Table 2.
Overview of systematic reviews reporting evidence about the consequences of caring
| Study | Date | Studies in review (n) | Data range of included studies | Population (care recipient) | Type of consequence/impact reported | Do studies within the review compare presence/level of impact with non-carer samples? | Does the review identify evidence about impact for specific carer subgroups relating to age, sex, socioeconomic status and geographical location? | Synthesis | Indicative risk of bias |
| Amer Nordin et al30 | 2019 | 19 | 1990–2017 | Older people | ‘Caregiver burden’, quality of life, perceived difficulty assisting recipient | No | No | Narrative | High |
| Bom et al31 | 2019 | 15 | 2009–2017 | Older people | Mental health, physical health | Yes, controls matched for caregiver health | Sex, SES, location (European region) | Narrative | High |
| Ge and Mordiffi32 | 2017 | 7 | 1999–2014 | Older people with cancer | ‘Caregiver burden’ prevalence and severity | No | Sex, SES, age | Narrative | Moderate |
| Jansen et al33 | 2018 | 14 | 1994–2016 | Older cancer survivors | Prevalence and predictors of ‘caregiver burden’, depression, anxiety, self-esteem, distress, communication issues, stress and QoL | Yes, general population | Sex, SES | Narrative | High |
| Namasivayam-MacDonald and Shune34 | 2018 | 4 | 2002–2017 | Older people | ‘Caregiver burden’ associated with feeding difficulties | No | No | Narrative | High |
| Ringer et al35 | 2017 | 9 | 1997–2012 | Older people with frailty | ‘Caregiver burden’, negative reactions to caregiving | Unclear | No | Narrative | Moderate |
QoL, quality of life; SES, socioeconomic status.