A Meta-Analysis of Smoking Cessation Interventions with Individuals in Substance Abuse Treatment Or Recovery
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Smoking Cessation Treatment at Substance Abuse Rehabilitation Programs
SMOKING CEssATION TREATMENT AT SUBSTANCE ABUSE REHABILITATION PROGRAMS Malcolm S. Reid, PhD, New York University School of Medicine, Department of Psychiatry; Jeff Sel- zer, MD, North Shore Long Island Jewish Healthcare System; John Rotrosen, MD, New York University School of Medicine, Department of Psychiatry Cigarette smoking is common among persons with drug and alcohol n Nicotine is a highly use disorders, with prevalence rates of 80-90% among patients in sub- addictive substance stance use disorder treatment programs. Such concurrent smoking may that meets all of produce adverse behavioral and medical problems, and is associated the criteria for drug with greater levels of substance use disorder. dependence. CBehavioral studies indicate that the act of cigarette smoking serves as a cue for drug and alcohol craving, and the active ingredient of cigarettes, nicotine, serves as a primer for drug and alcohol abuse (Sees and Clarke, 1993; Reid et al., 1998). More critically, longitudinal studies have found tobacco use to be the number one cause of preventable death in the United States, and also the single highest contributor to mortality in patients treated for alcoholism (Hurt et al., 1996). Nicotine is a highly addictive substance that meets all of the criteria for drug dependence, and cigarette smoking is an especially effective method for the delivery of nicotine, producing peak brain levels within 15-20 seconds. This rapid drug delivery is one of a number of common properties that cigarette smok- ing shares with hazardous drug and alcohol use, such as the ability to activate the dopamine system in the reward circuitry of the brain. -
Exploring Matrix Effects on Binding Properties and Characterization of Cotinine Molecularly Imprinted Polymer on Paper-Based Scaffold
Article Exploring Matrix Effects on Binding Properties and Characterization of Cotinine Molecularly Imprinted Polymer on Paper-Based Scaffold Nutcha Larpant 1, Yaneenart Suwanwong 2, Somchai Boonpangrak 3 and Wanida Laiwattanapaisal 4,5,* 1 Graduate Program in Clinical Biochemistry and Molecular Medicine, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok 10330, Thailand; [email protected] 2 Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok 10330, Thailand; [email protected] 3 Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakhon Pathom 73170, Thailand; [email protected] 4 Department of Clinical Chemistry, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok 10330, Thailand 5 Electrochemistry and Optical Spectroscopy Center of Excellence, Chulalongkorn University, Bangkok 10330, Thailand * Correspondence: [email protected] Received: 22 January 2019; Accepted: 20 March 2019; Published: 26 March 2019 Abstract: Commercially available sorbent materials for solid-phase extraction are widely used in analytical laboratories. However, non-selective binding is a major obstacle for sample analysis. To overcome this problem, molecularly imprinted polymers (MIPs) were used as selective adsorbent materials prior to determining target analysts. In this study, the use of non-covalent molecularly imprinted polymers (MIPs) for cotinine adsorption on a paper-based scaffold was studied. Fiberglass paper was used as a paper scaffold for cotinine-selective MIP adsorption with the use of 0.5% agarose gel. The effects of salt, pH, sample matrix, and solvent on the cotinine adsorption and extraction process were investigated. Under optimal conditions, the adsorption isotherm of synthesized MIPs increased to 125.41 µg/g, whereas the maximum adsorption isotherm of non-imprinted polymers (NIPs) was stable at 42.86 µg/g. -
Substance Abuse: the Pharmacy Educator’S Role in Prevention and Recovery
Substance Abuse: The Pharmacy Educator’s Role in Prevention and Recovery Curricular Guidelines for Pharmacy: Substance Abuse and Addictive Disease i Curricular Guidelines for Pharmacy: Substance Abuse and Addictive Disease1,2 BACKGROUND OF THE CURRICULUM DEVELOPMENT PROJECT In 1988, the AACP Special Interest Group (SIG) on Pharmacy Student and Faculty Impairment (renamed Substance Abuse Education and Assistance) undertook the development of curricular guidelines for colleges/schools of pharmacy to facilitate the growth of educational opportunities for student pharmacists. These Curricular Guidelines for Pharmacy Education: Substance Abuse and Addictive Disease were published in 1991 (AJPE. 55:311-16. Winter 1991.) One of the charges of the Special Committee on Substance Abuse and Pharmacy Education was to review and revise the 1991 curricular guidelines. Overall, the didactic and experiential components in the suggested curriculum should prepare the student pharmacist to competently problem-solve issues concerning alcohol and other drug abuse and addictive diseases affecting patients, families, colleagues, themselves, and society. The guidelines provide ten educational goals, while describing four major content areas including: psychosocial aspects of alcohol and other drug use; pharmacology and toxicology of abused substances; identification, intervention, and treatment of people with addictive diseases; and legal/ethical issues. The required curriculum suggested by these guidelines addresses the 1 These guidelines were revised by the AACP Special Committee on Substance Abuse and Pharmacy Education. Members drafting the revised guidelines were Edward M. DeSimone (Creighton University), Julie C. Kissack (Harding University), David M. Scott (North Dakota State University), and Brandon J. Patterson (University of Iowa). Other Committee members were Paul W. Jungnickel, Chair (Auburn University), Lisa A. -
Barriers and Solutions to Addressing Tobacco Dependence in Addiction Treatment Programs
Barriers and Solutions to Addressing Tobacco Dependence in Addiction Treatment Programs Douglas M. Ziedonis, M.D., M.P.H.; Joseph Guydish, Ph.D., M.P.H.; Jill Williams, M.D.; Marc Steinberg, Ph.D.; and Jonathan Foulds, Ph.D. Despite the high prevalence of tobacco use among people with substance use disorders, tobacco dependence is often overlooked in addiction treatment programs. Several studies and a meta-analytic review have concluded that patients who receive tobacco dependence treatment during addiction treatment have better overall substance abuse treatment outcomes compared with those who do not. Barriers that contribute to the lack of attention given to this important problem include staff attitudes about and use of tobacco, lack of adequate staff training to address tobacco use, unfounded fears among treatment staff and administration regarding tobacco policies, and limited tobacco dependence treatment resources. Specific clinical-, program-, and system-level changes are recommended to fully address the problem of tobacco use among alcohol and other drug abuse patients. KEY WORDS: Alcohol and tobacco; alcohol, tobacco, and other drug (ATOD) use, abuse, dependence; addiction care; tobacco dependence; smoking; secondhand smoke; nicotine; nicotine replacement; tobacco dependence screening; tobacco dependence treatment; treatment facility-based prevention; co-treatment; treatment issues; treatment barriers; treatment provider characteristics; treatment staff; staff training; AODD counselor; client counselor interaction; smoking cessation; Tobacco Dependence Program at the University of Medicine and Dentistry of New Jersey obacco dependence is one of to the other. The common genetic vul stance use was considered a potential the most common substance use nerability may be located on chromo trigger for the primary addiction. -
NINDS Custom Collection II
ACACETIN ACEBUTOLOL HYDROCHLORIDE ACECLIDINE HYDROCHLORIDE ACEMETACIN ACETAMINOPHEN ACETAMINOSALOL ACETANILIDE ACETARSOL ACETAZOLAMIDE ACETOHYDROXAMIC ACID ACETRIAZOIC ACID ACETYL TYROSINE ETHYL ESTER ACETYLCARNITINE ACETYLCHOLINE ACETYLCYSTEINE ACETYLGLUCOSAMINE ACETYLGLUTAMIC ACID ACETYL-L-LEUCINE ACETYLPHENYLALANINE ACETYLSEROTONIN ACETYLTRYPTOPHAN ACEXAMIC ACID ACIVICIN ACLACINOMYCIN A1 ACONITINE ACRIFLAVINIUM HYDROCHLORIDE ACRISORCIN ACTINONIN ACYCLOVIR ADENOSINE PHOSPHATE ADENOSINE ADRENALINE BITARTRATE AESCULIN AJMALINE AKLAVINE HYDROCHLORIDE ALANYL-dl-LEUCINE ALANYL-dl-PHENYLALANINE ALAPROCLATE ALBENDAZOLE ALBUTEROL ALEXIDINE HYDROCHLORIDE ALLANTOIN ALLOPURINOL ALMOTRIPTAN ALOIN ALPRENOLOL ALTRETAMINE ALVERINE CITRATE AMANTADINE HYDROCHLORIDE AMBROXOL HYDROCHLORIDE AMCINONIDE AMIKACIN SULFATE AMILORIDE HYDROCHLORIDE 3-AMINOBENZAMIDE gamma-AMINOBUTYRIC ACID AMINOCAPROIC ACID N- (2-AMINOETHYL)-4-CHLOROBENZAMIDE (RO-16-6491) AMINOGLUTETHIMIDE AMINOHIPPURIC ACID AMINOHYDROXYBUTYRIC ACID AMINOLEVULINIC ACID HYDROCHLORIDE AMINOPHENAZONE 3-AMINOPROPANESULPHONIC ACID AMINOPYRIDINE 9-AMINO-1,2,3,4-TETRAHYDROACRIDINE HYDROCHLORIDE AMINOTHIAZOLE AMIODARONE HYDROCHLORIDE AMIPRILOSE AMITRIPTYLINE HYDROCHLORIDE AMLODIPINE BESYLATE AMODIAQUINE DIHYDROCHLORIDE AMOXEPINE AMOXICILLIN AMPICILLIN SODIUM AMPROLIUM AMRINONE AMYGDALIN ANABASAMINE HYDROCHLORIDE ANABASINE HYDROCHLORIDE ANCITABINE HYDROCHLORIDE ANDROSTERONE SODIUM SULFATE ANIRACETAM ANISINDIONE ANISODAMINE ANISOMYCIN ANTAZOLINE PHOSPHATE ANTHRALIN ANTIMYCIN A (A1 shown) ANTIPYRINE APHYLLIC -
Vol. 1, Issue 1
Methamphetamine Topical Brief Series: Vol. 1, Issue 1 What is countries involved in World War II provided amphetamine to soldiers Methamphetamine? for performance enhancement and the drug was used by “actors, artists, Methamphetamine is an addictive, athletes, politicians, and the public stimulant drug that affects the alike.”5 central nervous system. It is typically used in powder or pill form and can By the 1960s, media coverage be ingested orally, snorted, smoked, began drawing simplistic, negative or injected. Methamphetamine is connections between amphetamine known as meth, blue, ice, speed, and and crime, and government officials 1 crystal among other names. The term discussed public safety and drugs amphetamine has been used broadly as a social concern.6 Over-the- to refer to a group of chemicals that counter amphetamines were have similar, stimulating properties available until 1959,7 and by 1970 and methamphetamine is included in all amphetamines were added to 2 this group. According to the National the controlled substances list as Institute on Drug Abuse (NIDA), Schedule II drugs. Schedule II drugs “Methamphetamine differs from required a new prescription with amphetamine in that, at comparable each fill and strict documentation doses, much greater amounts of the by doctors and pharmacists.8 drug get into the brain, making it a The reduction in a legal supply 3 more potent stimulant.” of amphetamine led to increased black-market production and sale From the 1930s to the 1960s, of various types of amphetamine U.S. pharmaceutical -
Effect of Varenicline Combined with Medical Management on Alcohol Use Disorder with Comorbid Cigarette Smoking
Table of Contents I. Summary of Changes to the Statistical Plan …………………. 2. II. Summary of Changes to the Protocol………………………… 2. III. Original Protocol at Trial Initiation ………………………… 5. 1 Downloaded From: https://jamanetwork.com/ on 09/28/2021 I. Summary of changes to the statistical analysis plan The original statistical analysis plan is described in the original protocol below beginning on page 20. In the original statistical analysis plan the stratification factor sex was omitted unintentionally from the primary model specification for the main outcome (percent heavy drinking days, PHDD) although sex was identified as a potential moderator in an exploratory aim. At the analysis stage, we included both stratification factors (site and sex) and their interactions with treatment in the model for PHDD consistent with prior hypothesis that men and women differ in their smoking and drinking behavior and treatment response, and with good statistical practice. Baseline percent heavy drinking days was specified as a covariate in the original analysis plan but in response to comments by the statistical reviewer was dropped as a covariate and included in the final mixed model analyses reported in the paper. In order to make the baseline and end-point measures comparable, baseline percent heavy drinking days and end-point percent heavy drinking days were both summarized over 8 week periods. This 8-week duration was pre-planned for the end-point measure but modified from the original intention to use 30 days of the baseline period. Unstructured variance-covariance matrix was used for the errors since variances at baseline and end-point were different. -
OPRM1 Genetic Polymorphisms Are Associated with the Plasma Nicotine Metabolite Cotinine Concentration in Methadone Maintenance Patients: a Cross Sectional Study
Journal of Human Genetics (2013) 58, 84–90 & 2013 The Japan Society of Human Genetics All rights reserved 1434-5161/13 www.nature.com/jhg ORIGINAL ARTICLE OPRM1 genetic polymorphisms are associated with the plasma nicotine metabolite cotinine concentration in methadone maintenance patients: a cross sectional study Yu-Ting Chen1, Hsiao-Hui Tsou2, Hsiang-Wei Kuo1, Chiu-Ping Fang1, Sheng-Chang Wang1, Ing-Kang Ho1,3,4, Yao-Sheng Chang1, Chia-Hui Chen1, Chin-Fu Hsiao2, Hsiao-Yu Wu2, Keh-Ming Lin1, Andrew CH Chen5, Jyy-Jih Tsai-Wu6 and Yu-Li Liu1,7,8 Majority of the heroin-dependent patients smoke cigarettes. Although it has been reported that the OPRM1 genetic polymorphism is associated with the brain mu-opioid receptor binding potential in cigarette smokers, there is no direct evidence showing the impact of plasma cotinine, a nicotine metabolite, on treatment responses to methadone maintenance treatment (MMT). In this study, we aimed to test the hypothesis that the genetic polymorphisms in the OPRM1 are associated with the methadone treatment responses and the severity of cigarette smoking directly measured by the plasma concentration of cotinine in a Taiwanese MMT cohort. Fifteen OPRM1 single-nucleotide polymorphisms (SNPs) were selected and genotyped on DNA samples of 366 MMT patients. Plasma concentrations of cotinine were measured by cotinine enzyme-linked immunosorbent assay. The plasma cotinine concentration had positive correlation with concentrations of methadone (P ¼ 0.042) and its metabolite 2-ethylidene-1,5-dimethyl-3,3-diphenyl-pyrrolidine (P ¼ 0.037). Methadone treatment non-responders, defined by a positive urine morphine test, had a higher plasma concentration of cotinine (P ¼ 0.005), but a lower plasma concentration-to- dose ratio of both R- and S-methadone (P ¼ 0.001 and 0.012, respectively) than the responders. -
Drug Use and Gender
Drug Use and Gender Tammy L. Anderson, Ph.D. University of lllinois, Chicago, lL GENDER DIFFERENCES IN study-report a greater occurrence ofillicit substance use DRUG USE AND ABUSE among males than among females. Both surveys have consistently documented this pattern over the years. Looking at the world through a "gender lens" began According to the 1997 NHSDA survey, men reported a in most areas of social science during the second wave of higher rate of illicit substance use (any illicit drug) than the women's movement, or the late 1960s through the women, 8.5 percent to 4.5 percent, nearly double. Men 1970s. During this time feminist researchers began report higher rates of cocaine use .9 percent versus .5 questioning science's conclusions by pointing to percent. alcohol use (58 percent versus 45 percent), binge male-oriented biases in research questions, hypotheses, drinking (23 percent versus 8 percent), and heavy drinking and designs. (8.7 percent versus 2.1 percent). The same pattern was Unfortunately, the "gender lens" did not appear in observed in marijuana use (Office of Applied Studies substance use research until the early 1980s. Prior to the [OAS] tee7). 1970s, most studies of alcohol and other drug use were Johnston. O'Malley, and Bachman (1997) the conducted among males. Early studies that included at University of Michigan yearly women suffered from the "add women and stir compile data on the substance use of 8th. 10th, and 12th graders, college students, approach." Females were added to samples, but no and young adults in the MTF study. -
Nicotine Metabolism and CYP2D6 Phenotype in Smokers
Vol. 10, 261–263, March 2001 Cancer Epidemiology, Biomarkers & Prevention 261 Short Communication Nicotine Metabolism and CYP2D6 Phenotype in Smokers Neil E. Caporaso,1 Caryn Lerman, Janet Audrain, CYP2D6 (debrisoquine hydroxylase) has been studied as a Neil R. Boyd, David Main, Haleem J. Issaq, putative lung cancer susceptibility factor, and it has been pro- Bill Utermahlan, Roni T. Falk, and Peter Shields posed that this enzyme may contribute to the metabolism of Division of Cancer Epidemiology and Genetics, National Cancer Institute, nicotine, thereby influencing the amount a person smokes and Bethesda, Maryland 20892 [N. E. C., R. T. F.]; Lombardi Cancer Research the delivery of carcinogens. Some in vitro (1) and population Center, Georgetown University, Washington, D.C. 20007 [C. L., J. A., (2) studies have suggested a role for CYP2D6 in nicotine N. R. B., D. M.]; Laboratory of Chemical Synthesis and Analysis, Frederick metabolism, although recent work indicates CYP2A6 is the Cancer Research Center, Frederick, Maryland 21701 [H. J. I., B. U.]; and Laboratory of Human Carcinogenesis, Division of Cancer Etiology, NIH, most important P-450 in nicotine metabolism (3, 4). The National Cancer Institute, Bethesda, Maryland 20892 [P. S.] CYP2D6 MP2 is determined by administering DM (5) and determining the ratio of urinary metabolites. A low ratio of unchanged drug:metabolite identifies extensive metabolizers, Abstract whereas PMs exhibit a high ratio. The hypothesis that a poly- We tested the hypothesis that the polymorphic enzyme morphic gene influences nicotine disposition is important be- CYP2D6 is related to nicotine metabolism in 261 healthy cause addicted smokers engage in smoking behavior in such a subjects enrolling in a smoking cessation clinic. -
Escreen Panel Descriptions
eScreen Panel Descriptions Service Description eScreen-9Panel-1205 Cocaine 300/150 Amphetamines 1000/500 Barbiturates 300/300 Ben- zodiazepines 300/300 Marijuana 50/15 Opiates 2000/2000 Phencycli- dine (PCP) 25/25 Propoxyphene 300/300 Methadone 300/300 eScreen-1065 Tramadol standalone test eScreen-10Panel-1204 Amphetamines 1000/500 Cocaine 300/150 Marijuana 50/15 Opiate 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Propoxyphene 300/300 Methadone 300/300 Methaqualone 300/300 pH/nitrites eScreen-10Panel-3125-Other Amphetamines 500/250 Cocaine 150/100 Marijuana 50/15 Opiate 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Methadone 300/300 Oxycodone 100/100 Ecstasy 1000/250 eScreen-1208 Amphetamines 1000/500 Cocaine 300/150 Marijuana 50/15 Opiates 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Propoxyphene 300/300 Methadone 300/300 Methaqualone 300/300 Urine ethanol 0.04 g%/0.04 g% eScreen-1224 Amphetamines 1000/500 Cocaine 300/150 Marijuana 50/15 Opiates 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Propoxyphene 300/300 Methadone 300/300 Methaqualone 300/300 Cotinine 500/500 pH/nitrites eScreen-1232 Amphetamines 1000/500 Cocaine 300/150 Marijuana 50/15 Opiate 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Propoxyphene 300/300 Methadone 300/300 Methaqualone 300/300 Oxycodone 100/100 Meperidine 100/100 eScreen-1309 Amphetamines 500/250 Cocaine 150/100 Marijuana 50/15 Opiate 2000/2000 PCP 25/25 Barbiturate 300/300 Benzodiazepine 300/300 Propoxyphene 300/300 Methadone -
Chronic Smokeless Tobacco Consumption Contributes to the Development of Renal Diseases in the Human Male Volunteers
Journal of Analytical & Pharmaceutical Research Research Article Open Access Chronic smokeless tobacco consumption contributes to the development of renal diseases in the human male volunteers Abstract Volume 7 Issue 6 - 2018 Smokeless tobacco may able to induce microalbuminuria. The present study S Fareeda Begum,1 G Nagajothi,2 K investigates the relation between nicotine and cotinine with renal function in gutkha Swarnalatha,1 C Suresh Kumar,1 Narendra and khaini users. Methods: The levels of nicotine and cotinine were estimated by HPLC 1 methods and other urine variables were detected by spectrophotometric methods. Maddu 1 Current smokeless tobacco users have shown that significantly elevated levels of Department of Biochemistry, Sri Krishnadevaraya University, India nicotine, cotinine, and epinephrine excretion in the urine than non-tobacco users. 2Department of Corporate Secretaryship, Queen Mary’s Renal function was assessed by glomerular filtration rate (GFR), levels of urea, and College (Autonomous), India creatinine. Among the kidney function measures that we examined, microalbuminuria, decreased glomerular filtration rate, and creatinine clearance were found associated Correspondence: Narendra Maddu, Assistant Professor, with gutkha and khaini users. Significantly decreased proteinuria, urea and increased Department of Biochemistry, Sri Krishnadevaraya University, levels of uric acid and creatinine excretion with the concomitant increase in plasma Ananthapuramu-515003, Andhra Pradesh, India, Tel 91+ total proteins, urea, and decreased uric acid levels were observed in the group I and 9441983797, Email group II users compared to group III users. The products of smokeless tobacco are regarded as good predictors of assessing the free radical levels in the cells. The active Received: June 01, 2018 | Published: November 26, 2018 markers of nitroxidative stress have been elevated progressively with the uptake of nicotine and exposure.