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有备而来的患者:新诊断的风湿病患者对互联网信息的搜寻

Prepared patients: internet information seeking by new rheumatology patients.

作者信息

Hay M Cameron, Cadigan R Jean, Khanna Dinesh, Strathmann Cynthia, Lieber Eli, Altman Roy, McMahon Maureen, Kokhab Morris, Furst Daniel E

机构信息

Miami University, Oxford, OH 45056, USA.

出版信息

Arthritis Rheum. 2008 Apr 15;59(4):575-82. doi: 10.1002/art.23533.

Abstract

OBJECTIVE

To investigate to what extent and why new rheumatology patients access medical information online prior to first appointments and secondarily to ask whether they discuss information gained from the Internet with physicians.

METHODS

Research was conducted in a teaching rheumatology clinic with a nonrandom sample of 120 English-speaking adults presenting for first appointments in rheumatology. Quantitative and qualitative data were gained in pre- and postappointment patient surveys and interviews, including online information gathering prior to first appointment, demographics, health status, information usage in patient-physician interactions, and satisfaction. Data were analyzed for significant relationships across variables and for qualitative insights into quantitative outcome measures.

RESULTS

Of all patients, 87.5% looked up their symptoms or suspected condition prior to their first appointment and 62.5% of all patients sought that information on the Internet. Only 20% of online information seekers discussed that information with their physicians. Age and sex were significant predictors of Internet information seeking. Physician and patient appointment satisfaction was significantly higher when Internet information was discussed; however, most patients did not discuss their information seeking because they primarily feared being perceived as challenging their physician.

CONCLUSION

The majority of patients research their conditions online prior to initial appointments, but are unlikely to discuss that research with physicians even though discussion is related to higher satisfaction. Physicians may want to consider strategies for enabling communication about online research.

摘要

目的

调查初诊前新的风湿病患者在多大程度上以及为何会在网上获取医疗信息,其次是询问他们是否会与医生讨论从互联网上获得的信息。

方法

在一家教学风湿病诊所进行研究,对120名前来首次就诊的讲英语的成年患者进行非随机抽样。通过预约前和预约后的患者调查及访谈收集定量和定性数据,包括首次预约前的在线信息收集、人口统计学、健康状况、医患互动中的信息使用情况以及满意度。对数据进行分析,以找出变量之间的显著关系,并对定量结果指标进行定性分析。

结果

在所有患者中,87.5%的患者在首次预约前查找过自己的症状或疑似病症,62.5%的患者在互联网上查找过该信息。在查找过在线信息的患者中,只有20%的人与医生讨论过该信息。年龄和性别是互联网信息查找的显著预测因素。当讨论互联网信息时,医生和患者的预约满意度显著更高;然而,大多数患者不讨论他们查找的信息,主要是因为他们担心被认为是在挑战医生。

结论

大多数患者在首次预约前会在网上研究自己的病情,但即使讨论与更高的满意度相关,他们也不太可能与医生讨论该研究。医生可能需要考虑制定策略,以便就在线研究进行沟通。

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