United BioSource Corporation, Lexington, MA 02420, USA.
Pharmacoepidemiol Drug Saf. 2012 Jan;21 Suppl 1:236-9. doi: 10.1002/pds.2331.
The Food and Drug Administration's (FDA) Mini-Sentinel pilot program aims to conduct active surveillance to refine safety signals that emerge for marketed medical products. A key facet of this surveillance is to develop and understand the validity of algorithms for identifying health outcomes of interest (HOIs) from administrative and claims data. This paper summarizes the process and findings of the algorithm review of erythema multiforme and related conditions.
PubMed and Iowa Drug Information Service searches were conducted to identify citations applicable to the erythema multiforme HOI. Level 1 abstract reviews and Level 2 full-text reviews were conducted to find articles that used administrative and claims data to identify erythema multiforme, Stevens-Johnson syndrome, or toxic epidermal necrolysis and that included validation estimates of the coding algorithms.
Our search revealed limited literature focusing on erythema multiforme and related conditions that provided administrative and claims data-based algorithms and validation estimates. Only four studies provided validated algorithms and all studies used the same International Classification of Diseases code, 695.1. Approximately half of cases subjected to expert review were consistent with erythema multiforme and related conditions.
Updated research needs to be conducted on designing validation studies that test algorithms for erythema multiforme and related conditions and that take into account recent changes in the diagnostic coding of these diseases.
食品和药物管理局(FDA)的 Mini-Sentinel 试点计划旨在进行主动监测,以完善针对已上市医疗产品的安全信号。这种监测的一个关键方面是开发和理解从行政和索赔数据中识别感兴趣的健康结果(HOI)的算法的有效性。本文总结了多形红斑和相关疾病算法审查的过程和结果。
进行了 PubMed 和爱荷华药物信息服务搜索,以确定适用于多形红斑 HOI 的引用。进行了一级摘要审查和二级全文审查,以查找使用行政和索赔数据识别多形红斑、史蒂文斯-约翰逊综合征或中毒性表皮坏死松解症并包含编码算法验证估计的文章。
我们的搜索结果表明,专注于多形红斑和相关疾病的文献很少,这些文献提供了基于行政和索赔数据的算法和验证估计。只有四项研究提供了经过验证的算法,所有研究都使用了相同的国际疾病分类代码 695.1。经过专家审查的大约一半病例与多形红斑和相关疾病一致。
需要对设计验证研究进行更新,以测试多形红斑和相关疾病的算法,并考虑这些疾病诊断编码的最新变化。