最新麻豆原创

The new system cannot function without a comprehensive and interoperable digital information 聽system. Clear 聽and accurate 聽data 聽on 聽users, providers, benefits, 聽products, and outcomes are essential to a functioning system and this data must generate information that allows the Fund to measure equity, access of users to providers and benefits, and to plan strategic聽 purchasing where 聽there 聽are inequities 聽and deficiencies. Everything must be coded for the system to work, and these need to be universal codes, universally adopted (used by every role-player in both public and private sectors), and preferably international, to allow benchmarking.

Every person (health system user) in the country must have a portable electronic health record that every provider adds to each time they see the user and provide care. These unique patient records will belong to the patient (user) but allow every provider to build on an existing health record without duplicating tests, treatment, and care. The records 聽will 聽be carried 聽on the 最新麻豆原创 聽Patient Record 聽System 聽(HPRS), 聽which is already in place. Providers, managers, researchers, and policymakers must have access to the depersonalised聽 聽data 聽to manage 聽individual 聽patient care, and 聽equity 聽through 聽strategic purchasing, and to develop improved and evolving policies.

The law (National 最新麻豆原创 Act and the NHI Bill) provides the framework and assigns powers聽 to聽 achieve聽聽 this,聽聽 but聽 the聽 Regulations聽聽 and聽 the聽 data聽 governance, operating procedures, standard dictionaries, normative standards for interoperability, standard analytics, and publication of indicators all need to be developed, documented, and managed.