Interventions to improve outcomes for caregivers of patients with advanced cancer: a meta-analysis

Author:

Chow Ronald12ORCID,Mathews Jean J3,Cheng Emily YiQin12ORCID,Lo Samantha1,Wong Joanne1,Alam Sorayya4,Hannon Breffni125ORCID,Rodin Gary1267ORCID,Nissim Rinat127ORCID,Hales Sarah127,Kavalieratos Dio8ORCID,Quinn Kieran L269ORCID,Tomlinson George256ORCID,Zimmermann Camilla1256ORCID

Affiliation:

1. Department of Supportive Care, Princess Margaret Cancer Centre, University Health Network , Toronto, ON, Canada

2. Temerty Faculty of Medicine, University of Toronto , Toronto, ON, Canada

3. Division of Palliative Medicine, Department of Medicine and Department of Oncology, Queen’s University , Kingston, ON, Canada

4. Palliative Medicine, Sobell House, Oxford University Hospitals NHS Foundation Trust , Oxford, UK

5. Department of Medicine, University Health Network , Toronto, ON, Canada

6. Dalla Lana School of Public Health, University of Toronto , Toronto, ON, Canada

7. Centre for Mental Health, University Health Network , Toronto, ON, Canada

8. Division of Palliative Medicine, Department of Family and Preventive Medicine, Emory University , Atlanta, GA, USA

9. Division of General Internal Medicine and Palliative Care, Department of Medicine, Sinai Health System, Temmy Latner Centre for Palliative Care , Toronto, ON, Canada

Abstract

Abstract Background Family caregivers of patients with advanced cancer often have poor quality of life (QOL) and mental health. We examined the effectiveness of interventions offering support for caregivers of patients with advanced cancer on caregiver QOL and mental health outcomes. Methods We searched Ovid MEDLINE, EMBASE, Cochrane CENTRAL, and Cumulative Index to Nursing and Allied Health Literature databases from inception through June 2021. Eligible studies reported on randomized controlled trials for adult caregivers of adult patients with advanced cancer. Meta-analysis was conducted for primary outcomes of QOL, physical well-being, mental well-being, anxiety, and depression, from baseline to follow-up of 1-3 months; secondary endpoints were these outcomes at 4-6 months and additional caregiver burden, self-efficacy, family functioning, and bereavement outcomes. Random effects models were used to generate summary standardized mean differences (SMD). Results Of 12 193 references identified, 56 articles reporting on 49 trials involving 8554 caregivers were eligible for analysis; 16 (33%) targeted caregivers, 19 (39%) patient–caregiver dyads, and 14 (29%) patients and their families. At 1- to 3-month follow-up, interventions had a statistically significant effect on overall QOL (SMD = 0.24, 95% confidence interval [CI] = 0.10 to 0.39); I2 = 52.0%), mental well-being (SMD = 0.14, 95% CI = 0.02 to 0.25; I2 = 0.0%), anxiety (SMD = 0.27, 95% CI = 0.06 to 0.49; I2 = 74.0%), and depression (SMD = 0.34, 95% CI = 0.16 to 0.52; I2 = 64.4) compared with standard care. In narrative synthesis, interventions demonstrated improvements in caregiver self-efficacy and grief. Conclusions Interventions targeting caregivers, dyads, or patients and families led to improvements in caregiver QOL and mental health. These data support the routine provision of interventions to improve well-being in caregivers of patients with advanced cancer.

Funder

Canadian Institutes of Health Research

Harold and Shirley Lederman Chair in Psychosocial Oncology and Palliative Care

Chair among the University of Toronto, Princess Margaret Cancer Centre

University Health Network

Princess Margaret Cancer Foundation

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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