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1.
J Foot Ankle Res ; 13(1): 39, 2020 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-32600388

RESUMEN

PURPOSE: Stroke-related changes in foot structure and function affect balance and mobility and quantifying foot function following stroke could offer clinically useful information to inform rehabilitation. The aim of this work was to explore the feasibility of undertaking plantar pressure assessment during barefoot walking in people with stroke, and evaluate the repeatability of the assessment protocol and regional footprint analysis as a measure of dynamic foot characteristics. MATERIALS & METHODS: Plantar pressure analysis was undertaken using a pressure platform (Tekscan HR Mat) on two test sessions, approximately two weeks apart (mean = 15.64 ± 11.64 days). Peak plantar pressure (kPa) and contact area (cm2) for foot regions were extracted and repeatability analysis undertaken. Descriptive evaluation of field notes and experiences of the participants was undertaken to inform the feasibility of the data collection protocol. RESULTS: Twenty-one participants (61.8 ± 9.2 years; 11 male, 10 female; 8 right-sided, 13 left-sided stroke) were recruited and 18 returned for retesting. Full data capture was achieved from 14 participants. Peak pressure and contact area demonstrated moderate to good repeatability for at the toes (ICC 0.76 and 0.58 respectively) and good to excellent repeatability for the other foot regions (ICC ≥ 0.82). CONCLUSION: The protocol adopted in this study was feasible and yielded good to excellent repeatability for the foot regions, except the toes. The challenges with data collection in our study cohort could help inform future studies adopting similar protocols. This work also has relevance for use of pressure technology in clinical practice for assessing and monitoring foot function following stroke.


Asunto(s)
Acelerometría/estadística & datos numéricos , Evaluación de la Discapacidad , Accidente Cerebrovascular/fisiopatología , Caminata/fisiología , Anciano , Fenómenos Biomecánicos , Estudios de Factibilidad , Femenino , Pie/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Placa Plantar/fisiopatología , Presión , Reproducibilidad de los Resultados
2.
Foot (Edinb) ; 25(3): 159-63, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26205998

RESUMEN

BACKGROUND: Previous studies have demonstrated that stimulating the cutaneous plantar sensory receptors of the foot through textured insoles improves human balance and walking. This study investigated the effect of medial and lateral zoned textured insoles using tibialis anterior/peroneus longus surface electromyographic activity and Centre-of-Pressure as indicators of postural stability while walking. METHODS: 15 asymptomatic subjects were tested using a within-subject randomised repeated measures design. The effect of lateral and medial zoned insoles of varying heights (control, 2, 4 and 6mm) on stability while walking under normal and impaired visual conditions was assessed. RESULTS: Impaired vision resulted in an increase in foot CoP variability while walking (p<0.05). The laterally zoned insole was associated with a significant (repeated measures ANOVA p<0.05) increase in the rate of medial-lateral CoP change. CONCLUSION: These findings suggest that the site of stimulation of the plantar foot cutaneous receptors may increase postural instability during walking. This should be considered in the design of insoles that aim to improve balance and reduce falls risk. The importance of vision in balance control has been highlighted and using impaired vision may serve as a way of trialling clinical products in the healthy population.


Asunto(s)
Ortesis del Pié , Músculo Esquelético/fisiología , Equilibrio Postural/fisiología , Caminata/fisiología , Adulto , Electromiografía , Retroalimentación Sensorial , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estimulación Física , Adulto Joven
4.
BMJ ; 318(7193): 1246-50, 1999 May 08.
Artículo en Inglés | MEDLINE | ID: mdl-10231255

RESUMEN

OBJECTIVE: To determine whether an educational package could influence the management of menorrhagia, increase the appropriateness of choice of non-hormonal treatment, and reduce referral rates from primary to secondary care. DESIGN: Randomised controlled trial. SETTING: General practices in East Anglia. SUBJECTS: 100 practices (348 doctors) in primary care were recruited and randomised to intervention (54) and control (46). INTERVENTIONS: An educational package based on principles of "academic detailing" with independent academics was given in small practice based interactive groups with a visual presentation, a printed evidence based summary, a graphic management flow chart, and a follow up meeting at 6 months. OUTCOME MEASURES: All practices recorded consultation details, treatments offered, and outcomes for women with regular heavy menstrual loss (menorrhagia) over 1 year. RESULTS: 1001 consultation data sheets for menorrhagia were returned. There were significantly fewer referrals (20% v 29%; odds ratio 0. 64; 95% confidence interval 0.41 to 0.99) and a significantly higher use of tranexamic acid (odds ratio 2.38; 1.61 to 3.49) in the intervention group but no overall difference in norethisterone treatment compared with controls. There were more referrals when tranexamic acid was given with norethisterone than when it was given alone. Those practices reporting fewer than 10 cases showed the highest increase in prescribing of tranexamic acid. CONCLUSIONS: The educational package positively influenced referral for menorrhagia and treatment with appropriate non-hormonal drugs.


Asunto(s)
Educación Médica Continua , Medicina Familiar y Comunitaria/educación , Menorragia/terapia , Antiinflamatorios no Esteroideos/uso terapéutico , Antifibrinolíticos/uso terapéutico , Competencia Clínica , Toma de Decisiones , Inglaterra , Femenino , Estudios de Seguimiento , Humanos , Ácido Mefenámico , Menorragia/tratamiento farmacológico , Noretindrona/uso terapéutico , Congéneres de la Progesterona/uso terapéutico , Derivación y Consulta/estadística & datos numéricos , Ácido Tranexámico/uso terapéutico
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