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首页> 外文期刊>The journal of clinical psychiatry >First-year Medicare Part D prescription drug benefits: medication access and continuity among dual eligible psychiatric patients.
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First-year Medicare Part D prescription drug benefits: medication access and continuity among dual eligible psychiatric patients.

机译:第一年Medicare D部分处方药的好处:双重合格精神病患者的药物可及性和连续性。

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OBJECTIVE: This study provides national data on medication access and continuity problems experienced during the first year of the Medicare Part D prescription drug program, which was implemented on January 1, 2006, among a national sample of Medicare and Medicaid "dual eligible" psychiatric patients. METHOD: Practice-based research methods were used to collect clinician-reported data across the full range of public and private psychiatric treatment settings. A random sample of psychiatrists was selected from the American Medical Association Physician Masterfile. Among these physicians, 1,490 provided clinically detailed data on a systematically selected sample of 2,941 dual eligible psychiatric patients. RESULTS: Overall, 43.3% of patients were reported to be unable to obtain clinically indicated medication refills or new prescriptions in 2006 because they were not covered or approved; 28.9% discontinued or temporarily stopped their medication(s) as a result of prescription drug coverage or management issues; and 27.7% were reported to be previously stable on their medications but were required to switch medications. Adjusting for case mix to control for sociodemographic and clinical confounders, the predicted probability of an adverse event among patients with medication access problems was 0.64 compared to 0.36 for those without access problems (P < .0001). All prescription drug utilization management features studied were associated with increased medication access problems (P < .0001). Adjusting for patient case mix, patients with "step therapy" (P < .0001), limits on medication number/dosing (P < .0001), or prior authorization (P < .0001) had 2.4 to 3.4 times the increased likelihood of an adverse event. CONCLUSIONS: More effective Part D policies and management practices are needed to promote clinically safer and appropriate pharmacotherapy for psychiatric patients to enhance treatment outcomes.
机译:目的:本研究提供了关于2006年1月1日实施的Medicare D部分处方药计划的第一年中遇到的药物可及性和连续性问题的国家数据,该数据来自Medicare和Medicaid“双重合格”精神病患者的国家样本。方法:以实践为基础的研究方法被用来收集整个公共和私人精神病学治疗环境中临床医生报告的数据。从美国医学会医师主档案中选择了随机的精神科医生样本。在这些医生中,有1,490位提供了系统地选择的2,941名双重合格精神病患者样本的临床详细数据。结果:总体而言,2006年有43.3%的患者因未得到覆盖或批准而无法获得临床指示的药物补充剂或新处方; 28.9%的人由于处方药承保范围或管理问题而停药或暂时停药;据报道,有27.7%的人以前对其药物稳定,但需要换药。调整病例组合以控制社会人口统计学和临床​​混杂因素,有药物治疗问题的患者中发生不良事件的预计概率为0.64,而没有药物治疗问题的患者为0.36(P <.0001)。研究的所有处方药利用管理功能均与增加的药物使用问题相关(P <.0001)。根据患者的病情调整,采用“分步治疗”(P <.0001),限制用药次数/剂量(P <.0001)或事先批准(P <.0001)的患者的发生可能性增加2.4到3.4倍不良事件。结论:需要更有效的D部分政策和管理措施,以促进精神病患者临床上更安全,更适当的药物治疗,从而提高治疗效果。

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