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对活体肾供体评估中使用APOL1基因检测聊天机器人的态度:一项焦点小组研究。

Attitudes Toward Use of an APOL1 Genetic Testing Chatbot in Living Kidney Donor Evaluation: A Focus Group Study.

作者信息

Rogers James L, Gacki-Smith Jessica, Yacat Rochell, Wicklund Catherine, Duquette Debra, Friedewald John, Cooper Matthew, Gilbert Alexander, Agrawal Akansha, Gordon Elisa J

机构信息

Vanderbilt School of Medicine, Nashville, Tennessee, USA.

Center for Health Services and Outcomes Research, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

出版信息

Clin Transplant. 2024 Dec;38(12):e70026. doi: 10.1111/ctr.70026.

Abstract

BACKGROUND

Living kidney donor (LKD) candidates of African ancestry are increasingly asked to undergo Apolipoprotein L1 (APOL1) genetic testing during the donor evaluation process to better understand their risk of kidney disease. LKD candidates' attitudes about using a clinical chatbot on APOL1 remain unknown. This study builds on prior work to culturally adapt the Gia (Genetic Information Assistant) chatbot on APOL1 by assessing donor, recipient, and community member attitudes about the Gia chatbot for enhancing the integration of APOL1 testing into the LKD clinical evaluation workflow.

METHODS

This study involved focus groups and a post-focus group survey in two US cities about the APOL1 Gia chatbot. Qualitative data were analyzed via thematic analysis, and descriptive statistics were used for demographic data.

RESULTS

We conducted 10 focus groups including 54 participants (25 LKDs, 23 community members, and 6 living donor kidney transplant recipients of African ancestry). Five themes emerged: (1) participants supported LKD candidates using the Gia chatbot before the nephrologist clinic visit, (2) participants were interested in undergoing APOL1 testing after using Gia, (3) APOL1 testing costs may influence LKD candidates' willingness to get tested, (4) patients of African ancestry may hold varying preferences for using chatbots in the healthcare setting, and (5) individual-level barriers may limit the use of Gia in the healthcare setting.

CONCLUSIONS

Individuals of African ancestry were highly receptive to integrating the APOL1 chatbot into LKD candidate clinical evaluation, which bodes well for integrating chatbots into the APOL1 clinical genetic testing process.

摘要

背景

在供体评估过程中,越来越多非洲裔的活体肾供体(LKD)候选人被要求进行载脂蛋白L1(APOL1)基因检测,以便更好地了解他们患肾病的风险。LKD候选人对使用关于APOL1的临床聊天机器人的态度尚不清楚。本研究基于之前的工作,通过评估供体、受体和社区成员对Gia(基因信息助手)聊天机器人的态度,对关于APOL1的Gia聊天机器人进行文化适应性调整,以促进将APOL1检测纳入LKD临床评估工作流程。

方法

本研究在两个美国城市开展了关于APOL1 Gia聊天机器人的焦点小组讨论和焦点小组讨论后调查。通过主题分析对定性数据进行分析,使用描述性统计分析人口统计学数据。

结果

我们进行了10个焦点小组讨论,包括54名参与者(25名LKD、23名社区成员和6名非洲裔活体供肾移植受者)。出现了五个主题:(1)参与者支持LKD候选人在肾病科门诊就诊前使用Gia聊天机器人;(2)参与者在使用Gia后有兴趣进行APOL1检测;(3)APOL1检测费用可能影响LKD候选人进行检测的意愿;(4)非洲裔患者在医疗环境中使用聊天机器人可能有不同偏好;(5)个人层面的障碍可能限制Gia在医疗环境中的使用。

结论

非洲裔个体对将APOL1聊天机器人纳入LKD候选人临床评估高度接受,这对于将聊天机器人纳入APOL1临床基因检测过程是个好兆头。

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