Table 3.
Reasons for asking patients about their socioeconomic circumstances
| Reasons | Citations |
|---|---|
| Reasons relating to individual healthcare encounters | |
| Clinicians can refer patients to social resources | [10, 16–38] |
| Clinicians can engage directly with patients’ social needs | [18, 34, 39, 40] |
| Clinicians can acknowledge patients’ socially-determined risk of disease (specifically cardiovascular disease risk) | [41–49] ( [16, 23, 35, 50–52]) |
| More clinical resources can be allocated to patients facing adverse social conditions | [26, 42, 53–57] |
| Clinical management plans can be adapted to patients’ socioeconomic context | [11, 16, 32, 38, 58–70] |
| Clinicians can better understand non-adherence to management plans | [26, 58, 66, 71, 72] |
| Communication and relationships can be improved between patients and clinicians | [54, 73–76] |
| Patient preferences | [27, 77, 78] |
| Reasons relating to health service provision and organisation | |
| Healthcare use by different socioeconomic groups can be better monitored | [26, 31, 43, 79–89] |
| More healthcare resources can be allocated to populations with greater need | [35, 90–93] |
| Healthcare services can be better adapted to population needs | [10, 16, 23, 26, 32, 42, 43, 60, 68, 87, 92, 94] |
| Deprivation payments can be more accurately allocated | [55, 82, 90, 95–97] |
| Reasons relating to population-level research and policies | |
| Health research can be improved | [13, 16, 35, 45, 46, 60, 73, 82, 89, 98–104] |
| Public health policies can be better-informed | [10, 23, 32, 42, 44, 57, 66, 81, 105–107] |
| Health and social care can be better integrated | [29, 31, 101] |