altretamine
(al-tret-a-meen)
Classification
Therapeutic: antineoplastics
Pregnancy Category D
| High Alert |
|
altretamine Classification |
| ROUTE | ONSET | PEAK | DURATION |
| PO | unknown | 3–4 wk | 6 wk |
Nausea and vomiting of gradual onset frequently occur. Tolerance may develop after several weeks of therapy. Treatment includes antiemetics or dosage reduction and, rarely, discontinuation. Monitor amount of emesis and notify physician if emesis exceeds guidelines to prevent dehydration.Monitor for bone marrow depression throughout therapy. Although the patient is often asymptomatic, symptoms include anemia (unusual tiredness), leukopenia (fever, chills, sore throat, cough or hoarseness, lower back or side pain, painful or difficult urination), and thrombocytopenia (bleeding gums, bruising, petechiae, guaiac stools, urine, and emesis). Notify physician if these symptoms occur.Avoid IM injections and taking rectal temperatures. Apply pressure to venipuncture sites for 10 min.Assess patient for signs of neurotoxicity including CNS effects (anxiety, clumsiness, confusion, dizziness, mental depression, weakness, seizures) and peripheral neuropathy (numbness, tingling, paresthesia) prior to initiation of each course and routinely throughout therapy. Pyridoxine may minimize peripheral neuropathy; usually reversible on discontinuation of altretamine. If neurotoxicity continues after dosage reduction, discontinue therapy.Lab Test Considerations:
Monitor CBC and platelets prior to each course of therapy, monthly, and as clinically indicated. The nadir of leukopenia and thrombocytopenia occurs in 3–4 wk with 21-day therapy and recovers in 6 wk with intermittent dosing; with continuous dosing the nadir occurs in 6–8 wk. Dose should be held for 14 or more days and resumed at 50 mg/m2/day 4 times daily for any of the following: GI intolerance unresponsive to conventional therapy, WBC <2000 mm3, granulocytes <1000 mm3, platelet count <75,000 mm3, or progressive neurologic toxicity.
High Alert: Fatalities have occurred with chemotherapeutic agents. Before administering, clarify all ambiguous orders; double check single, daily, and course-of-therapy dose limits; have second practitioner independently double check original order and dose calculations.PO: Administer doses after meals and at bedtime to reduce nausea and vomiting.Instruct patient to notify health care professional promptly if fever; sore throat; signs of infection; bleeding gums; bruising; petechiae; blood in stools, urine, or emesis; increased fatigue, dyspnea, or orthostatic hypotension occurs. Caution patient to avoid crowds and persons with known infections. Instruct patient to use soft toothbrush and electric razor and to avoid falls. Caution patient not to drink alcoholic beverages or take medications containing aspirin or NSAIDs; may precipitate GI bleeding.Instruct patient to report promptly any numbness or tingling in extremities.Instruct patient not to receive any vaccinations without advice of health care professional.Advise patient of the need for contraception.Emphasize the need for periodic lab tests to monitor for side effects.Decrease in size or spread of malignancy.