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      Poor survival with extracorporeal membrane oxygenation in acute respiratory distress syndrome (ARDS) due to coronavirus disease 2019 (COVID-19): Pooled analysis of early reports

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          Abstract

          Dear Editor, The novel coronavirus disease 2019 (COVID-19) can induce acute respiratory distress syndrome (ARDS), which can progress to refractory pulmonary failure. In such cases, extracorporeal membrane oxygenation (ECMO) may be considered as a rescue therapy. In a study of ECMO for ARDS in patients with Middle East Respiratory Syndrome Coronavirus (MERS-CoV), a similar coronavirus disease emerged in 2012, a significant decrease of in-hospital mortality rate and length of intensive care unit (ICU) stay was found in patients treated with ECMO compared to those managed with conventional therapy [1]. However, with COVID-19, concerns have been raised about high mortality rate observed in an early report which included data on ECMO in infected patients [2]. It has been suggested that the compounded immunologic insult by both infection and extracorporeal circuit may counterbalance or even offset survival benefits [2]. In this article, we aimed to evaluate ECMO mortality as reported in early COVID-19 epidemiological studies. An electronic search of Medline (PubMed interface), Scopus and Web of Science, was executed employing the keywords “mortality” OR “death” OR “ECMO” AND “coronavirus 2019” OR “COVID-19” OR “2019-nCoV” OR “SARS-CoV-2”, between 2019 and present time (i.e., March 13, 2020). No language restrictions were applied. The title, abstract and full text of all articles captured with these search criteria were assessed, and those reporting the rate of mortality in COVID-19 patients receiving ECMO were included in pooled analysis. The reference list of all identified studies was also analyzed (forward and backward citation tracking) to detect additional articles. Data on the number of patients with ARDS and treated with ECMO, and the mortality rate for each was extracted. The obtained data was pooled using a random effects model, with estimation of odds ratio (OR) and its 95% confidence interval (95% CI) for mortality in patients with or without ECMO support. Statistical analysis was performed using MetaXL, software Version 5.3 (EpiGear International Pty Ltd., Sunrise Beach, Australia). The study was carried out in accordance with the declaration of Helsinki and local legislation. Overall, 87 articles were initially identified based on our electronic and reference search, which after screening by tile, abstract, and full text, 83 were excluded for the following reasons: not related to COVID-19 (n = 27), review articles (n = 9), did not provide relevant data (n = 37), and editorials (n = 10). Thus, a total of 4 studies [[3], [4], [5], [6]] were finally included in our pooled analysis, comprising 562 COVID-19 patients, 234 (41.6%)of which developed ARDS. All studies were from China. Table 1 presents essential study characteristics. Table 1 Characteristics of included studies. Table 1 Authors Age (yrs): a # of patients: n = (# ARDS patients) Conventional ARDS Therapy: n= Conventional ARDS Therapy Survivors: n (%) ECMO: n= ECMO -Survivors: n (%) Ruan Q et al. 2020 Survivors: 67 (15–81)Non-Survivors: 50 (44–81) 150 (62) 55 7 (12.7%) 7 0 (0%) Wu et al. 2020 51 (43–60) 210 (84) 83 40 (48.2) 1 0 (%) Yang X et al. 2020 59.7 (13.3) 52 (35) 29 9 (31.0%) 6 1 (16.6%) Zhou F et al. 2020 56.0 (46.0–67.0) 191 (59) 56 9 (16.1%) 3 0 (0%) a Data presented as mean (SD) or median (IQR). ARDS – Acute Respiratory Distress Syndrome. Among the 234 ARDS patients, 17 (7.2%) underwent ECMO. The mortality rate was 94.1% in the ECMO patients and 70.9% in conventional therapy patients. The results of the pooled analysis is presented in Fig. 1 . The pooled odds of mortality in ECMO versus conventional therapy was not significantly different (OR: 2.00, 95%CI: 0.49–8.16). There was no observable heterogeneity (I2 = 0%, Cochran's Q, p-value = .99). Fig. 1 Forest Plots for Odds of Mortality in COVID-19 Patients Receiving of ECMO Therapy versus Conventional Therapy. Fig. 1 The results of this analysis using currently available literature would suggest that ECMO does not seemingly produce neither harm or benefit in COVID-19 patients progressing to ARDS. A few limitations shall be noted, however. Patients may have variable levels of ARDS severity, with those receiving ECMO being potentially more critically ill in some cases, which may have impacted the mortality rates. Nonetheless, the mortality rate in the conventional therapy group was relatively high (70.9%). Data on baseline characteristics and disease courses were not provided on ECMO patients. Lastly, the sample size of ECMO patients was considerably small (n = 17). However, when compared to the largest report of MERS patients receiving ECMO (n = 17), COVID-19 patients seem to have substantially higher mortality to-date (94.1% vs. 65.0%), raising questions about real utility of ECMO in this outbreak [1]. Further research is urgently needed. We encourage authors of future COVID-19 reports to provide more data specifically on the ECMO patients in order to aid in optimal patient selection in a limited resource setting. Funding None. Declaration of Competing Interest None.

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          Most cited references5

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          Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

          Summary Background Since December, 2019, Wuhan, China, has experienced an outbreak of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Epidemiological and clinical characteristics of patients with COVID-19 have been reported but risk factors for mortality and a detailed clinical course of illness, including viral shedding, have not been well described. Methods In this retrospective, multicentre cohort study, we included all adult inpatients (≥18 years old) with laboratory-confirmed COVID-19 from Jinyintan Hospital and Wuhan Pulmonary Hospital (Wuhan, China) who had been discharged or had died by Jan 31, 2020. Demographic, clinical, treatment, and laboratory data, including serial samples for viral RNA detection, were extracted from electronic medical records and compared between survivors and non-survivors. We used univariable and multivariable logistic regression methods to explore the risk factors associated with in-hospital death. Findings 191 patients (135 from Jinyintan Hospital and 56 from Wuhan Pulmonary Hospital) were included in this study, of whom 137 were discharged and 54 died in hospital. 91 (48%) patients had a comorbidity, with hypertension being the most common (58 [30%] patients), followed by diabetes (36 [19%] patients) and coronary heart disease (15 [8%] patients). Multivariable regression showed increasing odds of in-hospital death associated with older age (odds ratio 1·10, 95% CI 1·03–1·17, per year increase; p=0·0043), higher Sequential Organ Failure Assessment (SOFA) score (5·65, 2·61–12·23; p<0·0001), and d-dimer greater than 1 μg/mL (18·42, 2·64–128·55; p=0·0033) on admission. Median duration of viral shedding was 20·0 days (IQR 17·0–24·0) in survivors, but SARS-CoV-2 was detectable until death in non-survivors. The longest observed duration of viral shedding in survivors was 37 days. Interpretation The potential risk factors of older age, high SOFA score, and d-dimer greater than 1 μg/mL could help clinicians to identify patients with poor prognosis at an early stage. Prolonged viral shedding provides the rationale for a strategy of isolation of infected patients and optimal antiviral interventions in the future. Funding Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences; National Science Grant for Distinguished Young Scholars; National Key Research and Development Program of China; The Beijing Science and Technology Project; and Major Projects of National Science and Technology on New Drug Creation and Development.
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            Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study

            Summary Background An ongoing outbreak of pneumonia associated with the severe acute respiratory coronavirus 2 (SARS-CoV-2) started in December, 2019, in Wuhan, China. Information about critically ill patients with SARS-CoV-2 infection is scarce. We aimed to describe the clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia. Methods In this single-centered, retrospective, observational study, we enrolled 52 critically ill adult patients with SARS-CoV-2 pneumonia who were admitted to the intensive care unit (ICU) of Wuhan Jin Yin-tan hospital (Wuhan, China) between late December, 2019, and Jan 26, 2020. Demographic data, symptoms, laboratory values, comorbidities, treatments, and clinical outcomes were all collected. Data were compared between survivors and non-survivors. The primary outcome was 28-day mortality, as of Feb 9, 2020. Secondary outcomes included incidence of SARS-CoV-2-related acute respiratory distress syndrome (ARDS) and the proportion of patients requiring mechanical ventilation. Findings Of 710 patients with SARS-CoV-2 pneumonia, 52 critically ill adult patients were included. The mean age of the 52 patients was 59·7 (SD 13·3) years, 35 (67%) were men, 21 (40%) had chronic illness, 51 (98%) had fever. 32 (61·5%) patients had died at 28 days, and the median duration from admission to the intensive care unit (ICU) to death was 7 (IQR 3–11) days for non-survivors. Compared with survivors, non-survivors were older (64·6 years [11·2] vs 51·9 years [12·9]), more likely to develop ARDS (26 [81%] patients vs 9 [45%] patients), and more likely to receive mechanical ventilation (30 [94%] patients vs 7 [35%] patients), either invasively or non-invasively. Most patients had organ function damage, including 35 (67%) with ARDS, 15 (29%) with acute kidney injury, 12 (23%) with cardiac injury, 15 (29%) with liver dysfunction, and one (2%) with pneumothorax. 37 (71%) patients required mechanical ventilation. Hospital-acquired infection occurred in seven (13·5%) patients. Interpretation The mortality of critically ill patients with SARS-CoV-2 pneumonia is considerable. The survival time of the non-survivors is likely to be within 1–2 weeks after ICU admission. Older patients (>65 years) with comorbidities and ARDS are at increased risk of death. The severity of SARS-CoV-2 pneumonia poses great strain on critical care resources in hospitals, especially if they are not adequately staffed or resourced. Funding None.
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              COVID-19, ECMO, and lymphopenia: a word of caution

              Extracorporeal membrane oxygenation (ECMO) can serve as life-saving rescue therapy for refractory respiratory failure in the setting of acute respiratory distress syndrome, such as that induced by coronavirus disease 2019 (COVID-19). In the study by Yang and colleagues, 1 who compared clinical characteristics and outcomes in patients with severe COVID-19, five (83%) of six patients receiving ECMO died. Although this sample was small, and specific baseline characteristics and disease courses were almost unknown, it raises concerns about potential harms of ECMO therapy for COVID-19. Lymphocyte count has been associated with increased disease severity in COVID-19.1, 2 Patients who died from COVID-19 are reported to have had significantly lower lymphocyte counts than survivors. 2 As such, we need to consider the potential compounding immunological insults involved with initiation of an extracorporeal circuit in these patients. During ECMO, substantial decreases in the number and function of some populations of lymphocytes is commonplace. 3 As it might be hypothesised that repletion of lymphocytes could be key to recovery from COVID-19, lymphocyte count should be closely monitored in these patients receiving ECMO. Ruan and colleagues 2 also showed that interleukin-6 (IL-6) concentrations differed significantly between survivors and non-survivors of COVID-19, with non-survivors having up to 1·7-times higher values. During ECMO, IL-6 concentrations are consistently elevated and inversely correlated with survival in children and adults. 4 Those that survived ECMO were able to normalise their IL-6 concentrations, whereas those that died had persistently elevated values. Moreover, elevated IL-6 concentrations in lung induced by initiation of ECMO have been convincingly shown to be associated with parenchymal damage in animal models of venovenous ECMO. 5 While not to discourage the use of ECMO, based on the abovementioned observations, the immunological status of patients should be considered when selecting candidates for ECMO. More reports are needed to understand the potential benefits or harms of extracorporeal life support in severe COVID-19 and future authors should be encouraged to provide more data for this subset of patients. Lastly, clinicians should consider tracking both lymphocyte count and IL-6 during ECMO to monitor patient status and prognosis. © 2020 National Institute of Allergy and Infectious Diseases, National Institutes of Health/Science Photo Library 2020 Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
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                Author and article information

                Contributors
                Journal
                J Crit Care
                J Crit Care
                Journal of Critical Care
                Elsevier Inc.
                0883-9441
                1557-8615
                1 April 2020
                1 April 2020
                :
                Affiliations
                [a ]Cardiac Intensive Care Unit, The Heart Institute, Cincinnati Children's Hospital Medical Center, OH, USA
                [b ]Section of Clinical Biochemistry, Department of Neuroscience, Biomedicine and Movement, University of Verona, Verona, Italy
                Author notes
                [* ]Corresponding author at: Cardiac Intensive Care Unit, The Heart Institute, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA. Brandon.henry@ 123456cchmc.org
                Article
                S0883-9441(20)30542-6
                10.1016/j.jcrc.2020.03.011
                7118619
                32279018
                4b0ad193-8818-4634-9a91-d366aae3c80c
                © 2020 Elsevier Inc. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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                Emergency medicine & Trauma
                extracorporeal life support,acute respiratory distress syndrome,coronavirus,covid-19

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