Intensive care unit-acquired weakness: a review from molecular mechanisms to its impact in COVID-2019

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Miniatura
Fecha
2022-09
Profesor/a Guía
Facultad/escuela
Idioma
en
Título de la revista
ISSN de la revista
Título del volumen
Editor
Page Press Publications
Nombre de Curso
Licencia CC
Licencia CC
https://creativecommons.org/licenses/by/4.0/deed.es
Resumen
Intensive Care Unit-Acquired Weakness (ICU-AW) is a generalized and symmetric neuromuscular dysfunction associated with critical illness and its treatments. Its incidence is approximately 80% in intensive care unit patients, and it manifests as critical illness polyneuropathy, critical illness myopathy, and muscle atrophy. Intensive care unit patients can lose an elevated percentage of their muscle mass in the first days after admission, producing short- and long-term sequelae that affect patients’ quality of life, physical health, and mental health. In 2019, the world was faced with coronavirus disease 2019 (COVID-19), caused by the acute respiratory syndrome coronavirus 2. COVID-19 produces severe respiratory disorders, such as acute respiratory distress syndrome, which increases the risk of developing ICU-AW. COVID-19 patients treated in intensive care units have shown early diffuse and symmetrical muscle weakness, polyneuropathy, and myalgia, coinciding with the clinical presentation of ICU-AW. Besides, these patients require prolonged intensive care unit stays, invasive mechanical ventilation, and intensive care unit pharmacological therapy, which are risk factors for ICU-AW. Thus, the purposes of this review are to discuss the features of ICU-AW and its effects on skeletal muscle. Further, we will describe the mechanisms involved in the probable development of ICU-AW in severe COVID-19 patients.
Notas
Indexación: Scopus.
Palabras clave
ICU-acquired weakness (ICU-AW), Coronavirus Disease 2019, Skeletal Muscle Atrophy, Critical Illness
Citación
European Journal of Translational Myology. Volume 32, Issue 3. 29 September 2022. Article number 10511
DOI
DOI: 10.4081/ejtm.2022.10511
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