Each year, more babies are treated for RDS with CUROSURF than any other natural surfactant.1
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CUROSURF delivers more surfactant in a smaller overall volume for efficient instillation that may help to minimize complications.2-6
Clinical studies have not established that lower volume results in superior efficacy or safety based on clinically relevant end points.
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CUROSURF goes to work fast, improving oxygenation within 5 minutes.7,8
Physiological end points (eg, faster reduction in FiO2) have not been proven to impact key clinical outcomes such as mortality due to RDS.
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In clinical studies, most infants required only one dose, which can reduce complications associated with reintubation and subsequent mechanical ventilation.5-7
Clinical studies have not established that fewer doses or longer dosing intervals result in superior safety or efficacy based on clinically relevant end points.
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Experience a smooth process evaluating CUROSURF in your NICU with a comprehensive support program from Cornerstone Therapeutics.
Indication
CUROSURF® (poractant alfa) Intratracheal Suspension is indicated for the treatment (rescue) of respiratory distress syndrome (RDS) in premature infants. CUROSURF reduces mortality and pneumothoraces associated with RDS.
Important Safety Information
CUROSURF is intended for intratracheal use only. THE ADMINISTRATION OF EXOGENOUS SURFACTANTS, INCLUDING CUROSURF, CAN RAPIDLY AFFECT OXYGENATION AND LUNG COMPLIANCE. Therefore, infants receiving CUROSURF should receive frequent clinical and laboratory assessments so that oxygen and ventilatory support can be modified in response to respiratory changes.
CUROSURF should only be administered by those trained and experienced in the care, resuscitation, and stabilization of preterm infants.
TRANSIENT ADVERSE EFFECTS SEEN WITH THE ADMINISTRATION OF CUROSURF INCLUDE BRADYCARDIA, HYPOTENSION, ENDOTRACHEAL TUBE BLOCKAGE, AND OXYGEN DESATURATION. These events require stopping CUROSURF administration and taking appropriate measures to alleviate the condition. After the patient is stable, dosing may proceed with appropriate monitoring.
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