Program - Sunday 21 October 2007 |
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All conference attendants please use Angelsea Road!
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8:00-12:00 |
Pre-Congress Short Courses |
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See Short Courses Program |
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12:00–13:00 |
Grand Opening & Contributed Poster Presentations – Session I Viewing |
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13:00-13:30 |
Welcome from the ISPOR President |
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Diana I. Brixner RPh, PhD, 2007-2008 ISPOR President, Associate Professor and Chair, Department of Pharmacotherapy, Executive Director Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, Utah, USA
Introduction and Congress Objectives
Program Committee Co-Chairs:
Michael Drummond PhD, ISPOR 2006-2007 President and Professor of Health Economics, Centre for Health Economics, University of York, York, 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 |
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13:30-15:00 |
First Plenary Session |
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IS SMALL BEAUTIFUL? CHALLENGES FACING IRELAND IN ADOPTING THE FOURTH HURDLE
| Moderator: |
Dr. Tony Holohan, Deputy Chief Medical Officer, Department of Health & Children, Dublin, Ireland |
| Speakers: |
Michael Barry PhD, MD, Clinical Director, National Centre for Pharmacoeconomics, St. James's Hospital & Senior Lecturer in Clinical Pharmacology, Trinity College Dublin, Dublin Ireland
John McLaughlin, Managing Director, sanofi-aventis Ireland Ltd., Dublin, Ireland
Ross Hattaway, Assistant Principal Officer, Primary Care II, Department of Health and Children, Dublin, Ireland |
Ireland is the latest in a growing list of European countries requiring pharmacoeconomic data to help inform decisions on the reimbursement of drugs. Although a relatively small European country, Ireland has a considerable level of pharmaceutical investment, both in research and manufacturing. In this session, the main challenges in adopting the Fourth Hurdle will be discussed, including setting priorities for evaluation, developing the necessary analytic skills and balancing the needs of the health sector with those of the broader economy. |
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15:00-15:30 |
Break, Exhibits & Contributed Poster Presentations – Session I Viewing |
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View Poster Presentations in Session I |
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15:30-16:30 |
Contributed Workshops I (7 workshops in 4 categories) |
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CLINICAL OUTCOMES STUDY METHODOLOGY
W1: OUTCOMES RESEARCH- ITS ROLE IN RISK MANAGEMENT
DISCUSSION LEADERS: John Parkinson, PhD, Head, GPRD, MHRA, London, UK; Tjeerd P Van Staa, MD, PhD, Head of Research, GPRD, London, UK; Frank De Vries, PhD, Lecturer, Utrecht University, Institute for Pharmaceutical Science, Utrecht, Holland, The Netherlands.
W2: RISK FACTORS THAT CHANGE OVER TIME: HOW TO ESTIMATE THEIR IMPACT ON THE OCCURRENCE OF HEALTH OUTCOMES?
DISCUSSION LEADERS: K Jack Ishak, PhD, Director, Biostatistics, Caro Research Institute, Montreal, QC, Canada; Krista F. Huybrechts, MS, Senior Researcher, Caro Research Institute, Concord, MA, USA; J. Jaime Caro, MDCM, FRCPC, FAC, President & Scientific Director, Caro Research Institute, Concord, MA, USA.
COST STUDY METHODOLOGY
W3: THE USE OF EPISODES OF CARE TO DEFINE AND MEASURE UNITS OF HEALTH CARE COSTS
DISCUSSION LEADERS: William Crown, PhD, President, i3 Innovus, Waltham, MA, USA; Steven Wickstrom, MS, Senior Director of Research and Development, Ingenix, Eden Prairie, MN, USA.
HEALTH CARE POLICY AND FORMULARY DEVELOPMENT USING OUTCOMES RESEARCH
W4: CONDITIONAL REIMBURSEMENT FOR HOSPITAL BASED DRUGS IN THE NETHERLANDS: POLICY MEASURE, COST-EFFECTIVENESS CRITERIUM, FUTURE OUTCOMES RESEARCH, METHODOLOGICAL AND CLINICAL CHALLENGES
DISCUSSION LEADERS: Gepke Delwel, PhD, Policy Advisor, CVZ Healthcare Insurance Board, Diemen, The Netherlands; Johan L Severens, PhD, Professor of Health Technology Assessment, Academic Hospital Maastricht, Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht, The Netherlands; Carin A Uyl-de Groot, PhD, Professor, iMTA/VUMC, Rotterdam, The Netherlands.
W5: VALUE AND COST-EFFECTIVENESS: US AND EUROPEAN PERSPECTIVES
DISCUSSION LEADERS: Sean D. Sullivan, PhD, Professor, University of Washington, Department of Pharmacy, Seattle, WA, USA; Brian W. Bresnahan, PhD, Senior Fellow, University of Washington, Department of Pharmacy, PORPP, Seattle, WA, USA; Peter J. Neumann, ScD, Professor, Tufts-New England Medical Center, Institute for Clinical Research and Health Policy Studies, Boston, MA, USA; Louis P. Garrison, PhD, Professor of Pharmacy, University of Washington, Department of Pharmacy, Seattle, WA, USA.
PATIENT-REPORTED OUTCOMES STUDY METHODOLOGY (INCLUDING PREFERENCE-BASED & COMPLIANCE STUDIES)
W6: INTERVENTIONS THAT ENHANCE MEDICATION COMPLIANCE AND PERSISTENCE: THEORETICAL GROUNDING, AND ECONOMIC ASSESSMENT
DISCUSSION LEADERS: Dyfrig Hughes, PhD, Senior Research Fellow, University of Wales, Bangor, Centre for Economics and Policy in Health, Bangor, UK; Femida Gwadry Sridhar, PhD, RPH, MSc, Assistant Professor, University of Western Ontario & McMaster University, ON, Canada; Rachel Elliott, PhD, Professor, University of Nottingham, Division of Social Research in Medicines and Health School of Pharmacy, Nottingham, UK; Warren Cowell, MSc, Health Economist, Roche Products Ltd, Healthcare Management, Welwyn Garden City, UK; Sangeeta Budhia, PhD, Consultant, Heron Evidence Development, Letchworth Garden City, Hertfordshire, UK.
W7: COMPLIANCE, ADHERENCE, AND PERSISTENCE IN HEALTH OUTCOMES RESEARCH: WHY, WHEN, AND WHAT'S THE RIGHT CHOICE
DISCUSSION LEADERS: B Tang, MD, PhD, Associate Director, Centocor, Inc, Horsham, PA, USA; M I Rahman, MD, MPH, Senior Director of Pharmacoepidemiology, Centocor, Inc, Horsham, PA, USA |
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16:30-17:00 |
Break, Exhibits & Contributed Poster Presentations – Session I Viewing |
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17:00-18:00 |
Contributed Workshops - Session II ( 7 workshops in 4 categories ) |
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CLINICAL OUTCOMES STUDY METHODOLOGY
W8: USE OF ELECTRONIC MEDICAL RECORD (EMR) DATA IN OUTCOMES RESEARCH
DISCUSSION LEADERS: Gary M Oderda, PharmD, MPH, Professor, University of Utah, College of Pharmacy, Department of Pharmacotherapy, Salt Lake City, UT, USA; Michael Lieberman, MD, MS, Informatics Director, GE Medical Systems, Hillsboro, OR, USA; Carl V. Asche, PhD, Research Associate Professor, University of Utah, College of Pharmacy, Outcomes Research Center, Department of Pharmacotherapy, Salt Lake City, UT, USA; Diana Brixner, RPh, PhD, Associate Professor and Chair, Department of Pharmacotherapy, Executive Director Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, UT, USA
COST STUDY METHODOLOGY
W9: THROUGH A GLASS DARKLY: TRANSPARENCY IN DECISION-ANALYTIC MODELS
DISCUSSION LEADERS: Nancy Neil, PhD, Senior Director, Health Economics, ICON Clinical Research, Lifecycle Sciences Group, San Francisco, CA, USA; Michael Chambers, MA, MSc, Director of Health Economics, GlaxoSmithKline, Global Health Outcomes, Uxbridge, Middlesex, UK.
W10: ADHERENCE TO CLINICAL GUIDELINES: A KEY CONCEPT IN CLINICAL AND ECONOMIC MODELS FOR DIAGNOSTIC DEVICES
DISCUSSION LEADERS: Won Chan Lee, PhD, Director, Abt Associates Inc, Health Economic Research and Quality of Life Evaluation Services, Bethesda, MD, USA; Yu-Chen Yeh, MS, Lead Pharmacoeconomist, Abt Associates Inc, Health Economic Research & Quality of Life Evaluation Services, Lexington, MA, USA; Mary Jo Williams, BS, Principal, Health Economics, Medtronic, Gastroenterology and Urology, Shoreview, MN, USA.
HEALTH CARE POLICY AND FORMULARY DEVELOPMENT USING OUTCOMES RESEARCH
W11: FACTORS TO CONSIDER IN SELECTING A STUDY DESIGN FOR POST-LAUNCH RESEARCH – STRATEGIC, METHODOLOGIC AND PRACTICAL CONSIDERATIONS
DISCUSSION LEADERS: Deborah Marshall, PhD, Vice President, Global Health Economics and Outcomes, i3 Innovus, Burlington, ON, Canada; Monique Martin, MBA, Health Economist, i3 Innovus, Health Outcomes, Uxbridge, Middlesex, UK; Mike F Drummond, PhD, Professor of Health Economics, Centre for Health Economics, University of York, York, UK.
W12: THE IMPLICATIONS OF VALUE BASED PRICING FOR THE PRICING AND REIMBURSEMENT OF PHARMACEUTICALS.
DISCUSSION LEADERS: Keith Tolley, MPhil, Research Director, Mapi Values, Market Access Unit, Bollington, Cheshire, UK; Francis Pang, MSc, Phil, DM, European Health Economics Manager, Takeda Pharmaceutical Company Limited, Global Research and Development Centre (Europe), London, UK; Ulrich Oron, MSc, RPh, MBA, Associate Director Market Access, Mapi Values Netherlands, Houten, The Netherlands.
PATIENT-REPORTED OUTCOMES STUDY METHODOLOGY (INCLUDING PREFERENCE-BASED & COMPLIANCE STUDIES)
W13: SPECIFYING THE CONCEPTUAL FRAMEWORK OF AN INSTRUMENT: TWO TOOLS TO MAKE YOUR LIFE EASIER
DISCUSSION LEADERS: Pennifer Erickson, PhD, Co-founder, OLGA, State College, PA, USA; Richard J Willke, PhD, Senior Director/Group Leader, Pfizer Inc, Worldwide Outcomes Research, Bridgewater, NJ, USA.
W14: FROM MINIMAL IMPORTANT DIFFERENCE TO CUMULATIVE RESPONSE CURVES: KEYS TO THE INTERPRETATION OF PRO RESULTS
DISCUSSION LEADERS: Benoit Arnould, MSc, MA, Director, Patient Scales for Clinical Practice, Mapi Values France, Patient Scales for Clinical Practice, Lyon, France; Muriel Viala, MSc, Senior Research Analyst, Mapi Values France, Lyon, France; Gilles Berdeaux, MD, Associate Director, Alcon France, Rueil-Malmaison, France; Aude Roborel de Climens, PhD, Research Associate, Mapi Values France, Lyon, France. |
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18:00-20:00 |
Exhibitors’ Open House Reception, Poster Presentations – Session I Viewing |
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