Suppr超能文献

使用含丙胺卡因的乳膏和硬膜外丙胺卡因后早产儿的毒性高铁血红蛋白浓度。

Toxic methaemoglobin concentrations in premature infants after application of a prilocaine-containing cream and peridural prilocaine.

作者信息

Frey B, Kehrer B

机构信息

Intensive Care Unit, Ostschweizer Kinderspital, CH-9006 St Gallen, Switzerland.

出版信息

Eur J Pediatr. 1999 Oct;158(10):785-8. doi: 10.1007/s004310051204.

Abstract

UNLABELLED

We report on a retrospective analysis of eight episodes of toxic methaemoglobinaemia in seven premature infants after the combined exposure to prilocaine by EMLA cream (12.5 mg prilocaine) and caudal anaesthesia (5.4-6.7 mg/kg prilocaine). The causative relationship between prilocaine and the infants' deterioration came to our attention through an anonymous voluntary incident-reporting system. The highest methaemoglobin concentration found was 30.6% (5.5 h after anaesthesia). All infants were symptomatic (mottled skin, paleness, cyanosis, poor peripheral perfusion) and two were exposed to unnecessary diagnostic and therapeutic procedures for unspecified deterioration in their conditions. Pharmacokinetic evaluation indicated a single compartment first-order elimination with a methaemoglobin half-life of 8 h. Normal levels (<1%) were reached 36 h after exposure to prilocaine.

CONCLUSION

Whereas local skin application of prilocaine to premature babies is safe, peridural administration is not because premature infants are more sensitive to methaemoglobin inducing agents and tolerate methaemoglobinaemia less well.

摘要

未标注

我们报告了对7名早产儿发生的8次中毒性高铁血红蛋白血症事件的回顾性分析,这些婴儿在联合使用EMLA乳膏(含12.5毫克丙胺卡因)和骶管麻醉(5.4 - 6.7毫克/千克丙胺卡因)后出现了高铁血红蛋白血症。通过一个匿名自愿事件报告系统,我们注意到了丙胺卡因与婴儿病情恶化之间的因果关系。发现的最高高铁血红蛋白浓度为30.6%(麻醉后5.5小时)。所有婴儿均出现症状(皮肤花斑、苍白、发绀、外周灌注不良),其中两名婴儿因病情不明原因恶化而接受了不必要的诊断和治疗程序。药代动力学评估表明为单室一级消除,高铁血红蛋白半衰期为8小时。接触丙胺卡因36小时后达到正常水平(<1%)。

结论

虽然将丙胺卡因局部应用于早产儿皮肤是安全的,但硬膜外给药则不然,因为早产儿对高铁血红蛋白诱导剂更敏感,对高铁血红蛋白血症的耐受性也较差。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验