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为艾滋病毒/艾滋病患者提供优质护理:患者视角

Quality Care for People with HIV/AIDS: patients' perspectives.

作者信息

Davis-Michaud Mary, Yurk Robin, Lansky David, Asch Steven, Wu Albert W

机构信息

Medical Service, Portland VA Medical Center, Portland, Oregon, USA.

出版信息

HIV Clin Trials. 2004 Nov-Dec;5(6):406-15. doi: 10.1310/GQ98-PGK7-0T97-47XH.

Abstract

PURPOSE

To explore patient preferences to aid in the development of quality measures to assess quality of health care for people living with human immunodeficiency virus/acquired immunodeficiency disease (HIV/AIDS).

METHOD

This study involved three 2-hour focus groups with 29 people living with HIV/AIDS in Portland, Oregon, and San Francisco, California. Eighteen quality of care indicators for HIV/AIDS health care were presented to each group and quantitative rankings were obtained. Aggregated weightings were used to rank and prioritize the quality measures for further exploration.

RESULTS

Participants identified 38 themes relevant to high-quality care for HIV/AIDS. Patients ranked the following candidate measures most important: effective relationship with provider, prevention of opportunistic infections, involvement in care and treatment decisions, being offered antiretroviral treatment, and access to health care services. We observed attitudinal differences among focus group participants that corresponded to gender and race/ethnicity.

CONCLUSION

Participants favored quality information that rated the experience of care and outcome measures including indicators of access to services, standard treatments, and competence of the providers. Patient perspectives can inform the development of quality measures that are meaningful to consumers and can assist in the design of services that meet patients' demographic and socioeconomic needs.

摘要

目的

探讨患者偏好,以协助制定质量指标,用于评估感染人类免疫缺陷病毒/获得性免疫缺陷综合征(HIV/AIDS)患者的医疗保健质量。

方法

本研究在俄勒冈州波特兰市和加利福尼亚州旧金山对29名HIV/AIDS患者进行了3次为时2小时的焦点小组访谈。向每个小组展示了18项HIV/AIDS医疗保健的护理质量指标,并获得了定量排名。使用汇总权重对质量指标进行排名和优先排序,以便进一步探讨。

结果

参与者确定了38个与HIV/AIDS高质量护理相关的主题。患者将以下候选指标列为最重要的:与医护人员建立有效的关系、预防机会性感染、参与护理和治疗决策、提供抗逆转录病毒治疗以及获得医疗保健服务。我们观察到焦点小组参与者之间的态度差异与性别和种族/民族相关。

结论

参与者倾向于能对护理体验和结果指标(包括获得服务的指标、标准治疗以及医护人员的能力)进行评分的质量信息。患者的观点可为制定对消费者有意义的质量指标提供参考,并有助于设计满足患者人口统计学和社会经济需求的服务。

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