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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Thom, Howard
University of Bristol
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (3/3 displayed)
- 2022A clinical tool to identify older women with back pain at high risk of osteoporotic vertebral fractures (Vfrac)citations
- 2022Systematic Review of Cost-Effectiveness Models in Prostate Cancercitations
- 2021Exploratory Comparison of Healthcare costs and benefits of the UK’s Covid-19 response with four European countriescitations
Places of action
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article
A clinical tool to identify older women with back pain at high risk of osteoporotic vertebral fractures (Vfrac)
Abstract
Background: Osteoporotic vertebral fractures (OVFs) identify people at high risk of future fractures, but despite this, less than a third come to clinical attention. The objective of this study was to develop a clinical tool to aid healthcare professionals decide which older women with back pain should have a spinal radiograph. <br/><br/>Methods: A population-based cohort of 1635 women aged 65+ years with self-reported back pain in the previous four months were recruited from primary care. Exposure data were collected through self-completion questionnaires and physical examination including descriptions of back pain and traditional risk factors for osteoporosis.Outcome was the presence/absence of OVFs on spinal radiographs. Logistic regression models identified independent predictors of OVFs, with the Area Under the (Receiver Operating) Curve (AUC) calculated for the final model, and a cut-point identified.<br/><br/>Results: Mean age was 73.9 years and 209 (12.8%) had OVFs. The final Vfrac model comprised 15 predictors of OVF, with an AUC of 0.802 (95%CI 0.764-0.840). Sensitivity was 72.4% and specificity 72.9%. Vfrac identified 93% of those with >1 OVF and two-thirds of those with one OVF. Performance was enhanced by inclusion of self-reported back pain descriptors, removal of which reduced AUC to 0.742 (95%CI 0.696-0.788) and sensitivity to 66.5%. Health economic modelling to support a future trial was favourable.<br/><br/>Conclusions: The Vfrac clinical tool appears valid and is improved by the addition of self-reported back pain symptoms. The tool now requires testing to establish real-world clinical and cost-effectiveness.<br/>