Safran D G, Graham J D, Osberg J S
Health Institute, New England Medical Center, Boston, MA 02111.
Health Serv Res. 1994 Feb;28(6):729-50.
We determine the extent to which noninstitutionalized long-term care patients receive assistance from family members and friends, and evaluate the effect of this assistance on use of outpatient rehabilitative and personal care services.
Over 12 months, primary data were collected from 289 patients in noninstitutional settings after inpatient rehabilitation at three Boston-area rehabilitation hospitals. Data on patients' acute and rehabilitative stays were obtained from medical record reviews. Patients provided primary data on sociodemographics, living arrangements, social supports, functional status, health behaviors, life events, and use of outpatient services during the study period. The latter was verified and service charge data obtained from the care providers.
The study was longitudinal and observational. Patient-provided information was obtained at one, six, and twelve months postdischarge. ANALYTIC METHODS: Multivariate Tobit regression was used to evaluate the effect of social supports on patients' use of rehabilitative and personal care services, controlling for sociodemographics and functional status. Service use was measured as charges incurred during the 12-month study period.
Results confirm the primary role of family and friends in providing daily personal care and identify the availability of that support as a key determinant of expenditures on community-based personal care services. Social supports do not predict outpatient rehabilitative service use.
Differing eligibility criteria seem appropriate for outpatient rehabilitative and personal care services. The current emphasis on functional status in determining rehabilitative service eligibility appears appropriate; but we find that considering patients' social supports would be both meaningful and appropriate in determining personal care service eligibility. This approach would avert the expense of making personal care services universally available, while facilitating assistance for patients whose functional and social status put them at increased risk of institutional placement.
我们确定非机构化长期护理患者从家庭成员和朋友那里获得帮助的程度,并评估这种帮助对门诊康复和个人护理服务使用情况的影响。
在12个月的时间里,从波士顿地区三家康复医院住院康复后处于非机构环境中的289名患者收集了原始数据。患者急性和康复住院的数据通过病历审查获得。患者提供了关于社会人口统计学、生活安排、社会支持、功能状态、健康行为、生活事件以及研究期间门诊服务使用情况的原始数据。后者经过核实,并从护理提供者那里获得了服务收费数据。
该研究为纵向观察性研究。在出院后1个月、6个月和12个月获取患者提供的信息。分析方法:使用多元托比特回归来评估社会支持对患者康复和个人护理服务使用情况的影响,同时控制社会人口统计学和功能状态。服务使用情况以12个月研究期间产生的费用来衡量。
结果证实了家庭成员和朋友在提供日常个人护理方面的主要作用,并确定这种支持的可获得性是社区个人护理服务支出的关键决定因素。社会支持并不能预测门诊康复服务的使用情况。
对于门诊康复和个人护理服务,不同的资格标准似乎是合适的。目前在确定康复服务资格时强调功能状态似乎是合适的;但我们发现,在确定个人护理服务资格时考虑患者的社会支持既合理又恰当。这种方法将避免普遍提供个人护理服务的费用,同时便于为那些功能和社会状态使其进入机构安置风险增加的患者提供帮助。