Clinical review: intensive care unit acquired weakness
A substantial number of patients admitted to the ICU because of an acute illness, complicated surgery, severe trauma, or burn injury will develop a de novo form of muscle weakness during the ICU stay that is referred to as "intensive care unit acquired weakness" (ICUAW). This ICUAW evoked...
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description | A substantial number of patients admitted to the ICU because of an acute illness, complicated surgery, severe trauma, or burn injury will develop a de novo form of muscle weakness during the ICU stay that is referred to as "intensive care unit acquired weakness" (ICUAW). This ICUAW evoked by critical illness can be due to axonal neuropathy, primary myopathy, or both. Underlying pathophysiological mechanisms comprise microvascular, electrical, metabolic, and bioenergetic alterations, interacting in a complex way and culminating in loss of muscle strength and/or muscle atrophy. ICUAW is typically symmetrical and affects predominantly proximal limb muscles and respiratory muscles, whereas facial and ocular muscles are often spared. The main risk factors for ICUAW include high severity of illness upon admission, sepsis, multiple organ failure, prolonged immobilization, and hyperglycemia, and also older patients have a higher risk. The role of corticosteroids and neuromuscular blocking agents remains unclear. ICUAW is diagnosed in awake and cooperative patients by bedside manual testing of muscle strength and the severity is scored by the Medical Research Council sum score. In cases of atypical clinical presentation or evolution, additional electrophysiological testing may be required for differential diagnosis. The cornerstones of prevention are aggressive treatment of sepsis, early mobilization, preventing hyperglycemia with insulin, and avoiding the use parenteral nutrition during the first week of critical illness. Weak patients clearly have worse acute outcomes and consume more healthcare resources. Recovery usually occurs within weeks or months, although it may be incomplete with weakness persisting up to 2 years after ICU discharge. Prognosis appears compromised when the cause of ICUAW involves critical illness polyneuropathy, whereas isolated critical illness myopathy may have a better prognosis. In addition, ICUAW has shown to contribute to the risk of 1-year mortality. Future research should focus on new preventive and/or therapeutic strategies for this detrimental complication of critical illness and on clarifying how ICUAW contributes to poor longer-term prognosis. |
doi_str_mv | 10.1186/s13054-015-0993-7 |
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This ICUAW evoked by critical illness can be due to axonal neuropathy, primary myopathy, or both. Underlying pathophysiological mechanisms comprise microvascular, electrical, metabolic, and bioenergetic alterations, interacting in a complex way and culminating in loss of muscle strength and/or muscle atrophy. ICUAW is typically symmetrical and affects predominantly proximal limb muscles and respiratory muscles, whereas facial and ocular muscles are often spared. The main risk factors for ICUAW include high severity of illness upon admission, sepsis, multiple organ failure, prolonged immobilization, and hyperglycemia, and also older patients have a higher risk. The role of corticosteroids and neuromuscular blocking agents remains unclear. ICUAW is diagnosed in awake and cooperative patients by bedside manual testing of muscle strength and the severity is scored by the Medical Research Council sum score. In cases of atypical clinical presentation or evolution, additional electrophysiological testing may be required for differential diagnosis. The cornerstones of prevention are aggressive treatment of sepsis, early mobilization, preventing hyperglycemia with insulin, and avoiding the use parenteral nutrition during the first week of critical illness. Weak patients clearly have worse acute outcomes and consume more healthcare resources. Recovery usually occurs within weeks or months, although it may be incomplete with weakness persisting up to 2 years after ICU discharge. Prognosis appears compromised when the cause of ICUAW involves critical illness polyneuropathy, whereas isolated critical illness myopathy may have a better prognosis. In addition, ICUAW has shown to contribute to the risk of 1-year mortality. Future research should focus on new preventive and/or therapeutic strategies for this detrimental complication of critical illness and on clarifying how ICUAW contributes to poor longer-term prognosis.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>EISSN: 1364-8535</identifier><identifier>EISSN: 1366-609X</identifier><identifier>DOI: 10.1186/s13054-015-0993-7</identifier><identifier>PMID: 26242743</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Action Potentials - physiology ; Animal cognition ; Autonomic Nervous System Diseases - physiopathology ; Autophagy ; Autophagy - physiology ; Biomarkers - blood ; Blood Glucose - physiology ; Care and treatment ; Cognitive ability ; Critical care ; Critical Illness ; Cytokines ; Electromyography ; Health aspects ; Hospital Mortality ; Hospital patients ; Hospitalization ; Humans ; Hyperglycemia ; Illnesses ; Immobilization ; Incidence ; Intensive care ; Intensive Care Units ; Length of Stay ; Medical research ; Medicine, Experimental ; Mortality ; Multiple organ dysfunction syndrome ; Muscle function ; Muscle Strength - physiology ; Muscle Weakness - diagnosis ; Muscle Weakness - physiopathology ; Muscle Weakness - therapy ; Patient outcomes ; Patients ; Permeability ; Physical Therapy Modalities ; Proteins ; Quality of life ; Respiration, Artificial ; Respiratory distress syndrome ; Review ; Risk Factors ; Rodents ; Sepsis ; Sepsis - physiopathology ; Sepsis - therapy ; Studies ; Ventilators</subject><ispartof>Critical care (London, England), 2015-08, Vol.19 (1), p.274-274, Article 274</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Hermans and Van den Berghe. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-74474a8b1886499fa0abcb137297c82307375238ec7cc628884afb48112a4d153</citedby><cites>FETCH-LOGICAL-c588t-74474a8b1886499fa0abcb137297c82307375238ec7cc628884afb48112a4d153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526175/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526175/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26242743$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hermans, Greet</creatorcontrib><creatorcontrib>Van den Berghe, Greet</creatorcontrib><title>Clinical review: intensive care unit acquired weakness</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>A substantial number of patients admitted to the ICU because of an acute illness, complicated surgery, severe trauma, or burn injury will develop a de novo form of muscle weakness during the ICU stay that is referred to as "intensive care unit acquired weakness" (ICUAW). This ICUAW evoked by critical illness can be due to axonal neuropathy, primary myopathy, or both. Underlying pathophysiological mechanisms comprise microvascular, electrical, metabolic, and bioenergetic alterations, interacting in a complex way and culminating in loss of muscle strength and/or muscle atrophy. ICUAW is typically symmetrical and affects predominantly proximal limb muscles and respiratory muscles, whereas facial and ocular muscles are often spared. The main risk factors for ICUAW include high severity of illness upon admission, sepsis, multiple organ failure, prolonged immobilization, and hyperglycemia, and also older patients have a higher risk. The role of corticosteroids and neuromuscular blocking agents remains unclear. ICUAW is diagnosed in awake and cooperative patients by bedside manual testing of muscle strength and the severity is scored by the Medical Research Council sum score. In cases of atypical clinical presentation or evolution, additional electrophysiological testing may be required for differential diagnosis. The cornerstones of prevention are aggressive treatment of sepsis, early mobilization, preventing hyperglycemia with insulin, and avoiding the use parenteral nutrition during the first week of critical illness. Weak patients clearly have worse acute outcomes and consume more healthcare resources. Recovery usually occurs within weeks or months, although it may be incomplete with weakness persisting up to 2 years after ICU discharge. Prognosis appears compromised when the cause of ICUAW involves critical illness polyneuropathy, whereas isolated critical illness myopathy may have a better prognosis. In addition, ICUAW has shown to contribute to the risk of 1-year mortality. Future research should focus on new preventive and/or therapeutic strategies for this detrimental complication of critical illness and on clarifying how ICUAW contributes to poor longer-term prognosis.</description><subject>Action Potentials - physiology</subject><subject>Animal cognition</subject><subject>Autonomic Nervous System Diseases - physiopathology</subject><subject>Autophagy</subject><subject>Autophagy - physiology</subject><subject>Biomarkers - blood</subject><subject>Blood Glucose - physiology</subject><subject>Care and treatment</subject><subject>Cognitive ability</subject><subject>Critical care</subject><subject>Critical Illness</subject><subject>Cytokines</subject><subject>Electromyography</subject><subject>Health aspects</subject><subject>Hospital Mortality</subject><subject>Hospital patients</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Hyperglycemia</subject><subject>Illnesses</subject><subject>Immobilization</subject><subject>Incidence</subject><subject>Intensive care</subject><subject>Intensive Care Units</subject><subject>Length of Stay</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Mortality</subject><subject>Multiple organ dysfunction syndrome</subject><subject>Muscle function</subject><subject>Muscle Strength - physiology</subject><subject>Muscle Weakness - diagnosis</subject><subject>Muscle Weakness - physiopathology</subject><subject>Muscle Weakness - therapy</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Permeability</subject><subject>Physical Therapy Modalities</subject><subject>Proteins</subject><subject>Quality of life</subject><subject>Respiration, Artificial</subject><subject>Respiratory distress syndrome</subject><subject>Review</subject><subject>Risk Factors</subject><subject>Rodents</subject><subject>Sepsis</subject><subject>Sepsis - physiopathology</subject><subject>Sepsis - therapy</subject><subject>Studies</subject><subject>Ventilators</subject><issn>1364-8535</issn><issn>1466-609X</issn><issn>1364-8535</issn><issn>1366-609X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kk1rFTEUhoNY7If-ADcy4KabaXPyHRdCuVgVCt1UcBcyuWdq6txMm8zc4r83w63VikgWCcnzvic5eQl5DfQEwKjTApxK0VKQLbWWt_oZOQChVKuo_fq8rrkSrZFc7pPDUm4oBW0Uf0H2mWKCacEPiFoNMcXghybjNuL9uyamCVOJW2yCz9jMKU6ND3dzzLhu7tF_T1jKS7LX-6Hgq4f5iHw5_3C1-tReXH78vDq7aIM0Zmq1EFp404ExSljbe-q70AHXzOpgGKeaa8m4waBDUMwYI3zfCQPAvFiD5Efk_c73du42uA6YpuwHd5vjxucfbvTRPT1J8Zu7HrdOSKZALwbHDwZ5vJuxTG4TS8Bh8AnHuTjQlFGjKRcVffsXejPOOdXnObASpBWS2v9SWjNBubTmN3XtB3Qx9WO9XVhKuzMpQNZPYbpSJ_-g6ljjJoYxYR_r_hMB7AQhj6Vk7B87AdQtkXC7SLgaCbdEwi2aN3-28FHxKwP8J7Ugrcs</recordid><startdate>20150805</startdate><enddate>20150805</enddate><creator>Hermans, Greet</creator><creator>Van den Berghe, Greet</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150805</creationdate><title>Clinical review: intensive care unit acquired weakness</title><author>Hermans, Greet ; Van den Berghe, Greet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-74474a8b1886499fa0abcb137297c82307375238ec7cc628884afb48112a4d153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Action Potentials - physiology</topic><topic>Animal cognition</topic><topic>Autonomic Nervous System Diseases - physiopathology</topic><topic>Autophagy</topic><topic>Autophagy - physiology</topic><topic>Biomarkers - blood</topic><topic>Blood Glucose - physiology</topic><topic>Care and treatment</topic><topic>Cognitive ability</topic><topic>Critical care</topic><topic>Critical Illness</topic><topic>Cytokines</topic><topic>Electromyography</topic><topic>Health aspects</topic><topic>Hospital Mortality</topic><topic>Hospital patients</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Hyperglycemia</topic><topic>Illnesses</topic><topic>Immobilization</topic><topic>Incidence</topic><topic>Intensive care</topic><topic>Intensive Care Units</topic><topic>Length of Stay</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Mortality</topic><topic>Multiple organ dysfunction syndrome</topic><topic>Muscle function</topic><topic>Muscle Strength - physiology</topic><topic>Muscle Weakness - diagnosis</topic><topic>Muscle Weakness - physiopathology</topic><topic>Muscle Weakness - therapy</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Permeability</topic><topic>Physical Therapy Modalities</topic><topic>Proteins</topic><topic>Quality of life</topic><topic>Respiration, Artificial</topic><topic>Respiratory distress syndrome</topic><topic>Review</topic><topic>Risk Factors</topic><topic>Rodents</topic><topic>Sepsis</topic><topic>Sepsis - physiopathology</topic><topic>Sepsis - therapy</topic><topic>Studies</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hermans, Greet</creatorcontrib><creatorcontrib>Van den Berghe, Greet</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hermans, Greet</au><au>Van den Berghe, Greet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical review: intensive care unit acquired weakness</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2015-08-05</date><risdate>2015</risdate><volume>19</volume><issue>1</issue><spage>274</spage><epage>274</epage><pages>274-274</pages><artnum>274</artnum><issn>1364-8535</issn><eissn>1466-609X</eissn><eissn>1364-8535</eissn><eissn>1366-609X</eissn><abstract>A substantial number of patients admitted to the ICU because of an acute illness, complicated surgery, severe trauma, or burn injury will develop a de novo form of muscle weakness during the ICU stay that is referred to as "intensive care unit acquired weakness" (ICUAW). This ICUAW evoked by critical illness can be due to axonal neuropathy, primary myopathy, or both. Underlying pathophysiological mechanisms comprise microvascular, electrical, metabolic, and bioenergetic alterations, interacting in a complex way and culminating in loss of muscle strength and/or muscle atrophy. ICUAW is typically symmetrical and affects predominantly proximal limb muscles and respiratory muscles, whereas facial and ocular muscles are often spared. The main risk factors for ICUAW include high severity of illness upon admission, sepsis, multiple organ failure, prolonged immobilization, and hyperglycemia, and also older patients have a higher risk. The role of corticosteroids and neuromuscular blocking agents remains unclear. ICUAW is diagnosed in awake and cooperative patients by bedside manual testing of muscle strength and the severity is scored by the Medical Research Council sum score. In cases of atypical clinical presentation or evolution, additional electrophysiological testing may be required for differential diagnosis. The cornerstones of prevention are aggressive treatment of sepsis, early mobilization, preventing hyperglycemia with insulin, and avoiding the use parenteral nutrition during the first week of critical illness. Weak patients clearly have worse acute outcomes and consume more healthcare resources. Recovery usually occurs within weeks or months, although it may be incomplete with weakness persisting up to 2 years after ICU discharge. Prognosis appears compromised when the cause of ICUAW involves critical illness polyneuropathy, whereas isolated critical illness myopathy may have a better prognosis. In addition, ICUAW has shown to contribute to the risk of 1-year mortality. Future research should focus on new preventive and/or therapeutic strategies for this detrimental complication of critical illness and on clarifying how ICUAW contributes to poor longer-term prognosis.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26242743</pmid><doi>10.1186/s13054-015-0993-7</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials - physiology Animal cognition Autonomic Nervous System Diseases - physiopathology Autophagy Autophagy - physiology Biomarkers - blood Blood Glucose - physiology Care and treatment Cognitive ability Critical care Critical Illness Cytokines Electromyography Health aspects Hospital Mortality Hospital patients Hospitalization Humans Hyperglycemia Illnesses Immobilization Incidence Intensive care Intensive Care Units Length of Stay Medical research Medicine, Experimental Mortality Multiple organ dysfunction syndrome Muscle function Muscle Strength - physiology Muscle Weakness - diagnosis Muscle Weakness - physiopathology Muscle Weakness - therapy Patient outcomes Patients Permeability Physical Therapy Modalities Proteins Quality of life Respiration, Artificial Respiratory distress syndrome Review Risk Factors Rodents Sepsis Sepsis - physiopathology Sepsis - therapy Studies Ventilators |
title | Clinical review: intensive care unit acquired weakness |
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