Bridgepoint Collaboratory for Research and Innovation, Bridgepoint Health, Toronto, ON, Canada; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada.
Health Expect. 2013 Dec;16(4):e111-23. doi: 10.1111/hex.12085. Epub 2013 May 27.
This study investigated what is important in care delivery from the perspective of hospital inpatients with complex chronic disease, a currently understudied population.
One-on-one semi-structured interviews were conducted with inpatients at a continuing care/rehabilitation hospital (n = 116) in Canada between February and July 2011.
The study design was mixed methods and reports on patient characteristics and care delivery experiences. Basic descriptive statistics were run using SPSS version 17, and thematic analysis on the transcripts was conducted using NVivo9 software.
Patients had an average of 5 morbidities and several illness symptoms including activity of daily living impairments, physical pain and emotional disturbance. Three broad themes (each with one or more subthemes) were generated from the data representing important components of care delivery: components of the care plan (a comprehensive assessment, supported transitions and a bio-psycho-social care package); care capacity and quality (optimal staff to patient ratios, quicker response times, better patient-provider communication and consistency between providers) and the patient-provider relationships (characterized by respect and dignity).
As health systems throughout the industrialized world move to sustain health budgets while optimizing quality of care, it is critical to better understand this population, so that appropriate metrics, services and policies can be developed. The study has generated a body of evidence on the important components of care delivery from the perspectives of a diverse group of chronically ill individuals who have spent a considerable amount of time in the health-care system. Moving forward, exploration around the appropriate funding models and skill mix is needed to move the evidence into changed practice.
本研究从患有复杂慢性病的住院患者的角度出发,探讨了护理服务中重要的内容。这些患者是目前研究较少的人群。
2011 年 2 月至 7 月期间,在加拿大的一家持续护理/康复医院中对 116 名住院患者进行了一对一的半结构化访谈。
本研究设计为混合方法研究,报告了患者特征和护理服务体验。使用 SPSS 版本 17 进行了基本描述性统计,使用 NVivo9 软件对转录本进行了主题分析。
患者平均有 5 种合并症和多种疾病症状,包括日常生活活动障碍、身体疼痛和情绪困扰。从数据中生成了三个广泛的主题(每个主题都有一个或多个子主题),代表了护理服务的重要组成部分:护理计划的组成部分(全面评估、支持过渡和生物心理社会护理套餐);护理能力和质量(最佳的员工与患者比例、更快的响应时间、更好的医患沟通以及提供者之间的一致性)以及医患关系(以尊重和尊严为特征)。
随着工业化世界各国的医疗保健系统都在维持医疗预算的同时优化护理质量,因此了解这一人群至关重要,以便制定适当的指标、服务和政策。该研究从经历过大量医疗保健系统治疗的不同慢性病患者的角度生成了关于护理服务重要组成部分的证据。下一步,需要探索适当的资金模型和技能组合,将证据转化为实践。