Pub Date : 2025-11-01Epub Date: 2025-03-03DOI: 10.1097/ADM.0000000000001471
Jennifer A Ross, William Riccardelli, Sharon Levy
With the expansion of the "medical cannabis" or "medical marijuana" market, there is significant confusion surrounding cannabinoid terminology. This commentary provides definitions for cannabinoid terminology, examines US Food and Drug Administration (FDA)-approved and non-FDA-approved medications with cannabinoids as the main ingredient, and discusses how vague terminology may lead to a public misperception regarding the lack of evidence-based medical indications for cannabis.
{"title":"The Confusing Terminology of \"Medical Cannabis\" and Cannabinoid Products.","authors":"Jennifer A Ross, William Riccardelli, Sharon Levy","doi":"10.1097/ADM.0000000000001471","DOIUrl":"10.1097/ADM.0000000000001471","url":null,"abstract":"<p><p>With the expansion of the \"medical cannabis\" or \"medical marijuana\" market, there is significant confusion surrounding cannabinoid terminology. This commentary provides definitions for cannabinoid terminology, examines US Food and Drug Administration (FDA)-approved and non-FDA-approved medications with cannabinoids as the main ingredient, and discusses how vague terminology may lead to a public misperception regarding the lack of evidence-based medical indications for cannabis.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":"637-639"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143542217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: The objective of the study was to conduct a systematic review of the available literature on non-medical use of mephentermine, including its pattern of use, associated complications, and treatment approaches.
Methods: We conducted a systematic search across PubMed, Scopus, EMBASE, Web of Science, and EBSCO, to identify studies reporting non-medical mephentermine use. Two independent reviewers screened the studies, and methodological quality was assessed using the Joanna Briggs Institute tools. Extracted data included demographics, use patterns, psychiatric and physical complications, cooccurring substance use, and treatment approaches.
Results: Of 695 retrieved studies, 23 full-text studies met inclusion criteria (4 case series, 19 case reports, 30 cases). The majority (n = 28, 93.3%) were from India, all male (age: 19-39 y, mean = 27.9). Most used mephentermine for performance enhancement (63%), primarily through intravenous injection (77.8%). Psychiatric comorbidities were reported in 60%, with psychosis (43.3%) being the most common. Cooccurring substance use (40%) included alcohol, tobacco, and anabolic steroids. Treatment was largely symptomatic, with antipsychotics and benzodiazepines being most frequently prescribed.
Conclusions: Non-medical mephentermine use appears to be rising, particularly among athletes and bodybuilders, with notable psychiatric complications. Targeted education and clinical awareness are needed. Further research should explore addiction potential, long-term effects, and treatment strategies.
目的:本研究的目的是对现有的非医疗使用甲苯丙胺的文献进行系统回顾,包括其使用模式、相关并发症和治疗方法。方法:我们对PubMed、Scopus、EMBASE、Web of Science和EBSCO进行了系统检索,以确定报告非医疗使用甲基苯丙胺的研究。两名独立审稿人对研究进行了筛选,并使用乔安娜布里格斯研究所的工具对方法质量进行了评估。提取的数据包括人口统计、使用模式、精神和身体并发症、同时发生的物质使用和治疗方法。结果:检索到的695项研究中,23项全文研究符合纳入标准(4个病例系列,19个病例报告,30个病例)。大多数患者(n = 28, 93.3%)来自印度,均为男性(年龄19-39岁,平均27.9岁)。大多数使用甲芬特明来提高成绩(63%),主要通过静脉注射(77.8%)。60%的患者报告有精神疾病合并症,其中精神病(43.3%)最为常见。同时发生的物质使用(40%)包括酒精、烟草和合成代谢类固醇。治疗主要是对症治疗,抗精神病药物和苯二氮卓类药物是最常用的处方。结论:非医用甲基苯丙胺的使用似乎正在上升,尤其是在运动员和健美运动员中,并伴有明显的精神并发症。需要有针对性的教育和临床意识。进一步的研究应该探索成瘾的可能性、长期影响和治疗策略。
{"title":"Non-medical Mephentermine Use: A Systematic Review of Literature.","authors":"Vinit Patel, Harsha, Arun Kumar, Rizwana Quraishi, Ravindra Rao","doi":"10.1097/ADM.0000000000001485","DOIUrl":"10.1097/ADM.0000000000001485","url":null,"abstract":"<p><strong>Objectives: </strong>The objective of the study was to conduct a systematic review of the available literature on non-medical use of mephentermine, including its pattern of use, associated complications, and treatment approaches.</p><p><strong>Methods: </strong>We conducted a systematic search across PubMed, Scopus, EMBASE, Web of Science, and EBSCO, to identify studies reporting non-medical mephentermine use. Two independent reviewers screened the studies, and methodological quality was assessed using the Joanna Briggs Institute tools. Extracted data included demographics, use patterns, psychiatric and physical complications, cooccurring substance use, and treatment approaches.</p><p><strong>Results: </strong>Of 695 retrieved studies, 23 full-text studies met inclusion criteria (4 case series, 19 case reports, 30 cases). The majority (n = 28, 93.3%) were from India, all male (age: 19-39 y, mean = 27.9). Most used mephentermine for performance enhancement (63%), primarily through intravenous injection (77.8%). Psychiatric comorbidities were reported in 60%, with psychosis (43.3%) being the most common. Cooccurring substance use (40%) included alcohol, tobacco, and anabolic steroids. Treatment was largely symptomatic, with antipsychotics and benzodiazepines being most frequently prescribed.</p><p><strong>Conclusions: </strong>Non-medical mephentermine use appears to be rising, particularly among athletes and bodybuilders, with notable psychiatric complications. Targeted education and clinical awareness are needed. Further research should explore addiction potential, long-term effects, and treatment strategies.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":"19 6","pages":"685-692"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495179","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-03-07DOI: 10.1097/ADM.0000000000001476
Blythe Bynum, Katherine M Mahoney, Tachianna Griffiths, Arden McAllister, Courtney Schreiber, Sarita Sonalkar, Nia Bhadra-Heintz
Objectives: People with childbearing potential and opioid use disorder (OUD) have high rates of unintended pregnancies. Addiction medicine providers occupy an important role in diagnosing and counseling those who become pregnant; however, no guidelines exist to facilitate these conversations. We sought to explore participant experiences with pregnancy options counseling while in opioid use disorder treatment clinics.
Methods: We conducted semistructured interviews with people who became pregnant while in OUD treatment, regardless of pregnancy outcome. The interview domains included (1) interactions with health care upon pregnancy discovery, (2) pregnancy options counseling provision, and (3) factors affecting pregnancy decision. A codebook was formulated through an iterative process using a P3 framework (practice, provider, patient). All interviews were double-coded and analyzed for content and themes.
Results: Eighteen participants completed interviews between December 2022 and April 2023. Participants reported valuing nonjudgmental communication when providers disclose unexpected pregnancy results, as well as the need for unbiased and trustworthy information regarding the impact of OUD and OUD treatment on their options. They also identified the unique stigma and bias experienced by pregnant people with OUD.
Conclusions: Although no guidelines exist to guide pregnancy options counseling in addiction medicine settings, efforts should be made to integrate all pregnancy options counseling-parenting, adoption, and abortion-and/or referrals into the care of pregnant patients at OUD treatment centers. Effective discussions should be conducted in a nonbiased and nonjudgmental fashion. Our findings can be used to develop patient-centered counseling aimed at improving pregnancy decision-making while in treatment for OUD.
{"title":"Navigating Choices: Pregnancy Options Counseling Experiences in Individuals With Opioid Use Disorder.","authors":"Blythe Bynum, Katherine M Mahoney, Tachianna Griffiths, Arden McAllister, Courtney Schreiber, Sarita Sonalkar, Nia Bhadra-Heintz","doi":"10.1097/ADM.0000000000001476","DOIUrl":"10.1097/ADM.0000000000001476","url":null,"abstract":"<p><strong>Objectives: </strong>People with childbearing potential and opioid use disorder (OUD) have high rates of unintended pregnancies. Addiction medicine providers occupy an important role in diagnosing and counseling those who become pregnant; however, no guidelines exist to facilitate these conversations. We sought to explore participant experiences with pregnancy options counseling while in opioid use disorder treatment clinics.</p><p><strong>Methods: </strong>We conducted semistructured interviews with people who became pregnant while in OUD treatment, regardless of pregnancy outcome. The interview domains included (1) interactions with health care upon pregnancy discovery, (2) pregnancy options counseling provision, and (3) factors affecting pregnancy decision. A codebook was formulated through an iterative process using a P3 framework (practice, provider, patient). All interviews were double-coded and analyzed for content and themes.</p><p><strong>Results: </strong>Eighteen participants completed interviews between December 2022 and April 2023. Participants reported valuing nonjudgmental communication when providers disclose unexpected pregnancy results, as well as the need for unbiased and trustworthy information regarding the impact of OUD and OUD treatment on their options. They also identified the unique stigma and bias experienced by pregnant people with OUD.</p><p><strong>Conclusions: </strong>Although no guidelines exist to guide pregnancy options counseling in addiction medicine settings, efforts should be made to integrate all pregnancy options counseling-parenting, adoption, and abortion-and/or referrals into the care of pregnant patients at OUD treatment centers. Effective discussions should be conducted in a nonbiased and nonjudgmental fashion. Our findings can be used to develop patient-centered counseling aimed at improving pregnancy decision-making while in treatment for OUD.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":"661-667"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143573057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-04-07DOI: 10.1097/ADM.0000000000001484
Michelle R Lofwall, Edward V Nunes, Sharon L Walsh, Genie L Bailey, Michael Frost, Natalie R Budilovsky-Kelley, Elin Banke Nordbeck, Susanna Meyner, Peter Almgren, Stefan Peterson, Fredrik Tiberg
Objectives: CAM2038 weekly and monthly extended-release buprenorphine (BPN) formulations are effective for treating opioid use disorder (OUD). Little is known about the effect of dose on patient outcomes, particularly under blinded and flexible dosing conditions. We evaluated the number of dose changes and the impact of (1) dose on treatment outcomes and (2) baseline primary opioid use (heroin vs prescription opioids) and route of use (injection or not) on the dose.
Methods: This was a post hoc analysis of an outpatient randomized double-blind, double-dummy trial comparing weekly (first 12 wk) and monthly (second 12 wk) CAM2038 to SL-BPN (24 wk) for OUD treatment. Dosing was flexible and guided by clinical response. Maximum doses were 32 mg weekly/160 mg monthly CAM2038 and 24 mg/32 mg SL-BPN in the first and second 12 weeks, respectively. Effect of each dose was evaluated using four outcomes: urine drug test (UDT) opioid results, Clinical Opiate Withdrawal Scale scores, Subjective Opiate Withdrawal Scale scores, and need- and desire-to-use opioid visual analogue scales. Associations between baseline route of use and primary opioid used and study dose were investigated.
Results: After titration to 16 mg SL-BPN/24 mg weekly CAM2038, most participants had 0-1 dose adjustments in both first and second 12 weeks. All doses were utilized. Number of adjustments was not associated with retention. Withdrawal, craving, and opioid-positive UDTs decreased for all CAM2038 and SL-BPN doses. There were few clinically significant associations between dose and primary opioid used/route of use.
Conclusions: Results support current practice guidelines, emphasizing the importance of individualized dosing based on patient response.
{"title":"Dosing to Effect With Weekly and Monthly Subcutaneous and Daily Sublingual Buprenorphine: Post Hoc Analysis of a Phase 3 Clinical Trial.","authors":"Michelle R Lofwall, Edward V Nunes, Sharon L Walsh, Genie L Bailey, Michael Frost, Natalie R Budilovsky-Kelley, Elin Banke Nordbeck, Susanna Meyner, Peter Almgren, Stefan Peterson, Fredrik Tiberg","doi":"10.1097/ADM.0000000000001484","DOIUrl":"10.1097/ADM.0000000000001484","url":null,"abstract":"<p><strong>Objectives: </strong>CAM2038 weekly and monthly extended-release buprenorphine (BPN) formulations are effective for treating opioid use disorder (OUD). Little is known about the effect of dose on patient outcomes, particularly under blinded and flexible dosing conditions. We evaluated the number of dose changes and the impact of (1) dose on treatment outcomes and (2) baseline primary opioid use (heroin vs prescription opioids) and route of use (injection or not) on the dose.</p><p><strong>Methods: </strong>This was a post hoc analysis of an outpatient randomized double-blind, double-dummy trial comparing weekly (first 12 wk) and monthly (second 12 wk) CAM2038 to SL-BPN (24 wk) for OUD treatment. Dosing was flexible and guided by clinical response. Maximum doses were 32 mg weekly/160 mg monthly CAM2038 and 24 mg/32 mg SL-BPN in the first and second 12 weeks, respectively. Effect of each dose was evaluated using four outcomes: urine drug test (UDT) opioid results, Clinical Opiate Withdrawal Scale scores, Subjective Opiate Withdrawal Scale scores, and need- and desire-to-use opioid visual analogue scales. Associations between baseline route of use and primary opioid used and study dose were investigated.</p><p><strong>Results: </strong>After titration to 16 mg SL-BPN/24 mg weekly CAM2038, most participants had 0-1 dose adjustments in both first and second 12 weeks. All doses were utilized. Number of adjustments was not associated with retention. Withdrawal, craving, and opioid-positive UDTs decreased for all CAM2038 and SL-BPN doses. There were few clinically significant associations between dose and primary opioid used/route of use.</p><p><strong>Conclusions: </strong>Results support current practice guidelines, emphasizing the importance of individualized dosing based on patient response.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":"676-684"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12577654/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143795385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-05-01DOI: 10.1097/ADM.0000000000001491
Matthew E Sloan, Anthony Ngoy, Ke Bin Xiao, Bryce Barker, Leslie Buckley, Marina Fodor, Kate Hardy, Christian S Hendershot, Meldon Kahan, Sandra La Fleur, Bernard Le Foll, Mitchell Manicone, Marcos Sanches, Emily Simpkin, Lena C Quilty, Jennifer Wyman, Victor M Tang, Nikki Bozinoff
Objectives: Alcohol use is one of the leading causes of death and disability globally; however, access to evidence-based care for alcohol use disorder (AUD) is limited. Although telemedicine-based interventions promise to expand treatment access, there are no validated telemedicine-based interventions for alcohol withdrawal management. In this single-arm study, we sought to determine the feasibility of delivering symptom-triggered alcohol withdrawal management over telemedicine.
Methods: Thirty actively drinking participants with AUD and a history of alcohol withdrawal were recruited to participate. Participants were scheduled for 3 days of symptom-triggered withdrawal management using the Clinical Institute Withdrawal Assessment for Alcohol Scale Revised delivered by a trained clinician over a telemedicine platform. Primary outcomes were retention in treatment and need for transfer to a higher level of care (eg, the emergency room). Satisfaction with the treatment protocol and relapse to any alcohol use 30 days following treatment initiation were also assessed.
Results: In total, 93.3% of participants completed all 3 days of alcohol withdrawal management. No participants required transfer to a higher level of care. Satisfaction with treatment was high, with an average Client Satisfaction Questionnaire-8 score of 30.9 (SD = 1.5) out of 32. After the follow-up period, 56.7% of participants remained abstinent from alcohol.
Conclusions: Our study provides preliminary evidence that symptom-triggered alcohol withdrawal management over telemedicine is feasible and satisfactory for patients. If these findings are replicated, they could have important implications for access to alcohol withdrawal management services, especially in remote, rural, and underserved regions that lack specialized withdrawal management facilities.
{"title":"Symptom-Triggered Alcohol Withdrawal Management Delivered Over Telemedicine.","authors":"Matthew E Sloan, Anthony Ngoy, Ke Bin Xiao, Bryce Barker, Leslie Buckley, Marina Fodor, Kate Hardy, Christian S Hendershot, Meldon Kahan, Sandra La Fleur, Bernard Le Foll, Mitchell Manicone, Marcos Sanches, Emily Simpkin, Lena C Quilty, Jennifer Wyman, Victor M Tang, Nikki Bozinoff","doi":"10.1097/ADM.0000000000001491","DOIUrl":"10.1097/ADM.0000000000001491","url":null,"abstract":"<p><strong>Objectives: </strong>Alcohol use is one of the leading causes of death and disability globally; however, access to evidence-based care for alcohol use disorder (AUD) is limited. Although telemedicine-based interventions promise to expand treatment access, there are no validated telemedicine-based interventions for alcohol withdrawal management. In this single-arm study, we sought to determine the feasibility of delivering symptom-triggered alcohol withdrawal management over telemedicine.</p><p><strong>Methods: </strong>Thirty actively drinking participants with AUD and a history of alcohol withdrawal were recruited to participate. Participants were scheduled for 3 days of symptom-triggered withdrawal management using the Clinical Institute Withdrawal Assessment for Alcohol Scale Revised delivered by a trained clinician over a telemedicine platform. Primary outcomes were retention in treatment and need for transfer to a higher level of care (eg, the emergency room). Satisfaction with the treatment protocol and relapse to any alcohol use 30 days following treatment initiation were also assessed.</p><p><strong>Results: </strong>In total, 93.3% of participants completed all 3 days of alcohol withdrawal management. No participants required transfer to a higher level of care. Satisfaction with treatment was high, with an average Client Satisfaction Questionnaire-8 score of 30.9 (SD = 1.5) out of 32. After the follow-up period, 56.7% of participants remained abstinent from alcohol.</p><p><strong>Conclusions: </strong>Our study provides preliminary evidence that symptom-triggered alcohol withdrawal management over telemedicine is feasible and satisfactory for patients. If these findings are replicated, they could have important implications for access to alcohol withdrawal management services, especially in remote, rural, and underserved regions that lack specialized withdrawal management facilities.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":"708-715"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12352377/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144024762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-02-17DOI: 10.1097/ADM.0000000000001469
Ty S Schepis, Philip T Veliz, Brady T West, Vita V McCabe, Eric Hulsey, Luisa Kcomt, Sean Esteban McCabe
Purpose: Youth (children and adolescents under 18 yrs) exposed to parental substance use disorder (SUD) are at high risk for poor outcomes that include substance use, psychopathology, and child welfare involvement. With the changing SUD criteria from DSM-IV to DSM-5, revised estimates of youth exposed to parental SUD in the home are needed to provide more recent estimates and investigate whether the change from DSM-IV to DSM-5 may change estimated SUD exposure.
Methods: Nationally representative data from the 2020 National Survey on Drug Use and Health were used. Weighted counts of youth exposed to parental nonnicotine SUD in the home were estimated using both DSM-IV and DSM-5 criteria, which were assessed for every substance used by the parent in the past year; further analyses estimated counts by parental race/ethnicity, sex, household income, urbanicity, and substance leading to the SUD diagnosis.
Results: Parents with DSM-IV SUD had an estimated 9,341,336 youth in their households, versus an estimated 16,937,783 using DSM-5 criteria (81.3% greater). Larger increases were observed in Asian (262.9%) or multiracial (161.9%) parents versus parents of other racial/ethnic groups and in parents with cannabis use disorder (246.4%), with smaller increases observed in parents with alcohol use disorder (71.2%).
Discussion: The change from DSM-IV to DSM-5 criteria resulted in a large increase in youth exposed to parental SUD. The health needs of these youth will require large-scale planning to limit poor outcomes in the roughly 17 million exposed youth; family-based interventions may help limit harms to all members of the family.
{"title":"US Youth Exposed to Parental Substance Use Disorder in the Home: A Comparison of DSM-IV and DSM-5 Criteria.","authors":"Ty S Schepis, Philip T Veliz, Brady T West, Vita V McCabe, Eric Hulsey, Luisa Kcomt, Sean Esteban McCabe","doi":"10.1097/ADM.0000000000001469","DOIUrl":"10.1097/ADM.0000000000001469","url":null,"abstract":"<p><strong>Purpose: </strong>Youth (children and adolescents under 18 yrs) exposed to parental substance use disorder (SUD) are at high risk for poor outcomes that include substance use, psychopathology, and child welfare involvement. With the changing SUD criteria from DSM-IV to DSM-5, revised estimates of youth exposed to parental SUD in the home are needed to provide more recent estimates and investigate whether the change from DSM-IV to DSM-5 may change estimated SUD exposure.</p><p><strong>Methods: </strong>Nationally representative data from the 2020 National Survey on Drug Use and Health were used. Weighted counts of youth exposed to parental nonnicotine SUD in the home were estimated using both DSM-IV and DSM-5 criteria, which were assessed for every substance used by the parent in the past year; further analyses estimated counts by parental race/ethnicity, sex, household income, urbanicity, and substance leading to the SUD diagnosis.</p><p><strong>Results: </strong>Parents with DSM-IV SUD had an estimated 9,341,336 youth in their households, versus an estimated 16,937,783 using DSM-5 criteria (81.3% greater). Larger increases were observed in Asian (262.9%) or multiracial (161.9%) parents versus parents of other racial/ethnic groups and in parents with cannabis use disorder (246.4%), with smaller increases observed in parents with alcohol use disorder (71.2%).</p><p><strong>Discussion: </strong>The change from DSM-IV to DSM-5 criteria resulted in a large increase in youth exposed to parental SUD. The health needs of these youth will require large-scale planning to limit poor outcomes in the roughly 17 million exposed youth; family-based interventions may help limit harms to all members of the family.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":"19 6","pages":"722-725"},"PeriodicalIF":3.2,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12810740/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-31DOI: 10.1097/ADM.0000000000001604
Kirsten E Smith, Siva Rama Raju Kanumuri, Abhisheak Sharma, Rachel Rattenni, Robert LeComte, Christopher R McCurdy, Edward W Boyer, Eric C Strain
Background: 7-Hydroxymitragynine (7-OH) is a highly selective mu opioid receptor agonist with binding affinity greater than morphine. Although trace amounts of 7-OH are found in kratom, it is formed by metabolism in humans after kratom ingestion. Novel semi-synthetic 7-OH products are manufactured by mono-oxidation of kratom's primary alkaloid, mitragynine. Formulations include sublingual tablets, powders, and liquid shots. We report a case of a study participant with self-reported 7-OH use.
Case presentation: A 23-year-old man using kratom for 3 years was enrolled into a clinical trial evaluating kratom pharmacokinetics, behavioral pharmacology, and withdrawal. He typically used 1.5-2g of kratom whole-leaf powder 6 times/day. Following scheduled kratom product self-administration during the study, several outcomes were atypical, including blunted subjective kratom effects. He reported recent initiation of a "new kratom product" ("Opia") identified as semi-synthetic 7-OH; he was using 20 mg 3 times/day for 4 days before study admission. Mitragynine (29.7 ng/mL) plasma concentration peaked at 1.5 hours post kratom self-administration, while 7-OH Cmax (11.7 ng/mL) occurred before self-administration, confirming prior ingestion of 7-OH. The participant reported withdrawal symptoms and requested early discharge from the study, but refused the study protocol kratom "rescue dose," stating he preferred to take his "stronger" product.
Discussion: Clinicians must obtain detailed self-reports from patients who report any kratom use. As 7-OH products are misleadingly marketed as kratom, and as both long-time kratom consumers and kratom-naive individuals may experiment with these novel products, improved assessment methods are urgently needed in the absence of real-time confirmatory testing.
{"title":"Complicating Factors Surrounding Concurrent Use of Kratom and a Novel 7-hydroxymitragynine Product Among a Participant Enrolled in a Kratom Clinical Trial.","authors":"Kirsten E Smith, Siva Rama Raju Kanumuri, Abhisheak Sharma, Rachel Rattenni, Robert LeComte, Christopher R McCurdy, Edward W Boyer, Eric C Strain","doi":"10.1097/ADM.0000000000001604","DOIUrl":"https://doi.org/10.1097/ADM.0000000000001604","url":null,"abstract":"<p><strong>Background: </strong>7-Hydroxymitragynine (7-OH) is a highly selective mu opioid receptor agonist with binding affinity greater than morphine. Although trace amounts of 7-OH are found in kratom, it is formed by metabolism in humans after kratom ingestion. Novel semi-synthetic 7-OH products are manufactured by mono-oxidation of kratom's primary alkaloid, mitragynine. Formulations include sublingual tablets, powders, and liquid shots. We report a case of a study participant with self-reported 7-OH use.</p><p><strong>Case presentation: </strong>A 23-year-old man using kratom for 3 years was enrolled into a clinical trial evaluating kratom pharmacokinetics, behavioral pharmacology, and withdrawal. He typically used 1.5-2g of kratom whole-leaf powder 6 times/day. Following scheduled kratom product self-administration during the study, several outcomes were atypical, including blunted subjective kratom effects. He reported recent initiation of a \"new kratom product\" (\"Opia\") identified as semi-synthetic 7-OH; he was using 20 mg 3 times/day for 4 days before study admission. Mitragynine (29.7 ng/mL) plasma concentration peaked at 1.5 hours post kratom self-administration, while 7-OH Cmax (11.7 ng/mL) occurred before self-administration, confirming prior ingestion of 7-OH. The participant reported withdrawal symptoms and requested early discharge from the study, but refused the study protocol kratom \"rescue dose,\" stating he preferred to take his \"stronger\" product.</p><p><strong>Discussion: </strong>Clinicians must obtain detailed self-reports from patients who report any kratom use. As 7-OH products are misleadingly marketed as kratom, and as both long-time kratom consumers and kratom-naive individuals may experiment with these novel products, improved assessment methods are urgently needed in the absence of real-time confirmatory testing.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145431015","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-31DOI: 10.1097/ADM.0000000000001606
Marc Galanter, William L White, Brooke Hunter
Objective: Although 11% of all US drug overdose deaths have been attributed to methamphetamine, there are limited treatments for it that have a substantial impact on clinical outcomes. Online access to the community-based fellowship Narcotics Anonymous (NA) may offer support for remission for some persons with methamphetamine use disorder (MUD). Our objective was to characterize the role that online NA participation can play in remission of MUD.
Methods: Persons who accessed a website for participating in online NA meetings were offered the option of participating in an anonymous, structured survey consisting of items related to their clinical status, substance use, and prior experience with the website. Responses of those who designated their primary drug problem as methamphetamine were analyzed.
Results: Of the 1645 respondents who accessed the NA online meeting site in 2023, 356 indicated that methamphetamine was their principal drug problem. Levels of remission by respondents who reported turning to the website primarily for MUD were analyzed for those: (1) new to the online site (44%), (2) longtime abstinent (mean 2.3 y), or (3) still using methamphetamine (13%). Respondents' subjective experiences, such as their belief in the 12 Steps, spiritual awakening, and level of relief provided from distress, were also associated with remission.
Conclusions: Online NA meetings can provide support for promoting abstinence for some persons with MUD, and can be studied relative to their clinical status. Such meetings can therefore be useful for professional referral, and their function and utility merit further investigation.
{"title":"Online Narcotics Anonymous: An Option for Addressing Methamphetamine Use Disorder.","authors":"Marc Galanter, William L White, Brooke Hunter","doi":"10.1097/ADM.0000000000001606","DOIUrl":"10.1097/ADM.0000000000001606","url":null,"abstract":"<p><strong>Objective: </strong>Although 11% of all US drug overdose deaths have been attributed to methamphetamine, there are limited treatments for it that have a substantial impact on clinical outcomes. Online access to the community-based fellowship Narcotics Anonymous (NA) may offer support for remission for some persons with methamphetamine use disorder (MUD). Our objective was to characterize the role that online NA participation can play in remission of MUD.</p><p><strong>Methods: </strong>Persons who accessed a website for participating in online NA meetings were offered the option of participating in an anonymous, structured survey consisting of items related to their clinical status, substance use, and prior experience with the website. Responses of those who designated their primary drug problem as methamphetamine were analyzed.</p><p><strong>Results: </strong>Of the 1645 respondents who accessed the NA online meeting site in 2023, 356 indicated that methamphetamine was their principal drug problem. Levels of remission by respondents who reported turning to the website primarily for MUD were analyzed for those: (1) new to the online site (44%), (2) longtime abstinent (mean 2.3 y), or (3) still using methamphetamine (13%). Respondents' subjective experiences, such as their belief in the 12 Steps, spiritual awakening, and level of relief provided from distress, were also associated with remission.</p><p><strong>Conclusions: </strong>Online NA meetings can provide support for promoting abstinence for some persons with MUD, and can be studied relative to their clinical status. Such meetings can therefore be useful for professional referral, and their function and utility merit further investigation.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-29DOI: 10.1097/ADM.0000000000001605
Ilana Hull, Megan Gates, Kelly Dimattio, Lois Bangiolo, Kenichi Tamama, Christine E Bishop
The emergence of medetomidine, a potent veterinary alpha-2 adrenergic receptor agonist, as a common fentanyl adulterant in many areas of the United States poses new threats to pregnant women who use illicit opioids and their neonates. We present a case of severe withdrawal seen in a postpartum woman and her neonate after exposure to fentanyl adulterated with medetomidine up to the time of delivery. The case demonstrates the need for obstetric and pediatric providers to be aware of this emerging trend to allow for early recognition and prompt treatment of the potentially life-threatening symptoms of medetomidine withdrawal, which differs from traditional withdrawal patterns, and highlights the importance of communication and coordination between obstetric and pediatric teams caring for this population.
{"title":"A Case of Maternal and Neonatal Withdrawal After Exposure to Fentanyl Adulterated With Medetomidine.","authors":"Ilana Hull, Megan Gates, Kelly Dimattio, Lois Bangiolo, Kenichi Tamama, Christine E Bishop","doi":"10.1097/ADM.0000000000001605","DOIUrl":"10.1097/ADM.0000000000001605","url":null,"abstract":"<p><p>The emergence of medetomidine, a potent veterinary alpha-2 adrenergic receptor agonist, as a common fentanyl adulterant in many areas of the United States poses new threats to pregnant women who use illicit opioids and their neonates. We present a case of severe withdrawal seen in a postpartum woman and her neonate after exposure to fentanyl adulterated with medetomidine up to the time of delivery. The case demonstrates the need for obstetric and pediatric providers to be aware of this emerging trend to allow for early recognition and prompt treatment of the potentially life-threatening symptoms of medetomidine withdrawal, which differs from traditional withdrawal patterns, and highlights the importance of communication and coordination between obstetric and pediatric teams caring for this population.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145389847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1097/ADM.0000000000001599
Letizia Biso, Marianna Lebosi, Marco Bonaso, Marco Carli, Marco Scarselli
Objectives: Cocaine use disorder (CUD) is a chronic condition, often associated with attention deficit hyperactivity disorder (ADHD). No medications have been approved for the treatment of CUD, but methylphenidate (MPH) has been explored as a potential candidate. We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of MPH in patients with CUD with and without ADHD.
Methods: Following PRISMA guidelines, we developed a search string for PubMed, ISI Web of Science, and Scopus databases. We included randomized and nonrandomized clinical studies that used MPH in CUD treatment.
Results: Twenty studies were included in the systematic review, 6 of them were included in the meta-analysis. In the meta-analysis, MPH did not reduce craving (ES: -0.33, 95% CI: 1.69 to 1.03; Z = -0.473; P = 0.636) or cocaine use (ES: -0.01, 95% CI: -0.35 to 0.33) (Z= -0.084; P = 0.933) compared with placebo. However, the route of administration and the presence of ADHD associated with CUD influenced the outcomes on cocaine craving measures. Similarly, although the results were inconclusive, a trend toward the reduction of cocaine consumption was observed in patients with ADHD treated with MPH. Regarding safety, MPH can be used in patients with CUD up to 90 mg/d and monitoring the cardiovascular parameters is strictly required.
Conclusions: Evidence on the efficacy of MPH for the treatment of CUD is still limited and inconclusive. However, there might be a rationale for its use in patients with both CUD and ADHD, therefore, further clinical studies are needed in this particular category.
目的:可卡因使用障碍(CUD)是一种慢性疾病,通常与注意缺陷多动障碍(ADHD)有关。目前还没有药物被批准用于治疗CUD,但哌醋甲酯(MPH)已被视为潜在的候选药物。我们进行了一项系统回顾和荟萃分析,以评估MPH在合并和不合并ADHD的CUD患者中的疗效和安全性。方法:根据PRISMA指南,我们开发了PubMed、ISI Web of Science和Scopus数据库的搜索字符串。我们纳入了使用MPH治疗CUD的随机和非随机临床研究。结果:20项研究纳入系统评价,其中6项纳入meta分析。在荟萃分析中,与安慰剂相比,MPH没有减少渴望(ES: -0.33, 95% CI: 1.69至1.03;Z= -0.473; P = 0.636)或可卡因使用(ES: -0.01, 95% CI: -0.35至0.33)(Z= -0.084; P = 0.933)。然而,给药途径和与CUD相关的ADHD的存在影响了可卡因渴望测量的结果。同样,尽管结果不确定,但在MPH治疗的ADHD患者中观察到可卡因消费量减少的趋势。在安全性方面,对于CUD≥90 mg/d的患者,可使用MPH,并严格要求监测心血管参数。结论:关于MPH治疗CUD疗效的证据仍然有限且不确定。然而,它在ADHD和CUD患者中使用可能是有道理的,因此,需要对这一特定类别进行进一步的临床研究。
{"title":"Methylphenidate for the Treatment of Cocaine Use Disorder: A Systematic Review and Meta-analysis.","authors":"Letizia Biso, Marianna Lebosi, Marco Bonaso, Marco Carli, Marco Scarselli","doi":"10.1097/ADM.0000000000001599","DOIUrl":"https://doi.org/10.1097/ADM.0000000000001599","url":null,"abstract":"<p><strong>Objectives: </strong>Cocaine use disorder (CUD) is a chronic condition, often associated with attention deficit hyperactivity disorder (ADHD). No medications have been approved for the treatment of CUD, but methylphenidate (MPH) has been explored as a potential candidate. We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of MPH in patients with CUD with and without ADHD.</p><p><strong>Methods: </strong>Following PRISMA guidelines, we developed a search string for PubMed, ISI Web of Science, and Scopus databases. We included randomized and nonrandomized clinical studies that used MPH in CUD treatment.</p><p><strong>Results: </strong>Twenty studies were included in the systematic review, 6 of them were included in the meta-analysis. In the meta-analysis, MPH did not reduce craving (ES: -0.33, 95% CI: 1.69 to 1.03; Z = -0.473; P = 0.636) or cocaine use (ES: -0.01, 95% CI: -0.35 to 0.33) (Z= -0.084; P = 0.933) compared with placebo. However, the route of administration and the presence of ADHD associated with CUD influenced the outcomes on cocaine craving measures. Similarly, although the results were inconclusive, a trend toward the reduction of cocaine consumption was observed in patients with ADHD treated with MPH. Regarding safety, MPH can be used in patients with CUD up to 90 mg/d and monitoring the cardiovascular parameters is strictly required.</p><p><strong>Conclusions: </strong>Evidence on the efficacy of MPH for the treatment of CUD is still limited and inconclusive. However, there might be a rationale for its use in patients with both CUD and ADHD, therefore, further clinical studies are needed in this particular category.</p>","PeriodicalId":14744,"journal":{"name":"Journal of Addiction Medicine","volume":" ","pages":""},"PeriodicalIF":3.2,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145354906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}