Synchronized Nasal Intermittent Positive-Pressure Ventilation and Neonatal Outcomes

被引:64
|
作者
Bhandari, Vineet [1 ]
Finer, Neil N. [5 ]
Ehrenkranz, Richard A.
Saha, Shampa [6 ]
Das, Abhik [6 ]
Walsh, Michele C. [4 ]
Engle, William A. [3 ]
Van Meurs, Krisa P. [2 ]
机构
[1] Yale Univ, Sch Med, Dept Pediat, Div Perinatal Med, New Haven, CT 06520 USA
[2] Stanford Univ, Lucile Packard Childrens Hosp, Dept Pediat, Palo Alto, CA 94304 USA
[3] Indiana Univ, Riley Hosp Children, Dept Pediat, Indianapolis, IN 46204 USA
[4] Case Western Reserve Univ, Dept Pediat, Cleveland, OH 44106 USA
[5] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[6] Res Triangle Inst, Res Triangle Pk, NC 27709 USA
基金
美国国家卫生研究院;
关键词
premature newborn; respiratory distress syndrome; noninvasive ventilation; CYSTIC PERIVENTRICULAR LEUKOMALACIA; RESPIRATORY-DISTRESS-SYNDROME; BIRTH-WEIGHT INFANTS; AIRWAY PRESSURE; BRONCHOPULMONARY DYSPLASIA; PREMATURE-INFANTS; RANDOMIZED-TRIAL; MANDATORY VENTILATION; HYPOCAPNIA; EXTUBATION;
D O I
10.1542/peds.2008-1302
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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 <= 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. Pediatrics 2009; 124: 517-526
引用
收藏
页码:517 / 526
页数:10
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