Drug Guide

Generic Name

Poractant Alfa

Brand Names Curosurf

Classification

Therapeutic: Respiratory therapy - surfactant replacement in neonates

Pharmacological: Pulmonary surfactant

FDA Approved Indications

  • Treatment of neonatal respiratory distress syndrome (NRDS) in preterm infants

Mechanism of Action

Poractant Alfa is a natural surfactant that reduces surface tension in the alveoli, thereby improving lung compliance and gas exchange in neonates with surfactant deficiency.

Dosage and Administration

Adult: Not indicated for adult use

Pediatric: Administer via intratracheal instillation as prescribed. Typical dose varies, usually a dose of 2.5 mL/kg (120 mg/kg) is given initially, with additional doses if necessary.

Geriatric: Not applicable (specifically used in neonates)

Renal Impairment: No dose adjustment required, but monitoring advised

Hepatic Impairment: No specific data; use caution and monitor as appropriate

Pharmacokinetics

Absorption: Not applicable; administered directly into the lungs

Distribution: Lung tissue

Metabolism: Metabolized locally in the lungs

Excretion: Pulmonary clearance over time, excreted via mucociliary pathways and swallowed

Half Life: Varies; typically cleared from alveoli in hours to days

Contraindications

  • Known hypersensitivity to surfactant preparations or any component of Curosurf

Precautions

  • Use with caution in infants with congenital heart disease or persistent pulmonary hypertension. Ensure proper dosing and administration by trained personnel.

Adverse Reactions - Common

  • Chronic lung disease (bronchopulmonary dysplasia) (Rare)
  • Air leak syndromes (pneumothorax, pneumomediastinum) (Rare)

Adverse Reactions - Serious

  • Anaphylactic reactions (Very rare)
  • Pulmonary hemorrhage (Rare)

Drug-Drug Interactions

  • None established

Drug-Food Interactions

  • None known

Drug-Herb Interactions

  • None known

Nursing Implications

Assessment: Monitor for improvement in oxygenation, ventilation parameters, and signs of adverse reactions.

Diagnoses:

  • Impaired gas exchange related to surfactant deficiency
  • Risk for respiratory distress

Implementation: Administer via endotracheal tube as prescribed, maintain sterile technique, monitor vital signs and oxygenation.

Evaluation: Assess for improved lung compliance and oxygenation, monitor for adverse reactions.

Patient/Family Teaching

  • Explain the purpose of surfactant therapy and possible side effects.
  • Assist family in understanding the procedure and potential risks.
  • Advise on signs of respiratory distress or adverse reactions to watch for after administration.

Special Considerations

Black Box Warnings:

  • None

Genetic Factors: None specific

Lab Test Interference: None known

Overdose Management

Signs/Symptoms: Respiratory deterioration, oxygenation failure

Treatment: Supportive care; ensure adequate ventilation; no specific antidote; treat symptoms accordingly.

Storage and Handling

Storage: Store unopened vials at 2°C to 8°C (36°F to 46°F). Do not freeze.

Stability: Stable until the expiry date when stored properly. Use immediately after opening or discard if not used promptly.

This guide is for educational purposes only and is not intended for clinical use.