Schatz Michael, Zeiger Robert S, Vollmer William M, Mosen David, Apter Andrea J, Stibolt Thomas B, Leong Albin, Johnson Michael S, Mendoza Guillermo, Cook E Francis
Kaiser Permanente Medical Center, 7060 Clairemont Mesa Blvd, San Diego, CA 92111, USA.
Am J Manag Care. 2006 Aug;12(8):478-84.
To validate a risk stratification scheme using computerized pharmacy data to predict emergency hospital utilization for persistent asthma.
Retrospective cohort.
The development sample consisted of 1079 HMO members aged 18 to 56 years with persistent asthma. The scale used medication cut-points as predictors for next-year emergency hospital utilization in a stepwise logistic regression model. Prediction properties were evaluated in a validation sample of 24 370 patients aged 18 to 56 years in a separate persistent-asthma database.
Increasing use of beta-agonists (odds ratio [OR] of 2.2 for 5-13 vs 0-4 canisters; OR of 2.4 for >13 vs 5-13 canisters) and oral corticosteroids (OR of 2.6 for >2 vs 0-2 dispensing events) in the first year independently predicted emergency hospital utilization in the second year. Assigning 1 point for exceeding each of the above 3 medication thresholds led to a 4-level medication intensity scale that was significantly (P <.0001) related to validated measures of asthma symptom severity, asthma control, and asthma quality of life in the development sample. In the validation sample, this scheme identified a high-risk group that was 6 times more likely than the low-risk group to require subsequent emergency hospital care, with overall sensitivity of 65% and specificity of 54%. This scale did not perform as well as a scale based on both baseline emergency hospital care and pharmacy data.
This simple risk stratification scheme can be used for populations with persistent asthma for whom computerized pharmacy data, but not computerized prior utilization data, are available.
验证一种使用计算机化药房数据预测持续性哮喘患者急诊住院率的风险分层方案。
回顾性队列研究。
开发样本包括1079名年龄在18至56岁之间的持续性哮喘健康维护组织成员。该量表在逐步逻辑回归模型中使用药物切点作为预测下一年急诊住院率的指标。在另一个持续性哮喘数据库中,对24370名年龄在18至56岁的患者的验证样本进行预测性能评估。
第一年β受体激动剂使用量增加(5 - 13罐与0 - 4罐相比的比值比[OR]为2.2;>13罐与5 - 13罐相比的OR为2.4)以及口服糖皮质激素使用量增加(>2次与0 - 2次配药事件相比的OR为2.6)独立预测了第二年的急诊住院率。超过上述3种药物阈值中的每一个都给予1分,形成了一个4级药物强度量表,该量表与开发样本中哮喘症状严重程度、哮喘控制和哮喘生活质量的验证指标显著相关(P <.0001)。在验证样本中,该方案识别出一个高风险组,该组需要后续急诊住院治疗的可能性比低风险组高6倍,总体敏感性为65%,特异性为54%。该量表的表现不如基于基线急诊住院治疗和药房数据的量表。
这种简单的风险分层方案可用于有持续性哮喘且可获取计算机化药房数据但无法获取计算机化既往使用数据的人群。