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在公共医疗系统中实施孕期药物使用普遍筛查。

Implementation of universal screening for substance use in pregnancy in a public healthcare system.

作者信息

White Alesha, Afsari Macy, Balakrishnan Harini, Chapa Emilia, Kim Meredith, Mehra Shubhangi, Faucher Mary Ann, Miller Joyce, Cordova Polly, Duryea Elaine L, Nelson David B, Ambia Anne M, Mcintire Donald D, Adhikari Emily H

机构信息

Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX (White, Afsari, Balakrishnan, Chapa, Kim, Mehra, Duryea, Nelson, Ambia, Mcintire, Adhikari).

Department of Obstetrics and Gynecology at Parkland Health, Dallas, TX (White, Duryea, Nelson, Ambia, Adhikari, Faucher, Miller, Cordova).

出版信息

AJOG Glob Rep. 2024 Jul 27;4(3):100384. doi: 10.1016/j.xagr.2024.100384. eCollection 2024 Aug.

DOI:10.1016/j.xagr.2024.100384
PMID:39263682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11388400/
Abstract

OBJECTIVE

Screening questionnaires are one option for identification of at-risk substance use and substance use disorder (SUD) during pregnancy. We report the experience of a single institution following universal implementation of a brief screening tool for self-reported substance use at the first prenatal encounter.

STUDY DESIGN

This is a prospective implementation study evaluating screening for substance use in pregnancy in a large safety net healthcare system. Universal screening with the National Institute of Drug Abuse (NIDA) Quick Screen V1.0 was integrated into the electronic medical record (EMR) and administered at the first point of contact with the healthcare system. SUD was identified initially with diagnosis within the EMR by a healthcare provider and was confirmed with toxicology (maternal or neonatal) results corroborating a pattern of substance use and maternal and neonatal ICD-10 codes for SUD. Patients identified with SUD were then classified as moderate or severe SUD based on criteria established by the Diagnostic and Statistical Manual of Mental Disorders, 5th edition. We measured rates of NIDA implementation across different healthcare settings, evaluated NIDA concordance with ascertainment of SUD, and compared adverse pregnancy outcomes associated with moderate and severe SUD.

RESULTS

From July 28, 2021, through June 25, 2022, 14,634 unique pregnant individuals accessed care at ambulatory and acute care sites. Universal implementation of the NIDA Quick Screen identified at-risk substance use in 2146 (14.7%) of those who accessed our system, or 17.1% of 12,550 screened across the system, with greater screen completion in ambulatory over acute care settings. SUD was identified in 256 (1.7%) of 14,634 individuals and moderate or severe SUD was identified in 184 (1.3%). Among those with moderate or severe SUD, 90 (48.9%) were NIDA positive, 22 (12.0%) NIDA negative, and 72 (39.1%) unscreened. Of 94 individuals with NIDA discordance or who were unscreened 76 (81%) accessed initial care through an acute care setting. Of 96 individuals with opioid use disorder, 68 (70.8%) were treated with medication-assisted therapy, and 56 (58.3%) were screened with the NIDA Quick Screen. Among delivered individuals with available outcomes, those with moderate or severe SUD were less likely to seek prenatal care (71 (76%) vs 9852 (98%), <0.001)) and more likely to deliver before 37 weeks, (18 (20%) vs 909 (9%), RR (95% CI) 2.13 (1.40, 3.24)) compared to individuals without SUD. Neonates exposed to moderate or severe SUD were more likely to have birth weight <10th centile for gestational age (20 (22%) vs 1147 (12%), RR (95% CI) 1.92 (1.29, 2.85)) and require admission to the neonatal intensive care unit (NICU) (19 (21%) vs 964 (10%), RR (95%) 1.95 (1.30, 2.93)).

CONCLUSION

Universal screening was implemented across a large public healthcare system at a high rate, with higher rates of implementation in ambulatory settings. NIDA successfully identified at-risk substance use in 17% of the SUD cohort but failed to identify more than 50% of patients with moderate or severe SUD. Patients with moderate and severe SUD accessed care primarily through the emergency department and experienced higher rates of adverse obstetric and neonatal outcomes. Future efforts to identify, engage, and retain this highest-risk group are needed.

摘要

目的

筛查问卷是孕期识别高危物质使用和物质使用障碍(SUD)的一种方法。我们报告了一家机构在首次产前检查时普遍实施自我报告物质使用简短筛查工具后的经验。

研究设计

这是一项前瞻性实施研究,评估大型安全网医疗系统中孕期物质使用的筛查情况。使用美国国立药物滥用研究所(NIDA)快速筛查V1.0进行普遍筛查已整合到电子病历(EMR)中,并在与医疗系统首次接触时进行。最初由医疗服务提供者在EMR中诊断出SUD,并通过毒理学(母体或新生儿)结果证实存在物质使用模式以及SUD的母体和新生儿ICD-10编码。然后根据《精神疾病诊断与统计手册》第5版制定的标准,将确诊为SUD的患者分为中度或重度SUD。我们测量了不同医疗环境中NIDA实施率,评估NIDA与SUD确诊的一致性,并比较了与中度和重度SUD相关的不良妊娠结局。

结果

从2021年7月28日至2022年6月25日,14634名独特的孕妇在门诊和急症护理场所接受了治疗。NIDA快速筛查的普遍实施在14634名就诊者中的2146人(14.7%)中识别出高危物质使用,占全系统筛查的12550人的17.1%,门诊环境中的筛查完成率高于急症护理环境。在14634名个体中,256人(1.7%)被诊断为SUD,184人(1.3%)被诊断为中度或重度SUD。在中度或重度SUD患者中,90人(48.9%)NIDA呈阳性,22人(1

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6c/11388400/1ae629dbe4a1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6c/11388400/8259aad7d6e8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6c/11388400/1ae629dbe4a1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6c/11388400/8259aad7d6e8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6c/11388400/1ae629dbe4a1/gr2.jpg

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