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Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study
AIMS: Most devices for treating ambulatory Class II and III heart failure are linked to electrical pulses. However, a steady electric potential gradient is also necessary for appropriate myocardial performance and may be disturbed by structural heart diseases. We investigated whether chronic applica...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006737/ https://www.ncbi.nlm.nih.gov/pubmed/33559358 http://dx.doi.org/10.1002/ehf2.13242 |
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author | Kosevic, Dragana Wiedemann, Dominik Vukovic, Petar Ristic, Velibor Riebandt, Julia Radak, Una Brandes, Kersten Goettel, Peter Duengen, Hans‐Dirk Tahirovic, Elvis Kottmann, Tatjana Voss, Hans Werner Zdravkovic, Marija Putnik, Svetozar Schmitto, Jan D. Mueller, Johannes Rame, Jesus Eduardo Peric, Miodrag |
author_facet | Kosevic, Dragana Wiedemann, Dominik Vukovic, Petar Ristic, Velibor Riebandt, Julia Radak, Una Brandes, Kersten Goettel, Peter Duengen, Hans‐Dirk Tahirovic, Elvis Kottmann, Tatjana Voss, Hans Werner Zdravkovic, Marija Putnik, Svetozar Schmitto, Jan D. Mueller, Johannes Rame, Jesus Eduardo Peric, Miodrag |
author_sort | Kosevic, Dragana |
collection | PubMed |
description | AIMS: Most devices for treating ambulatory Class II and III heart failure are linked to electrical pulses. However, a steady electric potential gradient is also necessary for appropriate myocardial performance and may be disturbed by structural heart diseases. We investigated whether chronic application of electrical microcurrent to the heart is feasible and safe and improves cardiac performance. The results of this study should provide guidance for the design of a two‐arm, randomized, controlled Phase II trial. METHODS AND RESULTS: This single‐arm, non‐randomized pilot study involved 10 patients (9 men; mean age, 62 ± 12 years) at two sites with 6 month follow‐up. All patients had New York Heart Association (NYHA) Class III heart failure and non‐ischaemic dilated cardiomyopathy, with left ventricular ejection fraction (LVEF) <35%. A device was surgically placed to deliver a constant microcurrent to the heart. The following tests were performed at baseline, at hospital discharge, and at six time points during follow‐up: determination of LVEF and left ventricular end‐diastolic/end‐systolic diameter by echocardiography; the 6 min walk test; and assessment of NYHA classification and quality of life (36‐Item Short‐Form Health Survey questionnaire). Microcurrent application was feasible and safe; no device‐related or treatment‐related adverse events occurred. During follow‐up, rapid and significant signal of efficacy (P < 0.005) was present with improvements in LVEF, left ventricular end‐diastolic diameter, left ventricular end‐systolic diameter, and distance walked. For eight patients, NYHA classification improved from Class III to Class I (for seven, as early as 14 days post‐operatively); for one, to Class II; and for one, to Class II/III. 36‐Item Short‐Form Health Survey questionnaire scores also improved highly significantly. CONCLUSIONS: Chronic application of microcurrent to the heart is feasible and safe and leads to a rapid and lasting improvement in heart function and a near normalization of heart size within days. The NYHA classification and quality of life improve just as rapidly. |
format | Online Article Text |
id | pubmed-8006737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80067372021-04-01 Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study Kosevic, Dragana Wiedemann, Dominik Vukovic, Petar Ristic, Velibor Riebandt, Julia Radak, Una Brandes, Kersten Goettel, Peter Duengen, Hans‐Dirk Tahirovic, Elvis Kottmann, Tatjana Voss, Hans Werner Zdravkovic, Marija Putnik, Svetozar Schmitto, Jan D. Mueller, Johannes Rame, Jesus Eduardo Peric, Miodrag ESC Heart Fail Original Research Articles AIMS: Most devices for treating ambulatory Class II and III heart failure are linked to electrical pulses. However, a steady electric potential gradient is also necessary for appropriate myocardial performance and may be disturbed by structural heart diseases. We investigated whether chronic application of electrical microcurrent to the heart is feasible and safe and improves cardiac performance. The results of this study should provide guidance for the design of a two‐arm, randomized, controlled Phase II trial. METHODS AND RESULTS: This single‐arm, non‐randomized pilot study involved 10 patients (9 men; mean age, 62 ± 12 years) at two sites with 6 month follow‐up. All patients had New York Heart Association (NYHA) Class III heart failure and non‐ischaemic dilated cardiomyopathy, with left ventricular ejection fraction (LVEF) <35%. A device was surgically placed to deliver a constant microcurrent to the heart. The following tests were performed at baseline, at hospital discharge, and at six time points during follow‐up: determination of LVEF and left ventricular end‐diastolic/end‐systolic diameter by echocardiography; the 6 min walk test; and assessment of NYHA classification and quality of life (36‐Item Short‐Form Health Survey questionnaire). Microcurrent application was feasible and safe; no device‐related or treatment‐related adverse events occurred. During follow‐up, rapid and significant signal of efficacy (P < 0.005) was present with improvements in LVEF, left ventricular end‐diastolic diameter, left ventricular end‐systolic diameter, and distance walked. For eight patients, NYHA classification improved from Class III to Class I (for seven, as early as 14 days post‐operatively); for one, to Class II; and for one, to Class II/III. 36‐Item Short‐Form Health Survey questionnaire scores also improved highly significantly. CONCLUSIONS: Chronic application of microcurrent to the heart is feasible and safe and leads to a rapid and lasting improvement in heart function and a near normalization of heart size within days. The NYHA classification and quality of life improve just as rapidly. John Wiley and Sons Inc. 2021-02-09 /pmc/articles/PMC8006737/ /pubmed/33559358 http://dx.doi.org/10.1002/ehf2.13242 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Articles Kosevic, Dragana Wiedemann, Dominik Vukovic, Petar Ristic, Velibor Riebandt, Julia Radak, Una Brandes, Kersten Goettel, Peter Duengen, Hans‐Dirk Tahirovic, Elvis Kottmann, Tatjana Voss, Hans Werner Zdravkovic, Marija Putnik, Svetozar Schmitto, Jan D. Mueller, Johannes Rame, Jesus Eduardo Peric, Miodrag Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title | Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title_full | Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title_fullStr | Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title_full_unstemmed | Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title_short | Cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
title_sort | cardio‐microcurrent device for chronic heart failure: first‐in‐human clinical study |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006737/ https://www.ncbi.nlm.nih.gov/pubmed/33559358 http://dx.doi.org/10.1002/ehf2.13242 |
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