54 to 0.74) ( Beaton et al 2010). In workers with OA, RA-WIS demonstrated moderate to high correlations to both work-oriented learn more (r = 0.55 to 0.77) and disease-oriented (r = 0.70 to 0.79) constructs ( Tang et al 2010a). Predictive validity: The suggested 17 or more cut-point

was found to predict transition in work status (relative risk = 1.05, p = 0.04); but the optimal cutoff point for prediction of work transition was found to be > 13 (AUC 0.68, sensitivity = 51%, specificity = 83%) in a population of injured workers with chronic upper extremity disorders ( Tang et al 2010b). Responsiveness: RA-WIS has been shown to exhibit small to moderate SRMs and ES in identifying improved or deteriorated work ability ( Beaton et al 2010). Dimensionality: In the developmental study Rasch analysis suggested that all 23 items represent a

single construct, hence the scale can be considered unidimensional in a worker population with RA ( Gilworth et al 2003). These findings were later confirmed in a sample of workers with OA by Tang and associate where he found RA-WIS achieved adequate fit to the Rasch model in its original 23-item form ( Tang et al 2010a). However, in workers PFT�� order with work related upper limb disorders, Tang and associates have found significant deviations from the Rasch model requirements. They have proposed a 17 item format of the RA-WIS that satisfied RASCH model requirments of unidimensionality, local dependence, and absence of DIF ( Tang et al 2011). Work instability is a common problem in muscuoskeletal disorders. This necessitates appropriate outcome measures to predict and identify workers who are at-risk of work instability so that

treatment plans and work accommodations can be targeted more effectively. RA-WIS is brief and easily scored and shows preliminary evidence of reliable and valid. These factors suggest it may fit the needs and demands of clinical practice. More validation studies are needed to enhance confidence in its use across clinical populations and as a predictive measure. “
“Latest update: June 2013. Non-specific serine/threonine protein kinase Next update: Not stated. Patient group: All people aged over 65 years and people aged 50 to 64 who are admitted to hospital and have an underlying condition that places them at a greater risk of falling. Intended audience: Healthcare and other professionals and staff who care for older people who are at risk of falling. Additional versions: This guideline replaces and updates ‘Falls’ (NICE Clinical Guideline 21) published in 2004. Expert working group: A 14-member group including medical specialists, a physiotherapist, nurse, patient safety experts and consumer representatives from the United Kingdom (UK) comprised the guideline development group. Funded by: The National Institute for Health and Care Excellence (NICE), UK. Consultation with: Stakeholders included AGILE – Chartered Physiotherapists Working with Older People UK, National Osteoporosis Society, NHS, Royal College of Nursing.