Kiefer Miranda K, Cowen Jamie, Hinely Katherine A, Rood Kara M
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, The Ohio State University College of Medicine, Columbus, OH (Dr Kiefer, Ms Hinely, and Dr Rood).
The Ohio State University College of Medicine, Columbus, OH (Ms Cowen).
AJOG Glob Rep. 2024 Jan 19;4(2):100313. doi: 10.1016/j.xagr.2024.100313. eCollection 2024 May.
Although urine drug testing can have vast legal and social ramifications, its interpretation during pregnancy and after birth remains not well understood. Fentanyl metabolism is altered by an individual's genetics, history of opioid use, and liver function. However, little is known about the clearance of fentanyl or its primary metabolite, norfentanyl, in the peripartum period.
We sought to identify and describe cases of delayed urine norfentanyl clearance in the pregnancy and postpartum period within our institution.
This study described 3 cases of delayed urine norfentanyl clearance in pregnant and postpartum individuals in a colocated obstetrics, postpartum, and addiction medicine program. This program included prescriptions for medication for opioid use disorder and weekly urine drug testing with fentanyl immunoassay with reflex confirmation testing with liquid chromatography-tandem mass spectrometry for positive results with a limit of detection of 2.5 ng/mL.
Low levels of norfentanyl (<16.3 ng/mL) were detected in urine 294 days, 126 days, and 231 days after the last fentanyl use. Patient self-reported abstinence was supported by consistently negative urine fentanyl levels throughout the collection period, compliant weekly urine drug tests that were otherwise only positive for buprenorphine, and negative fentanyl and norfentanyl in umbilical cord toxicology.
Despite compliance in a medication for opioid use disorder program, the presence of norfentanyl in urine has significant consequences on the maternal-child dyad in the postpartum period. Caution should be used when using low levels of norfentanyl to determine an individual's abstinence, as it can lead to further discrimination against women in medication for opioid use disorder programs.
尽管尿液药物检测可能会产生广泛的法律和社会影响,但其在孕期及产后的解读仍未得到充分理解。芬太尼的代谢会因个体的基因、阿片类药物使用史及肝功能而发生改变。然而,关于围产期芬太尼或其主要代谢产物去甲芬太尼的清除情况,人们知之甚少。
我们试图在本机构内识别并描述孕期及产后尿液中去甲芬太尼清除延迟的病例。
本研究描述了在一个综合的产科、产后及成瘾医学项目中,3例孕期及产后个体尿液中去甲芬太尼清除延迟的病例。该项目包括开具阿片类药物使用障碍的药物处方,以及每周进行尿液药物检测,采用芬太尼免疫分析法,阳性结果需通过液相色谱 - 串联质谱法进行反射确认检测,检测限为2.5 ng/mL。
在最后一次使用芬太尼后的294天、126天和231天,尿液中检测到低水平的去甲芬太尼(<16.3 ng/mL)。患者自我报告已戒除毒品,这得到了整个收集期内尿液芬太尼水平持续呈阴性的支持,每周的尿液药物检测结果符合要求,否则仅丁丙诺啡呈阳性,且脐带毒理学检测中芬太尼和去甲芬太尼均为阴性。
尽管在阿片类药物使用障碍项目中遵守了规定,但尿液中去甲芬太尼的存在对产后母婴二元组有重大影响。在使用低水平的去甲芬太尼来确定个体是否戒除毒品时应谨慎,因为这可能会导致在阿片类药物使用障碍项目中对女性的进一步歧视。