Mosby's 2014 Nursing Drug Reference (259 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

HIGH ALERT
methadone (Rx)

(meth′a-done)

Dolophine, Metadol
, Methadose

Func. class.:
Opioid analgesic

Chem. class.:
Synthetic diphenylheptane derivative

 

Controlled Substance Schedule II

Do not confuse:
methadone
/methylphenidate

ACTION:

Depresses pain impulse transmission at the spinal cord level by interacting with opioid receptors; produces CNS depression

USES:

Severe pain, opioid withdrawal

CONTRAINDICATIONS:

Hypersensitivity to this product or chlorobutanol (inj); asthma, ileus

 

Black Box Warning:

Respiratory depression

Precautions:
Pregnancy (C), breastfeeding, children <18 yr, geriatric patients, addictive personality, increased intracranial pressure, MI (acute), severe heart disease, respiratory depression, pulmonary/renal/hepatic disease, respiratory insufficiency, torsades de pointes, COPD

 

Black Box Warning:

QT prolongation, pain, substance abuse, potential for overdose, poisoning, accidental exposure

DOSAGE AND ROUTES
Calculator
Severe pain

• Adult:
PO/SUBCUT/IM/IV
2.5-10 mg q8-12hr prn

Opioid withdrawal

• Adult including pregnant woman:
20-30 mg initially unless low opioid tolerance expected; additional 5-10 mg q2-4hr as needed after initial dose; if symptoms continue, may give for ≤5 days

Renal disease

• Adult:
may need to be modified

Available forms:
Inj 10 mg/ml; tabs 5, 10 mg; oral sol 5, 10 mg/5 ml, 10 mg/ml

Administer:
IM route

• 
Rotating inj sites, give deep in large muscle mass (IM)

SUBCUT route

• 
Pain and induration may occur at site

SIDE EFFECTS

CNS:
Drowsiness, dizziness, confusion, headache, sedation
, euphoria,
seizures

CV:
Palpitations, bradycardia, change in B/P,
cardiac arrest, shock,
hypotension,
torsades de pointes, QT prolongation

EENT:
Tinnitus, blurred vision, miosis, diplopia

GI:
Nausea, vomiting, anorexia, constipation, cramps
, biliary tract spasm

GU:
Increased urinary output, dysuria, urinary retention, impotence

INTEG:
Rash
, urticaria, bruising, flushing, diaphoresis, pruritus

RESP:
Respiratory depression, respiratory arrest

PHARMACOKINETICS

Metabolized by liver; excreted by kidneys; crosses placenta; excreted in breast milk; half-life 8-59 hr, extended interval with continued dosing; 90% bound to plasma proteins

PO:
Onset 30-60 min, peak 1-1.5 hr, duration 6-8 hr, cumulative 22-48 hr; PO half as active as INJ

SUBCUT/IM:
Onset 10-20 min, peak 1½-2 hr, duration 4-6 hr, cumulative 22-48 hr

INTERACTIONS

 
Unpredictable reactions: MAOIs; do not use together

• 
Do not use within 2 wk of selegiline

Increase:
effects with other CNS depressants—alcohol, opiates, sedative/hyp
notics, antipsychotics, skeletal muscle relaxants

Increase:
toxicity—CYP3A4 inhibitors (aprepitant, antiretroviral protease inhibitors, clarithromycin, danazol, delavirdine, diltiazem, erythromycin, fluconazole, FLUoxetine, fluroxamine, imatinib, ketoconazole, mibefradil, nefazodone, telithromycin, voriconazole)

Increase:
QT prolongation—class IA antiarrhythmics (disopyramide, procainamide, quiNIDine), class III antiarrhythmics (amiodarone, dofetilide, ibutilide, sotalol), astemizole, arsenic trioxide, cisapride, chloroquine, clarithromycin, levomethadye, pentamidine, some phenothiazines, pimozide, terfenadine

Decrease:
analgesia—rifampin, phenytoin, nalbuphine, pentazine

Decrease:
methadone effect—CYP3A4 inducers (barbiturates, bosentan, carBAMazepine, efavirenz, phenytoins, nevira-pine, rifabutin, rifampin), withdrawal symptoms may occur

Drug/Food

• 
Avoid use with grapefruit juice

Drug/Herb

• 
Avoid use with St. John’s wort; withdrawal may result

Increase:
CNS depression—chamomile, hops, kava, valerian

Drug/Lab Test

Increase:
amylase, lipase

NURSING CONSIDERATIONS
Assess:

• 
Pain:
type, location, intensity, grimacing before, 1½-2 hr after administration; use pain scoring

• 
I&O ratio; check for decreasing output; may indicate urinary retention

• 
CNS changes: dizziness, drowsiness, hallucinations, euphoria, LOC, pupil reaction

• 
Allergic reactions: rash, urticaria

 

Black Box Warning:

Respiratory dysfunction:
respiratory depression, character, rate, rhythm; notify prescriber if respirations are <10/min

 

Black Box Warning:

QT prolongation:
may be dose related or use with other products that increase QT

 

Black Box Warning:

Accidental exposure: make sure product is not accessible to children, pets

 

Black Box Warning:

Overdose, poisoning: advise persons involved in correct use

 

Black Box Warning:

Substance abuse: may occur but has less psychological dependence than other opiate agonists

• 
Opioid detoxification: no analgesia occurs, only prevention of withdrawal symptoms

 

Black Box Warning:

B/P, pulse, ECG; hypotension, palpitations may occur

• 
Bowel changes, bulk, fluids, laxatives should be used for constipation

Perform/provide:

• 
Storage in light-resistant container at room temp

• 
Assistance with ambulation

Evaluate:

• 
Therapeutic response: decrease in pain, successful opioid withdrawal

Teach patient/family:

• 
To report any symptoms of CNS changes, allergic reactions

• 
That physical dependency may result from extended use

 
That withdrawal symptoms may occur: nausea, vomiting, cramps, fever, faintness, anorexia

• 
To maintain proper hydration; to avoid alcohol use

TREATMENT OF OVERDOSE:

Naloxone (Narcan) 0.2-0.8 mg IV, O
2
, IV fluids, vasopressors

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

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