19 results on '"Ardine de Wit, G."'
Search Results
2. Estimating the health impact of delayed elective care during the COVID-19 pandemic in the Netherlands
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Oosterhoff, Marije, Kouwenberg, Lisanne H.J.A., Rotteveel, Adrienne H., Vliet, Ella D. van, Stadhouders, N.W., Ardine de Wit, G., Giessen, Anoukh van, Oosterhoff, Marije, Kouwenberg, Lisanne H.J.A., Rotteveel, Adrienne H., Vliet, Ella D. van, Stadhouders, N.W., Ardine de Wit, G., and Giessen, Anoukh van
- Abstract
Item does not contain fulltext
- Published
- 2023
3. Discrete choice experiment versus swing-weighting:A head-to-head comparison of diabetic patient preferences for glucose-monitoring devices
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Whichello, Chiara, Smith, Ian, Veldwijk, Jorien, Ardine de Wit, G., Rutten- van Molken, Maureen P.M.H., de Bekker-Grob, Esther W., Whichello, Chiara, Smith, Ian, Veldwijk, Jorien, Ardine de Wit, G., Rutten- van Molken, Maureen P.M.H., and de Bekker-Grob, Esther W.
- Abstract
Introduction Limited evidence exists for how patient preference elicitation methods compare directly. This study compares a discrete choice experiment (DCE) and swing-weighting (SW) by eliciting preferences for glucose-monitoring devices in a population of diabetes patients. Methods A sample of Dutch adults with type 1 or 2 diabetes (n = 459) completed an online survey assessing their preferences for glucose-monitoring devices, consisting of both a DCE and a SW exercise. Half the sample completed the DCE first; the other half completed the SW first. For the DCE, the relative importance of the attributes of the devices was determined using a mixed-logit model. For the SW, the relative importance of the attributes was based on ranks and points allocated to the ‘swing’ from the worst to the best level of the attribute. The preference outcomes and self-reported response burden were directly compared between the two methods. Results Participants reported they perceived the DCE to be easier to understand and answer compared to the SW. Both methods revealed that cost and precision of the device were the most important attributes. However, the DCE had a 14.9-fold difference between the most and least important attribute, while the SW had a 1.4-fold difference. The weights derived from the SW were almost evenly distributed between all attributes. Conclusions The DCE was better received by participants, and generated larger weight differences between each attribute level, making it the more informative method in our case study. This method comparison provides further evidence of the degree of method suitability and trustworthiness.
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- 2023
4. Diabetes patient preferences for glucose-monitoring technologies:results from a discrete choice experiment in Poland and the Netherlands
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Smith, Ian P, Whichello, Chiara Lauren, Veldwijk, Jorien, van Molken, Maureen, Groothuis-Oudshoorn, Catharina G.M., Vos, Rimke C, de Bekker-Grob, Esther, Ardine de Wit, G., Smith, Ian P, Whichello, Chiara Lauren, Veldwijk, Jorien, van Molken, Maureen, Groothuis-Oudshoorn, Catharina G.M., Vos, Rimke C, de Bekker-Grob, Esther, and Ardine de Wit, G.
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Introduction New glucose-monitoring technologies have different cost–benefit profiles compared with traditional finger-prick tests, resulting in a preference-sensitive situation for patients. This study aimed to assess the relative value adults with diabetes assign to device attributes in two countries. Research design and methods Adults with type 1 or 2 diabetes from the Netherlands (n=226) and Poland (n=261) completed an online discrete choice experiment. Respondents choose between hypothetical glucose monitors described using seven attributes: precision, effort to check, number of finger pricks required, risk of skin irritation, information provided, alarm function and out-of-pocket costs. Panel mixed logit models were used to determine attribute relative importance and to calculate expected uptake rates and willingness to pay (WTP). Results The most important attribute for both countries was monthly out-of-pocket costs. Polish respondents were more likely than Dutch respondents to choose a glucose-monitoring device over a standard finger prick and had higher WTP for a device. Dutch respondents had higher WTP for device improvements in an effort to check and reduce the number of finger pricks a device requires. Conclusion Costs are the primary concern of patients in both countries when choosing a glucose monitor and would likely hamper real-world uptake. The costs-benefit profiles of such devices should be critically reviewed.
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- 2023
5. Preventive exercises reduced injury-related costs among adult male amateur soccer players: a cluster-randomised trial
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Krist, Mark R., van Beijsterveldt, Anna M.C., Backx, Frank J.G., and Ardine de Wit, G.
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- 2013
- Full Text
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6. “Please, you go first!” preferences for a COVID-19 vaccine among adults in the Netherlands
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Mouter, N. (author), de Ruijter, A.M. (author), Ardine de Wit, G. (author), Lambooij, Mattijs S. (author), van Wijhe, Maarten (author), van Exel, Job (author), Kessels, Roselinde (author), Mouter, N. (author), de Ruijter, A.M. (author), Ardine de Wit, G. (author), Lambooij, Mattijs S. (author), van Wijhe, Maarten (author), van Exel, Job (author), and Kessels, Roselinde (author)
- Abstract
Background: Vaccination is generally considered the most direct way to restoring normal life after the outbreak of COVID-19, but the available COVID-19 vaccines are simultaneously embraced and dismissed. Mapping factors for vaccine hesitancy may help the roll-out of COVID-19 vaccines and provide valuable insights for future pandemics. Objectives: We investigate how characteristics of a COVID-19 vaccine affect the preferences of adult citizens in the Netherlands to take the vaccine directly, to refuse it outright, or to wait a few months and first look at the experiences of others. Methods: An online sample of 895 respondents participated between November 4th and November 10th, 2020 in a discrete choice experiment including the attributes: percentage of vaccinated individuals protected against COVID-19, month in which the vaccine would become available and the number of cases of mild and severe side effects. The data was analysed by means of panel mixed logit models. Results: Respondents found it important that a safe and effective COVID-19 vaccine becomes available as soon as possible. However, the majority did not want to be the first in line and would rather wait for the experiences of others. The predicted uptake of a vaccine with the optimal combination of attributes was 87%, of whom 55% preferred to take the vaccine after a waiting period. This latter group tends to be lower-educated. Older respondents gave more weight to vaccine effectiveness than younger respondents. Conclusions: The willingness to take a COVID-19 vaccine is high among adults in the Netherlands, but a considerable proportion prefers to delay their decision to vaccinate until experiences of others are known. Offering this wait-and-see group the opportunity to accept the invitation at a later moment may stimulate vaccination uptake. Our results further suggest that vaccination campaigns targeted at older citizens should focus on the effectiveness of the vaccine., Transport and Logistics
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- 2022
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7. “Please, you go first!”:preferences for a COVID-19 vaccine among adults in the Netherlands
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Mouter, Niek, de Ruijter, Annamarie, Ardine de Wit, G., Lambooij, Mattijs S., van Wijhe, Maarten, van Exel, Job, Kessels, Roselinde, Mouter, Niek, de Ruijter, Annamarie, Ardine de Wit, G., Lambooij, Mattijs S., van Wijhe, Maarten, van Exel, Job, and Kessels, Roselinde
- Abstract
Background: Vaccination is generally considered the most direct way to restoring normal life after the outbreak of COVID-19, but the available COVID-19 vaccines are simultaneously embraced and dismissed. Mapping factors for vaccine hesitancy may help the roll-out of COVID-19 vaccines and provide valuable insights for future pandemics. Objectives: We investigate how characteristics of a COVID-19 vaccine affect the preferences of adult citizens in the Netherlands to take the vaccine directly, to refuse it outright, or to wait a few months and first look at the experiences of others. Methods: An online sample of 895 respondents participated between November 4th and November 10th, 2020 in a discrete choice experiment including the attributes: percentage of vaccinated individuals protected against COVID-19, month in which the vaccine would become available and the number of cases of mild and severe side effects. The data was analysed by means of panel mixed logit models. Results: Respondents found it important that a safe and effective COVID-19 vaccine becomes available as soon as possible. However, the majority did not want to be the first in line and would rather wait for the experiences of others. The predicted uptake of a vaccine with the optimal combination of attributes was 87%, of whom 55% preferred to take the vaccine after a waiting period. This latter group tends to be lower-educated. Older respondents gave more weight to vaccine effectiveness than younger respondents. Conclusions: The willingness to take a COVID-19 vaccine is high among adults in the Netherlands, but a considerable proportion prefers to delay their decision to vaccinate until experiences of others are known. Offering this wait-and-see group the opportunity to accept the invitation at a later moment may stimulate vaccination uptake. Our results further suggest that vaccination campaigns targeted at older citizens should focus on the effectiveness of the vaccine.
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- 2022
8. The Predictive Value of Discrete Choice Experiments in Public Health: An Exploratory Application
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Salampessy, Benjamin H., Veldwijk, Jorien, Jantine Schuit, A., van den Brekel-Dijkstra, Karolien, Neslo, Rabin E. J., Ardine de Wit, G., and Lambooij, Mattijs S.
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- 2015
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9. Patient Preferences for Lung Cancer Treatment: A Qualitative Study Protocol Among Advanced Lung Cancer Patients
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Durosini, Ilaria, Janssens, Rosanne, Arnou, Reinhard, Veldwijk, Jorien, Smith, Meredith Y., Monzani, Dario, Smith, Ian, Galli, Giulia, Garassino, Marina, Katz, Eva G., Bailo, Luca, Louis, Evelyne, Vandevelde, Marie, Nackaerts, Kristiaan, Ardine de Wit, G., Pravettoni, Gabriella, Huys, Isabelle, Durosini, Ilaria, Janssens, Rosanne, Arnou, Reinhard, Veldwijk, Jorien, Smith, Meredith Y., Monzani, Dario, Smith, Ian, Galli, Giulia, Garassino, Marina, Katz, Eva G., Bailo, Luca, Louis, Evelyne, Vandevelde, Marie, Nackaerts, Kristiaan, Ardine de Wit, G., Pravettoni, Gabriella, and Huys, Isabelle
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Introduction: Lung cancer is the deadliest and most prevalent cancer worldwide. Lung cancer treatments have different characteristics and are associated with a range of benefits and side effects for patients. Such differences may raise uncertainty among drug developers, regulators, payers, and clinicians regarding the value of these treatment effects to patients. The value of conducting patient preference studies (using qualitative and/or quantitative methods) for benefits and side effects of different treatment options has been recognized by healthcare stakeholders, such as drug developers, regulators, health technology assessment bodies, and clinicians. However, evidence-based guidelines on how and when to conduct and use these studies in drug decision-making are lacking. As part of the Innovative Medicines Initiative PREFER project, we developed a protocol for a qualitative study that aims to understand which treatment characteristics are most important to lung cancer patients and to develop attributes and levels for inclusion in a subsequent quantitative preference survey. Methods: The study protocol specifies a four-phased approach: (i) a scoping literature review of published literature, (ii) four focus group discussions with stage III and IV Non-Small Cell Lung Cancer patients, (iii) two nominal group discussions with stage III and IV Non-Small Cell Lung Cancer patients, and (iv) multi-stakeholder discussions involving clinicians and preference experts. Discussion: This protocol outlines methodological and practical steps as to how qualitative research can be applied to identify and develop attributes and levels for inclusion in patient preference studies aiming to inform decisions across the drug life cycle. The results of this study are intended to inform a subsequent quantitative preference survey that assesses patient trade-offs regarding lung cancer treatment options. This protocol may assist researchers, drug developers, and decision-makers in designing, IMI-PREFER
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- 2021
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10. Groot draagvlak onder Nederlanders voor een 'vaccinatiebewijs light: Beleidsrapport over de hoofdresultaten van een keuze-experiment naar de voorkeuren van Nederlanders voor vaccinatiebeleid
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Mouter, Niek, Boxebeld, Sander, Kessels, Roselinde, van Wijhe, Maarten, Ardine de Wit, G., Lambooij, Mattijs, van Exel, Job, and Health Economics (HE)
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SDG 3 - Good Health and Well-being - Published
- 2020
11. Developing a vaccination evaluation model to support evidence-based decision making on national immunization programs
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Kimman, Tjeerd G., Boot, Hein J., Berbers, Guy A.M., Vermeer-de Bondt, Patricia E., Ardine de Wit, G., and de Melker, Hester E.
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- 2006
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12. Towards a more efficient diabetes control in primary care: six-monthly monitoring compared with three-monthly monitoring in type 2 diabetes - The EFFIMODI trial. Design of a randomised controlled patient-preference equivalence trial in primary care
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Ardine de Wit G, Gorter Kees J, van den Donk Maureen, Wermeling Paulien R, van der Graaf Yolanda, and Rutten Guy EHM
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Medicine (General) ,R5-920 - Abstract
Abstract Background Scientific evidence for the frequency of monitoring of type 2 diabetes patients is lacking. If three-monthly control in general practice could be reduced to six-monthly control in some patients, this would on the one hand reduce the use of medical services including involvement of practice nurses, and thus reduce costs, and on the other hand alleviate the burden of people with type 2 diabetes. The goal of this study is to make primary diabetes care as efficient as possible for patients and health care providers. Therefore, we want to determine whether six-monthly monitoring of well-controlled type 2 diabetes patients in primary care leads to equivalent cardiometabolic control compared to the generally recommended three-monthly monitoring. Methods and design The study is a randomised controlled patient-preference equivalence trial. Participants are asked if they prefer three-monthly (usual care) or six-monthly diabetes monitoring. If they do not have a preference, they are randomised to a three-monthly or six-monthly monitoring group. Patients are eligible for the study if they are between 40 and 80 years old, diagnosed with type 2 diabetes more than one year ago, treated by a general practitioner, not on insulin treatment, and with HbA1c ≤7.5%, systolic blood pressure ≤145 mmHg and total cholesterol ≤5.2 mmol/l. The intervention group (six-monthly monitoring) will receive the same treatment with the same treatment targets as the control group (three-monthly monitoring). The intervention period will last one and a half year. After the intervention, the three-monthly and six-monthly monitoring groups are compared on equivalence of cardiometabolic control. Secondary outcome measures are HbA1c, blood pressure, cholesterol level, Body Mass Index, smoking behaviour, physical activity, loss of work due to illness, health status, diabetes-specific distress, satisfaction with treatment and adherence to medications. We will use intention-to-treat analysis with repeated measures. For outcomes that have only baseline and final measurements, we will use ANCOVA. Depending on the results, a cost-minimisation analysis or an incremental cost-effectiveness analysis will be done. Discussion This study will provide valuable information on the most efficient control frequency of well-controlled type 2 diabetes patients in primary care. Trial registration Current Controlled Trials ISRCTN93201802
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- 2010
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13. Economic evaluation of a tight-control treatment strategy using an imaging device (handscan) for monitoring joint inflammation in early rheumatoid arthritis
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Nair, SC, Welsing, PM, Jacobs, JW, van, Laar JM, Rensen, WH, Ardine, de Wit G, Bijlsma, JW, Lafeber, FP, Other departments, Constitutional and Administrative Law, Criminal Law, Kooijmans Institute, and Empirical and Normative Studies
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health care economics and organizations - Abstract
To evaluate the cost-effectiveness of a tight-control treatment strategy using the handscan (TCHS) compared to using only clinical assessments (TC) and compared to a general non-tight-control treatment strategy (usual care; UC) in early rheumatoid arthritis (RA). Data from 299 early RA patients from the CAMERA trial were used. Clinical outcomes were extrapolated to Quality Adjusted Life Years (QALYs) and costs using a Markov model. Costs and QALYs were compared between the TC and UC treatment strategy arm of the CAMERA trial and a simulated tight-control treatment strategy using the handscan (TCHS). Incremental Cost-Effectiveness Ratios (ICERs) were calculated and several scenario analyses performed. All analyses were performed probabilistically to obtain confidence intervals and costs-effectiveness planes and acceptability curves. In TCHS, €4,660 (95% CI -€11,516 to €2,045) was saved and 0.06 (95% CI 0.01 to 0.11) QALYs were gained when compared to UC, with an ICER of €77,670 saved per QALY gained. Ninety-one percent (91%) of simulations resulted in less costs and more QALYs. TCHS resulted in comparable costs or even limited savings €642 (95% CI -€6,903 to €5,601)) and comparable QALYs to TC. In all scenario analyses, TCHS and TC were found to be cost effective as compared to UC. A tight-control treatment strategy is highly cost-effective compared to a non-tight-control approach in early RA. Using the handscan as a monitoring device might facilitate implementation of tight-control treatment strategy at comparable costs and with comparable effects. This approach should be investigated further
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- 2015
14. Cost-Effectiveness of Treatment of Acute Otorrhea in Children With Tympanostomy Tubes
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van Dongen, Thijs M.A., primary, Schilder, Anne G.M., additional, Venekamp, Roderick P., additional, Ardine de Wit, G., additional, and van der Heijden, Geert J.M.G., additional
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- 2015
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15. Towards a more efficient diabetes control in primary care: six-monthly monitoring compared with three-monthly monitoring in type 2 diabetes - The EFFIMODI trial. Design of a randomised controlled patient-preference equivalence trial in primary care
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Wermeling, Paulien R, primary, van den Donk, Maureen, additional, Gorter, Kees J, additional, Ardine de Wit, G, additional, van der Graaf, Yolanda, additional, and Rutten, Guy EHM, additional
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- 2010
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16. Unrelated medical care in life years gained and the cost utility of primary prevention: in search of a ‘perfect’ cost–utility ratio
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van Baal, Pieter H. M., primary, Feenstra, Talitha L., additional, Hoogenveen, Rudolf T., additional, Ardine de Wit, G., additional, and Brouwer, Werner B. F., additional
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- 2007
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17. Rationale and design of the costs, health status and outcomes in community-acquired pneumonia (CHOCAP) study in elderly persons hospitalized with CAP.
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Mangen, Marie-Josée J., Bonten, Marc J. M., and Ardine de Wit, G.
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COMMUNITY-acquired pneumonia ,DISEASES in older people ,MEDICAL care costs ,HEALTH status indicators ,HEALTH outcome assessment ,HOSPITAL patients ,RANDOMIZED controlled trials ,MEDICAL decision making - Abstract
Background Vaccine effectiveness is usually determined in randomized controlled trials (RCT) and if effective, additional information, e.g. on cost-effectiveness, is required to allow evidencebased decision making. A prerequisite for proper health economic modelling is the availability of good quality data on health care resources use, health outcomes and quality-oflife (QoL) data. The "Collecting health outcomes and economic data on hospitalized Community Acquired Pneumonia (CHO-CAP) - a prospective cohort study" is executed alongside the Community Acquired Pneumonia Immunization Trial with Adults (CAPiTA trial) to capture health outcomes and economic data of elderly hospitalized with CAP and matched controls without CAP. Methods/Design CAPiTA is a placebo-controlled double-blind RCT evaluating the effectiveness of a 13- valent conjugated pneumococcal vaccine in preventing vaccine-type pneumococcal CAP in 84,496 elderly in the Netherlands. Participants of CAPiTA, who consented and provided information on health status (EQ-5D) and socio-demographic background at the time of vaccination, constitute the source population of CHO-CAP and are eligible for the nested matched cohort study. CHO-CAP patients hospitalized with CAP form the "diseased" cohort and the "non-diseased" cohort consists of unaffected persons (i.e. no CAP). Observations in the diseased cohort and in matched controls from the non-diseased cohort are used to determine excess costs and QoL changes attributable to CAP. Based on an estimated 2,000 CAPiTA participants being hospitalized with CAP and an assumed CHO-CAP participation rate of 30% of all CAPiTA participants (+25,000), 600 CAP episodes are expected among CHO-CAP participants (the "diseased" cohort). For each patient with CAP, two non-diseased CHO-CAP subjects will be selected from the CHO-CAP cohort, with matching for age, gender and EQ-5D baseline-score. Data on healthcare and non-healthcare resources use, quality-of-life (using EQ-5D and SF-36 questionnaires) and selected health outcomes will be collected at 0, 1, 6 and 12 months after hospitalization for CAP. The CHO-CAP study was approved by the Central Committee on Research involving Human Subjects in the Netherlands. Discussion With an expected 600 CAP episodes this study will be one of the biggest prospectively studied cohorts of hospitalized elderly with CAP with regard to resources use and Qol data. Strengths of this study further include collection of out-of-pocket costs of patients and productivity losses of both patients and their caregivers and the follow-up period of up to one year post-discharge. This study is therefore expected to add more in-depth knowledge on the short and longer term outcomes of pneumonia in elderly. [ABSTRACT FROM AUTHOR]
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- 2013
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18. Dietary patterns in relation to quality-adjusted life years in the EPIC-NL cohort.
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Fransen, Heidi P., Beulens, Joline W. J., May, Anne M., Struijk, Ellen A., Boer, Jolanda M. A., Ardine de Wit, G., Charlotte Onland-Moret, N., van der Schouw, Yvonne T., Bas Bueno-de-Mesquita, H., Hoekstra, Jeljer, and Peeters, Petra H. M.
- Subjects
- *
DISEASE incidence , *NON-communicable diseases , *FOOD habits , *QUESTIONNAIRES , *COHORT analysis - Abstract
Background: Dietary patterns have been associated with the incidence or mortality of individual non-communicable diseases, but their association with disease burden has received little attention. Objective: The aim of our study was to relate dietary patterns to health expectancy using quality-adjusted life years (QALYs) as outcome parameter. Methods: Data from the EPIC-NL study were used, a prospective cohort study of 33,066 healthy men and women aged 20-70 years at recruitment. A lifestyle questionnaire and a validated food frequency questionnaire were administered at study entry (1993-1997). Five dietary patterns were studied: three a priori patterns (the modified Mediterranean Diet Score (mMDS), the WHO-based Healthy Diet Indicator (HDI) and the Dutch Healthy Diet index (DHD-index)) and two a posteriori data-based patterns. QALYs were used as a summary health measure for healthy life expectancy, combining a person's life expectancy with a weight reflecting loss of quality of life associated with having chronic diseases. Results: The mean QALYs of the participants were 74.9 (standard deviation 4.4). A higher mMDS and HDI were associated with a longer life in good health. Participants who had a high mMDS score (6-9) had 0.17 [95% CI, 0.05; 0.30] more QALYs than participants with a low score (0-3), equivalent to two months longer life in good health. Participants with a high HDI score also had more QALYs (0.15 [95% CI, 0.03; 0.27]) than participants with a low HDI score. Conclusion A Mediterranean-type diet and the Healthy Diet Indicator were associated with approximately 2 months longer life in good health. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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19. Economic evaluation of a tight-control treatment strategy using an imaging device (handscan) for monitoring joint inflammation in early rheumatoid arthritis.
- Author
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Nair SC, Welsing PM, Jacobs JW, van Laar JM, Rensen WH, Ardine de Wit G, Bijlsma JW, and Lafeber FP
- Subjects
- Adult, Antirheumatic Agents therapeutic use, Cost-Benefit Analysis, Female, Humans, Male, Markov Chains, Middle Aged, Netherlands, Outcome and Process Assessment, Health Care, Patient Acuity, Quality-Adjusted Life Years, Arthritis, Rheumatoid diagnosis, Arthritis, Rheumatoid economics, Arthritis, Rheumatoid therapy, Drug Monitoring economics, Drug Monitoring methods, Methotrexate therapeutic use, Patient Care Management economics, Patient Care Management methods
- Abstract
Objectives: To evaluate the cost-effectiveness of a tight-control treatment strategy using the handscan (TCHS) compared to using only clinical assessments (TC) and compared to a general non-tight-control treatment strategy (usual care; UC) in early rheumatoid arthritis (RA)., Methods: Data from 299 early RA patients from the CAMERA trial were used. Clinical outcomes were extrapolated to Quality Adjusted Life Years (QALYs) and costs using a Markov model. Costs and QALYs were compared between the TC and UC treatment strategy arm of the CAMERA trial and a simulated tight-control treatment strategy using the handscan (TCHS). Incremental Cost-Effectiveness Ratios (ICERs) were calculated and several scenario analyses performed. All analyses were performed probabilistically to obtain confidence intervals and costs-effectiveness planes and acceptability curves., Results: In TCHS, €4,660 (95% CI -€11,516 to €2,045) was saved and 0.06 (95% CI 0.01 to 0.11) QALYs were gained when compared to UC, with an ICER of €77,670 saved per QALY gained. Ninety-one percent (91%) of simulations resulted in less costs and more QALYs. TCHS resulted in comparable costs or even limited savings €642 (95% CI -€6,903 to €5,601)) and comparable QALYs to TC. In all scenario analyses, TCHS and TC were found to be cost effective as compared to UC., Conclusions: A tight-control treatment strategy is highly cost-effective compared to a non-tight-control approach in early RA. Using the handscan as a monitoring device might facilitate implementation of tight-control treatment strategy at comparable costs and with comparable effects. This approach should be investigated further.
- Published
- 2015
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