Information needs preferences of Chinese colorectal cancer patients receiving chemotherapy: A discrete choice experiment

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Linlin Li, Xueli Liu, Wanjun Zhou, Yawen Zhang, Xinqiong Zhang
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引用次数: 0

Abstract

Objective

The study aims to investigate the information needs and preferences of colorectal cancer (CRC) patients undergoing chemotherapy using a discrete choice experiment (DCE) to optimize and improve the information support strategy for these patients.

Methods

Between May and July 2023, 165 patients with CRC who were receiving chemotherapy at a single hospital in China completed the questionnaire. The survey instruments included a general information questionnaire, a DCE questionnaire, and the Brief Health Literacy Screening Scale. A conditional logit model was used with Stata 16.0 software to analyze patients' preferences.

Results

A total of 159 valid questionnaires were collected, and the questionnaire response rate was 96.4%. All 7 included attributes had an impact on patients' information needs preference (P < 0.05). Among them, information providers, knowledge content, and social support had high relative importance, which were 12.16%, 7.57% and 2.25%, respectively. Patients showed a preference for attending doctors (β = 1.9439, P < 0.05) and primary nurses (β = 1.7985, P < 0.05). Providing knowledge related to disease basis, treatment, and health promotion also had a significant impact (β = 1.6224, P < 0.05).

Conclusions

Healthcare professionals should be the primary information source for patients and improve the accessibility of information by establishing professional information platforms or identifying reliable channels. It is recommended to provide continuous information on treatment and health promotion to CRC patients at various stages of chemotherapy. Attention should be paid to identifying and providing measures to alleviate the economic and psychological burden and to meet the social support needs of patients.

中国结直肠癌化疗患者的信息需求偏好:离散选择实验
方法2023年5月至7月,165名在中国某医院接受化疗的结直肠癌(CRC)患者填写了调查问卷。调查工具包括一般信息问卷、DCE问卷和简明健康素养筛查量表。结果 共收集到 159 份有效问卷,问卷回收率为 96.4%。所有 7 个属性都对患者的信息需求偏好有影响(P < 0.05)。其中,信息提供者、知识内容和社会支持的相对重要性较高,分别为 12.16%、7.57% 和 2.25%。患者偏好主治医生(β = 1.9439,P < 0.05)和初级护士(β = 1.7985,P < 0.05)。结论医护人员应成为患者的主要信息来源,并通过建立专业信息平台或确定可靠渠道来提高信息的可及性。建议在化疗的不同阶段为 CRC 患者提供持续的治疗和健康促进信息。应注意确定和提供减轻患者经济和心理负担的措施,满足患者的社会支持需求。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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