Author: Güder, Gülmisal; Wilkesmann, Joana; Scholz, Nina; Leppich, Robert; Düking, Peter; Sperlich, Billy; Rost, Christian; Frantz, Stefan; Morbach, Caroline; Sahiti, Floran; Stefenelli, Ulrich; Breunig, Margret; Störk, Stefan
Title: Establishing a cardiac training group for patients with heart failure: the “HIP-in-Würzburg†study Cord-id: fhgvjrzc Document date: 2021_6_22
ID: fhgvjrzc
Snippet: BACKGROUND: Exercise training in heart failure (HF) is recommended but not routinely offered, because of logistic and safety-related reasons. In 2020, the German Society for Prevention&Rehabilitation and the German Society for Cardiology requested establishing dedicated “HF training groups.†Here, we aimed to implement and evaluate the feasibility and safety of one of the first HF training groups in Germany. METHODS: Twelve patients (three women) with symptomatic HF (NYHA class II/III) and a
Document: BACKGROUND: Exercise training in heart failure (HF) is recommended but not routinely offered, because of logistic and safety-related reasons. In 2020, the German Society for Prevention&Rehabilitation and the German Society for Cardiology requested establishing dedicated “HF training groups.†Here, we aimed to implement and evaluate the feasibility and safety of one of the first HF training groups in Germany. METHODS: Twelve patients (three women) with symptomatic HF (NYHA class II/III) and an ejection fraction ≤ 45% participated and were offered weekly, physician-supervised exercise training for 1 year. Patients received a wrist-worn pedometer (M430 Polar) and underwent the following assessments at baseline and after 4, 8 and 12 months: cardiopulmonary exercise test, 6-min walk test, echocardiography (blinded reading), and quality of life assessment (Kansas City Cardiomyopathy Questionnaire, KCCQ). RESULTS: All patients (median age [quartiles] 64 [49; 64] years) completed the study and participated in 76% of the offered 36 training sessions. The pedometer was worn ≥ 1000 min per day over 86% of the time. No cardiovascular events occurred during training. Across 12 months, NT-proBNP dropped from 986 pg/ml [455; 1937] to 483 pg/ml [247; 2322], and LVEF increased from 36% [29;41] to 41% [32;46]%, (p for trend = 0.01). We observed no changes in exercise capacity except for a subtle increase in peak VO(2)% predicted, from 66.5 [49; 77] to 67 [52; 78]; p for trend = 0.03. The physical function and social limitation domains of the KCCQ improved from 60 [54; 82] to 71 [58; 95, and from 63 [39; 83] to 78 [64; 92]; p for trend = 0.04 and = 0.01, respectively. Positive trends were further seen for the clinical and overall summary scores. CONCLUSION: This pilot study showed that the implementation of a supervised HF-exercise program is feasible, safe, and has the potential to improve both quality of life and surrogate markers of HF severity. This first exercise experiment should facilitate the design of risk-adopted training programs for patients with HF.
Search related documents:
Co phrase search for related documents- activity level and additional investigation: 1
- activity level and long term study: 1
- activity monitor and additional investigation: 1
- activity monitor and long term study: 1
- activity time and acute coronary syndrome: 1
- activity time and additional group: 1
- activity time and long term study: 1, 2, 3
- acute coronary syndrome and adjusted medication: 1
- acute coronary syndrome and lvedd end diastolic diameter: 1
- acute coronary syndrome and lvef ventricular ejection fraction: 1, 2, 3, 4, 5, 6
Co phrase search for related documents, hyperlinks ordered by date