Running Head: SEDATIVE-HYPNOTICS and ADDICTION 1

Total Page:16

File Type:pdf, Size:1020Kb

Running Head: SEDATIVE-HYPNOTICS and ADDICTION 1 Running Head: SEDATIVE-HYPNOTICS AND ADDICTION 1 Sedative-Hypnotics and Addiction Michelle Reynolds John Carroll University SEDATIVE-HYPNOTICS AND ADDICTION 2 Abstract This study examined the history and effects sedative-hypnotics have, both physically and psychologically, as well as the effect on society. Sedative-hypnotics are one of the oldest classifications of drugs, and as such, one of the most commonly abused drugs. They depress the central nervous system, many times inducing a feeling of relaxation and pleasure. There are many reasons a person might become addicted to sedative-hypnotics, but the most common issue is medication (sometimes self-medication) for insomnia, anxiety, and/ or pain relief. Many sedative-hypnotic addicts are also addicted to other substances, usually opioids. Polydrug use is common with sedative-hypnotics, which is usually where the danger lies for users. Treatment for sedative-hypnotic addicts is a process of weaning the addict off the substance, in combination with intensive psychological counseling to reinforce healthy thoughts and behaviors. Due to the legality of many sedative-hypnotics, this large social issue will most likely continue to be a problem for many years to come. SEDATIVE-HYPNOTICS AND ADDICTION 3 History of sedative-hypnotics Sedative-hypnotics are one of the most commonly used and abused drugs in the United States today (Kane, 2013). In the broadest sense of the definition of sedative-hypnotics, this classification of drugs includes anything that depresses the central nervous system, including ethanol alcohol and marijuana. These drugs might be used to calm an anxious person, promote sleep, relieve pain, and even anesthetize for a medical procedure. However, when many of these drugs are used, fine and gross motor activities are affected and consciousness can become a struggle to maintain; in more severe cases with higher dosages, unconsciousness, paralysis, and even death can occur. Sedative-hypnotics can also severely affect an unborn fetus, causing birth defects and behavioral problems for the babies. The focus of this paper will be mainly on the sedative-hypnotic pills that are commonly illicitly used, including the two major categories of barbiturates and benzodiazepines; however, methaqualone, ethchlorvynol, chloral hydrate, and mebrobamate are also members of the sedative-hypnotic study. The brand names for the most common names of sedative-hypnotics include Seconal, Valium, Ativan, Nembutal, Quaaludes, and Xanax (Division of Alcohol and Drug Abuse, 1993). Methaqualone (brand names: Quaaludes, Sopors), originally prescribed to treat anxiety and to promote sleep, was “one of the most commonly abused drugs and [could] cause both physical and psychological dependence” (Division of Alcohol and Drug Abuse, 1993). There are also legal, over-the-counter types of sedative-hypnotics that are readily available to the general public (Kane, 2013). Antihistamines, decongestants, and sleep aids are SEDATIVE-HYPNOTICS AND ADDICTION 4 considered sedative-hypnotics because of the general drowsiness caused by many of the products. The use of sedative-hypnotics throughout history is long and for drugs like alcohol and marijuana, celebrated. Early societies used synthetic sedative-hypnotics, such as ethanol analogues, piperidinedione derivitives, and potassium bromide, which commonly caused bromism, a disease characterized by excessive sedation and delirium (National Institute on Drug Abuse, 2012). Barbiturates were also a popular method of pain and anxiety relief. Ciraulo & Knapp (2011) noted that “barbiturates have been clinically available since the 1900s and were widely the most prescribed agents for anxiety until the introduction of meprobamate in 1955 and, subsequently, the advent of benzodiazepines with chlordiazepoxide in 1957” (Ciraulo & Knapp, 2011). Benzodiazepines became the preferred sedative-hypnotic of choice for many people because the risk of overdose and toxic effects of barbiturates was so high. Today, sedative-hypnotics are used in many capacities, both legally and illegally. Some are used to treat anxiety and relieve pain. Others are used medically to prepare for surgery (Kane, 2013). Barbiturates seem to produce greater mood enhancement and self-administration than benzodiazepines, in recent studies. The toxic threshold, however, is so high for barbiturates that unacceptable side effects are commonly seen among barbiturates (Longo & Johnson, 2000). As with many substances that are intended to be medications, many sedative-hypnotics that are prescribed are used illicitly, which can cause addiction and adverse effects on the user (Longo & Johnson, 2000). SEDATIVE-HYPNOTICS AND ADDICTION 5 Effects on society Because of the legality of many sedative-hypnotics, they are very commonly abused and misused. A 1990 study for the American Psychiatric Association found that “11 to 15 percent of the adult population has taken a benzodiazepine one or more times during the preceding year” (Salzman, 1990). The Substance Abuse and Mental Health Services Administration also found that an estimated 2.6% of the U.S. population 12 years of age or older used tranquilizers or sedatives illicitly, compared with a total of 15.3% of the population who used any substance illegally” (SAMHSA, 2010). However, good news has been found, despite increased media reports of deaths due to sedative-hypnotics. SAMHSA also found that in 2010, of the 2.8% of the total U.S. population diagnosed with substance abuse or dependence, less than half a percent were diagnosed for drug use/abuse related to sedatives or tranquilizers (SAMHSA, 2010). Polydrug use is also common among users of benzodiazepines. Longo and Johnson (2000) found that “an estimated 80 percent of benzodiazepine abuse is part of polydrug use, most commonly with opioids… Studies indicate that 3 to 41 percent of alcoholic persons report that they abused benzodiazepines at some time, often to modulate intoxication or withdrawal effects” (Longo & Johnson, 2000). Sedative-hypnotics and benzodiazepine overdoses tend not to be fatal; however, when another drug is coingested with a sedative-hypnotic, the risk of death is increased exponentially. Combinations of sedative-hypnotics and opioids or alcohol commonly depress the respiratory system, leading to fatal effects (Ciraulo & Oldham, 2013). A major effect that sedative-hypnotics have had on society in general is facilitation of date rape. A study by the Canadian Sexual Assault Centre found that of the 1,400 women who reported that they were raped, almost 25% of them were facilitated through surreptitious drug SEDATIVE-HYPNOTICS AND ADDICTION 6 administration, usually benzodiazepines, such as flunitrazepam (Rohypnol) or gamma hydroxybutyrate acid (GHB) (Weir, 2001). However, alcohol and marijuana are also sedative- hypnotics and are commonly used to “lower sexual inhibition and enhance the possibility of unwanted sexual intercourse” (Weir, 2001). Rape treatment centers in the U.S. found that 69% of urine samples submitted by victims of suspected drug-facilitated rapes showed the presence of alcohol and marijuana was found in another 18% of samples, as compared to only 4% for GHB and flunitrazepam (Weir, 2001). Nevertheless, in today’s society, women are being strongly cautioned to watch their drinks and never leave their drinks unattended, to prevent unwanted drug administration. Physiological effects of sedative-hypnotics Sedative-hypnotics can cause both physical and psychological dependence. The Missouri Department of Mental Health notes “When regular users stop using large doses of these drugs suddenly, they may develop physical withdrawal symptoms ranging from restlessness, insomnia and anxiety, to convulsions and death. When users become psychologically dependent, they feel as if they need the drug to function. Finding and using the drug becomes the main focus in life” (Missouri Department of Mental Health, 1993). Geoff Kane notes that sedative-hypnotics work “by augmenting the effects of gamma- aminobutyric acid (GABA)… Boosting GABA both calms the brain and increases dopamine in the nucleus accumbens” (Kane, 2013). This reward of increased dopamine means that the user is more likely to have pleasurable effects from the drug and thus, repeat the experience. Studies show that sedative-hypnotics are addictive and long-term use of the medication can cause SEDATIVE-HYPNOTICS AND ADDICTION 7 tolerance levels to rise and withdrawal symptoms to occur if the user suddenly stops the medication (Kane, 2013; Scher, 2014). Babies born to mothers who abuse sedatives during pregnancy may be physically dependent on drugs and show symptoms of withdrawal after birth. Their symptoms “may include breathing problems, feeding difficulties, disturbed sleep, sweating, irritability, and fever” (UnityPoint Health). Benzodiazepines can also be found in a using mother’s breast milk, and so are usually inappropriate for breast-feeding mothers to use. It is also noted that newborns who have been exposed to sedative-hypnotics may demonstrate floppy baby syndrome and withdrawal symptoms. Using sedative-hypnotics during pregnancy also carry an increased risk of cleft lip and other malformations to the fetus (Ciraulo & Oldham, 2013). Sedative-hypnotics have a profound effect on the psychomotor skills of the user. Both quantitative and qualitative studies have found delayed reaction times among sedative-hypnotic users, especially the elderly, who generally have lower metabolisms and greater susceptibility to central nervous
Recommended publications
  • Benzodiazepine & Alcohol Co-Ingestion
    The Journal of COLLEGIATE EMERGENCY MEDICAL SERVICES ISSN: 2576-3687 (Print) 2576-3695 (Online) Journal Website: https://www.collegeems.com Benzodiazepine & Alcohol Co-Ingestion: Implications for Collegiate-Based Emergency Medical Services David Goroff & Alexander Farinelli Keywords: alcohol, benzodiazepines, collegiate-based emergency medical services, toxicology Citation (AMA Style): Goroff D, Farinelli A. Benzodiazepine and Alcohol Co-In- gestion. J Coll Emerg Med Serv. 2018; 1(2): 19-23. https://doi.org/10.30542/ JCEMS.2018.01.02.04 Electronic Link: https://doi.org/10.30542/JCEMS.2018.01.02.04 Published Online: August 8, 2018 Published in Print: August 13, 2018 (Volume 1: Issue 2) Copyright: © 2018 Goroff & Farinelli. This is an OPEN ACCESS article distributed under the terms of the Creative Commons Attribu- tion 4.0 International (CC BY 4.0) License, which permits unrestrict- ed use, distribution, and reproduction in any medium, provided the original author and source are credited. The full license is available at: https://creativecommons.org/licenses/by/4.0/ CLINICAL REVIEW Benzodiazepine & Alcohol Co-Ingestion: Implications for Collegiate-Based Emergency Medical Services David Goroff, MS, NRP & Alexander Farinelli, BS, NRP ABSTRACT KEYWORDS: alcohol, The co-ingestion of benzodiazepines and alcohol presents a unique challenge to colle- benzodiazepines, collegiate- giate EMS providers, due to the pharmacological interaction of the two substances and based emergency medical the variable patient presentations. Given the likelihood that collegiate EMS providers services, toxicology will be called to treat a patient who has co-ingested benzodiazepines and alcohol, this Corresponding Author and review discusses the relevant pharmacology, clinical presentation, and treatment of these Author Affiliations:Listed co-ingestion patients.
    [Show full text]
  • Acute Poisoning: Understanding 90% of Cases in a Nutshell S L Greene, P I Dargan, a L Jones
    204 REVIEW Postgrad Med J: first published as 10.1136/pgmj.2004.027813 on 5 April 2005. Downloaded from Acute poisoning: understanding 90% of cases in a nutshell S L Greene, P I Dargan, A L Jones ............................................................................................................................... Postgrad Med J 2005;81:204–216. doi: 10.1136/pgmj.2004.024794 The acutely poisoned patient remains a common problem Paracetamol remains the most common drug taken in overdose in the UK (50% of intentional facing doctors working in acute medicine in the United self poisoning presentations).19 Non-steroidal Kingdom and worldwide. This review examines the initial anti-inflammatory drugs (NSAIDs), benzodiaze- management of the acutely poisoned patient. Aspects of pines/zopiclone, aspirin, compound analgesics, drugs of misuse including opioids, tricyclic general management are reviewed including immediate antidepressants (TCAs), and selective serotonin interventions, investigations, gastrointestinal reuptake inhibitors (SSRIs) comprise most of the decontamination techniques, use of antidotes, methods to remaining 50% (box 1). Reductions in the price of drugs of misuse have led to increased cocaine, increase poison elimination, and psychological MDMA (ecstasy), and c-hydroxybutyrate (GHB) assessment. More common and serious poisonings caused toxicity related ED attendances.10 Clinicians by paracetamol, salicylates, opioids, tricyclic should also be aware that severe toxicity can result from exposure to non-licensed pharmaco-
    [Show full text]
  • Benzodiazepine (Benzo) Advisory
    BENZODIAZEPINE (BENZO) ADVISORY Drug checking within the Interior Health region continues to detect benzodiazepines (benzos) in multiple drug samples in several communities across the region. Benzodiazepines have been found in a variety of substances most often sold as “down”, heroin, or fentanyl. There has been a wide range of colours and textures identified. Risk: Benzodiazepines mixed with opioids carry a high risk of overdose and can cause prolonged sedation, sleepiness, muscle relaxation, slurred speech, loss of consciousness, black outs/memory loss. Overdose Response: Responding to overdoses involving BOTH Opioids and Benzos is more complex. Naloxone does not work on Benzos, BUT naloxone will work on the opioid overdose symptoms. After giving breaths and naloxone, the person may begin breathing normally, but may not wake up. More doses of naloxone should only be given if the person is not breathing normally (less than 10 breaths a minute). If the person is breathing normally but remains unconscious, place in recovery position and stay with them until emergency services arrive. Call to action: Reinforce overdose prevention messaging: don’t use alone, start small – go low and slow, use overdose prevention services. Talk to clients about getting their drugs tested for benzodiazepines. Benzo testing is currently available at the following the locations: o ASK Wellness: Kamloops – 778-257-1292 o Supervised Consumption Service: Kelowna o UBCO Harm Reduction Program: Kelowna, Penticton, Vernon 250-864-1431 o Vernon Overdose Prevention Site: 250-503-3737 o ANKORS: Cranbrook - 250-426-3383 o ANKORS: Nelson - 250-505-5506 o MHSU Overdose Prevention Nurses - Penticton - 250-462-1050 Ensure that service providers and peer responders are aware of how to recognize and respond to overdoses involving benzos.
    [Show full text]
  • Benzodiazepine Overdose
    BRITISH MEDICAL JOURNAL VOLUME 290 16 MARCH 1985 805 Br Med J (Clin Res Ed): first published as 10.1136/bmj.290.6471.805 on 16 March 1985. Downloaded from benzodiazepine dependent animals.'2 In man oral Ro 15- Benzodiazepine overdose: 1788 (200 mg) antagonises the effects of diazepam on are antagonists psychomotor performance without decreasing its bio- specific availability'3"' and reverses the benzodiazepine effects on useful? rapid eye movement sleep.'5 Given intravenously (10 mg) it immediately reverses the deep sedation induced by intravenous flunitrazepam (2 mg) and the impaired per- Benzodiazepines are remarkably non-toxic. Taken alone, formance caused by intravenous midazolam.'6 Ro 15-1788 is even large doses rarely produce serious effects. Self almost devoid of intrinsic effects in oral doses of 600 mg,'3 poisoners commonly take mixtures of drugs, however, and though it may depress stage 4 sleep.'5 Electroencephalo- benzodiazepines are included in 40% of drug overdoses in graphic frequency analysis and evoked potentials both show Britain.' Because of additive effects large doses of benzo- a stimulant effect after intravenous Ro 15-1788 (5 mg); diazepines taken with other depressants may aggravate or some people report mild anxiety and "pressure to move,"'7 precipitate respiratory failure, especially in the elderly or suggesting slight inverse agonist activity. patients with pulmonary disease; they may also add to A few clinical trials of Ro 15-1788 in benzodiazepine hypotension and occasionally lead to fatal hypothermia in overdose have been reported. In one open study nine myxoedema.2 patients (aged 22-74) in deep coma due to benzodiazepines A patient suspected of having taken benzodiazepines with responded within one to two minutes to intravenous Ro 15- other drugs producing coma may present diagnostic 1788 (2-5-10 mg).'8 They opened their eyes and responded difficulties.
    [Show full text]
  • Toxicology and Overdoses Objectives Facts
    7/12/2018 #FSHP2018 #FSHP2018 Objectives • Discuss common drugs in overdoses, both legal and illegal Toxicology and Overdoses • Recognize reversal agents • Discuss administration techniques for reversal By: Kathy Moorman agents • Discuss tentative treatments for overdoses #FSHP2018 Why do we do what we do Top 9 Causes of Overdoses • Opioids • Benzodiazepines • Ethyl Alcohol • Amphetamines • Marijuana • Antihistamines • Acetaminophen • Pesticides • Anticonvulsants #FSHP2018 #FSHP2018 Facts • More than 30% of opioid overdoses also involve benzodiazepines • Every day over 115 Americans die of overdoses • Individuals who are prescribed both benzodiazepines and opioids are 10X more likely to die of an overdose. • Both opioids and benzodiazepines now have black box warnings issued by the FDA recommending they not be prescribed together. National Institute of Drug Abuse rev 3/18 #FSHP2018 #FSHP2018 1 7/12/2018 OPIOID Toxicity • Opioids include: HYDROmorphone, MORphine, What do you use to reverse opioids? meperidine, fentanyl, oxycontin and others • Answer: Naloxone • Symptoms of overdose include drowsiness, slow breathing, pinpoint pupils, cyanosis (blueish skin due to poor circulation), loss of consciousness, and death. • Due to their addictive potential and easy accessibility opioid addiction is a growing problem. • Antidote for an acute opioid overdose in the emergency room is Narcan(naloxone), which is an opioid antagonist. #FSHP2018 #FSHP2018 Naloxone (Narcan®) Benzodiazepines • Comes as a 2mg/2ml syringe or 1mg/ml vial • Can be administered
    [Show full text]
  • Benzodiazepines and Opioids
    CLINICAL BULLETIN: BENZODIAZEPINES AND OPIOIDS June 8, 2021 Visit www.bccsu.ca/opioid-use-disorder for the latest version IN THIS BULLETIN • Benzodiazepines Detected in Street Drugs • Symptoms of Benzodiazepine Overdose • How to Respond to an Opioid Overdose Involving Benzodiazepines • Management of Benzodiazepine-Opioid Withdrawal • Implications for Substance Use Disorder Treatment • Harm Reduction and Education • Additional Resources ɤ BC’s drug checking services have seen a rapid increase in benzodiazepine-positive street opioids ɤ In January 2021, benzodiazepines were detected in more than 20% of street opioid samples tested in Vancouver ɤ Vancouver Island Drug Checking Project found benzodiazepines and etizolam in 59% of expected opioid samples collected in March 2021 ɤ Benzodiazepines were detected in nearly 50% of suspected overdose deaths in January 2021, which is more than three times higher than the data reported only six months prior (16%) ɤ Opioid-benzodiazepine overdoses result in atypical and protracted overdose events that can be challenging to reverse This bulletin highlights the risks associated with the emergence of benzodiazepine-adulterated drugs in the street opioid supply and provides guidance for the care of individuals who have been exposed to benzodiazepines through the use of adulterated opioids. The scope of this bulletin is limited to individuals who have been exposed to benzodiazepines through the street opioid supply; care considerations for individuals who are prescribed benzodiazepines and those who meet the criteria for benzodiazepine use disorder is outside the scope of this document.a a Considerations for individuals prescribed benzodiazepines and those with benzodiazepine use disorder will be provided in a forthcoming document.
    [Show full text]
  • Acute Fatal Posthypoxic Leukoencephalopathy Following Benzodiazepine Overdose: a Case Report and Review of the Literature Salman Aljarallah and Fawaz Al-Hussain*
    Aljarallah and Al-Hussain BMC Neurology (2015) 15:69 DOI 10.1186/s12883-015-0320-6 CASE REPORT Open Access Acute fatal posthypoxic leukoencephalopathy following benzodiazepine overdose: a case report and review of the literature Salman Aljarallah and Fawaz Al-Hussain* Abstract Background: Among the rare neurological complications of substances of abuse is the selective cerebral white matter injury (leukoencephalopathy). Of which, the syndrome of delayed post hypoxic encephalopathy (DPHL) that follows an acute drug overdose, in addition to “chasing the dragon” toxicity which results from chronic heroin vapor inhalation remain the most commonly described syndromes of toxic leukoencephalopathy. These syndromes are reported in association with opioid use. There are very few cases in the literature that described leukoencephalopathy following benzodiazepines, especially with an acute and progressive course. In this paper, we present a patient who developed an acute severe fatal leukoencephalopathy following hypoxic coma and systemic shock induced by benzodiazepine overdose. Case presentation: A 19-year-old male was found comatose at home and brought to hospital in a deep coma, shock, hypoxia, and acidosis. Brain magnetic resonant imaging (MRI) revealed a strikingly selective white matter injury early in the course of the disease. The patient remained in a comatose state with no signs of neurologic recovery until he died few weeks later following an increase in the brain edema and herniation. Conclusion: Toxic leukoencephalopathy can occur acutely following an overdose of benzodiazepine and respiratory failure. This is unlike the usual cases of toxic leukoencephalopathy where there is a period of lucidity between the overdose and the development of white matter disease.
    [Show full text]
  • XANAX (Alprazolam) Tablets, for Oral Use, CIV Ritonavir
    HIGHLIGHTS OF PRESCRIBING INFORMATION When tapering, decrease dosage by no more than 0.5 mg every 3 days. These highlights do not include all the information needed to use XANAX Some patients may require an even slower dosage reduction. (2.3, 5.2) safely and effectively. See full prescribing information for XANAX. See the Full Prescribing Information for the recommended dosage in geriatric patients, patients with hepatic impairment, and with use with XANAX (alprazolam) tablets, for oral use, CIV ritonavir. (2.4, 2.5, 2.6) Initial U.S. Approval: 1981 --------------------- DOSAGE FORMS AND STRENGTHS --------------------- Tablets: 0.25 mg, 0.5 mg, 1 mg, and 2 mg (3) WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS; ABUSE, MISUSE, AND ADDICTION; and ------------------------------ CONTRAINDICATIONS ------------------------------ DEPENDENCE AND WITHDRAWAL REACTIONS Known hypersensitivity to alprazolam or other benzodiazepines. (4) See full prescribing information for complete boxed warning. Concomitant use with strong cytochrome P450 3A (CYP3A) inhibitors, except ritonavir. (4, 5.5, 7.1) Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death. ----------------------- WARNINGS AND PRECAUTIONS ----------------------- Reserve concomitant prescribing for use in patients for whom Effects on Driving and Operating Machinery: Patients receiving XANAX alternative treatment options are inadequate. Limit dosages and should be cautioned against operating machinery or driving a motor durations to the minimum required. Follow patients for signs and vehicle, as well as avoiding concomitant use of alcohol and other central symptoms of respiratory depression and sedation. (5.1, 7.1) nervous system (CNS) depressant drugs. (5.4) The use of benzodiazepines, including XANAX, exposes users to Neonatal Sedation and Withdrawal Syndrome (NOWS): Use of XANAX risks of abuse, misuse, and addiction, which can lead to overdose or during pregnancy can result in neonatal sedation and neonatal withdrawal death.
    [Show full text]
  • Evidence-Based Practices in Drug and Alcohol Treatment and Recovery
    Evidence-based Practices in Drug and Alcohol Treatment and Recovery June 2016 Contents Introduction 2 Principles and goals of substance abuse treatment 4 Evaluation and determination of therapeutic service need 5 Withdrawal management services—management of acute intoxication and withdrawal 8 Alcohol 8 Benzodiazepines 9 Opioids 9 Medication-assisted therapies 9 Stimulants (cocaine and amphetamine) 10 Cannabis withdrawal 10 Hallucinogens (LSD, mescaline, psilocybin, and related drugs) 10 Phencyclidine (PCP) 11 Volatile substances (inhalants) 11 Club drugs 11 Designer drugs 11 Anabolic-androgenic steroids (AAS) 12 Interventions—substance abuse treatment and recovery 13 Psychosocial treatments 13 Somatic treatments (Psychopharmacotherapy) 14 Medication-assisted treatment (MAT) 15 Levels of care 18 Conclusion 19 References 20 ©2016 Magellan Health, Inc—Evidence-based Practices in Drug and Alcohol Treatment and Recovery 1 Introduction The use of illicit drugs, e g , marijuana, cocaine, physiological symptoms indicating that the heroin, hallucinogens, inhalants, and nonmedical individual continues using the substance despite use of prescription-type psychotherapeutic drugs, substance-related problems” (DSM-5, 2013) SUDs and alcohol is both a significant public health occur when recurrent use of the substance results problem and a challenge in the U S A national in a pathological pattern of related behaviors, e g , report, Behavioral Health Trends in the United impaired control and social impairment The 2014 States: Results from the 2014 National
    [Show full text]
  • Common Antidotes Used in the ICU
    SURIYAWUT SURIYA/SHUTTERSTOCK SURIYAWUT Common antidotes used in the ICU By Carrie L. Griffiths, PharmD, BCCCP, FCCM; Arzu Patel, BS; and Kristie A. Hertel, MSN, RN, CCRN, ACNP-BC Abstract: When ingested, some common household products can be poisonous, and, when taken improperly, both prescription and over- the-counter medications can result in overdoses. This article describes several common toxicities encountered in the ICU and their respec- tive antidotes. Keywords: acetaminophen, antidote, benzodiazepine, beta-blocker, calcium channel blocker, digoxin, digoxin immune fab, flumazenil, fomepizole, hyperinsulinemia-euglycemia therapy (HIET), naloxone, N-acetylcysteine, opioids, toxic alcohols www.nursingcriticalcare.com July l Nursing2020CriticalCare l 9 Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved. Common antidotes used in the ICU According to the 2018 National for overdose include advanced sites. That is, digoxin immune Poison Data System Annual age, metabolic disorders, and fab binds to digoxin, removing it Report, there were 2,099,751 drug interactions.4 Medications from its tissue binding sites, and human exposures to substances such as verapamil, atorvastatin, the bound drug is then pushed ranging from household cleaning omeprazole, potassium-depleting into the extracellular fluid. As products to prescription medica- diuretics, alprazolam, erythromy- a result, it is unable to exert its tions.1 In the critical care setting, cin, and tetracycline may lead to effect on its target tissues, revers- patients present with a variety of increased serum concentrations ing adverse events associated conditions, including intentional of digoxin.6,7 with overdose.7 or unintentional poisonings or Mechanism of toxicity. Adverse reactions. There have overdoses. Antidotes are used to Digoxin’s mechanism of action been reported allergic reactions counteract the toxicity of poisons.
    [Show full text]
  • Use of Flumazenil in the Treatment of Drug Overdose
    Critical Care Medicine Issue: Volume 24(2), February 1996, pp 199-206 Copyright: © Williams & Wilkins 1996. All Rights Reserved. Publication Type: [Clinical Investigation] ISSN: 0090-3493 Accession: 00003246-199602000-00004 [Clinical Investigation] Use of flumazenil in the treatment of drug overdose: A double-blind and open clinical study in 110 patients Weinbroum, Avi MD; Rudick, Valeri MD; Sorkine, Patrick MD; Nevo, Ygal MD; Halpern, Pinchas MD; Geller, Eran MD; Niv, David MD Author Information From the Departments of Anesthesiology and Critical Care Medicine (Drs. Weinbroum, Rudick, Sorkine, Nevo, and Niv), and Emergency Room (Dr. Halpern), Tel-Aviv- Elias Sourasky Medical Center and the Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, and the Surgical Intensive Care Unit (Dr. Geller), Palo Alto Veterans Administration Medical Center and the Stanford University School of Medicine, Palo Alto, CA. This study was supported, in part, by institutional departmental funds. Address requests for reprints to: Avi Weinbroum, MD, Department of Anesthesiology and Critical Care Medicine, Tel-Aviv-Elias Sourasky Medical Center, 6 Weizman Street, Tel-Aviv 64239, Israel. Abstract Objectives: To assess the efficacy, usefulness, safety, and dosages of flumazenil required when flumazenil is used in the diagnosis of benzodiazepine-induced coma (vs. other drug-induced coma), and to reverse or prevent the recurrence of unconsciousness. Design: A two-phase study: a controlled, randomized, doubleblind study followed by a prospective, open study. Setting: An 800-bed, teaching, university-affiliated hospital. Patients: Unconscious patients (n equals 110) suspected of benzodiazepine overdose, graded 2 to 4 on the Matthew and Lawson coma scale, were treated with flumazenil, the specific benzodiazepine receptor antagonist.
    [Show full text]
  • Sedative Hypnotics Leon Gussow and Andrea Carlson
    CHAPTER 165 Sedative Hypnotics Leon Gussow and Andrea Carlson BARBITURATES three times therapeutic, the neurogenic, chemical, and hypoxic Perspective respiratory drives are progressively suppressed. Because airway reflexes are not inhibited until general anesthesia is achieved, Barbiturates are discussed in do-it-yourself suicide manuals and laryngospasm can occur at low doses. were implicated in the high-profile deaths of Marilyn Monroe, Therapeutic oral doses of barbiturates produce only mild Jimi Hendrix, Abbie Hoffman, and Margaux Hemingway as well decreases in pulse and blood pressure, similar to sleep. With toxic as in the mass suicide of 39 members of the Heaven’s Gate cult in doses, more significant hypotension occurs from direct depression 1997. Although barbiturates are still useful for seizure disorders, of the myocardium along with pooling of blood in a dilated they rarely are prescribed as sedatives, with the availability of safer venous system. Peripheral vascular resistance is usually normal or alternatives, such as benzodiazepines. Mortality from barbiturate increased, but barbiturates interfere with autonomic reflexes, poisoning declined from approximately 1500 deaths per year in which then do not adequately compensate for the myocardial the 1950s to only two fatalities in 2009.1 depression and decreased venous return. Barbiturates can precipi- Barbiturates are addictive, producing physical dependence and tate severe hypotension in patients whose compensatory reflexes a withdrawal syndrome that can be life-threatening. Whereas tol- are already maximally stimulated, such as those with heart failure erance to the mood-altering effects of barbiturates develops or hypovolemic shock. Barbiturates also decrease cerebral blood rapidly with repeated use, tolerance to the lethal effects develops flow and intracerebral pressure.
    [Show full text]