Practice Standard for the Administration
of Exogenous Surfactant (Survanta)
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Surfactant Use for Respiratory Distress Syndrome (RDS) in Preterm Infants - First Dose
- Prophylactic treatment for preventing or ameliorating the
severity of RDS is recommended for all inborn infants with a
gestational age of < 27 weeks. Treatment should be accomplished as soon
after delivery as possible, following intubation and
clinical ascertainment of proper endotracheal tube
placement.
- Inborn infants > 27 weeks and < 30 weeks gestation should receive
surfactant without delay if they require intubation and supplemental oxygen for respiratory failure.
- Infants > 30 weeks gestation should receive surfactant therapy if they require mechanical
ventilation and have a diagnosis of RDS.
Surfactant Use for RDS in Preterm Infants - Additional Doses
- Infants < 30 weeks gestation with the diagnosis of RDS should receive a second dose of surfactant
as a bolus 6-12 hours after the first dose if they continue intubated on mechanical ventilation, regardless of the inspired oxygen concentration.
- Infants > 30 weeks gestation with the diagnosis of RDS should receive a second dose of surfactant as a bolus
6-12 hours after the first dose if they continue intubated on mechanical ventilation and require > 30% inspired oxygen. If
the infant remains intubated with an inspired oxygen concentration between 21-29%, one should consider a second dose of surfactant.
- One may consider continued treatment with additional doses of surfactant (total of 4 doses maximum) for preterm infants with RDS and worsening
oxygenation 6-12 hours after the second dose.
- The Survanta dose is 4 mL/kg/dose.
- There is no contraindication to following another type of
exogenous surfactant given at an outside institution
(e.g., Exosurf) with the NICU standard dose of Survanta.
- Generally speaking, initial treatment should not be
initiated if the infant is greater than 48 hours of
postnatal age.
- Treatment is not contraindicated by endotracheal tube
suction material that is blood streaked.
SELECTED REFERENCES
- Schwartz,RM,Luby, AM, Scanlon, JW, Kellogg, RJ: Effect of
surfactant on morbidity, mortality, and resource use in
newborn infants weighing 500 to 1500 g. N. Engl. J. Med.
1994;330:1476-1480.
- Horbar, JD, Wright, EC, Onstad, L, and the Members of the
National Institute of Child Health and Human Developement
Neonatal Research Network: Decreasing mortality
associated with the introduction of surfactant therapy:
an observational study of neonates weighing 601 to 1300
grams at birth. Pediatrics 1993;1992:191-196.
- Egberts, J, deWinter, JP, Sedin, G, deKleine, JK,
Broberger, U, van Bel, F, Curstedt, T, Robertson, B:
Comparison of prophylaxis and rescue treatment with
Cursourf in neonates less than 30 weeks' gestation: a
randomized trial. Pediatrics 1993;92:768-774.
- Kattwinkel, J, Bloom, BT, Delmore, P, Davis, CL, Farrell,
E, Friss, H, Jung, Al, King, K, Mueller, D: Prophylactic
administration of calf lung surfactant extract is more
effective than early treatment of respiratory distress
syndrome in neonates of 29 through 32 weeks' gestation.
Pediatrics 1993;92:90-98.
- Dunn, MS: Surfactant replacement therapy: prophylaxis or
treatment? Pediatrics 1993;148-149.
- Long, W, Corbet, A, Cotton, R, Courtney, S, McGuiness, G,
Walter, D, Watts, J, Smyth, J, Bard, H, Chernick, V: A
controlled trial of synthetic surfactant in infants
weighing 1250 g or more with respiratory distress
syndrome. N. Engl. J. Med. 1991;325:1696-1703.
- Dunn, MS, Shennan, AT, Zayack, D, Possmayer, F: Bovine
surfactant replacement therapy in neonates of less than
30 weeks' gestation: a randomized controlled trial of
prophylaxis versus treatment. Pediatrics1991;87:377-386.
- Long, W, Thompson, T, Sundell, H, Schumacher, R, Volberg,
F, Guthrie, R, and the American Exosurf Neonatal Study
Group: Effects of two rescue doses of a synthetic
surfactant on mortality rate and survival without
bronchopulmonary dysplasia in 700 to 1350 gram infants
with respiratory distress syndrome. J. Pediatr.
1991;118:595-605.
- Merritt, TA, Hallman, M, Berry, C, Pohjavuori, M,
Edwards, DK, Jaaskelainen, J, Grafe, MR, Vaucher, Y,
Wozniak, P, Heldt, G, Rapola, J: Randomized,
placebo-controlled trial of human surfactant given at
birth versus rescue administration in very low birth
weight infants with lung immaturity. J. Pediatr.
1991;118(4):581-594.
- Couser, RJ, Ferrara, TB, Ebert, J, Hoekstra, RE, Fangman,
JJ: Effects of exogenous surfactant therapy on dynamic
compliance during mechanical breathing in preterm infants
with hyaline membrane disease. J.Pediatr.
1990;116:119-124
AUTHORS
About NICU-WEB Authorship
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Primary Author |
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Dennis E. Mayock, M.D. |
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Professor |
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Contributing Authors |
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David Woodrum, M.D. |
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Professor |
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Thomas P. Strandjord, M.D. |
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Associate Professor |
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Peter Tarczy-Hornoch, M.D. |
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Professor |
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