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极低出生体重儿的肺动脉高压:特征与结局。

Pulmonary hypertension in extremely low birth weight infants: characteristics and outcomes.

机构信息

Department of Pediatrics, Division of Neonatology, Metro Health Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH, 44109, USA.

出版信息

World J Pediatr. 2014 Feb;10(1):46-52. doi: 10.1007/s12519-014-0464-2. Epub 2014 Jan 25.

DOI:10.1007/s12519-014-0464-2
PMID:24464663
Abstract

BACKGROUND

To determine the characteristics and outcomes of pulmonary arterial hypertension (PAH) in extremely low birth weight (ELBW) infants.

METHODS

A retrospective case-control study of all ELBW infants admitted to a level III neonatal intensive care unit (NICU) between January 1, 2003 and December 31, 2010.

RESULTS

During the study period, 450 ELBW infants were admitted. 6.4% (29/450) were diagnosed with PAH and were matched to 26 controls. The mean gestational age of infants with PAH and their controls were similar [24.5 ± 1.3 vs. 24.9 ± 1.8 weeks (P=0.26)]; however the cases were smaller at birth than were controls [640.7 ± 119.5 vs. 727.0 ± 184.5 g (P=0.04)]. The diagnosis of PAH was made at a mean postnatal age of 131.8 ± 53.7 days. Infants with PAH had a higher rate of intrauterine exposure to illicit maternal drug use [12/29 (41%) vs. 1/25 (4%); P=0.001], a longer duration of initial mechanical ventilation [74.9 ± 28.3 vs. 59.1 ± 27.8 days; P=0.04)], a higher incidence of severe BPD [23/29 (79%) vs. 13/26 (50%); P=0.02], and a greater NICU mortality rate [12/29 (41%) vs. 4/26 (15%); P=0.04].

CONCLUSION

PAH in ELBW infants is associated with maternal illicit drug use in pregnancy, longer exposure to mechanical ventilation, severe bronchopulmonary dysplasia and a significant increase in early mortality.

摘要

背景

确定极低出生体重(ELBW)婴儿中肺动脉高压(PAH)的特征和结局。

方法

对 2003 年 1 月 1 日至 2010 年 12 月 31 日期间入住三级新生儿重症监护病房(NICU)的所有 ELBW 婴儿进行回顾性病例对照研究。

结果

在研究期间,有 450 名 ELBW 婴儿入院。6.4%(29/450)被诊断为 PAH,并与 26 名对照匹配。PAH 婴儿及其对照的平均胎龄相似[24.5 ± 1.3 与 24.9 ± 1.8 周(P=0.26)];然而,病例组的出生体重小于对照组[640.7 ± 119.5 与 727.0 ± 184.5 g(P=0.04)]。PAH 的诊断平均在出生后 131.8 ± 53.7 天做出。PAH 婴儿宫内暴露于非法母亲药物的发生率更高[12/29(41%)与 1/25(4%);P=0.001],初始机械通气时间更长[74.9 ± 28.3 与 59.1 ± 27.8 天;P=0.04],严重支气管肺发育不良发生率更高[23/29(79%)与 13/26(50%);P=0.02],新生儿重症监护病房死亡率更高[12/29(41%)与 4/26(15%);P=0.04]。

结论

ELBW 婴儿的 PAH 与母亲妊娠期间非法药物使用、更长时间的机械通气暴露、严重支气管肺发育不良以及早期死亡率显著增加有关。

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Prospective analysis of pulmonary hypertension in extremely low birth weight infants.极低出生体重儿肺动脉高压的前瞻性分析。
Pediatrics. 2012 Mar;129(3):e682-9. doi: 10.1542/peds.2011-1827. Epub 2012 Feb 6.
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Prediction of bronchopulmonary dysplasia by postnatal age in extremely premature infants.预测极早产儿支气管肺发育不良的出生后年龄。
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Echocardiographic detection of pulmonary hypertension in extremely low birth weight infants with bronchopulmonary dysplasia requiring prolonged positive pressure ventilation.
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Tyrosine phosphorylation of Kv1.5 is upregulated in intrauterine growth retardation rats with exaggerated pulmonary hypertension.在患有严重肺动脉高压的宫内生长受限大鼠中,Kv1.5的酪氨酸磷酸化上调。
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