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1.
Psychol Neuropsychiatr Vieil ; 5(2): 121-5, 2007 Jun.
Artículo en Francés | MEDLINE | ID: mdl-17556218

RESUMEN

Alzheimer's disease has major social and family consequences. However, therapeutic strategies are still limited. Non-pharmacological therapeutic approaches are known to be useful to protect the intellectual abilities of the patients, or at least, to slow down their decline. Therefore, it is important to pay attention to the consequences of sensory impairment in these old patients. Indeed, sensory troubles, mainly concerning hearing, may have an impact on the cognitive and behavioral symptoms. Several studies showed that the management of hearing impairment could afford cognitive and behavioral benefits in demented subjects as well as for the non-demented people. These results are encouraging, and suggest that hearing management should be applied to all hearing impaired patients with Alzheimer's disease.


Asunto(s)
Enfermedad de Alzheimer/epidemiología , Enfermedad de Alzheimer/fisiopatología , Audífonos , Trastornos de la Audición/epidemiología , Trastornos de la Audición/terapia , Anciano , Humanos
2.
J Alzheimers Dis ; 58(1): 123-137, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28387664

RESUMEN

BACKGROUND/OBJECTIVE: This study evaluated the cognitive benefit of hearing aids (HA) in older patients with Alzheimer's disease (AD) and hearing loss (HL) after a 6- and 12-month period of utilization. METHODS: A multicenter double-blind randomized placebo-controlled trial was conducted in patients aged more than 65 years. A group was equipped with active HA for 6 months (active group) and a second group had placebo HA for 6 months (placebo group) followed by a secondary activation phase for a further 6 months (semi crossover procedure). Both groups were retested after a 12-month period. The primary endpoint was the change from baseline of the Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS Cog) after a 6-month period in both groups and after 6 months of secondary HA activation in the placebo group. A smaller cognitive decline should be obtained with HA use; an increase in ADAS Cog score of less than 6 points was defined a success. RESULTS: Fifty-one patients aged 68 to 99 years were included; 38 attended the 6-month visit: 18 in the active group and 20 in the placebo group. At 6 months, 14 (82.4%) successes were noticed in the active group, and 15 (88.2%) in the placebo group (p = 1.0); delta ADAS Cog in the active group was 1.8±5.3 and 1.3±5.3 in the placebo group (p = 0.8). In the placebo group, after the secondary HA activation, no significant improvement was observed. CONCLUSION: No significant effect of HA use was observed after 6 months of follow-up in patients with AD and HL.


Asunto(s)
Enfermedad de Alzheimer/complicaciones , Trastornos del Conocimiento/etiología , Audífonos , Pérdida Auditiva/complicaciones , Pérdida Auditiva/rehabilitación , Anciano , Anciano de 80 o más Años , Enfermedad de Alzheimer/rehabilitación , Audiometría , Trastornos del Conocimiento/rehabilitación , Estudios Cruzados , Método Doble Ciego , Femenino , Humanos , Masculino , Pruebas Neuropsicológicas
3.
J Alzheimers Dis ; 58(1): 109-121, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28269769

RESUMEN

BACKGROUND: It has been suggested that age-related hearing loss (ARHL) and Alzheimer's disease (AD) are commonly associated. OBJECTIVE: The Alzheimer Disease, Presbycusis and Hearing Aids (ADPHA) clinical trial assessed the influence of hearing aids (HAs) on patients affected by ARHL and AD, as judged by behavioral symptoms and functional abilities, as well as patient and caregiver quality of life (QoL). METHODS: A multicenter double-blind randomized placebo-controlled trial, with a semi-crossover procedure over 12 months, was conducted from 2006 to 2012. For the first 6 months, the active group was treated with active HAs and the placebo group with inactive HAs. For the last 6 months, HAs in the placebo group were activated. Assessment was conducted at baseline, 6 months, and 12 months. We performed intergroup and intragroup comparisons. Behavioral symptoms were assessed by neuropsychiatric inventory (NPI), functional abilities by instrumental activities of daily living, and QoL by Zarit, Alzheimer's disease related quality of life, and simplified Duke scales. RESULTS: Fifty-one patients were included and randomized: 22 in active group (mean NPI 17.6; mean age 83±6.2) and 26 in placebo group (mean NPI 25.8; mean age 82.3±7.2) were fitted with HAs. At 6-month follow-up, all scores worsened without significant difference between the two groups. In placebo group, activation of HAs had no effect on the change of these scores. CONCLUSION: These findings do not provide evidence of improvement in behavioral symptoms, functional status, or QoL of hearing impaired AD patients and their caregivers after 6 months of HA use. However, we cannot exclude that HAs may have a positive effect in patients aged less than 75 years.


Asunto(s)
Enfermedad de Alzheimer/psicología , Cuidadores/psicología , Demencia/psicología , Audífonos , Pérdida Auditiva , Calidad de Vida/psicología , Actividades Cotidianas/psicología , Anciano , Anciano de 80 o más Años , Enfermedad de Alzheimer/fisiopatología , Demencia/fisiopatología , Método Doble Ciego , Femenino , Estudios de Seguimiento , Audífonos/psicología , Pérdida Auditiva/etiología , Pérdida Auditiva/fisiopatología , Pérdida Auditiva/psicología , Pérdida Auditiva/rehabilitación , Humanos , Masculino , Pruebas Neuropsicológicas , Evaluación de Resultado en la Atención de Salud , Cooperación del Paciente , Escalas de Valoración Psiquiátrica , Estudios Retrospectivos , Factores de Tiempo
4.
Int J Audiol ; 44(10): 567-73, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16315447

RESUMEN

Presented are results relevant to extending the utility of the auditory steady-state response (ASSR) in threshold estimation at high-frequency carriers and to the accuracy of thresholds estimated using modulation frequencies near 40 versus 80 Hz. Initially, efforts were directed at confirming various findings reported in the literature apropos effects of several basic ASSR parameters. Results supplement others' observations suggesting that ASSR detection limits overestimate behavioral thresholds for conventional audiometric (carrier) frequencies from 500 to 4000 Hz. Further investigation revealed even greater errors of threshold estimates for 8000 and 12000 Hz, by about 14 and 22 dB on average, respectively. Although suggesting high-frequency ASSR testing to be efficacious, technical advances and additional work is needed to establish clinical utility. Comparison of effects of modulation frequency suggested ASSR thresholds with 40 Hz modulation to fall closer to behavioral threshold than those estimated at 80 Hz. Consequently, when circumstances permit, 40 Hz ASSR testing may be the method of choice (e.g. in the assessment of malingers, who may be tested awake/alert).


Asunto(s)
Umbral Auditivo , Potenciales Evocados Auditivos , Trastornos de la Audición/diagnóstico , Pruebas Auditivas/métodos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Audiometría , Femenino , Humanos , Masculino , Persona de Mediana Edad , Programas Informáticos
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