Dementia Diagnosis and Prognosis EMILY MORGAN, MD 2020 OHSU INTERNAL MEDICINE and GERIATRICS Objectives

Total Page:16

File Type:pdf, Size:1020Kb

Dementia Diagnosis and Prognosis EMILY MORGAN, MD 2020 OHSU INTERNAL MEDICINE and GERIATRICS Objectives Dementia Diagnosis and Prognosis EMILY MORGAN, MD 2020 OHSU INTERNAL MEDICINE AND GERIATRICS Objectives Define dementia and mild cognitive impairment Identify and differentiate the 5 most common types of dementia Explore key elements of treatment and prognosis in dementia BILL Creator:Raul Rodriguez Copyright:© Fotoluminate LLC Bill 82 year old man, recently moved to assisted living after his wife died 12 months ago. His daughter has noticed increasing “forgetfulness” in the past 2-3 years. Bill has good days and bad days, but his family notices he has been neglecting his appearance recently. No agitation or delusions, but occasional visual hallucinations. No loss of appetite or weight loss. He has had 2 falls in the last 3 months. Never smoked, rarely drinks. Meds: HCTZ, baby aspirin, multivitamin and occasional diphenhydramine for insomnia. Dementia defined by DSM-V: Major Neurocognitive Disorder Deficit in at least one objective assessment of: ◦ Complex attention ◦ Executive ability ◦ Learning and memory ◦ Language ◦ Visuo-constructional-perceptual ability ◦ Social cognition Deficits must interfere with independence (ADLs/IADLs) Mild cognitive impairment defined: Minor Neurocognitive Disorder Minor cognitive decline from a previous level of performance in one or more of the stated domains No interference with function but greater effort and compensatory strategies may be required to maintain independence Why is MCI important? 50% progress to dementia within 7 years There are interventions that can potential prevent or slow the rate of conversion to dementia ◦ Controlling vascular risk factors (OSA) ◦ Exercise (Tai chi) ◦ Diet (Mediterranean) ◦ Socialization (avoiding isolation) Must rule out depression and delirium when assessing for dementia! 6 types of dementia Alzheimer’s Vascular Lewy Body Frontotemporal Alcohol related HIV Associated Dementia 5% 15% 45% 20% 15% Alzheimers Vascular Mixed LBD FTD Alzheimer’s Dementia Impairment in learning and memory plus one: ◦ Complex attention ◦ Executive function ◦ Language ◦ Visuo-constructional-perceptual ability ◦ Social cognition Vascular Dementia New cognitive deficit + Focal neurological signs and symptoms +/- Brain imaging evidence of cerebrovascular disease Judged to be temporally related to the dementia MIXED vascular-Alzheimer’s dementia Vascular insults are very common in Alzheimer’s disease 20% of patients have evidence of both vascular and Alzheimer’s pathology Lewy Body Dementia New cognitive deficits + 2/3 symptoms: Parkinsonian findings: shuffling gait, rigidity, dysphagia >>>tremor Fluctuation in LOC and cognition Well formed visual hallucinations LBD – suggestive findings REM sleep disorders Severe antipsychotic sensitivity: Exaggerated extrapyramidal symptoms Increased rigidity and bradykinesia Frontotemporal Dementia A TALE OF 2 DEMENTIAS Frontotemporal Dementia: Behavioral variant Decline in personal or social interpersonal conduct Impaired reasoning and difficulty with tasks out of proportion to impairments in memory Frontotemporal Dementia: progressive aphasia variant Deficits in language out of proportion to memory impairment ◦ Motor speech ◦ Word comprehension or object recognition ◦ Word retrieval or speech errors (substitution) Alcohol related dementia Deficiency in thiamine (Vitamin B1) The toxic effects of alcohol on brain cells The biological stress of repeated intoxication and withdrawal Alcohol-related cerebrovascular disease Head injuries from falls sustained when inebriated Alcohol related dementia Learning and memory most effected Confabulation - making up information not remembered People with alcohol related dementia many benefit from extended treatment with oral thiamine and magnesium With treatment: ¼ will completely recover ½ will improve without complete recovery ¼ will remain unchanged HIV Associated Dementia Late stage disease: CD4<200 and high viral loads Characterized by symptoms of cognitive, motor, and behavioral disturbances Behavioral changes including apathy and social withdrawal Motor changes include gait impairment, falls, impaired fine motor skills No quick screening test validated – MoCA likely the best, also Modified HIV Dementia Scale https://aidsetc.org/guide/hiv-associated-neurocognitive-disorders Quick memory Screen The Mini Cog ◦ 3 item recall ◦ Clock draw Validated for diagnosis of dementia AND for MCI Tests 5 brain domains Tests 6 brain domains Helps to assess driving ability MoCA < 18 Abnormal trails B Abnormal clock MMSE (proprietary- $1.68/use) Tests 4 brain domains: ◦ orientation, memory, visual-spatial, verbal fluency USE ONLY FOR FOLLOWING DEMENTIA OVER TIME Physical Exam Neurologic Exam: ◦ Sensory, Reflexes, Strength, Motor Coordination ◦ E/o Parkinsonism? ◦ Gait assessment: Timed Get up and Go (TUG) Lab studies TSH Vitamin B12 (MMA) Consider HIV and RPR If none recently: CBC and metabolic panel Neuroimaging Non contrast CT scan or MRI For any patients under age 65 Or patients over age 65 with: ◦ Atypical presentation ◦ Unclear diagnosis ◦ Rapid unexplained deterioration ◦ Unexplained focal neurological symptoms ◦ History of head injury ◦ Urinary incontinence or gait ataxia early in illness ◦ Suspicion of undiagnosed CV disease BILL Creator:Raul Rodriguez Copyright:© Fotoluminate LLC Bill SLUMS Orientation 3/3 Calculation 1/3 Naming 2/3 Object Recall 3/5 Attention 1/2 Clock 0/4 Shapes 2/2 Story Recall 4/8 Total 16/30 Bill Gait – wide based, mild shuffling, TUG>15 sec Tone – mild cog wheeling on L side No tremor, normal facial movements On further questioning, Bill has a long hx of “insomnia” caused by restless sleep. He has vivid dreams, often acting them out in his sleep. Lewy Body Dementia Now that my patient has a diagnosis, what next? ◦ Staging Dementia for treatment ◦ Behavioral symptoms assessment ◦ Driving assessment ◦ Home safety evaluation ◦ Caregiver burden ◦ Goals of care planning Staging dementia Mild Moderate MoCA 20-16 Advanced Decline in MoCA 15-10 End stage IADLs, mild Decline in behavioral ADLs, MoCA <10 symptoms Increasing FAST staging behavioral Needing 24 for hospice symptoms hour care care A review of Reviews – what works? Exercise Patient+Caregiver QOL interventions AChE-I Memantine Laver K, Dyer S, Whitehead C, Clemson L, Crotty M. Interventions to delay functional decline in people with dementia: a systematic review of systematic reviews. BMJ Open. 2016;6(4):e010767. Published 2016 Apr 27. doi:10.1136/bmjopen-2015-010767 Cholinesterase Inhibitors Most studies with statistically significant difference favoring cholinesterase inhibitors –Delay in progression of up to 7 months in mild dementia –Delay of 2-5 months in moderate dementia –Statistically significant improvement in behavioral symptoms in mild and moderate dementia –Effective for all dementia types except FTD Raina 2008, Rodda 2009 When to stop? A Systematic Review of Practice Guidelines and Recommendations for Discontinuation of Cholinesterase Inhibitors in Dementia. Renn BN, Asghar-Ali AA, Thielke S, et al. Am J Geriatr Psychiatry. 2017;26(2):134-147. Risk for Health Events After Deprescribing Acetylcholinesterase Inhibitors in Nursing Home Residents With Severe Dementia Journal of the American Geriatrics Society, First published: 26 November 2019, DOI: (10.1111/jgs.16241) Memantine Memantine for Alzheimer's Disease: An Updated Systematic Review and Meta-analysis. Kishi et al. J Alz Disease, 2017. Memantine showed a significant improvement Cognitive 95% CI (-0.34, -0.15) p < 0.00001 Behavioral 95% CI (-0.34, -0.07) p = 0.003 Memantine Studies in vascular, LBD, and FTD trend toward benefit Dual therapy with AChE-I or monotherapy Dose: 5mg daily -10 mg bid eGFR of 30-60, max dose is 10 mg daily Stop if eGFR below 30 Mild Dementia Alzheimer’s Vascular Lewy Body FTD mixed Trial AChE-I Control vascular risk Trial AChE-I (NO AChE-I) factors PT/OT Trial memantine Trial AChE-I Driving and safety Driving and assessment Safety assessment Exercise (Tai chi) Mediterranean diet Socialization Mild Dementia Conversations with patient and family: What are your wishes? What’s it going to look like? Assisted living options Advance Directive Plan to stop driving Moderate Dementia AlzheimerSs Vascular mixed Lewy Body FTD Trial AChE-I Control vascular Trial AChE-I Trial memantine risk factors Trial memantine Trial memantine Trial AChE-I Trial memantine Moderate Dementia Conversations with patient and family: What is our safety plan? Neuropsychiatric symptoms Yes and… approach to communication Memory care options POLST Advanced Dementia Alzheimer’s Vascular Lewy Body FTD mixed Consider Consider Consider Trial memantine stopping AChE-I stopping AChE-I stopping AChE-I Trial memantine Trial memantine Trial memantine Advanced Dementia Conversations with caregiver: 24 hour caregiving Planning for end stages ◦ Loss of mobility ◦ Loss of verbal interaction ◦ Complete Incontinence ◦ Dysphagia ◦ Weight loss References Laver K, Dyer S, Whitehead C, Clemson L, Crotty M. Interventions to delay functional decline in people with dementia: a systematic review of systematic reviews. BMJ Open. 2016;6(4):e010767. Published 2016 Apr 27. doi:10.1136/bmjopen-2015-010767 Lockhart IA, Orme ME, Mitchell SA. The efficacy of licensed-indication use of donepezil and memantine monotherapies for treating behavioural and psychological symptoms of dementia in patients with Alzheimer’s disease: systematic review and meta-analysis. Dement Geriatr Cogn Dis Extra. 2011;1(1):212–27. McShane R, Areosa Sastre A, Minakaran N. Memantine for dementia. Cochrane Database Syst Rev. 2006;2:CD003154.
Recommended publications
  • Diagnosis, Treatment, and Prognosis of Glioma Five New Things
    Diagnosis, treatment, and prognosis of glioma Five new things s the profession of neurology becomes in- creasingly subspecialized, it becomes more A and more difficult for general neurologists to feel comfortable with every category of disease. At no time is this felt more keenly than when an imaging procedure has been performed on a pa- tient for a seizure, headache, or focal neurologic complaint and a brain tumor is discovered. In con- trast to consulting with a patient with a movement disorder or neuromuscular disease, there is no time to craft the discussion and discuss a differential diag- nosis. As with demyelinating disease or stroke, the scan result dictates an immediate conversation with the patient, but in contrast to those disorders this takes place from the perspective of a provider who understands that the eventual outcome for the pa- tient is likely to be guarded. How to give that message with tact, candor, and some optimism could be the sole topic of this article but, instead, we focus on 5 new ideas that are changing the management of brain tumor patients in the hopes that these points might prove useful during those times. Lynne P. Taylor, MD PROGNOSIS AND GLIOMA SUBTYPES In his pioneering work “Death Foretold,” Dr. Nicholas Chris- takis1 says “prognosis gives diagnosis its affective component, striking fear in patients and physicians Address correspondence and alike.” There has traditionally been a lot of therapeutic nihilism about the treatment of glioblastoma, but reprint requests to Dr. Lynne P. that is now changing. Previously believed to be one homogeneous group of tumors based on clinicopath- Taylor, X7NEU, Virginia Mason Medical Center, 1100 9th ologic and histologic assessments, we are now finding that subgroups exist within these tumors that one Avenue, Seattle, WA 98101 day may allow us to better predict which chemotherapy option is best for each individual patient.
    [Show full text]
  • Neuroinflammation and Functional Connectivity in Alzheimer's Disease: Interactive Influences on Cognitive Performance
    Research Articles: Neurobiology of Disease Neuroinflammation and functional connectivity in Alzheimer's disease: interactive influences on cognitive performance https://doi.org/10.1523/JNEUROSCI.2574-18.2019 Cite as: J. Neurosci 2019; 10.1523/JNEUROSCI.2574-18.2019 Received: 5 October 2018 Revised: 25 March 2019 Accepted: 11 April 2019 This Early Release article has been peer-reviewed and accepted, but has not been through the composition and copyediting processes. The final version may differ slightly in style or formatting and will contain links to any extended data. Alerts: Sign up at www.jneurosci.org/alerts to receive customized email alerts when the fully formatted version of this article is published. Copyright © 2019 Passamonti et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. 1 Neuroinflammation and functional connectivity in Alzheimer’s disease: 2 interactive influences on cognitive performance 3 4 L. Passamonti1*, K.A. Tsvetanov1*, P.S. Jones1, W.R. Bevan-Jones2, R. Arnold2, R.J. Borchert1, 5 E. Mak2, L. Su2, J.T. O’Brien2#, J.B. Rowe1,3# 6 7 Joint *first and #last authorship 8 9 10 Authors’ addresses 11 1Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK 12 2Department of Psychiatry, University of Cambridge, Cambridge, UK 13 3Cognition and Brain Sciences Unit, Medical Research Council, Cambridge,
    [Show full text]
  • Study Guide Medical Terminology by Thea Liza Batan About the Author
    Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails ­proficiency­in­communicating­with­healthcare­professionals­such­as­physicians,­nurses,­ or dentists.
    [Show full text]
  • Neurocognitive and Functional Impairment in Adult and Paediatric Tuberculous Meningitis [Version 1; Peer Review: 2 Approved]
    Wellcome Open Research 2019, 4:178 Last updated: 20 MAY 2021 REVIEW Neurocognitive and functional impairment in adult and paediatric tuberculous meningitis [version 1; peer review: 2 approved] Angharad G. Davis 1-3, Sam Nightingale4, Priscilla E. Springer 5, Regan Solomons 5, Ana Arenivas6,7, Robert J. Wilkinson 2,8,9, Suzanne T. Anderson10,11*, Felicia C. Chow 12*, Tuberculous Meningitis International Research Consortium 1University College London, Gower Street, London, WC1E 6BT, UK 2Francis Crick Institute, Midland Road, London, NW1 1AT, UK 3Institute of Infectious Diseases and Molecular Medicine. Department of Medicine, University of Cape Town, Observatory, 7925, South Africa 4HIV Mental Health Research Unit, University of Cape Town,, Observatory, 7925, South Africa 5Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa 6The Institute for Rehabilitation and Research Memorial Hermann, Department of Rehabilitation Psychology and Neuropsychology,, Houston, Texas, USA 7Baylor College of Medicine, Department of Physical Medicine and Rehabilitation, Houston, Texas, USA 8Department of Infectious Diseases, Imperial College London, London, W2 1PG, UK 9Wellcome Centre for Infectious Disease Research in Africa, Institute of Infectious Diseases and Molecular Medicine at Department of Medicine, University of Cape Town, Observatory, 7925, South Africa 10MRC Clinical Trials Unit at UCL, University College London, London, WC1E 6BT, UK 11Evelina Community, Guys and St Thomas’
    [Show full text]
  • Melanoma Review
    Philip J. Bergman DVM, MS, PhD Diplomate ACVIM-Oncology Director, Clinical Studies, VCA Antech Medical Director, Katonah-Bedford Veterinary Center (#893) 546 North Bedford Rd., Bedford Hills, NY 10507 Office 914-241-7700, Fax 914-241-7708 Adjunct Associate, Memorial Sloan-Kettering Cancer Center, NYC MELANOMA REVIEW Melanomas in dogs have extremely diverse biologic behaviors depending on a variety of factors. A greater understanding of these factors significantly helps the clinician to delineate in advance the appropriate staging, prognosis and treatments. The primary factors which determine the biologic behavior of a melanoma in a dog are site, size, stage and histologic parameters. Unfortunately, even with an understanding of all of these factors, there will be occasional melanomas which have an unreliable biologic behavior; hence the desperate need for additional research into this relatively common (~ 4% of all canine tumors), heterogeneous, but frequently extremely malignant tumor. This review will assume the diagnosis of melanoma has already been made, which in of itself can be fraught with difficulty, and will focus on the aforementioned biologic behavior parameters, the staging and the treatment of canine melanoma. Biologic Behavior The biologic behavior of canine melanoma is extremely variable and best characterized based on anatomic site, size, stage and histologic parameters. On divergent ends of the spectrum would be a 0.5 cm haired-skin melanoma with an extremely low grade likely to be cured with simple surgical removal vs. a 5.0 cm high-grade malignant oral melanoma with a poor-grave prognosis. Similar to the development of a rational staging, prognostic and therapeutic plan for any tumor, two primary questions must be answered; what is the local invasiveness of the tumor and what is the metastatic propensity? The answers to these questions will determine the prognosis, and to be discussed later, the treatment.
    [Show full text]
  • Cancer Treatment and Survivorship Facts & Figures 2019-2021
    Cancer Treatment & Survivorship Facts & Figures 2019-2021 Estimated Numbers of Cancer Survivors by State as of January 1, 2019 WA 386,540 NH MT VT 84,080 ME ND 95,540 59,970 38,430 34,360 OR MN 213,620 300,980 MA ID 434,230 77,860 SD WI NY 42,810 313,370 1,105,550 WY MI 33,310 RI 570,760 67,900 IA PA NE CT 243,410 NV 185,720 771,120 108,500 OH 132,950 NJ 543,190 UT IL IN 581,350 115,840 651,810 296,940 DE 55,460 CA CO WV 225,470 1,888,480 KS 117,070 VA MO MD 275,420 151,950 408,060 300,200 KY 254,780 DC 18,750 NC TN 470,120 AZ OK 326,530 NM 207,260 AR 392,530 111,620 SC 143,320 280,890 GA AL MS 446,900 135,260 244,320 TX 1,140,170 LA 232,100 AK 36,550 FL 1,482,090 US 16,920,370 HI 84,960 States estimates do not sum to US total due to rounding. Source: Surveillance Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute. Contents Introduction 1 Long-term Survivorship 24 Who Are Cancer Survivors? 1 Quality of Life 24 How Many People Have a History of Cancer? 2 Financial Hardship among Cancer Survivors 26 Cancer Treatment and Common Side Effects 4 Regaining and Improving Health through Healthy Behaviors 26 Cancer Survival and Access to Care 5 Concerns of Caregivers and Families 28 Selected Cancers 6 The Future of Cancer Survivorship in Breast (Female) 6 the United States 28 Cancers in Children and Adolescents 9 The American Cancer Society 30 Colon and Rectum 10 How the American Cancer Society Saves Lives 30 Leukemia and Lymphoma 12 Research 34 Lung and Bronchus 15 Advocacy 34 Melanoma of the Skin 16 Prostate 16 Sources of Statistics 36 Testis 17 References 37 Thyroid 19 Acknowledgments 45 Urinary Bladder 19 Uterine Corpus 21 Navigating the Cancer Experience: Treatment and Supportive Care 22 Making Decisions about Cancer Care 22 Cancer Rehabilitation 22 Psychosocial Care 23 Palliative Care 23 Transitioning to Long-term Survivorship 23 This publication attempts to summarize current scientific information about Global Headquarters: American Cancer Society Inc.
    [Show full text]
  • Cognitive Impairment/Dementia – Summary
    Cognitive Impairment/Dementia Care Guide December 2014 SUMMARY GOALS Early identification of affected patients Prevention of victimization Reduce symptom severity Improve quality of life ALERTS Victimized patients Increase in rules violation behaviors Worsening personal hygiene Anxiety and agitation, especially at night Complete Advance Directive-Durable Power of Attorney for Health Care (DPAHC) early in course of disease Prison environment may mask symptoms DIAGNOSTIC CRITERIA/EVALUATION Definition - Mild Cognitive Impairment (MCI) Cognitive decline greater than expected for age and education level without significantly interfering with activities of daily life. Evidence of memory impairment Preservation of general cognitive and functional abilities Absence of diagnosed dementia Definition - Dementia Cognitive impairment with: significant decline from previous level of performance in one or more cognitive domains (complex attention, executive function, learning and memory, language, social cognition, perceptual motor) interference with independence in daily activities Not occurring exclusively with delirium Not better explained by another disorder Neurobehavioral abnormalities History - MCI and Dementia patients may have similar historical findings which contribute to the ultimate diagnosis: Poor adherence to rules and routines Personal hygiene problems Impaired comprehension History of head injury, substance abuse, or other medical contributors Differential Diagnosis – Mild Cognitive Impairment (MCI) Medication
    [Show full text]
  • The Cognitive Basis of Dyslexia in School-Aged Children: a Multiple Case
    The cognitive basis of dyslexia The cognitive basis of dyslexia in school-aged children: a multiple case study in a transparent orthography Agnieszka Dębska1*, Magdalena Łuniewska1,2*, Julian Zubek2, Katarzyna Chyl1, Agnieszka Dynak1,2, Gabriela Dzięgiel-Fivet1, Joanna Plewko1, Katarzyna Jednoróg1, Anna Grabowska3 * these authors contributed equally to the paper 1Laboratory of Language Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland 2 Faculty of Psychology, University of Warsaw, Warsaw, Poland 3Faculty of Psychology, SWPS University of Social Sciences and Humanities, Warsaw, Poland Laboratory of Language Neurobiology Nencki Institute of Experimental Biology, Polish Academy of Sciences ul. Pasteura 3, 02-093 Warszawa, Poland Conflict of Interest Statement None of the authors has to declare a conflict of interest. Supplementary materials 1. Tables and Figures 2. Supplementary materials S1, S2, S3 and S4 1 The cognitive basis of dyslexia The cognitive basis of dyslexia in school-aged children: a multiple case study in a transparent orthography Research highlights ● This study tested the (co)existence of cognitive deficits in dyslexia in phonological awareness, rapid naming, visual and selective attention, auditory skills, and implicit learning. ● The most frequent deficits in Polish children with dyslexia included a phonological (51%) and a rapid naming deficit (26%), which coexisted in 14% of children. ● Despite the severe reading impairment, 26% of children with dyslexia presented no deficits in measured cognitive abilities. ● RAN explains reading skills variability across the whole spectrum of reading ability; phonological skills explain variability best among average and good readers but not poor readers. Abstract This study focused on the role of numerous cognitive skills such as phonological awareness (PA), rapid automatized naming (RAN), visual and selective attention, auditory skills, and implicit learning in developmental dyslexia.
    [Show full text]
  • Mild Cognitive Impairment (Mci) and Dementia February 2017
    CareCare Process Process Model Model FEBRUARY MONTH 2015 2017 DIAGNOSIS AND MANAGEMENT OF Mild Cognitive Impairment (MCI) and Dementia minor update - 12 / 2020 The Intermountain Cognitive Care Development Team developed this care process model (CPM) to improve the diagnosis and treatment of patients with cognitive impairment across the staging continuum from mild impairment to advanced dementia. It is primarily intended as a tool to assist primary care teams in making the diagnosis of dementia and in providing optimal treatment and support to patients and their loved ones. This CPM is based on existing guidelines, where available, and expert opinion. WHAT’S INSIDE? Why Focus ON DIAGNOSIS AND MANAGEMENT ALGORITHMS OF DEMENTIA? Algorithm 1: Diagnosing Dementia and MCI . 6 • Prevalence, trend, and morbidity. In 2016, one in nine people age 65 and Algorithm 2: Dementia Treatment . .. 11 older (11%) has Alzheimer’s, the most common dementia. By 2050, that Algorithm 3: Driving Assessment . 13 number may nearly triple, and Utah is expected to experience one of the Algorithm 4: Managing Behavioral and greatest increases of any state in the nation.HER,WEU One in three seniors dies with Psychological Symptoms . 14 a diagnosis of some form of dementia.ALZ MCI AND DEMENTIA SCREENING • Costs and burdens of care. In 2016, total payments for healthcare, long-term AND DIAGNOSIS ...............2 care, and hospice were estimated to be $236 billion for people with Alzheimer’s MCI TREATMENT AND CARE ....... HUR and other dementias. Just under half of those costs were borne by Medicare. MANAGEMENT .................8 The emotional stress of dementia caregiving is rated as high or very high by nearly DEMENTIA TREATMENT AND PIN, ALZ 60% of caregivers, about 40% of whom suffer from depression.
    [Show full text]
  • The History of Medicine a Beginner’S Guide
    The History of Medicine A Beginner’s Guide Mark Jackson A Oneworld Paperback Published in North America, Great Britain & Australia by Oneworld Publications, 2014 Copyright © Mark Jackson 2014 The right of Mark Jackson to be identified as the Author of this work has been asserted by him in accordance with the Copyright, Designs and Patents Act 1988 All rights reserved Copyright under Berne Convention A CIP record for this title is available from the British Library ISBN 978-1-78074-520-6 eISBN 978-1-78074-527-5 Typeset by Siliconchips Services Ltd, UK Printed and bound in Denmark by Nørhaven Oneworld Publications 10 Bloomsbury Street London WC1B 3SR England Stay up to date with the latest books, special offers, and exclusive content from Oneworld with our monthly newsletter Sign up on our website www.oneworld-publications.com For Ciara, Riordan and Conall ‘A heart is what a heart can do.’ Sir James Mackenzie, 1910 Contents List of illustrations viii Preface x Introduction xiii 1 Balance and flow: the ancient world 1 2 Regimen and religion: medieval medicine 25 3 Bodies and books: a medical Renaissance? 50 4 Hospitals and hope: the Enlightenment 84 5 Science and surgery: medicine in the nineteenth century 120 6 War and welfare: the modern world 159 Conclusion 197 Timeline 201 Further reading 214 Index 221 List of illustrations Figure 1 Chinese acupuncture chart Figure 2 Vessel for cupping (a form of blood-letting) discov- ered in Pompeii, dating from the first century CE Figure 3 Text and illustration on ‘urinomancy’ or urine analysis Figure 4 Mortuary crosses placed on the bodies of plague victims, c.
    [Show full text]
  • Canine Multicentric Lymphoma
    MEDICAL ONCOLOGY Canine Multicentric Lymphoma WHAT IS LYMPHOMA? Lymphoma is a cancer of the cells of the immune system called lymphocytes. Lymphocytes are present throughout the body, so dogs can develop lymphoma in multiple organs. Lymphoma most often affects lymph nodes, but can also affect the liver, spleen, bone marrow, and other sites. Lymphoma is typically diagnosed using aspirates collected from enlarged lymph nodes. In some cases, diagnosis may require sampling of bone marrow or other organs, tissue biopsy, or molecular testing (flow cytometry, PARR). Once a diagnosis is made, staging tests are recommended to assess the extent of disease. Complete staging includes blood and urine testing, non-invasive imaging (chest X-rays, abdominal ultrasound), and additional aspirates. This evaluation provides prognostic information, a baseline for monitoring, and information regarding organ function and involvement. Results may influence treatment recommendations or help anticipate potential complications. Lymphoma is categorized into five stages, depending on the extent of the disease in the body: single lymph node enlargement (stage I), regional lymph node enlargement (stage II), generalized lymph node enlargement (stage III), liver and/or spleen involvement (stage IV), and bone marrow and blood involvement (stage V). Patients are further categorized into a substage, with substage “a” being patients who show no clinical signs of illness and “b” being patients who show signs of illness (such as vomiting, weight loss, lethargy, fever, decreased appetite, etc.). WHAT IS THE DIFFERENCE BETWEEN B CELL AND T CELL LYMPHOMA? In addition to staging and substaging, lymphoma can be further characterized based on the type of lymphocyte (T cell or B cell) that becomes cancerous.
    [Show full text]
  • Prognosis: How Do We Estimate It and Why Is It Important?
    Prognosis: How do we estimate it and why is it important? Allie Halpern, MS4 Palliative Medicine Service August 27, 2014 prog·no·sis noun \präg-ˈnō-səs\ : a doctor's opinion about how someone will recover from an illness or injury : a judgment about what is going to happen in the future Prognosis: The Definition < http://www.merriam-webster.com/dictionary/prognosis> Many cultures recognize impending death. In the holy city of Varanasi (Hindu capital of India), families and priests bring dying people to end their lives in charity hospices. When asked how they know when to bring patients to the hospice the family members and priests answered, "when the patient no longer wanted to eat or drink". A 14-day stay is allowed but 10% died on the day of admission, 84% in the first week, and all by 17 days. Our system is very different from this, but still faces the same prognostication concerns. http://www.independent.co.uk/news/world/asia/varanasi-the-last-stop-before-nirvana-1805245.html Basu, M. Hotel Dealth. CNN Interactive Online. http://www.cnn.com/interactive/2014/04/world/india-hotel-death/index.html Survival Estimation in Palliative Care. Prtenoy, RK and Bruera E. Topics in Palliative Care. Volume 4. Oxford University Press, Mar 30, 2000. Photograph by Atul Loke/Panos Pictures for CNN. http://www.cnn.com/interactive/2014/04/world/india-hotel-death/index.html Prognosis: Why Bother? Patient autonomy and need to know: Palliative care patients recognize that their disease is progressing inexorably, but deserve to share the physician's estimation of life expectancy in order to make their own end of life decisions, both practical and spiritual.
    [Show full text]