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药品不良反应自愿报告态度调查

Attitudinal survey of voluntary reporting of adverse drug reactions.

作者信息

Eland I A, Belton K J, van Grootheest A C, Meiners A P, Rawlins M D, Stricker B H

机构信息

Pharmaco-epidemiology Unit, Departments of Internal Medicine and Epidemiology and Biostatistics, Erasmus University Medical School, Rotterdam, The Netherlands.

出版信息

Br J Clin Pharmacol. 1999 Oct;48(4):623-7. doi: 10.1046/j.1365-2125.1999.00060.x.

Abstract

AIMS

Voluntary adverse drug reaction (ADR) reporting schemes have operated since the early sixties in many Western countries. It is generally recognized, however, that only a small proportion of ADRs is actually reported. The current survey was conducted to assess attitudes towards reporting of ADRs, and to study which types of ADRs are reported.

METHODS

A questionnaire seeking reasons for nonreporting was sent to a random sample of 10% of medical practitioners in The Netherlands in October 1997. After 6 weeks, a reminder was sent to those who had not responded.

RESULTS

One thousand four hundred and forty-two (73%) questionnaires were returned, of which 94% were complete. The percentage of GPs (51%) which had ever reported an ADR to the national reporting centre was significantly higher than the percentage of specialists (35%), who reported more often to the pharmaceutical industry (34% vs 48%). 86% of GPs, 72% of surgical specialists and 81% of medical specialists had ever diagnosed an ADR, which they had not reported. Uncertainty as to whether the reaction was caused by a drug (72%), the ADR being trivial (75%) or too well known (93%) were the most important reasons for not reporting. 18% were not aware of the need to report ADRs, 22% did not know how to report ADRs, 38% did not have enough time, 36% thought that reporting was too bureaucratic and only 26% of Dutch physicians knew which ADRs to report. A serious ADR, an unlabelled ADR, an ADR to a new drug, history of reporting of one or more ADRs, and specialty were all independently associated with reporting of 16 hypothetical ADRs. Surgical and medical specialists tended to report less often than GPs.

CONCLUSIONS

There is a considerable degree of underreporting, which might partly be explained by lack of knowledge and misconceptions about spontaneous reporting of adverse drug reactions.

摘要

目的

自20世纪60年代初以来,许多西方国家都实行了自愿性药品不良反应(ADR)报告制度。然而,人们普遍认识到,实际报告的ADR只是一小部分。本次调查旨在评估对ADR报告的态度,并研究报告的ADR类型。

方法

1997年10月,向荷兰10%的执业医师随机抽样发送了一份询问未报告原因的问卷。6周后,向未回复的人发送了提醒。

结果

共收回1442份(73%)问卷,其中94%完整。曾向国家报告中心报告过ADR的全科医生(51%)比例显著高于专科医生(35%),专科医生向制药行业报告的频率更高(34%对48%)。86%的全科医生、72%的外科专科医生和81%的内科专科医生曾诊断出ADR但未报告。反应是否由药物引起不确定(72%)、ADR轻微(75%)或太常见(93%)是未报告的最重要原因。18%的人不知道需要报告ADR,22%的人不知道如何报告ADR,38%的人没有足够时间,36%的人认为报告过于官僚化,只有26%的荷兰医生知道应报告哪些ADR。严重ADR、未标注的ADR、新药的ADR、有一个或多个ADR的报告史以及专业都与16种假设的ADR的报告独立相关。外科和内科专科医生报告的频率往往低于全科医生。

结论

存在相当程度的报告不足,这可能部分是由于对药品不良反应自发报告缺乏了解和存在误解。

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