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  • Hendry, Gordon J  (4)
  • 1
    In: Journal of Foot and Ankle Research, Wiley, Vol. 7, No. 1 ( 2014-01)
    Abstract: An increased awareness of patients' and parents' care preferences regarding foot care is desirable from a clinical perspective as such information may be utilised to optimise care delivery. The aim of this study was to examine parents' preferences for, and valuations of foot care and foot‐related outcomes in juvenile idiopathic arthritis (JIA). Methods A discrete choice experiment (DCE) incorporating willingness‐to‐pay (WTP) questions was conducted by surveying 42 parents of children with JIA who were enrolled in a randomised‐controlled trial of multidisciplinary foot care at a single UK paediatric rheumatology outpatients department. Attributes explored were: levels of pain; mobility; ability to perform activities of daily living (ADL); waiting time; referral route; and footwear. The DCE was administered at trial baseline. DCE data were analysed using a multinomial‐logit‐regression model to estimate preferences and relative importance of attributes of foot care. A stated‐preference WTP question was presented to estimate parents' monetary valuation of health and service improvements. Results Every attribute in the DCE was statistically significant ( p 〈 0.01) except that of cost ( p = 0.118), suggesting that all attributes, except cost, have an impact on parents' preferences for foot care for their child. The magnitudes of the coefficients indicate that the strength of preference for each attribute was (in descending order): improved ability to perform ADL, reductions in foot pain, improved mobility, improved ability to wear desired footwear, multidisciplinary foot care route, and reduced waiting time. Parents' estimated mean annual WTP for a multidisciplinary foot care service was £1,119.05. Conclusions In terms of foot care service provision for children with JIA, parents appear to prefer improvements in health outcomes over non‐health outcomes and service process attributes. Cost was relatively less important than other attributes suggesting that it does not appear to impact on parents' preferences.
    Type of Medium: Online Resource
    ISSN: 1757-1146 , 1757-1146
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2440706-9
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  • 2
    In: Journal of Foot and Ankle Research, Wiley, Vol. 2, No. 1 ( 2009-01)
    Abstract: Foot and ankle problems are a common but relatively neglected manifestation of juvenile idiopathic arthritis. Studies of medical and non‐medical interventions have shown that clinical outcome measures can be improved. However existing data has been drawn from small non‐randomised clinical studies of single interventions that appear to under‐represent the adult population suffering from juvenile idiopathic arthritis. To date, no evidence of combined therapies or integrated care for juvenile idiopathic arthritis patients with foot and ankle problems exists. Methods/design An exploratory phase II non‐pharmacological randomised controlled trial where patients including young children, adolescents and adults with juvenile idiopathic arthritis and associated foot/ankle problems will be randomised to receive integrated podiatric care via a new foot care programme, or to receive standard podiatry care. Sixty patients (30 in each arm) including children, adolescents and adults diagnosed with juvenile idiopathic arthritis who satisfy the inclusion and exclusion criteria will be recruited from 2 outpatient centres of paediatric and adult rheumatology respectively. Participants will be randomised by process of minimisation using the Minim software package. The primary outcome measure is the foot related impairment measured by the Juvenile Arthritis Disability Index questionnaire's impairment domain at 6 and 12 months, with secondary outcomes including disease activity score, foot deformity score, active/limited foot joint counts, spatio‐temporal and plantar‐pressure gait parameters, health related quality of life and semi‐quantitative ultrasonography score for inflammatory foot lesions. The new foot care programme will comprise rapid assessment and investigation, targeted treatment, with detailed outcome assessment and follow‐up at minimum intervals of 3 months. Data will be collected at baseline, 6 months and 12 months from baseline. Intention to treat data analysis will be conducted. A full health economic evaluation will be conducted alongside the trial and will evaluate the cost effectiveness of the intervention. This will consider the cost per improvement in Juvenile Arthritis Disability Index, and cost per quality adjusted life year gained. In addition, a discrete choice experiment will elicit willingness to pay values and a cost benefit analysis will also be undertaken. Trial Registration Trial registration number: UKCRN5045
    Type of Medium: Online Resource
    ISSN: 1757-1146 , 1757-1146
    Language: English
    Publisher: Wiley
    Publication Date: 2009
    detail.hit.zdb_id: 2440706-9
    Location Call Number Limitation Availability
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  • 3
    In: Journal of Foot and Ankle Research, Wiley, Vol. 4, No. S1 ( 2011-01)
    Type of Medium: Online Resource
    ISSN: 1757-1146 , 1757-1146
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 2440706-9
    Location Call Number Limitation Availability
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  • 4
    In: Journal of Foot and Ankle Research, Wiley, Vol. 4, No. S1 ( 2011-01)
    Type of Medium: Online Resource
    ISSN: 1757-1146 , 1757-1146
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 2440706-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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