about
Predictors of long-term care utilization by Dutch hospital patients aged 65+Evaluating an integrated neighbourhood approach to improve well-being of frail elderly in a Dutch community: a study protocol.Lifetime health effects and medical costs of integrated stroke services - a non-randomized controlled cluster-trial based life table approach.Quality of life of nursing home residents with dementia: validation of the German version of the ICECAP-OExtending life for people with a terminal illness: a moral right and an expensive death? Exploring societal perspectives.Exploring views on what is important for patient-centred care in end-stage renal disease using Q methodologyAre all health gains equally important? An exploration of acceptable health as a reference point in health care priority settingAssessing health-related quality-of-life changes in informal caregivers: an evaluation in parents of children with major congenital anomaliesValuing QALYs in Relation to Equity Considerations Using a Discrete Choice ExperimentBalancing equity and efficiency in the Dutch basic benefits package using the principle of proportional shortfallA long life in good health: subjective expectations regarding length and future health-related quality of life.Unrelated medical costs in life-years gained: should they be included in economic evaluations of healthcare interventions?Measuring Health Spillovers for Economic Evaluation: A Case Study in Meningitis.The value of a QALY: individual willingness to pay for health gains under risk.Attitudes to medication after kidney transplantation and their association with medication adherence and graft survival: a 2-year follow-up study.Discounting future health gains: an empirical enquiry into the influence of growing life expectancy.Societal discounting of health effects in cost-effectiveness analyses: the influence of life expectancy.Expectations regarding length and health related quality of life: some empirical findings.Discounting in decision making: the consistency argument revisited empirically.A short note on measuring subjective life expectancy: survival probabilities versus point estimatesAre some QALYs more equal than others?Care for a break? An investigation of informal caregivers' attitudes toward respite care using Q-methodology.Caring for and caring about: disentangling the caregiver effect and the family effect.Economic valuation of informal care: conjoint analysis applied in a heterogeneous population of informal caregivers.The value of informal care--a further investigation of the feasibility of contingent valuation in informal caregivers.Medical consumption and costs during a one-year follow-up of patients with LUTS suggestive of BPH in six european countries: report of the TRIUMPH study.Patient views on determinants of compliance with tuberculosis treatment in the eastern cape, South Africa: an application of q-methodology.Is "end of life" a special case? Connecting Q with survey methods to measure societal support for views on the value of life-extending treatments.Preferences for health care and self-management among Dutch adolescents with chronic conditions: a Q-methodological investigation.Subjective caregiver burden of parents of adults with Duchenne muscular dystrophy.Perseverance Time of Informal Caregivers for Institutionalized Elderly: Construct Validity and Test-Retest Reliability of a Single-Question Instrument.Perceptions of team workers in youth care of what makes teamwork effective.Putting your money where your mouth is: parents' valuation of good oral health of their children.Measuring health and well-being effects in family caregivers of children with craniofacial malformations.A dollar is a dollar is a dollar--or is it?Process utility from providing informal care: the benefit of caring.Burden of informal caregiving for stroke patients. Identification of caregivers at risk of adverse health effects.Acceptability of less than perfect health states.Economic valuation of informal care: the contingent valuation method applied to informal caregiving.Instruments for assessing the burden of informal caregiving for stroke patients in clinical practice: a comparison of CSI, CRA, SCQ and self-rated burden.
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P50
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Nederlands onderzoeker
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P106
P27
P31
P496
0000-0002-4178-1777