Solomon Daniel H, Schneeweiss Sebastian, Glynn Robert J, Levin Raisa, Avorn Jerry
Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Am J Med. 2003 Dec 15;115(9):715-20. doi: 10.1016/j.amjmed.2003.08.025.
Little is known about which factors influence the widespread use of selective cyclooxygenase (COX)-2 inhibitors. We examined the relative effects of patient risk factors for gastrointestinal toxicity, other patient characteristics, and physician prescribing preferences on the decision to prescribe a selective COX-2 inhibitor.
We retrospectively studied a cohort of 28,190 Medicare beneficiaries who were continuously enrolled in a large, state-run pharmacy benefits program that reimbursed for selective COX-2 inhibitors and nonselective nonsteroidal anti-inflammatory drugs (NSAIDs) without restrictions. Half of the study sample filled a prescription for a selective COX-2 inhibitor and the other half for a nonselective NSAID. Multivariable logistic regression models were developed to predict COX-2 inhibitor use.
Seventeen percent of patients using a COX-2 inhibitor had no identifiable risk factor for NSAID-associated gastrointestinal toxicity, compared with 23% of those using a nonselective NSAID. Established risk factors (age > or =75 years, history of gastrointestinal hemorrhage or peptic ulcer disease, or concomitant warfarin or oral glucocorticoid use) were all significant predictors of COX-2 inhibitor use, but a multivariable model including only these risk factors discriminated poorly between the two patient groups (C statistic = 0.55). Adding other patient clinical and demographic characteristics to the model somewhat improved this association (C statistic = 0.66); however, when physician prescribing preference was included, the model had excellent ability to discriminate between the two treatment groups (C statistic = 0.83).
Established risk factors for NSAID-associated gastrointestinal toxicity were poor predictors of who was prescribed a selective COX-2 inhibitor; in contrast, physician prescribing preference was an important determinant.
关于哪些因素影响选择性环氧化酶(COX)-2抑制剂的广泛使用,目前所知甚少。我们研究了胃肠道毒性的患者风险因素、其他患者特征以及医生的处方偏好对开具选择性COX-2抑制剂决策的相对影响。
我们回顾性研究了28190名医疗保险受益人的队列,这些人连续参加了一个大型的国营药房福利计划,该计划对选择性COX-2抑制剂和非选择性非甾体抗炎药(NSAIDs)无限制报销。研究样本的一半开具了选择性COX-2抑制剂的处方,另一半开具了非选择性NSAIDs的处方。建立多变量逻辑回归模型来预测COX-2抑制剂的使用情况。
使用COX-2抑制剂的患者中,17%没有可识别的与NSAID相关的胃肠道毒性风险因素,而使用非选择性NSAIDs的患者中这一比例为23%。既定的风险因素(年龄≥75岁、胃肠道出血或消化性溃疡病史、或同时使用华法林或口服糖皮质激素)都是COX-2抑制剂使用的显著预测因素,但仅包含这些风险因素的多变量模型在两组患者之间的区分能力较差(C统计量=0.55)。在模型中加入其他患者的临床和人口统计学特征后,这种关联有所改善(C统计量=0.66);然而,当纳入医生的处方偏好时,该模型在区分两个治疗组方面具有出色的能力(C统计量=0.83)。
与NSAID相关的胃肠道毒性的既定风险因素对谁会开具选择性COX-2抑制剂的预测能力较差;相比之下,医生的处方偏好是一个重要的决定因素。