General
Pronunciation
a-se-teel-SIS-teen
Trade Name(s)
Acetadote
Mucomyst
Mucosil
Pregnancy CategoryCategory BTher. class.antidotes
(for acetaminophen toxicity)
mucolytic
Indications
PO: Antidote for the management of potentially hepatotoxic overdosage of acetaminophen (should be administered within 24 hours of ingestion)
IV: Antidote for the management of potentially hepatotoxic overdosage of acetaminophen (should be administered within 810 hours of ingestion)
Inhaln: Mucolytic in the management of conditions associated with thick viscid mucous secretions
Unlabelled Use(s): Prevention of radiocontrast-induced renal dysfunction (oral)
Action
PO: Decreases the buildup of a hepatotoxic metabolite in acetaminophen overdosage
IV: Decreases the buildup of a hepatotoxic metabolite in acetaminophen overdosage
Inhaln: Degrades mucus, allowing easier mobilization and expectoration
Therapeutic Effect(s): PO: Prevention or lessening of liver damage following acetaminophen overdose
Inhaln: Lowers the viscosity of mucus
Pharmacokinetics
Absorption: Absorbed from the GI tract following oral administration. Action is local following inhalation; remainder may be absorbed from pulmonary epithelium
Distribution: Crosses the placenta; 0.47 L/kg
Protein Binding: 83% bound to plasma proteins
Metabolism and Excretion: Partially metabolized by the liver, 22% excreted renally
Half-life: Adults 5.6 hr (
in hepatic impairment)newborns 11 hr
TIME/ACTION PROFILE
| ROUTE | ONSET | PEAK | DURATION |
| PO (antidote) | unknown | 3060 min | 4 hr |
| Inhalation (mucolytic) | 1 min | 510 min | short |
Contraindication/Precautions
Contraindicated in:
Hypersensitivity
Use Cautiously in:
Severe respiratory insufficiency, asthma or history of bronchospasm
History of GI bleeding (oral only)
OB: Lactation: Safety not established
Adverse Reactions/Side Effects
CNS: drowsiness.
CV: vasodilation.
EENT: rhinorrhea.
Resp: bronchospasm, bronchial/tracheal irritation, chest tightness, increased secretions.
GI: nausea, vomiting, stomatitis.
Derm: pruritus, rash, urticaria, clamminess.
Misc: allergic reactions (primarily with IV), including anaphylaxis, ANGIOEDEMA, chills, fever.
*CAPITALS indicates life-threatening.
*italic indicates most frequent.
Interactions
Drug-Drug
Activated charcoal may adsorb orally administered acetylcysteine and decrease its effectiveness as an antidote
Route/Dosage
Acetaminophen Overdose
PO (Adults and Children): 140 mg/kg initially, followed by 70 mg/kg q 4 hr for 17 additional doses.
IV (Adults and Children):
Loading dose 150 mg/kg over 15 min initially followed by
First maintenance dose 50 mg/kg over 4 hr, then
second maintenance dose 100 mg/kg over 16 hr.
Mucolytic Inhaln (Adults and Children):
Nebulization via face mask35 ml of 20% solution or 610 ml of the 10% solution 34 times daily (range 110 ml of 20% solution or 220 ml of 10% solution q 26 hr);
nebulization via tent or croupettevolume of 1020% solution required to maintain heavy mist;
direct instillation12 ml of 1020% solution q 14 hr;
intratracheal instillation via tracheostomy12 ml of 1020% solution q 14 hr (up to 25 ml of 20% solution via tracheal catheter into particular segments of the bronchopulmonary tree).
Unlabeled Use (prevention of radiocontrast-induced renal dysfunction) PO (Adults): 600 mg twice daily for 2 days, beginning the day before the procedure.
Availability
Solution for inhalation: 10% in 4-, 10-, and 30-ml vials, 20% in 4-, 10-, 30-, and 100mL vials
Solution for injection: 20% in 30mL vials
Assessment
Antidote in Acetaminophen Overdose
Assess type, amount, and time of acetaminophen ingestion. Assess plasma acetaminophen levels. Initial levels are drawn at least 4 hr after ingestion of acetaminophen. Plasma level determinations may be difficult to interpret following ingestion of extended-release preparations. Do not wait for results to administer dose
» IV: Assess for anaphylactoid reaction. Erythema and flushing are common, usually occurring 3060 min after initiating infusion, and may resolve with continued administration. If rash, hypotension, wheezing, dyspnea occur, initiate treatment for anaphylaxis (antihistamine and epinephrine). Acetylcysteine infusion should be interrupted until symptoms resolve and carefully restarted. If anaphylactoid reaction recurs, discontinue acetylcysteine and use alternative form of treatment
» Monitor AST, ALT, and bilirubin levels along with prothrombin time every 24 hr for 96 hr in patients with plasma acetaminophen levels indicating potential hepatotoxicity
» Monitor cardiac and renal function (creatinine, BUN), serum glucose, and electrolytes. Maintain fluid and electrolyte balance, correct hypoglycemia, and administer vitamin K1 or fresh frozen plasma or clotting factor concentrate if prothrombin time ratio exceeds 1.5 or 3, respectively
» Assess patient for nausea, vomiting, and urticaria. Notify physician if these occur
Mucolytic Assess respiratory function (lung sounds, dyspnea) and color, amount, and consistency of secretions before and immediately following treatment to determine effectiveness of therapy
Potential Nursing Diagnoses
Risk for self-directed violence (Indications)
Ineffective airway clearance (Indications)
Deficient knowledge, related to medication regimen (Patient/Family Teaching)
Implementation
After opening, solution for inhalation may turn light purple; does not alter potency. Refrigerate open vials and discard after 96 hr
» Drug reacts with rubber and metals (iron, nickel, copper); avoid contact with these substances
PO: Acetaminophen Overdose First empty stomach contents by inducing emesis or lavage. Dilute 20% solution with cola, water, or juice to a final concentration of 1:3 for patients weighing up to 20 kg or with enough diluent to make a 5% solution for patients weighing more than 20 kg, to increase palatability. May be administered by duodenal tube if patient is unable to swallow. If patient vomits loading dose or maintenance doses within 1 hr of administration, readminister dose
IV Adminstration: Intermittent Infusion:
Most effective if administered within 8 hrs of acetaminophen ingestion. Dilute in D5W. For loading dose: Dilute 150 mg/kg in 200 mL. For 1st Maintenance Dose: Dilute 50 mg/kg in 500 mL. For 2nd Maintenance Dose: Dilute 100 mg/kg in 1000 ML. Adjust fluid volume for patients <40 kg or requiring fluid restriction. Vials are single-use. Discard after using. Reconstituted solution is stable for 24 hr at room temperature
Rate:
Administer Loading Dose over 15 min
Administer 1st Maintenance Dose over 4 hr
Administer 2nd Maintenance Dose over 16 hr
Inhaln:
Mucolytic Encourage adequate fluid intake (20003000 ml/day) to decrease viscosity of secretions
For nebulization, the 20% solution may be diluted with 0.9% NaCl for injection or inhalation or sterile water for injection or inhalation. May use 10% solution undiluted. May be administered by nebulization, or 12 ml may be instilled directly into airway. During administration, when 25% of medication remains in nebulizer, dilute with equal amount of 0.9% NaCl or sterile water
An increased volume of liquefied bronchial secretions may occur following administration. Have suction equipment available for patients unable to effectively clear airways
If bronchospasm occurs during treatment, discontinue and consult health care professional regarding possible addition of bronchodilator to therapy. Patients with asthma or hyperactive airway disease should be given a bronchodilator prior to acetylcysteine to prevent bronchospasm
Rinse patient's mouth and wash face following treatment, as drug leaves a sticky residue
Patient/Family Teaching
Acetaminophen Overdose: Explain purpose of medication to patient
Inhaln: Instruct patient to clear airway by coughing deeply before taking aerosol treatment
» Inform patient that unpleasant odor of this drug becomes less noticeable as treatment progresses and medicine dissipates
Evaluation/Desired Outcomes
Decreased acetaminophen levels
» No further increase in hepatic damage during acetaminophen overdose therapy
Decreased dyspnea and clearing of lung sounds when used as a mucolytic
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