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beractant (be-rak-tant)
Survanta
Classification
Therapeutic: anti-RDS agents
Pharmacologic: pulmonary surfactants
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Treatment and prophylaxis of respiratory distress syndrome (RDS, hyaline membrane disease) in premature infants.
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Replaces endogenous pulmonary surfactant in premature infants, allowing normal surface activity in alveoli. Consists of natural bovine lung extract. Therapeutic Effects: Decreased incidence, mortality, and complications from RDS.
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Adverse Reactions/Side Effects
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Resp: oxygen desaturation (as a result of administration process). CV: transient bradycardia.
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PHYSICAL THERAPY IMPLICATIONS
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Examination and Evaluation
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Monitor oxygen saturation levels following administration. Notify physician or nursing staff immediately about a sudden decrease is oxygen saturation.
Assess heart rate, and report a sustained decrease in heart rate (bradycardia).
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When indicated, implement chest physical therapy interventions such as positioning, suctioning, and chest percussion/vibration to maintain respiratory function and augment drug effects in premature infants.
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Absorption: Administered directly to site of action. Systemic absorption not known.
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Distribution: Rapidly distributes to lung tissue.
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Metabolism and Excretion: Enters surfactant pathways in which recycling and reutilization occur.
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Contraindications/Precautions
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Contraindicated in: No known contraindications.
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Use Cautiously in: No known cautions. Nosocomial infections may be more common.
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Intratracheal (Infants, Premature): 100 mg phospholipids/kg birth weight (4 mL/kg birth weight); 4 doses may be given in first 48 hr of life, no closer than q 6 hr apart.
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Intratracheal suspension: 25 mg phospholipid/mL—4-mL and 8-mL vials.