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社会人口统计学差异对产后症状报告的看法。

Sociodemographic Differences in Perspectives on Postpartum Symptom Reporting.

机构信息

School of Nursing, Columbia University, New York, New York, United States.

Department of Population Health Sciences, Weill Cornell Medicine, New York, New York, United States.

出版信息

Appl Clin Inform. 2024 Aug;15(4):692-699. doi: 10.1055/s-0044-1788328. Epub 2024 Aug 21.

Abstract

OBJECTIVE

The overall goal of this work is to create a patient-reported outcome (PRO) and decision support system to help postpartum patients determine when to seek care for concerning symptoms. In this case study, we assessed differences in perspectives for application design needs based on race, ethnicity, and preferred language.

METHODS

A sample of 446 participants who reported giving birth in the past 12 months was recruited from an existing survey panel. We sampled participants from four self-reported demographic groups: (1) English-speaking panel, Black/African American race, non-Hispanic ethnicity; (2) Spanish-speaking panel, Hispanic-ethnicity; (3) English-speaking panel, Hispanic ethnicity; (4) English-speaking panel, non-Black race, non-Hispanic ethnicity. Participants provided survey-based feedback regarding interest in using the application, comfort reporting symptoms, desired frequency of reporting, reporting tool features, and preferred outreach pathway for concerning symptoms.

RESULTS

Fewer Black participants, compared with all other groups, stated that they had used an app for reporting symptoms ( = 0.02), were least interested in downloading the described application ( < 0.05), and found a feature for sharing warning sign information with friends and family least important ( < 0.01). Black and non-Hispanic Black participants also preferred reporting symptoms less frequently as compared with Hispanic participants (English and Spanish-speaking; all  < 0.05). Spanish-speaking Hispanic participants tended to prefer calling their professional regarding urgent warning signs, while Black and English-speaking Hispanic groups tended to express interest in using an online chat or patient portal (all  < 0.05) CONCLUSION:  Different participant groups described distinct preferences for postpartum symptom reporting based on race, ethnicity, and preferred languages. Tools used to elicit PROs should consider how to be flexible for different preferences or tailored toward different groups.

摘要

目的

本项工作的总体目标是开发一种患者报告结局(PRO)和决策支持系统,以帮助产后患者确定何时因出现令人担忧的症状而寻求医疗。本病例研究评估了基于种族、民族和首选语言的应用设计需求的观点差异。

方法

从现有的调查小组中招募了 446 名过去 12 个月内分娩的参与者。我们从四个自我报告的人口统计学群体中抽取了参与者:(1)英语小组,黑人/非裔美国人种族,非西班牙裔;(2)西班牙语小组,西班牙裔;(3)英语小组,西班牙裔;(4)英语小组,非黑人种族,非西班牙裔。参与者提供了基于调查的反馈,内容涉及对使用应用程序的兴趣、报告症状的舒适度、报告频率、报告工具功能、以及对令人担忧症状的首选联络途径的偏好。

结果

与所有其他群体相比,黑人参与者表示他们曾使用过应用程序报告症状的比例较少( = 0.02),对下载描述应用程序的兴趣最低( < 0.05),并认为与朋友和家人分享警告信号信息的功能最不重要( < 0.01)。与西班牙裔参与者相比,黑人参与者和非西班牙裔黑人参与者表示报告症状的频率也较低(均  < 0.05)。讲西班牙语的西班牙裔参与者倾向于选择致电他们的专业人员报告紧急警告信号,而黑人和讲英语的西班牙裔群体则倾向于对使用在线聊天或患者门户感兴趣(均  < 0.05)。

结论

不同的参与者群体根据种族、民族和首选语言描述了不同的产后症状报告偏好。用于引出 PRO 的工具应考虑如何灵活适应不同的偏好,或针对不同群体进行定制。

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