Clark Richard C, Maxwell Simon R J, Kerr Sheena, Cuthbert Melinda, Buchanan Duncan, Steinke Doug, Webb David J, Bateman Nicholas D
Information Services Division (National Health Service, Scotland), Edinburgh, UK.
Drug Saf. 2007;30(4):357-66. doi: 10.2165/00002018-200730040-00008.
Adverse drug reaction (ADR) reporting makes a vital contribution to pharmacovigilance, although the factors that influence the reporting rate remain unclear. The aim of this study was to investigate whether the variation in the rate of reporting of suspected ADRs in different regions of Scotland was explained by differences in local prescribing practice and to quantify the extent of this influence.
Population and primary care prescribing data were obtained for ten geographical areas based on the 15 administrative regions of the National Health Service in Scotland. All reports of suspected ADRs received from within Scotland for 2000 and 2001 were available from the regional monitoring centre (Committee on Safety of Medicines, Scotland). The primary analysis was based on 14 medications that appeared in the 'top ten' list for the frequency of reported ADRs for either year. Reporting rates for each area were expressed both in terms of population (reports per million people) and in terms of estimated exposure to those medications in primary care (reports per 1000 prescriptions). For each analysis, the Pearson correlation coefficient between reporting and prescribing data was calculated using SPSS software.
The 'top ten' medications accounted for 1715 of 2817 (60.9%, 95% CI 59.1, 62.7) ADR reports but only 2.2 million out of a total of 128 million primary care prescriptions (1.7%). Although there was a 3-fold geographical variation in the per-population ADR reporting rate, there was a close correlation between local reporting of ADRs and prescribing of the index medications (p = 0.66, p = 0.04, respectively). This implies that 44% of the observed variation in reporting rate can be attributed to variation in prescribing within the same population.
Spontaneous ADR reporting in Scotland over the 2 years studied was highly concentrated on a small number of medications that were under intensive surveillance. Although there was a 3-fold variation in reporting rates from individual geographic areas when corrected for the size of the population, primary care prescribing data showed nearly half of this local variation in reporting rates could be explained by differences in prescribing. This study highlights the importance of considering prescribing practice when interpreting spontaneous ADR reporting data.
药物不良反应(ADR)报告对药物警戒至关重要,尽管影响报告率的因素尚不清楚。本研究的目的是调查苏格兰不同地区疑似ADR报告率的差异是否由当地处方习惯的差异所解释,并量化这种影响的程度。
基于苏格兰国民健康服务体系的15个行政区,获取了10个地理区域的人口和基层医疗处方数据。2000年和2001年从苏格兰境内收到的所有疑似ADR报告可从区域监测中心(苏格兰药品安全委员会)获得。主要分析基于在这两年中ADR报告频率“排名前十”的14种药物。每个地区的报告率既以人口为基础表示(每百万人口的报告数),也以基层医疗中这些药物的估计暴露量为基础表示(每1000张处方的报告数)。对于每项分析,使用SPSS软件计算报告数据与处方数据之间的Pearson相关系数。
“排名前十”的药物占2817份ADR报告中的1715份(60.9%,95%置信区间59.1, 62.7),但在总共1.28亿份基层医疗处方中仅占220万份(1.7%)。尽管每人口ADR报告率存在3倍的地理差异,但ADR报告率与索引药物的处方之间存在密切相关性(分别为p = 0.66,p = 0.04)。这意味着观察到的报告率差异中有44%可归因于同一人群中处方的差异。
在所研究的两年中,苏格兰的自发ADR报告高度集中在少数受到密切监测的药物上。尽管在根据人口规模校正后,各个地理区域的报告率存在3倍差异,但基层医疗处方数据显示,报告率的这种局部差异近一半可由处方差异来解释。本研究强调了解读自发ADR报告数据时考虑处方习惯的重要性。