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HHS Walks the Middle Ground in Final Ruling on Nondiscrimination Drug Access and Formulary Construction Still Unguided

机译:HHS在非歧视性药物获取和配方建设的最终裁决中仍处于中间地位

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摘要

New federal standards aimed at preventing discrimination in all fed-I eral health plans and programs1 disappointed patient advocacy groups that had hoped for requirements dictating expansive formularies. They wanted the Department of Health and Human Services (HHS) to instruct Medicare, Med-icaid, marketplace and community health plans, and others receiving federal funds that certain formulary restrictions, such as placing expensive drugs on the highest tiers, were discriminatory. But the HHS declined to adopt such standards. That was a victory for insurance companies and their pharmacy benefit managers. But neither did the HHS establish a "safe harbor" where drug benefit access practices approved by P&T committees would be deemed compliant with the new antidiscrimination standards.
机译:旨在防止所有联邦卫生计划和计划中出现歧视的新联邦标准1使希望通过要求制定扩大处方的要求的患者拥护团体失望。他们希望卫生与公众服务部(HHS)指示Medicare,Med-icaid,市场和社区卫生计划,以及其他接受联邦资金的计划,指出某些配方限制(例如将昂贵的药物放在最高级别上)具有歧视性。但是HHS拒绝采用此类标准。对于保险公司及其药房福利经理而言,这是一次胜利。但是,HHS既未建立“安全港”,也不会认为P&T委员会批准的药品利益获取做法符合新的反歧视标准。

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