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Program - Tuesday 23 October 2007
 

All conference attendants please use Angelsea Road!

8:00-9:00
Exhibits & Contributed Poster Presentations – Session III Viewing
8:30–9:30
Issue Panel – Session I (5 contributed panels)
 

USE OF HEALTH ECONOMIC / PHARMACOECONOMIC INFORMATION BY DECISION-MAKERS ISSUES

IP1: PHARMACOECONOMICS IN IRELAND, SCOTLAND AND WALES: A CELTIC PERSPECTIVE ON THE APPRAISAL OF PHARMACEUTICALS
Moderator: Mike F Drummond, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK
Panelist(s): Dyfrig Hughes, PhD, Senior Research Fellow, University of Wales, Bangor, UK; Keith Tolley, MPhil, Research Director, Mapi Values, Bollington, Cheshire, UK; Mairin Ryan, BSc, Pharm, PhD, Health Information & Quality Authority, Lecturer in Pharmacoeconomics, Trinity College Dublin, Dublin, Ireland

IP2: WHAT IS THE ROLE OF COST-EFFECTIVENESS DATA IN THERAPEUTIC INNOVATION AND INEQUALITIES OF HEALTH CARE?
Moderator: John Hutton, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK
Panelist(s): Uwe Siebert, PhD, MPH, MSc, Professor of Public Health, University for Health Sciences, Medical Informatics and Technology, Vienna, Austria; Mark JC Nuijten, MD, PhD, MBA, Consultant, Ars Accessus Medica/Erasmus University Rotterdam, Amsterdam, The Netherlands; Elly A. Stolk PhD, Senior Research Associate, Institute for Medical Technology Assessment, Erasmus Medical Center, Rotterdam, The Netherlands

CLINICAL OUTCOMES/TREATMENT GUIDELINES ISSUES

IP3: INSTITUTIONAL DEVELOPMENTS IN HEALTH TECHNOLOGY ASSESSMENT AT MICRO AND MACRO LEVELS – IS RAISING STANDARDS THROUGH COMMON METHODOLOGIES AN ISSUE?
Moderator: Finn Boerlum Kristensen, MD, PhD, Director, National Board of Health, Copenhagen, Denmark
Panelist(s): Cari Almazan, Catalan Agency for Health Technology Assessment and Research (CAHTA), Barcelona, Spain; Americo Cicchetti, PhD, Professor of Health Care Management, Catholic University of Sacred Heart, Rome, Italy; Harri Sintonen, PhD, Professor, Department of Public Health, University of Helsinki, Helsinki, Finland

HEALTH CARE REIMBURSEMENT / COVERAGE ISSUES

IP4: REIMBURSEMENT DECISION PROCESSES IN EUROPE – IS THERE A POSSIBILTY OF PARTIALLY HARMONIZED APPROACH?
Moderator: Fabian Waechter, MD, MSc, Medical Assessor, Project Manager, AGES PharmMed - the Austrian Medicines Agency, Wien, Austria
Panelist(s): Richard Bergström, Vice Director, LIF Sweden, Stockholm, Sweden

HEALTH POLICY ISSUES

IP5: VALUE-BASED PRICING: SOLUTION OR ILLUSION?
Moderator: Mark Sculpher, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK.
Panelist(s): Martin Buxton, BSc, Professor of Economics and Director, Health Economics Research Group, Brunel University, London,UK; William Comanor, PhD, Professor, Department of Health Services, UCLA School of Public Health, Los Angeles, CA, USA; John O'Donnell, PhD, Sr. Director Health Policy, External Medical Affairs, AstraZeneca Pharmaceuticals, Wilmington, DE, USA.

   
9:30-10:00
Break, Exhibits & Contributed Poster Presentations – Session III Viewing
  View Poster Presentations in Session III
10:00-11:00
Issue Panel – Session II (5 contributed panels)
 

USE OF HEALTH ECONOMIC / PHARMACOECONOMIC INFORMATION BY DECISION-MAKERS ISSUES

IP6: THE HTA “REVOLUTION” IN EUROPE: THE FUTURE IS BRIGHT, THE FUTURE IS COST-EFFECTIVENESS?
Moderator: Keith Tolley, MPhil, Research Director, Mapi Values, Bollington, Cheshire, UK
Panelist(s): Carole Longson, PhD, Director, National Institute for Health and Clinical Excellence (NICE), London, UK; Michael Barry, PhD, MD, Clinical Director, National Centre for Pharmacoeconomics, St. James’s Hospital & Senior Lecturer in Clinical Pharmacology, Trinity College Dublin, Dublin, Ireland; Hilda Bastian, Head of Department; Health Information, Institute for Quality and Efficiency in Health Care (IQWiG), Cologne, Germany

HEALTH POLICY ISSUES

IP7: THE GERMAN WAY IN DEFINING AND APPLYING COST-EFFECTIVENESS-ANALYSES – REFLECTIONS FROM INTERNATIONAL EXPERIENCE
Moderator: Johann M Von der Schulenburg, PhD, Professor of Health Economics, Leibniz University Hannover, Hannover, Germany
Panelist(s): Peter T Sawicki, MD, Director, Institute for Quality and Efficiency in Health Care (IQWiG), Cologne, Germany; John Hutton, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK; Ulf Persson, PhD, Program Director, The Swedish Institute for Health Economics, IHE, Lund, Sweden

IP8: DISPARITIES IN ACCESS TO CANCER CARE – THE KAROLINSKA REPORT
Moderator: Frans Rutten, PhD, Professor, Institute for Medical Technology Assessment (iMTA), Rotterdam, The Netherlands
Panelist(s): Nils Wilking, MD, PhD, Associate Professor, Karolinska Institute, Stockholm, Sweden; Bengt Jönsson, PhD, Professor, Stockholm School of Economics, Stockholm, Sweden; Mark JC Nuijten, MD, PhD, MBA, Consultant, Ars Accessus Medica/Erasmus University Rotterdam, Amsterdam, The Netherlands

PHARMACOECONOMIC / HEALTH ECONOMIC STUDY METHODOLOGY ISSUES

IP9: IMPLEMENTING "GOOD REGISTRY PRACTICE" - NEWLY DEFINED BEST PRACTICE RECOMMENDATIONS FOR THE DESIGN, USE, AND EVALUATION OF PATIENT REGISTRIES
Moderator: Richard Gliklich, MD, President, Outcome, Cambridge, MA, USA
Panelist(s): Kathryn Starzyk, MS, Associate Director of Scientific Affairs, Outcome, Cambridge, MA, USA; Sarah Garner, PhD, MRPharmS, Technical Adviser, National Institute for Health and Clinical Excellence (NICE), London, UK

MEDICAL DEVICE, DIAGNOSTICS AND BIOTECHNOLOGY ISSUES

IP10: ARE MEDICAL DEVICES MORE CHALLENGING TO EVALUATE THAN DRUGS?
Moderator: Mike F Drummond, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK
Panelist(s): Rosanna Tarricone, DrPH, Economic Affairs Director, EUCOMED, Brussels, Belgium; Adrian Griffin, MSc, BSc, Director of Health Outcomes, Johnson & Johnson, High Wycombe, Buckinghamshire, UK; Rod Taylor, PhD, MSc, Reader, PenTAG, Peninsular Medical School, Exeter, UK

   
11:30-13:00
Lunch, Exhibits & Contributed Poster Presentations – Session III Viewing
11:45-12:45
Educational Symposium sponsored by i3 Innovus
Can We Afford to Pay for Innovation?


How to balance delivering cost-effective health care, maximizing health, and stimulating continued research and development

Moderator:
Bengt Jönsson, DPhil, Professor, Health Economics, Stockholm School of Economics and Principal Consultant, i3 Innovus

Speakers:
Peter Hertzman, PhD, Director Corporate Affairs, Amgen Nordic
Thomas B. Cueni, Secretary General, Interpharma AG, Chair of European Federation of Pharmaceutical Industries and Associations Economic and Social Policy Committee (ESPC)
Alistair McGuire, DPhil, Professor of Health Economics, London School of Economics, Health and Social Care and Principal Consultant, i3 Innovus

Description:
The development of innovations in healthcare represent an important component of the current therapeutic arsenal, but budget constraints create tensions between delivering cost-effective health care, maximizing health, and stimulating continued research and development.  There are concerns that health technology assessment will stifle innovation in health care.  Major innovative breakthroughs are typically the result of smaller incremental steps, and failure to support incremental innovations may diminish the overall pace of innovation. When is innovation really innovative?  And how should we value innovation?

13:00-14:20
Third Plenary Session

CONDITIONAL REIMBURSEMENT BASED ON FUTURE RESEARCH

Moderator: Michael Drummond PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK
Speakers: Mark Sculpher PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK
Adrian Towse MA, MPhil, Director, Office of Health Economics, London, UK
Dr. Kalipso Chalkidou, Associate Director, Research and Development, National Institute for Health and Clinical Excellence (NICE), London, UK
Dr. Gepke Delwel, Senior Policy Advisor, CVZ Health Care Insurance Board, The Netherlands
Reimbursement agencies frequently face the problem that there is considerable uncertainty surrounding the cost-effectiveness of new drugs. The objectives of this session are to explore the desirability and feasibility of recommending use of the product conditional on further research being carried out. The key issues include the design, funding and monitoring of such research and the nature of any ‘risk-sharing’ scheme that may be associated with it.
14:20-14:30
Contributed Research Award Presentations
14:30-14:45
Break, Exhibits & Contributed Poster Presentations – Session III Viewing
14:45-15:45
Contributed Workshops - Session III (5 workshops in 4 categories)

CLINICAL OUTCOMES STUDY METHODOLOGY

W15: MIXED TREATMENT COMPARISON: A PRACTICAL APPROACH
DISCUSSION LEADERS: Sibilia Quilici, MSc, Senior Analyst, i3 Innovus, Health Outcomes, Uxbridge, Middlesex, UK; Keith Abrams, PhD, Professor of Medical Statistics, University of Leicester, Centre for Biostatistics & Genetic Epidemiology, Leicester, UK.

COST STUDY METHODOLOGY

W16: PROGRAMME BUDGETING AND MARGINAL ANALYSIS – ITS PLACE IN HEALTH ECONOMICS
DISCUSSION LEADERS: Monique Martin, MSc, MBA, Vice-President UK Operations, i3 Innovus, Uxbridge, Middlesex, UK; Alistair McGuire, PhD, Chair in Health Economics, London School of Economics, Health and Social Care, London, UK.

HEALTH CARE POLICY AND FORMULARY DEVELOPMENT USING OUTCOMES RESEARCH

W17: THE COST-EFFECTIVENESS THRESHOLD: A HURDLE FOR INNOVATION?
DISCUSSION LEADERS: Mark JC Nuijten, MD, PhD, MBA, Consultant, Ars Accessus Medica/Erasmus University Rotterdam, Amsterdam, The Netherlands; Rogier M Klok, PharmD, PhD, Health Outcomes Officer, Wyeth

W18: TRANSLATING CLINICAL TRIAL DATA TO LOCAL ENVIRONMENTS: THE VALIDITY OF EXTRAPOLATING DATA FOR HTA SUBMISSIONS
DISCUSSION LEADERS: Phil McEwan, PhD, Director, Cardiff Research Consortium, Cardiff, South Glamorgan, UK; Phil James, BSc, Director, CHKS, Alcester, Warwickshire, UK; Peter Sharplin, MSocSc, Head of Pharmaceutical Development, Cardiff Research Consortium, Cardiff, South Glamorgan, UK;

PATIENT-REPORTED OUTCOMES STUDY METHODOLOGY (INCLUDING PREFERENCE-BASED & COMPLIANCE STUDIES)

W19: IS THERE A CONSENSUS ON BEST-PRACTICE METHODS FOR STATED-PREFERENCE STUDIES?
DISCUSSION LEADERS: Semra Ozdemir, MS, Research Economist, RTI International, Research Triangle Park, NC, USA; F. Reed Johnson, PhD, Senior Fellow and Principal Economist, RTI International, Research Triangle Park, NC, USA; A. Brett Hauber, PhD, Senior Economist and Head, RTI International, Research Triangle Park, NC, USA

   
15:45-16:00
Break, Exhibits & Contributed Poster Presentations – Session III Viewing
16:00-17:00
Contributed Workshops - Session IV (5 workshops in 4 categories)

CLINICAL OUTCOMES STUDY METHODOLOGY

W20: ASSESSING THE EFFECTIVENESS OF COUNTER MATCHING AS A TOOL FOR IMPROVING THE EFFICIENCY OF THE NESTED CASE CONTROL DESIGN IN EFFECTIVENESS STUDIES
DISCUSSION LEADERS: Victor A Kiri, MSc, PhD, Director of Pharmacoepidemiology, PAREXEL International, Peri Approval Clinical Excellence (PACE), Uxbridge, London, Middlesex, UK; Camille Maringe, MSc, Epidemiology Fellow, GlaxoSmithKline R&D, Worldwide Epidemiology, London, Middlesex, UK.

COST STUDY METHODOLOGY

W21: ANALYSIS OF SECOND ORDER UNCERTAINTY FOR PATIENT-LEVEL SIMULATION MODELS USING META-MODELS
DISCUSSION LEADERS: Jeremy VM Chancellor, MSc, Director, i3 Innovus, Health Economics and Outcomes, Uxbridge, Middlesex, UK; Patrick Mollon, MD, MBA, MSc, Senior Associate Director, Pfizer Ltd, Outcomes Research, Sandwich, Kent, UK; Samuel Aballéa, MSc, Lead Research Analyst, i3 Innovus, Health Economics and Outcomes, Uxbridge, Middlesex, UK.

W22: THE IMPACT OF DIFFERENT RESOURCE COST DEFINITIONS ON RESULTS, INTERPRETATIONS, AND COMPARABILITY OF HEALTH ECONOMIC STUDIES
DISCUSSION LEADERS: Sandra L. Tunis, PhD, Senior Research Scientist, IMS Health Consulting, Health Economics and Outcomes Research, Noblesville, IN, USA; Elise M. Pelletier, MS, Director, IMS Health Consulting, Health Economics and Outcomes Research, Watertown, MA, USA; Meaghan St. Charles, MS, Research Scientist, IMS Health Consulting, Health Economics and Outcomes Research, Noblesville, IN, USA; Phil McEwan, PhD, Director, Cardiff Research Consortium, Cardiff, South Glamorgan, UK.

HEALTH CARE POLICY AND FORMULARY DEVELOPMENT USING OUTCOMES RESEARCH

W23: OPPORTUNITIES AND BARRIERS FOR ASSESSMENT OF EMERGING HEALTH TECHNOLOGIES: THE CASE OF PHARMACOGENETICS
DISCUSSION LEADERS: Katherine Payne, PhD, Health Economist, Manchester University, Academic Unit of Medical Genetics, Manchester, UK; Hans-Peter Dauben, MD, Head, International Affairs, German Institute for Medical Documentation and Information, Cologne, Germany; Emma Gutierrez de Mesa, PhD, Scientific Officer, European Commission, DG-JRC, IPTS, Seville, Spain.

PATIENT-REPORTED OUTCOMES STUDY METHODOLOGY (INCLUDING PREFERENCE-BASED & COMPLIANCE STUDIES)

W24: INTRODUCTION TO PROBABILISTIC CHOICE MODELS FOR THE MEASUREMENT OF HEALTH STATES
DISCUSSION LEADERS: Paul Krabbe, PhD, Senior Researcher, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands