Neurologic Outcomes of Survivors of COVID-19–Associated Acute Respiratory Distress Syndrome Requiring Intubation

To describe 3-6-month neurologic outcomes of survivors of COVID-19-associated acute respiratory distress syndrome, invasively ventilated in the ICU. A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020). Two academic hospital ICUs, Pa...

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Veröffentlicht in:Critical care medicine 2022-08, Vol.50 (8), p.e674-e682
Hauptverfasser: Jaquet, Pierre, Legouy, Camille, Le Fevre, Lucie, Grinea, Alexandra, Sinnah, Fabrice, Franchineau, Guillaume, Patrier, Juliette, Marzouk, Mehdi, Wicky, Paul-Henri, Alexis Geoffroy, Pierre, Arnoult, Florence, Vledouts, Serafima, de Montmollin, Etienne, Bouadma, Lila, Timsit, Jean-François, Sharshar, Tarek, Sonneville, Romain
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container_end_page e682
container_issue 8
container_start_page e674
container_title Critical care medicine
container_volume 50
creator Jaquet, Pierre
Legouy, Camille
Le Fevre, Lucie
Grinea, Alexandra
Sinnah, Fabrice
Franchineau, Guillaume
Patrier, Juliette
Marzouk, Mehdi
Wicky, Paul-Henri
Alexis Geoffroy, Pierre
Arnoult, Florence
Vledouts, Serafima
de Montmollin, Etienne
Bouadma, Lila
Timsit, Jean-François
Sharshar, Tarek
Sonneville, Romain
description To describe 3-6-month neurologic outcomes of survivors of COVID-19-associated acute respiratory distress syndrome, invasively ventilated in the ICU. A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020). Two academic hospital ICUs, Paris, France. Adult COVID-19-associated acute respiratory distress syndrome survivors, invasively ventilated in the ICU, were eligible for a neurologic consultation between 3 and 6 months post ICU discharge. Follow-up by face-to-face neurologic consultation. The primary endpoint was favorable functional outcome defined by a modified Rankin scale score less than 2, indicating survival with no significant disability. Secondary endpoints included mild cognitive impairment (Montreal Cognitive Assessment score < 26), ICU-acquired weakness (Medical Research Council score < 48), anxiety and depression (Hospital Anxiety and Depression score > 7), and posttraumatic stress disorder (posttraumatic stress disorder checklist for Diagnostic and Statistical Manual of Mental Disorders 5 score > 30). Of 54 eligible survivors, four non-French-speaking patients were excluded, eight patients were lost-to-follow-up, and one died during follow-up. Forty-one patients were included. Time between ICU discharge and neurologic consultation was 3.8 months (3.6-5.9 mo). A favorable functional outcome was observed in 16 patients (39%) and mild cognitive impairment in 17 of 33 patients tested (52%). ICU-acquired weakness, depression or anxiety, and posttraumatic stress disorder were reported in six of 37 cases (16%), eight of 31 cases (26%), and two of 27 cases (7%), respectively. Twenty-nine patients (74%) required rehabilitation (motor, cognitive, or psychologic). ICU and hospital lengths of stay, tracheostomy, and corticosteroids were negatively associated with favorable outcome. By contrast, use of alpha-2 agonists during ICU stay was associated with favorable outcome. COVID-19-associated acute respiratory distress syndrome requiring intubation led to slight-to-severe functional disability in about 60% of survivors 4 months after ICU discharge. Cognitive impairment, muscle weakness, and psychologic symptoms were frequent. A large multicenter study is warranted to allow identification of modifiable factors for improving long-term outcome.
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A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020). Two academic hospital ICUs, Paris, France. Adult COVID-19-associated acute respiratory distress syndrome survivors, invasively ventilated in the ICU, were eligible for a neurologic consultation between 3 and 6 months post ICU discharge. Follow-up by face-to-face neurologic consultation. The primary endpoint was favorable functional outcome defined by a modified Rankin scale score less than 2, indicating survival with no significant disability. Secondary endpoints included mild cognitive impairment (Montreal Cognitive Assessment score &lt; 26), ICU-acquired weakness (Medical Research Council score &lt; 48), anxiety and depression (Hospital Anxiety and Depression score &gt; 7), and posttraumatic stress disorder (posttraumatic stress disorder checklist for Diagnostic and Statistical Manual of Mental Disorders 5 score &gt; 30). Of 54 eligible survivors, four non-French-speaking patients were excluded, eight patients were lost-to-follow-up, and one died during follow-up. Forty-one patients were included. Time between ICU discharge and neurologic consultation was 3.8 months (3.6-5.9 mo). A favorable functional outcome was observed in 16 patients (39%) and mild cognitive impairment in 17 of 33 patients tested (52%). ICU-acquired weakness, depression or anxiety, and posttraumatic stress disorder were reported in six of 37 cases (16%), eight of 31 cases (26%), and two of 27 cases (7%), respectively. Twenty-nine patients (74%) required rehabilitation (motor, cognitive, or psychologic). ICU and hospital lengths of stay, tracheostomy, and corticosteroids were negatively associated with favorable outcome. By contrast, use of alpha-2 agonists during ICU stay was associated with favorable outcome. COVID-19-associated acute respiratory distress syndrome requiring intubation led to slight-to-severe functional disability in about 60% of survivors 4 months after ICU discharge. Cognitive impairment, muscle weakness, and psychologic symptoms were frequent. A large multicenter study is warranted to allow identification of modifiable factors for improving long-term outcome.</description><identifier>ISSN: 0090-3493</identifier><identifier>EISSN: 1530-0293</identifier><identifier>DOI: 10.1097/CCM.0000000000005500</identifier><identifier>PMID: 35132020</identifier><language>eng</language><publisher>United States: Lippincott Williams &amp; Wilkins</publisher><subject>Adult ; COVID-19 - complications ; COVID-19 - therapy ; Humans ; Intensive Care Units ; Intubation, Intratracheal ; Online Clinical Investigations ; Prospective Studies ; Quality of Life ; Respiratory Distress Syndrome - etiology ; Respiratory Distress Syndrome - therapy ; Stress Disorders, Post-Traumatic - epidemiology ; Stress Disorders, Post-Traumatic - therapy ; Survivors - psychology</subject><ispartof>Critical care medicine, 2022-08, Vol.50 (8), p.e674-e682</ispartof><rights>Lippincott Williams &amp; Wilkins</rights><rights>Copyright © 2022 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.</rights><rights>Copyright © 2022 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. 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A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020). Two academic hospital ICUs, Paris, France. Adult COVID-19-associated acute respiratory distress syndrome survivors, invasively ventilated in the ICU, were eligible for a neurologic consultation between 3 and 6 months post ICU discharge. Follow-up by face-to-face neurologic consultation. The primary endpoint was favorable functional outcome defined by a modified Rankin scale score less than 2, indicating survival with no significant disability. Secondary endpoints included mild cognitive impairment (Montreal Cognitive Assessment score &lt; 26), ICU-acquired weakness (Medical Research Council score &lt; 48), anxiety and depression (Hospital Anxiety and Depression score &gt; 7), and posttraumatic stress disorder (posttraumatic stress disorder checklist for Diagnostic and Statistical Manual of Mental Disorders 5 score &gt; 30). Of 54 eligible survivors, four non-French-speaking patients were excluded, eight patients were lost-to-follow-up, and one died during follow-up. Forty-one patients were included. Time between ICU discharge and neurologic consultation was 3.8 months (3.6-5.9 mo). A favorable functional outcome was observed in 16 patients (39%) and mild cognitive impairment in 17 of 33 patients tested (52%). ICU-acquired weakness, depression or anxiety, and posttraumatic stress disorder were reported in six of 37 cases (16%), eight of 31 cases (26%), and two of 27 cases (7%), respectively. Twenty-nine patients (74%) required rehabilitation (motor, cognitive, or psychologic). ICU and hospital lengths of stay, tracheostomy, and corticosteroids were negatively associated with favorable outcome. By contrast, use of alpha-2 agonists during ICU stay was associated with favorable outcome. COVID-19-associated acute respiratory distress syndrome requiring intubation led to slight-to-severe functional disability in about 60% of survivors 4 months after ICU discharge. Cognitive impairment, muscle weakness, and psychologic symptoms were frequent. 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A bicentric prospective study during the two first waves of the pandemic (March to May and September to December, 2020). Two academic hospital ICUs, Paris, France. Adult COVID-19-associated acute respiratory distress syndrome survivors, invasively ventilated in the ICU, were eligible for a neurologic consultation between 3 and 6 months post ICU discharge. Follow-up by face-to-face neurologic consultation. The primary endpoint was favorable functional outcome defined by a modified Rankin scale score less than 2, indicating survival with no significant disability. Secondary endpoints included mild cognitive impairment (Montreal Cognitive Assessment score &lt; 26), ICU-acquired weakness (Medical Research Council score &lt; 48), anxiety and depression (Hospital Anxiety and Depression score &gt; 7), and posttraumatic stress disorder (posttraumatic stress disorder checklist for Diagnostic and Statistical Manual of Mental Disorders 5 score &gt; 30). Of 54 eligible survivors, four non-French-speaking patients were excluded, eight patients were lost-to-follow-up, and one died during follow-up. Forty-one patients were included. Time between ICU discharge and neurologic consultation was 3.8 months (3.6-5.9 mo). A favorable functional outcome was observed in 16 patients (39%) and mild cognitive impairment in 17 of 33 patients tested (52%). ICU-acquired weakness, depression or anxiety, and posttraumatic stress disorder were reported in six of 37 cases (16%), eight of 31 cases (26%), and two of 27 cases (7%), respectively. Twenty-nine patients (74%) required rehabilitation (motor, cognitive, or psychologic). ICU and hospital lengths of stay, tracheostomy, and corticosteroids were negatively associated with favorable outcome. By contrast, use of alpha-2 agonists during ICU stay was associated with favorable outcome. COVID-19-associated acute respiratory distress syndrome requiring intubation led to slight-to-severe functional disability in about 60% of survivors 4 months after ICU discharge. Cognitive impairment, muscle weakness, and psychologic symptoms were frequent. A large multicenter study is warranted to allow identification of modifiable factors for improving long-term outcome.</abstract><cop>United States</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>35132020</pmid><doi>10.1097/CCM.0000000000005500</doi><oa>free_for_read</oa></addata></record>
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subjects Adult
COVID-19 - complications
COVID-19 - therapy
Humans
Intensive Care Units
Intubation, Intratracheal
Online Clinical Investigations
Prospective Studies
Quality of Life
Respiratory Distress Syndrome - etiology
Respiratory Distress Syndrome - therapy
Stress Disorders, Post-Traumatic - epidemiology
Stress Disorders, Post-Traumatic - therapy
Survivors - psychology
title Neurologic Outcomes of Survivors of COVID-19–Associated Acute Respiratory Distress Syndrome Requiring Intubation
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