Department of Medicines Policy and Standards The WHO Model List of Essential Medicines – Palliative Care update Suzanne Hill World Health Organisation.

Slides:



Advertisements
Similar presentations
1 MDG Target 8.E gap analysis Dr Hans Hogerzeil Director, Department of Essential Medicines and Pharmaceutical Policies, World Health Organization October.
Advertisements

February 2006 WHO's Contribution to Scaling Up towards Universal Access to HIV/AIDS Prevention, Care and Treatment Department of HIV/AIDS.
Technical cooperation with countries Technical Cooperation for essential drugs and traditional medicines September 2005.
The concept of essential drugs and the
The concept of essential drugs and the
Medication Management
WHO update on: Guidelines for the selection of RH medicines and prequalification of priority RH medicines Medicines Policy and Standards Health Technology.
Key elements to develop a national strategic plan for TB control Malgosia Grzemska Stop TB Department WHO, Geneva, Switzerland EURO/TBTEAM Regional Workshop.
Essential Medicines List: Concept and Procedures 1 |1 | WHO Essential Medicines List Concept and Process WHO Essential Medicines List Concept and Process.
MEDICINES SELECTION & FORMULARY MANAGEMENT
Role of Pharmacoeconomics in a Developing country context Gavin Steel for Anban Pillay Cluster Manager: Health Economics National Department of Health.
Rational Use of Injections within National Drug Policies World health organisation Essential Drugs and Medicines Policy Safe Injection Global Network Cairo.
PSK Annual Conference 2008 Palliative care medicine: A balanced approach to opioid availability and safe use in Kenya Presenter: Dr. Bilha Kiama-Murage.
1 EFCA - 21th March 2002 Raul Mateus Paula. 2 This presentation underlines: The key objectives of the Relex Reform The division of the responsibilities.
25 Years of Essential Medicines Jonathan D. Quick, MD, MPH Hans V. Hogerzeil, MD, PhD WHO Essential Drugs and Medicines Policy May 2002.
CADTH Therapeutic Reviews
The ICH E5 Question and Answer Document Status and Content Robert T. O’Neill, Ph.D. Director, Office of Biostatistics, CDER, FDA Presented at the 4th Kitasato-Harvard.
Effectiveness Evaluation for Therapeutic Drugs for Non-Food Animals
Clinical Trials of Traditional Herbal Medicines In India Y.K.Gupta Professor & Head, Department of Pharmacology, All India Institute of Medical Sciences,
1 Drug and Therapeutics Committee Session 10. Standard Treatment Guidelines.
Can there be essential medicines for rare diseases? Hans V. Hogerzeil, MD, PhD, FRCP Edin Director Medicines Policy and Standards World Health Organization.
Working as an ICTC Team ICTC Team Training. What is a team A group of people working in an organisation can be called a team “when there is interdependency.
From Evidence to EMS Practice: Building the National Model Eddy Lang, MD, CFPC (EM), CSPQ SMBD-Jewish General Hospital, McGill University Montreal, Canada.
Essential Medicines Technical Briefing Seminar 1 |1 | Access to essential medicines for NCDs WHO EMP and NVI Departments Access to essential medicines.
Generating evidence for change: Implementing the post-ICIUM research agenda Dennis Ross-Degnan, ScD Harvard Medical School and Harvard Pilgrim Health Care.
National Medicine Policy
Selection of essential medicines
Occupational health nursing
Dr. Tahereh Safarnavadeh Clinical Pharmacist The Formulary Process In the Name of GOD.
The Concept of Essential Medicines and the WHO Model List of Essential Medicines Technical Briefing Seminar 29 th October 2013 Department of Essential.
Summary of ICIUM Chronic Care Track Prepared by: Ricardo Perez-Cuevas Veronika Wirtz David Beran.
Improving Access and Quality Use of Medicines in Palliative Care within National Drug Policy, Regulatory, and Funding Frameworks Debra Rowett, Tania Shelby-James,
10/15/ :127 Pharmaceutical Management for Underserved Populations 1 Drug Management Cycle: Selection Essential Drugs Treatment Guidelines Formularies.
The Global Fund - Proposal Process & Round 8 February 19, 2008.
Selection of essential medicines Hans V. Hogerzeil, MD, PhD, FRCP Edin Director Medicines Policy and Standards September 2005 Department of Medicines Policy.
Organization and guideline development April 2010 ACCC The Netherlands.
ACCESS TO MEDICINES - POLICY AND ISSUES
Supporting Informed Formulary Decision Making: CADTH’s Common Drug Review Denis Bélanger, Director, CADTH New Brunswick Stroke Summit November 27, 2010,
University of Wisconsin Pain & Policy Studies Group World Health Organization Collaborating Center for Pain Policy and Palliative Care Action Plan for:
ABSTRACT Title: Developing National Formularies Based on the WHO Model Formulary Authors: Tisocki K 3, Laing RL 1, Hogerzeil H 1, Mehta DK 2, Ryan RSM.
BASELINE SURVEYS AND MONITORING OF PHARMACEUTICAL SITUATION IN COUNTRIES. Joseph Serutoke NPO/EDM WHO Uganda November 2002.
Social Pharmacy Lecture no. 6 Rational use of drugs Dr. Padma GM Rao
Single Convention on Narcotic Drugs Establishes a regulatory system for narcotic drugs government authorization is required for participation in the trade.
Promoting Drug and Therapeutics Committees in the Developing World
04_DirectorReport_PCC/1 9/2004 Rita Kabra_/1 Access to essential medicines for Maternal and Newborn Health Dr Rita Kabra Making Pregnancy Safer WHO/EDM.
PATIENT-CENTERED OUTCOMES RESEARCH INSTITUTE PCORI Board of Governors Meeting Washington, DC September 24, 2012 Anne Beal, MD, MPH, Chief Operating Officer.
Selection of essential medicines Suzanne Hill September 2006 Department of Medicines Policy and Standards TBS 2006.
COMPARATIVE ANALYSIS OF SELECTED ESSENTIAL DRUG LISTS AZIZ JAFAROV/RICHARD LAING.
Selection of essential medicines Richard Laing and Deidre Dimancesco TBS 2011 Department of Essential Medicines & Pharmaceutical Policies TBS 2008.
Portfolio Committee for Health Medicines and Related Substances Amendment Bill (06/08/08) IMSA represents Research Based Pharmaceutical Companies.
'Hot topics' ESSENTIAL MEDICINES FOR CHILDREN Suzanne Hill September 2006.
Rational Selection of Essential Medicines Tim Reed World health Assembly May 2014.
Guidelines Recommandations. Role Ideal mediator for bridging between research findings and actual clinical practice Ideal tool for professionals, managers,
Prepared by: Imon Rahman Lecturer Department of Pharmacy BRAC University.
Training for organisations participating in Peer Review of Paediatric Diabetes.
WHO Estonia country office Marge Reinap Head of WHO Country Office in Estonia.
Health Technology Assessment
WHO Essential Drugs and Medicines Policy
Health Technology Assessment
CH 20: PAIN NATIONAL DEPARTMENT OF HEALTH PRIMARY HEALTHCARE 2014
WHO Essential Drugs and Medicines Policy
ABSTRACT   Qualitative and Quantitative Assessment of the Essential Medicines List of Delhi State: A Time Series Analysis. Gupta U, Sangeeta S, Baishya.
Essential Drugs and Medicines Policy
Background Cancers are among the leading causes of morbidity and mortality worldwide, responsible for 18.1 million new cases and 9.6 million deaths in.
Essential Drugs and Medicines Policy
Supporting Implementation of the EDL
Access to Essential Medicines
Towards International Harmonized Nomenclature for Medical Devices
Access to Essential Medicines
WHO Department of Essential Medicines and Health Products
Presentation transcript:

Department of Medicines Policy and Standards The WHO Model List of Essential Medicines – Palliative Care update Suzanne Hill World Health Organisation April 2006

Department of Medicines Policy and Standards Essential medicines n The concept of essential medicines A limited range of carefully selected essential medicines leads to better health care, better drug management, and lower costs n Definition of essential medicines Essential medicines are those that satisfy the priority health care needs of the population (2002)

Department of Medicines Policy and Standards Essential medicines n Are selected on the basis of  disease prevalence,  evidence of comparative efficacy, safety and cost- effectiveness n Are intended to be  Used in the context of functioning health systems  Available at all times in adequate amounts,  in the appropriate dosage forms,  with assured quality  at a price the individual and the community can afford

Department of Medicines Policy and Standards ‘Levelled’ lists  Core and complementary  Complementary medicines require specialist facilities or services  Default position is 'core'

Department of Medicines Policy and Standards The Essential Medicines Target SS All the drugs in the world Registered medicines National list of essential medicines Levels of use Supplementary specialist medicines CHW dispensary Health center Hospital Referral hospital Private sector

Department of Medicines Policy and Standards How many?  Ideally the best in each class for the purpose  Multiplicity confuses and may not help access  List one, up to 2-3 alternatives  Clear message  Flexibility in procurement  Competition between generics, rather than within class

Department of Medicines Policy and Standards Updating the list

Department of Medicines Policy and Standards Adding new medicines to the WHO Model List of Essential Medicines 1. Identification of public-health need for a medicine 2. Development of the medicine; phase I - II - III trials 3. Regulatory approval in a number of countries > Effective and safe medicine on the market 4.More experience under different field circumstances; post- marketing surveillance 5.Price indication for public sector use 6.Review by WHO disease programme; define comparative effectiveness and safety in real-life situations, comparative cost-effectiveness and public health relevance > Medicine included in WHO treatment guideline 7.Submission to WHO Expert Committee on Essential Medicines > Medicine included in WHO Model List

Department of Medicines Policy and Standards Role of treatment cost and global cost-effectiveness analyses 1. High cost alone should not exclude an essential medicine 2. Cost-effectiveness (C/E) comparisons are made among alternative medicines within the same therapeutic group 3. Price information from existing UN sources are used; all information sources will be identified 4. 'Formal' cost effectiveness analysis not yet required because methods for international analysis are not developed

Department of Medicines Policy and Standards Application review process 1.Application on WHO Medicines web site 2. Specialist assessment of comparative efficacy, safety and cost- effectiveness 3. Review of assessments by Expert Committee member (“presenter”); formulation of draft recommendation 4. Review of draft recommendation by relevant Expert Advisory Panel members; and posted on WHO Medicines web site 5. Review by presenter, prepares final draft recommendation 6. Discussion of draft recommendation and proposed text for WHO Model Formulary by the Expert Committee

Department of Medicines Policy and Standards Requirements for application  Who is applying  What the product is (INN, formulation)  What it is for  Availability and regulatory status  Supporting evidence:  Public health need  Comparative effectiveness and safety  Cost  Proposal for formulary text

Department of Medicines Policy and Standards Clinical guidelines and the model list of essential medicines List of common diseases and complaints Training and Supervision Financing and Supply of drugs Treatment guidelines Treatment choice Prevention and care Essential medicines list / National formulary

Department of Medicines Policy and Standards Updating WHO guidelines 1. Guideline development group with wide representation 2. Careful consideration of conflict of interest 3. Systematic search for evidence 4. Evaluation of quality of evidence 5. Systematic cost-effectiveness analysis 6. for WHO: evaluation of public health considerations 7. Graded recommendations with linked references 8. External review of draft recommendations Systematic and transparent process

Department of Medicines Policy and Standards So what does this mean for palliative care?

Department of Medicines Policy and Standards Guidelines and the list n The 14 th list recommends that everything in 'Cancer Pain Relief' be available. n Is that right?

Department of Medicines Policy and Standards Conditions covered n Pain in cancer patients n Analgesics, adjuvants ……… other symptoms? n Nausea/hiccups/dry mouth etc etc

Department of Medicines Policy and Standards Current medicines BASIC DRUGS  Aspirin  Paracetamol  ibuprofen  indometacin  Codeine  Morphine  Naloxone  Amitriptyline  Carbamazapine  Prednisolone  Dexamathasone ALTERNATIVES  Choline magnesium trisalcylate  Diflunisal  Naproxen  Diclofenac  Dihydrocodeine  Dextropropoxyphene  Standardised opium  Tramadol  Methadone  Hydromorphone  Oxycodone  Levorphanol  Pethidine  Buprenorphine  Imipramine  Valproic acid  Prednisone  Betamethasone

Department of Medicines Policy and Standards Current medicines BASIC DRUGS n Aspirin n Paracetamol n ibuprofen n Indometacin ? n Codeine n Morphine n Naloxone n Amitriptyline n Carbamazapine n Prednisolone n Dexamathasone ALTERNATIVES n Choline magnesium trisalcylate n Diflunisal n Naproxen n Diclofenac n Dihydrocodeine n Dextropropoxyphene ? n Standardised opium n Tramadol n Methadone n Hydromorphone n Oxycodone n Levorphanol n Pethidine  n Buprenorphine n Imipramine n Valproic acid n Prednisone n Betamethasone ?

Department of Medicines Policy and Standards Questions  What should be done to the guidelines?  Cancer pain control update?  General palliative care?  Population specific guidelines?  How can the guidelines be updated?  To do a WHO guideline =$200K minimum  Can this meeting 'scope' the guidelines?  Should the palliative care section of the Model EML change? To list the specific drugs?  What are the priority medicines for addition and deletion?  Who and how will the applications be prepared?

Department of Medicines Policy and Standards timelines  Guidelines  'rapid advice' takes 4 months  Full guidelines take 12 months  EML  Next meeting March 2007  Applications close October  Need for experts to advise the Committee