HealthCore, Inc., Wilmington, DE 19801, USA.
Pharmacoepidemiol Drug Saf. 2010 Jun;19(6):596-603. doi: 10.1002/pds.1924.
To validate administrative claims codes with medical chart review for myocardial infarction (MI), ischemic stroke, and severe upper gastrointestinal (UGI) bleed events in a large, commercially-insured US population.
These validation studies were part of a larger study examining the risk of MI, ischemic stroke, and severe UGI bleeds in patients receiving a new prescription of selective cyclooxygenase (COX)-2 inhibitors (coxibs) and non-over-the-counter (OTC) non-steroidal anti-inflammatory drugs (NSAIDs), between 1 July 2002 and 30 September 2004. Patients from the study cohort and other health plan members from the HealthCore Integrated Research Database(SM) (HIRD) experiencing these events were selected for these studies. The positive predictive value (PPV) of each of the claims code algorithms, using medical chart review as the gold standard, was calculated.
Two hundred charts per event were abstracted. The PPV for MI was 88.4% (177/200; 95%CI, 83.2-92.5%); PPV for ischemic stroke was 87.4% (175/200; 95%CI, 82.0-91.7%); PPV for severe UGI bleed was 56.5% (109/193; 95%CI, 49.2-63.6%). Refining the ischemic stroke claims algorithm resulted in a PPV of 95.5% (95%CI, 91.0-98.2%); refining the claims algorithm for severe UGI bleed resulted in a PPV of 87.8% (95%CI, 78.7-94.0%).
The results suggest that, for certain adverse events, claims data can serve as the basis for pharmacoepidemiology research and drug safety surveillance in the US.
在一个大型的、商业保险覆盖的美国人群中,通过医学图表审查来验证与心肌梗死(MI)、缺血性卒中和严重上消化道(UGI)出血事件相关的行政索赔代码。
这些验证研究是一项更大研究的一部分,该研究旨在检查在 2002 年 7 月 1 日至 2004 年 9 月 30 日期间接受新处方选择性环氧化酶(COX)-2 抑制剂(昔布)和非处方(OTC)非甾体抗炎药(NSAIDs)的患者中发生 MI、缺血性卒中和严重 UGI 出血的风险。这些研究选择了来自研究队列的患者和 HealthCore 综合研究数据库(SM)(HIRD)中经历这些事件的其他健康计划成员。使用医学图表审查作为金标准,计算了每种索赔代码算法的阳性预测值(PPV)。
每例事件提取 200 份图表。MI 的 PPV 为 88.4%(177/200;95%CI,83.2-92.5%);缺血性卒中的 PPV 为 87.4%(175/200;95%CI,82.0-91.7%);严重 UGI 出血的 PPV 为 56.5%(109/193;95%CI,49.2-63.6%)。改进缺血性卒中和严重 UGI 出血的索赔算法分别导致 PPV 为 95.5%(95%CI,91.0-98.2%)和 87.8%(95%CI,78.7-94.0%)。
结果表明,对于某些不良事件,索赔数据可以作为美国药物流行病学研究和药物安全监测的基础。