Tabali Manuela, Jeschke Elke, Bockelbrink Angelina, Witt Claudia M, Willich Stefan N, Ostermann Thomas, Matthes Harald
Research Institute and Community Hospital Havelhoehe, Berlin, Germany.
BMC Public Health. 2009 Jul 31;9:274. doi: 10.1186/1471-2458-9-274.
Recent studies have shown that adverse drug reactions (ADRs) are underreported. This may be particularly true of ADRs associated with complementary and alternative medicine (CAM). Data on CAM-related ADRs, however, are sparse.Objective was to evaluate the impact of an educational intervention and monitoring programme designed to improve physician reporting of ADRs in a primary care setting.
A prospective multicentre study with 38 primary care practitioners specialized in CAM was conducted from January 2004 through June 2007. After 21 month all physicians received an educational intervention in terms of face-to-face training to assist them in classifying and reporting ADRs. The study centre monitored the quantity and quality of ADR reports and analysed the results.To measure changes in the ADR reporting rate, the median number of ADR reports and interquartile range (IQR) were calculated before and after the educational intervention. The pre-intervention and post-intervention quality of the reports was assessed in terms of changes in the completeness of data provided for obligatory items. Interrater reliability between the physicians and the study centre was calculated using Cohen's kappa with a 95% confidence interval (CI). We used Mann Whitney U-test for testing continuous data and chi-square test was used for categorical data. The level of statistical significance was set at P < 0.05.
A total of 404 ADRs were reported during the complete study period. An initial 148% increase (P = 0.001) in the number of ADR reports was observed after the educational intervention. Compared to baseline the postinterventional number of ADR reportings was statistically significant higher (P < 0.005) through the first 16 months after the intervention but not significant in the last 4-month period (median: 8.00 (IQR [2.75; 8.75]; P = 0.605). The completeness of the ADR reports increased from 80.3% before to 90.7% after the intervention. The completeness of the item for classifying ADRs as serious or non-serious increased significantly (P < 0.001) after the educational intervention. The quality of ADR reports increased from kappa 0.15 (95% CI: 0.08; 0.29) before to 0.43 (95% CI: 0.23; 0.63) after the intervention.
The results of the present study demonstrate that an educational intervention can increase physician awareness of ADRs. Participating physicians were able to incorporate the knowledge they had gained from face-to-face training into their daily clinical practice. However, the effects of the intervention were temporary.
最近的研究表明,药物不良反应(ADR)报告不足。与补充和替代医学(CAM)相关的ADR可能尤其如此。然而,关于CAM相关ADR的数据很少。目的是评估一项教育干预和监测计划对改善基层医疗环境中医师报告ADR的影响。
2004年1月至2007年6月,对38名专门从事CAM的基层医疗从业者进行了一项前瞻性多中心研究。21个月后,所有医生都接受了面对面培训形式的教育干预,以帮助他们对ADR进行分类和报告。研究中心监测ADR报告的数量和质量并分析结果。为了衡量ADR报告率的变化,计算了教育干预前后ADR报告的中位数和四分位间距(IQR)。根据强制性项目提供数据的完整性变化评估报告干预前和干预后的质量。使用Cohen's kappa计算医生与研究中心之间的评分者间信度,并给出95%置信区间(CI)。我们使用Mann Whitney U检验来检验连续数据,使用卡方检验来检验分类数据。统计学显著性水平设定为P < 0.05。
在整个研究期间共报告了404例ADR。教育干预后,观察到ADR报告数量最初增加了148%(P = 0.001)。与基线相比,干预后前16个月ADR报告数量在统计学上显著更高(P < 0.005),但在最后4个月期间不显著(中位数:8.00(IQR [2.75;8.75];P = 0.605)。ADR报告的完整性从干预前的80.3%提高到干预后的90.7%。教育干预后,将ADR分类为严重或非严重项目的完整性显著提高(P < 0.001)。ADR报告的质量从干预前的kappa 0.15(95% CI:0.08;0.29)提高到干预后的0.43(95% CI:0.23;0.63)。
本研究结果表明,教育干预可以提高医生对ADR的认识。参与的医生能够将他们从面对面培训中学到的知识应用到日常临床实践中。然而,干预的效果是暂时的。