Lack of accessible and agreed standards: No agreed standard data quality framework (that is straightforward to apply) and no defined data coding/mapping standard |
Shortfalls of “SNOMED Clinical Terms” in practical applications |
Lack of resourcing and activities to support primary care providers to implement data quality improvements at point of data capture |
The ‘resource drain’ for researchers or data custodians to implement a comprehensive data quality framework |
Inconsistencies or lack of transparency around data transformation related to data extraction tools, leading to data quality issues including inconsistent or inaccurate results |
Uncertainty among data custodians on types and definitions of data ‘de-identification’, leading to the possibility of secondary users re-identifying individuals in datasets |
Technical limitations of received data structures and data tools limiting data recipients’ ability to analyse and report received data |