Natalie C Benda, Ruth M Masterson Creber, Roberta Scheinmann, Stephanie Nino de Rivera, Eric Costa Pimentel, Robin B Kalish, Laura E Riley, Alison Hermann, Jessica S Ancker
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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.</p><p><strong>Results: </strong> Fewer Black participants, compared with all other groups, stated that they had used an app for reporting symptoms (<i>p</i> = 0.02), were least interested in downloading the described application (<i>p</i> < 0.05), and found a feature for sharing warning sign information with friends and family least important (<i>p</i> < 0.01). Black and non-Hispanic Black participants also preferred reporting symptoms less frequently as compared with Hispanic participants (English and Spanish-speaking; all <i>p</i> < 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 <i>p</i> < 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.</p>","PeriodicalId":48956,"journal":{"name":"Applied Clinical Informatics","volume":"15 4","pages":"692-699"},"PeriodicalIF":2.1000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11338653/pdf/","citationCount":"0","resultStr":"{\"title\":\"Sociodemographic Differences in Perspectives on Postpartum Symptom Reporting.\",\"authors\":\"Natalie C Benda, Ruth M Masterson Creber, Roberta Scheinmann, Stephanie Nino de Rivera, Eric Costa Pimentel, Robin B Kalish, Laura E Riley, Alison Hermann, Jessica S Ancker\",\"doi\":\"10.1055/s-0044-1788328\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong> 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.</p><p><strong>Methods: </strong> 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.</p><p><strong>Results: </strong> Fewer Black participants, compared with all other groups, stated that they had used an app for reporting symptoms (<i>p</i> = 0.02), were least interested in downloading the described application (<i>p</i> < 0.05), and found a feature for sharing warning sign information with friends and family least important (<i>p</i> < 0.01). Black and non-Hispanic Black participants also preferred reporting symptoms less frequently as compared with Hispanic participants (English and Spanish-speaking; all <i>p</i> < 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 <i>p</i> < 0.05) CONCLUSION: Different participant groups described distinct preferences for postpartum symptom reporting based on race, ethnicity, and preferred languages. 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引用次数: 0
摘要
目标:这项工作的总体目标是创建一个患者报告结果(PRO)和决策支持系统,帮助产后患者确定何时就相关症状寻求治疗。在本案例研究中,我们评估了基于种族、民族和首选语言的应用设计需求观点差异:方法:我们从一个现有的调查小组中招募了 446 名在过去 12 个月中生育过的参与者。我们从四个自我报告的人口统计群体中抽取了参与者:(1) 英语小组,黑人/非洲裔美国人,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。参与者通过调查就以下方面提供了反馈意见:使用应用程序的兴趣、报告症状的舒适度、希望报告的频率、报告工具的功能以及有关症状的首选外联途径:与所有其他组别相比,只有较少的黑人参与者表示他们使用过用于报告症状的应用程序(p = 0.02),他们对下载所述应用程序的兴趣最小(p p p p
Sociodemographic Differences in Perspectives on Postpartum Symptom Reporting.
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 (p = 0.02), were least interested in downloading the described application (p < 0.05), and found a feature for sharing warning sign information with friends and family least important (p < 0.01). Black and non-Hispanic Black participants also preferred reporting symptoms less frequently as compared with Hispanic participants (English and Spanish-speaking; all p < 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 p < 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.
期刊介绍:
ACI is the third Schattauer journal dealing with biomedical and health informatics. It perfectly complements our other journals Öffnet internen Link im aktuellen FensterMethods of Information in Medicine and the Öffnet internen Link im aktuellen FensterYearbook of Medical Informatics. The Yearbook of Medical Informatics being the “Milestone” or state-of-the-art journal and Methods of Information in Medicine being the “Science and Research” journal of IMIA, ACI intends to be the “Practical” journal of IMIA.