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支气管肺发育不良可预测极低出生体重儿的不良发育和临床结局。

Bronchopulmonary dysplasia predicts adverse developmental and clinical outcomes in very-low-birthweight infants.

作者信息

Jeng Suh-Fang, Hsu Chyong-Hsin, Tsao Po-Nien, Chou Hung-Chieh, Lee Wang-Tso, Kao Hsin-An, Hung Han-Yang, Chang Jui-Hsing, Chiu Nan-Chang, Hsieh Wu-Shiun

机构信息

School of Physical Therapy, College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Dev Med Child Neurol. 2008 Jan;50(1):51-7. doi: 10.1111/j.1469-8749.2007.02011.x.

Abstract

This study examined the developmental and clinical outcomes in very-low-birthweight (VLBW; < or =1500g) infants with and without bronchopulmonary dysplasia (BPD) throughout infancy, and assessed if BPD predicted poor developmental outcome beyond the effects of other risk factors. One hundred and three VLBW infants (53 males, 50 females; mean gestational age 28wks [SD 2] birthweight 1041g [SD 261]) were graded for severity of BPD according to the American National Institutes of Health (NIH) consensus definition. Neuro-development was assessed using the Neonatal Neurobehavioral Examination-Chinese version, at 36 and 39 weeks' postmenstrual age, and the 2nd edition of the Bayley Scales of Infant Development at 6 and 12 months' corrected age. Clinical outcome was measured by means of rehospitalization for pulmonary causes and treatment with pulmonary medications. Compared with infants without BPD, infants with BPD had higher rates of clinical morbidity, and those with severe BPD further exhibited higher incidences of developmental delay throughout infancy. BPD predicts poor 1-year developmental and clinical outcomes in VLBW infants for which effects are well correlated to the NIH consensus definition.

摘要

本研究调查了患有和未患支气管肺发育不良(BPD)的极低出生体重(VLBW;≤1500g)婴儿在整个婴儿期的发育和临床结局,并评估了BPD是否能在其他风险因素的影响之外预测不良发育结局。根据美国国立卫生研究院(NIH)的共识定义,对103例VLBW婴儿(53例男性,50例女性;平均胎龄28周[标准差2],出生体重1041g[标准差261])的BPD严重程度进行分级。在孕龄36周和39周时,使用中文版新生儿神经行为检查评估神经发育情况,在矫正年龄6个月和12个月时,使用贝利婴儿发育量表第二版进行评估。通过因肺部原因再次住院和使用肺部药物治疗来衡量临床结局。与未患BPD的婴儿相比,患BPD的婴儿临床发病率更高,而患有严重BPD的婴儿在整个婴儿期发育迟缓的发生率更高。BPD可预测VLBW婴儿1岁时不良的发育和临床结局,其影响与NIH共识定义密切相关。

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