Differences in reproductive health discussions in an urban Hispanic population with SLE: lessons from the field

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Martha Delgado, Jack Rodman, Meredith Xepoleas, Michael Weisman, Leanna Marderian Wise
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Abstract

Objective Management of reproductive health-related issues is crucial for patients with SLE, given this is a disease that primarily affects women of childbearing age. Little is known as to how the 2020 American College of Rheumatology (ACR) Reproductive Health in Rheumatic Disease Guideline is experienced by an underserved, primarily Hispanic population and their physicians as it relates to pregnancy planning and contraception conversations. Given this population experiences high rates of unplanned pregnancies and worse SLE outcomes compared with the non-Hispanic white population, it is crucial to understand how reproductive health is discussed in this setting. Methods A survey based on the 2020 ACR Reproductive Health Guideline was created and distributed in English and Spanish in the outpatient setting to 151 patients with SLE to determine patients’ beliefs, experiences and limitations with reproductive health discussions. Associations between categorical variables were evaluated using Pearson’s χ2 or Fisher’s exact test, as appropriate, and differences in continuous variables were assessed using Wilcoxon rank-sum test. Results English language survey respondents were significantly more likely to report having conversations regarding contraception, pregnancy planning and peripartum medication use than the Spanish survey respondents. Two-thirds of all respondents relied on the rheumatologist as a top source of reproductive health information. Conclusion Disparities exist regarding reproductive health conversations on multiple topics between English-speaking and Spanish-speaking populations with SLE. Further understanding is needed to clarify why reproductive health conversations occur at lower frequencies in Spanish-speaking SLE populations. Data are available upon reasonable request.
患有系统性红斑狼疮的城市西班牙裔人群在生殖健康讨论方面的差异:来自实地的经验教训
目的 鉴于系统性红斑狼疮是一种主要影响育龄妇女的疾病,因此对系统性红斑狼疮患者进行生殖健康相关问题的管理至关重要。对于美国风湿病学会(ACR)2020 年《风湿病生殖健康指南》,服务不足的人群(主要是西班牙裔人群)及其医生是如何理解其与怀孕计划和避孕对话相关的内容的,我们知之甚少。与非西班牙裔白人相比,该人群的计划外怀孕率较高,系统性红斑狼疮的治疗效果也较差,因此了解在这种情况下如何讨论生殖健康问题至关重要。方法 根据 2020 年 ACR 生殖健康指南制作了一份调查问卷,并在门诊环境中以英语和西班牙语向 151 名系统性红斑狼疮患者分发,以确定患者对生殖健康讨论的信念、经验和限制。分类变量之间的关联酌情使用皮尔逊χ2 或费雪精确检验进行评估,连续变量之间的差异使用 Wilcoxon 秩和检验进行评估。结果 英语调查对象在避孕、计划怀孕和围产期用药方面进行交谈的比例明显高于西班牙语调查对象。三分之二的受访者将风湿免疫科医生作为生殖健康信息的首要来源。结论 系统性红斑狼疮患者中讲英语和讲西班牙语的人群在就多个话题进行生殖健康对话方面存在差异。我们需要进一步了解为何讲西班牙语的系统性红斑狼疮患者进行生殖健康对话的频率较低。如有合理要求,可提供相关数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus Science & Medicine
Lupus Science & Medicine RHEUMATOLOGY-
CiteScore
5.30
自引率
7.70%
发文量
88
审稿时长
15 weeks
期刊介绍: Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.
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