Fife Guidelines for Benzodiazepine Prescribing in Benzodiazepine Dependence

Total Page:16

File Type:pdf, Size:1020Kb

Fife Guidelines for Benzodiazepine Prescribing in Benzodiazepine Dependence NHS Fife Guidelines for Benzodiazepine Prescribing in Benzodiazepine Dependence Dr. A. Baldacchino, Liz. Hutchings, Addiction Services Issued: April 2013 Review Date: April 2016 1 Approved by NHS Fife ADTC on behalf of NHS Fife Date June 2013 Contents Flowchart for Benzodiazepine Withdrawal ……………………………………………………………3 Establishing type of dependence. ...........................................................................................4 Assessment of Benzodiazepine Dependence..............................................................................5 Management of dependence in therapeutic dose users............................................................6 Management of dependence in prescribed high dose users. ...................................................7 Management of dependence in illicit and recreational users. ..................................................8 Psychological support. .................................................................................................................9 Pharmacological support............................................................................................................10 Appendices Appendix 1 Example Patient Letter (regular user).................................................11 Appendix 2 Information leaflets and advice from the internet................................13 Appendix 3 DRUG DIARY.....................................................................................14 Appendix 4 Benzodiazepine conversion table.......................................................15 Appendix 5 Withdrawal regimes for therapeutic dose users..................................16 Appendix 6 Withdrawal regimes for high dose users ............................................18 Appendix 7 Self-help guides for psychological support.........................................20 Dr. A. Baldacchino, Liz. Hutchings, Addiction Services Issued: April 2013 Review Date: April 2016 2 Approved by NHS Fife ADTC on behalf of NHS Fife Date June 2013 Flowchart for Benzodiazepine Withdrawal Patient taking benzodiazepine Assess. Establish dependence and pattern of usage Prescribed therapeutic dose Prescribed high dose Recreational high dose and dependence dependence abuse Monitor benzodiazepine use for Complete drug diary for at 2 3 months & complete at least least weeks two drug screens. Establish boundaries, set goals Is patient topping up Is minimum intervention prescription with illicitly obtained appropriate? Patient ready to reduce usage? benzodiazepine? Yes No No Yes Yes No Advise self-reduction of illicitly Continue to support reduction obtained benzodiazepine to Letter and FAQs using motivational interviewing. prescribed or therapeutic level. Do not Brief intervention Consider referral to prescribe doses of diazepam to Self-help booklet DAPL/FIRST/Psychology compensate for illicitly obtained drugs Agree gradual dose reduction converting to diazepam with twice daily Yes Patient reduced use to 30-40mg No dosing if appropriate. equivalent diazepam? Prescribe 2mg or 5mg diazepam only Reduce daily dose by about 1/8th (range 1/10th to ¼) every 2 or 3 weeks Withdrawal Symptoms? No Yes Maintain at present dose until symptoms improve-avoid increasing the dosage again Continue reduction at agreed Address any underlying mental rate health problems offering psychological or pharmacological support Renegotiate rate of reduction if required STOP COMPLETELY (Time needed can vary from 4 weeks to a year or more) Dr. A. Baldacchino, Liz. Hutchings, Addiction Services Issued: April 2013 Review Date: April 2016 3 Approved by NHS Fife ADTC on behalf of NHS Fife Date June 2013 Following the introduction of benzodiazepines in the 1960s as the treatment of choice for anxiety and insomniaFife Guidelines and their widespread for Benzodiazepine use from the Prescribing1970s onwards in it Benzodiazepinehas been recognised Dependence that long term use can result in physical and psychological dependence as well as tolerance to their use. In addition to patients prescribed benzodiazepines the illicit use, particularly by opioid drug users is a major problem for users in and out of drug treatment. High doses of prescribed and illicit benzodiazepines are taken and users become extremely tolerant to the sedative effects. Benzodiazepine withdrawal syndrome is characterised by insomnia, anxiety, loss of appetite and body- weight, tremor, perspiration, tinnitus, and perceptual disturbances. Abrupt withdrawal may produce confusion, toxic psychosis, convulsions, or a condition resembling delirium tremens. For this reason patients exhibiting dependence should undergo gradual withdrawal of the benzodiazepine. Establishing type of dependence. Patients may exhibit dependency on a therapeutic dose or non-therapeutic dose – the latter group being subdivided into “prescribed high dose dependence” and “recreational high dose abuse and dependence” groups. Therapeutic Dose Prescribed High Dose Illicit and Recreational Use Dependence Dependence (eg ≥30mg diazepam) Dependence Characteristics of Therapeutic Dose Dependence – Patient may have: • taken benzodiazepines in prescribed low doses for months or years. • gradually come to “need” benzodiazepines in order to carry out normal activities of daily living. • continued to take their medication even though original indication has disappeared. • experienced withdrawal symptoms when they try to reduce or stop the drugs. • contacted the prescriber frequently to request repeat prescriptions. • experienced anxiety if there is a delay to the next prescription. • increased the dosage since the original prescription • experienced anxiety symptoms, panics, agoraphobia, insomnia, depression and increasing physical symptoms despite continuing to take benzodiazepines. Characteristics of Prescribed High Dose Dependence – patient requiring ever larger doses may: • try to persuade doctor to escalate doses and/or number of tablets on the prescription. • present at hospital or register at further practices to obtain more tablets • combine benzodiazepine misuse with excessive alcohol consumption or other sedative drugs • be highly anxious, depressed or have personality disorder • tend not to use illicit drugs, but may obtain benzodiazepines from relatives or acquaintances. Characteristics of Recreational High Dose Abuse & Dependence – • Often develops as polydrug abusers attempt to enhance the effect of opioids or to “come down” from stimulants. • A very high tolerance develops making it difficult to detect the actual scale of drug consumption. • Users may be taking well in excess of 100mg daily in a single dose to maximise the effect. • There may be a concurrent alcohol problem and the user may have been introduced to benzodiazepines during previous alcohol detoxification Dr. A. Baldacchino, Liz. Hutchings, Addiction Services Issued: April 2013 Review Date: April 2016 4 Approved by NHS Fife ADTC on behalf of NHS Fife Date June 2013 Assessment of Benzodiazepine Dependence 1. Establish PATTERN of benzodiazepine usage 2. Establish DEPENDENCE if 3 or more or the following are present in the same 12-month period: Date of onset of usage ……………………………… 3 to 5 indicators – mild to moderate dependence Benzodiazepines used ………………………………. 5 to 7 indicators – moderate to severe dependence i) Tolerance – a need for increased amounts to achieve desired effect OR Average daily dose and dose intervals …………….. - diminished effect with continued use of same amount Previous successful withdrawal from use? ………… ii) Withdrawal – previous attempts to cut down result in withdrawal symptoms OR - substance is taken to prevent withdrawal symptoms If yes, longest period of abstinence? ……………… iii) Substance taken in larger amounts or over longer period than originally intended Any other drug or alcohol used?.............................. iv) Persistent desire or unsuccessful effort to cut down or control use v) Great deal of time spent obtaining substance or recovering from its effects vi) Important activities (social, work related or recreational) given up or reduced vii) Continued use of drug despite clear evidence of harmful effects 4. Establish CATEGORY of dependence: DSM-IV Diagnostic Criteria for Substance Dependence Therapeutic Dose Dependence Started for a reason and continued 3. Additional considerations (to inform but not prevent detox): High Dose Dependence Concomitant severe medical or psychiatric illness Started as a prescription and then escalated No other drug or alcohol problems History of severe withdrawal (including PROVEN history of seizures) Recreational High Dose Abuse & Dependence Completion of drug diary (for at least 2 weeks, up to 3 months may be appropriate) Used and abused by people who use drugs: illicit, POM or OTC and/or alcohol Confirmation of dependence by drug screening (urine but consider oral fluid) See page 4 for more detail Level of motivation to change Dr. A. Baldacchino, Liz. Hutchings, Addiction Services Issued: April 2013 Review Date: April 2016 5 Approved by NHS Fife ADTC on behalf of NHS Fife Date June 2013 Management of dependence in therapeutic dose users Management can include minimal interventions, gradual dose reduction and gradual dose reduction with additional psychological support. Minimal interventions (1 and 2 below) are suitable in early/mild dependence. 1. Write to the patient: explain problems associated with long-term benzodiazepine use and the need to reduce their prescription encouraging a gradual reduction or cessation if possible. (appx 1) 2. Brief Intervention:
Recommended publications
  • Methylphenidate Hydrochloride
    Application for Inclusion to the 22nd Expert Committee on the Selection and Use of Essential Medicines: METHYLPHENIDATE HYDROCHLORIDE December 7, 2018 Submitted by: Patricia Moscibrodzki, M.P.H., and Craig L. Katz, M.D. The Icahn School of Medicine at Mount Sinai Graduate Program in Public Health New York NY, United States Contact: [email protected] TABLE OF CONTENTS Page 3 Summary Statement Page 4 Focal Point Person in WHO Page 5 Name of Organizations Consulted Page 6 International Nonproprietary Name Page 7 Formulations Proposed for Inclusion Page 8 International Availability Page 10 Listing Requested Page 11 Public Health Relevance Page 13 Treatment Details Page 19 Comparative Effectiveness Page 29 Comparative Safety Page 41 Comparative Cost and Cost-Effectiveness Page 45 Regulatory Status Page 48 Pharmacoepial Standards Page 49 Text for the WHO Model Formulary Page 52 References Page 61 Appendix – Letters of Support 2 1. Summary Statement of the Proposal for Inclusion of Methylphenidate Methylphenidate (MPH), a central nervous system (CNS) stimulant, of the phenethylamine class, is proposed for inclusion in the WHO Model List of Essential Medications (EML) & the Model List of Essential Medications for Children (EMLc) for treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) under ICD-11, 6C9Z mental, behavioral or neurodevelopmental disorder, disruptive behavior or dissocial disorders. To date, the list of essential medications does not include stimulants, which play a critical role in the treatment of psychotic disorders. Methylphenidate is proposed for inclusion on the complimentary list for both children and adults. This application provides a systematic review of the use, efficacy, safety, availability, and cost-effectiveness of methylphenidate compared with other stimulant (first-line) and non-stimulant (second-line) medications.
    [Show full text]
  • Drug & Alcohol Testing Program
    Pottawattmie County Drug & Alcohol Testing Program Appendix A Table of Contents POLICY STATEMENT ...................................................................................................................................... 3 SCOPE ............................................................................................................................................................ 4 EDUCATION AND TRAINING .......................................................................................................................... 4 DESIGNATED EMPLOYER REPRESENTATIVE (DER): ....................................................................................... 5 DUTY TO COOPERATE ................................................................................................................................... 5 EMPLOYEE ADMISSION OF ALCOHOL AND CONTROLLED SUBSTANCE USE: (49 CFR Part 382.121) ... 6 PROHIBITED DRUGS AND ILLEGALLY USED CONTROLLED SUBSTANCES: ..................................................... 7 PROHIBITED BEHAVIOR AND CONDUCT: ...................................................................................................... 8 DRUG & ALCOHOL TESTING REQUIREMENTS (49 CFR, Part 40 & 382) ............................................... 10 DRUG & ALCOHOL TESTING CIRCUMSTANCES (49 CFR Part 40 & 382) .............................................. 12 A. Pre-Employment Testing: .................................................................................................... 12 B. Reasonable Suspicion Testing: .........................................................................................
    [Show full text]
  • Guidelines for the Forensic Analysis of Drugs Facilitating Sexual Assault and Other Criminal Acts
    Vienna International Centre, PO Box 500, 1400 Vienna, Austria Tel.: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org Guidelines for the Forensic analysis of drugs facilitating sexual assault and other criminal acts United Nations publication Printed in Austria ST/NAR/45 *1186331*V.11-86331—December 2011 —300 Photo credits: UNODC Photo Library, iStock.com/Abel Mitja Varela Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Guidelines for the forensic analysis of drugs facilitating sexual assault and other criminal acts UNITED NATIONS New York, 2011 ST/NAR/45 © United Nations, December 2011. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. List of abbreviations . v Acknowledgements .......................................... vii 1. Introduction............................................. 1 1.1. Background ........................................ 1 1.2. Purpose and scope of the manual ...................... 2 2. Investigative and analytical challenges ....................... 5 3 Evidence collection ...................................... 9 3.1. Evidence collection kits .............................. 9 3.2. Sample transfer and storage........................... 10 3.3. Biological samples and sampling ...................... 11 3.4. Other samples ...................................... 12 4. Analytical considerations .................................. 13 4.1. Substances encountered in DFSA and other DFC cases .... 13 4.2. Procedures and analytical strategy...................... 14 4.3. Analytical methodology .............................. 15 4.4.
    [Show full text]
  • Substance Abuse and Dependence
    9 Substance Abuse and Dependence CHAPTER CHAPTER OUTLINE CLASSIFICATION OF SUBSTANCE-RELATED THEORETICAL PERSPECTIVES 310–316 Residential Approaches DISORDERS 291–296 Biological Perspectives Psychodynamic Approaches Substance Abuse and Dependence Learning Perspectives Behavioral Approaches Addiction and Other Forms of Compulsive Cognitive Perspectives Relapse-Prevention Training Behavior Psychodynamic Perspectives SUMMING UP 325–326 Racial and Ethnic Differences in Substance Sociocultural Perspectives Use Disorders TREATMENT OF SUBSTANCE ABUSE Pathways to Drug Dependence AND DEPENDENCE 316–325 DRUGS OF ABUSE 296–310 Biological Approaches Depressants Culturally Sensitive Treatment Stimulants of Alcoholism Hallucinogens Nonprofessional Support Groups TRUTH or FICTION T❑ F❑ Heroin accounts for more deaths “Nothing and Nobody Comes Before than any other drug. (p. 291) T❑ F❑ You cannot be psychologically My Coke” dependent on a drug without also being She had just caught me with cocaine again after I had managed to convince her that physically dependent on it. (p. 295) I hadn’t used in over a month. Of course I had been tooting (snorting) almost every T❑ F❑ More teenagers and young adults die day, but I had managed to cover my tracks a little better than usual. So she said to from alcohol-related motor vehicle accidents me that I was going to have to make a choice—either cocaine or her. Before she than from any other cause. (p. 297) finished the sentence, I knew what was coming, so I told her to think carefully about what she was going to say. It was clear to me that there wasn’t a choice. I love my T❑ F❑ It is safe to let someone who has wife, but I’m not going to choose anything over cocaine.
    [Show full text]
  • Withdrawing Benzodiazepines in Primary Care
    PC\/ICU/ ADTiriC • CNS Drugs 2009,-23(1): 19-34 KtVltW MKIIWLC 1172-7047/I»/O(X)1«119/S4W5/C1 © 2009 Adis Dato Intocmation BV. All rights reserved. Withdrawing Benzodiazepines in Primary Care Malcolm Luder} Andre Tylee^ and ]ohn Donoghue^ 1 Institute of Psychiatry, King's College London, London, England 2 John Moores University, Liverpool, Scotland Contents Abstract ' 19 1. Benzodiazepine Usage 22 2. Interventions 23 2.1 Simple interventions 23 2.2 Piiarmacoiogicai interventions 25 2.3 Psychoiogical Interventions 26 2.4 Meta-Anaiysis ot Various interventions 27 3. Outcomes 28 4. Practicai Issues 29 5. Otiier Medications 30 5.1 Antidepressants 30 5.2 Symptomatic Treatments 30 6. Conciusions 31 Abstract The use of benzodiazepine anxiolytics and hypnotics continues to excite controversy. Views differ from expert to expert and from country to country as to the extent of the problem, or even whether long-term benzodiazepine use actually constitutes a problem. The adverse effects of these drugs have been extensively documented and their effectiveness is being increasingly questioned. Discontinua- tion is usually beneficial as it is followed by improved psychomotor and cognitive functioning, particularly in the elderly. The potential for dependence and addic- tion have also become more apparent. The licensing of SSRIs for anxiety disorders has widened the prescdbers' therapeutic choices (although this group of medications also have their own adverse effects). Melatonin agonists show promise in some forms of insomnia. Accordingly, it is now even more imperative that long-term benzodiazepine users be reviewed with respect to possible discon- tinuation. Strategies for discontinuation start with primary-care practitioners, who are still the main prescdbers.
    [Show full text]
  • XANAX® Alprazolam Tablets, USP
    XANAX® alprazolam tablets, USP CIV WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death [see Warnings, Drug Interactions]. Reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. Limit dosages and durations to the minimum required. Follow patients for signs and symptoms of respiratory depression and sedation. DESCRIPTION XANAX Tablets contain alprazolam which is a triazolo analog of the 1,4 benzodiazepine class of central nervous system-active compounds. The chemical name of alprazolam is 8-Chloro-1-methyl-6-phenyl-4H-s-triazolo [4,3-α] [1,4] benzodiazepine. The structural formula is represented to the right: Alprazolam is a white crystalline powder, which is soluble in methanol or ethanol but which has no appreciable solubility in water at physiological pH. Each XANAX Tablet, for oral administration, contains 0.25, 0.5, 1 or 2 mg of alprazolam. XANAX Tablets, 2 mg, are multi-scored and may be divided as shown below: 1 Reference ID: 4029640 Inactive ingredients: Cellulose, corn starch, docusate sodium, lactose, magnesium stearate, silicon dioxide and sodium benzoate. In addition, the 0.5 mg tablet contains FD&C Yellow No. 6 and the 1 mg tablet contains FD&C Blue No. 2. CLINICAL PHARMACOLOGY Pharmacodynamics CNS agents of the 1,4 benzodiazepine class presumably exert their effects by binding at stereo specific receptors at several sites within the central nervous system. Their exact mechanism of action is unknown. Clinically, all benzodiazepines cause a dose-related central nervous system depressant activity varying from mild impairment of task performance to hypnosis.
    [Show full text]
  • 124.210 Schedule IV — Substances Included. 1
    1 CONTROLLED SUBSTANCES, §124.210 124.210 Schedule IV — substances included. 1. Schedule IV shall consist of the drugs and other substances, by whatever official name, common or usual name, chemical name, or brand name designated, listed in this section. 2. Narcotic drugs. Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation containing any of the following narcotic drugs, or their salts calculated as the free anhydrous base or alkaloid, in limited quantities as set forth below: a. Not more than one milligram of difenoxin and not less than twenty-five micrograms of atropine sulfate per dosage unit. b. Dextropropoxyphene (alpha-(+)-4-dimethylamino-1,2-diphenyl-3-methyl-2- propionoxybutane). c. 2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol, its salts, optical and geometric isomers and salts of these isomers (including tramadol). 3. Depressants. Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation which contains any quantity of the following substances, including its salts, isomers, and salts of isomers whenever the existence of such salts, isomers, and salts of isomers is possible within the specific chemical designation: a. Alprazolam. b. Barbital. c. Bromazepam. d. Camazepam. e. Carisoprodol. f. Chloral betaine. g. Chloral hydrate. h. Chlordiazepoxide. i. Clobazam. j. Clonazepam. k. Clorazepate. l. Clotiazepam. m. Cloxazolam. n. Delorazepam. o. Diazepam. p. Dichloralphenazone. q. Estazolam. r. Ethchlorvynol. s. Ethinamate. t. Ethyl Loflazepate. u. Fludiazepam. v. Flunitrazepam. w. Flurazepam. x. Halazepam. y. Haloxazolam. z. Ketazolam. aa. Loprazolam. ab. Lorazepam. ac. Lormetazepam. ad. Mebutamate. ae. Medazepam. af. Meprobamate. ag. Methohexital. ah. Methylphenobarbital (mephobarbital).
    [Show full text]
  • S1 Table. List of Medications Analyzed in Present Study Drug
    S1 Table. List of medications analyzed in present study Drug class Drugs Propofol, ketamine, etomidate, Barbiturate (1) (thiopental) Benzodiazepines (28) (midazolam, lorazepam, clonazepam, diazepam, chlordiazepoxide, oxazepam, potassium Sedatives clorazepate, bromazepam, clobazam, alprazolam, pinazepam, (32 drugs) nordazepam, fludiazepam, ethyl loflazepate, etizolam, clotiazepam, tofisopam, flurazepam, flunitrazepam, estazolam, triazolam, lormetazepam, temazepam, brotizolam, quazepam, loprazolam, zopiclone, zolpidem) Fentanyl, alfentanil, sufentanil, remifentanil, morphine, Opioid analgesics hydromorphone, nicomorphine, oxycodone, tramadol, (10 drugs) pethidine Acetaminophen, Non-steroidal anti-inflammatory drugs (36) (celecoxib, polmacoxib, etoricoxib, nimesulide, aceclofenac, acemetacin, amfenac, cinnoxicam, dexibuprofen, diclofenac, emorfazone, Non-opioid analgesics etodolac, fenoprofen, flufenamic acid, flurbiprofen, ibuprofen, (44 drugs) ketoprofen, ketorolac, lornoxicam, loxoprofen, mefenamiate, meloxicam, nabumetone, naproxen, oxaprozin, piroxicam, pranoprofen, proglumetacin, sulindac, talniflumate, tenoxicam, tiaprofenic acid, zaltoprofen, morniflumate, pelubiprofen, indomethacin), Anticonvulsants (7) (gabapentin, pregabalin, lamotrigine, levetiracetam, carbamazepine, valproic acid, lacosamide) Vecuronium, rocuronium bromide, cisatracurium, atracurium, Neuromuscular hexafluronium, pipecuronium bromide, doxacurium chloride, blocking agents fazadinium bromide, mivacurium chloride, (12 drugs) pancuronium, gallamine, succinylcholine
    [Show full text]
  • Calculating Equivalent Doses of Oral Benzodiazepines
    Calculating equivalent doses of oral benzodiazepines Background Benzodiazepines are the most commonly used anxiolytics and hypnotics (1). There are major differences in potency between different benzodiazepines and this difference in potency is important when switching from one benzodiazepine to another (2). Benzodiazepines also differ markedly in the speed in which they are metabolised and eliminated. With repeated daily dosing accumulation occurs and high concentrations can build up in the body (mainly in fatty tissues) (2). The degree of sedation that they induce also varies, making it difficult to determine exact equivalents (3). Answer Advice on benzodiazepine conversion NB: Before using Table 1, read the notes below and the Limitations statement at the end of this document. Switching benzodiazepines may be advantageous for a variety of reasons, e.g. to a drug with a different half-life pre-discontinuation (4) or in the event of non-availability of a specific benzodiazepine. With relatively short-acting benzodiazepines such as alprazolam and lorazepam, it is not possible to achieve a smooth decline in blood and tissue concentrations during benzodiazepine withdrawal. These drugs are eliminated fairly rapidly with the result that concentrations fluctuate with peaks and troughs between each dose. It is necessary to take the tablets several times a day and many people experience a "mini-withdrawal", sometimes a craving, between each dose. For people withdrawing from these potent, short-acting drugs it has been advised that they switch to an equivalent dose of a benzodiazepine with a long half life such as diazepam (5). Diazepam is available as 2mg tablets which can be halved to give 1mg doses.
    [Show full text]
  • Prescription Medications: Misuse, Abuse, Dependence, and Addiction
    Substance Abuse Treatment May 2006 Volume 5 Issue 2 ADVISORYNews for the Treatment Field Prescription Medications: Misuse, Abuse, Dependence, and Addiction How serious are prescription Older adults are particularly vulnerable to misuse and medication use problems? abuse of prescription medications. Persons ages 65 and older make up only 13 percent of the population but Development and increased availability of prescription account for one-third of all medications prescribed,3 drugs have significantly improved treatment of pain, and many of these prescriptions are for psychoactive mental disorders, anxiety, and other conditions. Millions medications with high abuse and addiction liability.4 of Americans use prescription medications safely and Data from the National Survey on Drug Use and Health responsibly. However, increased availability and vari- indicate that nonmedical use of prescription medications ety of medications with psychoactive effects (see Table was the second most common form of substance abuse 1) have contributed to prescription misuse, abuse, among adults older than 55.5 dependence, and addiction. In 2004,1 the number of Americans reporting abuse2 of prescription medications Use of prescription medications in ways other than was higher than the combined total of those reporting prescribed can have a variety of adverse health conse- abuse of cocaine, hallucinogens, inhalants, and heroin. quences, including overdose, toxic reactions, and serious More than 14.5 million persons reported having used drug interactions leading to life-threatening conditions, prescription medications nonmedically within the past such as respiratory depression, hypertension or hypoten- year. Of this 14.5 million, more than 2 million were sion, seizures, cardiovascular collapse, and death.6 between ages 12 and 17.
    [Show full text]
  • Benzodiazepines Factsheet
    Benzodiazepines This factsheet gives information about benzodiazepine medication. This medication is sometimes used to treat anxiety. Your doctor may prescribe this medication if your anxiety has become severe or if you are very distressed. Benzodiazepines are a type of medication that are used to treat anxiety. You may get side effects from taking this kind of medication. If you get side effects that you are worried about, you should see your doctor. You can become addicted to benzodiazepines. Therefore, you should not take them for longer than one month. You may get withdrawal symptoms when you stop taking benzodiazepines. You should talk to your doctor before you stop taking them. Your doctor may gradually take you off your medication if you have been taking them for a long time. This factsheet covers: 1. What are benzodiazepines? 2. Are there different types of benzodiazepines? 3. Are there any side effects? 4. What if I want to I stop taking benzodiazepines? 5. Do benzodiazepines affect other medication? 6. Does alcohol affect my benzodiazepines? 7. Can I drive when taking benzodiazepines? 8. What else should I consider before taking benzodiazepines? 1 1. What are benzodiazepines? Your doctor may offer you benzodiazepines if you have symptoms of anxiety which are causing you a lot of distress or if you are having difficulty sleeping. Benzodiazepines are a type of sedative and are mostly used as short-term treatment. They work by making the calming chemicals released by your body more powerful. You should not take benzodiazepines for longer than one month. If you take them for longer, you can become tolerant to them (meaning you need more to have the same effect), and you may also become dependent (addicted) to them.
    [Show full text]
  • An Overview of Outpatient and Inpatient Detoxification
    An Overview of Outpatient and Inpatient Detoxification Motoi Hayashida, M.D., Sc.D. lcohol detoxification can be defined as a period facility, where they reside for the duration of of medical treatment, usually including counsel- treatment, which may range from 5 to 14 days. A ing, during which a person is helped to overcome The process of detoxification in either setting initially physical and psychological dependence on alcohol (Chang involves the assessment and treatment of acute with- and Kosten 1997). The immediate objectives of alcohol drawal symptoms, which may range from mild (e.g., detoxification are to help the patient achieve a substance- tremor and insomnia) to severe (e.g., autonomic free state, relieve the immediate symptoms of withdrawal, hyperactivity, seizures, and delirium) (Swift 1997). and treat any comorbid medical or psychiatric conditions. Medications often are provided to help reduce a patient’s These objectives help prepare the patient for entry into withdrawal symptoms. Benzodiazepines (e.g., diazepam long-term treatment or rehabilitation, the ultimate goal of detoxification (Swift 1997). The objectives of long- and chlordiazepoxide) are the most commonly used term treatment or rehabilitation include the long-term drugs for this purpose, and their efficacy is well estab- maintenance of the alcohol-free state and the incor- lished (Swift 1997). Benzodiazepines not only reduce poration of psychological, family, and social interven- alcohol withdrawal symptoms but also prevent alcohol tions to help ensure its persistence (Swift 1997). withdrawal seizures, which occur in an estimated 1 to Alcohol detoxification can be completed safely and 4 percent of withdrawal patients (Schuckit 1995).
    [Show full text]