A Pilot Study of Memantine Effects on Protracted Withdrawal (Syndrome of Anhedonia) in Heroin Addicts

2002 ◽  
Vol 1 (4) ◽  
pp. 143-146 ◽  
Author(s):  
E. M. Krupitsky ◽  
D. V. Masalov ◽  
A. M. Burakov ◽  
T. Y. Didenko ◽  
T. N. Romanova ◽  
...  
2002 ◽  
Vol 12 ◽  
pp. 400
Author(s):  
E. Krupitsky ◽  
D. Masalov ◽  
A. Burakov ◽  
T. Romanova ◽  
T. Didenko ◽  
...  

2021 ◽  
Author(s):  
Mary Beth Sutter ◽  
Hannah Watson ◽  
Nicole Yonke ◽  
Sherry Weitzen ◽  
Lawrence Leeman

Abstract Background Neonatal Opioid Withdrawal Syndrome (NOWS) is a significant public health issue and while millions of neonates are affected each year, an optimal pharmacologic weaning protocol has yet to be demonstrated. In this study, we compare hospital length of stay (LOS) and length of treatment (LOT) for treatment of neonatal opioid withdrawal (NOWS) with morphine versus methadone. Methods This was a single-site, open-label, randomized controlled pilot study conducted from October 2016-June 2018. Infants were eligible if their primary in-utero drug exposure was heroin, oral opioids, or methadone and they were born at greater than or equal to 34 weeks gestation. Infants were excluded for serious medical comorbidities and primary in-utero exposure to buprenorphine. Results 61 infants were enrolled; 30 were randomized to methadone treatment, and 31 to morphine treatment. Overall 46% of infants required treatment for NOWS. LOS and LOT for infants treated with morphine was 17.9 days and 14.7 days respectively, compared to 16.1 days and 12.8 days for babies treated with methadone (p=0.5, p=0.54). Infants treated with morphine received lower total morphine equivalents than those treated with methadone (9.7 vs. 33, p<0.01). Three treated infants in the methadone group required transfer to the Neonatal Intensive Care Unit, versus no infants in the morphine group. Conclusions Infants treated with morphine versus methadone had no significant differences in LOS or LOT in this pilot study. Infants treated with methadone received up to 3 times the opioid based on morphine equivalents as infants treated with morphine and had more transfers to the NICU for over sedation. Clinical Trial Registration: Morphine Versus Methadone for Opiate Exposed Infants With Neonatal Abstinence Syndrome NCT02851303, initated 01/08/2016 https://clinicaltrials.gov/ct2/show/NCT02851303.


2002 ◽  
Vol 30 (6) ◽  
pp. 561-565 ◽  
Author(s):  
Giovanni B. Moneta ◽  
Oi-Chu Wong

The authors examined how heroin addicts' affect varies in relation to perceived levels of challenges and skills in daily activities. Fourteen male residents of a therapeutic community completed 21 end-of-day diaries measuring affect. Unexpectedly, addicts had comparable positive affect to, and less negative affect, than a nonclinical student sample. Positive affect correlated with the imbalance of challenges and skills. Heroin addicts deviate from the flow model of healthy functioning as they optimize affect in states of either overcontrol or lack of control.


2020 ◽  
Vol 1 (3) ◽  
pp. 124-135
Author(s):  
Elisha M. Wachman ◽  
Alice Wang ◽  
Breanna C. Isley ◽  
Jeffery Boateng ◽  
Jacob A. Beierle ◽  
...  

Aims: Epigenetic variation of DNA methylation of the mu-opioid receptor gene (OPRM1) has been identified in the blood and saliva of individuals with opioid use disorder (OUD) and infants with neonatal opioid withdrawal syndrome (NOWS). It is unknown whether epigenetic variation in OPRM1 exists within placental tissue in women with OUD and whether it is associated with NOWS outcomes. In this pilot study, we aimed to 1) examine the association between placental OPRM1 DNA methylation levels and NOWS outcomes, and 2) compare OPRM1 methylation levels in opioid-exposed versus non-exposed control placentas. Methods: Placental tissue was collected from eligible opioid (n = 64) and control (n = 29) women after delivery. Placental DNA was isolated and methylation levels at six cytosine-phosphate-guanine (CpG) sites within the OPRM1 promoter were quantified. Methylation levels were evaluated for associations with infant NOWS outcome measures: need for pharmacologic treatment, length of hospital stay (LOS), morphine treatment days, and treatment with two medications. Regression models were created and adjusted for clinical co-variates. Methylation levels between opioid and controls placentas were also compared. Results: The primary opioid exposures were methadone and buprenorphine. Forty-nine (76.6%) of the opioid-exposed infants required pharmacologic treatment, 10 (15.6%) two medications, and average LOS for all opioid-exposed infants was 16.5 (standard deviation 9.7) days. There were no significant associations between OPRM1 DNA methylation levels in the six CpG sites and any NOWS outcome measures. No significant differences were found in methylation levels between the opioid and control samples. Conclusions: No significant associations were found between OPRM1 placental DNA methylation levels and NOWS severity in this pilot cohort. In addition, no significant differences were seen in OPRM1 methylation in opioid versus control placentas. Future association studies examining methylation levels on a genome-wide level are warranted.


Pain Medicine ◽  
2015 ◽  
Vol 16 (5) ◽  
pp. 839-848 ◽  
Author(s):  
Da Ma ◽  
Ji-Sheng Han ◽  
Quan-Heng Diao ◽  
Gui-Fa Deng ◽  
Xing-Jie Ping ◽  
...  

2012 ◽  
Vol 263 (3) ◽  
pp. 197-203 ◽  
Author(s):  
Ulrich Frischknecht ◽  
Derik Hermann ◽  
Milena Heinrich ◽  
Mareen Hoerst ◽  
Wolfgang Weber-Fahr ◽  
...  

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