From: A systematic review of reasons for and against asking patients about their socioeconomic contexts
Reasons | Citations |
---|---|
Reasons relating to individual healthcare encounters | |
 Clinicians can refer patients to social resources | [10, 16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38] |
 Clinicians can engage directly with patients’ social needs | |
 Clinicians can acknowledge patients’ socially-determined risk of disease (specifically cardiovascular disease risk) | |
 More clinical resources can be allocated to patients facing adverse social conditions | |
 Clinical management plans can be adapted to patients’ socioeconomic context | |
 Clinicians can better understand non-adherence to management plans | |
 Communication and relationships can be improved between patients and clinicians | |
 Patient preferences | |
Reasons relating to health service provision and organisation | |
 Healthcare use by different socioeconomic groups can be better monitored | |
 More healthcare resources can be allocated to populations with greater need | |
 Healthcare services can be better adapted to population needs | |
 Deprivation payments can be more accurately allocated | |
Reasons relating to population-level research and policies | |
 Health research can be improved | [13, 16, 35, 45, 46, 60, 73, 82, 89, 98,99,100,101,102,103,104] |
 Public health policies can be better-informed | |
 Health and social care can be better integrated |