Opioid Management

Total Page:16

File Type:pdf, Size:1020Kb

Load more

Just the facts on Opioid Management Opioid Classifications Prudent Prescription Practice Using Evidence-Based Medicine (EBM) Pure-agonists Partial agonists- Mixed agonists- Central acting Opioid Misuse/Abuse antagonists antagonists analgesics Think twice about the risk of misuse versus Took from Dealer, friend/family stranger, Natural or synthetic Stimulate analgesic Limited use in chronic Emerging class of medical necessity with each script: 5% or other agents that don’t have a opioid receptors with pain because of ceiling synthetic opioids that Almost 90% of prescription painkiller misuse 12% ceiling for analgesic little effect on toxicity, effect for analgesia inhibit reuptake of and abuse comes from drugs prescribed legally efficacy or antagonize lower abuse potential which does not increase serotonin and to users or their friends and family. Most of the effects of other opioids but added side effects with dose escalation norepinephrine prescriptions come from primary care and Bought from friend/family 11% internal medicine doctors, not specialists. Obtained free from friend/family 55% Healthcare provider accountability: Precribed by Short-Acting Long-Acting The Centers for Disease Control has urged doctor 17% “Normal-release” or “immediate-release”, often used “Controlled-release”, “extended-release”, or States to ensure providers follow evidence- for intermittent or breakthrough pain and combined “sustained-release”, highly potent and can stabilize based treatment guidelines for the safe and with other analgesics like acetaminophen or aspirin. medication levels for round-the-clock analgesia. effective use of prescription painkillers. Duration of action is 3-4 hours. Increased risk of hypogonadism. EBM Takeaways from Official Disability Guidelines (ODG) Acute Pain Subacute Pain Routine long-term opioid Not recommended therapy for non-malignant except for short-term Increasing duration of Chronic Pain pain is NOT recommended. use for severe cases, Evidence does not support use may lead to Recommended only not to exceed two dependency and overall effectiveness and as 2nd/3rd line option indicates risk of numerous weeks. Patients higher prevalence of at doses ≤ 120 mg adverse effects, including should be warned of work disability, risks and side effects. daily oral morphine psychological dependence depression, anxiety, (MED) equivalent in with difficultly weaning. and substance abuse. cases not at risk of misuse or diversion. 18,000 Annual Deaths in the USA from 16,000 Opioid Pain Relievers (OPR) 14,000 OPR deaths now far exceed 12,000 those from heroin/cocaine. Consider one- 10,000 Overdose and death month limit for 8,000 risk increases non-malignant 6,000 significantly pain patients 4,000 with higher 2,000 doses. 0 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 Year Steps before therapeutic opioid trial: ODG Opioid Drug Formulary: Opioids should only be part of a tailored treatment plan. Prior to First-Line: (Yes or No) starting, consider alternatives, and screen for risk of addiction, Brand Name Generic Name Status abuse or adverse outcome using tools like “Opioid Risk Tool” or Abstral Fentanyl transmucosal N “Screener & Opioid Assessment for Patients with Pain-Revised”. Actiq® Fentanyl lollipop N Obtain history of alcohol/substance abuse use. Opioids may not be Avinza® Morphine ER N helpful for conversion or somatization disorder, or pain from Buprenex® Buprenorphine (injection for detox) Y psychological factors (anxiety, depression, history of substance Butrans™ Buprenorphine(transdermal) N Codeine Codeine Y abuse). While patients may misuse opioids for these, there are Combunox Oxycodone/ibuprofen N better alternatives. Document the basis for any clinical decision to ConZip Tramadol ER N withhold opioids on inconsistencies in history, presentation, Darvocet® Propoxyphene/acetaminophen N behaviors, or physical findings for patients requesting them. Darvon® Propoxyphene hcl N Darvon-N® Propoxyphene napsylate N • Determine if pain is nociceptive or neuropathic (neuropathic Demerol® Meperidine N may require higher dose, though opioids would not be first-line Dilaudid® Hydromorphone Y therapy) and if there are underlying psychological issues. Duragesic® Fentanyl transdermal Y • A therapeutic trial of opioids should not be employed until the Embeda Morphine ER / Naltrexone Y Exalgo Hydromorphone ER N patient has failed a trial of non-opioid analgesics. Fentora® Fentanyl buccal N • Doctor and patient should set goals; continued use of opioids Fioricet® Butalbital (a barbiturate) N should be contingent on meeting those goals. Kadian® Morphine ER N • Baseline pain and functional assessments should be made to Lazanda Fentanyl nasal spray N include social, physical, psychological, daily/work activities, Levo-Dromoran® Levorphanol Y history of pain treatment, and effect of pain and function. Lortab® Hydrocodone/acetamin. Y Methadose® Methadone (link to rules) N • Assess likelihood patient could be weaned from opioids if there Morphine Morphine Y is no improvement in pain and function. Morphine Morphine ER Y • Conduct physical and psychological assessment; if subjective Nucynta™ Tapentadol N complaints don’t correlate w/imaging or physical findings or if Onsolis™ Fentanyl buccal film N psychosocial concerns exist, obtain specialist opinion. Opana® Oxymorphone N • Discuss risks and benefits with the patient or caregiver. Oxecta Oxycodone N OxyContin® Oxycodone ER N • Use written consent or pain agreement to document patient OxyIR® Oxycodone Y education, treatment plan, and informed consent. Percocet® Oxycodone/acetaminophen Y • Conduct urine drug screen for opioid misuse, illegal drug use. Percodan® Oxycodone/aspirin N • Check State Prescription Monitoring Program for duplicate Prialt® Ziconotide (morphine pump) N prescribers or inconsistent prescription fills. Suboxone® Buprenorphine (for pain) N Suboxone® Buprenorphine/Naloxone (detox) Y Subsys® Fentanyl sublingual spray N Subutex® Buprenorphine (for detox) Y When to continue opioids: Talwin Pentazocine lactate N Talwin NX Pentazocine/Naloxone N • If the patient has returned to work. Tylenol #3 Codeine/acetaminophen Y • If the patient has improved functioning and pain. Ultracet® Tramadol/Acetaminophen Y Ultram ER® Tramadol ER Y Ultram® Tramadol Y Vicodin® Hydrocodone/acetaminophen Y When to discontinue opioids: Vicoprofen® Hydrocodone/ibuprofen N Determine if treatment failure is due to correctable causes such as under-dosing or an inappropriate schedule. If not, weaning should Provided with permission, occur under direct medical supervision as slow taper. Official Disability Guidelines (ODG) Published by Work Loss Data Institute • Continuing pain with intolerable adverse effects. • Lack of significant benefit (persistent pain or no improved function despite doses of opiates up to 120 mg/day MED). • Resolution of pain, or patient requests discontinuing. • If serious non-adherence is occurring. • Evidence of illegal activity (diversion, forgery, or stealing). • Car accident or arrest related to opioids, alcohol, or illicit drugs; suicide attempt; aggressive or threatening behavior. • Repeat violations from opioid contract or evidence of abuse/addiction. Consider referral to addiction specialist. www.worklossdata.com .
Recommended publications
  • Could Mycolactone Inspire New Potent Analgesics? Perspectives and Pitfalls

    Could Mycolactone Inspire New Potent Analgesics? Perspectives and Pitfalls

    toxins Review Could Mycolactone Inspire New Potent Analgesics? Perspectives and Pitfalls 1 2 3, 4, , Marie-Line Reynaert , Denis Dupoiron , Edouard Yeramian y, Laurent Marsollier * y and 1, , Priscille Brodin * y 1 France Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR8204-CIIL-Center for Infection and Immunity of Lille, F-59000 Lille, France 2 Institut de Cancérologie de l’Ouest Paul Papin, 15 rue André Boquel-49055 Angers, France 3 Unité de Microbiologie Structurale, Institut Pasteur, CNRS, Univ. Paris, F-75015 Paris, France 4 Equipe ATIP AVENIR, CRCINA, INSERM, Univ. Nantes, Univ. Angers, 4 rue Larrey, F-49933 Angers, France * Correspondence: [email protected] (L.M.); [email protected] (P.B.) These three authors contribute equally to this work. y Received: 29 June 2019; Accepted: 3 September 2019; Published: 4 September 2019 Abstract: Pain currently represents the most common symptom for which medical attention is sought by patients. The available treatments have limited effectiveness and significant side-effects. In addition, most often, the duration of analgesia is short. Today, the handling of pain remains a major challenge. One promising alternative for the discovery of novel potent analgesics is to take inspiration from Mother Nature; in this context, the detailed investigation of the intriguing analgesia implemented in Buruli ulcer, an infectious disease caused by the bacterium Mycobacterium ulcerans and characterized by painless ulcerative lesions, seems particularly promising. More precisely, in this disease, the painless skin ulcers are caused by mycolactone, a polyketide lactone exotoxin. In fact, mycolactone exerts a wide range of effects on the host, besides being responsible for analgesia, as it has been shown notably to modulate the immune response or to provoke apoptosis.
  • Ketamine: an Update for Its Use in Complex Regional Pain Syndrome

    Ketamine: an Update for Its Use in Complex Regional Pain Syndrome

    xperim & E en l ta a l ic P in h Bentley et al., Clin Exp Pharmacol 2015, 5:2 l a C r m f Journal of DOI: 10.4172/2161-1459.1000169 o a l c a o n l o r g u y o J ISSN: 2161-1459 Clinical and Experimental Pharmacology Commentry Open Access Ketamine: An Update for Its Use in Complex Regional Pain Syndrome and Major Depressive Disorder William E Bentley*, Michael Sabia, Michael E Goldberg and Irving W Wainer Cooper University Hospital, Camden, New Jersey, United States of America Abstract In recent years, there has been significant research in regard to the efficacy of ketamine in regards to treating Complex Regional Pain Syndrome (CRPS) and Major Depressive Disorder (MDD). Many patients have had substantial symptomatic relief; however, not all patients have had positive results. This has prompted current research with evidence to suggest certain biomarkers exist that would infer which patients will/will not respond to ketamine treatment. Current biomarkers of interest include D-Serine (D-Ser) and magnesium, which will be discussed. Whether or not D-Ser and/or magnesium levels should be checked and possibly dictate therapy is an area of future research. It is also possible that downstream metabolites of ketamine are the key to successful therapy. Keywords: Complex regional pain syndrome; Major Depressive thoughts; and slowing of speech and action. These changes must last a Disorder(MDD); Ketamine minimum of 2 weeks and interfere considerably with work and family relations” [6]. Treatment options include antidepressant medications, Complex Regional Pain Syndrome (CRPS) and Major Depressive cognitive behavioral therapy, and interpersonal therapy.
  • ACPA Guide to Pain Management

    ACPA Guide to Pain Management

    [Document title] [Document subtitle] Abstract [Draw your reader in with an engaging abstract. It is typically a short summary of the document. When you’re ready to add your content, just click here and start typing.] ACPA [Email address] 1 ACPA Resource Guide To Chronic Pain Management An Integrated Guide to Medical, Interventional, Behavioral, Pharmacologic and Rehabilitation Therapies 2019 Edition American Chronic Pain Association P.O. Box 850 Rocklin, CA 95677 Tel 800-533-3231 Fax 916-652-8190 E-mail [email protected] Web Site http://www.theacpa.org Copyright 2019 American Chronic Pain Association, Inc. All rights reserved. No portion of this book may be reproduced without permission of the American Chronic Pain Association, Inc. 2 Table of Contents A STATEMENT FROM THE ACPA BOARD OF DIRECTORS ...........................................................................................................................5 INTRODUCTION ........................................................................................................................................................................................................6 OVERVIEW OF CHRONIC PAIN TREATMENT ..................................................................................................................................................8 WHAT DOES SUCCESSFUL PAIN TREATMENT LOOK LIKE? .......................................................................................................................8 PAIN TYPES, SOURCES & CLASSIFICATION .....................................................................................................................................................9
  • Membrane Stabilizer Medications in the Treatment of Chronic Neuropathic Pain: a Comprehensive Review

    Membrane Stabilizer Medications in the Treatment of Chronic Neuropathic Pain: a Comprehensive Review

    Current Pain and Headache Reports (2019) 23: 37 https://doi.org/10.1007/s11916-019-0774-0 OTHER PAIN (A KAYE AND N VADIVELU, SECTION EDITORS) Membrane Stabilizer Medications in the Treatment of Chronic Neuropathic Pain: a Comprehensive Review Omar Viswanath1,2,3 & Ivan Urits4 & Mark R. Jones4 & Jacqueline M. Peck5 & Justin Kochanski6 & Morgan Hasegawa6 & Best Anyama7 & Alan D. Kaye7 Published online: 1 May 2019 # Springer Science+Business Media, LLC, part of Springer Nature 2019 Abstract Purpose of Review Neuropathic pain is often debilitating, severely limiting the daily lives of patients who are affected. Typically, neuropathic pain is difficult to manage and, as a result, leads to progression into a chronic condition that is, in many instances, refractory to medical management. Recent Findings Gabapentinoids, belonging to the calcium channel blocking class of drugs, have shown good efficacy in the management of chronic pain and are thus commonly utilized as first-line therapy. Various sodium channel blocking drugs, belonging to the categories of anticonvulsants and local anesthetics, have demonstrated varying degrees of efficacy in the in the treatment of neurogenic pain. Summary Though there is limited medical literature as to efficacy of any one drug, individualized multimodal therapy can provide significant analgesia to patients with chronic neuropathic pain. Keywords Neuropathic pain . Chronic pain . Ion Channel blockers . Anticonvulsants . Membrane stabilizers Introduction Neuropathic pain, which is a result of nervous system injury or lives of patients who are affected. Frequently, it is difficult to dysfunction, is often debilitating, severely limiting the daily manage and as a result leads to the progression of a chronic condition that is, in many instances, refractory to medical This article is part of the Topical Collection on Other Pain management.
  • Intrathecal Drug Infusions

    Intrathecal Drug Infusions

    INTRATHECAL DRUG INFUSIONS RATIONAL USE OF POLYANALGESIA TIMOTHY R. DEER, MD • PRESIDENT AND CEO, THE CENTER FOR PAIN RELIEF, CHARLESTON, WEST VIRGINIA • CLINICAL PROFESSOR OF ANESTHESIOLOGY, WEST VIRGINIA UNIVERSITY • BOARD OF DIRECTORS, INTERNATIONAL NEUROMODULATION SOCIETY • IMMEDIATE PAST CHAIR, AMERICAN SOCIETY OF ANESTHESIOLOGISTS, COMMITTEE ON PAIN MEDICINE • BOARD OF DIRECTORS; AMERICAN ACADEMY OF PAIN MEDICINE AND AMERICAN SOCIETY OF INTERVENTIONAL PAIN PHYSICIANS 2 INS 2009 • SYMPOSIUM ON INTRATHECAL DRUG DELIVERY • DISCLOSURES IN INTRATHECAL DRUG DELIVERY • CONSULTANT: INSET, JOHNSON AND JOHNSON. Intrathecal Pump for Pain ! 1 mg intrathecal morphine = 300 mg oral morphine CONFIDENTIAL Krames ES. J Pain Symptom Manage. 1996 Jun;11(6):333-52 4 Objectives • Review current options for pump infusions • Build on the talks of Dr. Levy and Dr. Abejon • Use a case based approach to discuss the issues • Make conclusions regarding the algorithm of Intrathecal analgesia Clinical Decision Making • Regulatory Approval in your country • Case reports • Lectures and anecdotal information • Retrospective analysis • Double-blind, randomized, prospective studies • Physician innovation with no available evidence • Consensus Statements 2000 Guidelines for Intraspinal Infusion 2007 Polyanalgesic Consensus Guidelines for Management of Pain by Intraspinal Drug Delivery Line 1 Morphine or Hydromorphone or Ziconotide Fentanyl or Clonodine alone OR one of the following 2-drug Line 2 combinations: • Morphine (or Hydromorphone) + Ziconotide • Morphine (or
  • Drug and Medication Classification Schedule

    Drug and Medication Classification Schedule

    KENTUCKY HORSE RACING COMMISSION UNIFORM DRUG, MEDICATION, AND SUBSTANCE CLASSIFICATION SCHEDULE KHRC 8-020-1 (11/2018) Class A drugs, medications, and substances are those (1) that have the highest potential to influence performance in the equine athlete, regardless of their approval by the United States Food and Drug Administration, or (2) that lack approval by the United States Food and Drug Administration but have pharmacologic effects similar to certain Class B drugs, medications, or substances that are approved by the United States Food and Drug Administration. Acecarbromal Bolasterone Cimaterol Divalproex Fluanisone Acetophenazine Boldione Citalopram Dixyrazine Fludiazepam Adinazolam Brimondine Cllibucaine Donepezil Flunitrazepam Alcuronium Bromazepam Clobazam Dopamine Fluopromazine Alfentanil Bromfenac Clocapramine Doxacurium Fluoresone Almotriptan Bromisovalum Clomethiazole Doxapram Fluoxetine Alphaprodine Bromocriptine Clomipramine Doxazosin Flupenthixol Alpidem Bromperidol Clonazepam Doxefazepam Flupirtine Alprazolam Brotizolam Clorazepate Doxepin Flurazepam Alprenolol Bufexamac Clormecaine Droperidol Fluspirilene Althesin Bupivacaine Clostebol Duloxetine Flutoprazepam Aminorex Buprenorphine Clothiapine Eletriptan Fluvoxamine Amisulpride Buspirone Clotiazepam Enalapril Formebolone Amitriptyline Bupropion Cloxazolam Enciprazine Fosinopril Amobarbital Butabartital Clozapine Endorphins Furzabol Amoxapine Butacaine Cobratoxin Enkephalins Galantamine Amperozide Butalbital Cocaine Ephedrine Gallamine Amphetamine Butanilicaine Codeine
  • Future Local Anesthetics: Neurotoxins?

    Future Local Anesthetics: Neurotoxins?

    FUTURE PERSPECTIVE Future local anesthetics: Neurotoxins? Prasanna Vadhanan C. MD*, Adhinarayanan S, DA, DNB** *Associate Professor, Department of Anesthesiology, Vinayaka Mission’s Medical College & Hospitals (VMMCH),Karaikal (India) **Associate Professor, Department of Anesthesiology, Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), Puducherry (India) Correspondence: Dr. Prasanna Vadhanan, Associate Professor, Department of Anesthesiology, Vinayaka Mission’s Medical College & Hospitals (VMMCH), Karaikal (India) ABSTRACT This review article gives a look into the efforts being made to develop local anesthetics from new molecules, thus offering a better safety profile. Neurotoxins are a varied group of compounds, both chemically and pharmacologically. These encompass a wide group of drugs which acts on various ionic channels like sodium, potassium, calcium and chloride channels. The differences between current agents and the new group are presented. Tetrodotoxin and saxitoxin (STX) are the two more prominent groups of neurotoxins. Their characteristics are outlined. Key words: Local anesthetics; Neurotoxins; Tetrodotoxin; Saxitoxin Citation: Vadhanan P, Adhinarayanan S. Future local anesthetics: Neurotoxins?. Anaesth Pain & Intensive Care 2014;18(3):308-312 INTRODUCTION properties The use of cocaine by Koller in 1884 heralded a new class 1. No or minimal systemic toxicity of drugs which would later prove indispensable in routine 2. Longer shelf life anesthesia practice. Local anesthetic agents are one of the 3. Better sensory motor separation most widely used drugs for providing and or supplementing 4. Prolonged action analgesia . Lignocaine (1943) and bupivacaine (1963), 5. Stability quickly replaced cocaine and procaine because of their 6. No tissue irritation better safety profile. Even with the introduction of newer 7. Easily metabolized local anesthetics like ropivacaine and levobupivacaine, the By the current knowledge of NaV isoforms, it would be search for the ideal local anesthetic is still on.
  • Conotoxins As Tools to Understand the Physiological Function of Voltage-Gated Calcium (Cav) Channels

    Conotoxins As Tools to Understand the Physiological Function of Voltage-Gated Calcium (Cav) Channels

    marine drugs Review Conotoxins as Tools to Understand the Physiological Function of Voltage-Gated Calcium (CaV) Channels David Ramírez 1,2, Wendy Gonzalez 1,3, Rafael A. Fissore 4 and Ingrid Carvacho 5,* 1 Centro de Bioinformática y Simulación Molecular, Universidad de Talca, 3460000 Talca, Chile; [email protected] (D.R.); [email protected] (W.G.) 2 Instituto de Ciencias Biomédicas, Universidad Autónoma de Chile, 3460000 Talca, Chile 3 Millennium Nucleus of Ion Channels-Associated Diseases (MiNICAD), Universidad de Talca, 3460000 Talca, Chile 4 Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003, USA; rfi[email protected] 5 Department of Biology and Chemistry, Faculty of Basic Sciences, Universidad Católica del Maule, 3480112 Talca, Chile * Correspondence: [email protected]; Tel.: +56-71-220-3518 Received: 8 August 2017; Accepted: 4 October 2017; Published: 13 October 2017 Abstract: Voltage-gated calcium (CaV) channels are widely expressed and are essential for the completion of multiple physiological processes. Close regulation of their activity by specific inhibitors and agonists become fundamental to understand their role in cellular homeostasis as well as in human tissues and organs. CaV channels are divided into two groups depending on the membrane potential required to activate them: High-voltage activated (HVA, CaV1.1–1.4; CaV2.1–2.3) and Low-voltage activated (LVA, CaV3.1–3.3). HVA channels are highly expressed in brain (neurons), heart, and adrenal medulla (chromaffin cells), among others, and are also classified into subtypes which can be distinguished using pharmacological approaches. Cone snails are marine gastropods that capture their prey by injecting venom, “conopeptides”, which cause paralysis in a few seconds.
  • 2 12/ 35 74Al

    2 12/ 35 74Al

    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date 22 March 2012 (22.03.2012) 2 12/ 35 74 Al (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61K 9/16 (2006.01) A61K 9/51 (2006.01) kind of national protection available): AE, AG, AL, AM, A61K 9/14 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, (21) International Application Number: DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, PCT/EP201 1/065959 HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, (22) International Filing Date: KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, 14 September 201 1 (14.09.201 1) ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PE, PG, PH, PL, PT, QA, RO, RS, RU, (25) Filing Language: English RW, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, (26) Publication Language: English TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 61/382,653 14 September 2010 (14.09.2010) US (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant (for all designated States except US): GM, KE, LR, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, NANOLOGICA AB [SE/SE]; P.O Box 8182, S-104 20 ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, Stockholm (SE).
  • Prescription Medications, Drugs, Herbs & Chemicals Associated With

    Prescription Medications, Drugs, Herbs & Chemicals Associated With

    Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus American Tinnitus Association Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form, or by any means, without the prior written permission of the American Tinnitus Association. ©2013 American Tinnitus Association Prescription Medications, Drugs, Herbs & Chemicals Associated with Tinnitus American Tinnitus Association This document is to be utilized as a conversation tool with your health care provider and is by no means a “complete” listing. Anyone reading this list of ototoxic drugs is strongly advised NOT to discontinue taking any prescribed medication without first contacting the prescribing physician. Just because a drug is listed does not mean that you will automatically get tinnitus, or exacerbate exisiting tinnitus, if you take it. A few will, but many will not. Whether or not you eperience tinnitus after taking one of the listed drugs or herbals, or after being exposed to one of the listed chemicals, depends on many factors ‐ such as your own body chemistry, your sensitivity to drugs, the dose you take, or the length of time you take the drug. It is important to note that there may be drugs NOT listed here that could still cause tinnitus. Although this list is one of the most complete listings of drugs associated with tinnitus, no list of this kind can ever be totally complete – therefore use it as a guide and resource, but do not take it as the final word. The drug brand name is italicized and is followed by the generic drug name in bold.
  • Practical Considerations in Analgesic Selection for Chronic Noncancer Pain

    Practical Considerations in Analgesic Selection for Chronic Noncancer Pain

    Primary Care Pain Management in Pennsylvania: Optimizing Treatment, Minimizing Risk PRACTICAL CONSIDERATIONS IN ANALGESIC SELECTION FOR CHRONIC NONCANCER PAIN MARY LYNN MCPHERSON, PHARMD, MA, BCPS, CPE UNIVERSITY OF MARYLAND SCHOOL OF PHARMACY . LEARNING OBJECTIVES 1. Given an actual or simulated patient with chronic noncancer pain, demonstrate consideration of patient- and drug-related variables in selecting opioid analgesics. 2. Demonstrate competence in basic opioid conversion calculations and opioid dosage titration. 3. Given an actual or simulated patient with chronic noncancer pain, recommend appropriate coanalgesic. WHAT IS PAIN? ¡ “Total” Pain (Dame Cicely Saunders) ¡ Physical (due to disease or treatments) ¡ Psychological (anger, fear of suffering, depression, past experience of illness) ¡ Social (loss of role, status, job; financial concerns, worries about future/ family, dependency) ¡ Spiritual (anger, loss of faith, finding meaning, fear of the unknown ¡ An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage (IASP). ¡ “Pain is whatever the person experiencing it says it is” (McCaffery). www.iasp-pain.org/AM/Template.cfm?Sec8on=Home&Template=/CM/ContentDisplay.cfm&ContentID=8705 PATHOGENESIS OF PAIN Pain Nocicep8ve Neuropathic Central or Visceral Somac Peripheral Type of pain How patient’s describe it Analgesics Nociceptive • May be sharp or dull, often aching in nature Responds well to somatic pain • Familiar pain (e.g., toothache) primary analgesics
  • Current and Evolving Standards of Care for Patients with Neuropathic Pain Southern Pain Society 2020

    Current and Evolving Standards of Care for Patients with Neuropathic Pain Southern Pain Society 2020

    Current and Evolving Standards of Care For Patients with Neuropathic Pain Southern Pain Society 2020 Miroslav Backonja, MD Department of Anesthesiology and Pain Medicine Department of Neurology University of Washington – Seattle Objectives • Definition of neuropathic pain (NP) and its implications • Application of new assessment approaches to NP and their implications for treatment • An example of diabetic neuropathy pain to demonstrate challenges in assessing and treating NP • Standards and practice of NP treatment • Developments in treatment of NP Neuropathic Pain Pain caused by a lesion or disease of the somatosensory nervous system. Treede et al. Neurology 2008 Jensen et al Pain 2011 https://www.iasp-pain.org/Education/Content.aspx?ItemNumber=1698 1 Neuropathic Pain Pain caused by a lesion or disease of the somatosensory nervous system. Central Sensitization Treede et al. Neurology 2008 Jensen et al Pain 2011 Peripheral Sensitization https://www.iasp-pain.org/Education/Content.aspx?ItemNumber=1698 Neuropathic Pain – Implications of definition - It is necessary to perform neurological somatosensory exam across the range of fiber types, including small fibers (e.g. such as test for cold and hot) to establish the diagnosis of neuropathic pain - NP is a positive and confirmatory diagnosis, not diagnosis of exclusion -In NP, history and neurological sensory exam reveal a mix of positive phenomena (e.g. allodynia) and negative (e.g. deficits) phenomena across the range of sensory modalities Question for the audience: • By raising your hands,