Key result
A randomized trial of peritoneal ultrafiltration for severe heart failure was stopped early due to inadequate recruitment, enrolling only 10 of the planned 130 participants.
Why the study?
Peritoneal ultrafiltration has been used for severe heart failure, but evidence demonstrating its benefit is lacking.
Does peritoneal ultrafiltration improve 6-minute walk test distance in patients with severe diuretic-resistant heart failure and CKD stage 3/4?
RCT (n=10)
randomized
Yes
Does peritoneal ultrafiltration improve 6-minute walk test distance in patients with severe diuretic-resistant heart failure and CKD stage 3/4?
The PDHF trial highlights the severe logistical and clinical challenges, including patient frailty and cross-specialty coordination, in recruiting severe heart failure patients for invasive peritoneal ultrafiltration studies.
Answers are grounded in this paper and cite their sources.
Early termination leaves peritoneal ultrafiltration efficacy untested in severe HF; underscores recruitment barriers for future invasive trials.
Peritoneal ultrafiltration (PuF) has been employed for severe heart failure (HF), but evidence for its benefit is lacking. The Peritoneal Dialysis for Heart Failure (PDHF) study was a multicenter prospective randomized controlled trial which aimed to investigate this issue. The trial stopped early due to inadequate recruitment. We describe methods, trial activity, and lessons learned.The trial aimed to recruit 130 participants with severe diuretic-resistant HF (New York Heart Association [NYHA] 3/4) and chronic kidney disease (CKD) stage 3/4 on optimal medical treatment for ≥ 4 weeks from 6 UK centers. Participants were randomized to either continuation of conventional HF treatment or to additionally receiving PuF (1 overnight exchange using Icodextrin dialysate). Primary outcome was change in 6-minute walk test (6MWT) between baseline and 28 weeks (end of trial). Secondary outcomes were changes in patient reported quality of life as assessed by the Kansas City Cardiomyopathy Questionnaire, short form 36 (SF 36) health survey results, hospitalization, and mortality.Over a 2-year period, 290 patients were screened from which only 20 met inclusion criteria and 10 were recruited. Reasons for ineligibility were fluctuating estimated glomerular filtration rate (eGFR), suboptimal HF treatment, frailty, and patients being too unwell for randomization. Barriers to recruitment included patient frailty, with some participants considered only when they were at end of life, unwillingness to engage in an invasive therapy, and suboptimal coordination between cardiology and renal services. This is a challenging patient group in which to perform research, and lessons learned from the peritoneal dialysis (PD)-HF trial will be helpful in the planning of future studies in this area.
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Dukka et al. (2019) conducted an RCT in severe diuretic-resistant heart failure and chronic kidney disease stage 3/4 (n=10). Peritoneal ultrafiltration (PuF) vs. continuation of conventional HF treatment was evaluated on change in 6-minute walk test (6MWT) between baseline and 28 weeks. A randomized trial of peritoneal ultrafiltration for severe heart failure was stopped early due to inadequate recruitment, enrolling only 10 of the planned 130 participants.
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