Johns Hopkins University School of Nursing, Baltimore, MD.
Johns Hopkins University School of Nursing, Baltimore, MD.
Am J Geriatr Psychiatry. 2014 Jun;22(6):587-97. doi: 10.1016/j.jagp.2012.11.005. Epub 2013 Jul 25.
To examine prevalence of modifiable risk factors and their contribution to patient quality of life (QoL) as rated by dementia patients and family caregivers.
Cross-sectional.
Home environment.
88 patients and their caregivers.
Modifiable characteristics of home environments, patients, and caregivers were observed or obtained through interview. Demographics and ratings of patients' QoL were obtained from patients and caregivers.
Patients had mean Mini-mental Status Examination (MMSE) score = 17.7 ± 4.6, (range: 10-28) on an average 7.7 ± 2.4 neuropsychiatric behaviors, 6.0 ± 3.1 health conditions and moderate functional challenges; 70.7% (N = 58) had fall risk; 60.5% (N = 52) had sleep problems at least once weekly; and 42.5% (N = 37) had pain. An average of 8.1 ± 5.2 home hazards and 5.4 ± 4.1 adaptations were observed; 51.7% had unmet device/navigation needs. Patients' and caregivers' QoL ratings were unrelated to MMSE; and patients' self-rated QoL was higher than rated by caregivers. Number of health conditions and unmet device/navigation needs were inversely associated with patient self-rated QoL, and number of health conditions, frequency of behaviors, and level of negative communications were inversely associated with caregiver's assessment of patient QoL. Positive endorsement of caregiving was positively associated with caregiver's appraisal of patient QoL. Other factors were unrelated.
Most patients lived at home with high fall risk, unmanaged behavioral symptoms, pain, sleep disturbances, environmental challenges, and multiple hazards. Except for health, factors associated with lower QoL differed for patients and caregivers. Results suggest need to improve QoL by addressing modifiable risk factors and tailoring interventions to patient and caregiver perspectives.
调查可改变的风险因素的流行程度及其对痴呆症患者和家庭照顾者评定的患者生活质量(QoL)的贡献。
横断面研究。
家庭环境。
88 名患者及其照顾者。
通过观察或访谈获得家庭环境、患者和照顾者的可改变特征。从患者和照顾者那里获得患者的人口统计学和 QoL 评分。
患者的平均简易精神状态检查(MMSE)得分为 17.7 ± 4.6(范围:10-28),平均有 7.7 ± 2.4 种神经精神行为、6.0 ± 3.1 种健康状况和中度功能挑战;70.7%(N = 58)有跌倒风险;60.5%(N = 52)每周至少有一次睡眠问题;42.5%(N = 37)有疼痛。观察到平均 8.1 ± 5.2 种家庭危害和 5.4 ± 4.1 种适应措施;51.7%有未满足的设备/导航需求。患者和照顾者的 QoL 评分与 MMSE 无关;患者的自我报告 QoL 评分高于照顾者的评分。健康状况的数量和未满足的设备/导航需求与患者自我报告的 QoL 呈负相关,健康状况的数量、行为的频率和负面交流的程度与照顾者对患者 QoL 的评估呈负相关。积极认可照顾与照顾者对患者 QoL 的评估呈正相关。其他因素与 QoL 无关。
大多数患者在家中生活,有较高的跌倒风险、未管理的行为症状、疼痛、睡眠障碍、环境挑战和多种危害。除健康状况外,患者和照顾者的 QoL 相关因素不同。结果表明,需要通过解决可改变的风险因素和根据患者和照顾者的观点调整干预措施来提高 QoL。