What proportion of patients refuse consent to data collection from their records for research purposes?

被引：0

作者：

Baker, R ^{[1
]}

Shiels, C ^{[1
]}

Stevenson, K ^{[1
]}

Fraser, R ^{[1
]}

Stone, M ^{[1
]}

机构：

[1] Univ Leicester, Dept Gen Practice & Primary Hlth Care, Clin Goverance Res & Dev Unit, Leicester LE1 7RH, Leics, England

来源：

BRITISH JOURNAL OF GENERAL PRACTICE | 2000年 / 50卷 / 457期

关键词：

patient consent; general practice records; research; asthma; angina;

D O I：

暂无

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

In a randomised trial of the implementation of guidelines for asthma and angina, we sent questionnaires that included a request for consent to collect data from the patient's clinical records to 5069 patients in 81 general practices. Of these 3429 (67.6%) responded, of whom 335 (9.8% [95%, CI = 8.8%-10.8%]) refused consent. We conclude that consent should always be sought unless a research ethics committee has waived this requirement for pressing reasons.

引用

页码：655 / 656

页数：2

共 50 条

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