Developmental outcomes in persistent pulmonary hypertension treated with nitric oxide therapy

Developmental outcomes in persistent pulmonary hypertension treated with nitric oxide therapy
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DOI:
10.1111/j.1442-200x.2008.02664.x
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发表时间:
2009-02-01
影响因子:
1.4
通讯作者:
Harada, Kensuke
Harada, Kensuke
中科院分区:
医学4区
文献类型:
--
作者:
Hosono, Shigeharu;Ohno, Tutomu;Harada, Kensuke

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本研究的目的是评估新生儿持续性肺动脉高压(PPHN)引入吸入型一氧化氮(i-NO)治疗前后3年的听觉和神经发育结局,并检测影响预后不良的临床因素。对26例肺氧合指数(OI) >= 25的PPHN幸存者进行回顾性历史队列研究(未给予i-NO治疗的13例为对照组;给予i-NO治疗的13例为i-NO组)。评估6个月和12个月时的听觉脑干反应(ABR)和3岁时的神经发育结果。i-NO组患儿6月龄ABR异常1例,对照组患儿6例(P = 0.04)。1岁时,i-NO组仍有1例,对照组6例中仍有2例存在ABR异常。在i-NO组中,有2名儿童出现神经发育异常,而在3年随访中,对照组有5名儿童出现神经发育异常。对照组2例,i-NO组3岁时无听力损失。睡眠不足(P = 0.04)和肌酸磷酸激酶升高(P = 0.04)是神经发育异常的预测指标。通过引入i-NO治疗来避免过度的低呼吸可能会减少ABR和神经发育异常。
The aim of the present study was to assess 3 year auditory and neurodevelopmental outcomes of persistent pulmonary hypertension of the newborn (PPHN) before and after introducing inhaled nitric oxide (i-NO) therapy, and to detect the clinical factors affecting poor outcome.A retrospective historical cohort study of 26 survivors with PPHN with oxygenation index (OI) >= 25 (13 infants without i-NO therapy, control group; 13 with i-NO therapy, i-NO group) was performed. Auditory brainstem response (ABR) at 6 and 12 months and neurodevelopmental outcomes at 3 years of age were evaluated.ABR abnormalities at 6 months were observed in one infant in the i-NO group and six in the control group (P = 0.04). At 1 year, one infant in the i-NO group and two of six infants in the control group still had ABR abnormality. In the i-NO group, two children had abnormal neurodevelopmental outcomes, as compared with five children in the control group at 3 year follow up. Two children in the control group and no children in the i-NO group had hearing loss at 3 years of age. Hypocapnea (P = 0.04) and elevated creatine phosphokinase (P = 0.04) were found to be most predictive for neurodevelopmental abnormality.Avoidance of excessive hypocapnea via introduction of i-NO therapy might reduce both ABR and neurodevelopmental abnormalities.