HIQA is currently undertaking a programme of work to set a number of health information standards. The aim of a health information standard is to standardise the collection and recording of health information so that it can be shared in the most effective way possible in order to ensure a high-quality, safe service. This standardised approach promotes safety and progressive quality improvements in the health and social care environment and promotes the safety of people using services.
As part of our programme of work, we are revising the National Standard for a Demographic Dataset for Health and Social Care (Version 2 of this standard was published in 2016). A National Standard for a Demographic Dataset defines the core set of data elements required to identify an individual uniquely, in order to provide safe, quality care and support. The standard applies to individuals of any age (children and adults) who are receiving care and treatment in a health and social care service that collects and records demographic details. Examples of data elements comprising a demographic dataset include forename, surname and date of birth.