Are responders to patient health surveys representative of those invited to participate? An analysis of the Patient-Reported Outcome Measures Pilot from the Australian Orthopaedic Association National Joint Replacement Registry.
Ian A HarrisKara CashmanMichelle LorimerYi PengIlana AckermanEmma L HeathStephen E GravesPublished in: PloS one (2021)
Patients undergoing total joint replacement who provide direct electronic PROMs data are younger, healthier and more likely to be female than non-responders, but these differences are small, particularly for post-operative data collection. The addition of telephone call follow up to electronic contact does not provide a more representative sample. Electronic-only follow up of patients undergoing joint replacement provides a satisfactory representation of the population invited to participate.
Keyphrases
- patients undergoing
- patient reported
- cross sectional
- electronic health record
- patient reported outcomes
- public health
- healthcare
- big data
- mental health
- quality improvement
- case report
- study protocol
- randomized controlled trial
- machine learning
- risk assessment
- health information
- data analysis
- neural network
- double blind