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新生儿重症监护病房中早产儿邻苯二甲酸二(2-乙基己基)酯暴露情况

Exposure to di-(2-ethylhexyl) phthalate among premature neonates in a neonatal intensive care unit.

作者信息

Calafat Antonia M, Needham Larry L, Silva Manori J, Lambert George

机构信息

Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, Georgia 30341, USA.

出版信息

Pediatrics. 2004 May;113(5):e429-34. doi: 10.1542/peds.113.5.e429.

Abstract

OBJECTIVE

Premature neonates who spend time in a neonatal intensive care unit may be at increased risk of adverse health effects from exposure to di-(2-ethylhexyl) phthalate (DEHP) because of their increased risk of high exposure, their small body size, and their physical condition. DEHP, a reproductive toxicant in animals, is a major component in polyvinyl chloride (PVC) plastics, which are frequently used in medical tubing and blood storage bags. DEHP is not covalently bound to PVC, and it may be easily released from the PVC medical devices. The objective of this study was to determine whether premature infants who undergo medical procedures, such as blood transfusions, intravenous therapy, enteral and parenteral nutrition support, and dialysis, are at increased risk of exposure to DEHP than the general population. Because of their smaller size, children and especially premature and small infants may receive a larger dose of DEHP on a milligram per kilogram basis than adults when the same-size medical device is used for all ages.

METHODS

Premature neonates who seemed to have the potential to be on intravenous infusion for >2 weeks and were expected to survive were eligible for enrollment in the study. We assessed exposure to DEHP in 6 premature newborns by measuring in 41 urine samples the levels of 3 DEHP metabolites: mono-(2-ethylhexyl) phthalate (mEHP), mono-(2-ethyl-5-hydroxyhexyl) phthalate (mEHHP), and mono-(2-ethyl-5-oxohexyl) phthalate (mEOHP).

RESULTS

mEHHP and mEOHP were detected in all 41 urine samples, and mEHP was detected in 33. Because only 33 of the samples had detectable amounts for all 3 metabolites, statistical analyses were limited to those 33. The levels of all 3 DEHP metabolites varied widely, and the urinary mean and median concentrations of mEOHP and mEHHP were 1 order of magnitude higher than those for mEHP. Furthermore, the geometric mean urinary concentrations of mEOHP (1617 ng/mL), mEHHP (2003 ng/mL), and mEHP (100 ng/mL) in these 6 premature infants who underwent intensive therapeutic interventions were found to be severalfold higher than in the US general population (for mEHP, geometric mean in those 6 years and older was 3.43 ng/mL).

CONCLUSIONS

This study provides the first quantitative evidence confirming that newborns who undergo intensive therapeutic medical interventions are exposed to higher concentrations of DEHP than the general population. Although the overall benefits of medical procedures using PVC devices outweigh the risks associated with exposure to DEHP, more research is needed to determine whether infants and children who undergo intensive therapeutic interventions using DEHP-containing devices are at higher risk for altered health outcomes than infants and children who undergo similar treatments but are not potentially exposed to DEHP.

摘要

目的

在新生儿重症监护病房接受治疗的早产儿,由于其高暴露风险增加、体型小以及身体状况,接触邻苯二甲酸二(2-乙基己基)酯(DEHP)可能会增加健康不良影响的风险。DEHP是一种动物生殖毒性物质,是聚氯乙烯(PVC)塑料的主要成分,PVC塑料常用于医疗管材和储血袋。DEHP并非与PVC共价结合,它可能很容易从PVC医疗设备中释放出来。本研究的目的是确定接受输血、静脉治疗、肠内和肠外营养支持以及透析等医疗程序的早产儿,接触DEHP的风险是否高于普通人群。由于体型较小,当所有年龄段使用相同尺寸的医疗设备时,儿童尤其是早产儿和小婴儿每千克体重可能比成年人接受更大剂量的DEHP。

方法

似乎有可能进行超过2周静脉输注且预期存活的早产儿符合本研究的入组条件。我们通过检测41份尿液样本中3种DEHP代谢物的水平,评估了6例早产新生儿接触DEHP的情况,这3种代谢物分别是单-(2-乙基己基)邻苯二甲酸酯(mEHP)、单-(2-乙基-5-羟基己基)邻苯二甲酸酯(mEHHP)和单-(2-乙基-5-氧代己基)邻苯二甲酸酯(mEOHP)。

结果

在所有41份尿液样本中均检测到mEHHP和mEOHP,33份样本中检测到mEHP。由于只有33份样本可检测到所有3种代谢物,统计分析仅限于这33份样本。所有3种DEHP代谢物的水平差异很大,mEOHP和mEHHP的尿平均浓度和中位数浓度比mEHP高1个数量级。此外,在这6例接受强化治疗干预的早产儿中,mEOHP(1617 ng/mL)、mEHHP(2003 ng/mL)和mEHP(100 ng/mL)的几何平均尿浓度比美国普通人群高几倍(对于mEHP,6岁及以上人群的几何平均值为3.43 ng/mL)。

结论

本研究提供了首个定量证据,证实接受强化治疗性医疗干预的新生儿接触的DEHP浓度高于普通人群。尽管使用PVC设备进行医疗程序的总体益处超过了接触DEHP相关的风险,但仍需要更多研究来确定,与接受类似治疗但未潜在接触DEHP的婴幼儿相比,使用含DEHP设备进行强化治疗干预的婴幼儿健康结局改变的风险是否更高。

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