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      Veno-venous extra-corporeal membrane oxygenation in a COVID-19 patient with cold-agglutinin haemolytic anaemia: A case report

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          Abstract

          Overview

          The use of extra-corporeal membrane oxygenation (ECMO) therapy to treat severe COVID-19 patients with acute respiratory failure is increasing worldwide. We reported herein the use of veno-venous ECMO in a patient with cold agglutinin haemolytic anaemia (CAHA) who suffered from severe COVID-19 infection.

          Description

          A 64-year-old man presented to the emergency department (ED) with incremental complaints of dyspnoea and cough since one week. His history consisted of CAHA, which responded well to corticosteroid treatment. Because of severe hypoxemia, urgent intubation and mechanical ventilation were necessary. Despite deep sedation, muscle paralysis and prone ventilation, P/F ratio remained low. Though his history of CAHA, he still was considered for VV-ECMO. As lab results pointed to recurrence of CAHA, corticosteroids and rituximab were started. The VV-ECMO run was short and rather uncomplicated. Although, despite treatment, CAHA persisted and caused important complications of intestinal ischemia, which needed multiple surgical interventions. Finally, the patient suffered from progressive liver failure, thought to be secondary to ischemic cholangitis. One month after admission, therapy was stopped and patient passed away.

          Conclusion

          Our case report shows that CAHA is no contraindication for VV-ECMO, even when both titre and thermal amplitude are high. Although, the aetiology of CAHA and its response to therapy will determine the final outcome of those patients.

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          Most cited references12

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          Extracorporeal membrane oxygenation for COVID-19: a systematic review and meta-analysis

          Background There are several reports of extracorporeal membrane oxygenation (ECMO) use in patients with coronavirus disease 2019 (COVID-19) who develop severe acute respiratory distress syndrome (ARDS). We conducted a systematic review and meta-analysis to guide clinical decision-making and future research. Methods We searched MEDLINE, Embase, Cochrane and Scopus databases from 1 December 2019 to 10 January 2021 for observational studies or randomised clinical trials examining ECMO in adults with COVID-19 ARDS. We performed random-effects meta-analyses and meta-regression, assessed risk of bias using the Joanna Briggs Institute checklist and rated the certainty of evidence using the GRADE approach. Survival outcomes were presented as pooled proportions while continuous outcomes were presented as pooled means, both with corresponding 95% confidence intervals [CIs]. The primary outcome was in-hospital mortality. Secondary outcomes were duration of ECMO therapy and mechanical ventilation, weaning rate from ECMO and complications during ECMO. Results We included twenty-two observational studies with 1896 patients in the meta-analysis. Venovenous ECMO was the predominant mode used (98.6%). The pooled in-hospital mortality in COVID-19 patients (22 studies, 1896 patients) supported with ECMO was 37.1% (95% CI 32.3–42.0%, high certainty). Pooled mortality in the venovenous ECMO group was 35.7% (95% CI 30.7–40.7%, high certainty). Meta-regression found that age and ECMO duration were associated with increased mortality. Duration of ECMO support (18 studies, 1844 patients) was 15.1 days (95% CI 13.4–18.7). Weaning from ECMO (17 studies, 1412 patients) was accomplished in 67.6% (95% CI 50.5–82.7%) of patients. There were a total of 1583 ECMO complications reported (18 studies, 1721 patients) and renal complications were the most common. Conclusion The majority of patients received venovenous ECMO support for COVID-19-related ARDS. In-hospital mortality in patients receiving ECMO support for COVID-19 was 37.1% during the first year of the pandemic, similar to those with non-COVID-19-related ARDS. Increasing age was a risk factor for death. Venovenous ECMO appears to be an effective intervention in selected patients with COVID-19-related ARDS. PROSPERO CRD42020192627. Supplementary Information The online version contains supplementary material available at 10.1186/s13054-021-03634-1.
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            Cold agglutinin disease.

            Cold agglutinin disease is a rare and poorly understood disorder affecting 15% of patients with autoimmune hemolytic anemia. We reviewed the clinical and pathologic features, prognosis, and management in the literature and describe our institutional experience to improve strategies for accurate diagnosis and treatment. Retrospective analysis identified 89 patients from our institution with cold agglutinin disease from 1970 through 2012. Median age at symptom onset was 65 years (range, 41 to 83 years), whereas the median age at diagnosis was 72 years (range, 43 to 91 years). Median survival of all patients was 10.6 years, and 68 patients (76%) were alive 5 years after the diagnosis. The most common symptom was acrocyanosis (n = 39 [44%]), and many had symptoms triggered by cold (n = 35 [39%]) or other factors (n = 20 [22%]). An underlying hematologic disorder was detected in 69 patients (78%). Thirty-six patients (40%) received transfusions during their disease course, and 82% received drug therapy. Rituximab was associated with the longest response duration (median, 24 months) and the lowest proportion of patients needing further treatment (55%). Our institution's experience and review of the literature confirms that early diagnostic evaluation and treatment improves outcomes in cold agglutinin disease.
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              How I manage patients with cold agglutinin disease

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                Author and article information

                Journal
                Perfusion
                Perfusion
                spprf
                PRF
                Perfusion
                SAGE Publications (Sage UK: London, England )
                0267-6591
                1477-111X
                21 September 2022
                21 September 2022
                : 02676591221127932
                Affiliations
                [1 ]Department of Critical Care, Ringgold 60201, universityUniversitair Ziekenhuis Brussel; , Laarbeeklaan, Belgium
                [2 ]Department of Anaesthesia and Perioperative Care, universityUniversitair Ziekenhuis Brussel (UZB), , Ringgold 60201; Laarbeeklaan, Belgium
                [3 ]Faculty of Medicine and Pharmacy, Ringgold 60201, universityVrije Universiteit Brussel; , Belgium
                [4 ]Department of Haematology, Ringgold 60201, universityUniversitair Ziekenhuis Brussel (UZB; ), Laarbeeklaan, Belgium
                [5 ]Department of Cardiac Surgery, universityUniversitair Ziekenhuis Brussel (UZB), , Ringgold 60201; Laarbeeklaan, Belgium
                [6 ]Department of Cardiology, Ringgold 60201, universityUniversitair Ziekenhuis Brussel; , Laarbeeklaan, Belgium
                [7 ]Biomedical Research Institute, Faculty of Medicine and Life Sciences, Ringgold 60201, universityHasselt University; , Hasselt, Belgium
                [8 ]Department of Intensive Care, Ringgold 60201, universityErasme Hospital; , Brussels, Belgium
                Author notes
                [*]Matthias Raes, Department of Intensive care, Laarbeeklaan 101, 1090 Brussels, Belgium. Email: matthias.raes@ 123456uzbrussel.be
                Author information
                https://orcid.org/0000-0002-6809-6921
                https://orcid.org/0000-0002-5437-1689
                Article
                10.1177_02676591221127932
                10.1177/02676591221127932
                9490382
                36128692
                7d05a8e7-412d-4bb5-87ef-5d392c5209bd
                © The Author(s) 2022

                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
                Funding
                Funded by: Hasselt University;
                Award ID: BOF19PD04
                Categories
                Case Report
                Custom metadata
                corrected-proof
                ts10

                venovenous,extra-corporeal membrane oxygenation,cold agglutinins,case report,haemolytic anaemia,covid-19

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