Literature DB >> 19651577

Synchronized nasal intermittent positive-pressure ventilation and neonatal outcomes.

Vineet Bhandari1, Neil N Finer, Richard A Ehrenkranz, Shampa Saha, Abhik Das, Michele C Walsh, William A Engle, Krisa P VanMeurs.   

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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Year:  2009        PMID: 19651577      PMCID: PMC2924622          DOI: 10.1542/peds.2008-1302

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  50 in total

1.  A randomized trial of nasopharyngeal-synchronized intermittent mandatory ventilation versus nasopharyngeal continuous positive airway pressure in very low birth weight infants after extubation.

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3.  Comparing the effects of nasal synchronized intermittent positive pressure ventilation (nSIPPV) and nasal continuous positive airway pressure (nCPAP) after extubation in very low birth weight infants.

Authors:  C Moretti; C Gizzi; P Papoff; S Lampariello; M Capoferri; G Calcagnini; G Bucci
Journal:  Early Hum Dev       Date:  1999-12       Impact factor: 2.079

4.  A prospective randomized, controlled trial comparing synchronized nasal intermittent positive pressure ventilation versus nasal continuous positive airway pressure as modes of extubation.

Authors:  M N Khalaf; N Brodsky; J Hurley; V Bhandari
Journal:  Pediatrics       Date:  2001-07       Impact factor: 7.124

5.  Effects of hypocarbia on the development of cystic periventricular leukomalacia in premature infants treated with high-frequency jet ventilation.

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6.  Efficacy of nasal intermittent positive pressure ventilation in treating apnea of prematurity.

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7.  Thoracoabdominal motion in newborns during ventilation delivered by endotracheal tube or nasal prongs.

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8.  Randomized trial of permissive hypercapnia in preterm infants.

Authors:  G Mariani; J Cifuentes; W A Carlo
Journal:  Pediatrics       Date:  1999-11       Impact factor: 7.124

9.  Randomized trial of nasal synchronized intermittent mandatory ventilation compared with continuous positive airway pressure after extubation of very low birth weight infants.

Authors:  K J Barrington; D Bull; N N Finer
Journal:  Pediatrics       Date:  2001-04       Impact factor: 7.124

10.  Nasal continuous positive airway pressure and early surfactant therapy for respiratory distress syndrome in newborns of less than 30 weeks' gestation.

Authors:  H Verder; P Albertsen; F Ebbesen; G Greisen; B Robertson; A Bertelsen; L Agertoft; B Djernes; E Nathan; J Reinholdt
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2.  Factors affecting nasal intermittent positive pressure ventilation failure and impact on bronchopulmonary dysplasia in neonates.

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Review 3.  The new bronchopulmonary dysplasia.

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Review 4.  Recent Advances in Bronchopulmonary Dysplasia: Pathophysiology, Prevention, and Treatment.

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6.  SNIPPV vs NIPPV: does synchronization matter?

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7.  The role of surfactant in respiratory distress syndrome.

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8.  Gastric pneumatosis in a premature neonate.

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9.  Flow-synchronized nasal intermittent positive pressure ventilation for infants <32 weeks' gestation with respiratory distress syndrome.

Authors:  C Gizzi; P Papoff; I Giordano; L Massenzi; C S Barbàra; M Campelli; V Panetta; R Agostino; C Moretti
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10.  Need for supplemental oxygen at discharge in infants with bronchopulmonary dysplasia is not associated with worse neurodevelopmental outcomes at 3 years corrected age.

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