针对子宫腺肌症患者的微信辅助电子症状测量。

IF 3.3 3区 医学 Q2 MEDICAL INFORMATICS
Wei Xu, Xin Zhang, Fan Xu, Yuan Yuan, Ying Tang, Qiuling Shi
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引用次数: 0

摘要

目的:症状评估是子宫腺肌症合理治疗的核心。通过基于微信小程序的入口,我们旨在建立一个有效的子宫腺肌症症状评估量表(AM-SAS),以准确、及时地识别症状管理需求,并最终警惕疾病复发:方法:通过对子宫腺肌症患者的深入访谈以及对微信医患交流群的自然语言处理,建立了子宫腺肌症相关症状项目库。专家小组对该清单进行了缩减,最终形成了临时的 AM-SAS。将 AM-SAS 制作成微信小程序并发送给患者,通过经典测验理论和项目反应理论检验其心理效度和临床适用性:共纳入338名子宫腺肌症患者(29人参与访谈,179人参与开发,130人参与外部验证)和86名妇科医生。基于微信的症状评估符合率超过 90%。通过 Rasch 分析,AM-SAS 具有单维性、良好的内部一致性(Cronbach's alphas 均高于 0.8)和测试-再测可靠性(类内相关系数在 0.65 至 0.84 之间)。贫血组和血红蛋白正常组患者的症状严重程度得分存在差异(3.04 ± 3.17 vs. 5.68 ± 3.41,P 结论:AM-SAS 是一种基于电子 PRO 的症状严重程度评分系统:基于PRO的电子AM-SAS是监测AM相关症状的重要工具。作为临床试验中多种症状的结果测量,AM-SAS 可以识别出出院后需要大量护理的患者,并捕捉到患者可能被忽视的重大有益变化:本试验经重庆医科大学机构审查委员会和三家参与医院(南充市中心医院医学伦理委员会、西南医科大学附属医院医学伦理委员会和海扶医院医学伦理委员会)批准,并在中国临床试验注册中心注册(注册号为ChiCTR2000038590),注册日期为2020年10月26日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WeChat assisted electronic symptom measurement for patients with adenomyosis.

Purpose: Symptom assessment is central to appropriate adenomyosis management. Using a WeChat mini-program-based portal, we aimed to establish a valid symptom assessment scale of adenomyosis (AM-SAS) to precisely and timely identify needs of symptom management and ultimately, to alert disease recurrence.

Methods: A combination of intensive interviews of patients with adenomyosis and natural language processing on WeChat clinician-patient group communication was used to generate a pool of symptom items-related to adenomyosis. An expert panel shortened the list to form the provisional AM-SAS. The AM-SAS was built in a Wechat mini-programmer and sent to patients to exam the psychotically validity and clinical applicability through classic test theory and item response theory.

Results: Total 338 patients with adenomyosis (29 for interview, 179 for development, and 130 for external validation) and 86 gynecologists were included. The over 90% compliance to the WeChat-based symptom evaluate. The AM-SAS demonstrated the uni-dimensionality through Rasch analysis, good internal consistency (all Cronbach's alphas above 0.8), and test-retest reliability (intraclass correlation coefficients ranging from 0.65 to 0.84). Differences symptom severity score between patients in the anemic and normal hemoglobin groups (3.04 ± 3.17 vs. 5.68 ± 3.41, P < 0.001). In external validation, AM-SAS successfully detected differences in symptom burden and physical status between those with or without relapse.

Conclusion: Electronic PRO-based AM-SAS is a valuable instrument for monitoring AM-related symptoms. As an outcome measure of multiple symptoms in clinical trials, the AM-SAS may identify patients who need extensive care after discharge and capture significant beneficial changes of patients may have been overlooked.

Trial registration: This trial was approved by the institutional review board of the Chongqing Medical University and three participating hospitals (Medical Ethics Committee of Nanchong Central Hospital, Medical Ethics Committee of Affiliated Hospital of Southwest Medical University, and Medical Ethics Committee of Haifu Hospital) and registered in the Chinese Clinical Trial Registry (registration number ChiCTR2000038590), date of registration was 26/10/2020.

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来源期刊
CiteScore
7.20
自引率
5.70%
发文量
297
审稿时长
1 months
期刊介绍: BMC Medical Informatics and Decision Making is an open access journal publishing original peer-reviewed research articles in relation to the design, development, implementation, use, and evaluation of health information technologies and decision-making for human health.
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