Evaluation of routinely collected records for dementia outcomes in UK: a prospective cohort study.
Shabina A HayatRobert LubenKay-Tee KhawNicholas WarehamCarol BraynePublished in: BMJ open (2022)
Use of different types of record linkage from varying parts of the UK's health system reveals differences in recorded dementia diagnosis, indicating that dementia can be identified to varying extents in different parts of the NHS system. However, there is considerable variation, and limited overlap in those identified. We present potential selection biases that might occur depending on whether cause of death, or primary and secondary care data sources are used. With the expansion of using routinely collected health data, researchers must be aware of these potential biases and inaccuracies, reporting carefully on the likely extent of limitations and challenges of the data sources they use.
Keyphrases
- mild cognitive impairment
- electronic health record
- healthcare
- cognitive impairment
- big data
- public health
- drinking water
- human health
- mental health
- palliative care
- emergency department
- type diabetes
- cross sectional
- patient safety
- dna methylation
- genome wide
- quality improvement
- insulin resistance
- adipose tissue
- health information
- hiv testing
- men who have sex with men