OBJECTIVES: To examine differences between users and non-users of community services in caregivers of persons with dementia (PWD). A profile of who used services versus did not use services was developed. DESIGN AND SAMPLE: Existing cross-sectional data from the NINR funded National Caregiver Training Project (data collected 1995-1997) were used. The sample (N = 241) of caucasian, well-educated caregivers reflected a mix of spouse and adult caregivers with a mean age of 64.8 years. MEASURES: Variables measured included caregiver social support, burden, and depression as well as problem behavior of PWD. RESULTS: The majority of caregivers did not attend support groups (73%) or use respite services (79%). Among caregivers who did not use services, 78% lived with the recipient and 77% were spouses. The profile of non-users compared to users revealed that non-users were significantly older, more depressed, and received less social support. On the other hand, non-users provided fewer hours of care per week to recipients who had less cognitive and functional deterioration and fewer behavior problems. CONCLUSIONS: These findings provide public health nurses with knowledge about service use in caregivers of PWD. Recommendations regarding caregiver needs for assistance and increased use of services before a crisis ensues are presented.
OBJECTIVES: To examine differences between users and non-users of community services in caregivers of persons with dementia (PWD). A profile of who used services versus did not use services was developed. DESIGN AND SAMPLE: Existing cross-sectional data from the NINR funded National Caregiver Training Project (data collected 1995-1997) were used. The sample (N = 241) of caucasian, well-educated caregivers reflected a mix of spouse and adult caregivers with a mean age of 64.8 years. MEASURES: Variables measured included caregiver social support, burden, and depression as well as problem behavior of PWD. RESULTS: The majority of caregivers did not attend support groups (73%) or use respite services (79%). Among caregivers who did not use services, 78% lived with the recipient and 77% were spouses. The profile of non-users compared to users revealed that non-users were significantly older, more depressed, and received less social support. On the other hand, non-users provided fewer hours of care per week to recipients who had less cognitive and functional deterioration and fewer behavior problems. CONCLUSIONS: These findings provide public health nurses with knowledge about service use in caregivers of PWD. Recommendations regarding caregiver needs for assistance and increased use of services before a crisis ensues are presented.
Authors: Geoffrey Tremont; Jennifer D Davis; Brian R Ott; Rachel Galioto; Cara Crook; George D Papandonatos; Richard H Fortinsky; Pedro Gozalo; Duane S Bishop Journal: J Am Geriatr Soc Date: 2016-12-23 Impact factor: 5.562
Authors: Raquel Martín-García; Guillermo Martín-Avila; María De la Rubia-Marcos; Raquel Maroto-Rodríguez; Celia Ortega-Angulo; María Teresa Carreras Rodriguez; Francisco Abad Santos; Ana Beatriz Gago Veiga Journal: Dement Geriatr Cogn Dis Extra Date: 2016-03-16
Authors: Connie Lethin; Helena Leino-Kilpi; Brenda Roe; Maria Martin Soto; Kai Saks; Astrid Stephan; Sandra Zwakhalen; Adelaida Zabalegui; Staffan Karlsson Journal: BMC Geriatr Date: 2016-01-29 Impact factor: 3.921
Authors: Ana María Rodríguez-González; Eva Rodríguez-Míguez; Ana Duarte-Pérez; Eduardo Díaz-Sanisidro; Ángel Barbosa-Álvarez; Ana Clavería Journal: Aten Primaria Date: 2016-07-14 Impact factor: 1.137