Mosby's 2014 Nursing Drug Reference (402 page)

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topiramate (Rx)

(toh-pire′ah-mate)

Topamax, Topamax Sprinkle, Topiragen

Func. class.:
Anticonvulsant—miscellaneous

Chem. class.:
Monosaccharide derivative

ACTION:

May prevent seizure spread as opposed to an elevation of seizure threshold, increases GABA activity

USES:

Partial seizures in adults and children 2-16 yr old; tonic-clonic seizures; seizures with Lennox-Gastaut syndrome; migraine prophylaxis

Unlabeled uses:
Infantile spasms, bipolar disorder, alcohol dependence, absence seizures, neuropathic pain, cluster headaches, mania

CONTRAINDICATIONS:

Hypersensitivity, metabolic acidosis, pregnancy (D)

Precautions:
Breastfeeding, children, renal/hepatic disease, acute myopia, secondary closed-angle glaucoma, behavioral disorders, COPD, dialysis, encephalopathy, status asthmaticus, status epilepticus, surgery, paresthesias, maculopathy

DOSAGE AND ROUTES
Calculator
Adjunctive therapy for seizures

• Adult/adolescent/child

10 yr:
PO
25-50 mg/day initially, titrate by 25-50 mg/wk, up to 200-400 mg/day in 2 divided doses

• Child 2-9 yr:
PO
week 1: 25 mg in
PM
, then 25 mg bid if tolerated (week 2), then increase by 25-50 mg/day each week as tolerated over 5 to 7-wk titration period, maintenance given in 2 divided doses; <11 kg, minimum 150 mg/day, max 250 mg/day; 12-22 kg, minimum 200 mg/day, max 300 mg/day; 23-31 kg, minimum 200 mg/day, max 350 mg/day; 32-38 kg, minimum 250 mg/day, max 350 mg/day; >38 kg, minimum 250 mg/day, max 400 mg/day

Migraine prophylaxis

• Adult:
PO
25 mg/day initially, increase by 25 mg/day/wk up to 100 mg/day in 2 divided doses

Renal dose

• Adult:
PO
CCr <70 ml/min, give 1/2 dose

Atonic/atypical absence/myoclonic seizures (unlabeled)

• Adult/adolescent >16 yr:
PO
50 mg/day, titrate slowly by 50 mg/wk to 100-300 mg tid

• Child 2-16 yr:
PO
0.5-1 mg/kg, max 25 mg, initially daily × 7 days then increase by 0.5-1 mg/kg/day weekly up to 3-6 mg/kg/day in divided doses

Refractory infantile spasms (unlabeled)

• Child:
PO
25 mg/day, may increase by 25 mg q2-3days until spasms controlled, max 24 mg/kg/day

Alcoholism (unlabeled)

• Adult:
PO
25 mg/day, titrated to max 300 mg/day in divided doses

Neuropathic pain (unlabeled)

• Adult:
PO
12.5-25 mg q day or bid × 4 wk then double dose q4wk to max 100-200 mg/day in divided doses

Bipolar disorder (unlabeled)

• Adult:
PO
25 mg/day then increase by 25-mg increments to 200 mg/day

Available forms:
Tabs 25, 50, 100, 200 mg; sprinkle caps 15, 25 mg

Administer:

• 
Swallow tabs whole; do not break, crush, or chew tabs; very bitter

• 
May take without regard to meals

• 
Sprinkle cap can be given whole or opened and sprinkled on soft food; do not chew, drink water after sprinkle

SIDE EFFECTS

CNS:
Dizziness, fatigue
, cognitive disorders, insomnia,
anxiety
, depression, paresthesia,
memory loss, tremor
, motor retardation,
suicidal ideation

EENT:
Diplopia,
vision abnormality

GI:
Diarrhea,
anorexia, nausea, dyspepsia
, abdominal pain, constipation, dry mouth,
pancreatitis

GU:
Breast pain, dysmenorrhea, menstrual disorder

INTEG:
Rash

MISC:
Weight loss, leukopenia, metabolic acidosis, increased body temperature;
unexplained death (epilepsy)

RESP:
Upper respiratory tract infection, pharyngitis, sinusitis

PHARMACOKINETICS

Well absorbed, peak 2 hr, terminal half-life 19-25 hr, excreted in urine (55%-97% unchanged), crosses placenta, excreted in breast milk, protein binding (9%-17%), steady state 4 days

INTERACTIONS

Increase:
renal stones—carbonic anhydrase inhibitors

Increase:
effect of amitriptyline

Increase:
CNS depression—alcohol, CNS depressants

Increase:
topiramate levels—metformin, hydrochlorothiazide, lamoTRIgine

Decrease:
levels of oral contraceptives, estrogen, digoxin, valproic acid, lithium, risperiDONE

Decrease:
topiramate levels—phenytoin, carBAMazepine, valproic acid, probenecid

NURSING CONSIDERATIONS
Assess:

• 
Seizures:
location, type, duration, aura

• 
Bipolar disorder:
mood, behavior

• 
Renal studies: urinalysis, BUN, urine creatinine q3mo; symptoms of renal colic

• 
Hepatic studies: ALT, AST, bilirubin if patient receiving long-term treatment

• 
CBC during long-term therapy (anemia); serum bicarbonate (metabolic acidosis)

• 
Migraines: pain location, duration; alleviating factors

 
Mental status: mood, sensorium, affect, behavioral changes,
suicidal thoughts/behaviors;
if mental status changes, notify prescriber

• 
Body weight, evidence of cognitive disorder

Perform/provide:

• 
Storage at room temp away from heat, light

• 
Assistance with ambulation during early part of treatment; dizziness occurs

• 
Seizure precautions: padded side rails, move objects that may harm patient

Evaluate:

• 
Therapeutic response: decreased seizure activity

Teach patient/family:

• 
To carry emergency ID stating patient’s name, products taken, condition, prescriber’s name and phone number

• 
To avoid driving, other activities that require alertness

• 
Not to discontinue medication quickly after long-term use

• 
To notify prescriber immediately of blurred vision, periorbital pain

• 
To maintain adequate fluid intake

• 
About administration procedure and expected results

• 
To use nonhormonal contraceptive; that effect of oral contraceptives is decreased, pregnancy (D)

• 
To drink plenty of fluids to prevent kidney stones

• 
May need to increase amount of food consumed, weight loss may occur

Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

HIGH ALERT
topotecan (Rx)

(toh-poh-tee′kan)

Hycamtin

Func. class.:
Antineoplastic, natural; topoisomerase inhibitor

Chem. class.:
Camptothecin analog

ACTION:

Antitumor product with topoisomerase-I–inhibitory activity; topoisomerase I relieves torsional strain
in DNA by causing single-strand breaks; also causes double-strand DNA damage

USES:

Metastatic ovarian cancer after failure of traditional chemotherapy; relapsed small-cell lung cancer; cervical cancer

Unlabeled uses:
Non–small-cell lung cancer (NSCLC), rhabdomyosarcoma

CONTRAINDICATIONS:

Pregnancy (D), breastfeeding, hypersensitivity, severe bone marrow depression

 

Black Box Warning:

Neutropenia

Precautions:
Children, renal disease, gelatin hypersensitivity

DOSAGE AND ROUTES
Calculator
Metastatic carcinoma of the ovary after failure of first or subsequent chemotherapy; SCLC-sensitive disease after failure of first-line therapy

• Adult:
IV INF
1.5 mg/m
2
over 30 min daily × 5 days starting on day 1 of 21-day course × 4 courses; may be reduced to 0.25 mg/m
2
for subsequent courses if severe neutropenia occurs; relapsed small-cell lung cancer (SCLC) in those with a prior complete or partial response, ≥45 days from end of first-line treatment.
PO
2.3 mg/m
2
/day on days 1-5 of 21-day course

Renal dose

• Adult:
IV
CCr 20-39 ml/min, 0.75 mg/m
2
/day × 5 days starting on day 1 of 21-day course

Available forms:
Lyophilized powder for inj 4 mg; caps 0.25, 1 mg

Administer:
PO route

• 
Do not break, crush, chew, or open caps; protect from light

• 
Take without regard to food

Intermittent IV infusion route

• 
Visually inspect for particulate matter and discoloration prior to use

• 
Reconstitute each 4 mg-vial with 4 ml sterile water for injection; use immediately, no preservative

• 
Withdraw the appropriate volume of the reconstituted solution; dilute further, dilute in 0.9% NaCl or D5W prior to administration

• 
The reconstituted solution is yellow or yellow-green

• 
Topotecan injection diluted for infusion is stable at room temperature with normal light for 24 hr

• 
Infuse over 30 min

SIDE EFFECTS

CNS:
Arthralgia,
asthenia, headache
, myalgia,
pain
, weakness

GI:
Abdominal pain, constipation
, diarrhea, obstruction,
nausea
, stomatitis,
vomiting;
increased ALT, AST; anorexia

HEMA:
Neutropenia, leukopenia, thrombocytopenia, anemia, sepsis

INTEG:
Total alopecia

RESP:
Dyspnea, cough,
interstitial lung disease

PHARMACOKINETICS

Rapidly and completely absorbed, excreted in urine and feces as metabolites, half-life 2.8 hr, 7%-35% bound to plasma proteins

INTERACTIONS

• 
Avoid use with P-glycoprotein, breast cancer resistance protein inhibitors (amiodarone, clarithromycin, diltiazem, erythromycin, indinavir), quiNIDine, testosterone, verapamil, tamoxifen, itraconazole, mefloquine, RU-486, niCARdipine, vaccines, toxoids

Increase:
myelosuppression when used with CISplatin

Increase:
bleeding risk—NSAIDs, anticoagulants, thrombolytics, platelet inhibitors

Drug/Food

• 
Avoid use with grapefruit juice

NURSING CONSIDERATIONS
Assess:

• 
Hepatic studies: AST, ALT, alk phos, which may be elevated; creatinine, BUN

 

Black Box Warning:

CBC, differential, platelet count weekly; withhold product if WBC is <3500/mm
3
or platelet count is <100,000/mm
3
; notify prescriber of results; product should be discontinued

• 
Buccal cavity for dryness, sores or ulcerations, white patches, oral pain, bleeding, dysphagia

• 
Interstitial lung disease (ILD):
fever, cough, dyspnea, hypoxia, may be fatal

Perform/provide:

• 
Storage of caps in refrigerator; IV INF unopened at room temp; protect both from light

• 
Increased fluid intake to 2-3 L/day to prevent dehydration unless contraindicated

• 
Rinsing of mouth tid-qid with water, club soda; brushing of teeth bid-tid with soft brush or cotton-tipped applicator for stomatitis; use unwaxed dental floss

Evaluate:

• 
Therapeutic response: decreased tumor size, spread of malignancy

Teach patient/family:

• 
That total alopecia may occur; that hair grows back but is different in color and texture

• 
To avoid foods with citric acid or hot or rough texture if stomatitis is present; to drink adequate fluids

• 
To report stomatitis and any bleeding, white spots, ulcerations in mouth; to examine mouth daily; to report symptoms

 

Black Box Warning:

To report signs of anemia: fatigue, headache, faintness, SOB, irritability

• 
To use effective contraception during treatment and for ≤6 mo after, pregnancy (D); to avoid breastfeeding

• 
To avoid OTC products without approval of prescriber

• 
To avoid driving or other activities requiring alertness

• 
To avoid vaccines, toxoids

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