4.5 Article

Home-Based Exercise in Patients Awaiting Liver Transplantation: A Feasibility Study

Journal

LIVER TRANSPLANTATION
Volume 25, Issue 7, Pages 995-1006

Publisher

WILEY
DOI: 10.1002/lt.25442

Keywords

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Funding

  1. University Hospitals Birmingham Charity (United Kingdom)
  2. MRC [MR/P021220/1, MR/K00414X/1] Funding Source: UKRI

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Frailty is associated with increased mortality both before and after liver transplantation (LT). There are no standardized exercise programs, in particular home-based exercise programs (HBEPs), for patients awaiting LT. The aim was to investigate the feasibility of such a program in patients awaiting LT. Patients were randomly selected from the Birmingham LT waiting list and provided with a 12-week HBEP, including average daily step (ADS) targets and twice-weekly resistance exercises. Feasibility was based on patient eligibility (>= 66% of waiting list), target recruitment (>= 90% of n = 20), safety (no related serious adverse events), and adherence (>= 66% adherence to 6-week HBEP). Measures of aerobic (incremental shuttle walk test [ISWT], ADS), functional capacity (short physical performance battery test [SPPBT]), and health-related quality of life (EuroQol 5-Dimension 5-Level (EQ-5D-5L) and hospital anxiety and depression score [HADS]) were taken at baseline and at 6 and 12 weeks. 18 patients (50% male; median age, 55 years) were recruited. All domains of the study feasibility criteria were met. ISWT improved after 6 weeks (50 m; P <= 0.01) and 12 weeks (210 m; P <= 0.01), despite withdrawal of the telephone health calls. Similarly, improvements were seen in ADS (2700/day; P <= 0.01) and the SPPBT (2.5; P = 0.02) after 12 weeks. There was no difference in HADS (median difference [MD] -3; P = 0.69), but EQ-5D-5L after 12 weeks (17.5%; P = 0.04). In conclusion, a 12-week HBEP, incorporating both easy-to-apply resistance and aerobic exercises, is safe and feasible in patients awaiting LT. Measures of aerobic and functional capacity demonstrate trends toward improvement that warrant further investigation in a randomized controlled trial.

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