Exam 3 Peds GI Flashcards

(81 cards)

1
Q

When is an infant’s GI tract mature?

A

Age 2

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2
Q

Why is the mouth an optimal point of infection entrance?

A

?

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3
Q

What prevents regurgitation of stomach contents into the esophagus?

A

Lower esophageal sphincter (LES)

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4
Q

When is the LES developed?

A

1 month

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5
Q

What is the stomach capacity for newborns?

A

10-20 mL

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6
Q

What is the stomach capacity for infants?

A

200 mL

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7
Q

What is the stomach capacity for a 16 year old?

A

1,500 mL

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8
Q

When do pancreatic enzymes reach adult levels?

A

2 years

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9
Q

Liver at birth

A

Large, easily palpated

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10
Q

If infants have small bowel loss what happens?

A

Chronic problems with absorption and diarrhea

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11
Q

Small intestines at birth

A

Not fully functionally mature, rapid growth spurts

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12
Q

Physical exam order

A

Inspect and observe
Auscultation
Percussion
Palpation

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13
Q

2 categories of food sensitivity

A

Allergy/hypersensitivity

Intolerance

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14
Q

Systemic effects of food sensitivity

A

Anaphylactic, growth failure

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15
Q

GI effects of food sensitivity

A

Abdominal pain, vomiting, cramping, diarrhea

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16
Q

Respiratory effects of food sensitivity

A

Cough, wheezing, rhinitis, infiltrates

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17
Q

Cutaneous effects of food sensitivity

A

Urticaria, rash, atopic dermatitis

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18
Q

What can help prevent food sensitivity?

A
Breastfeeding
No solids for first 6 mo
No whole milk until 12 mo
No eggs until 24 mo
No peanuts, nuts, fish, seafood for 36 mo
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19
Q

How do you identify possible reactions to food?

A

Add one new food at 5 day intervals

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20
Q

Cow’s Milk Allergy

A

Adverse systemic and local GI reaction to cow’s milk protein

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21
Q

When can cow’s milk allergy be seen?

A

Within the first 4 months of life

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22
Q

What are GI symptoms of cow’s milk allergy?

A

Diarrhea, committing, colic, abd pain

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23
Q

What are respiratory symptoms of cow’s milk allergy?

A

Rhinitis, wheezing, sneezing, eczema, excessive crying, pallor

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24
Q

How do you diagnose cow’s milk allergy?

A

Occult blood
Serum IgE levels
Allergy testing
Milk restriction followed by challenge test

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25
Treatment of cow's milk allergy
Elimination of cow’s milk based formula | Continue until one year old, then small amounts are reintroduced
26
Nursing care management for cow's milk allergy
Prevent and reduce exposure of infants to cow’s milk protein (through exclusive breastfeeding for the first 4-6 months) Help parents identify signs and symptoms Teach parents when introduce solid foods to be aware of those that contain milk Educate on re-introduction of milk products after one year
27
Happens much more quickly in infants and children than adults due to differences in A&P
Dehydration
28
Why must dehydration be recognized quickly?
To prevent hypovolemic shock
29
Occurs whenever the total output of fluid exceeds the total intake
Dehydration
30
Causes of dehydration
``` Vomiting/Diarrhea Decreased oral intake High fever DKA Burns, insensible losses Increased renal excretion ```
31
Fluid balance and losses compared with older children and adults
Infants have a greater need for water and have more alterations in fluid and electrolyte balance
32
Expanded extracellular compartment lasts how long?
Age 2
33
Expanded extracellular compartment
Constitutes more than half of their total body water, causes greater and more rapid water loss
34
Fluid losses are divided into what 3 types?
1. Insensible 2. Urinary 3. Fecal
35
Insensible fluid losses
Fever increases fluid loss Increased Body Surface Area (BSA) in infants and children increase fluid loss Basal metabolic rate is higher than adults Kidneys are immature and cannot concentrate urine
36
Nursing assessment for fluid loss
Mental status Fontanel Eyes Oral mucosa Skin turgor Heart rate Blood pressure Extremities – capillary refill Urine output – specific gravity Table 41-1 – mild vs. moderate vs. severe *Must accurately measure intake and output Intake – anything that goes in the mouth/IV/tube feedings Output – anything that comes out – urine, stool, emesis, sweat, drainage
37
Nursing care management for insensible fluid loss
Must restore fluid volume Replace ongoing losses 1:1 Offer at frequent intervals and small amount Do NOT manage by encouraging intake of clear liquids other than ORS or BRATT diet IV fluids – used for severe dehydration or shock Observe for s/s of dehydration Need at least 1 cc/kg/hr of urine output Probiotics may decrease the extent of diarrhea Lactobacillus (Culturelle)
38
Constipation
Alteration in the frequency, consistency, or ease of passing stool Passing hard, dry stools, often painful Liquid stools around hard stools Bowel habits vary between children Meconium stools ``` Assessment signs and symptoms What are normal bowel habits?? Abdominal distention Inspect for any anal fissures Bowel sounds ``` KUB and stool studies
39
Nursing care management for constipation
Change dietary habits Increase high-fiber foods and fluids Eliminate constipating foods Behavior modification Positive reinforcement Scheduled times to sit on toilet
40
Hirschprung's Dz
Absence of ganglion cells in the bowel Also called congenital aganglionic megacolon Causes inadequate peristalsis in part of the intestine Males affected 4x more than females Associated with Down syndrome
41
Therapeutic management for Hirschsprung's Dz
Surgical resection of aganglionic bowel to relieve obstruction and restore normal bowel motility 1st surgery to create ostomy 2nd surgery to “pull-through” the healed intestines to rectum and close ostomy
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Nursing care management for Hirschsprung's Dz
Provide Postoperative Care Observe for complications of enterocolitis ``` Provide Ostomy Care Ensure proper function of stoma Daily ostomy care Skin care Diet: avoid foods that produce excess gas and constipation ``` Patient and Family education Explain surgical procedure Educate on stoma care Medications
43
GERD
Passage of gastric contents into the esophagus Occurs during episodes of transient relaxation of LES Common during first year of life
44
Nursing assessment for GERD
Assess for signs and symptoms and risk factors Ask parents what they observed Physical exam May appear malnourished Assess for aspiration and breathing patterns Diagnosis Upper GI/EGD pH probe – gold standard Hemoccult stool
45
Therapeutic management for GERD
``` Modify feeding habits Appropriate positioning Elevate HOB during feeding and for 30 min - 1 hour after Smaller more frequent feeds Thicken feeds with rice cereal Avoid foods known to cause reflux Medications Histamine-2 blockers (Zantac, Pepcid) Proton Pump Inhibitors (Nexium) Prokinetics (Reglan) ``` Surgical intervention Nissen fundoplication
46
Nursing care management for GERD
Promote safe feeding techniques Monitor vomiting Weight daily Maintain patent airway Risk for aspiration and ALTE Post-operative care ``` Parent education Feeding Positioning Medications NG care/Apnea monitor ```
47
Hypertrophic Pyloric Stenosis
The circular muscle of the pylorus becomes hypertrophied creating a gastric outlet obstruction Compensatory dilation, hypertrophy, and hyperperistalsis of stomach Infant usually presents at 2-5 weeks old with a history of projectile nonbilious vomiting Other symptoms include: Hard, moveable “olive” mass is the RUQ, no pain Hunger soon after vomiting Wt loss, dehydration, and electrolyte disturbancesCircular muscle thickens  severe narrowing of the pyloric canal (olive shaped mass)  obstruction  vomiting  dehydrated, lethargic, malnourished
48
Nursing care management for Hypertrophic Pyloric Stenosis
Requires surgical intervention (pyloromyotomy) Preop care: Assess laboratory values/physical exam for dehydration Restore hydration and electrolyte balance Monitor VS - dehydration Strict intake and output - NPOPostop care: May have vomiting, pain feedings begun 4-6 hours post op (clears then formula) Monitor tolerance of feedings Incision site care Strict intake and output Provide emotional support for anxious family
49
Intussusception
Occurs when a proximal segment of bowel “telescopes” into a more distal segment Pulls the mesentery with it Most common at ileocecal valve Can result in lymphatic and venous congestion and bowel wall edema Leads to obstruction, infarction, and perforation Venous engorgement leads to leaking of blood and mucous into intestinal lumen Forms the classic “currant jelly” stools
50
Nursing assessment for intussusception
``` Look for common signs and symptoms Sudden onset of intermittent abd pain Child screaming and drawing knees to abdomen but comfortable in between episodes Distended, tender abdomen Vomiting/Diarrhea Currant-jelly stools or bloody ``` Palpate the abdomen for sausage-shaped mass in the upper-mid abdomen Ultrasound, Pneumo/Saline/Barium enema Surgical reduction
51
Nursing care management for intussusception
IV fluids/NPO Monitor for adequate hydration and nutrition May need abx and NG tube before intervention Monitor for return of normal bowel function after enema or surgery Passage of a normal brown stool usually indicates that the intussusception has reduced itself Can d/c home once tolerating feedings Reoccurs in 1 out of 10 patients
52
Cleft lip and cleft palate
Facial malformations that occur during embryonic development Frequently occurs with other anomalies Can occur individually or together and can be unilateral or bilaterally ``` Causes include Maternal smoking and alcohol consumption Prenatal infection Medications used during pregnancy- anticonvulsants Advanced maternal age ``` Involves the care of a multidisciplinary team
53
Cleft lip
Can involve only the lip or extend into the nostril Can be diagnosed by prenatal ultrasound or at birth by classic appearance Significant emotional reaction in parents Repaired surgically at 2-3 months old Z-plasty or Millard technique
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Cleft palate
Can involve both the hard and soft palate Not as obvious as cleft lip Can be seen when mouth examined Management directed at: closure of cleft prevention of complications normal growth and development Repaired surgically at 6- 12 months
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Nursing care management for cleft lip/palate
Immediate problems related to feeding and parent reaction Encourage infant-parent bonding, provide emotional support ``` Feeding can be difficult, must educate parents Infants have a reduced ability to suck Must feed in upright position Need to start feeding as soon as possible after birth Special cleft lip/palate nipple used Burp frequently Breastfeeding usually most effective Risk for aspiration Risk for failure to grow ```
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Preop care for cleft lip/palate
Preoperative Educate parents on what to expect Place elbow restraints on infant
57
Cleft palate postop care
Allowed to lie on abdomen after surgery May resume feeds after surgery Usually through syringe or soft sipee cup Sent home on soft diet Avoid the use of tongue depressors, thermometers, pacifiers, spoons, or straws Packing in place – will remove after 2 to 3 days Watch for respiratory complications, risk for aspiration Suction with extreme caution! Elbow restraints in place to prevent injury to mouth and continued for 7-10 days Pain medication as needed – want to avoid crying
58
Complications/Prognosis of cleft lip and palate
Feeding difficulties Upper respiratory infections Altered dentition Delayed speech development, will need speech therapy Chronic otitis media, possible hearing loss Long-term social adjustment
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Ingestion of injurious agents
``` Very common in pediatrics Cosmetics and personal care products Cleaning products Plants Foreign bodies, toys Medications ``` Often occur in the home or relatives house Infants and toddlers explore their environment through oral experimentation Very curious Imitation
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Emergency tx for ingestion of injurious agents
Call Poison Control Center Will develop a plan of care Treat the child first, not the poison Immediate concern is life support Vital signs, respiratory, circulation Gastric Decontamination Specific antidotes for certain poisons Would like to originally prevent Parents need education on how to prevent recurrence
61
Heavy metal poisoning
Ingestion of a variety of substances Lead Iron Mercury Treatment involves chelation therapy
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Tracheoesophageal Fistula (TEF)
Failure of the trachea and the esophagus to separate Proximal- ends in a blind pouch Distal- connected to the trachea or bronchus Commonly associated with VATER or VACTERL
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Biliary Atresia
Inflammatory Process that causes intrahepatic and extrahepatic bile duct fibrosis with eventual obstruction
64
Biliary Atresia tx
Hepatic portoenterostomy Intestine anastomosed to help bile drainage Liver transplant later Nutrition support
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Omphalocele
Protrusion of intra-abdominal viscera- out pouching from umbilical cord- contents covered in peritoneum without skin Surgical Repair
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Nursing care for omphalocele
``` Protect sac from drying or trauma Keep soaked with saline soaked dressings Maintain temperature Prophylactic antibiotics After surgery- bowel decompression, pain management ```
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Gatroschisis
Protrusion of intra-abdominal contents- no peritoneal sac covering the exposed bowel Surgical repair Sometimes requires gradual reduction of contents into the abdomen
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Nursing care for Gatroschisis
Same as Omphalocele EXCEPT: NG decompression Observe exposed bowel for necrosis or color change Post op- Monitor lower extremities- pulses and perfusion Siloh Pouch
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Total Parenteral Nutrition
``` Why do we need TPN? Side effects/Adverse events Know the patho behind patient’s illness to know what is in the TPN Evaluate patients response Weight gain Bloating Electrolyte imbalance Central access unless less than 12.5% dextrose Sometimes they will add meds Liver testing Other metabolic labs ```
70
What is the treatment of choice for mild dehydration?
Oral rehydration treatment
71
After initial rehydration what may be used as maintenance fluid therapy?
ORS and alternate with formula/breastmilk or regular diet
72
Meds for fluid loss
If bacteria or parasitic causes may need antibiotics or antiparasitics Metronidazole, Vancomycin *Antidiarrheals not recommended Educate parents- Rotavirus oral vaccine (3 doses at 2, 4, and 6 months)
73
Meds for constipation
Medications and enemas Stool Softeners (colace) Laxatives (Miralax, Milk of Magnesia, Lactulose) Pediatric Fleets Enema, Milk and Molasses enema
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Health history for Hirschsprung's Dz
Newborn stool patterns
75
Physical exam for Hirschsprung's Dz
Inspect and palpate abdomen for distention
76
Lab and diagnostic tests for Hirschsprung's Dz
Barium enema Rectal biopsy to evaluate for absence of ganglion cells Absence of ganglion cells causes contraction which leads to obstruction Stool collects = distention, leading to ischemia and enterocolitis
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GERD clinical manifestations in infants
Spitting up, forceful vomiting Excessive crying, arching of back Wt loss, growth failure Respiratory problems, ALTE
78
GERD clinical manifestations in children
Heartburn, abdominal pain, non cardiac chest pain | Chronic cough, dysphagia, recurrent PNA
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Postoperative CL Repair
Must protect the operative site!! Place elbow restraints Prevent infant from rolling onto abdomen Will be supine immediately after surgery then can go into infant seat Adequate pain relief – want to avoid crying Clear liquids once recovered from anesthesia
80
Clinical manifestations of TEF
``` Excessive salivation Coughing Choking Cyanosis Apnea/ respiratory distress Abdominal distention Immediately NPO Prone position to aid in the drainage of secretions Low intermittent suction in the blind pouch via a catheter One surgery or several staged surgeries ```
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Clinical manifestations of Biliary Atresia
``` Jaundice Dark urine Light color (tan) stool Hepatomegaly Poor weight gain Growth retardation Pruritus Irritability ```