Burden of Disease: What Is It and Why Is It Important for Safer Food?
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Communicable Disease Chart
COMMON INFECTIOUS ILLNESSES From birth to age 18 Disease, illness or organism Incubation period How is it spread? When is a child most contagious? When can a child return to the Report to county How to prevent spreading infection (management of conditions)*** (How long after childcare center or school? health department* contact does illness develop?) To prevent the spread of organisms associated with common infections, practice frequent hand hygiene, cover mouth and nose when coughing and sneezing, and stay up to date with immunizations. Bronchiolitis, bronchitis, Variable Contact with droplets from nose, eyes or Variable, often from the day before No restriction unless child has fever, NO common cold, croup, mouth of infected person; some viruses can symptoms begin to 5 days after onset or is too uncomfortable, fatigued ear infection, pneumonia, live on surfaces (toys, tissues, doorknobs) or ill to participate in activities sinus infection and most for several hours (center unable to accommodate sore throats (respiratory diseases child’s increased need for comfort caused by many different viruses and rest) and occasionally bacteria) Cold sore 2 days to 2 weeks Direct contact with infected lesions or oral While lesions are present When active lesions are no longer NO Avoid kissing and sharing drinks or utensils. (Herpes simplex virus) secretions (drooling, kissing, thumb sucking) present in children who do not have control of oral secretions (drooling); no exclusions for other children Conjunctivitis Variable, usually 24 to Highly contagious; -
Better Together TNVR and Public Health APHA 11-13-18.Pdf
Better Together: TNVR and Public Health 11/13/2018 Presenter Disclosures Introduction Better Together TNVR and public health Peter J. Wolf and G. Robert Weedon • TNVR: trap-neuter-vaccinate-return G. Robert Weedon, DVM, MPH Clinical Assistant Professor and Service Head (Retired) Shelter Medicine, College of Veterinary Medicine University of Illinois • Emphasis on the “V” Peter J. Wolf, MS Research/Policy Analyst – Vaccination Best Friends Animal Society Have no relationships to disclose • Emphasizes the public health aspect of TNVR programs • Vaccinating against rabies as a means of protecting the health of the public Introduction TNVR TNVR • Why TNVR? • Why TNVR? – The only humane way to – More than half of impounded cats are euthanized deal with the problem of due to shelter crowding, shelter-acquired disease free-roaming (feral, or feral behavior animal welfareTNVR public health community) cats – TNVR, an alternative to shelter impoundment, – When properly applied, improves cat welfare and reduces the size of cat TNVR has been shown to colonies control/reduce populations rabies prevention of free-roaming cats Levy, J. K., Isaza, N. M., & Scott, K. C. (2014). Effect of high-impact targeted trap-neuter-return and adoption Levy, J. K., Isaza, N. M., & Scott, K. C. (2014). Effect of high-impact targeted trap-neuter-return and adoption of community cats on cat intake to a shelter. The Veterinary Journal, 201(3), 269–274. of community cats on cat intake to a shelter. The Veterinary Journal, 201(3), 269–274. TNVR TNVR TNVR • Why TNVR? • Why -
797 Circulating Tumor DNA and Circulating Tumor Cells for Cancer
Medical Policy Circulating Tumor DNA and Circulating Tumor Cells for Cancer Management (Liquid Biopsy) Table of Contents • Policy: Commercial • Coding Information • Information Pertaining to All Policies • Policy: Medicare • Description • References • Authorization Information • Policy History • Endnotes Policy Number: 797 BCBSA Reference Number: 2.04.141 Related Policies Biomarkers for the Diagnosis and Cancer Risk Assessment of Prostate Cancer, #336 Policy1 Commercial Members: Managed Care (HMO and POS), PPO, and Indemnity Plasma-based comprehensive somatic genomic profiling testing (CGP) using Guardant360® for patients with Stage IIIB/IV non-small cell lung cancer (NSCLC) is considered MEDICALLY NECESSARY when the following criteria have been met: Diagnosis: • When tissue-based CGP is infeasible (i.e., quantity not sufficient for tissue-based CGP or invasive biopsy is medically contraindicated), AND • When prior results for ALL of the following tests are not available: o EGFR single nucleotide variants (SNVs) and insertions and deletions (indels) o ALK and ROS1 rearrangements o PDL1 expression. Progression: • Patients progressing on or after chemotherapy or immunotherapy who have never been tested for EGFR SNVs and indels, and ALK and ROS1 rearrangements, and for whom tissue-based CGP is infeasible (i.e., quantity not sufficient for tissue-based CGP), OR • For patients progressing on EGFR tyrosine kinase inhibitors (TKIs). If no genetic alteration is detected by Guardant360®, or if circulating tumor DNA (ctDNA) is insufficient/not detected, tissue-based genotyping should be considered. Other plasma-based CGP tests are considered INVESTIGATIONAL. CGP and the use of circulating tumor DNA is considered INVESTIGATIONAL for all other indications. 1 The use of circulating tumor cells is considered INVESTIGATIONAL for all indications. -
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. -
Medical Microbiology and Infectious Diseases 22% Specialists in 2017 = 11%3
Medical Microbiology & Infectious Diseases Profile Updated December 2019 1 Table of Contents Slide . General Information 3-5 . Total number & number/100,000 population by province, 2019 6 . Number/100,000 population, 1995-2019 7 . Number by gender & year, 1995-2019 8 . Percentage by gender & age, 2019 9 . Number by gender & age, 2019 10 . Percentage by main work setting, 2019 11 . Percentage by practice organization, 2017 12 . Hours worked per week (excluding on-call), 2019 13 . On-call duty hours per month, 2019 14 . Percentage by remuneration method 15 . Professional & work-life balance satisfaction, 2019 16 . Number of retirees during the three year period of 2016-2018 17 . Employment situation, 2017 18 . Links to additional resources 19 2 General information Microbiology and infectious diseases focuses on the diagnosis and treatment of infectious diseases; thus, it is concerned with human illness due to micro-organisms. Since such disease can affect any and all organs and systems, this specialist must be prepared to deal with any region of the body. The specialty of Medical Microbiology and Infectious Disease consists primarily of four major spheres of activity: 1. the provision of clinical consultations on the investigation, diagnosis and treatment of patients suffering from infectious diseases; 2. the establishment and direction of infection control programs across the continuum of care; 3. public health and communicable disease prevention and epidemiology; 4. the scientific and administrative direction of a diagnostic microbiology laboratory. Source: Pathway evaluation program 3 General information Once you’ve completed medical school, it takes an additional 5 years of Royal College-approved residency training to become certified in medical microbiology and infectious disease. -
Diagnostic Tests Diagnostic Tests Attempt to Classify Whether Somebody Has a Disease Or Not Before Symptoms Are Present
community project encouraging academics to share statistics support resources All stcp resources are released under a Creative Commons licence stcp-rothwell-diagnostictests Diagnostic Tests Diagnostic tests attempt to classify whether somebody has a disease or not before symptoms are present. We are interested in detecting the disease early, while it is still curable. However, there is a need to establish how good a diagnostic test is in detecting disease. In this situation a 2x2 table similar to the below would be produced to test how effective a diagnostic test is at predicting the outcome of interest. A number of different measures can be calculated from this information. True Diagnosis Disease +ve Disease -ve Total Test Results +ve a b a+b -ve c d c+d a+c b+d N = This is the proportion of diseased individuals that are correctly Sensitivity: ( ) identified by the test as having the disease. (+ | ) + = This is the proportion of non-diseased individuals that Specificity: ( ) are correctly identified by the test as not having the disease. ( | ) + = This is the proportion − of individuals with Positive Predictive Value**: ( ) positive test results that are correctly diagnosed and actually have the disease. ( | + ) + = This is the proportion of individuals with Negative Predictive Value**: ( ) negative test results that are correctly diagnosed and do not have the disease. ( | + ) − © Joanne Rothwell Reviewer: Chris Knox University of Sheffield University of Sheffield Medical Statistics – diagnostic tests Positive Likelihood Ratio: = This gives a ratio of the test being positive + for patients with disease compared with those without disease. Aim to be much greater − than 1 for a good test. -
Diabetic Foot and Gangrene
11 Diabetic Foot and Gangrene Jude Rodrigues and Nivedita Mitta Department of Surgery, Goa Medical College, India 1. Introduction “Early intervention in order to prevent potential disaster in the management of Diabetic foot is not only a great responsibility, but also a great opportunity” Despite advances in our understanding and treatment of diabetes mellitus, diabetic foot disease still remains a terrifying problem. Diabetes is recognized as the most common cause of non-traumatic lower limb amputation in the western world, with individuals over 20 times more likely to undergo an amputation compared to the rest of the population. There is growing evidence that the vascular contribution to diabetic foot disease is greater than was previously realised. This is important because, unlike peripheral neuropathy, Peripheral Arterial Occlusive Disease (PAOD) due to atherosclerosis, is generally far more amenable to therapeutic intervention. PAOD, has been demonstrated to be a greater risk factor than neuropathy in both foot ulceration and lower limb amputation in patients with diabetes. Diabetes is associated with macrovascular and microvascular disease. The term peripheral vascular disease may be more appropriate when referring to lower limb tissue perfusion in diabetes, as this encompasses the influence of both microvascular dysfunction and PAOD. Richards-George P. in his paper about vasculopathy on Jamaican diabetic clinic attendees showed that Doppler measurements of ankle/brachial pressure index (A/BI) revealed that 23% of the diabetics had peripheral occlusive arterial disease (POAD) which was mostly asymptomatic. This underscores the need for regular Doppler A/BI testing in order to improve the recognition, and treatment of POAD. -
Defining Malaria Burden from Morbidity and Mortality Records, Self Treatment Practices and Serological Data in Magugu, Babati District, Northern Tanzania
Tanzania Journal of Health Research Volume 13, Number 2, April 2011 Defining malaria burden from morbidity and mortality records, self treatment practices and serological data in Magugu, Babati District, northern Tanzania CHARLES MWANZIVA1*, ALPHAXARD MANJURANO2, ERASTO MBUGI3, CLEMENT MWEYA4, HUMPHREY MKALI5, MAGGIE P. KIVUYO6, ALEX SANGA7, ARNOLD NDARO1, WILLIAM CHAMBO8, ABAS MKWIZU9, JOVIN KITAU1, REGINALD KAVISHE11, WIL DOLMANS10, JAFFU CHILONGOLA1 and FRANKLIN W. MOSHA1 1Kilimanjaro Clinical Research Institute, P. O. Box 2236, Moshi, Tanzania 2Joint Malaria Programme, Moshi, Tanzania 3Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania 4Tukuyu Medical Research Centre, Tukuyu, Tanzania 5Tabora Medical Research Centre, Tabora, Tanzania 6Ngongongare Medical Research Station, Usa River, Tanzania 7St. John University of Tanzania, Dodoma, Tanzania 8Amani Medical Research Centre, Muheza, Tanzania 9Magugu Health Centre, Babati, Manyara, Tanzania 10 Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands Abstract: Malaria morbidity and mortality data from clinical records provide essential information towards defining disease burden in the area and for planning control strategies, but should be augmented with data on transmission intensity and serological data as measures for exposure to malaria. The objective of this study was to estimate the malaria burden based on serological data and prevalence of malaria, and compare it with existing self-treatment practices in Magugu in Babati District of northern Tanzania. Prospectively, 470 individuals were selected for the study. Both microscopy and Rapid Diagnostic Test (RDT) were used for malaria diagnosis. Seroprevalence of antibodies to merozoite surface proteins (MSP- 119) and apical membrane antigen (AMA-1) was performed and the entomological inoculation rate (EIR) was estimated. To complement this information, retrospective data on treatment history, prescriptions by physicians and use of bed nets were collected. -
Risk, Overdiagnosis and Ethical Justifications
Health Care Analysis (2019) 27:231–248 https://doi.org/10.1007/s10728-019-00369-7 ORIGINAL ARTICLE Risk, Overdiagnosis and Ethical Justifcations Wendy A. Rogers1 · Vikki A. Entwistle2 · Stacy M. Carter3 Published online: 4 May 2019 © The Author(s) 2019 Abstract Many healthcare practices expose people to risks of harmful outcomes. However, the major theories of moral philosophy struggle to assess whether, when and why it is ethically justifable to expose individuals to risks, as opposed to actually harming them. Sven Ove Hansson has proposed an approach to the ethical assessment of risk imposition that encourages attention to factors including questions of justice in the distribution of advantage and risk, people’s acceptance or otherwise of risks, and the scope individuals have to infuence the practices that generate risk. This paper investigates the ethical justifability of preventive healthcare practices that expose people to risks including overdiagnosis. We applied Hansson’s framework to three such practices: an ‘ideal’ breast screening service, a commercial personal genome testing service, and a guideline that lowers the diagnostic threshold for hypertension. The framework was challenging to apply, not least because healthcare has unclear boundaries and involves highly complex practices. Nonetheless, the framework encouraged attention to issues that would be widely recognised as morally pertinent. Our assessment supports the view that at least some preventive healthcare practices that impose risks including that of overdiagnosis are not ethically justifable. Further work is however needed to develop and/or test refned assessment criteria and guid‑ ance for applying them. Keywords Overdiagnosis · Risk · Uncertainty · Harm · Ethics · Risk evaluation * Wendy A. -
Diseases of Poverty and the 10/90 Gap Diseases of Poverty and the 10/90 Gap Diseases of Poverty and the 10/90 Gap
Diseases of poverty and the 10/90 gap Diseases of poverty and the 10/90 Gap Diseases of poverty and the 10/90 Gap Written by Philip Stevens, Director of Health Projects, International Policy Network November 2004 International Policy Network Third Floor, Bedford Chambers The Piazza London WC2E 8HA UK t : +4420 7836 0750 f: +4420 7836 0756 e: [email protected] w : www.policynetwork.net © International Policy Network 2004 Designed and typeset in Latin 725 by MacGuru Ltd [email protected] Cover design by Sarah Hyndman Printed in Great Britain by Hanway Print Centre 102–106 Essex Road Islington N1 8LU All rights reserved. Without limiting the rights under copyright reserved above, no part of this publication may be reproduced, stored or introduced into a retrieval system, or transmitted, in any form or by any means (electronic, mechanical, photocopying, recording or otherwise) without the prior written permission of both the copyright owner and the publisher of this book. Diseases of poverty and the 10/90 Gap Introduction: What is the 10/90 Gap? Figure 1 Number of daily deaths from diseases7 Activists claim that only 10 per cent of global health research is devoted to conditions that account for 90 Respiratory 10,814 per cent of the global disease burden – the so-called infections 1 ‘10/90 Gap’. They argue that virtually all diseases HIV/ 7,852 AIDS prevalent in low income countries are ‘neglected’ Diarrhoeal 5,482 and that the pharmaceutical industry has invested diseases almost nothing in research and development (R&D) Tuberculosis 4,504 for these diseases. -
Human Resource for Health Migration: an Analysis from the Perspective of Utilitarianism Rupesh Gautam University of Southern Denmark, [email protected]
Online Journal of Health Ethics Volume 12 | Issue 1 Article 5 Human Resource for Health Migration: An Analysis from the Perspective of Utilitarianism Rupesh Gautam University of Southern Denmark, [email protected] Pawan Acharya University of Southern Denmark, [email protected] Follow this and additional works at: http://aquila.usm.edu/ojhe Recommended Citation Gautam, R., & Acharya, P. (2016). Human Resource for Health Migration: An Analysis from the Perspective of Utilitarianism. Online Journal of Health Ethics, 12(1). http://dx.doi.org/10.18785/ ojhe.1201.05 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Online Journal of Health Ethics by an authorized administrator of The Aquila Digital Community. For more information, please contact [email protected]. Human Resource for Health Migration: An Analysis from the Perspective of Utilitarianism Introduction Medical brain drain or health-worker migration is a part of what has been labeled a global health workforce crisis and is characterized by the migration of trained and skilled health workers (doctors, nurses, and midwives) from low-income countries to high-income countries. It leads to loss in human capital for the developing countries, uneven distribution of those professionals between the affluent and poor countries and more severe suffering for the latter, due to the heavy disease burden (Kollar & Buyx, 2013; WHO, 2006). According to an estimate by WHO, a healthcare system is considered unable to deliver essential health services if it operates with fewer than 23 health workers (doctors, nurses, or midwives) for every 10,000 members of its population (WHO, 2006). -
Why Neglected Tropical Diseases Matter in Reducing Poverty 1.42 MB
July 2013 Working Paper 03 Why neglected tropical diseases matter in reducing poverty Fiona Samuels and Romina Rodríguez Pose • Neglected tropical diseases (NTDs) have a direct impact on the achievement This and other Development of the Millennium Development Goals (MDGs). Without addressing these Progress materials are available at Key diseases, the broader aim of poverty alleviation is unlikely to be achieved. developmentprogress.org messages • Straightforward and highly cost-effective strategies are available to control Development Progress is an ODI project and eventually eradicate or eliminate NTDs. that aims to measure, understand and communicate where and how progress • Success in controlling, eliminating or eradicating NTDs depends on has been made in development. partnerships between multiple constituencies that enable countries to adapt international guidelines to local contexts, integrate NTD programmes into ODI is the UK’s leading independent think tank on international development health systems and engage communities in implementation. and humanitarian issues. Further ODI materials are available at odi.org.uk Introduction indicators specific to them (Molyneux, 2008). While neglected tropical diseases (NTDs) One possible explanation for have been recognised for centuries – international disinterest is that NTDs indeed as ‘biblical plagues’ – NTDs have, almost exclusively affect the developing as the name implies, remained below the world (though this is also true for malaria) radar of most international and national and are not likely to spread far beyond; policy-makers. indeed, many NTDs have disappeared This relative neglect can be seen in completely in the developed world due examining the Millennium Development to improved hygiene and sanitation Goal (MDG) framework: while NTDs standards.