Margaret Pepper Dean, Helen Mistler, Lori Moore, Nicole Lewis, Martin Olsen
{"title":"Increased Prevalence of Skeletal Anomalies on Ultrasound Evaluation of Buprenorphine-Exposed Human Fetuses.","authors":"Margaret Pepper Dean, Helen Mistler, Lori Moore, Nicole Lewis, Martin Olsen","doi":"10.14423/SMJ.0000000000001776","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>In this study, buprenorphine was the primary source of maternal opioid exposure at the time of initial prenatal evaluation. Current recommendations advise that level II ultrasounds be performed in patients with substance use disorders. For some patients, distance, transportation, and costs associated with obtaining ultrasounds from a specialist pose significant barriers. This study was thus undertaken to evaluate the value of level II ultrasounds in buprenorphine-exposed pregnancies.</p><p><strong>Methods: </strong>In a retrospective chart review comparing 1188 substance-exposed patients with 1261 nonexposed, anomaly data were collected from level I and level II anatomy scans, problem lists on prenatal flowsheets, and visit notes. If anomalies were detected, then they were further classified by the affected organ system. Two proportion tests were used to compare the exposed and unexposed groups. When the assumptions were not met, a Fisher exact test and the Benjamini-Hochberg method were used to adjust for multiple testing.</p><p><strong>Results: </strong>Buprenorphine-exposed fetuses have increased rates of composite skeletal anomalies when compared with nonexposed fetuses (P< 0.005). No statistically significant difference, however, was found between groups for any other system or for any specific skeletal anomaly. No statistical difference was found related to buprenorphine dose.</p><p><strong>Conclusions: </strong>This is the first report of skeletal anomalies in buprenorphine-exposed human fetuses. Causality is unproven, but this report is consistent with prior human and animal studies in which maternal opioid use has been linked to significant impairments in bone growth and development. Our findings suggest that anatomic surveys of fetuses exposed to buprenorphine should be performed by individuals with expertise in the detection of fetal skeletal anomalies.</p>","PeriodicalId":22043,"journal":{"name":"Southern Medical Journal","volume":"118 1","pages":"39-44"},"PeriodicalIF":1.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Southern Medical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14423/SMJ.0000000000001776","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: In this study, buprenorphine was the primary source of maternal opioid exposure at the time of initial prenatal evaluation. Current recommendations advise that level II ultrasounds be performed in patients with substance use disorders. For some patients, distance, transportation, and costs associated with obtaining ultrasounds from a specialist pose significant barriers. This study was thus undertaken to evaluate the value of level II ultrasounds in buprenorphine-exposed pregnancies.
Methods: In a retrospective chart review comparing 1188 substance-exposed patients with 1261 nonexposed, anomaly data were collected from level I and level II anatomy scans, problem lists on prenatal flowsheets, and visit notes. If anomalies were detected, then they were further classified by the affected organ system. Two proportion tests were used to compare the exposed and unexposed groups. When the assumptions were not met, a Fisher exact test and the Benjamini-Hochberg method were used to adjust for multiple testing.
Results: Buprenorphine-exposed fetuses have increased rates of composite skeletal anomalies when compared with nonexposed fetuses (P< 0.005). No statistically significant difference, however, was found between groups for any other system or for any specific skeletal anomaly. No statistical difference was found related to buprenorphine dose.
Conclusions: This is the first report of skeletal anomalies in buprenorphine-exposed human fetuses. Causality is unproven, but this report is consistent with prior human and animal studies in which maternal opioid use has been linked to significant impairments in bone growth and development. Our findings suggest that anatomic surveys of fetuses exposed to buprenorphine should be performed by individuals with expertise in the detection of fetal skeletal anomalies.
期刊介绍:
As the official journal of the Birmingham, Alabama-based Southern Medical Association (SMA), the Southern Medical Journal (SMJ) has for more than 100 years provided the latest clinical information in areas that affect patients'' daily lives. Now delivered to individuals exclusively online, the SMJ has a multidisciplinary focus that covers a broad range of topics relevant to physicians and other healthcare specialists in all relevant aspects of the profession, including medicine and medical specialties, surgery and surgery specialties; child and maternal health; mental health; emergency and disaster medicine; public health and environmental medicine; bioethics and medical education; and quality health care, patient safety, and best practices. Each month, articles span the spectrum of medical topics, providing timely, up-to-the-minute information for both primary care physicians and specialists. Contributors include leaders in the healthcare field from across the country and around the world. The SMJ enables physicians to provide the best possible care to patients in this age of rapidly changing modern medicine.