Please use this identifier to cite or link to this item: doi:10.22028/D291-40447
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Title: Safety and feasibility of electrical muscle stimulation in patients undergoing autologous and allogeneic stem cell transplantation or intensive chemotherapy
Author(s): Bewarder, M
Klostermann, A
Ahlgrimm, M
Bittenbring, J T
Pfreundschuh, M
Wagenpfeil, Stefan
Kaddu-Mulindwa, D
Language: English
Title: Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
Volume: 27
Issue: 3
Pages: 1013–1020
Publisher/Platform: Springer
Year of Publication: 2019
Free key words: Electric muscle stimulation
Supportive care
Stem cell transplantation
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: Intensive chemotherapy, with or without following autologous or allogeneic stem cell transplantation (HSCT), is often the only curative treatment option for patients with hematological malignancies and leave many survivors physically and psychologically impaired. Electrical muscle stimulation (EMS) is a proven tool to improve physical performance in seniors and patients with chronic diseases. We therefore investigated the safety and feasibility of EMS in 45 patients undergoing autologous HSCT (n = 13), allogeneic HSCT (n = 11) and intensive chemotherapy (n = 21). Furthermore, physical (assessed by 6-min walking distance (6MWD) and short physical performance battery (SPPB)) and psychological performance (assessed by multidimensional fatigue inventory (MFI) and the EORTC QOL-C30 questionnaire) were measured before chemotherapy (T1) and at discharge from hospital (T2). Four patients died due to septic shock, two withdrew consent before the start of EMS training and five stopped EMS training during the study because of chemotherapy-related complications, loss of motivation or loss of ability to use EMS autonomously. Thirty-four out of 45 (76%) patients used EMS throughout the study period and participated in physical and psychological tests at time points 1 and 2. EMS-related adverse events were hematoma (n = 1) and muscle pain (n = 2). No bleeding events > 1 according to the WHO bleeding scale occurred. Decline in 6MWD from T1 to T2 was 24 m. The SPPB score stayed the same with 11 points at T1 and T2. Most MFI subscales showed stable fatigue levels and quality of life (QoL) did not decrease significantly throughout therapy. EMS is feasible and safe in patients undergoing intensive chemotherapy. Trial registration: NCT03467087.
DOI of the first publication: 10.1007/s00520-018-4390-z
URL of the first publication: https://link.springer.com/article/10.1007/s00520-018-4390-z
Link to this record: urn:nbn:de:bsz:291--ds-404473
hdl:20.500.11880/36347
http://dx.doi.org/10.22028/D291-40447
ISSN: 0941-4355
1433-7339
Date of registration: 1-Sep-2023
Faculty: M - Medizinische Fakultät
Department: M - Medizinische Biometrie, Epidemiologie und medizinische Informatik
Professorship: M - Prof. Dr. Stefan Wagenpfeil
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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