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Type 1 diabetes
Characterized by destruction of pancreatic beta cells, usually leading to an absolute insulin deficiency
aka low insulin levels
type 2 diabetes
Arises because of insulin resistance combined with relative insulin deficiency
normal insulin levels but it’s resistant to glucose and can’t take it into cell
sample diet menu for a child with diabetes mellitus
PB&J: fruit spread instead of jelly/jam
Mac and cheese: instead of regular pasta, use chickpeas or veggie noodles
food management in diabetes happens in 2 ways
Constant carbohydrate
Carbohydrate (“carb”) counting
constant carbohydrate
Same amount of carbohydrates for each meal so we can see how much insulin is needed
Usually a starting place and then move to carbohydrate counting
carb counting
Counting the grams of carbs in foods to be eaten
Insulin given matches the number of grams of carbohydrate
good for calculating I/C ratio
I/C ratio
insulin to carb ratio
usually one unit of insulin for each 10 g of carbohydrate
corrects what you’re abt to eat
I/C ratio protocol
Check blood sugar 2 hours after meals
Adjust I/C ratio as needed
May vary with each meal
more insulin may be needed at dinner bc we eat more
correction factor (CF)
The Correction Factor tells you how many points the blood sugar will be lowered by 1 unit of rapid acting insulin.
corrects glucose before you eat
how to use CF ratio
Used in combination with the I/C Ratio calculation to correct high blood sugars before meals.
The CF can vary at different meals/times of day according to the person’s needs.
CF factor calculation
blood glucose- target (will be given)= amount of correct
amount to correct/ correction factor (will be given)= correction bolus
if blood sugar is below target, don’t give correction amount, just I/C amount (aka amount for when your about to eat)
glucose levels
70-100
80-100 in older kids
we don’t want it below 120
s/s of hyperglycemia
glucose in urine
lots of H2O drinking
tachycardia
polyuria
tachypnea
thirsty*
ketones in blood and urine*
sweet breath*
disoriented*
unconscious*
*= DKA s/s
why are there ketones in urine with DKA
since insulin can;’t bring insulin into cell or there is an insulin deficiency, body uses protein then fat
fat gets broken down into ketones in blood (acid) which goes into urine & lungs (sweet breath)
Urine testing for ketones
not routinely used EXCEPT testing is helpful when done every 3 hours during illness and whenever the glucose level is 240 mg/dL or higher when illness is not present
insulin pumps
reserved for the kids who are the most fragile
rapid insulin
eat within 15-20 mins of getting it
regular insulin
eat within 30 mins of getting it
drinking w diabetes
be careful bc alcohol has a LOT of sugar and can affect glucose for 24 hrs
check sugar regularly before, during, and 24 hours after drinking
Why do we rotate the injections sites?
bc absorption rate is different depending on site
buttock is best place but kids don’t rlly like it
fast absorption= short duration

education w insulin pumps
they can shower pump but not go in pool
and don’t spend too long in the sun bc it can affect the medicine
tx for hypoglycemia
rule of 15
rule of 15
15 grams of a simple carb
check glucose in 15 mins
rule of 15: simple carbs
hard candy
juice
glucose tab
glucose gel*
why are glucose gels the best
bc they don’t need to be conscious to take it and you can just squirt it in their cheek
rule of 15: check glucose in 15 mins
once its in therapuetic range, give complex carb w protein to maintain level
ex: crackers w PB or cheese
sick day guidelines (aka when a kid w diabetes is sick)
seek medical attention for fever or signs of infection
monitor serum glucose levels more often
required dose of insulin may be increased
don’t skip doses of insulin
continue to maintain food and fluid intake
monitor urine for ketones
1st action in hypoglycemia
get blood sugar
quick assessment
s/s of hypoglycemia
cold clammy skin
tachycardia
dizziness
sweating
feeling shaky and irritable
hypoglycemia in a hospital setting
give glucagon sub q or dextrose bolus (D-5W) then constant infusion to keep it elevated
questions to ask when someone comes in w suspected hypoglycemia
What were you doing before
when was the last time he took his insulin
was he doing something strenuous or sleeping
did he take his glucose that morning
VS in hypoglycemia
if VS are not stable even after giving carbs and dextrose, give more carbs
regular insulin peak
2-3 hours
long acting insulin peak
no peak
What would you teach diabetics about alcohol use and managing diabetes?
check glucose before, during, and for at least 24 hours after
Hydrate while drinking
Have some food with the alcohol
Drink light beer or a seltzer bc it is lower in sugar
Can add diet sodas instead of the regular sodas and drink (diet rum and coke instead of rum and coke)
questions to ask when someone comes in w suspected hyperglycemia
When was the last time insulin was taken
How much and what type of insulin did they take
Has this happened before
are they vomiting? How often?
When is the last time they voided
Dip urine to see if there is ketones - see if the parents did that
questions to ask when someone comes in w suspected hyperglycemia w N/V: When is the last time they voided
worried abt dehydration, especially if they’ve been vomiting
no pee= dehydration
VS and electrolytes w DKA
BP = low (bc of dehydration)
HR = higher because trying to compensate for the dehydration
RR = high because compensating for the acidosis (Kussmaul)
Temp = high because of possible infection or the dehydration
Potassium = high because of trying to lessen the acidosis
contraindicated orders in DKA
LR
NPH insulin
Private room
indicated orders in DKA
bed rest with bathroom privileges
Continuous ECG monitoring
CBC, BMP stat
Intake and output with urinary output every hour
Glucose checks every hour
regular insulin IV infusion
DKA results from
progressive deterioration with dehydration
electrolyte imbalance
acidosis
coma
signs of DKA
vomiting more than twice in a 6hr period
more than 5 diarrheal stools in a day
change in mental status
high temp
sugar >400
ketones in urine
acetone breath
signs of bacterial infection
dyspnea
oliguria
dysuria (UTI signs)
IV insulin
needs 2 nurse sign off
How fast can you bring down a glucose level?
No more than 80-100 per hour
thats why we give dextrose w insulin drip once glucose hits 300 range
is someone has hyperkalemia with DKA was should we do
Continuous ECG monitoring to pick up any arrhythmias
Elevated potass can give you muscle weakness
Make sure we give insulin and IVF as ordered bc if glucose goes up usually potass goes up
Monitor for falls and seizures
Resp status
precocious puberty
Onset of puberty is too early
secondary sexual characteristics
precocious puberty ages
Too early for boy: <9 yrs
African American girl: before 6
White: before age of 7
3 types of precocious puberty
central precocious puberty (80%)
peripheral precocious puberty
incomplete precocious puberty
how is central precocious puberty treated
leuprolide acetate
Lupron
Depot
leuprolide acetate
Slows prepubertal growth to normal rates
Treatment is discontinued at the age at which normal pubertal changes would resume
thyroid dysfunction in kids is
usually hypothyroidism
hypothyroidism
Low levels can lead to low growth (especially of brain)= developmental delays
Part of newborn screening (thyroid levels)
Juvenile hypothyroidism
Rarely occurs from dietary iodine insufficiency in the US
Early detection important: it is part of the newborn screening test
Juvenile hypothyroidism s/s
Decelerated growth
Myxedematous skin changes
Dry skin
Sparse hair
Periorbital edema
Constipation
sleepiness
Mental decline
Juvenile hypothyroidism s/s in infants
“quiet baby”
prolonged jaundice
constipation
tx for hypothyroidism
synthroid (levothyroxine) (to replace hormones)
hyperthyroidism (Grave’s disesae)
Seen in babies w moms who have hyperthyroidism
increased levels of T4 and T3
suppressed TSH levels
s/s of hyperthyroidism
Enlarged thyroid gland and exophthalmos
tx for hyperthyroidism
Antithyroid drugs (PTU & methimazole)
watch leukopenia w/ methimazole
Subtotal thyroidectomy
Ablation with radioiodine
Labs for thyroid dysfunction kids:
Total T4
Total TSH
Not rlly T3
Signs that show meds are working in thyroid dysfunction
TSH should be normal (goes up when T4 goes low)
T4 should also be normal
Thyrotoxicosis or thyroid storm/crisis
Life threatening
Sudden release of thyroid hormones
s/s of Thyrotoxicosis or thyroid storm/crisis
Acute onset of:
severe irritability and restlessness
vomiting & diarrhea
hyperthermia
hypertension
tachycardia
goiter
Hypertrophy of the thyroid gland
congenital goiter
Usually results from maternal ingestion of antithyroid
drugs or iodides during pregnancy
acquired goiter
from increased secretion of pituitary TSH
how to get rid of goiter
Replacement of thyroid hormone (synthroid)
priority in goiter
airway
diabetes insipidus
disorder of the posterior pituitary gland
Too little ADH (vasopressin)
Pee too much
s/s of Diabetes insipidus
Bed wetting (first s/s)
polyuria
polydypsia
Diabetes insipidus in infants
Irritability is relieved with feedings of water but not milk
Dehydration often occurs
Therapuetic management for DI
replacement of vasopressin
Strict I&O
SIADH
Too much ADH
s/s of SIADH
Hypotonicity (delusional hyponatremia)
Fluid retention (no urine output)
Anorexia
N/V
irritability
personality changes
therapeutic management of SIADH
restrict fluid
Strict I&O
Seizure precautions
Hyperpituitarism
Excessive GH before closure of the epiphyseal shafts results in proportional overgrowth of the long bones until the individual reaches a height of 8ft or more
Also accompanied by rapid & increased development of muscle and viscera
If over secretion of GH occurs after the closure of epiphyseal then they develop acromegaly
Grow fast during puberty and then not during adult hood
can be caused by tumor
s/s of Hyperpituitarism
Acromegaly (overgrowth of head, mouth, lips, nose, tongue, jaw, and sinuses)
Separation and malocclusion of teeth in enlarged jaw
thickened deeply creased skin
increased facial hair
disproportion of face and cerebral division of skull
dx of Hyperpituitarism
H&PE and evidence of inc GH
therapeutic management of Hyperpituitarism
surgical removal of tumor (if present)
destruction of pituitary tissue by radiation and radioactive implants
Hypopituitarism
diminished or deficient secretion of pituitary hormones
gonadotropin deficiency (absent or regressed secondary sex characteristics)
growth hormone deficiency (stunted somatic growth)
thyroid stimulating hormone (hypothyroidism)
adrenocorticotropic hormone deficiency (adrenal hypofunction)
s/s of Hypopituitarism
usually grow normal during 1st yr and then follow a slow growth curve that is under the 3rd percentile
may appear overweight or obese
dentition
sexual maturation is delayed, but otherwise normal unless gonadotropin hormone deficient
Hypopituitarism: dentition
the development, arrangement, and number of teeth in the mouth
dx of Hypopituitarism
absent or subnormal reserves of pituitary GH (GH stimulation test)
growth failure
an absolute height of less than -2 standard deviation for age or a linear growth velocity consistently less than -1 SD for age
s/s of Growth Hormone deficiency
Short stature but proportional height and weight
Delayed epiphyseal closure
delayed bone age proportional to height
Premature aging common in later life
Increased insulin sensitivity
Hypopituitarism tx
give GH supplements to make bones grow
discontinued when growth velocity is < 1 in/year and bone age is 14 I n girls and 16 in boys