Nemours Center for Cancer and Blood Disorders, Wilmington, Delaware.
Nemours/AI duPont Hospital for Children & Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, Pennsylvania.
Pediatr Blood Cancer. 2018 Nov;65(11):e27306. doi: 10.1002/pbc.27306. Epub 2018 Jul 14.
Management of pediatric cancer entails frequent laboratory and radiology testing to monitor response to treatment, side effects, and possible relapse of disease. Little is known about how caregivers of children with cancer would like to receive results of these tests and whether on-line patient portals may meet those preferences.
One-on-one semistructured interviews were conducted with 19 caregivers of children with cancer purposively sampled for breadth on demographic characteristics. Inductive qualitative content coding/analysis was utilized to distill caregiver's preferred methods for test result acquisition and their views of using an on-line patient portal to do so.
The relative prioritization of speed of information and mode of communication (i.e., "in person," by phone, etc.) revealed three preference styles. Factors including type of testing, type of result, and the time course within their child's care modified these preferences, and the desire to reduce anxiety played a central role. Caregivers recognized advantages of portal use including getting results "fast," being able to visualize trends in results, "keeping a record," and not interfering with clinic flow. Perceived disadvantages included the results being "complicated" or easily misunderstood, and learning results prior to disclosure by care team.
This study provides insight into the importance of understanding of how caregivers want test results and how they utilize the portal. Preferences for result acquisition vary on many factors and include the desire to decrease anxiety. As portal use increases, we have a duty to integrate this technology responsibly.
儿童癌症的治疗需要频繁进行实验室和影像学检查,以监测治疗反应、副作用和疾病复发的可能性。对于癌症患儿的照顾者希望如何接收这些检查结果,以及在线患者门户是否能满足这些需求,我们知之甚少。
采用目的性抽样方法,对 19 名癌症患儿的照顾者进行了一对一的半结构式访谈,以广泛了解其人口统计学特征。采用归纳式定性内容编码/分析方法,提炼出照顾者获取检测结果的首选方法及其对使用在线患者门户获取结果的看法。
信息获取速度和沟通方式(即“面对面”、电话等)的相对优先级揭示了三种偏好风格。包括检测类型、检测结果类型以及患儿治疗过程中的时间因素等因素,都对这些偏好产生了影响,减轻焦虑的愿望起到了核心作用。照顾者认识到使用门户的好处包括“快速”获取结果、能够观察结果趋势、“保存记录”以及不干扰诊所流程。被认为的缺点包括结果“复杂”或容易被误解,以及在医疗团队披露结果之前了解结果。
本研究深入了解了照顾者获取检测结果的方式以及他们如何利用门户的重要性。获取结果的偏好因多种因素而异,包括减轻焦虑的愿望。随着门户使用的增加,我们有责任负责任地整合这项技术。