Wieland Susan, Dickersin Kay
Department of Community Health, Center for Gerontology and Health Care Research, Brown University, Providence, RI 02912, USA.
J Clin Epidemiol. 2005 Jun;58(6):560-7. doi: 10.1016/j.jclinepi.2004.11.018. Epub 2005 Apr 18.
To explore development of possible approaches leading to a sensitive and precise Medline search to identify observational studies of the association between oral contraceptives and breast cancer, an adverse event.
We compared the results of a series of Medline searches to a gold standard comprising 58 reports from a 1996 systematic review examining the relationship between oral contraceptives and the development of breast cancer. Sensitivity (the proportion of gold standard publications identified) and precision (the proportion of retrieved publications that were included in the gold standard) were calculated for each Medline search.
We identified all 58 articles when the search was not limited by terms related to oral contraceptives, but precision was less than 1% (58 of 6,120). Indexing was problematic when oral contraceptives or hormones were not mentioned in the title or abstract (n = 8) or full text (n = 2).
Search strategies identifying all relevant studies were possible but arguably impractical; additional research is needed to generalize our findings. Authors and editors should ensure that all interventions and outcomes examined are reported and indexers should make sure they are indexed. Central registration of observational studies and all variables they examined should be considered to assure identification of studies examining adverse events associated with health interventions.
探索可能的方法,以开展敏感且精确的医学索引数据库(Medline)检索,从而识别关于口服避孕药与乳腺癌(一种不良事件)之间关联的观察性研究。
我们将一系列Medline检索结果与一个金标准进行比较,该金标准包含1996年一项关于口服避孕药与乳腺癌发生关系的系统评价中的58篇报告。针对每次Medline检索,计算敏感性(识别出的金标准出版物的比例)和精确性(检索到的被纳入金标准的出版物的比例)。
当检索不受与口服避孕药相关术语限制时,我们识别出了所有58篇文章,但精确性低于1%(6120篇中的58篇)。当标题、摘要(n = 8)或全文(n = 2)中未提及口服避孕药或激素时,索引存在问题。
识别所有相关研究的检索策略是可行的,但可能不切实际;需要进一步研究以推广我们的发现。作者和编辑应确保报告所有研究的干预措施和结果,索引人员应确保对其进行索引。应考虑对观察性研究及其所考察的所有变量进行集中注册,以确保识别出考察与健康干预相关不良事件的研究。