute Appendicitis is inflammation of vermiform appendix (blind sac at the end of cecum), caused by bacterial infection.

Most common organsim is E. Coli.

Most common ab surgery in childhood.

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15
Q

What can acute appendictis lead to?

A

Acute episodes can quickly progress to perfortation and peritonitis.

early signs are often mistaken for other illnesses.

Rarely occurs in children less than 2 years old.

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16
Q

Appendictis Assessment

A

Pain
◦Initially pain generalized or periumbilical
◦Pain descends to lower right quadrant with most intense pain at McBurney point
◦Colicky abdominal pain & tenderness◦Rebound tenderness, guarding (very painful) (Rovsing sign)
◦Referred pain indicates presence of peritoneal irritation

  • }Nausea, vomiting & anorexia usually after onset of pain
  • }May see diarrhea/constipation, lethargy, poor feeding, irritability
  • }Labs include: Elevated WBC (15,00 to 20,000) with elevated % bands (shift to the left) indicating inflammatory process
  • }Increasing erythrocyte sedimentation rate may indicate worsening condition.
  • }Ultrasound or CT may be used to confirm
  • }Diagnosis not always straightforward and delay may lead to perforation

Temp

  • ◦Low grade (non perforation)
  • ◦ >39 C (102.2 F) may indicate perforation or viral illness
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17
Q

How do you know when perforation occurred?

A
  1. Signs of peritonitis, plus increased fever, and sudden relief from pain after peroration.
  2. Ab distention usually increases with return of pain diffuse, and accompanied by rigid guarding of abs
  3. Tachycardia
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18
Q
A
19
Q

What does peritonitis Assessment include? (5)

A
  1. Distended abs
  2. Rigid, boardlike abdomen
  3. Diminishing bowel sounds
  4. Inability to pass gas or feces
  5. fever
20
Q

How would you treat a ruptured appendix?

A

Pt may be on medical management, which invovles: broad spectrum antibiotic, NG tube for feeding, IV fluids.

Or srugical treatment, where post op care involves: zosyn, pain meds, NPO, and may have drain

hospitalization is long, 2~3 weeks for ruptured appendix

21
Q

What’s the difference between Ulcerative Colitis and Crohn’s Disease?

A

Ulcerative Colitis is limited to colon and rectum

Crohn’s Disease invovles any part of the GI, from mouth to anus

22
Q

What is the dif between cleft lip and cleft palate?

A

Cleft lip is failure of the oral cavitt fusing.

Clef palate is the failure of the fusion of palatal structures.

Both may occur separately, but more often together.

23
Q

What may cleft lip and cleft palate be associated with you?

A
  1. omphalocele
  2. TE fistula
  3. Skeletal dysplasia
24
Q

What are two priorities of Post op cleft lip repair?

A
  1. Airway position: upright position to prevent aspiration of secretions. Supine to prevent rubbing suture line.
  2. Protect Suture Line: Logan bar, lip protection device, Arm/Elbow Restraints, comfort measure to decrease crying, Cleanse suture line since infection/inflammation interferes with healing and cosmetic effects.
25
Q

What is TE fisutla?

A

Congenital condition with an abnormal opening between trachea and esophagus and/or blind pouches of trachea and esophagus

26
Q

What are clinical manifestations of TEF? What are 3 cardinal symptoms?

A

Clinical manifestation: excessive frothy mucous, drooling, choking, sneezing & coughing with feeds, regurgitation through mouth and nose, cyanosis, apnea and inability to pass catheter into stomach.

Three cardinal symptoms: Coughing, Choking, Cyanosis

27
Q

What is a hernia?

A

Protrusion of bowel through abnomrla opening in the abdominal wall (umbilicus and inguinal canal are common locations in children)

28
Q

What are hydroceles?

A

Abdominal fluid in scrotal sac. Typically resolves on it’s own.

29
Q

What’s the difference between Incarcertaed hernia, strangualted hernia and inguinal hernia?

A

Incarcerated hernia cannot be easily reduced.

Strangulated hernia is one in which the blood supply to herniated organ is impaired EMERGENCY.

Inguinal hernia can be repaired while asymptomatic, less complications.

30
Q

What is Hypertrophic Pyloric Stenosis?

A

When an infant has pyloric stenosis, the muscles in the pylorus have become enlarged and cause narrowing within the pyloric channel to the point where food is prevented from emptying out of the stomach.

31
Q

What is intussusception?

A

Intussusception is telescoping/invagination of one portion of the bowel into another, resulting in obstruction.

32
Q

S/S of intussusception?

A

Causes inflammation, edema, decreased blood supply to intestine, bower necrosis, hemorrhage, perforation and peritonitis

33
Q

Intussusception Assessment

A

}Acute onset

}Severe colicky abdominal pain with vomiting and currant jelly stools (blood & mucous)

}Palpable sausage shaper mass in URQ

}Abdomen tender and distended

}Classic symptoms may not appear in many children

}Diagnostic tests include abdominal radiographand ultrasound

34
Q

How is Intussusception treated?

A
  • }Hydrostatic reduction (if no perforation) guided by ultrasound with air or water soluble contrast
  • }Force of air pressure or water soluble contrast may relieve obstruction without need for surgical intervention

}Pre-operatively/Pre-reduction

  • ◦Monitor for signs perforation/peritonitis

}Post-operatively/Post-reduction

  • ◦Routine post-op care (pain meds, antibiotics, +/- NG to LIWS, NPO until bowel function)
  • ◦IV replacement of gastric output volumes
  • ◦Monitor for return of normal colored stools and signs of obstruction recurrence (most common first 24 hours)
35
Q

what is an imperforate anus?

A

failure of the membrane separating the rectum from the anus to absorb during fetal life

36
Q

What’s the primary assessment of anorectal anomaly?

A

Failures to pass meconium in first 24 to 48 hours is primary assessment

37
Q

What are 3 Malabsorption Syndromes?

A
  1. Carb/lactose intolerance
  2. Celiac Disease
  3. Short Gut/ Short Bowel
38
Q

What are assessment findings and interventions of carb/lactose intolerance?

A

Assessment Findings

  • –Loose, foul smelling stools
  • –Colicky, fussy behavior
  • –Excessive spitting or vomiting with feeds
  • –FTT
  • –Sugar in stools

Interventions

  • –Soy based formulas (may need to try several)
39
Q

What is Celiac Disease?

A

Auto immune response to gluten, a protein substance found in rye, oat, wheat &barley

40
Q

Assessment and intervention of Celiac Disease?

A

Assessment

  • –Large greasy strong smelling stools (steatorrhea)
  • –Abdominal pain and distention
  • –FTT/small size
  • –Excessive fat in stools
  • –Deficiency in absorption of vitamins and minerals
  • –May develop intolerance to carbohydrates & protein

Interventions

  • –Gluten free diet (rice/corn only)
  • –Patient teaching to recognize food sources of gluten (food labels starch/wheat)
  • –Need for life long dietary modifications
  • –High risk for bowel cancer in adulthood if diet not followed
41
Q

What is Short Bowel Syndrome?

A

Decreased mucosal surface area, usually a result of extensive small bower resection. Leads to:

  • ◦Decreased absorption of fluids, electrolytes & nutrients
  • ◦Need for Total Parenteral Nutrition (TPN) via Central Venous Line
42
Q

What are causes of Short Bowel Syndrome?

A

}Causes Include:

◦NEC, volvulus, intestinal atresia, gastroschisis

43
Q

What are assessments and monitoring steps for lead?

A

Assessment & Monitoring

  • }Monitor CBC, chem panel & lead levels
  • }Therapeutic response (high lead levels in urine)
  • }Monitor intake and output
44
Q
A