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

被引:209
|
作者
Calafat, AM
Needham, LL
Silva, MJ
Lambert, G
机构
[1] Ctr Dis Control & Prevent, Div Sci Lab, Natl Ctr Environm Hlth, Atlanta, GA 30341 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pediat, Ctr Childhood Neurotoxicol & Exposure Assessment, Piscataway, NJ 08854 USA
关键词
DEHP; phthalate; plasticizer; urine; biomarker;
D O I
10.1542/peds.113.5.e429
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:E429 / E434
页数:6
相关论文
共 50 条
  • [21] ALTERATION OF HEPATIC PHOSPHOLIPIDS IN RATS AND MICE BY FEEDING DI-(2-ETHYLHEXYL)ADIPATE AND DI-(2-ETHYLHEXYL)PHTHALATE
    YANAGITA, T
    SATOH, M
    NOMURA, H
    ENOMOTO, N
    SUGANO, M
    LIPIDS, 1987, 22 (08) : 572 - 577
  • [22] The impact of Di-(2-ethylhexyl) Phthalate and Mono(2-ethylhexyl) Phthalate in placental development, function, and pathophysiology
    Daniel Martinez-Razo, Luis
    Martinez-Ibarra, Alejandra
    Ricardo Vazquez-Martinez, Edgar
    Cerbon, Marco
    ENVIRONMENT INTERNATIONAL, 2021, 146 (146)
  • [23] REPRODUCTIVE HAZARDS OF DI-(2-ETHYLHEXYL)-PHTHALATE: IN VITRO AND IN VIVO EXPOSURE TO MOUSE
    Huang, X. -F.
    Li, Y.
    Zhang, H. -Q.
    Shi, H. -J.
    FERTILITY AND STERILITY, 2012, 98 (03) : S33 - S33
  • [24] POLAR METABOLITES OF DI-(2-ETHYLHEXYL)PHTHALATE IN THE RAT
    ALBRO, PW
    TONDEUR, I
    MARBURY, D
    JORDAN, S
    SCHROEDER, J
    CORBETT, JT
    BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 760 (02) : 283 - 292
  • [25] REVIEW OF BIOLOGICAL EFFECTS OF DI-(2-ETHYLHEXYL) PHTHALATE
    THOMAS, JA
    DARBY, TD
    WALLIN, RF
    GARVIN, PJ
    MARTIS, L
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1978, 45 (01) : 1 - 27
  • [26] Toxicity and Mechanism of Di-(2-ethylhexyl) Phthalate on Testis
    Feng An-Ni
    Sun Ren-Ren
    Xiao Yu-Bo
    Zeng Zhao-Ming
    Mo Zhong-Cheng
    Xie Yuan-Jie
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2024, 51 (03) : 555 - 563
  • [27] Cardiovascular Response of Rat Aorta to Di-(2-ethylhexyl) Phthalate (DEHP) Exposure
    Melissa Mariana
    Joana Feiteiro
    Elisa Cairrao
    Cardiovascular Toxicology, 2018, 18 : 356 - 364
  • [28] Di-(2-ethylhexyl) phthalate and autism spectrum disorders
    Testa, Chiara
    Nuti, Francesca
    Hayek, Joussef
    De Felice, Claudio
    Chelli, Mario
    Rovero, Paolo
    Latini, Giuseppe
    Papini, Anna Maria
    ASN NEURO, 2012, 4 (04): : 223 - 229
  • [29] VISCOELASTIC AND ULTRASONIC RELAXATION IN DI-(2-ETHYLHEXYL) PHTHALATE
    BARLOW, AJ
    ERGINSAV, A
    MCLACHLA.RJ
    SINGH, RP
    JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1974, 70 (07): : 1288 - 1293
  • [30] Cardiovascular Response of Rat Aorta to Di-(2-ethylhexyl) Phthalate (DEHP) Exposure
    Mariana, Melissa
    Feiteiro, Joana
    Cairrao, Elisa
    CARDIOVASCULAR TOXICOLOGY, 2018, 18 (04) : 356 - 364