Alterations In Endocrine Function Flashcards

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1
Q

The endocrine system is comprised of what: name them

A

Glands that secrete hormones. Pituitary, thyroid, parathyroid, adrenal, gonads, pancreas

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2
Q

There are two parts of the pituitary gland, the anterior and posterior. Which produces hormones?

A

The anterior pituitary produces seven hormones, while the posterior pituitary only stores two hormones

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3
Q

What seven hormones does the anterior pituitary secrete?

A

Growth hormones, thyroid stimulating hormone, corticotropin, follicle-stimulating hormone, Leutinizing hormones, prolactin, Melanocytes

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4
Q

What to hormones does the posterior pituitary store?

A

Oxytocin and antidiuretic hormone

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5
Q

What are the disorders of pituitary function?

A

Growth hormone deficiency, and diabetes insipidus

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6
Q

How is growth hormone deficiency characterized?

A

During infancy and childhood it is characterized by growth retardation, short stature, and delayed bone maturation

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7
Q

What are the causes of growth hormone deficiency?

A

Idiopathic, CNS infection, infarction of the pituitary gland, tumors

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8
Q

What are the clinical manifestations of growth hormone deficiency?

A

Appears infantile with small mandible and small teeth, Higher pitched voices, delayed sexual maturation

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9
Q

What are some diagnostic test that can be performed to determine if a person has growth hormone deficiency?

A

Wrist, provocative growth hormone tests

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10
Q

How is provocative growth hormone test done?

A

Various medications are used to stimulate the release of GH. Confirmation of GH deficiency based on two failures of the provocative stimuli test. Sleep specimens, exercise tests, IGF/1

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11
Q

What is the treatment for growth hormone deficiency?

A

Daily SQ/IM injections of growth hormone. Replacement is expensive starting at $35,000 a year. This is continued until they reach acceptable height or growth

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12
Q

What is diabetes insipidus?

A

A disorder of the posterior pituitary resulting in hyposecretion of ADH which produces a state of uncontrolled diaresis

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13
Q

What are causes of diabetes insipidus?

A

CNS trauma, brain tumor ( 50% of DI), infection, electrolyte in balance says, surgical procedure (hypophysectomy), Hypoxic brain damage, neoplasm, vascular anomaly, leukemia

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14
Q

What are clinical manifestations of diabetes insipidus?

A

Sudden onset of symptoms: polyuria, polydipsia, irritability, enuresis, dehydration

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15
Q

What diagnostic tests are performed to confirm diabetes insipidus

A

Serum electrolytes, serum and urine osmolality’s, measurement of plasma arginine vasopressin before and during fluid deprivation test

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16
Q

What is the treatment for diabetes insipidus?

A

Water replacement therapy, does naproxen acetate (DD a VP) this is only effective for neurogenic diabetes insipidus. The goal is urine osmolality of 2 to 3 mL/kilogram/hour. specific gravity 1.010 to 1.020. Sodium of 140 to 140 5MEQ/L

17
Q

What is nursing considerations for diabetes insipidus?

A

Is in the hospital, monitor INO, check urine specific gravity you. Teach parents DDAVP administration: daily weights, I and O especially during illness and when NPO. Child should wear ID bracelet

18
Q

What are the disorders of pancreatic function?

A

Diabetes mellitus type one, diabetes mellitus type two

19
Q

What is diabetes mellitus?

A

Disorder of carbohydrates, proteins, and fat metabolism

20
Q

What are the causes of diabetes mellitus?

A

Genetic factors, autoimmune factors (type one), viral infection

21
Q

What is the pathophysiology for diabetes mellitus?

A

Disturbances and carbohydrate, protein, fat metabolism. Deficiency of insulin or insulin resistance compromise of Body’s access to essential nutrients for fuel

22
Q

Symptoms develop rapidly in which type of diabetes mellitus?

A

Type one

23
Q

What are the signs and symptoms of type one diabetes mellitus?

A

The three poly’s: polydipsia, polyuria, polyphagia. Weakness, fatigue, enuresis, dehydration, weight loss and hunger, vision changes, frequent skin and UTIs, skin changes, blood glucose levels of 200 mg/dL

24
Q

What diagnostic tests are performed for type one diabetes confirmation?

A

To fasting plasma glucose test above one 26 mg/dL her. With normal fasting glucose: two blood glucose levels above 200 mg/dL her during a two hour glucose tolerance test. Other findings: acetone or glucose in the urine, diabetic retinopathy

25
Q

What are signs and symptoms of type two diabetes mellitus?

A

Vague, long-standing symptoms develop gradually. Severe viral infection, other endocrine diseases, recent stress or trauma, obesity, particularly in the abdominal region, acanthosis nigricans: Hyperpigmentation and thickening of the skin. It is rare to see three poly’s

26
Q

What diagnostic tests are done to support diabetes mellitus type two?

A

Obesity, acanthosis nigricans, glucose levels above 200 mg/dL

27
Q

What are complications of diabetes Mellitis?

A

Diabetic ketoacidosis (DK), hypoglycemia, nephropathy, retinopathy, neuropathy, complications can occur as early as 2 to 3 years after diagnosis

28
Q

What is a diabetic ketoacidosis?

A

It occurs when the body must burn fat and protein stores for energy due to no insulin

29
Q

What are signs and symptoms of diabetic ketoacidosis?

A

3 poly’s, abdominal or chest pain, nausea and vomiting, dehydration, weight loss, tachycardia, flushed ears and cheeks, Kuszmaul restorations, fruity breath, altered LOC, hyperglycemia, glycosuria, acidosis, Keytonuria

30
Q

What are symptoms of hypoglycemia

A

Lethargy, hunger, sweating, pallor, tremors, seizures, coma

31
Q

What are signs and symptoms of hyperglycemia

A

Sweet, fruity breath, dehydration, decrease sodium, bicarbonate, chloride, and phosphate levels, vomiting, abdominal pain, coma

32
Q

What is basal bolus therapy?

A

Basal insulin administered once per day (Lantos or glargine) or twice a day (Humulin or Ultralente). Bolus of rapid acting insulin (Humalog) administered with each meal or snack based on carb count. Also includes blood glucose monitoring 4 to 8 times per day, 12 AM and 3 AM once per week. Carb counting, exercise in daily routine

33
Q

What phenylketonuria?

A

An autosomal recessive disease that leads to mental retardation, seizures, and death. It is caused by a deficiency of liver enzyme which breaks down phenylalanine into tyrosine

34
Q

What are the clinical manifestations of phenylketonuria

A

Musty or mousy odor to body and urine, vomiting, irritability, hyperactivity, eczema like rash, seizures, lighter complexion the nonaffected siblings, hypertonic, hyper reflexive deep tendon reflexes

35
Q

What diagnostic tests are performed to diagnose phenylketonuria?

A

All infants are screened via blood test in newborn. After 48 hours of age. Child needs to have been on breastmilk or formula for at least two days

36
Q

What is the treatment for phenylketonuria?

A

You special formula (loft alas), diet low in phenylalanine for entire life, avoid high-protein foods and aspartame, use elemental medical foods

37
Q

What does the endocrine system do?

A

Regulate and integrate metabolic processes in the body