Fradgley Elizabeth A, Paul Christine L, Bryant Jamie, Roos Ian A, Henskens Frans A, Paul David J
Priority Research Centre for Health Behaviour, School of Medicine and Public Health & Hunter Medical Research Institute, University of Newcastle, Callaghan, Australia.
J Med Internet Res. 2014 Dec 19;16(12):e292. doi: 10.2196/jmir.3545.
With increasing attention given to the quality of chronic disease care, a measurement approach that empowers consumers to participate in improving quality of care and enables health services to systematically introduce patient-centered initiatives is needed. A Web-based survey with complex adaptive questioning and interactive survey items would allow consumers to easily identify and prioritize detailed service initiatives.
The aim was to develop and test a Web-based survey capable of identifying and prioritizing patient-centered initiatives in chronic disease outpatient services. Testing included (1) test-retest reliability, (2) patient-perceived acceptability of the survey content and delivery mode, and (3) average completion time, completion rates, and Flesch-Kincaid reading score.
In Phase I, the Web-based Consumer Preferences Survey was developed based on a structured literature review and iterative feedback from expert groups of service providers and consumers. The touchscreen survey contained 23 general initiatives, 110 specific initiatives available through adaptive questioning, and a relative prioritization exercise. In Phase II, a pilot study was conducted within 4 outpatient clinics to evaluate the reliability properties, patient-perceived acceptability, and feasibility of the survey. Eligible participants were approached to complete the survey while waiting for an appointment or receiving intravenous therapy. The age and gender of nonconsenters was estimated to ascertain consent bias. Participants with a subsequent appointment within 14 days were asked to complete the survey for a second time.
A total of 741 of 1042 individuals consented to participate (71.11% consent), 529 of 741 completed all survey content (78.9% completion), and 39 of 68 completed the test-retest component. Substantial or moderate reliability (Cohen's kappa>0.4) was reported for 16 of 20 general initiatives with observed percentage agreement ranging from 82.1%-100.0%. The majority of participants indicated the Web-based survey was easy to complete (97.9%, 531/543) and comprehensive (93.1%, 505/543). Participants also reported the interactive relative prioritization exercise was easy to complete (97.0%, 189/195) and helped them to decide which initiatives were of most importance (84.6%, 165/195). Average completion time was 8.54 minutes (SD 3.91) and the Flesch-Kincaid reading level was 6.8. Overall, 84.6% (447/529) of participants indicated a willingness to complete a similar survey again.
The Web-based Consumer Preferences Survey is sufficiently reliable and highly acceptable to patients. Based on completion times and reading level, this tool could be integrated in routine clinical practice and allows consumers to easily participate in quality evaluation. Results provide a comprehensive list of patient-prioritized initiatives for patients with major chronic conditions and delivers practice-ready evidence to guide improvements in patient-centered care.
随着对慢性病护理质量的关注度不断提高,需要一种能让消费者参与改善护理质量并使卫生服务机构系统引入以患者为中心举措的测量方法。基于网络的具有复杂适应性提问和交互式调查项目的调查,将使消费者能够轻松识别并优先考虑详细的服务举措。
旨在开发并测试一种基于网络的调查,该调查能够识别以患者为中心的慢性病门诊服务举措并对其进行优先级排序。测试内容包括:(1)重测信度;(2)患者对调查内容和交付方式的可接受性;(3)平均完成时间、完成率以及弗莱什-金凯德阅读分数。
在第一阶段,基于结构化文献综述以及服务提供者和消费者专家小组的反复反馈,开发了基于网络的消费者偏好调查。触摸屏调查包含23项一般举措、110项通过适应性提问可得的具体举措以及一项相对优先级排序活动。在第二阶段,在4家门诊诊所内进行了一项试点研究,以评估该调查的信度特性、患者感知的可接受性和可行性。符合条件的参与者在等待预约或接受静脉治疗时被邀请完成调查。对未同意参与的参与者的年龄和性别进行了估计,以确定同意偏差。要求在14天内有后续预约的参与者再次完成调查。
1042名个体中有741名同意参与(同意率为71.11%),741名中有529名完成了所有调查内容(完成率为78.9%),68名中有39名完成了重测部分。20项一般举措中有16项报告了较高或中等的信度(科恩kappa系数>0.4),观察到的百分比一致性范围为82.1% - 100.0%。大多数参与者表示基于网络的调查易于完成(97.9%,531/543)且内容全面(93.1%,505/543)。参与者还报告交互式相对优先级排序活动易于完成(97.0%,189/195),并帮助他们决定哪些举措最为重要(84.6%,165/195)。平均完成时间为8.54分钟(标准差3.91),弗莱什-金凯德阅读水平为6.8。总体而言,84.6%(447/529)的参与者表示愿意再次完成类似的调查。
基于网络的消费者偏好调查具有足够的信度且患者高度可接受。基于完成时间和阅读水平,该工具可整合到常规临床实践中,使消费者能够轻松参与质量评估。研究结果为患有主要慢性病的患者提供了一份按患者优先级排序的举措综合清单,并提供了可直接应用于实践的证据,以指导以患者为中心的护理改进。