Siegert Richard J, Jackson Diana M, Playford E Diane, Fleminger Simon, Turner-Stokes Lynne
School of Public Health and Psychosocial Studies and School of Rehabilitation and Occupational Studies, AUT University, Auckland, New Zealand.
BMJ Open. 2014 Feb 28;4(2):e004231. doi: 10.1136/bmjopen-2013-004231.
Part A: To pilot the use of a register to identify and monitor patients with complex needs arising from long-term neurological conditions. Part B: To determine the extent to which patients' needs for health and social services are met following discharge to the community after inpatient rehabilitation; to identify which factors predict unmet needs and to explore the relationship between service provision and outcomes at 12 months.
A multicentre, prospective, cohort study surveying participants at 1, 6 and 12 months using postal/online questionnaires and telephone interview.
Consecutive discharges to the community from all nine tertiary, specialist, inpatient neurorehabilitation services in London over 18 months in 2010-2011.
Of 576 admissions 428 patients were recruited at discharge: 256 responded at 4 weeks, 212 at 6 months and 190 at 12 months.
Neurological Impairment Scale, The Needs and Provision Complexity Scale, The Northwick Park Dependency Scale, Community Integration Questionnaire, Zarit Burden Inventory.
n=322 (75%) expressed willingness to be registered, but in practice less than half responded to questionnaires at 6 and 12 months (49% and 44%, respectively), despite extensive efforts to contact them, with no significant differences between responders and non-responders. Significant unmet needs were identified within the first year following discharge, particularly in rehabilitation, social work support and provision of specialist equipment. Dependency for basic care and motor and cognitive impairment predicted services received, together accounting for 40% of the variance. Contra to expectation, patients whose rehabilitation needs were met were more dependent and less well integrated at 12 months post discharge than those with unmet needs.
Registration is acceptable to most patients, but questionnaires/telephone interviews may not be the most efficient way to reach them. When community resources are limited, service provision tends to be focused on the most dependent patients.
The study was registered with the NIHR Comprehensive Local Research Network: ID number 7503.
A部分:试行使用登记册来识别和监测因长期神经系统疾病而有复杂需求的患者。B部分:确定患者在住院康复后出院回到社区后,其健康和社会服务需求得到满足的程度;确定哪些因素可预测未满足的需求,并探讨12个月时服务提供与结果之间的关系。
一项多中心、前瞻性队列研究,在1、6和12个月时使用邮政/在线问卷及电话访谈对参与者进行调查。
2010年至2011年期间,伦敦所有9家三级专科住院神经康复服务机构连续18个月向社区的出院患者。
在576例入院患者中,428例患者在出院时被招募:256例在4周时做出回应,212例在6个月时做出回应,190例在12个月时做出回应。
神经功能缺损量表、需求与服务复杂性量表、诺斯威克公园依赖量表、社区融入问卷、扎里特负担量表。
n = 322(75%)表示愿意登记,但实际上在6个月和12个月时,尽管竭尽全力与他们联系,仍分别只有不到一半的人回复问卷(分别为49%和44%),回复者与未回复者之间无显著差异。出院后的第一年内发现了大量未满足的需求,尤其是在康复、社会工作支持和专业设备提供方面。基本护理依赖以及运动和认知障碍可预测所接受的服务,二者共同解释了40%的方差。与预期相反,康复需求得到满足的患者在出院后12个月时比需求未得到满足的患者更依赖他人且融入程度更低。
登记对大多数患者来说是可以接受的,但问卷/电话访谈可能不是联系他们的最有效方式。当社区资源有限时,服务提供往往集中于依赖性最强的患者。
该研究已在英国国家卫生研究院综合地方研究网络注册:识别号7503。