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Natural Versus Synthetic Surfactant Therapy in Respiratory Distress Syndrome of Prematurity

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Indian Journal of Pediatrics Aims and scope Submit manuscript

Abstract

Objectives

To compare the clinical efficacy and the cost of treatment between the newborns who received either a natural or a protein-free synthetic surfactant for respiratory distress syndrome (RDS) of prematurity.

Methods

This is a retrospective analytical study incorporating comparisons of clinical parameters and cost in newborns having RDS of prematurity who received either Survanta (bovine lung extract), a natural surfactant or Surfact (protein-free colfosceril palmitate), a synthetic surfactant.

Results

There were 100 newborns who received either of the natural (n = 52) or synthetic (n = 48) surfactant with mean (SD) gestational age and mean (SD) birth weight of 31.5 (2.6) wk, 1425 (461) g and 32.2 (2.2) wk, 1519 (413) g, respectively. Majority of the newborns (> 90%) received endotracheal surfactant within the first 24 h of life and had similar baseline characteristics in either group. No differences were noted in ventilator settings on admission and 24 h after surfactant/admission. Oxygen requirement, extubation age, complications, hospital stay, and mortality were similar across groups, except that the necrotizing enterocolitis was noted only in natural surfactant group. There was a significant pharmacy cost savings in synthetic surfactant group.

Conclusion

Synthetic surfactant was comparable to natural surfactant with regard to outcomes, like ventilator settings, hospital stay, and mortality. Pharmacy cost was less in synthetic surfactant group.

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Data Availability

Deidentified individual participant data will be made available. The data will be made available upon publication to researchers who provide a methodologically sound proposal for use in achieving the goals of the approved proposal. Proposals should be submitted to dipen_patel258@yahoo.co.in.

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Authors and Affiliations

Authors

Contributions

DVP, SCB, MS conceptualized and designed the study, coordinated and supervised data collection, carried out the final analysis, drafted the initial manuscript, and reviewed and revised the manuscript; CLP, KP designed the data collection instruments, collected data, carried out the initial analyses, and reviewed and revised the manuscript for important intellectual content; SMN conceptualized as well as designed the study and revisited the manuscript for important intellectual content; All authors approved the final manuscript as submitted and agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work were appropriately investigated and resolved. DVP will act as the guarantor for this paper.

Corresponding author

Correspondence to Dipen V. Patel.

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Ethical Approval

The study was approved by the Institutional Ethics Committee of H M Patel Center for Medical Care and Education, Karamsad, Gujarat.

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Patel, D.V., Bansal, S.C., Shah, M. et al. Natural Versus Synthetic Surfactant Therapy in Respiratory Distress Syndrome of Prematurity. Indian J Pediatr 89, 1086–1092 (2022). https://doi.org/10.1007/s12098-022-04166-4

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  • DOI: https://doi.org/10.1007/s12098-022-04166-4

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