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他汀类药物初始处方开具延迟:药物持续性不佳的一个潜在早期指标。

Delay in filling the initial prescription for a statin: a potential early indicator of medication nonpersistence.

作者信息

Yu Andrew Peng, Yu Yanni F, Nichol Michael B, Gwadry-Sridhar Femida

机构信息

Department of Pharmaceutical Economics and Policy, School of Pharmacy, University of Southern California, Los Angeles, California, USA.

出版信息

Clin Ther. 2008 Apr;30(4):761-74; discussion 716. doi: 10.1016/j.clinthera.2008.04.015.

Abstract

BACKGROUND

Identification of early predictors of medication nonpersistence may allow timely adherence-promoting interventions and potentially reduce the risk of negative health outcomes.

OBJECTIVE

This study was conducted to determine whether delay in filling an initial statin prescription predicts subsequent nonpersistence with medication.

METHODS

This observational study of a cohort of adult patients (>18 years) who newly initiated statin therapy between December 1997 and June 2000 employed data from the administrative claims database of a large US managed care organization. Patients initiating statin therapy had to have at least 18 months of continuous eligibility and no statin use in the 6-month period before the index prescription. A new measure, dispensation delay, was measured as the gap between the most recent physician or hospital visit and the fill date of the index prescription. Five categories of dispensation delay were created--no delay, 1 to 7 days, 8 to 30 days, 31 to 183 days, and >183 days. Nonpersistence was defined as a gap of >or=30 days in the statin prescription supply during the follow-up period. Cox proportional hazards regression was used to model the risk of the initial dispensation delay on the time to discontinuation, controlling for such variables as demographic characteristics, comorbidities, physician specialty, and previous health care utilization.

RESULTS

The final sample included 19,038 patients. Among all variables studied, the dispensation-delay variables were the most significant predictors of non-persistence, with a longer delay predicting a higher risk of early discontinuation. Patients with delays in filling the initial prescription of >30 days but <183 days were 30% more likely to discontinue therapy than those without delays (hazard ratio=1.30; 95% CI=1.20-1.40).

CONCLUSIONS

The delay in filling the first statin prescription significantly predicted future non-persistence. Use of this measure may allow early identification of patients at high risk for early discontinuation.

摘要

背景

识别药物治疗不依从性的早期预测因素可使我们及时采取促进依从性的干预措施,并有可能降低负面健康结果的风险。

目的

本研究旨在确定首次他汀类药物处方配药延迟是否可预测后续的药物治疗不依从性。

方法

这项观察性研究的队列对象为1997年12月至2000年6月期间新开始他汀类药物治疗的成年患者(>18岁),使用了美国一家大型管理式医疗组织的行政索赔数据库中的数据。开始他汀类药物治疗的患者必须至少连续参保18个月,且在索引处方前6个月内未使用过他汀类药物。一种新的测量指标,即配药延迟,被定义为最近一次医生就诊或住院时间与索引处方配药日期之间的间隔。配药延迟分为五类——无延迟、1至7天、8至30天、31至183天以及>183天。不依从性被定义为随访期间他汀类药物处方供应中断≥30天。采用Cox比例风险回归模型来模拟初始配药延迟对停药时间的风险,同时控制人口统计学特征、合并症、医生专业以及既往医疗服务利用等变量。

结果

最终样本包括19038名患者。在所有研究变量中,配药延迟变量是不依从性最显著的预测因素,延迟时间越长,早期停药风险越高。初始处方配药延迟>30天但<183天的患者比无延迟患者停药的可能性高30%(风险比=1.30;95%置信区间=1.20 - 1.40)。

结论

首次他汀类药物处方配药延迟显著预测了未来的不依从性。使用这一指标可能有助于早期识别有早期停药高风险的患者。

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