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1.
Medicine (Baltimore) ; 102(30): e34435, 2023 Jul 28.
Artículo en Inglés | MEDLINE | ID: mdl-37505139

RESUMEN

BACKGROUND: A minimal number of studies have documented the impact of Vestibular rehabilitation (VR) on the recovery rate of patients with bilateral vestibular hypofunction (BVH). OBJECTIVE: The purpose of this study was to investigate the effectiveness of structured VR programs on severity of dizziness, kinesiophobia, balance, fatigue, quality of sleep, activities of daily living (ADL) and quality of life (QoL) in subjects with chronic BVH. METHOD: Twenty-five participants diagnosed with BVH were included in the study. A structured VR program was applied in 50-minute sessions once a week and as a home exercise program 3 times a day over 8 weeks. Participants were evaluated for severity of dizziness with the visual analog scale, for kinesiophobia with the tampa scale of kinesiophobia, for balance with the Semitandem, tandem, and standing tests, for quality of sleep with the Pittsburgh sleep quality index, for ADL with the vestibular disorders activities of daily life, for QoL with dizziness handicap inventory and for fatigue with the fatigue severity scale at the baseline (T1), at 4th week (T2), 8th week (T3), and 20th week (T4) after study started. RESULTS: Significant difference in terms of Tandem Test and 1 Leg Stand Test was found in favor of T3-T4 Period (P < .05). There were significant improvements in terms of vestibular disorders activities of daily life, tampa scale of kinesiophobia, Pittsburgh sleep quality index and dizziness handicap inventory in favor of the T3 to T4 Period (P < .05). Significant difference in terms of visual analog scale was found in favor of T2 Period (P < .05). CONCLUSIONS: A twelve-week structured VR program may enhance severity of dizziness, kinesiophobia, balance, quality of sleep, ADL and QoL in participants with chronic BVH.


Asunto(s)
Mareo , Enfermedades Vestibulares , Humanos , Actividades Cotidianas , Calidad de Vida , Calidad del Sueño , Kinesiofobia , Vértigo , Terapia por Ejercicio , Fatiga , Equilibrio Postural
2.
J Int Adv Otol ; 16(1): 47-52, 2020 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-31287437

RESUMEN

OBJECTIVES: This study evaluated the efficacy of intratympanic steroid injection (ITSI)as initial treatment and therecovery speed for Bell's palsy (BP)inpatients with diabetes mellitus (DM)and/or hypertension (HT). MATERIALS AND METHODS: In total,90 patients with comorbid diseases diagnosed with BP received either ITSI (study group, n=61) or systemic steroid treatment (SST) (control group, n=29).The facial nerve function was assessed using the House-Brackmann (HB) grading system for up to 6 months or until complete recovery from BP. To investigate a relationship with the complete recovery time from BP, hematologic and baseline characteristic parameters were analyzed. RESULTS: The complete recovery rate of the ITSI and SST groups was 47.5% and 44.8% at the 1st month, 70.5% and 89.7% at the 3rd month, and 96.7% and 100% at the 6th month of the study, respectively. Lymphocyte and neutrophil values were significantly associated with the complete recovery time from BP. No major adverse events from ITSI itself were noticed during the procedure and during the follow-up of the treatment. CONCLUSION: Both treatment types have no superiorities over each other in initial treatment for BP in patients with comorbid diseases. ITSI is effective and safe and may avoid the unwanted side effects associated with systemic steroids inthese patients.


Asunto(s)
Parálisis de Bell/tratamiento farmacológico , Esteroides/uso terapéutico , Adulto , Anciano , Estudios de Casos y Controles , Comorbilidad , Complicaciones de la Diabetes , Diabetes Mellitus/epidemiología , Nervio Facial/fisiopatología , Femenino , Humanos , Hipertensión/complicaciones , Hipertensión/epidemiología , Inyección Intratimpánica/métodos , Masculino , Persona de Mediana Edad , Recuperación de la Función , Estudios Retrospectivos , Seguridad , Esteroides/administración & dosificación , Esteroides/efectos adversos , Resultado del Tratamiento
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