final exam
Antiemetics
Select Prototype Medications
Serotonin antagonists:
- Ondansetron
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Expected Pharmacological Action
Antiemetics prevent emesis (vomiting) by:
- Blocking serotonin receptors in the chemoreceptor trigger zone (CTZ).
- Antagonizing serotonin receptors on afferent vagal neurons from the upper GI tract to the CTZ.
Therapeutic Uses
Prevents emesis related to:
- Chemotherapy
- Radiation therapy
- Postoperative recovery.Off-label uses:
- Treatment of nausea and vomiting related to pregnancy.
- Childhood viral gastritis.Administration routes:
- PO (by mouth)
- IM (intramuscular)
- IV (intravenous)
Nursing Actions
For Ondansetron:
- Monitor for headache, diarrhea, dizziness.
- Treat headaches with non-opioid analgesics.
- Monitor stool patterns.
- Be aware of prolonged QT interval which can lead to torsades de pointes (serious dysrhythmia).
- Monitor ECG in clients with cardiac disorders/out with other QT-prolonging medications.
- Use cautiously in clients with electrolyte abnormalities.
Warnings, Contraindications/Precautions
Pregnancy:
- Safety not established for ondansetron, metoclopramide, scopolamine.Lactation:
- Avoid chronic use of promethazine during pregnancy; safety for ondansetron, metoclopramide, scopolamine not established.Specific Contraindications:
- Ondansetron contraindicated in long QT syndrome clients.
- Use cautiously for clients with urinary retention/obstruction, asthma, and narrow-angle glaucoma: dopamine antagonists, antihistamines, and anticholinergic antiemetics.
Nursing Administration
Antiemetics prevent or treat nausea and vomiting from various causes.
Nursing assessments can help identify underlying factors related to the use of appropriate medication.
For chemotherapy-induced nausea and vomiting (CINV), administer antiemetics prior to chemotherapy as this is more effective than treating nausea after its onset.
Combining three antiemetics is more effective than using a single antiemetic.
Ondansetron Administration
Administer IV 1 hour before chemotherapy or PO 1 hour before anesthesia to prevent nausea and vomiting.
For clients receiving radiation, administer PO three times daily.
Iron Preparations
Select Prototype Medications
Oral:
- Ferrous sulfate
Expected Pharmacological Action
Iron preparations provide iron needed for RBC development and oxygen transport.
Iron demand increases during growth (children, pregnancy) or RBC high demand (post blood loss).
Since iron is poorly absorbed, large amounts must be ingested to increase hemoglobin (Hgb) and hematocrit (Hct) levels.
Therapeutic Uses
Used to treat and prevent iron-deficiency anemia.
Types of Iron Preparations
Ferumoxytol: Limited to clients with chronic kidney disease, requires only two doses over 3–8 days.
SFGC (Sucrose-Formed Gluconate Complex): Used for long-term hemodialysis clients along with erythropoietin.
Iron Sucrose: Used for chronic kidney disease clients on erythropoietin and those not on dialysis.
Complications
GI distress (nausea, constipation, heartburn).
Nursing Actions
Administer medication with food if intolerable, although this greatly reduces absorption.
Monitor the client's bowel patterns and intervene accordingly.
Client Education
Stools may turn black or dark green while taking an iron preparation; this resolves with continued use.
For liquid form:
- Dilute with water or juice.
- Drink with a straw.
- Rinse mouth after swallowing to prevent teeth staining.
IM Injections
Administer deep IM using Z-track technique to avoid staining skin and other tissues.
- Avoid this route if possible due to risk of complications.
Anaphylaxis
Risk with parenteral iron dextran, triggered by dextran, not iron; minimal risk with other forms (SFGC, iron sucrose).
- IV route is safer than IM.
Nursing Actions
Administer test dose and observe closely; administer only slow infusion.
Be prepared with life-support equipment and epinephrine.
Hypotension
Can progress to circulatory collapse with parenteral administration.
Nursing Actions
Monitor vital signs during parenteral iron administration.
Fatal Iron Toxicity in Children
Can occur from overdose (2–10 g) of iron.
Nursing Actions
Monitor for manifestations such as severe GI symptoms, shock, acidosis, liver, and heart failure.
Use chelating agent deferoxamine parenterally to treat toxicity.
Gastric lavage can help remove iron from the stomach.
Avoid concurrent oral and parenteral iron administration.
Contraindications/Precautions
Warnings
Pregnancy:
- Ferrous sulfate and oral iron dextran are safe; parenteral safety not established.Lactation:
- Same as pregnancy.Contraindicated for clients with previous hypersensitivity to iron, anemias not from iron deficiency.
Caution with clients having peptic ulcer disease, regional enteritis, ulcerative colitis, and severe liver disease.
Interactions
Concurrent administration of antacids or tetracyclines reduces iron absorption.
Nursing Actions
Avoid antacids within 1 hour after iron administration.
Space iron administration 1 to 2 hours apart from tetracycline.
Vitamin C increases absorption but does so with GI side effects.
Client Education
Avoid caffeine and dairy during medication intake as they reduce iron absorption.
Nursing Administration
Client Education
Take iron on an empty stomach (1 hour before meals) for better absorption.
If GI side effects occur, take with food although absorption might be affected.
Space doses evenly throughout the day for optimal RBC production.
For liquid iron:
- Dilute and drink through a straw to avoid teeth staining.
Folic Acid
Select Prototype Medication
Folic Acid
Expected Pharmacological Action
Essential for DNA production and erythropoiesis (RBC, WBC, platelets).
Therapeutic Uses
Treatment of megaloblastic anemia due to folic acid deficiency.
Prevention of neural tube defects in early pregnancies; important for all women of childbearing age.
Treatment of malabsorption syndromes (sprue).
Supplement for alcohol use disorder (due to poor dietary intake of folic acid, and liver injury).
Contraindications/Precautions
Warnings
Pregnancy: Safe
Lactation: Use cautiously.
Avoid indiscriminate use due to risk of masking vitamin B12 deficiency symptoms.
Interactions
Folate levels reduced by methotrexate and sulfonamides.
Nursing Actions
Avoid concurrent use with these medications.
Folic acid can decrease phenytoin blood levels due to increased metabolism; monitor blood levels.
Nursing Administration & Care
Nursing Care
Assess for symptoms of megaloblastic anemia (pallor, easy fatigue, palpitations, paresthesia).
Obtain and monitor baseline folic acid, Hgb, Hct levels, RBC, and reticulocyte counts periodically.
Client Education
Increase intake of food sources high in folic acid (liver, leafy greens, citrus fruits, dried peas and beans).
Monitor risk factors for folic acid therapy need (heavy alcohol use, childbearing age).
Nursing Evaluation of Medication Effectiveness
Effectiveness indicated by:
- Folate levels within reference range.
- Return to expected RBC, reticulocyte count, Hgb, and Hct levels.
- Absence of anemia findings (no pallor, dyspnea, or easy fatigue).
- No neural tube defects in newborns.
Potassium Supplements
Select Prototype Medication
Potassium Chloride
Expected Pharmacological Action
Essential for nerve impulses conduction, maintaining acid/base balance, and electrical excitability of muscle.
Therapeutic Uses
Treat hypokalemia (potassium < 3.5 mEq/L).
Address potassium loss via diuretics (e.g., furosemide).
Correct potassium loss from prolonged vomiting, diarrhea, excessive laxative use, or GI fistula.
Complications
GI ulceration and distress (nausea, vomiting, diarrhea, abdominal discomfort, esophagitis).
Nursing Actions
Administer with meals or 8 oz of water to minimize GI complications and prevent ulceration.
- Important: Do not dissolve the tablet in the mouth to prevent ulceration.
Hyperkalemia
Rare with oral administration.
Nursing Actions
Monitor IV potassium clients for hyperkalemia manifestations (bradycardia, changes in ECG, etc.).
Severe hyperkalemia treatment: Calcium salt, glucose and insulin, sodium bicarbonate, sodium polystyrene sulfonate, peritoneal or hemodialysis.
Contraindications/Precautions
Contraindicated for severe kidney disease or hypoaldosteronism.
Interactions
Increased hyperkalemia risk with potassium-sparing diuretics (e.g., spironolactone) and ACE inhibitors (e.g., lisinopril).
Nursing Actions
Avoid concurrent use with these medications.
Absorption may be decreased by oxalates in spinach/rhubarb and phytates in bran/whole grains.
Nursing Administration
Oral Formulations
Mix powdered formulations in at least 90–240 mL of cold water or juice; drink slowly.
Effervescent tablets should be dissolved in 90–240 mL of cold water.
Client Education
Administer potassium chloride with meals or at least 8 oz of water to prevent GI adverse effects.
Do not crush or chew extended-release tablets; notify the provider if swallowing is difficult.
Magnesium Sulfate
Select Prototype Medication
Parenteral: Magnesium Sulfate
Expected Pharmacological Action
Activates many intracellular enzymes, binds mRNA to ribosomes, regulates muscle contractility and blood coagulation.
Therapeutic Uses
Magnesium supplements for clients with hypomagnesemia (magnesium < 1.3 mEq/L).
Oral magnesium for low magnesium levels and laxative use.
Parenteral magnesium for severe hypomagnesemia; IV for stopping preterm labor/anticonvulsant during labor.
Complications
Muscle weakness, flaccid paralysis, painful contractions, suppression of AV conduction, respiratory depression.
Nursing Actions
Monitor cardiac and neuromuscular status cautiously during IV administration.
Monitor blood magnesium levels.
Do not administer with neuromuscular-blocking agents to avoid respiratory issues.
Have calcium gluconate on hand to reverse magnesium effects.
Contraindications/Precautions
Warnings
Pregnancy: Avoid administering magnesium sulfate within 2 hours of delivery.
Lactation: Present in breast milk; monitor for toxicity.
Contraindicated for clients with AV block, rectal bleeding, nausea, vomiting, and abdominal pain.
Use carefully in renal/cardiac disease patients.
Interactions
Magnesium sulfate reduces absorption of tetracyclines and digoxin; monitor therapeutic effects.
Nursing Administration
Nursing Care
Monitor blood magnesium, calcium, phosphorus levels, blood pressure, heart rate, and respiratory rate during IV administration.
Assess for depressed/absent reflexes as signs of toxicity; always have calcium gluconate ready.
Client Education
Educate on dietary magnesium sources (whole grain cereals, nuts, legumes, green leafy vegetables, bananas).
Hormonal Contraceptives
Estrogen-Progestin Combinations
Combination oral contraceptives (OCs) contain estrogen and progestin.
Progestin-only OCs are known as mini-pills.
Combination OCs can be:
- Monophasic: The dosage remains constant throughout the cycle.
- Biphasic, Triphasic, Quadriphasic: The estrogen/progestin ratios are adjusted within the cycle to mimic normal menstrual cycles.
Select Prototype Medications
Combination OCs:
- Ethinyl estradiol and norethindrone
- Ethinyl estradiol and drospirenoneProgestin-only OC:
- NorethindroneTransdermal Patch:
- Ethinyl estradiol and norelgestrominVaginal Contraceptive Ring:
- Ethinyl estradiol and etonogestrelParenteral:
- Depot medroxyprogesterone acetate (IM and subcutaneous use)Etonogestrel Implants
Hormonal IUD
Expected Pharmacological Action
Oral contraceptives prevent conception by:
- Inhibiting ovulation
- Thickening cervical mucus
- Altering the endometrial lining to reduce fertilization chances.
Therapeutic Uses
Prevention of pregnancy
Treating:
- Premenstrual Dysphoric Disorder (PDD)
- Acne
- Fibrocystic breast disease
- Leiomyomas (to manage discomfort/bleeding)
- Reducing menstrual blood loss to help iron deficiency anemia
- Alleviating dysmenorrhea by reducing menstrual cramping
- Protection against endometrial and ovarian cancers.
Complications
Thromboembolic Events
Risks include myocardial infarction (MI), pulmonary embolism, thrombophlebitis, stroke; less likely with progestin-only OCs.
Client Education
Advise against smoking.
Report warmth, edema, tenderness, or pain in lower legs, chest pain, shortness of breath, severe headache.
Hypertension
Client Education
Monitor and report high blood pressure and vision changes.
Breakthrough or Irregular Uterine Bleeding
Client Education
Track the duration and frequency of breakthrough bleeding.
Evaluate for pregnancy if 2 or more menstrual periods are missed.
Breast Cancer
Nursing Actions
Avoid use with clients having or suspected to have breast cancer.
Hyperglycemia
Nursing Actions
Monitor glucose levels in diabetic clients; adjust antihyperglycemics as needed.
Hyperkalemia
Nursing Actions
Do not use combination OCs with drospirenone in clients at risk for hyperkalemia (renal/adrenal insufficiency).
Contraindications/Precautions
Warnings
Pregnancy: Contraindicated for hormonal contraceptives; progestin-only is safe.
Lactation: Combination OCs contraindicated; progestin-only is safe.
Reproductive Health: Notify provider if pregnancy is planned or suspected.
Contraindicated for clients who are:
- Smokers older than 35 years
- Have a history of thrombophlebitis/cardiovascular events
- Have suspected/known breast cancer
- Have liver conditions
- Experience abnormal vaginal bleedingUse cautiously:
- Hypertension
- Diabetes mellitus
- Gallbladder disease
- Uterine leiomyoma
- Seizures
- Migraine headaches.
Interactions
Effectiveness may decrease with carbamazepine, phenobarbital, ritonavir, rifampin, St. John's wort.
Some sources suggest that antibiotics may decrease oral contraceptive effectiveness.
Nursing Actions
Suggest secondary birth control method during antibiotic therapy for clients using hormonal contraceptives.
Oral contraceptives can decrease effects of:
- Warfarin
- Oral hypoglycemics.
Nursing Actions
Monitor INR, PT, and glucose levels; provider may adjust dosages as necessary; monitor for breakthrough bleeding.
Oral contraceptives can increase effects of:
- Theophylline
- Imipramine
- Tricyclic antidepressants
- Chlordiazepoxide
- Diazepam
Nursing Actions
Monitor for toxicity signs; provider may need to decrease dosage.
Nursing Administration
Nurses/administering personnel of childbearing age should avoid direct handling of hormonal medications to minimize reproductive system effects.
Rule out pregnancy before starting therapy.
Dosing
Most combination OCs administered cyclically in a 28-day regimen; extended-cycle OCs taken longer than 28 days.
Typical cycle: 84 days with 4 days of withdrawal bleeding.
For IM/subcutaneous contraception, administer under conditions indicating the patient is not pregnant (6 weeks postpartum if breastfeeding exclusively or within first 5 days postpartum if not).
Client Education
Quit smoking.
Report abdominal pain, chest pain, severe headaches, vision problems, or severe leg pain/swelling.
Take pills daily at the same time.
Traditional 28-day regimen: Take for 21 days, followed by 7 days of no medication (placebo if using inert pills).
For missed pills in first week: Take one pill as soon as possible; use backup contraception for 7 days.
For missed pills in second or third week: Take one pill as soon as possible, continue with active pills, skip placebo, and start the next pack.
For transdermal patches: Apply to the lower abdomen, upper arm, torso, or buttock; place a new patch weekly for 3 weeks, omit during the fourth week.
For vaginal rings: Insert and keep for 3 weeks, then remove for the fourth week. If out for more than 3 hours, use backup contraception for the next 7 days.
For contraceptive implants: Insert under the skin in the inner upper arm and change every 3 years.
IUDs replaced according to type (between 3–10 years, depending on the device type).