Late administration of surfactant replacement therapy increases surfactant protein-B content: a randomized pilot study

Roberta L Keller, Jeffrey D Merrill, Dennis M Black, Robin H Steinhorn, Eric C Eichenwald, David J Durand, Rita M Ryan, William E Truog, Sherry E Courtney, Philip L Ballard, Roberta A Ballard, Roberta L Keller, Jeffrey D Merrill, Dennis M Black, Robin H Steinhorn, Eric C Eichenwald, David J Durand, Rita M Ryan, William E Truog, Sherry E Courtney, Philip L Ballard, Roberta A Ballard

Abstract

Background: Surfactant dysfunction may contribute to the development of bronchopulmonary dysplasia (BPD) in persistently ventilated preterm infants. We conducted a multicenter randomized, blinded, pilot study to assess the safety and efficacy of late administration of doses of a surfactant protein-B (SP-B)-containing surfactant (calfactant) in combination with prolonged inhaled nitric oxide (iNO) in infants ≤1,000 g birth weight (BW).

Methods: We randomized 85 preterm infants ventilated at 7-14 d after birth to receive either late administration of surfactant (up to 5 doses) plus prolonged iNO or iNO alone. Large aggregate surfactant was isolated from daily tracheal aspirates (TAs) for measurement of SP-B content, total protein, and phospholipid (PL).

Results: Late administration of surfactant had minimal acute adverse effects. Clinical status as well as surfactant recovery and SP-B content in tracheal aspirate were transiently improved as compared to the controls; these effects waned after 1 d. The change in SP-B content with surfactant dosing was positively correlated with SP-B levels during treatment (r = 0.50, P = 0.02).

Conclusion: Low SP-B values increased with calfactant administration, but the relationship of this response to SP-B levels suggests that degradation is a contributing mechanism for SP-B deficiency and surfactant dysfunction. We conclude that late therapy with surfactant in combination with iNO is safe and transiently increases surfactant SP-B content, possibly leading to improved short- and long-term respiratory outcomes.

Trial registration: ClinicalTrials.gov NCT00569530.

Figures

Figure 1
Figure 1
Enrollment flow diagram for infants admitted to the nine study hospitals during the recruitment period, January 2008–October 2009.
Figure 2
Figure 2
Absolute change in surfactant parameters following study drug dosing (days 1–3). Data are median values for the Control (white bars, n = 43–47 from 20 infants) and Surfactant (black bars, n = 55–64 from 27 infants) groups. (a) Surfactant recovery, phospholipid (PL) normalized to total protein content of tracheal aspirate; (b) total protein in surfactant pellet as a percentage of PL; (c) surfactant protein-B (SP-B) content of surfactant pellet, normalized to PL; and (d) SP-B content normalized to total protein in surfactant pellet. P values are for comparison of the change between groups, *P = 0.04, **P ≤ 0.002.
Figure 3
Figure 3
Absolute change in surfactant parameters in infants treated with surfactant (n = 21) on day 1 vs. mean level of surfactant parameters on subsequent days prior to dosing (days 2–4). Surfactant protein-B (SP-B) content (%) normalized to total protein in surfactant: (a) vs. SP-B content r = 0.50, P = 0.02, and (b) surfactant recovery (μg phospholipid (PL)/μg tracheal aspirate protein): r = 0.05, P = 0.83.

References

    1. Ehrenkranz RA, Walsh MC, Vohr al. Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia Pediatrics 20051161353–60.
    1. Schmidt B, Roberts RS, Davis al. Long-term effects of caffeine therapy for apnea of prematurity N Engl J Med 20073571893–902.
    1. Laughon M, Allred EN, Bose al. Patterns of respiratory disease during the first 2 postnatal weeks in extremely premature infants Pediatrics 20091231124–31.
    1. Tyson JE, Wright LL, Oh al. Vitamin A supplementation for extremely-low-birth-weight infants. National Institute of Child Health and Human Development Neonatal Research Network N Engl J Med 19993401962–8.
    1. Schmidt B, Roberts RS, Davis al. Caffeine therapy for apnea of prematurity N Engl J Med 20063542112–21.
    1. Ballard RA, Truog WE, Cnaan al. Inhaled nitric oxide in preterm infants undergoing mechanical ventilation N Engl J Med 2006355343–53.
    1. Ballard RA. Inhaled nitric oxide in preterm infants–correction. N Engl J Med. 2007;357:1444–5.
    1. Hibbs AM, Walsh MC, Martin al. One-year respiratory outcomes of preterm infants enrolled in the nitric oxide (to prevent) chronic lung disease trial J Pediatr 2008153525–9.
    1. Zupancic JA, Hibbs AM, Palermo al. Economic evaluation of inhaled nitric oxide in preterm infants undergoing mechanical ventilation Pediatrics 20091241325–32.
    1. Walsh MC, Hibbs AM, Martin al. Two-year neurodevelopmental outcomes of ventilated preterm infants treated with inhaled nitric oxide J Pediatr 2010156556–61.e1.
    1. Merrill JD, Ballard RA, Cnaan al. Dysfunction of pulmonary surfactant in chronically ventilated premature infants Pediatr Res 200456918–26.
    1. Ballard PL, Merrill JD, Truog al. Surfactant function and composition in premature infants treated with inhaled nitric oxide Pediatrics 2007120346–53.
    1. Merrill JD, Ballard PL, Courtney al. Pilot trial of late booster doses of surfactant for ventilated premature infants J Perinatol 201131599–606.
    1. Günther A, Schmidt R, Harodt al. Bronchoscopic administration of bovine natural surfactant in ARDS and septic shock: impact on biophysical and biochemical surfactant properties Eur Respir J 200219797–804.
    1. Katz LA, Klein JM. Repeat surfactant therapy for postsurfactant slump. J Perinatol. 2006;26:414–22.
    1. Bissinger R, Carlson C, Michel Y, Dooley C, Hulsey T, Jenkins D. Secondary surfactant administration in neonates with respiratory decompensation. J Perinatol. 2008;28:192–8.
    1. Laughon M, Bose C, Moya al. A pilot randomized, controlled trial of later treatment with a peptide-containing, synthetic surfactant for the prevention of bronchopulmonary dysplasia Pediatrics 200912389–96.
    1. Bland RD, Albertine KH, Carlton al. Chronic lung injury in preterm lambs: abnormalities of the pulmonary circulation and lung fluid balance Pediatr Res 20004864–74.
    1. Altiok O, Yasumatsu R, Bingol-Karakoc al. Imbalance between cysteine proteases and inhibitors in a baboon model of bronchopulmonary dysplasia Am J Respir Crit Care Med 2006173318–326.
    1. Furue S, Kuwabara K, Mikawa al. Crucial role of group IIA phospholipase A(2) in oleic acid-induced acute lung injury in rabbits Am J Respir Crit Care Med 19991601292–302.
    1. Farver RS, Mills FD, Antharam VC, Chebukati JN, Fanucci GE, Long JR. Lipid polymorphism induced by surfactant peptide SP-B(1-25) Biophys J. 2010;99:1773–82.
    1. Shelley SA, Kovacevic M, Paciga JE, Balis JU. Sequential changes of surfactant phosphatidylcholine in hyaline-membrane disease of the newborn. N Engl J Med. 1979;300:112–6.
    1. Ikegami M, Whitsett JA, Martis PC, Weaver TE. Reversibility of lung inflammation caused by SP-B deficiency. Am J Physiol Lung Cell Mol Physiol. 2005;289:L962–70.
    1. Nakamura T, Malloy J, McCaig al. Mechanical ventilation of isolated septic rat lungs: effects on surfactant and inflammatory cytokines J Appl Physiol 200191811–20.
    1. Walker MG, Tessolini JM, McCaig L, Yao LJ, Lewis JF, Veldhuizen RA. Elevated endogenous surfactant reduces inflammation in an acute lung injury model. Exp Lung Res. 2009;35:591–604.
    1. Sato A, Whitsett JA, Scheule RK, Ikegami M. Surfactant protein-d inhibits lung inflammation caused by ventilation in premature newborn lambs. Am J Respir Crit Care Med. 2010;181:1098–105.
    1. Coalson JJ, Winter VT, Gerstmann DR, Idell S, King RJ, Delemos RA. Pathophysiologic, morphometric, and biochemical studies of the premature baboon with bronchopulmonary dysplasia. Am Rev Respir Dis. 1992;145 4 Pt 1:872–81.
    1. Coalson JJ, Winter VT, Siler-Khodr T, Yoder BA. Neonatal chronic lung disease in extremely immature baboons. Am J Respir Crit Care Med. 1999;160:1333–46.
    1. Bancalari E, Claure N. Non-invasive ventilation of the preterm infant. Early Hum Dev. 2008;84:815–9.
    1. Laughon M, Bose C, Allred al. Antecedents of chronic lung disease following three patterns of early respiratory disease in preterm infants Arch Dis Child Fetal Neonatal Ed 201196F114–20.
    1. Laughon MM, Langer JC, Bose al. Prediction of bronchopulmonary dysplasia by postnatal age in extremely premature infants Am J Respir Crit Care Med 20111831715–22.
    1. Davis JM, Parad RB, Michele T, Allred E, Price A, Rosenfeld W. Pulmonary outcome at 1 year corrected age in premature infants treated at birth with recombinant human CuZn superoxide dismutase. Pediatrics. 2003;111:469–76.
    1. Posencheg MA, Gow AJ, Truog al. Inhaled nitric oxide in premature infants: effect on tracheal aspirate and plasma nitric oxide metabolites J Perinatol 201030275–80.
    1. Walsh MC, Yao Q, Gettner al. Impact of a physiologic definition on bronchopulmonary dysplasia rates Pediatrics 20041141305–11.
    1. Bligh EG, Dyer WJ. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959;37:911–7.
    1. Bernhard W, Linck M, Creutzburg al. High-performance liquid chromatographic analysis of phospholipids from different sources with combined fluorescence and ultraviolet detection Anal Biochem 1994220172–80.
    1. Notter RH, Wang Z, Egan EA, Holm BA. Component-specific surface and physiological activity in bovine-derived lung surfactants. Chem Phys Lipids. 2002;114:21–34.

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