[Purpose] This study aims to describe a protocol based on neurocognitive therapeutic
exercises and determine its feasibility and usefulness for upper extremity functionality
when compared with a conventional protocol. [Subjects and Methods] Eight subacute stroke
patients were randomly assigned to a conventional (control group) or neurocognitive
(experimental group) treatment protocol. Both lasted 30 minutes, 3 times a week for 10
weeks and assessments were blinded. Outcome measures included: Motor Evaluation Scale for
Upper Extremity in Stroke Patients, Motricity Index, Revised Nottingham Sensory Assessment
and Kinesthetic and Visual Imagery Questionnaire. Descriptive measures and nonparametric
statistical tests were used for analysis. [Results] The results indicate a more favorable
clinical progression in the neurocognitive group regarding upper extremity functional
capacity with achievement of the minimal detectable change. The functionality results are
related with improvements on muscle strength and sensory discrimination (tactile and
kinesthetic). [Conclusion] Despite not showing significant group differences between pre
and post-treatment, the neurocognitive approach could be a safe and useful strategy for
recovering upper extremity movement following stroke, especially regarding affected hands,
with better and longer lasting results. Although this work shows this protocol’s
feasibility with the panel of scales proposed, larger studies are required to demonstrate
its effectiveness.
Background: The Nasal Obstruction Symptom Evaluation (NOSE) scale is a symptom-specific, self-completed questionnaire for assessing quality of life related to nasal obstruction or its treatment in patients with septal deviation. The aim of this study was to validate the Spanish adaptation of the NOSE, thus allowing comparison across studies and international multicenter projects. Methodology: Multicenter prospective instrument validation study. Guidelines for the cross-cultural adaptation process from the original English language scale into a Spanish language version were followed. The psychometric properties (reproducibility, reliability, validity, responsiveness) of the Spanish version ("NOSE-e" for "NOSE-espanol") were assessed in 58 consecutive patients undergoing septoplasty (both before and 3 months after surgery) and 58 matched asymptomatic controls. Results: Test-retest reliability and internal consistency reliability were adequate. The NOSE-e demonstrated satisfactory construct validity. Positive correlations between the NOSE-e scores and the score of a visual analog scale measuring the subjective sensation of nasal obstruction were found. The instrument showed excellent between-groups discrimination and high response sensitivity to change. Conclusions: The Spanish version of the NOSE (NOSE-e) is a valid tool for measuring the subjective severity of nasal obstruction, and its use is recommended.
The field of medical applications is currently one of the most dynamic in medicine due to the great potential for improving clinical practice they hold. However, clinicians' opinion around their usability in daily clinical care has not been thoroughly addressed. This study aimed to analyze the otolaryngologists response to a rhinoplasty application. It was designed as a survey of 21 otolaryngologists with regards to a rhinoplasty planning application for the iPhone with the capacity to project potential surgery outcomes through tactile morphing software compared to a photo tracing method used as the gold standard. The participants were asked to rate the usefulness of the two technologies on a visual analog scale from 0-10. Questions addressed included four topics: physician-patient communication; imaging process time; perceived usefulness for preoperative planning; and perceived usefulness for surgery. A one sample t-test was applied to compare the scores of both methods for each question. The test subjects (mean age 43.21 years) rated the utility of the iPhone application as superior to that of the photo tracing method (p < 0.05) concluding that the iPhone application could facilitate an immediate preliminary analysis of the options for nasal improvement.
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