Chinese General Practice ›› 2025, Vol. 28 ›› Issue (02): 228-233.DOI: 10.12114/j.issn.1007-9572.2024.0082
• Original Research·Quality Improvement in Health Services • Previous Articles Next Articles
Received:
2024-03-10
Revised:
2024-05-20
Published:
2025-01-15
Online:
2024-10-28
Contact:
CHEN Yahong
通讯作者:
陈亚红
作者简介:
作者贡献:
陈亚红提出临床问题需求,并与褚红玲共同讨论提出研究思路,即分析慢阻肺领域患者参与医疗质量改进的研究现状,为制订中国慢阻肺领域患者参与的实施策略提供参考依据;褚红玲负责进行范围综述的整体规划和文献检索;李姝润、李信麟负责文献筛选、资料提取、数据分析等;褚红玲和李姝润负责论文起草;李信麟参与论文草稿的修改;陈亚红负责最终版本修订,对论文负责;所有作者确认论文终稿。
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URL: https://www.chinagp.net/EN/10.12114/j.issn.1007-9572.2024.0082
序号 | 检索式 |
---|---|
#1 | "patient participation"[MeSH Terms] |
#2 | "patient preference"[MeSH Terms] |
#3 | "patient need"[Title/Abstract] |
#4 | "patient insight"[Title/Abstract] |
#5 | "patient perspective"[Title/Abstract] |
#6 | "patients' experience"[Title/Abstract] |
#7 | #1 OR #2 OR #3 OR #4 OR #5 OR #6 |
#8 | "pulmonary disease,chronic obstructive"[MeSH Terms] |
#9 | "Chronic Obstructive Pulmonary Disease"[Title/Abstract] |
#10 | "COPD"[Title/Abstract] |
#11 | #8 OR #9 OR #10 |
#12 | #7 AND #11 |
Table 1 Search strategy in PubMed
序号 | 检索式 |
---|---|
#1 | "patient participation"[MeSH Terms] |
#2 | "patient preference"[MeSH Terms] |
#3 | "patient need"[Title/Abstract] |
#4 | "patient insight"[Title/Abstract] |
#5 | "patient perspective"[Title/Abstract] |
#6 | "patients' experience"[Title/Abstract] |
#7 | #1 OR #2 OR #3 OR #4 OR #5 OR #6 |
#8 | "pulmonary disease,chronic obstructive"[MeSH Terms] |
#9 | "Chronic Obstructive Pulmonary Disease"[Title/Abstract] |
#10 | "COPD"[Title/Abstract] |
#11 | #8 OR #9 OR #10 |
#12 | #7 AND #11 |
项目 | 篇数(篇) | 占比(%) |
---|---|---|
国家 | ||
英国 | 6 | 16.22 |
美国 | 4 | 10.81 |
荷兰 | 4 | 10.81 |
德国 | 3 | 8.11 |
中国 | 3 | 8.11 |
澳大利亚 | 2 | 5.40 |
意大利 | 2 | 5.40 |
瑞典 | 2 | 5.40 |
其他国家(爱尔兰、巴西、丹麦、法国、加拿大、厄瓜多尔、日本、瑞士、泰国、西班牙、印度尼西亚) | 11 | 29.73 |
年份 | ||
2000—2011年 | 4 | 10.81 |
2012—2015年 | 9 | 24.32 |
2016—2018年 | 11 | 29.73 |
2019—2022年 | 14 | 37.84 |
患者参与的目的类别 | ||
为临床研究提供反馈 | 20 | 54.05 |
为医疗实践提供反馈 | 17 | 45.95 |
收集患者声音的方法 | ||
访谈 | 19 | 51.35 |
问卷调查 | 9 | 24.32 |
访谈+问卷调查 | 7 | 18.92 |
离散选择试验 | 2 | 5.41 |
Table 2 Overview of the included literatures related to the patient involvement among COPD
项目 | 篇数(篇) | 占比(%) |
---|---|---|
国家 | ||
英国 | 6 | 16.22 |
美国 | 4 | 10.81 |
荷兰 | 4 | 10.81 |
德国 | 3 | 8.11 |
中国 | 3 | 8.11 |
澳大利亚 | 2 | 5.40 |
意大利 | 2 | 5.40 |
瑞典 | 2 | 5.40 |
其他国家(爱尔兰、巴西、丹麦、法国、加拿大、厄瓜多尔、日本、瑞士、泰国、西班牙、印度尼西亚) | 11 | 29.73 |
年份 | ||
2000—2011年 | 4 | 10.81 |
2012—2015年 | 9 | 24.32 |
2016—2018年 | 11 | 29.73 |
2019—2022年 | 14 | 37.84 |
患者参与的目的类别 | ||
为临床研究提供反馈 | 20 | 54.05 |
为医疗实践提供反馈 | 17 | 45.95 |
收集患者声音的方法 | ||
访谈 | 19 | 51.35 |
问卷调查 | 9 | 24.32 |
访谈+问卷调查 | 7 | 18.92 |
离散选择试验 | 2 | 5.41 |
参与类别 | 参与程度 | ||
---|---|---|---|
咨询 | 参与 | 合作伙伴,共同领导 | |
患者参与直接的诊疗过程 | 患者接收诊疗信息,N=0 | 治疗中患者对治疗计划提出意愿和偏好,N=3 | 治疗决策是基于患者偏好、医学证据和临床判断,N=0 |
患者参与组织层面的设计与管理 | 调查了解患者的治疗体验,N=10 组织患者讨论他们关注的问题,N=2 | 纳入患者作为顾问或咨询委员会成员,N=0 参与医疗质量改进工具开发,N=2 | 患者参与质量改进委员会,N=0 患者参与决定如何分配卫生资源,N=0 |
患者参与临床研究 | 倾听患者需求,N=4 | 对干预措施提出意愿和偏好,N=10 参与评估工具开发,N=4 患者参与研究设计与实施讨论,N=2 | 患者参与推荐研究优先资助方向,N=0 患者参与干预措施应用决策,N=0 |
Table 3 Implementation of patient involvement in health care to improve quality of care among COPD
参与类别 | 参与程度 | ||
---|---|---|---|
咨询 | 参与 | 合作伙伴,共同领导 | |
患者参与直接的诊疗过程 | 患者接收诊疗信息,N=0 | 治疗中患者对治疗计划提出意愿和偏好,N=3 | 治疗决策是基于患者偏好、医学证据和临床判断,N=0 |
患者参与组织层面的设计与管理 | 调查了解患者的治疗体验,N=10 组织患者讨论他们关注的问题,N=2 | 纳入患者作为顾问或咨询委员会成员,N=0 参与医疗质量改进工具开发,N=2 | 患者参与质量改进委员会,N=0 患者参与决定如何分配卫生资源,N=0 |
患者参与临床研究 | 倾听患者需求,N=4 | 对干预措施提出意愿和偏好,N=10 参与评估工具开发,N=4 患者参与研究设计与实施讨论,N=2 | 患者参与推荐研究优先资助方向,N=0 患者参与干预措施应用决策,N=0 |
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