DROPERIDOL
(droe-per'i-dole)
Inapsine
Classifications: central nervous system agent; butyrophenone; antiemetic
Prototype: Haloperidol
Pregnancy Category: C

Availability

2.5 mg/mL injection

Actions

Butyrophenone derivative structurally and pharmacologically related to haloperidol. Antagonizes emetic effects of morphine-like analgesics and other drugs that act on chemoreceptor trigger zone. Mild alpha-adrenergic blocking activity and direct vasodilator effect may cause hypotension. Acts primarily at subcortical level to produce sedation.

Therapeutic Effects

Sedative property reduces anxiety and motor activity without necessarily inducing sleep; patient remains responsive. Potentiates other CNS depressants. Also has antiemetic properties.

Uses

To produce tranquilizing effect and to reduce nausea and vomiting during surgical and diagnostic procedures. Also for premedication, during induction, and as adjunct in maintenance of general or regional anesthesia. Principally used in fixed combination with the potent narcotic analgesic fentanyl (Innovar) to produce neuroleptanalgesia (quiescence, reduced motor activity, and indifference to pain and environmental stimuli) to permit carrying out a variety of diagnostic and minor surgical procedures.

Unlabeled Uses

IV antiemetic in cancer chemotherapy.

Contraindications

Known intolerance to droperidol. Safe use during pregnancy (category C), lactation, or in children <2 y is not established.

Cautious Use

Older adult, debilitated, and other poor-risk patients; Parkinson's disease; hypotension; liver, kidney, cardiac disease; cardiac bradyarrhythmias.

Route & Dosage

Premedication
Adult: IV/IM 2.5–10 mg 30–60 min preoperatively
Child: IV/IM 2–12 y, 0.088–0.165 mg/kg 30–60 min preoperatively

Maintenance of General Anesthesia
Adult: IV/IM Induction, 0.22–0.275 mg/kg; Maintenance, 1.25–2.5 mg
Child: IV/IM 2–12 y, 0.088–0.165 mg/kg

Administration

Intramuscular
Intravenous
  • IV administration to infants and children: Verify correct rate of IV injection with physician.

PREPARE: Direct: Give undiluted.  

ADMINISTER: Direct: Give at a rate of 10 mg or fraction thereof over 30–60 s.  

INCOMPATIBILITIES Solution/additive: Fluorouracil, furosemide, heparin, leucovorin, methotrexate, pentobarbital. Y-site: Fluorouracil, furosemide, heparin, leucovorin, methotrexate, nafcillin.

Adverse Effects (1%)

CNS: Postoperative drowsiness, extrapyramidal symptoms: dystonia, akathisia, oculogyric crisis; dizziness, restlessness, anxiety, hallucinations, mental depression. CV: Hypotension, tachycardia, irregular heartbeats (prolonged QTc interval even at low doses). Other: Chills, shivering, laryngospasm, bronchospasm.

Pharmacokinetics

Onset: 3–10 min. Peak: 30 min. Duration: 2–4 h; may persist up to 12 h. Distribution: Crosses placenta. Metabolism: Metabolized in liver. Elimination: Excreted in urine and feces.

Nursing Implications

Assessment & Drug Effects

Patient & Family Education


Common adverse effects in italic, life-threatening effects underlined; generic names in bold; classifications in SMALL CAPS; Canadian drug name; Prototype drug