Chap 52: Endocrine Disorders Flashcards

1
Q

what is a hypophysectomy, its surgical complications?

A

Removal of the pituitary gland. Surgical complications include: risk for increased ICP, potential for adrenal insufficiency, risk for altered fluid and electrolyte imbalance: r/t reduced ADH, secondary adrenal insufficiency: low Na, high K, Ca, and BUN.

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2
Q

What are the specific nursing interventions for a patient who has undergone a hypophysectomy?

A
  1. hourly neuro checks-24hrs then q4h. (mental status, pupils, vision, strength, including reflexes)
  2. STRICT I & O
  3. No coughing, tooth brushing, sneezing, bending at waist.
  4. Monitor for CSF discharge from nose.
  5. Monitor for DI or SIADH
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3
Q

What does the antidiuretic hormone do? What happens with hypo ADH levels? ?S/S and Rx

A

ADH: controls full body water.
Hypo S/S: high Na, Excessive urine output, extreme thirst, high K, acidosis
Rx: Central: Admin of DDAVP, (monit for S-T changes)
Renal: thiazide diuretics prostaglandin inhibitors: ibuprofen, indomethacin, and salt depletion.

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4
Q

What causes hyperpituitarism

A

hypersecretion of growth hormone or adrenocorticotropic hormones. Causes may include: pituitary tumor, hypothalamus trauma, radiation, vascular lesion, disease of hypothyroidism.

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5
Q

what are the S/S of hyperpituitarism?

A

Extreme weight loss, SIADH, Cushing’s Syndrome, Emaciation, galactorrhea, prolactinoma, acromegaly (adults), and gigantism (kids).

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6
Q

how is hyperpituitarism diagnosed and treated?

A

Diagnosed: blood tests, urine tests, high dose dexamethasone, suppression test, MRI, CT, OGTT, (normal: GH levels go down after drinking glucose) visual acuity, P/E. Rx: surgery, medication to shrink tumor, decrease prolactin levels, Bromocriptine, cabergoline (dopamine agonists), radiation

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7
Q

What is hypopituitarism and its causes?

A

Hypopituitarism is the under secretion/release of pituitary hormones. Causes: tumor, disease, hypothalmic disease, trauma, surgery, destruction of pituitary gland.

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8
Q

what are the S/S of hypopituitarism?

A

S/S: weight gain, lethargy, atrophy of all endorcine glands and organs, hair loss, impotence, hypometabolism, hypoglycemia

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9
Q

What is the Dx and Rx for hypopituitarism?

A

Dx: history and physical, visual acuity fields, CT, MRI, serum levels.
Rx: Replace hormone, surgery

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10
Q

what are the results of hyperpituitarism:

A

GH: Acromegaly, Gigantism ACTH: Cushing’s Syndrome,, Prolactin: galactorrhea, prolactinoma, ADH: SIADH, TSH: hyperactive thyroid, FSH: excess of sex hormones, LH: excess of sex hormones. Oxytocin: uterine contractions

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11
Q

what are the results of hypopituitarism?

A

GH: dwarfism, ACTH: Addison’s, TSH: low thyroid, FSH: low estrogen, testosterone, LH: low progesterone, testosterone, Prolactin: low breast milk, ADH: DI,

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12
Q

What are the causes and S/S of hypo ADH

A

Causes: primary: hypothalamus, posterior pit, deficit, Secondary: tumor, infection, brain injury, brain infarct.

S/S: full body dehydration, intense thirst DI, Increased Na, Increased urinary output, increased water loss.

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13
Q

how is too little ADH diagnosed and treated?

A

Dx: Labs, I&O, weight changes, decrease in specific gravity, decrease in urine osmolarity= <200mOsm/kg UO: >4L/24hr.

Rx: Central: DDAVP, Mon: S-T changes
Renal: Thiazide diuretics, prostaglandin inhibitors: ibuprofen, indomethacin, and salt depletion.

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14
Q

What is the cause and S/S of too much ADH: SIADH?

A

Cause: malignant tumors, lung cancer, increased doses nicotine. Tricylics and thiazides may trigger SIADH.

S/S: Water retention, I > O, weight gain, dilutional hyponatremia, low serum Na.

Monitor fluids, neuro, V/S, mucous membranes

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15
Q

How is SIADH diagnosed and treated?

A

Dx: Fluid retentioin, hyponatremia (unknown cause)
Rx; Stop cause, restrict fluids, may use HYPERtonic saline solution.

Low Na: seizures

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16
Q

What is hypothyroidism caused by? What are the S/S

A

causes: usually r/t autoimmune, thyroiditis, AB that cause hashimotos.
S/S: fatigue, hair loss, brittle nails, hoarseness, husky voice, thickened skin, slowed speech and mental acuity. MYXEDEMA: severe hypothyroidism

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17
Q

how is hypothyroid diagnosed and treated:

A

Dx: CRT, US, biopsy, TSH, (after injection; large response= hypothyroidism). Too little uptake of RAI.
Increase in TSH, Decrease in T3 and T4

Rx: Thyroid replacement, emergent Rx of hypoxia, rewarming, Rx of BP/HR,

18
Q

what are the s/s of Myxedema? causes

A

decreased temp, hr, bp, rr, tissue perfusion

causes: acute illnes/infection, surgery, anesthesia, hypothermia (pt with hashimotos)

19
Q

What are the causes and s/s of HYPER thyroidism?

A

Causes: t/t Graves disease, toxic nodules, thyroiditis.

S/S: tachy, weight loss, sleeplessness, anxiety, heat intolerance, hair changes, diarrhea, decreased menses, weakness, exopthalmos, goiter

20
Q

How is hyperthyroidism Dx and Rx

A

Dx: thyroid scan, thyroid antibodies, overproduction of T3, US, needle biopsy, CRT, RAI: excessive take up of RAI

Blood: decrease in TSH, increases in T3 and T4

Rx: monitor dysrhythmias, oxygen, give NS, steroids (IV and high dose), Thyroid hormone blockers: PTU, Iodine, decrease temp. AVOID ASPIRIN

21
Q

What are the s/s of Thyroid Storm?

A

Causes: stress, surgery, trauma, MI, PE, infection

S/S: agitation, delirium, fever, tachycardia

22
Q

what are increased risks for untreated hypothyroidism

A

increased pulm/card. risk, atherosclerosis, poor left vent function, pleural and pericardial effusions

23
Q

what are surgical complications for patients who have hypothyroidism

A

hypotension, regulating body temp, prob. with sedation/anesthesia, post op heart failure, alt. mental status, myxedema coma.

24
Q

patients who are treated with RAI need to avoid:

A

pregnant women, nursing mothers, children: time, distance, and space

25
Q

what are some extra precautions for patients who have RAI therapy

A

separate linens/utensils, rinse sink/tub X 3, increase water, flush X 3.

26
Q

What is Addison’s disease, S/S

A

Addison’s disease: hyposecretion of adrenal cortex hormones: glucocorticoids and mineralcorticoids cortisol, aldosterone,

S/S: bronze skin, hyponatremia, hypoglycemia, HYPERcalcemia, HYPERkalemia, lethargy, fatigue, weight loss, GI disturb. hypotension, menses/impotence

27
Q

What is the difference between primary and secondary adrenal insufficiency

A

Primary: the problem is within the adrenal cortex, Hyperkalemia, met. acidosis, low Na, low BP, hypoglycemia, pigmentation is affected
Secondary: pituitary gland is not secreting enough ACTH S/S: met. alkalosis, high Na, high BP, increase in testosterone, hypoglycermia, K is ok. No pigmentation issues, no increase in testosterone

28
Q

what are some causes for Addison’s disease

A

TB, histoplasmosis, abrupt cessation after long term >2weeks of glucocorticoids (steroids)

29
Q

What are S/S and causes for Addisonian Crisis

A

S/S: severe headache, profound fatigue, hypotension, dehydration, hyponatremia, hyperkalemia,

Causes: overexertion, stress, decreased salt intake

30
Q

what is Cushing’s Disease? what are some causes

A

Metabolic disorder in which there is hypersecretion of ACTH.
Causes: ant. pit oversecretion of ACTH, adrenal adenoma, glucocorticoid excess (meds)

31
Q

What is the difference between Cushing’s Disease and Cushing’s Syndrome?

A

Cushing’s Disease: met disorder in which the hypersecretion of ACTH from the pituitary. Etiology may pit tumor.
Cushing’s Syndrome: met. disorder in which the hypersecretion is from the Adrenal cortex, and is usually the result of abrupt cessation of glucocorticoids

32
Q

how is Addison’s Dx and Rx?

A

Dx: admin of ACTH stimulation test. Cortisol levels do not increase.
Rx: steroids, salt intake, prevent dehydration

33
Q

how is Cushing’s DX and Rx

A

Dx: Dexamethasone suppression test: High cortisol and low ACTH=adrenal disease
high ACTH + cortisol= pit or hypothalmic dsyfunction
Rx: radiation, surgery, adrenal enzyme inhibitors

34
Q

What are the S/S of Cushings:

A

S/S: skin striae, hirsuitism, balding, hypervolemia, edema, decrease in muscle mass, osteoporosis, mood swings, sleep difficulties, decreased WBC,
Labs: Hypernatremia, Hyperglycemia, Hypokalemia, Hypocalcemia

35
Q

What are the causes of hypoparathyroidism

A

injuries during thyroid/neck surgery, RAI treatment

36
Q

What are the S/S of hypoparathyroidism

A

cardiovascular: prolonged Q-T, increased risk of dysrhythmias
Neuromuscular: numbness, tingling of extremities, muscle cramping, tetany, bronchospasm, laryngospasm, brain fog, anxiety, depression, fatigue, irritability, memory loss, seizures
High phosphate/low calcium, normal Na

37
Q

what is the Dx and Rx for hypothyroidism

A

Dx: blood levels of Ca and PTH
Rx: Calcium and active Vit. D

38
Q

What are the causes of hyperparathyroidism

A

Primary: adenoma, Secondary: hyperplasia w/increased PTH to compensate for prolonged hypocalcemia. Tertiary: continuous stimulation

39
Q

What are the S/S of hyperparathyroidism

A

S/S: hypercalcemia, polyuria, lethargy, anorexia, polydipsia, nausea, constipation, low phosphate

Bones, Stones, Moans, and Groans: osteoporosi, kidney stones, depression, and constipation, anorexia, and nausea

40
Q

what is the Rx of hyperparathyroidism

A

NS, diuretics, phosphates, dialysis, calcitonin

41
Q

nursing interventions for hyperparathyroidism

A

increase hydration, water, walk, avoid HCTZ, treat depression