Frequently Asked Questions

This resource section is designed to provide you with helpful information about respiratory distress syndrome (RDS) in premature infants and CUROSURF. Find clinical resources and videos all in one convenient place.

Clinical Profile FAQs

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How is the clinical profile of CUROSURF different from Infasurf® (calfactant) and Survanta® (beractant)?1-3

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What are the uses of CUROSURF?

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How does surfactant therapy work in premature infants with RDS?



Dosing & Administration FAQs

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How do I administer CUROSURF?

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What is the recommended dosage for CUROSURF administration?

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Are there any nursing/NICU staff considerations or implications that should be taken into account when administering CUROSURF to preterm infants?



INSURE Strategy FAQs

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What is the INSURE strategy for surfactant administration?



Early Rescue FAQs

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What are the infant and maternal risk factors for RDS and CPAP failure in premature infants?

IMPORTANT SAFETY INFORMATION

CUROSURF® (poractant alfa) 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 to respond to respiratory changes.

CUROSURF should only be administered by those trained and experienced in the care, resuscitation, and stabilization of preterm infants.

Transient adverse reactions associated with 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.

Pulmonary hemorrhage, a known complication of premature birth and very low birth-weight, has been reported with CUROSURF. The rates of common complications of prematurity observed in a multicenter single-dose study that enrolled infants 700–2000 g birth weight with RDS requiring mechanical ventilation and FiO2 ≥ 0.60 are as follows for CUROSURF 2.5 mL/kg (200 mg/kg) (n=78) and control (n=66; no surfactant) respectively: acquired pneumonia (17% vs. 21%), acquired septicemia (14% vs. 18%), bronchopulmonary dysplasia (18% vs. 22%), intracranial hemorrhage (51% vs. 64%), patent ductus arteriosus (60% vs. 48%), pneumothorax (21% vs. 36%) and pulmonary interstitial emphysema (21% vs. 38%).

INDICATION

CUROSURF® (poractant alfa) Intratracheal Suspension is indicated for the rescue treatment of Respiratory Distress Syndrome (RDS) in premature infants. CUROSURF reduces mortality and pneumothoraces associated with RDS.

Please see Full Prescribing Information.

AAP=American Academy of Pediatrics; APGAR=appearance, pulse, grimace, activity, and respiration; CPAP=continuous positive airway pressure; FiO2=fraction of inspired oxygen; NICU=neonatal intensive care unit.

References: 1. CUROSURF® (poractant alfa) Intratracheal Suspension Prescribing Information, Chiesi USA, Inc. May 2021. 2. Survanta® (beractant) Intratracheal Suspension Prescribing Information, AbbVie, Inc. October 2020. 3. Infasurf® (calfactant) Intratracheal Suspension Prescribing Information, ONY, Inc, March 2018. 4. Taeusch HW, Lu K, Ramierez-Schrempp D. Acta Pharmacol Sin. 2002;23(suppl):11-15. 5. Ramanathan R, Rasmussen MR, Gerstmann DR, Finer N, Sekar K; North American Study Group. Am J Perinatol. 2004;21:109-119. 6. Wiseman LR, Bryson HM. Drugs. 1994;48:386-403. 7. IQVIA SMART—US Edition, National Sales Perspectives, All Channels. 2020. 8. US News and World Report website. https://health.usnews.com/best-hospitals/pediatric-rankings/neonatal-care. Accessed September 30, 2024. 9. Children’s Hospital Association website. https://www.childrenshospitals.org/Directories/Hospital-Directory. Accessed 9/30/2024. 10. US News and World Report website. https://health.usnews.com/health-news/best-childrens-hospitals/articles/best-childrens-hospitals-honor-roll-and-overview. Accessed September 30, 2024. 11. Malloy CA, Nicoski P, Muraskas JK. Acta Pediatr. 2005;94:779-784. 12. Bahadue FL, Soll R. Cochrane Database Syst Rev. 2012;11(11):CD001456. 13. Committee on Fetus and Newborn. Pediatrics. 2014;133(1):171-174. 14. Stevens TP, Harrington EW, Blennow M, Soll RF. Cochrane Database Syst Rev. 2007;2007(4):CD003063. 15. Verder H, Albertsen P, Ebbesen F, et al. Pediatrics. 1999;103(2):E24. 16. Dani C, Bertini G, Pezzati M, et al. Pediatrics. 2004;113(6)e560-e563. 17. Bohlin K, Gudmundsdottir T, Katz-Salamon M, et al. J Perinatol. 2007;27(7):422-427. 18. Leone F, Trevisanuto D, Cavallin F, et al. Minerva Pediatr. 2013;65(2):187-192. 19. Tian T, Wang L, Ye R, Liu J, Ren A. Pregnancy Hypertens. 2020;19:131-137. 20. Terfa ZG, Nantanda R, Lesosky M, et al. BMJ Open. 2022;12:e050729. 21. Dargaville PA, Aiyappan A, De Paoli AG, et al. Neonatology. 2013;104(1):8-14. 22. Nanda D, Nangia S, Thukral A, Yadav CP. Eur J Pediatr. 2020;179(4):603-610. 23. Schwartz RM, Luby AM, Scanlon JW, Kellogg RJ. N Engl J Med. 1994;330(21):1476-1480. 24. Sweet DG, Carnielli V, Greisen G, et al. Neonatology. 2019;115(4):432-450. 25. Ovesen P, Rasmussen S, Kesmodel U. Obstet Gynecol. 2011;118(2 pt 1):305-312.