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growth hormone deficiency
inhibits growth
primary site of dysfunction→ hypothalamus
diagnostic evaluation for growth hormone deficiency
family history
physical exam
growth patterns and health history
bone age films:
looking at the wrist
endocrine studies to detect deficiences
thyroid
growth hormones
GH stimulation
CT, MRI, Skull xray
looks for tumors that can impact growth
growth hormone deficiency- therapeutic management
biosynthetic growth hormone
somatropin (SQ injection)
other hormones replacements as needed- given at bedtimes daily
Thyroid hormone
Cortisone
Testosterone or estrogen and progesterone
GH deficiency: prognosis
GH replacement successful in 80% of affected children
Growth rate of 3.5 to 4 cm/ year before treatment and increase to 8-9 cm after treatment
Response varies based on
Age
Length of treatment
Frequency of doses
Dosages
Wt
GH receptors amount
GH deficiency: if untreated
Decreased growth
Delayed epiphyseal closure
Delayed bone age and sexual development
Premature aging
Pituitary Hyperfunction
Excess GH before closure of the epiphyseal shafts results in overgrowth of long bones
Pituitary Hyperfunction growth changes
Reach heights of 8 feet or more
Vertical growth and increased muscle
Weight is generally in proportion to height
Pituitary Hyperfunction: acromegaly
Excess GH after epiphyseal closure is called acromegaly
Typical facial features
Precocious puberty:
Secondary sexual development before age of 9 in boys and 7 ½ - 8 in girls
Occurs more in girls (breast development and growth in ht )
Precocious puberty: potential causes
Disorder of the gonads, adrenal glands, hypothalamic- pituitary gondadal axis
No causative factors in 80% to 90% of girls and 50% boys
precocious puberty treatments
treatment of specific cause is unknown
May be treated with Lupron
Slows prepubertal growth to normal rates
Treatment is discontinued at age for normal pubertal changes to resume
Psychologic support for child and family
Degree of dehydration
compare to weight before they’re sick to determine extent (% of body weight dehydrated)
Mild = 3-5% infant, 3-4% child
Moderate = 6-9% infant, 6-8% child
Severe = > 10% infant and child
dehydration: fluid loss in mL/kg/body wt (need to wt before sickness to compare
Mild = loss of 50 mL/kg
Severe = loss of 100 mL/kg
dehydration risks
electrolyte imbalance
dehydration causes
insensible water loss
urine
stool
vomiting
sweating
skin/ respiratory tract
dehydration symptoms
LOC,
irritability,
lethargy/lack of activity,
decreased response to stimulation,
decreased skin turgor/elasticity (wrinkles),
increased cap refill > 2 seconds,
increased HR,
sunken fontanelles in infants,
dry skin or mucous membranes,
coolness or mottling of extremities
mild dehydration symptoms
increased thirst,
dry mucous membranes (tacky – not a lot of saliva)
moderate dehydration symptoms
decreased tears,
loss of skin turgor,
dry mucous membrane,
normal-moderate to sunken fontanel,
cap refill 2-4 seconds
severe dehydration symptoms
weight loss (moderate),
tachycardia,
decreased BP,
extreme thirst,
tenting,
no tears and sunken eyes,
decreased urine output,
lethargy (decreased activity is a big issue)
diagnostic test for dehydration
Degree of dehydration – VS, cap refill, I&Os, BS
Type of illness
Clinical signs
Body weight
dehydration treatment
Oral rehydration first (PO or IV)
Ondansetron (Zofran) 🡪 decrease vomiting
Less expensive
Tylenol 🡪 break fever; ibuprofen only in 6 months+ (harder on the stomach though)
IV fluids if severe enough
Need education
Oral rehydration first (PO or IV) for dehydration
correct fluid imbalance, treat the cause
Only if alert/awake
Clear fluids first (ex. Pedialyte – recommended ratio for electrolytes OR Gatorade – for older kids)
IV fluids if severe enough-for dehydration
if severely dehydrated; unable to drink or drink enough to replace losses
Give small, frequent sips (want them to keep it down for a couple hours)
Via syringe or medicine cup – children may refuse to drink b/c of fear of vomiting again
If tolerating 🡪 progress to bland foods like crackers, bread, etc.
Calculation of maintenance fluid requirements in children
Purpose
Keep children hydrated and nourished, especially if child is NPO
Calculate child’s weight in kg
Allow 100 mL/kg for first 10 kg of body weight (in 24 hr period)
Allow 50 mL/kg for second 10 kg of body weight (additional)
Allow 20 mL/kg for remaining body weight (anything over 20 kg they need 20 mL more)
Add up totals and divide by 24 hrs to determine mL/hr
fluid balance- replacement
Insensible water losses- through skin, respiratory tract, urinating, defecating
If kids have high fever they will loss more fluid (12%)→ more intake of fluids
Urine and stool
fluid balance- increased requirements
Fever, tachypnea
need fluid to bring temperature down
12% increase per degree C
radiant warmer, phototherapy (preterm infants)--> increase fluids
Vomiting and diarrhea, DI, acidosis
Shock, burns, postoperative bowel surgery (have to wait/ listen for bowel sounds before eating to drinking)
fluid balance: decreased fluid requirements
Heart failure
Restrictions because they have too much fluids in the body
Increased ICP
Minimize excess fluid on the brain
Renal failure
Postop- you already get fluids through IV
GI assessment: history
pattern of elimination
What is normal for them
When did you last poops and what does it look like
round, skinny, loose and watery, hard and round
GI assessment: clinical exam and observation
Activity
Skin moisture
Mucous membranes
Lips
Do eyes appear sunken
Sunk frontalles
GI assessment: I and O
fluid balance is important, vomiting, diarrhea, breast milk not sufficient which causes decreased activity
First concern is are they dehydrated
GI assessment: wt and ht
Can’t grow properly if they have a malabsorption disorder (ex. pts with CF are short and skinny)
GI assessment: abdominal assessment
Inspect 🡪 are they distended, is it flat, does it appear enlarged, observe guarding behaviors
Circumference recorded if concerned about a potential tumor
Listen
Palpate
GI assessment: Lab tests
Stool exam
Color, amount, frequency, consistencies
O and P (ova & parasites)- look for infection
Stool Culture- looks for bacterial infections
Occult Blood Guaiac- look for blood (blue ring- blood in stool)
GI assessment: diagnositic procedures
Xray
Upper/lower GI (barium or air swallowed enema
Assess structure and function
Identify masses
May be given via NGT
Ultrasound- at invasive
MRI/CT- if there a mass
Endoscopy- in from the top
Colonoscopy- in from the bottom
Consequences of GI Dysfunction in Children:
malabsorption,
fluid and electrolyte disturbances,
malnutrition,
poor growth
vomiting causes
Acute infection, increased ICP (if they have a shunt 🡪 could be malfunction of the shunt), ingestions, food allergy/intolerance, GI obstruction, UTI, etc.
May be protective, stress induced, or learned behavior
vomiting symptoms
Forceful expulsion of stomach contents
vomiting assessment
hydration status (most important)
vomiting evaluation
Clinical evaluation
Urine analysis for ketones, specific gravity (would be elevated)
Labs – CO2 (would be elevated)
Metabolic acidosis
vomiting treatment
Give ondansetron (Zofran) to settle their stomach
Prevent complications with poisoning
Rehydration
Support of the child and family
diarrhea is caused by
abnormal intestinal water and electrolyte transport
Fecal-oral spread
Rotavirus, norovirus
Bacteria
Might be drinking too much 🡪 cut out milk to see if it’s a lactose issue
bacteria that cause diarrhea
E coli, salmonella, yersinia, C diff, clostridium, shigella, staph
Spread through food (contaminated or undercooked), contaminated water, pets
acute diarrhea
< 14 days, usually due to infection or antibiotics
chronic diarrhea
> 14 days, can be due to IBD, lactose intolerance, food allergy
Higher mortality and morbidity < 5 years
Higher incidence in low income houses and communities worldwide
diarrhea treatment
Understand and initiate appropriate treatment for mild, moderate, or severe dehydration
Rehydration*; monitor hydration (ORS guidelines)
Replace ongoing stool losses 1:1 ORS
Give in small amounts frequently (tsp, cup, syringe, NGT)
I&Os
Skin care
Maintenance fluid
Medications
Probiotics to restore good bacteria and provides bulk
Sometimes antibiotics
Education 🡪 prevention
Family support
diarrhea nutrition
Reintroduce normal diet after rehydration
Continue use of breast milk
constipation
symptom rather than a disease
constipation causes
Alteration in frequency, consistency, or ease of passage of stool
constipation is secondary to
Systemic disorders associated with it =
structural anomalies of intestine,
ectopic anus,
Hirschsprung disease,
lead poisoning,
children with spinal cord lesions (lose sensation and tone of rectum 🡪 prone to fecal retention/incontinence)
constipation is a associated with
antacids, diuretics, antiepileptics, antihistamines, opioids, iron supplements
idiopathic constipation
functional, not known cause
chronic constipation
may be due to environmental or psychosocial factors
Hard stool can cause anal fissures 🡪 pain causes stool withholding behaviors
constipation symptoms
Less than 3 stools/week, painful BMs, retained stool/stool incontinence (encopresis)
constipation symptoms in newborn
first meconium should be passed within 24-36 hrs of life, otherwise assess for…
Hirschsprung disease,
hypothyroidism,
meconium plug,
meconium ileus (CF)
constipation symptoms in infancy
Often related to diet
Constipation in exclusively BF infants is almost unknown
Infrequent stool may occur b/c of minimal residue from digested breast milk
Formula fed infants may develop constipation
constipation treatment
Increase fruit, vegetables, fluids (might use prune juice, Miralax, etc.)
constipation nutrition
Increase fiber, fluids, fruits/vegetables, exercise
Hirschsprung
Absence of ganglion cells in colon, causes decreased motility
stool accumulates, sphincter won’t relax- leads to obstruction
Hirschsprung s/s newborn
delayed meconium passage
bilious vomiting
refusing PO feeds
Abdominal distention
Hirschsprung s/s infant
FTT
Constipation
Diarrhea
vomiting
Hirschsprung s/s child
poor growth
abdominal distention
foul smelling
ribbon like stool
palpable mass (stool)
Hirschsprung diagnostic testing
CBC, Electrolytes
Rectal biopsy
determine whether ganglion cells are absent
Check for dehydrations
Hirschsprung surgery to correct
May need Daily anal dilations in future
Hirschsprung therapeutic management
Assist family with improving nutritional status
Low Fiber, High protein & calorie diet
TPN if needed
Surgery
Preoperative care-
saline enemas, antibiotics, Abdominal Circ
Postoperative care-
Daily anal dilations
Discharge planning and care
Hirschsprung two stages
Temporary ostomy
Second stage is the pull-through procedure
GER
gastric contents back up into the esophagus
Usually resolved during the first year of life
GER at risk
Preemies
CF
Chronic lung disease
neuro problems
GER diagnositic testing
UGI- checks for abnormal anatomy
24 hour PH probe- amount of reflux
Endoscopy-checks for narrowing in esophagus
GER presentation
vomiting/spitting up
Crying
Arching
Difficulty breathing/Apnea
FTT in infancy
GER children presentation
chronic cough, abdominal pain, chest pain
Therapeutic Management of GER/GERD: feeding alteration
Thickening feedings (1 tsp-TBSP rice cereal/oz formula)
AR formula= added rice (weigh it down to keep it int the cold stomach)
Upright positioning after
Frequent burping during feeds
Avoid overfeeding- small, frequent meals
Avoid offending foods
Maintain normal weight
Therapeutic Management of GER/GERD: meds
H2 receptor antagonists:
cimetidine (Tagamet), ranitidine (zantac), or famotidine (Pepcid)
Proton pump inhibitors:
esomeprazole (Nexium)
lansoprazole (Prevacid)
omeprazole (Prilosec)- reduce acid secretion, increase sphincter tone
Therapeutic Management of GER/GERD: surgery
Nissen fundoplication
Pyloric stenosis-
Constriction of the pyloric sphincter with obstruction of the gastric outlet
Pyloric stenosis- when does it occur
first few weeks of life
When baby is eating, food isn’t going to their stomach 🡪 they get hungry, they eat, they vomit, repeat (always hungry)
Pyloric stenosis- incidence
1 in 500 infants
Pyloric stenosis- diagnostic evaluation
Serum electrolytes
ABD ultrasound
Pyloric stenosis- clinical manifestations
Non-bilious projectile vomiting after eating
Constant hunger- eat and throwing up, never gets to their stomach
Olive shaped abd mass in RUQ & poss peristaltic movements
Failure to gain wt and S& S of dehydration
Pyloric stenosis- therapeutic management
surgery pylorotomy
Pyloric stenosis- nursing management
Surgery – pylorotomy (opens up pylorus/stomach to correct passage)
Preop care – correct dehydration
Postop care – feeding starts gradually
pyloric stenosis nutrition
Usually ravenous b/c they eat and then puke so it never makes it all the way down to satisfy their hunger needs
Intussusception Pathophysiology
Telescoping or invagination of one portion of intestine into another
Usually Toddlers
Intussusception classic triad of symptoms
Sudden onset of abdominal pain w/fever, vomiting and typically in toddlers
Abdominal mass “sausage like, RUQ”
Blood/mucous in stool- “currant-jelly stools” (late sign)
Intussusception Diagnostic evaluation:
US,
air enema
Can cure the issue so we don’t always know if this was the issue because air goes into the bowel and reinflates it
Intussusception therapeutic management
often cured by enema
Conservative treatment first
Air enema – usually cures it (radiologist guided; with or without contrast)
Hydrostatic (saline) enema (US guided)
Barium enema
Might surgically go in to see if bowel needs repair 🡪 surgical reduction and fixation or excision of nonviable segment of colon
Intussusception nutrition
Might not be eating b/c of pain and vomiting
Appendicitis
Inflammation due to obstruction of the lumen of the appendix by burdened stool, swollen lymph tissues or a parasite
Appendicitis clincial manifestations
Referred pain/ RLQ
Epigastric McBurney’s point
Fever, nausea, vomiting
Appendicitis diagnostic test
Detailed physical exam, history
Labs 🡪 CBC, electrolyte, UA
US of abdomen
Abdominal XR
CT (GOLD STANDARD**)
Appendicitis treatment sugery
Nonruptured 🡪 appendix is removed (laparoscopic, open surgery)
Ruptured 🡪 treat infection, clear them up, and schedule removal at a later time
Appendicitis surgery preop
NPO, IVF (fluid and electrolyte assessment), pain medications, support
Appendicitis postop
early ambulation,
pain management,
monitor temperature and surgical site (wound care),
start with clear liquids and advance as tolerated once NGT removed,
deep breathing,
assessment of BS,
supportive care
Discharge once having gas
Appendicitis treatment: perforation
IV antibiotics, NG to suction until BS return, surgical incision care
Family support; emotional support of child
Appendicitis nutrition
NPO
Clear liquids and advance as tolerated
GU physical assessment
Palpation, percussion
Not much to inspect besides urine sample
GU health history
Previous UTIs (on our radar if they’re recurrent), calculi (kidney stones), urinary stasis (not emptying bladder all the way), retention, pregnancy (have to urinate more frequently), STIs
Tea and soda can make kids more likely to have kidney stones (oscillate drinks) 🡪 need water and lemonade to decrease risk
Family history of enuresis/bed wetting (at least 2x a week for at least 3 months and at least 5 years old)
Urologic instrumentation
GU health history- medication list
Medications = antibiotics, anticholinergics, antispasmodics (decrease function of the bladder by relaxing muscles)
Desmopressin acetate = decreases urine volume
Imipramine hydrochloride = inhibits urination
Oxybutynin chloride = reduces bladder contractions
GU hygiene
harder for females if not wiping front to back
Need education on assisting females in keeping their perineal area clean
GU health history- pattern of elimination
voiding
In middle school/high school kids tend to hold their pee b/c they don’t want to leave their class
In elementary school the teachers do joint bathroom breaks at certain intervals
Expect kids to empty their bladder about 6x a day 🡪 need to tell kids this and potentially create a schedule