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      Extracorporeal Membrane Oxygenation for COVID-19: Updated 2021 Guidelines from the Extracorporeal Life Support Organization

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      * , , , , § , , , # , ** , †† , ‡‡ , §§ , ¶¶ , ∥∥ , ## , *** , ††† , ‡‡‡ , §§§ , ¶¶¶ , ∥∥∥ , ### , **** , †††† , ‡‡‡‡ , §§§§ , ¶¶¶¶ , †† , ‡‡
      Asaio Journal
      Lippincott Williams & Wilkins
      acute respiratory distress syndrome, coronavirus disease 2019, extracorporeal life support organization, extracorporeal life support program, extracorporeal membrane oxygenation, multisystem inflammatory syndrome in children, pandemic

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          This is an updated guideline from the Extracorporeal Life Support Organization (ELSO) for the role of extracorporeal membrane oxygenation (ECMO) for patients with severe cardiopulmonary failure due to coronavirus disease 2019 (COVID-19). The great majority of COVID-19 patients (>90%) requiring ECMO have been supported using venovenous (V-V) ECMO for acute respiratory distress syndrome (ARDS). While COVID-19 ECMO run duration may be longer than in non-COVID-19 ECMO patients, published mortality appears to be similar between the two groups. However, data collection is ongoing, and there is a signal that overall mortality may be increasing. Conventional selection criteria for COVID-19–related ECMO should be used; however, when resources become more constrained during a pandemic, more stringent contraindications should be implemented. Formation of regional ECMO referral networks may facilitate communication, resource sharing, expedited patient referral, and mobile ECMO retrieval. There are no data to suggest deviation from conventional ECMO device or patient management when applying ECMO for COVID-19 patients. Rarely, children may require ECMO support for COVID-19–related ARDS, myocarditis, or multisystem inflammatory syndrome in children (MIS-C); conventional selection criteria and management practices should be the standard. We strongly encourage participation in data submission to investigate the optimal use of ECMO for COVID-19.

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          Multisystem Inflammatory Syndrome in U.S. Children and Adolescents

          Abstract Background Understanding the epidemiology and clinical course of multisystem inflammatory syndrome in children (MIS-C) and its temporal association with coronavirus disease 2019 (Covid-19) is important, given the clinical and public health implications of the syndrome. Methods We conducted targeted surveillance for MIS-C from March 15 to May 20, 2020, in pediatric health centers across the United States. The case definition included six criteria: serious illness leading to hospitalization, an age of less than 21 years, fever that lasted for at least 24 hours, laboratory evidence of inflammation, multisystem organ involvement, and evidence of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) based on reverse-transcriptase polymerase chain reaction (RT-PCR), antibody testing, or exposure to persons with Covid-19 in the past month. Clinicians abstracted the data onto standardized forms. Results We report on 186 patients with MIS-C in 26 states. The median age was 8.3 years, 115 patients (62%) were male, 135 (73%) had previously been healthy, 131 (70%) were positive for SARS-CoV-2 by RT-PCR or antibody testing, and 164 (88%) were hospitalized after April 16, 2020. Organ-system involvement included the gastrointestinal system in 171 patients (92%), cardiovascular in 149 (80%), hematologic in 142 (76%), mucocutaneous in 137 (74%), and respiratory in 131 (70%). The median duration of hospitalization was 7 days (interquartile range, 4 to 10); 148 patients (80%) received intensive care, 37 (20%) received mechanical ventilation, 90 (48%) received vasoactive support, and 4 (2%) died. Coronary-artery aneurysms (z scores ≥2.5) were documented in 15 patients (8%), and Kawasaki’s disease–like features were documented in 74 (40%). Most patients (171 [92%]) had elevations in at least four biomarkers indicating inflammation. The use of immunomodulating therapies was common: intravenous immune globulin was used in 144 (77%), glucocorticoids in 91 (49%), and interleukin-6 or 1RA inhibitors in 38 (20%). Conclusions Multisystem inflammatory syndrome in children associated with SARS-CoV-2 led to serious and life-threatening illness in previously healthy children and adolescents. (Funded by the Centers for Disease Control and Prevention.)
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            Surviving Sepsis Campaign: guidelines on the management of critically ill adults with Coronavirus Disease 2019 (COVID-19)

            Background The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of a rapidly spreading illness, Coronavirus Disease 2019 (COVID-19), affecting thousands of people around the world. Urgent guidance for clinicians caring for the sickest of these patients is needed. Methods We formed a panel of 36 experts from 12 countries. All panel members completed the World Health Organization conflict of interest disclosure form. The panel proposed 53 questions that are relevant to the management of COVID-19 in the ICU. We searched the literature for direct and indirect evidence on the management of COVID-19 in critically ill patients in the ICU. We identified relevant and recent systematic reviews on most questions relating to supportive care. We assessed the certainty in the evidence using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach, then generated recommendations based on the balance between benefit and harm, resource and cost implications, equity, and feasibility. Recommendations were either strong or weak, or in the form of best practice recommendations. Results The Surviving Sepsis Campaign COVID-19 panel issued 54 statements, of which 4 are best practice statements, 9 are strong recommendations, and 35 are weak recommendations. No recommendation was provided for 6 questions. The topics were: (1) infection control, (2) laboratory diagnosis and specimens, (3) hemodynamic support, (4) ventilatory support, and (5) COVID-19 therapy. Conclusion The Surviving Sepsis Campaign COVID-19 panel issued several recommendations to help support healthcare workers caring for critically ill ICU patients with COVID-19. When available, we will provide new recommendations in further releases of these guidelines. Electronic supplementary material The online version of this article (10.1007/s00134-020-06022-5) contains supplementary material, which is available to authorized users.
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              COVID-19 and Cardiovascular Disease

              Coronavirus disease 2019 (COVID-19) is a global pandemic affecting 185 countries and >3 000 000 patients worldwide as of April 28, 2020. COVID-19 is caused by severe acute respiratory syndrome coronavirus 2, which invades cells through the angiotensin-converting enzyme 2 receptor. Among patients with COVID-19, there is a high prevalence of cardiovascular disease, and >7% of patients experience myocardial injury from the infection (22% of critically ill patients). Although angiotensin-converting enzyme 2 serves as the portal for infection, the role of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers requires further investigation. COVID-19 poses a challenge for heart transplantation, affecting donor selection, immunosuppression, and posttransplant management. There are a number of promising therapies under active investigation to treat and prevent COVID-19.
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                Author and article information

                Contributors
                Journal
                ASAIO J
                ASAIO J
                MAT
                Asaio Journal
                Lippincott Williams & Wilkins (Hagerstown, MD )
                1058-2916
                1538-943X
                26 February 2021
                May 2021
                : 67
                : 5
                : 485-495
                Affiliations
                From the [* ]Department of Emergency Medicine, University of Washington, Seattle, Washington
                []Division of Pulmonary Critical Care and Sleep Medicine, University of Washington, Seattle, Washington
                []General ICU, University Hospital of Parma, Parma, Italy
                [§ ]Department of Biomedical, Metabolic and Neural Sciences, University of Modena & Reggio Emilia, Modena, Italy
                []Extracorporeal Life Support Organization
                []Texas Children’s Hospital, Baylor College of Medicine, Houston, Texas
                [# ]Children’s Medical Center of Dallas, University of Texas Southwestern Medical Center, Dallas, Texas
                [** ]Emory University, Children’s Healthcare of Atlanta, Atlanta, Georgia
                [†† ]Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York
                [‡‡ ]Center for Acute Respiratory Failure, New York-Presbyterian Hospital, New York, New York
                [§§ ]University of Michigan, Ann Arbor, Michigan
                [¶¶ ]Department of Critical Care, Guy’s and St. Thomas’ NHS Foundation Trust, London, United Kingdom
                [∥∥ ]Centre for Human and Applied Physiological Sciences, Faculty of Life Sciences and Medicine, King’s College London, London, United Kingdom
                [## ]Institute of Cardiometabolism and Nutrition, INSERM, Sorbonne Université, Paris, France
                [*** ]Service de Médecine Intensive-Réanimation, Institut de Cardiologie, APHP Sorbonne Université Hôpital Pitié-Salpêtrière, Paris, France
                [††† ]Department of Cardio-Thoracic Surgery, Maastricht University Medical Centre, Cardiovascular Research Institute Maastricht, Maastricht, The Netherlands
                [‡‡‡ ]Department of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany
                [§§§ ]Nemours Children’s Health System, Wilmington, Delaware
                [¶¶¶ ]Congenital Heart Center, Departments of Surgery and Pediatrics, University of Florida, Gainesville, Florida
                [∥∥∥ ]Intensive Care Unit, Alfred Health Melbourne, Victoria, Australia
                [### ]Critical Care ECMO Service, King Saud Medical City, Ministry Of Health (MOH), Riyadh, Saudi Arabia
                [**** ]Fundación Cardiovascular de Colombia, Floridablanca, Santander, Colombia
                [†††† ]Service de Médecine Intensive-Réanimation, Institut de Cardiologie, AP-HP, Sorbonne Université Hôpital Pitié-Salpêtrière, Paris, France
                [‡‡‡‡ ]Sorbonne Université, GRC n°30, GRC RESPIRE, INSERM, UMRS_1166-ICAN, Institute of Cardiometabolism and Nutrition, Paris, France
                [§§§§ ]Adult Intensive Care Services, The Prince Charles Hospital, Brisbane, Queensland, Australia
                [¶¶¶¶ ]National University Hospital, Singapore.
                Author notes
                Correspondence: Jenelle Badulak, Department of Emergency Medicine, Division of Pulmonary Critical Care and Sleep Medicine, University of Washington, Harborview Medical Center, Box 359702, 325 Ninth Avenue, Seattle, WA 98104-2499. Email: badulakj@ 123456uw.edu .
                Article
                00003
                10.1097/MAT.0000000000001422
                8078022
                33657573
                283f9a75-d47c-4b19-a79e-b618d5078869
                Copyright © ELSO 2021

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : February 2021
                : February 2021
                Categories
                Management of COVID-19 Patients

                acute respiratory distress syndrome,coronavirus disease 2019,extracorporeal life support organization,extracorporeal life support program,extracorporeal membrane oxygenation,multisystem inflammatory syndrome in children,pandemic

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