Allied Health Research, Gold Coast Health, Gold Coast University Hospital, Southport, Queensland, Australia.
Menzies Health Institute Queensland, Griffith University, Southport, Queensland, Australia.
Health Expect. 2022 Dec;25(6):3096-3104. doi: 10.1111/hex.13617. Epub 2022 Oct 13.
Health consumers (patients, their family, friends and carers) are frequently using their smartphones to record hospital clinical encounters. However, there is limited research which has explored the social interaction surrounding this behaviour. Understanding the consumer perspective is key to informing policy and practice. This study explored consumer attitudes and experiences regarding patient-led recordings.
Semistructured interviews were undertaken with 20 hospital consumers. Participants were recruited via advertising, posters and invitation letters. Interviews were digitally recorded and transcribed. Data were analysed using thematic analysis.
Four main themes were identified relating to participant perspectives of patient-led recordings: (1) consumers viewed clinician consent as important, although they reported different experiences of the consent process, (2) consumers indicated that a clinician refusing the recording had the potential to undermine the consumer-clinician relationship, (3) consumers were both uninformed and misinformed regarding relevant policy and legislation and (4) consumers expressed a number of expectations regarding their rights to record and of the health service in supporting this practice.
Consumers want to record their clinical encounters with the consent of their clinician but are unprepared to navigate consent discussions. Health services and clinicians should inform consumers who want to record about their rights and responsibilities, to support the consent process and safe recording environments. Clinician refusal to consent to a patient-led recording may not lead to increased covert recording; however, clear communication about the reasons for refusing a recording is needed to protect the consumer-clinician relationship.
A health consumer was part of the research team and was involved in all stages of this study, including the design, data analysis and reviewing of the manuscript.
健康消费者(患者、其家属、朋友和护理人员)经常使用智能手机记录医院临床就诊情况。然而,针对这一行为的社会互动,相关研究甚少。了解消费者的观点是为政策和实践提供信息的关键。本研究探讨了消费者对患者主导的记录行为的态度和体验。
通过广告、海报和邀请函,对 20 名医院消费者进行了半结构化访谈。对参与者进行了数字录音和转录。使用主题分析对数据进行分析。
确定了与患者主导的记录相关的四个主要主题:(1)消费者认为临床医生的同意很重要,尽管他们报告了不同的同意过程体验;(2)消费者表示,临床医生拒绝记录可能会破坏医患关系;(3)消费者对相关政策和法规既不知情也存在误解;(4)消费者对他们记录的权利以及医疗服务支持这一做法表达了一系列期望。
消费者希望在临床医生同意的情况下记录他们的就诊情况,但他们还没有准备好进行同意讨论。医疗服务机构和临床医生应告知有记录意愿的消费者其权利和责任,以支持同意过程和安全的记录环境。临床医生拒绝同意患者主导的记录可能不会导致更多的秘密记录;然而,需要明确沟通拒绝记录的原因,以保护医患关系。
一名健康消费者是研究团队的一员,参与了本研究的所有阶段,包括设计、数据分析和审查手稿。