Malaria ~ Frequently Asked Questions
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Meeting Report
Meeting Report EXPERT CONSULTATION ON PLASMODIUM KNOWLESI MALARIA TO GUIDE MALARIA ELIMINATION STRATEGIES 1–2 March 2017 Kota Kinabalu, Malaysia Expert Consultation on Plasmodium Knowlesi Malaria to Guide Malaria Elimination Strategies 1–2 March 2017 Kota Kinabalu, Malaysia WORLD HEALTH ORGANIZATION REGIONAL OFFICE FOR THE WESTERN PACIFIC RS/2017/GE/05/(MYS) English only MEETING REPORT EXPERT CONSULTATION ON PLASMODIUM KNOWLESI MALARIA TO GUIDE MALARIA ELIMINATION STRATEGIES Convened by: WORLD HEALTH ORGANIZATION REGIONAL OFFICE FOR THE WESTERN PACIFIC Kota Kinabalu, Malaysia 1–2 March 2017 Not for sale Printed and distributed by: World Health Organization Regional Office for the Western Pacific Manila, Philippines September 2017 NOTE The views expressed in this report are those of the participants of the Expert Consultation on Plasmodium knowlesi Malaria to Guide Malaria Elimination Strategies and do not necessarily reflect the policies of the World Health Organization. This report has been prepared by the World Health Organization Regional Office for the Western Pacific for governments of Member States in the Region and for those who participated in the Expert Consultation on Plasmodium knowlesi Malaria to Guide Malaria Elimination Strategies, which was held in Kota Kinabalu, Malaysia from 1 to 2 March 2017. CONTENTS ABBREVIATIONS SUMMARY 1. INTRODUCTION ............................................................................................................................................. 1 2. PROCEEDINGS ............................................................................................................................................... -
Malaria Treatment in Africa
Malaria Treatment in Africa Africa Fighting Malaria Policy Paper May 2008 By Richard Tren, Philip Coticelli, Roger Bate and Kimberly Hess AFRICA FIGHTING MALARIA 1050 17th Street, NW P.O Box 17156 Suite 520 Congella Washington DC, 20036 4013 United States South Africa www.fightingmalaria.org Table of Contents I. Executive Summary.................................................................................................................3 II. Key Recommendations...........................................................................................................5 III. Introduction: Advocates Drive Reform..................................................................................6 IV. Private Sector Regulation......................................................................................................8 V. Public Funding for Drugs: Quantity vs. Quality....................................................................11 VI. Generic and Local Pharmaceutical Production.....................................................................15 VII. The Affordable Medicines Facility- malaria (AMFm) ........................................................19 VIII. What Africa Still Lacks: Functioning Health Systems.......................................................22 IX. Conclusion..........................................................................................................................25 X. Endnotes ..............................................................................................................................26 -
Manual for the Microscopical Diagnosis of Malaria in Man
NATIONAL INSTITUTE OP HEALTH Bulletin No. 180 MANUAL FOR THE MICROSCOPICAL DIAGNOSIS OF MALARIA IN MAN Federal Security Agency U. S. PUBLIC HEALTH SERVICE Washington, D. C. FEDERAL SECURITY AGENCY U. S. PUBLIC HEALTH SERVICE National Institute of Health Bulletin No. 180 MANUAL FOR THE MICROSCOPICAL DIAGNOSIS OF MALARIA IN MAN By AIMEE WILCOX, Assistant Technologist U. S. Public Health Service From the Division of Infectious Diseases National Institute of Health UNITED STATES GOVERNMENT PRINTING OFFICE WASHINGTON : 1942 For sale by the Superintendent ofDocuments, Washington, D. C. - - - - - - Price 30 cents ORGANIZATION OF THE NATIONAL INSTITUTE OF HEALTH Thomas Parran, Surgeon General, United States Public Health Service Dyer, R. E, Director, National Institute of Health Division of Biologics Control.—Chief, Senior Surgeon M. Y. Yeldee. Division of Chemistry.—Chief, Professor C. S. Hudson. Division of Chemotherapy.—Chief, Surgeon W. H. Sebrell, Jr. Division of Industrial Hygiene.—Chief, Medical Director J. G. Townsend. Division of Infectious Diseases. —Chief, Senior Surgeon Charles Armstrong. Division of Pathology.—Chief, Senior Surgeon R. D. Lillie. Division of Public Health Methods. —Chief, G. St.J. Perrott. Division of Zoology.-—Chief, Professor W. H. Wright. National Cancer Institute. —Chief, Pharmacologist Director Carl Voegtlin. FOREWORD This manual begins with a description of the morphology and life history of the parasites of the different species of malaria, a descrip- tion which is clear and thorough and should be useful to both the beginner in the subject and to one who may wish a concise review. The author uses throughout the terminology recommended by the Sub-Committee of the Health Organization of the League of Nations. -
WHO Guidelines for the Treatment of Malaria
GTMcover-production.pdf 11.1.2006 7:10:05 GUIDELINES FOR THE TREATMENT O F M A L A R I A GUIDELINES FOR THE TREATMENT OF MALARIA Guidelines for the treatment of malaria Guidelines for the treatment of malaria WHO Library Cataloguing-in-Publication Data Guidelines for the treatment of malaria/World Health Organization. Running title: WHO guidelines for the treatment of malaria. 1. Malaria – drug therapy. 2. Malaria – diagnosis. 3. Antimalarials – administration and dosage. 4. Drug therapy, Combination. 5. Guidelines. I. Title. II. Title: WHO guidelines for the treatment of malaria. ISBN 92 4 154694 8 (NLM classification: WC 770) ISBN 978 92 4 154694 2 WHO/HTM/MAL/2006.1108 © World Health Organization, 2006 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20, avenue Appia, 1211 Geneva 27, Switzerland (tel. +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press, at the above address (fax: +41 22 791 4806; e-mail: [email protected]). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. -
Laboratory Diagnosis of Malaria Infection – a Short Review of Methods
Laboratory diagnosis of malaria infection – A short review of methods Kesinee Chotivanich1 Kamolrat Silamut2 Nicholas P J Day2,3 1Department of Clinical Tropical Medicine, Faculty of Tropical Medicine. Mahidol University. Bangkok. Thailand 2Wellcome Trust-Mahidol University-Oxford Tropical Medicine Programme, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand 3Center for Clinical Vaccinology and Tropical Medicine, Nuffield Department of Clinical Medicine, Churchill Hospital, University of Oxford, Oxford, United Kingdom. Abstract diagnosis. Microscopic diagnosis of malaria is performed by staining Malaria is one of the most important tropical infectious diseases. The thick and thin blood films on a glass slide to visualize the malaria incidence of malaria worldwide is estimated to be 300–500 million parasite (2). Briefly, the patient’s finger is cleaned with alcohol, allowed clinical cases each year with a mortality of between one and three to dry and then the side of the fingertip is pricked with a sharp sterile million people worldwide annually. The accurate and timely diagnosis lancet or needle and two drops of blood are placed on a glass slide. To of malaria infection is essential if severe complications and mortality prepare a thick blood film, a blood spot is stirred in a circular motion are to be reduced by early specific antimalarial treatment. This review with the corner of the slide, taking care not make the preparation details the methods for the laboratory diagnosis of malaria infection. too thick, and allowed to dry without fixative. As they are unfixed the red cells lyse when a water based stain is applied. A thin blood film is Keywords: malaria, diagnosis, microscopy, rapid prepared by immediately placing the smooth edge of a spreader slide in the drop of blood, adjusting the angle between slide and spreader This article has previously been published in the Australian Journal of to 45°, and then smearing the blood with a swift and steady sweep Medical Science 2006; 27 (1): 11-15 and is reprinted here with kind along the surface. -
Treatment of Malaria: Guidelines for Clinicians
TREATMENT GUIDELINES Treatment of Malaria (Guidelines For Clinicians) If you wish to share your clinical experience, please contact us at: [email protected] Treatment Table The Treatment Table is available in PDF format at www.cdc.gov/malaria/pdf/treatmenttable.pdf Reporting We encourage clinicians to report all cases of laboratory-confirmed malaria to help CDC's surveillance efforts. Refer to our information on the Malaria Case Surveillance Report Form (http://www.cdc.gov/malaria/report.html). Evaluation and Diagnosis Because malaria cases are seen relatively rarely in North America, misdiagnosis by clinicians and laboratorians has been a commonly documented problem in published reports. However, malaria may be a common illness in areas where it is transmitted and therefore the diagnosis of malaria should routinely be considered for any febrile person who has traveled to an area with known malaria transmission in the past several months preceding symptom onset. Symptoms of malaria are generally non-specific and most commonly consist of fever, malaise, weakness, gastrointestinal complaints (nausea, vomiting, diarrhea), neurologic complaints (dizziness, confusion, disorientation, coma), headache, back pain, myalgia, chills, and/or cough. The diagnosis of malaria should also be considered in any person with fever of unknown origin regardless of travel history. Patients suspected of having malaria infection should be urgently evaluated. Treatment for malaria should not be initiated until the diagnosis has been confirmed by laboratory investigations. "Presumptive treatment" without the benefit of laboratory confirmation should be reserved for extreme circumstances (strong clinical suspicion, severe disease, impossibility of obtaining prompt laboratory confirmation, usually by microscopy). Laboratory diagnosis of malaria can be made through microscopic examination of thick and thin blood smears. -
Vaccines As a Preventive Modality for Malaria: a Review
Vaccines as a Preventive Modality for Malaria: A Review Alka K. Singh, Vivek M. Ghate, Shaila A. Lewis Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India Abstract Malaria is one among the several parasitic infections that continue to claim lives despite the tremendous progress in the techniques for diagnosis, prevention, and treatment. Although the figures of malaria-ridden patients are decreasing in all the countries due to the collective efforts from all sectors of the society, the tropical countries are REVIEW ARTICLE REVIEW still facing severe setbacks in the implementation of the health measures due to the emergence of resistant strains and non-availability of appropriate medications at the required time. An efficient strategy would be to develop vaccines to prevent malaria from occurring than treating it. This review reflects the significant progress made in the field of vaccines and the challenges associated with it. A comprehensive summary is provided for the various diagnostic tests available for detecting malaria and the aspects of treatment related to infections during pregnancy. Key words: Diagnosis, malaria, parasite, pregnancy, vaccine INTRODUCTION to the population accounting for the death of one child (under the age of 5 years) every 2 min.[4] plague of the poor - malaria is a deadly disease caused by parasites.[1,2] In the The World Health Assembly has adopted a “Global Technical year 2016, the number of new cases Strategy for Malaria 2016–2030” in the year 2015, which A gives guidance to all the countries in the efforts they are of malaria was reported to touch 216 million, as a result of which the total number of deaths putting in for malaria eradication. -
Analysis of Research and Development Priorities for Malaria – Working Paper
Global Malaria Programme Analysis of research and development priorities for malaria – working paper In collaboration with the WHO Global Observatory on Health R&D Framework for a national insecticide resistance monitoring and management plan for malaria vectors Global Malaria Programme World Health Organization 20 Avenue Appia CH-1211 Geneva 27 Switzerland Prepared in collaboration with the Barcelona Institute for Global Health, the Malaria Eradication Scientific Alliance and WHO Global Malaria Programme August 2018 © World Health Organization 2018 All rights reserved. The content of this document is not final, and the text may be subject to revisions before publication. The document may not be reviewed, abstracted, quoted, reproduced, transmitted, distributed, translated or adapted, in part or in whole, in any form or by any means without the permission of the World Health Organization. CONTENTS LIST OF FIGURES AND TABLES ................................................................................................................................................................. 3 ACKNOWLEDGMENTS ................................................................................................................................................................................... 4 ABBREVIATIONS ................................................................................................................................................................................................ 5 EXECUTIVE SUMMARY ................................................................................................................................................................................ -
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Plasmodium coatneyi in Rhesus Macaques Replicates the Multisystemic Dysfunction of Severe Malaria in Humans Alberto Moreno, Emory University Monica Cabrera-Mora, Emory University Anapatricia Garcia, Emory University Jack Orkin, Emory University Elizabeth Strobert, Emory University John W. Barnwell, Centers for Disease Control and Prevention Mary R Galinski, Emory University Journal Title: Infection and Immunity Volume: Volume 81, Number 6 Publisher: American Society for Microbiology | 2013-06-01, Pages 1889-1904 Type of Work: Article | Final Publisher PDF Publisher DOI: 10.1128/IAI.00027-13 Permanent URL: https://pid.emory.edu/ark:/25593/s78xt Final published version: http://dx.doi.org/10.1128/IAI.00027-13 Copyright information: © 2013, American Society for Microbiology. All Rights Reserved. Accessed October 6, 2021 3:29 PM EDT Plasmodium coatneyi in Rhesus Macaques Replicates the Multisystemic Dysfunction of Severe Malaria in Humans Alberto Moreno,a,b Monica Cabrera-Mora,a AnaPatricia Garcia,c,d Jack Orkin,e Elizabeth Strobert,e John W. Barnwell,f Mary R. Galinskia,b Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USAa; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USAb; Division of Pathology, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USAc; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Emory University Hospital, Atlanta, Georgia, USAd; Division of Animal Resources, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USAe; Malaria Branch, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, USAf Severe malaria, a leading cause of mortality among children and nonimmune adults, is a multisystemic disorder characterized by complex clinical syndromes that are mechanistically poorly understood. -
The Push for Local Production, Costs and Benefits – a Case Study of Uganda’S Quality Chemicals
The push for local production, costs and benefits – A case study of Uganda’s Quality Chemicals Africa Fighting Malaria Policy Paper September 2009 James Taylor1, Roger Bate2,3, Emily Putze2, Richard Tren3 1 Graduate Student, Columbia University (SIPA) 2 American Enterprise Institute 3 Africa Fighting Malaria 1 Abstract Many Africans lack access to essential medicines. There are myriad reasons for this: poverty, lack of awareness about the need for treatment, confusion over which drugs to take, technical and logistical challenges in procurement and distribution combined with a general lack of local healthcare staff and infrastructure, among other cultural and political factors. One additional problem is the relatively high price of drugs, which the international community has prioritized by encouraging competition from various generic producers often through compulsory licensing. The latest cost-reduction strategy is the push for local drug production. But, as shown by the start-up problems of Quality Chemicals Industries Limited in Uganda, many burdens and barriers to access continue to seriously hinder the success of such enterprises. Indirect government subsidies to exporters selling into African markets, and pressure by donors and lobbyists on innovator producers to offer developing countries subsidized prices, actually undermine the competitiveness and viability of these nascent firms. Furthermore, the focus on drug pricing and local production can actually undermine the overall aim to increase access to medicines. Introduction “Essential medicines save lives and improve health when they are available, affordable, of assured quality and properly used.”4 Still, a lack of access to these life-saving medicines in developing countries remains one of the most pressing global public health concerns. -
The President's Malaria Initiative Fourth Annual Report To
The President’s Malaria Initiative Sustaining Momentum Against Malaria: Saving Lives in Africa Fourth Annual Report April 2010 The President’s Malaria Initiative Sustaining Momentum Against Malaria: Saving Lives in Africa Fourth Annual Report April 2010 Cover photo A child carries the long-lasting insecticide-treated net her family received during a net distribution campaign in her village in Ghana. To reduce the intolerable burden of malaria, the President’s Malaria Initiative targets those most vulnerable to the infection – children under the age of five and pregnant women. Credit Lisa Kramer/PMI ii Sustaining Momentum Against Malaria: Saving Lives in Africa www.pmi.gov TABLE OF CONTENTS Abbreviations and Acronyms . .v Executive Summary . .2 Chapter 1: Prevention – Insecticide-Treated Mosquito Nets . .11 Chapter 2: Prevention – Indoor Residual Spraying . .17 Chapter 3: Prevention – Malaria in Pregnancy . .23 Chapter 4: Case Management – Diagnosis and Treatment . .29 Chapter 5: Health Systems, Integration, and Country Capacity . .35 Chapter 6: Partnerships . .41 Chapter 7: Outcomes and Impact . .47 Chapter 8: U.S. Government Malaria Research . .53 Appendix 1: PMI Funding FY 2006–FY 2010 . .59 Appendix 2: PMI Activity Summary . .60 Appendix 3: PMI Country-Level Targets . .69 Acknowledgments . .70 Sustaining Momentum Against Malaria: Saving Lives in Africa www.pmi.gov iii iv Sustaining Momentum Against Malaria: Saving Lives in Africa www.pmi.gov ABBREVIATIONS AND ACRONYMS ACT Artemisinin-based combination therapy AL Artemether-lumefantrine -
Tracking Number: DDTBMQ000044
Drug Development Tool (DDT) Tracking number: DDTBMQ000044 Submission: Drug Development Tool Biomarker Qualification Proposal, received by Center for Drug Evaluation and Research (CDER) DDT name: Plasmodium falciparum 18S ribosomal (r)RNA/rDNA A type Context of use: The submitter proposed the following context of use: Detection of the P. falciparum 18S rRNA/rDNA is a safety (and efficacy) endpoint for initiating treatment before clinical malaria symptoms appear in subjects who have undergone P. falciparum sporozoite controlled human malaria infection (CHMI) in non-endemic regions. The biomarker can be tested for at ≥6 days post-CHMI in human whole blood. The P. falciparum 18S rRNA/rDNA biomarker must have been measured with one or more specific nucleic acid amplification-based methods. This biomarker is intended to replace the use of thick blood smear (TBS) microscopy for this endpoint. The context of use was modified during Biomarker Qualification Review Team discussions as follows: A monitoring biomarker to inform initiation of rescue treatment with an anti-malarial drug following controlled human malaria infection (CHMI) with P. falciparum sporozoites in healthy subjects from non-endemic areas enrolled in clinical studies for vaccine and drug development against P. falciparum. Submitter: Dr Sean C. Murphy, M.D., Ph.D. University of Washington Medical Center, Seattle, WA Digitally signed by Shukal Bala -S DN: c=US, o=U S. Government, ou=HHS, ou=FDA, ou=People, cn=Shukal Bala -S, Reviewer: Shukal Bala, Ph.D. Shukal Bala -S 0.9.2342.19200300.100.1.1=1300068480 Microbiologist Date: 2018.05.10 14:34 51 -04'00' Division of Anti-Infective Products (DAIP), Office of Antimicrobial Products (OAP), CDER Through: Sumati Nambiar, M.D., M.P.H.