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Comparative Study
. 2009 Aug;124(2):517-26.
doi: 10.1542/peds.2008-1302. Epub 2009 Jul 27.

Synchronized nasal intermittent positive-pressure ventilation and neonatal outcomes

Collaborators, Affiliations
Comparative Study

Synchronized nasal intermittent positive-pressure ventilation and neonatal outcomes

Vineet Bhandari et al. Pediatrics. 2009 Aug.

Abstract

Background: Synchronized nasal intermittent positive-pressure ventilation (SNIPPV) use reduces reintubation rates compared with nasal continuous positive airway pressure (NCPAP). Limited information is available on the outcomes of infants managed with SNIPPV.

Objectives: To compare the outcomes of infants managed with SNIPPV (postextubation or for apnea) to infants not treated with SNIPPV at 2 sites.

Methods: Clinical retrospective data was used to evaluate the use of SNIPPV in infants <or=1250 g birth weight (BW); and 3 BW subgroups (500-750, 751-1000, and 1001-1250 g, decided a priori). SNIPPV was not assigned randomly. Bronchopulmonary dysplasia (BPD) was defined as treatment with supplemental oxygen at 36 weeks' postmenstrual age.

Results: Overall, infants who were treated with SNIPPV had significantly lower mean BW (863 vs 964 g) and gestational age (26.4 vs 27.9 weeks), more frequently received surfactant (85% vs 68%), and had a higher incidence of BPD or death (39% vs 27%) (all P < .01) compared with infants treated with NCPAP. In the subgroup analysis, SNIPPV was associated with lower rates of BPD (43% vs 67%; P = .03) and BPD/death (51% vs 76%; P = .02) in the 500- to 750-g infants, with no significant differences in the other BW groups. Logistic regression analysis, adjusting for significant covariates, revealed infants with 500-700-g BW who received SNIPPV were significantly less likely to have the outcomes of BPD (OR: 0.29 [95% CI: 0.11-0.77]; P = .01), BPD/death (OR: 0.30 [95% CI: 0.11-0.79]; P = .01), neurodevelopmental impairment (NDI) (OR: 0.29 [95% CI: 0.09-0.94]; P = .04), and NDI/death (OR: 0.18 [95% CI: 0.05-0.62]; P = .006).

Conclusion: SNIPPV use in infants at greatest risk of BPD or death (500-750 g) was associated with decreased BPD, BPD/death, NDI, and NDI/death when compared with infants managed with NCPAP.

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Figures

Figure 1
Figure 1
Blood gas values of Pco2 in infants in the SNIPPV vs. no-SNIPPV groups on postnatal days 1, 3, 7, 14, 21 and 28. Data expressed as mean ± SEM. Pco2 values were significantly lower on days 7, 21, and 28 in the SNIPPV group (all P ≤ .01).

Comment in

References

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