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通过让患者能够访问互联网上的医疗数据,增强接受体外受精治疗患者的能力。

Empowering patients undergoing in vitro fertilization by providing Internet access to medical data.

作者信息

Tuil Wouter S, Verhaak Chris M, Braat Didi D M, de Vries Robbé Pieter F, Kremer Jan A M

机构信息

Department of Obstetrics and Gynaecology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.

出版信息

Fertil Steril. 2007 Aug;88(2):361-8. doi: 10.1016/j.fertnstert.2006.11.197. Epub 2007 Apr 9.

DOI:10.1016/j.fertnstert.2006.11.197
PMID:17416366
Abstract

OBJECTIVE

To study the effect of an Internet-based personal health record on the empowerment of patients undergoing IVF.

DESIGN

Randomized clinical trial.

SETTING

Patients undergoing IVF and intracytoplasmic sperm injection (ICSI) in an academic research environment.

PATIENT(S): We selected patients who were undergoing an IVF or ICSI treatment, have an Internet connection, and speak fluent Dutch.

INTERVENTION(S): An Internet-based personal health record that provides patients with general and personal information concerning their given treatment and that also provides facilities for communication with fellow patients and physicians.

MAIN OUTCOME MEASURE(S): Patient empowerment (measured as a multidimensional concept consisting of self-efficacy, actual and perceived knowledge, and involvement in the decision process), patient satisfaction, meaning of infertility problems, social support, anxiety, and depression.

RESULT(S): A total of 91 female and 89 male participants were suitable for analysis. No significant differences were observed in per person change in patient empowerment. We did not find any significant differences regarding per person change in patient satisfaction, the meaning of infertility problems, social support, anxiety, and depression.

CONCLUSION(S): Usage of the personal health record did not have any effects on patient empowerment, but, at the same time, the study did not find that the personal health record had any significant adverse effects either.

摘要

目的

研究基于互联网的个人健康记录对接受体外受精(IVF)患者赋权的影响。

设计

随机临床试验。

地点

在学术研究环境中接受IVF和卵胞浆内单精子注射(ICSI)的患者。

患者

我们选择了正在接受IVF或ICSI治疗、能上网且荷兰语流利的患者。

干预措施

一种基于互联网的个人健康记录,为患者提供有关其特定治疗的一般和个人信息,并提供与其他患者和医生沟通的便利。

主要观察指标

患者赋权(作为一个多维概念来衡量,包括自我效能感、实际和感知的知识以及参与决策过程)、患者满意度、不孕问题的意义、社会支持、焦虑和抑郁。

结果

共有91名女性和89名男性参与者适合进行分析。在患者赋权的人均变化方面未观察到显著差异。在患者满意度、不孕问题的意义、社会支持、焦虑和抑郁的人均变化方面,我们也未发现任何显著差异。

结论

个人健康记录的使用对患者赋权没有任何影响,但同时,该研究也未发现个人健康记录有任何显著的不良影响。

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