Early administration of the second dose of surfactant (beractant) in the treatment of severe hyaline membrane disease

Citation
J. Figueras-aloy et al., Early administration of the second dose of surfactant (beractant) in the treatment of severe hyaline membrane disease, ACT PAEDIAT, 90(3), 2001, pp. 296-301
Citations number
20
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
ACTA PAEDIATRICA
ISSN journal
08035253 → ACNP
Volume
90
Issue
3
Year of publication
2001
Pages
296 - 301
Database
ISI
SICI code
0803-5253(200103)90:3<296:EAOTSD>2.0.ZU;2-T
Abstract
The aim of this study was to demonstrate that administration of the second dose of beractant 2 h after the first one is more effective than 6 h after the initial dose. The inclusion criteria for the recruitment of newborn inf ants were: age less than or equal to8 h, birthweight 600-2000 g, gestationa l age 23-36 wk, need for mechanical ventilation with inspiratory oxygen fra ction (FiO(2)) greater than or equal to0.4 and mean airway pressure (MAP) g reater than or equal to7 cmH(2)O to obtain arterial oxygen tension (PaO2) v alues between 70 and 80 mmHg, and thoracic X-ray compatible with hyaline me mbrane disease (HMD). Newborns with major congenital malformations, hydrops fetalis or seven pulmonary hypoplasia, or being treated with high-frequenc y oscillatory ventilation were excluded. In total, 57 premature newborns we re studied. 20 of them below 1000 g, who received 100 mg kg(-1) of beractan t in 2 aliquots and showed an inadequate response, i.e, after 2 h of the fi rst dose the newborn still needed a FiO(2) greater than or equal to 0.4 and a MAP greater than or equal to 7 cmH(2)O to achieve a PaO2 > 70 mmHg. The second dose was randomly administered 2 or 6 h from the first one. Conclusion: The 2 study groups were comparable except for a higher need of dopamine and seroalbumin in 2-h group. Evolution and complications were sim ilar. Twelve hours after the first dose, the percentage improvement in the arteriolar/alveolar ratio (a/ADO(2)) in the 2-h group was similar to that i n the 6-h group. However, in newborns below 1000 g, 12 h after the first do se the a/ADO(2) percentage improvement in the 2-h group was greater than in 6-h group (median of 103.6% vs 16.3%; p = 0.035). In premature infants bel ow 1000 g, it seems reasonable to advance the second dose of beractant if n eeded.