engleski

Quality dimensions od registries

The primary dimension of registries’ quality is the quality of the data. Data quality is influenced by a number of other identifiable registry features. Four basic categories of factors influencing registry’s quality are: • Governance, as an organizational foundation of patient registries, is mostly concerned with guidance and decision making. Adequate governance model makes sure to address issues such as overall direction and operations (procedures and processes), communication, scientific content, ethics, safety, data access, transparency, publications, change management and registry life-span planning. • Data quality is assured by defined requirements/standards for data collection and management. Data quality is also to be assessed against a list of dimensions which can be defined and measured. • Information quality is an output of a data collection process. It is measured by the amount and impact of scientific publications based on registry data. • Quality is also influenced by features like confidentiality, security, privacy and ethical issues. These influence a registry’s interoperability capability and information dissemination. Meeting ethical and legal requirements concerning privacy influences registry’s interoperability capability and information dissemination. Privacy component of the registry is measured by privacy impact assessments (PIAs). Integrally addressing advices indicated within stated categories during registry planning and creation but also while running a registry, should ensure high level of registry performance.

registries, interoperability, quality

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