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Ppt chapter 50
- 1. Chapter 50
Drugs Affecting Pituitary,
Thyroid, Parathyroid, and
Hypothalamic Function
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 2. Physiology
• Pituitary gland function
– Anterior lobe of the pituitary gland: It controls
the function of glucocorticoid hormone levels (ACTH),
body growth and metabolism (GH), function of the
thyroid gland (TSH), gonadal function (FSH and LH),
and milk production and breast growth (prolactin).
– Posterior lobe of the pituitary gland: It stores
and secretes two effector hormones (hormones that
produce an effect when stimulated): oxytocin and
vasopressin (also known as antidiuretic hormone
[ADH]).
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 3. Physiology (cont.)
• Thyroid gland function
– It controls cellular metabolism and promotes normal
growth and development.
• Parathyroid gland function
– PTH affects three target organs: bone, kidneys, and
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GI tract.
– The major controlling factor for PTH secretion is
serum calcium.
- 5. Pathophysiology
• Anterior pituitary gland dysfunction: It includes
growth hormone deficiency and excess.
• Posterior pituitary gland dysfunction: Major disorders
are diabetes insipidus (DI) and syndrome of inappropriate
antidiuretic hormone (SIADH).
• Thyroid gland dysfunction: Hyperfunctioning or
hypofunctioning gland, malfunctions that may be caused
by either a congenital defect or by a problem that occurs
later in life.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 6. Pathophysiology (cont.)
• Parathyroid gland dysfunction: Hormone is a major
regulator of serum calcium and phosphate.
– A decrease in serum calcium concentration is the
dominant regulator of PTH, with a response rate of
just a few seconds.
– A decrease in phosphate causes an indirect effect on
PTH by combining with calcium and decreasing serum
calcium concentrations.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 7. Growth Hormones
• GH deficiency, leading to short stature, was initially
treated with GH injections extracted from the pituitary
glands of cadavers.
• Presently, synthetic human GH (rhGH), produced from
recombinant DNA, is available.
• rhGH therapy is very expensive.
• Prototype drug: somatropin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 8. Somatropin: Core Drug Knowledge
• Pharmacotherapeutics
– Used as long-term replacement of inadequate
endogenous GH secretion
• Pharmacokinetics
– Administered: SC and IM. Excreted: liver and
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
kidneys.
• Pharmacodynamics
– It stimulates cell growth and cellular mitosis,
facilitates cellular uptake of amino acids for protein
synthesis, and promotes use of fatty acids for
energy.
- 9. Somatropin: Core Drug Knowledge (cont.)
• Contraindications and precautions
– Growth promotion in children with closed epiphyses
• Adverse effects
– Headache, hypertension, joint and back pain,
peripheral edema, muscle aches, and rhinitis
• Drug interactions
– Anabolic steroids, androgens, estrogens, or thyroid
hormones may accelerate epiphyseal maturation.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 10. Somatropin: Core Patient Variables
• Health status
– Assess medical history and contraindications to the
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
drug.
• Life span and gender
– Pregnancy Category C drug
• Lifestyle, diet, and habits
– Assess ability to adhere to medical regimen.
• Environment
– Assess the environment where the drug will be given.
- 11. Somatropin: Nursing Diagnoses and
Outcomes
• Delayed Growth and Development related to deficiency of
GH secretion
– Desired outcome: The patient will demonstrate an
increase in linear growth.
• Imbalanced nutrition: More (or Less) than Body
Requirements related to endocrine changes and rapid
changes in height and weight
– Desired outcome: The patient will receive adequate
nutrition for growth appropriate to age and need.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 12. Somatropin: Nursing Diagnoses and
Outcomes (cont.)
• Impaired Tissue Integrity related to pain and swelling at
injection site
– Desired outcome: The patient will not experience
pain and swelling at the injection site.
• Altered Comfort related to headache, joint and muscle
discomfort, secondary to somatropin effects
– Desired outcome: The patient will describe
measures to improve comfort.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 13. Somatropin: Planning and Interventions
• Maximizing therapeutic effects
– Hypothyroidism may develop during somatropin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
therapy.
– Patients who require chronic cycling peritoneal
dialysis should receive their doses of somatropin in
the morning, after the dialysis is completed.
• Minimizing adverse effects
– GH therapy may induce insulin resistance.
– Be alert for the development of a limp or complaints
of hip or knee pain, and tell parents to do the same.
- 14. Somatropin: Teaching, Assessment, and
Evaluation
• Patient and family education
– Explain that this drug is replacing an important
hormone (GH).
– Explain proper administration of medication.
• Ongoing assessment and evaluation
– In patients taking somatropin, evaluate thyroid
function at regular intervals because hypothyroidism
compromises rGH drug effects.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 15. Question
• Patients taking somatropin should have which lab values
monitored on a routine basis due to adverse effects of
the drug therapy?
– A. TSH
– B. CBC
– C. Glucose level
– D. Both A and C
– E. All of the above
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- 16. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• D. Both A and C
• Rationale: Somatropin can cause hypothyroidism and
glucose intolerance; therefore, these lab values
should be monitored during therapy.
- 17. Posterior Pituitary Hormone Regulators
• The posterior pituitary stores two hormones that are
produced in the hypothalamus: vasopressin and oxytocin.
• Desmopressin and vasopressin are synthetic analogues of
the naturally occurring posterior pituitary hormone.
• Prototype drug: desmopressin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 18. Desmopressin: Core Drug Knowledge
• Pharmacotherapeutics
– Manages central DI and nocturnal enuresis and
maintains homeostasis in hemophilia A
• Pharmacokinetics
– Administered: intranasally, orally, or parenterally (IV
or SC route). Metabolism: liver. Excreted: kidneys.
• Pharmacodynamics
– Interacts with V1 and V2 receptors
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 19. Desmopressin: Core Drug Knowledge
(cont.)
• Contraindications and precautions
– Hypersensitivity
• Adverse effects
– Abdominal pain, transient headache, nasal
congestion, nausea, rhinitis, and facial flushing
• Drug interactions
– Carbamazepine, chlorpromazine, and nonsteroidal
anti-inflammatory drugs
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 20. Desmopressin: Core Patient Variables
• Health status
– Assess for conditions that require drug therapy.
• Life span and gender
– Pregnancy Category B drug
• Lifestyle, diet, and habits
– Assess lifestyle activities and use of recreational
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
drugs.
• Environment
– Assess the environment where the drug will be given.
- 21. Desmopressin: Nursing Diagnoses and
Outcomes
• Risk for Fluid Volume Excess related to administration of
desmopressin, secondary to diabetes insipidus
– Desired outcome: The patient will not demonstrate
signs and symptoms of water intoxication and will
maintain urine specific gravity within a normal range.
• Risk for Ineffective Therapeutic Regimen Management
related to lack of knowledge of diabetes insipidus, disease
management, and signs and symptoms of complications
– Desired outcome: The patient will describe the
disease process, causes, and factors contributing to
symptoms and the regimen for disease or symptom
control, relate intent to practice health behaviors
needed or desired to control disease and prevent
complications, and report less anxiety from fear of the
unknown and loss of control.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 22. Desmopressin: Planning and
Interventions
• Maximizing therapeutic effects
– Establish baseline values for weight, blood pressure,
electrolytes, and urine specific gravity.
– Protect ADH solutions from agitation and
temperature extremes.
• Minimizing adverse effects
– Assess the patient for preexisting cardiovascular or
renal disorders and monitor patients carefully for
cardiac reactions from desmopressin.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 23. Desmopressin: Teaching, Assessment, and
Evaluation
• Patient and family education
– Provide information about drug therapy.
– Alcohol can alter the therapeutic response to
desmopressin.
• Ongoing assessment and evaluation
– Instruct patients taking desmopressin to monitor
urine specific gravity and intake and output as well
as to weigh themselves daily to determine drug
efficacy.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 24. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Question
• Desmopressin is used to treat
– A. Central DI
– B. Primary nocturnal enuresis
– C. Hemophilia A
– D. Both A and B
– E. All of the above
- 25. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• E. All of the above
• Rationale: Desmopressin is used to manage central
DI. Primary nocturnal enuresis and episodes of
spontaneous or trauma-induced bleeding. Parenteral
desmopressin maintains homeostasis in hemophilia A
and von Willebrand disease (type I).
- 26. Thyroid Drugs
• Thyroid hormones influence essentially every organ
system in the body.
• Thyroid disorders involve an alteration in the quantity of
thyroid hormone secretion, enlargement of the thyroid
gland (goiter), or both and are classified as either
hyperthyroidism or hypothyroidism.
• Hypothyroidism may be mistaken for the normal aging
process.
• The only treatment for hypothyroidism is lifelong
replacement of thyroid hormones that are adequate to
meet the individual’s metabolic needs.
• Prototype drug: levothyroxine (T4; Levothroid, Synthroid)
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 27. Levothyroxine: Core Drug Knowledge
• Pharmacotherapeutics
– Used as replacement therapy in hypothyroidism
• Pharmacokinetics
– Administered: oral. Metabolism: liver. Excreted: bile.
Onset: 6 to 8 hours.
• Pharmacodynamics
– Acts as replacement for natural thyroid hormone
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 28. Levothyroxine: Core Drug Knowledge
(cont.)
• Contraindications and precautions
– Hypersensitivity, thyrotoxicosis, and acute MI
complicated by hypothyroidism
• Adverse effects
– Hypertension, tachycardia, arrhythmias, anxiety,
headache, nervousness, GI irritation, sweating, and
heat intolerance
• Drug interactions
– Many drugs
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 29. Levothyroxine: Core Patient Variables
• Health status
– Assess for contraindications to therapy.
• Life span and gender
– Pregnancy Category A drug
• Lifestyle, diet, and habits
– Assess the ability to adapt to long-term therapy.
• Environment
– Assess the environment where the drug will be given.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 30. Levothyroxine: Nursing Diagnoses and
Outcomes
• Imbalanced nutrition: More than Body Requirements
related to dietary intake in excess of metabolic demands
secondary to hypothyroidism
– Desired outcome: The patient will maintain normal
body weight, describe reasons why weight gain may
occur, discuss nutritional needs related to age,
lifestyle, and diagnosis, and discuss the effects of
exercise and diet on weight control.
• Risk for Injury related to adverse drug reactions
– Desired outcome: The patient will not experience
adverse reactions to thyroid hormone replacement.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 31. Levothyroxine: Nursing Diagnoses and
Outcomes (cont.)
• Risk for Injury related to preexisting health status that
requires cautious use of a thyroid agent
– Desired outcome: The patient will not experience
complications of preexisting health conditions.
• Knowledge Deficit related to thyroid dysfunction and the
necessity for thyroid hormone replacement
– Desired outcome: The patient and family will
express accurate understanding of the teaching
regarding the disease process and the prescribed
thyroid hormone replacement therapy.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 32. Levothyroxine: Planning and Interventions
• Maximizing therapeutic effects
– Replacement therapy is a lifelong occurrence.
– During drug therapy, monitor cardiovascular
response and serum thyroid function.
• Minimizing adverse effects
– Young adults without evidence of coronary artery
disease can begin a full replacement dose of
levothyroxine.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 33. Levothyroxine: Teaching, Assessment,
and Evaluation
• Patient and family education
– Explain the purpose of drug therapy.
– Advise patients to avoid OTC drugs.
• Ongoing assessment and evaluation
– In patients taking levothyroxine, monitor serum
thyroid hormone levels periodically.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 34. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Question
• Levothyroxine is a Pregnancy Category ___ drug?
– A. A
– B. B
– C. C
– D. D
– E. X
- 35. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• A. A
• Rationale: Levothyroxine is in Pregnancy Category A.
• Thyroid hormone deficiency may have an adverse
effect on fetal nervous system development and on
the outcome of the pregnancy.
- 36. Antithyroid Compounds
• Hyperthyroidism is treated with thyroid-hormone
antagonist drugs, surgery, or radioactive iodine.
• The purpose of treatment is to reduce the amount of
functional thyroid tissue.
• Prototype drug: methimazole (MMI)
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 37. Methimazole: Core Drug Knowledge
• Pharmacotherapeutics
– Palliative treatment of hyperthyroidism
• Pharmacokinetics
– Administered: oral. Metabolism: liver. Excreted:
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
kidneys.
• Pharmacodynamics
– Inhibits the synthesis of thyroid hormones
- 38. Methimazole: Core Drug Knowledge
(cont.)
• Contraindications and precautions
– Hypersensitivity
• Adverse effects
– Hives, itching, rash, fever, arthralgia, joint swelling,
vertigo, drowsiness, nausea and vomiting, and
altered taste sensation
• Drug interactions
– Beta-blocking agents, theophylline, and warfarin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 39. Methimazole: Core Patient Variables
• Health status
– Assess for contraindications to therapy.
• Life span and gender
– Pregnancy Category D drug
• Lifestyle, diet, and habits
– Assess the ability to adapt to long-term therapy.
• Environment
– Assess the environment where the drug will be given.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 40. Methimazole: Nursing Diagnoses and
Outcomes
• Imbalanced nutrition: Less than Body Requirements
related to increased metabolic demands secondary to
hypothyroidism
– Desired outcome: The patient will describe reasons
why weight loss may occur and discuss nutritional
needs related to age, lifestyle, and diagnosis.
• Risk for Injury related to blood dyscrasias (e.g.,
granulocytosis) or to drowsiness and vertigo secondary
to adverse reactions of PTU
– Desired outcome: The patient will demonstrate no
adverse hematologic reactions to thyroid therapy.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 41. Methimazole: Nursing Diagnoses and
Outcomes (cont.)
• Nonadherence related to long-term use of the antithyroid
agent and need to take the prescribed medication
frequently
– Desired outcome: The patient will describe the
reasons for the therapeutic regimen, identify barriers
to adherence, and identify the behaviors that must
change to facilitate adherence.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 42. Methimazole: Planning and Interventions
• Maximizing therapeutic effects
– Ensure that the drug is being administered
appropriately.
• Minimizing adverse effects
– During drug therapy, arrange for periodic blood tests
to monitor for hematologic and thyroid functions.
– Monitor the patient’s bone marrow function.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 43. Methimazole: Teaching, Assessment, and
Evaluation
• Patient and family education
– Explain the purpose of therapy.
– If the drug is taken in divided doses, instruct patients
to take them every 8 hours around the clock.
• Ongoing assessment and evaluation
– Monitor serum thyroid hormone levels periodically to
evaluate the effectiveness of MMI and to assess the
need for replacement thyroid hormone because the
thyroid gland is suppressed.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 44. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Question
• Methimazole is a Pregnancy Category _____ drug.
– A. A
– B. B
– C. C
– D. D
– E. X
- 45. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• D. D
• Rationale: Methimazole is a Pregnancy Category D drug.
- 46. Antihypercalcemic, Calcium-Regulator
Drugs
• Antihypercalcemic drugs do not directly affect the
parathyroid gland or PTH but rather inhibit bone
resorption of calcium.
• These agents are frequently used in the treatment of
Paget disease.
• Individuals with symptomatic disease experience bone
pain and deformity, fractures, spinal cord compression,
or cranial and spinal cord entrapment.
• Prototype drug: calcitonin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 47. Calcitonin: Core Drug Knowledge
• Pharmacotherapeutics
– Treatment of symptomatic Paget disease
• Pharmacokinetics
– Administered: SC, IM, or intranasal. Metabolism:
kidneys. Excreted: kidneys.
• Pharmacodynamics
– A synthetic polypeptide with essentially the same
actions as calcitonin
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 48. Calcitonin: Core Drug Knowledge (cont.)
• Contraindications and precautions
– Allergic to salmon
• Adverse effects
– GI disturbances, skin rash, flushing of the face and
hands, and nasal irritation or rhinitis (if using the
nasal spray)
• Drug interactions
– Calcium supplements, antacids, vitamin D, and
theophylline
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 49. Calcitonin: Core Patient Variables
• Health status
– Determine if the drug can be administered safely.
• Life span and gender
– Pregnancy Category C drug
• Lifestyle, diet, and habits
– Assess the ability to comply with long-term therapy.
• Environment
– Assess the environment where the drug will be given.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 50. Calcitonin: Nursing Diagnoses and
Outcomes
• Imbalanced nutrition: Less than Body Requirements
related to GI effects of drug therapy
– Desired outcome: The patient will relate the
importance of good nutrition and ingest daily
nutritional requirements in accordance with activity
level and metabolic needs.
• Pain, Acute or Chronic related to complications of calcium
or phosphate imbalances (e.g., renal stones, pathologic
fractures, and osteoporosis)
– Desired outcome: The patient will practice pain
relief measures to avoid or manage the pain.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 51. Calcitonin: Planning and Interventions
• Maximizing therapeutic effects
– Be aware of the proper dosages of calcitonin.
– For Paget disease, it is necessary to give the drug by
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
injection.
• Minimizing adverse effects
– Watch for nausea, which is the most common
adverse effect with SC or IM administration.
– Rhinitis, nasal crusts, and dryness are the most
common adverse effects of nasal calcitonin.
- 52. Calcitonin: Teaching, Assessment, and
Evaluation
• Patient and family education
– Instruct patients on proper administration of the
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
drug.
– Explain adverse effects of drug therapy.
– Instruct patients to report twitching, muscle pain,
severe diarrhea, or dark urine.
• Ongoing assessment and evaluation
– Calcitonin can cause the serum calcium level to drop,
resulting in tetany and cardiac arrhythmias.
- 53. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Question
• When calcitonin is administered with vitamin D, there is
an increase in the therapeutic effect of calcitonin?
– A. True
– B. False
- 54. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• B. False
• Rationale: If calcitonin, salmon is taken with calcium
supplements, antacids, or vitamin D, there is a risk
of hypercalcemia, and therapeutic effect is
decreased.
- 55. Antihypocalcemic Drugs
• Vitamin D compounds regulate absorption of calcium and
phosphate.
• Vitamin D is considered a hormone, although it is not a
natural human hormone.
• Vitamin D metabolites control intestinal absorption of
dietary calcium, tubular reabsorption of calcium by the
kidney, and mobilization of calcium from the skeleton, in
conjunction with PTH.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 56. Antihypocalcemic Drugs (cont.)
• Vitamin D is also involved in magnesium metabolism.
• Vitamin D works together with PTH and calcitonin to
regulate calcium homeostasis.
• Prototype drug: calcitriol (1,25-dihydroxyvitamin D3,
Rocaltrol [capsules, solution], Calcijex [parenteral])
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 57. Calcitriol: Core Drug Knowledge
• Pharmacotherapeutics
– Management of hypocalcemia
• Pharmacokinetics
– Administered: oral or IV. Metabolism: liver. Excreted:
urine and feces.
• Pharmacodynamics
– Is a fat-soluble vitamin derived from natural sources
(fish liver oils) or from conversion of provitamins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 58. Calcitriol: Core Drug Knowledge (cont.)
• Contraindications and precautions
– Given carefully to patients at risk for hypercalcemia
and hypercalciuria
• Adverse effects
– Weakness, headache, nausea and vomiting, dry
mouth, constipation, and bone pain
• Drug interactions
– Thiazide diuretics
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 59. Calcitriol: Core Patient Variables
• Health status
– Assess past medical history and indications for the
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
drug.
• Life span and gender
– Pregnancy Category C drug
• Lifestyle, diet, and habits
– IV doses can be given following dialysis to increase
calcium levels.
- 60. Calcitriol: Nursing Diagnoses and
Outcomes
• Imbalanced nutrition: Less than Body Requirements related to
reduced absorption of fat-soluble vitamins
– Desired outcome: The patient will ingest a nutritionally
balanced diet to allow for normal absorption of fat-soluble
vitamins.
• Imbalanced nutrition: More than Body Requirements
– Desired outcome: The patient will identify sources of
dietary vitamin D and calcium.
• Acute Pain related to headache and general discomfort
secondary to drug effects
– Desired outcome: The patient will not experience undue
pain and discomfort as a result of drug therapy.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 61. Calcitriol: Planning and Interventions
• Maximizing therapeutic effects
– Calcitriol capsules should be swallowed whole, rather
than crushed or chewed.
– When high therapeutic doses are used, frequent
serum and urinary calcium, phosphate, and BUN
determinations are necessary.
• Minimizing adverse effects
– Chronic dialysis patients should avoid magnesium-containing
antacids while taking these drugs.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 62. Calcitriol: Teaching, Assessment, and
Evaluation
• Patient and family education
– Explain the purpose of drug therapy.
– Discuss the possible adverse effects of the drug.
• Ongoing assessment and evaluation
– Dosage adjustment is required for patients taking
calcitriol as soon as clinical improvement occurs.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
- 63. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Question
• Calcitriol dosing guidelines are established for all age
groups.
– A. True
– B. False
- 64. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Answer
• B. False
• Rationale: Dosing guidelines for patients with
hypoparathyroidism who are younger than 1 year or
patients with pseudohypoparathyroidism who are
younger than 6 years have not been established.