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Doxapram


General


Pronunciation

(DOKS a pram)


Brand Names: U.S.

  • Dopram

Indications


Use: Labeled Indications

Respiratory stimulant for respiratory depression secondary to anesthesia, mild-to-moderate drug-induced respiratory and CNS depression; acute hypercapnia secondary to COPD

Note: In general, the use of doxapram as a respiratory stimulant in adults is limited; alternate therapies are preferred.


Contraindications


Hypersensitivity to doxapram or any component of the formulation; significant cardiovascular impairment (eg, uncompensated heart failure, severe coronary artery disease); severe hypertension (including severe hypertension associated with hyperthyroidism or pheochromocytoma); cerebral edema, cerebral vascular accident, epilepsy, head injury; mechanical disorders of ventilation (eg, mechanical obstruction, muscle paresis, neuromuscular blockade, flail chest, pneumothorax, acute asthma, pulmonary fibrosis); pulmonary embolism


Dosing and Administration


Dosing: Adult

Note: Although manufacturer 's dosing recommendations are presented for these FDA-approved indications, use of doxapram has largely been replaced by alternate preferred agents.

Respiratory depression following anesthesia: IV:

Intermittent injection: Initial: 0.5-1 mg/kg; may repeat at 5-minute intervals (only in patients who demonstrate initial response); maximum total dose: 2 mg/kg

IV infusion: Initial: 5 mg/minute until adequate response or adverse effects seen; decrease to 1-3 mg/minute; maximum total dose: 4 mg/kg

Drug-induced CNS depression: IV:

Intermittent injection: Initial: Priming dose of 1-2 mg/kg; repeat after 5 minutes; may repeat at 1-2 hour intervals (until sustained consciousness); maximum: 3000 mg daily. May repeat in 24 hours if necessary.

IV infusion: Initial: Priming dose of 1-2 mg/kg repeated in 5 minutes. If no response, wait 1-2 hours and repeat priming dose. If some stimulation is noted, initiate infusion at 1-3 mg/minute (depending on size of patient/depth of CNS depression); suspend infusion if patient begins to awaken. Infusion should not be continued for >2 hours. May reinstitute infusion as described above, including bolus, after rest interval of 30 minutes to 2 hours; maximum: 3000 mg daily.

Acute hypercapnia secondary to COPD: IV infusion: Initial: Initiate infusion at 1-2 mg/minute (depending on size of patient/depth of CNS depression); may increase to maximum rate of 3 mg/minute; infusion should not be continued for >2 hours. Monitor arterial blood gases prior to initiation of infusion and at 30-minute intervals during the infusion (to identify possible development of acidosis/CO2 retention). Additional infusions are not recommended (per manufacturer).


Dosing: Geriatric

Refer to adult dosing.


Dosing: Pediatric

Children ≥12 years and Adolescents: Refer to adult dosing.


Dosing: Renal Impairment

No dosage adjustment provided in manufacturers labeling (has not been studied); however, use caution in severe impairment due to the potential for altered pharmacokinetics.


Dosing: Hepatic Impairment

No dosage adjustment provided in manufacturers labeling (has not been studied); however, use caution in severe impairment due to the potential for altered pharmacokinetics.


Reconstitution

To prepare an IV infusion:

Drug-induced CNS depression or postanesthesia: Mix doxapram 250 mg in 250 mL of D5W, D10W, or NS.

COPD-associated hypercapnia: Mix doxapram 400 mg in 180 mL of D5W, D10W, or NS (final concentration: 2 mg/mL).


Administration

Administer IV as an intermittent bolus or as an IV infusion. Avoid rapid infusion. Avoid extravasation.


Storage

Store intact vials at 20 � �C to 25 � �C (68 � �F to 77 � �F).


Dosage Forms/Strengths


Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Solution, Intravenous, as hydrochloride:

Dopram: 20 mg/mL (20 mL) [contains benzyl alcohol]

Generic: 20 mg/mL (20 mL)


Compatibility

Stable in D5W, D10W, NS.

Y-site administration: Incompatible with clindamycin.


Drug Interactions

AtoMOXetine: May enhance the hypertensive effect of Sympathomimetics. AtoMOXetine may enhance the tachycardic effect of Sympathomimetics. Monitor therapy

Cannabinoid-Containing Products: May enhance the tachycardic effect of Sympathomimetics. Exceptions: Cannabidiol. Monitor therapy

Doxofylline: Sympathomimetics may enhance the adverse/toxic effect of Doxofylline. Monitor therapy

Iobenguane I 123: Sympathomimetics may diminish the therapeutic effect of Iobenguane I 123. Avoid combination

Linezolid: May enhance the hypertensive effect of Sympathomimetics. Management: Reduce initial doses of sympathomimetic agents, and closely monitor for enhanced pressor response, in patients receiving linezolid. Specific dose adjustment recommendations are not presently available. Consider therapy modification

MAO Inhibitors: May enhance the hypertensive effect of Doxapram. Exceptions: Tedizolid. Monitor therapy

Sympathomimetics: May enhance the adverse/toxic effect of other Sympathomimetics. Monitor therapy

Tedizolid: May enhance the hypertensive effect of Sympathomimetics. Tedizolid may enhance the tachycardic effect of Sympathomimetics. Monitor therapy


Monitoring Parameters

Monitor heart rate, blood pressure, deep tendon reflexes, CNS status, ECG, arterial blood gases (COPD)


Adverse Reactions


Frequency not defined.

Cardiovascular: Cardiac arrhythmia, change in heart rate, chest pain, chest tightness, flattened T wave on ECG, flushing, increased blood pressure, phlebitis ventricular fibrillation, ventricular tachycardia

Central nervous system: Apprehension, clonus, disorientation, dizziness, hallucination, headache, hyperactivity, hyperreflexia, involuntary muscle movements, paresthesia, positive Babinski sign, seizure

Dermatologic: Burning sensation of skin, diaphoresis, pruritus

Endocrine & metabolic: Albuminuria

Gastrointestinal: Bowel urgency, diarrhea, hiccups, nausea, vomiting

Genitourinary: Urinary incontinence, urinary retention

Hematologic & oncologic: Decreased hematocrit, decreased hemoglobin, hemolysis, decreased red blood cells

Neuromuscular & skeletal: Fasciculations, laryngospasm, muscle spasm

Ophthalmic: Mydriasis

Renal: Increased blood urea nitrogen

Respiratory: Bronchospasm, cough, dyspnea, hyperventilation, hypoventilation (rebound), tachypnea

Miscellaneous: Fever

<1% (Limited to important or life-threatening): Agitation (emergence), prolonged Q-T interval on ECG (premature neonates), second degree atrioventricular block (premature neonates)


Warnings/Precautions


Concerns related to adverse effects:

- Cardiovascular effects: May cause dysrhythmias; monitor for disturbances of cardiac rhythm. If sudden hypotension develops during use, discontinue. Increases in blood pressure are generally modest; use is contraindicated in patients with severe hypertension.

- CNS stimulation: May cause severe CNS stimulation, including seizures; anticonvulsants (as well as oxygen and resuscitative equipment) should be available to manage potential excessive CNS stimulation.

Disease-related concerns:

- Cerebrovascular disease: Use with caution in patients with cerebrovascular disease; lowered pCO2 induced by hyperventilation produces cerebral vasoconstriction and decreased circulation.

- Hepatic impairment: Use with caution in patients with hepatic impairment.

- Renal impairment: Use with caution in patients with renal impairment.

- Respiratory disease: Do not use in patients on mechanical ventilation. Use with caution in treating pulmonary disease; a pressor effect on pulmonary circulation may result in a fall in arterial pO2. If sudden dyspnea develops during use, discontinue. Doxapram causes patients to increase the work of breathing; therefore, do not increase the rate of infusion in an attempt to lower the pCO2 in severely-ill COPD patients.

Concurrent drug therapy issues:

- MAO inhibitors (MAOIs): Use caution with coadministration; additive pressor effect may occur.

- Sympathomimetics: Use caution with coadministration; additive pressor effect may occur.

- Volatile anesthetics: If patient has received anesthesia with a volatile agent known to sensitize the myocardium to catecholamines, avoid use of doxapram until anesthetic has been eliminated to decrease the risk of ventricular tachycardia or ventricular fibrillation.

Dosage form specific issues:

- Benzyl alcohol and derivatives: Some dosage forms may contain benzyl alcohol; large amounts of benzyl alcohol ( ≥99 mg/kg/day) have been associated with a potentially fatal toxicity ( "gasping syndrome " �) in neonates; the "gasping syndrome " � consists of metabolic acidosis, respiratory distress, gasping respirations, CNS dysfunction (including convulsions, intracranial hemorrhage), hypotension and cardiovascular collapse (AAP [Inactive" 1997]; CDC, 1982); some data suggests that benzoate displaces bilirubin from protein binding sites (Ahlfors, 2001); avoid or use dosage forms containing benzyl alcohol with caution in neonates. See manufacturer 's labeling.

Other warnings/precautions:

- Administration: Avoid extravasation; doxapram may cause thrombophlebitis or local skin irritation. Hemolysis may result from rapid infusion.

- Appropriate use: Adequate airway required prior to use; consider airway protection in case of vomiting. Resuscitative equipment (in addition to anticonvulsants and oxygen) should be readily available; doxapram alone may not be sufficient to stimulate spontaneous breathing or provide sufficient arousal. Doxapram is neither an antagonist to skeletal muscle relaxants nor an opioid antagonist. Use with caution in patients with hypermetabolic states (eg, hyperthyroidism, pheochromocytoma).


Pregnancy Risk Factor

B


Pregnancy Considerations

Adverse events have not been observed in animal reproduction studies.


Actions


Pharmacology

Stimulates respiration through action on peripheral carotid chemoreceptors; respiratory center in medulla is also directly stimulated as dosage is increased


Distribution

Vd: Neonates: 4 to 7.3 L/kg


Metabolism

Extensive in the liver to active metabolite (keto-doxapram)


Excretion

Clearance: Neonates, premature: 0.44 to 0.7 L/hour/kg


Onset of Action

Respiratory stimulation: Single IV injection: 20 to 40 seconds; Peak effect: Single IV injection: 1 to 2 minutes


Duration of Action

Single IV injection: 5 to 12 minutes


Half-Life Elimination

Serum: Neonates, premature: 6.6 to 12 hours; Adults: Mean: 3.4 hours (range: 2.4 to 4.1 hours)


Patient and Family Education


Patient Education

- Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)

- Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.

Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for healthcare professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience and judgment in diagnosing, treating and advising patients.

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