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无并发症早产儿和患有特发性呼吸窘迫综合征的早产儿在新生儿早期的血浆次黄嘌呤和黄嘌呤水平。

Plasma hypoxanthine and xanthine levels in the early newborn period in problem-free preterm babies and those with idiopathic respiratory distress syndrome.

作者信息

Karmazsin L, Balla G

出版信息

Acta Paediatr Hung. 1985;26(1):1-9.

PMID:3986048
Abstract

The use of hypoxanthine measurements for quantitative monitoring of intrauterine asphyxia is generally accepted. A high level in blood or in CSF is a consequence of tissue hypoxia. Hypoxanthine and xanthine were measured by selective high pressure liquid chromatography in mature newborns, in healthy, symptom-free preterm babies, and in preterm babies affected by idiopathic respiratory distress syndrome. The measurements were carried out from peripheral venous blood within three hours after birth and at the age of 48-72 hours. In mature newborns the mean hypoxanthine level was 11.10 mumol/l in the early determinations, and 8.45 mumol/l in the second set of measurements. In unaffected prematures there were significantly higher levels, and the highest values (44.22 +/- 15.13 mumol/l) were encountered in premature babies subsequently dying of severe hypoxia. Xanthine showed a similar course. In addition to establishing normal values for prematures we desired to clarify the changes in the levels of purine metabolites during idiopathic respiratory distress and their prognostic value. Hypoxanthine and xanthine levels were found to be informative in postnatal hypoxia, especially together with other parameters.

摘要

使用次黄嘌呤测量来定量监测宫内窒息已被广泛接受。血液或脑脊液中次黄嘌呤水平升高是组织缺氧的结果。通过选择性高压液相色谱法测定了成熟新生儿、健康无症状早产儿以及患有特发性呼吸窘迫综合征的早产儿的次黄嘌呤和黄嘌呤水平。测量在出生后三小时内及48 - 72小时时从外周静脉血中进行。在成熟新生儿中,早期测定的次黄嘌呤平均水平为11.10 μmol/l,第二次测量时为8.45 μmol/l。在未受影响的早产儿中,次黄嘌呤水平明显更高,随后死于严重缺氧的早产儿中出现了最高值(44.22 ± 15.13 μmol/l)。黄嘌呤呈现类似的变化趋势。除了确定早产儿的正常值外,我们还希望阐明特发性呼吸窘迫期间嘌呤代谢产物水平的变化及其预后价值。发现次黄嘌呤和黄嘌呤水平在出生后缺氧情况中具有参考价值,尤其是与其他参数一起时。

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