剖析患者在以团队为基础的初级保健诊所(加拿大)的就医体验和连续性模式:潜类分析。

IF 4.5 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Nadia Deville-Stoetzel, Isabelle Gaboury, Djamal Berbiche, Mylaine Breton
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引用次数: 0

摘要

背景:获得初级医疗保健服务是减少健康不平等的核心杠杆。具有某些个人社会特征的人口群体更有可能在获得医疗服务方面遇到过多障碍。本研究确定了在以团队为基础的初级医疗诊所工作的家庭医生处登记的患者的就医概况和连续性体验,并探讨了这些概况与个人和组织特征之间的关联:在 2022 年 9 月至 2023 年 4 月期间进行了一次横断面电子调查。邀请了魁北克省 104 家团队初级医疗保健诊所中所有拥有电子邮件地址的注册成年患者参与调查。调查采用潜类分析法,根据获得医疗服务和连续性体验的九个组成部分来识别患者特征。多项式逻辑回归模型用于分析每个特征与个人社会人口统计学、感知健康状况、慢性病等十个特征以及与诊所区域和规模相关的两个特征之间的关联:根据 87 155 名患者的就医经历,确定了四种特征。"方便就医和持续就医"(42% 的受访者)的特点是几乎所有就医和持续就医要素都很方便。三种情况的特点是在就医和/或连续性方面存在不同的困难。"预约困难"(32%)的特点是病人需要多次尝试才能在其诊所获得预约。"连续性障碍"(9%)的特点是患者不得不重复他们档案中本应存在的信息。"就诊和连续性障碍"(16%)是指在就诊和连续性方面遇到的所有困难。女性性别和健康状况差会使属于与困难相关的三种情况的风险明显增加 1.5。新近抵达的移民(p = 0.036)、高中以下教育程度(p = 0.002)和在大型诊所注册(p 结论:这三种情况的风险都很高:这些结果凸显了与就医困难风险增加相关的个人社会和健康特征,如移民身份、教育水平和/或患有慢性病和心理健康状况不佳时的就医连续性困难。建议为新近抵达的移民和教育程度低的患者提供预约便利,为慢性病患者整合跨专业合作实践,并为有心理健康需求的患者改善护理协调和沟通。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Profiling patterns of patient experiences of access and continuity at team-based primary healthcare clinics (Canada): a latent class analysis.

Background: Access to primary healthcare services is a core lever for reducing health inequalities. Population groups living with certain individual social characteristics are disproportionately more likely to experience barriers accessing care. This study identified profiles of access and continuity experiences of patients registered with a family physician working in team-based primary healthcare clinics and explored the associations of these profiles with individual and organizational characteristics.

Methods: A cross-sectional e-survey was conducted between September 2022 and April 2023. All registered adult patients with an email address at 104 team-based primary healthcare clinics in Quebec were invited to participate. Latent class analysis was used to identify patient profiles based on nine components of access to care and continuity experiences. Multinomial logistic regression models were fit to analyze each profile's association with ten characteristics related to individual sociodemographics, perceived heath status, chronic conditions and two related to clinic area and size.

Results: Based on 87,155 patients who reported on their experience, four profiles were identified. "Easy access and continuity" (42% of respondents) was characterized by ease in almost all access and continuity components. Three profiles were characterized by diverging access and/or continuity difficulties. "Challenging booking" (32%) was characterized by patients having to try several times to obtain an appointment at their clinic. "Challenging continuity" (9%) was characterized by patients having to repeat information that should have been in their file. "Access and continuity barriers" (16%) was characterized by difficulties with all access and continuity components. Female gender and poor perceived health significantly increased the risk of belonging to the three profiles associated with difficulties by 1.5. Being a recently arrived immigrant (p = 0.036), having less than a high school education (p = 0.002) and being registered at a large clinic (p < 0.001) were associated with experiencing booking difficulties. Having at least one chronic condition (p = 0.004) or poor perceived mental health (p = 0.048) were associated with experiencing continuity difficulties.

Conclusions: These results highlight individual social and health characteristics associated with increased risk of experiencing healthcare access difficulties, such as immigration status and education level and/or continuity difficulties when having a chronic condition and poor perceived mental health. Facilitating appointment booking for recently arrived immigrants and patients with low education, integrating interprofessional collaboration practices for patients with chronic conditions and improving care coordination and communication for patients with mental health needs are recommended.

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来源期刊
CiteScore
7.80
自引率
4.20%
发文量
162
审稿时长
28 weeks
期刊介绍: International Journal for Equity in Health is an Open Access, peer-reviewed, online journal presenting evidence relevant to the search for, and attainment of, equity in health across and within countries. International Journal for Equity in Health aims to improve the understanding of issues that influence the health of populations. This includes the discussion of political, policy-related, economic, social and health services-related influences, particularly with regard to systematic differences in distributions of one or more aspects of health in population groups defined demographically, geographically, or socially.
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