Hindrik Vondeling
University of Southern Denmark
Publications 53
#1Kathryn M Antioch (Monash University)H-Index: 4
#2Michael Drummond (Ebor: University of York)H-Index: 72
Last.Hindrik VondelingH-Index: 14
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Economic evidence is influential in health technology assessment world-wide. Clinical Practice Guidelines (CPG) can enable economists to include economic information on health care provision. Application of economic evidence in CPGs, and its integration into clinical practice and national decision making is hampered by objections from professions, paucity of economic evidence or lack of policy commitment. The use of state-of-art economic methodologies will improve this. Economic evidence can be ...
7 CitationsSource
#1Jilles Fermont (University of Oxford)H-Index: 4
#2Karla Douw (UT: University of Twente)H-Index: 1
Last.Maarten Joost IJzerman (UT: University of Twente)H-Index: 40
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Objectives In 2001, Fuchs and Sox published a landmark study on the relative importance for patients of thirty preselected medical innovations in the United States. About a decade later, we replicated the study in the Netherlands in response to the continuing debate on rising healthcare costs. The aims were to provide an updated list of medical innovations, categorise these according to their impact and novelty, provide a ranking according to the perceived health benefit by Dutch clinical and he...
1 CitationsSource
#1Anne-Kirstine Dyrvig (University of Southern Denmark)H-Index: 4
#2Oke Gerke (University of Southern Denmark)H-Index: 20
Last.Hindrik Vondeling (UT: University of Twente)H-Index: 14
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IntroductionThe studies that constitute the knowledge base of evidence based medicine represent only 5%–50% of patients seen in routine clinical practice. Therefore, whether the available evidence applies to the implementation of a particular service often remains unclear. Chronic obstructive pulmonary disease (COPD) is no exception.MethodsIn this article, the effects of implementing a telemedicine intervention for COPD patients were analysed using data collected before, during, and after a rand...
2 CitationsSource
Last.Merel Ritskes-HoitingaH-Index: 19
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#1Anne-Kirstine Dyrvig (University of Southern Denmark)H-Index: 4
#2Kristian Kidholm (OUH: Odense University Hospital)H-Index: 11
Last.Hindrik Vondeling (University of Southern Denmark)H-Index: 14
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Rationale, aims and objectives The quality of the current literature on external validity varies considerably. An improved checklist with validated items on external validity would aid decision-makers in judging similarities among circumstances when transferring evidence from a study setting to an implementation setting. In this paper, currently available checklists on external validity are identified, assessed and used as a basis for proposing a new improved instrument. Method A systematic lite...
11 CitationsSource
Objectives: The European Network for Health Technology Assessment (EUnetHTA) Joint Action Project Framework, 2010–12, Work Package 7B (WP 7B), was aimed at facilitating collaboration between HTA agencies to avoid duplication of assessment efforts. A major task of WP 7B was to collect information on planned and ongoing (POP) projects by EUnetHTA agencies and to incorporate this information in a POP Database. We analyzed whether the Database served its intended purpose. Methods: A survey was sent ...
1 CitationsSource
#1Wija Oortwijn (Ecorys)H-Index: 11
#2Pieter Broos (Ecorys)H-Index: 1
Last.Lora Todorova (Novo Nordisk)H-Index: 2
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Objectives: The aim of this study was to develop and apply an instrument to map the level of health technology assessment (HTA) development at country level in selected countries. We examined middle-income countries (Argentina, Brazil, India, Indonesia, Malaysia, Mexico, and Russia) and countries well-known for their comprehensive HTA programs (Australia, Canada, and United Kingdom). Methods: A review of relevant key documents regarding the HTA process was performed to develop the instrument whi...
34 CitationsSource
#1Marianne SandveiH-Index: 2
#2Hindrik VondelingH-Index: 14
Last.Jens OlsenH-Index: 1
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1 Citations
#1Heidi Carmen Howard (University of Toulouse)H-Index: 23
#2E Swinnen (Katholieke Universiteit Leuven)H-Index: 1
Last.Pascal Borry (Katholieke Universiteit Leuven)H-Index: 34
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With the human genome project running from 1989 until its completion in 2003, and the incredible advances in sequencing technology and in bioinformatics during the last decade, there has been a shift towards an increase focus on studying common complex disorders which develop due to the interplay of many different genes as well as environmental factors. Although some susceptibility genes have been identified in some populations for disorders such as cancer, diabetes and cardiovascular diseases, ...
13 CitationsSource
Objectives: High-quality clinical evidence is most often lacking when novel high-risk devices enter the European market. At the same time, a randomized controlled trial (RCT) is often initiated as a requirement for obtaining market access in the US. Should coverage in Europe be postponed until RCT data are available? We studied the premarket clinical evaluation of innovative high-risk medical devices in Europe compared with the US, and with medicines, where appropriate. Methods: The literature a...
34 CitationsSource