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患者对肾脏替代治疗信息与教育的认知:欧洲肾脏患者联合会关于肾脏替代治疗信息与支持的独立调查

Patients' perceptions of information and education for renal replacement therapy: an independent survey by the European Kidney Patients' Federation on information and support on renal replacement therapy.

作者信息

Van Biesen Wim, van der Veer Sabine N, Murphey Mark, Loblova Olga, Davies Simon

机构信息

Renal Division, Ghent University Hospital, Ghent, Belgium.

Department of Medical Informatics, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

PLoS One. 2014 Jul 31;9(7):e103914. doi: 10.1371/journal.pone.0103914. eCollection 2014.

Abstract

BACKGROUND

Selection of an appropriate renal replacement modality is of utmost importance for patients with end stage renal disease. Previous studies showed provision of information to and free modality choice by patients to be suboptimal. Therefore, the European Kidney Patients' Federation (CEAPIR) explored European patients' perceptions regarding information, education and involvement on the modality selection process.

METHODS

CEAPIR developed a survey, which was disseminated by the national kidney patient organisations in Europe.

RESULTS

In total, 3867 patients from 36 countries completed the survey. Respondents were either on in-centre haemodialysis (53%) or had a functioning graft (38%) at the time of survey. The majority (78%) evaluated the general information about kidney disease and treatment as helpful, but 39% did not recall being told about alternative treatment options than their current one. Respondents were more often satisfied with information provided on in-centre haemodialysis (90%) and transplantation (87%) than with information provided on peritoneal dialysis (79%) or home haemodialysis (61%), and were more satisfied with information from health care professionals vs other sources such as social media. Most (75%) felt they had been involved in treatment selection, 29% perceived they had no free choice. Involvement in modality selection was associated with enhanced satisfaction with treatment (OR 3.13; 95% CI 2.72-3.60). Many respondents (64%) could not remember receiving education on how to manage their kidney disease in daily life. Perceptions on information seem to differ between countries.

CONCLUSIONS

Kidney patients reported to be overall satisfied with the information they received on their disease and treatment, although information seemed mostly to have been focused on one modality. Patients involved in modality selection were more satisfied with their treatment. However, in the perception of the patients, the freedom to choose an alternative modality showed room for improvement.

摘要

背景

对于终末期肾病患者而言,选择合适的肾脏替代治疗方式至关重要。既往研究表明,向患者提供信息并给予其自由选择治疗方式的情况并不理想。因此,欧洲肾病患者联合会(CEAPIR)探讨了欧洲患者对肾脏替代治疗方式选择过程中信息、教育及参与情况的看法。

方法

CEAPIR开展了一项调查,由欧洲各国的肾病患者组织进行分发。

结果

共有来自36个国家的3867名患者完成了该调查。调查时,受访者中53%正在接受中心血液透析,38%拥有功能良好的移植肾。大多数(78%)受访者认为关于肾病及治疗的总体信息很有帮助,但39%的受访者表示不记得曾被告知除当前治疗方式之外的其他替代治疗选项。受访者对中心血液透析(90%)和移植(87%)相关信息的满意度高于腹膜透析(79%)或家庭血液透析(61%)相关信息,且对来自医疗保健专业人员的信息比对社交媒体等其他来源的信息更满意。大多数(75%)受访者觉得自己参与了治疗方式的选择,29%的受访者认为自己没有自由选择权。参与治疗方式选择与对治疗的满意度提高相关(比值比3.13;95%置信区间2.72 - 3.60)。许多受访者(64%)不记得接受过关于如何在日常生活中管理肾病的教育。各国对信息的看法似乎存在差异。

结论

肾病患者报告称总体上对所获得的关于其疾病及治疗的信息感到满意,尽管信息似乎大多集中在一种治疗方式上。参与治疗方式选择的患者对其治疗更满意。然而,在患者看来,选择替代治疗方式的自由度仍有提升空间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32a3/4117591/50f970f3f4e5/pone.0103914.g001.jpg

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