Diabetes Mellitus Flashcards
Type 1
- Most common endocrine disorder of childhood
- Autoimmue
- Characterized by destruction of beta cells, usually leading to absolute insulin deficiency
-
Onset typically in childhood & adolescence
> can occur at any age
> peaks 10-15yrs - more prominent in caucasians
- abt 10% of world population
Type 2
- Arises bc of insulin resistance
- Onset usually after age 45
- Incrd incidence in Native American, Hispanic, & AA children
- Affected ppl may require insulin injections
Diabetes Mellitus - Patho
- W/ a deficiency of insulin, glucose is unable to enter cell & remians in blood, causing hyperglycemia
- When serum glucose exceeds renal threshold, glucose spills into urine(glycosuria)
- Cells break down protein for conversion to glucose by liver (glucogenesis)
- Insulin stimulates protein synthesis & free fatty acid storage in adipose tissues
-
Deficiency of insulin or insulin resistance compromise body tissues’ access to essentail nutrients for feul & storage
polydipsia, polyuria, polyphagia
Type 1- CMs
- Polyuria
- Polydipsia
- Polyphagia
- Glycosuria
- Weakness/fatigue
- Enuresis/nocturia
- Dehydration
- Wt loss
- Vision changes
- Frequent skin & UTI infections
- Skin changes (cool, dry, itchy)
- Headaches
- Hyperglycemia
- Diabetic ketosis
- DKA
Hyperglycemia
- Glucose >250mg/dl
- Gradual onset
- Lethargic/weak
- Confusion
- Thirsty
- N/V
- Flushed
- Deep/rapid breathing
-
Fruity breath
> acetone - Diminished reflexes
- Acidosis
-
Coma
hot and dry, sugar high
Hypoglycemia
- Glucose <60mg/dl
- Rapid onset
- Irritable
- Headaches
- Pallor
- Shallow breathing
- Shakey
- Tachycardia
- Palpations
- Sweating
- Confusion
- Shock
-
Coma
cold and clammy, need some candy
DM - Assessment
-
Long-term effects
> failure to grow at normal rate
> delayed maturation
> recurrrent infections
> neuropathy
> cardiovascular disease
> retinal disease
> renal disease
effects can occur a lot quicker if DM is uncontrolled
DM - Compliations
- Hypoglycemia
- Hyperglycemia
- DKA
- Hypokalemia
- Hyperkalemia
- Microvascular changes
- Cardiovascular changes
Diabetic Ketoacidosis
- When glucose is unavailable for cellular metabolism, the body breaks down alternative sources of energy; ketones are released, and excess ketons are eliminated in urine (ketonuria) or by the lungs (acetone breath)
- Ketones in blood are strong acids tht lower serum pH & produce ketoacidosis
- Pediatric emergency
-
Results from profressive deterioration w/ dehydration, electrolyte imbalance, acidosis, coma
> may cause death - Should be instituted in an ICU setting
- Undiagnosed T1 typically present in DKA
Most Common Times of DKA
- Run out of insulin
- Pump malfunction
- Infection
-
Stress
> released cortisol, dumping out sugar
DKA - Nurse Priority
- Fluids 1st
- Insulin drip
-
Electrolytes
> potassium - Once at 250, also give sugar
- Head & body cooling to slow perfusion, once controlled warm back up
DM - Diagnostic Evaluation
- Check risk factors
- Glycosuria w/ or w/out ketonuria
-
4 different tests to confirm DM
> 8hr fasting BG of 126mg/dl
> random BG 200mg/dl+
> oral glucose tolerance test of 200mg/dl or more in 2hr sample
> hgb A1C of 6.5% or more
Therapeutic Management of Diabetes Mellitus
-
Mutlisciplinary Approach
> parents, school nurse, teachers, anyone tht will be alone w/ child - Insulin therapy
-
Insulin preparations
> dosage
> methods of admin -
Monitoring
> blood glucose 3-5x/day
> glycosylated hgb
> urine
DM - Education
- Nutrition
-
Exercise
> snack before if exercise is >30 mins - Hypoglycemia
- Interdisciplinary management
- Pain management
-
Medical indentification
> bracelet identifier -
Sports
> snack before & during
> stress will incr BG
Sick Day Managment
- Always give insulin, even if child in not eating
- Test blood glucose q4
- Check for urinary ketons
- Follow normal meal plan if child is able
- Encourage liquids
- Encourage rest
- Notify PCP is moderate/high ketone lvls, vomiting, fruity breath, deep/rapid respirations, dcrs LOA, presistent hyperglycemia, not drinking or eating anything in 24hrs
Newborn Screening
MO law requires all babies born in the state to be screened for certain metabolic, genetic, & endocrine disorders as well as hearing loss & critical CHD. The newborn screening should be done btwn 24-48hrs of age (before d/c). The test screens for 76 conditions:
- Amino acid disorders (PKU, Maple syrup disease)
- Endocrine disorders (congenital adrenal hyperplasia)
- Hemoglobin disorders (SCD, thalassemia)
- Lysosomal storage disorders
- Organic acid conditions
- Fatty acid oxidation disorders (galactosemia, CF)