Fed Regist. 2012 Dec 7;77(236):72985-91.
The Department of Health and Human Services (HHS) is issuing this interim final rule with comment period to replace the Data Element Catalog (DEC) standard and the Quality Reporting Document Architecture (QRDA) Category III standard adopted in the final rule published on September 4, 2012 in the Federal Register with updated versions of those standards. This interim final rule with comment period also revises the Medicare and Medicaid Electronic Health Record (EHR) Incentive Programs by adding an alternative measure for the Stage 2 meaningful use (MU) objective for hospitals to provide structured electronic laboratory results to ambulatory providers, correcting the regulation text for the measures associated with the objective for hospitals to provide patients the ability to view online, download, and transmit information about a hospital admission, and making the case number threshold exemption for clinical quality measure (CQM) reporting applicable for eligible hospitals and critical access hospitals (CAHs) beginning with FY 2013. This rule also provides notice of CMS's intention to issue technical corrections to the electronic specifications for CQMs released on October 25, 2012.
美国卫生与公众服务部(HHS)正在发布此份带有意见征求期的暂行最终规则,以用这些标准的更新版本取代2012年9月4日在《联邦公报》上发布的最终规则中采用的数据元素目录(DEC)标准和质量报告文档架构(QRDA)第三类标准。此份带有意见征求期的暂行最终规则还对医疗保险和医疗补助电子健康记录(EHR)激励计划进行了修订,为医院在第二阶段有意义使用(MU)目标中向门诊医疗服务提供者提供结构化电子实验室结果增加了一项替代措施,纠正了与医院为患者提供在线查看、下载和传输有关住院信息能力的目标相关的监管文本,并使自2013财年起适用于合格医院和临界接入医院(CAH)的临床质量指标(CQM)报告的病例数阈值豁免生效。本规则还通知了医疗保险和医疗补助服务中心(CMS)打算对2012年10月25日发布的CQM电子规范发布技术更正。