Caregiver outcomes of the REACH-HF multicentre randomized controlled trial of home-based rehabilitation for heart failure with reduced ejection fraction.
Jennifer Wingham, Julia Frost, Nicky Britten and 12 others
PMID 31117815WHAT IT FOUND
Caregivers of people with heart failure showed no clear difference from usual care on anxiety, depression, burden or quality of life; only confidence in supporting self-care was higher.
Interviews described use of symptoms, emergency and medication guidance.
Key findings
01At 12 months, caregivers in the REACH-HF group had a higher adjusted mean confidence score for contributing to heart failure self-care than control caregivers, by 9.3 points on a 0 to 100 scale.
02Between-group comparisons showed no significant differences for caregiver anxiety, depression, family quality of life, caregiver burden or generic health-related quality of life at 12 months.
03In interviews, caregivers used the family and friends resource most for managing signs and symptoms, what to do in an emergency, when to call for help, and medication information.
STILL TO COME
How it was doneWhat they foundWhat it means for RNs
Read the rest of this summary
You get three full summaries a month, free, and we do not ask for a card. Search, the TL;DRs and your library stay unlimited either way.
What it does not show
The study was powered for patient outcomes, not caregiver outcomes, so real caregiver effects could be missed. Caregivers were allocated with their patients and were not randomised separately, so differences between caregiver groups could reflect selection or baseline imbalance. Control caregivers were older and had higher depression and anxiety scores and lower generic health-related quality of life at baseline. Many caregivers already had good functioning at baseline, leaving little room for measured improvement. No imputation was done for missing data, and 12-month outcome data were available for 45 of 53 REACH-HF caregivers and 37 of 44 control caregivers. The qualitative interviews were done only with REACH-HF caregivers, so they cannot compare views with control caregivers. The trial process evaluation found facilitators were less effective involving caregivers than patients, so the caregiver component may have been delivered unevenly. REACH-HF was a multi-component home programme, so the study cannot separate the effects of patient education, caregiver support, goal setting, the family resource and the walking element.
Declared interests
Funding came from the National Institute for Health Research. The supplied text does not state any author conflicts of interest.
The easy way to misread this
Do not conclude that REACH-HF improved caregiver wellbeing broadly. Only confidence in supporting self-care differed from control; anxiety, depression, burden and quality-of-life differences were not significant, and the study was powered for patient outcomes rather than caregivers.