NUR 370 Exam 2 - Endocrine Alterations Review Questions and Correct Answers
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Course
NUR 370
Institution
NUR 370
Total or partial deficiency of insulin; most common endocrine disorder of childhood Diabetes mellitus
Immune-mediated destruction of pancreatic beta cells - absolute insulin deficiency Type 1 diabetes
Insulin-resistance combined with relative insulin deficiency Type 2 diabetes
Genetic and enviro...
NUR 370 Exam 2 - Endocrine Alterations
Revie Questions and Correct Answers
Total or partial deficiency of insulin; most common endocrine disorder of childhood
✅Diabetes mellitus
Insulin-resistance combined with relative insulin deficiency ✅Type 2 diabetes
Genetic and environmental; Dx based on serum glucose levels ✅Etiology DM
Autoimmune disorder; recessive gene causes indv. to be vulnerable to trigger event
which starts process that gradually destroys beta cells in pancreas ✅Type 1 etiology
Excess sugar in the urine ✅Glycosuria
Abnormally large volumes of dilute urine ✅Polyuria
Large sensation of thirst ✅Polydipsia
Excessive hunger ✅Polyphagia
Large amounts of ketones in the urine ✅Ketonuria
Extremely high levels of blood acids called ketones. BS >>>> ✅Ketoacidosis
Deep, labored breathing pattern symptomatic of metabolic acidosis such as DKA
✅Kussmaul Respirations
Kidney disease or damage ✅Nephropathy
Damage to nerves (tingling, pain, numbness...) ✅Neuropathy
Damage to eye/retina that causes distortion in vision ✅Retinopathy
Insufficient insulin production leads to decreased transfer of glucose into cells, cause
increased concentration of glucose in blood stream; body uses fat and proteins for
energy ✅DM pathophysiology
, Similar to diabetes in adults but onset usually rapid- lethargy, weight loss, bedwetting,
irritable, fatigue, blurred vision, sores slow to heal, headache, flushed, dry skin, 3 Ps
✅DM clinical manifestations
Hospitalized ✅Where are children at time of DM diagnosis?
indv. plan for total dose and rapid/long acting; based on glucose levels from test; SubQ
injections 2+ times a day or by pump; adjusted during illness ✅DM insulin therapy
Balanced diet with cals enough to maintain energy needs and growth/dev. consistent
intake/timing; count carbs or use point system ✅DM nutrition
May need extra snack with activity ✅DM exercise
life-threatening potential; ICU for management; reduce BS via insulin; fluids for
dehydration; electrolyte replacement, especially K; be cautious with replacement to
avoid cerebral edema ✅DKA management for DM
Overwhelmed for first few days, need family support ✅DM nursing considerations
Patho, meal planning, insulin admin, glucose monitoring, hyper and hypo SS, exercise,
record keeping, hygiene, when to contact HCP ✅DM teaching
Growth hormone deficiency (GHD) ✅Hypotituitarism
normal initially, growth drops during 2nd year < 5th percentile ✅GHD short stature
appear well nourished ✅GHD height more affected than wt
normal skeletal proportions; bone age retarded and parallels height age ✅GHD
proportions
delay in appearance of permanent teeth d/t crowding from underdeveloped jaw ✅GHD
teeth
Delayed but normal ✅GHD sexual development
H&P, family history, deteriorating rate of growth on chart; bone age via radiographic;
pituitary funct. testing for growth hormone levels; differentiate b/w GHD and
constitutional growth delay ✅GHD diagnostic evaluation
Treat underlying problem ✅GHD secondary mananagement
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