A Comparison of Thrombosis and Hemorrhage Rates in Patients With Severe Respiratory Failure Due to Coronavirus Disease 2019 and Influenza Requiring Extracorporeal Membrane Oxygenation.
Adult
C-Reactive Protein
/ metabolism
COVID-19
/ therapy
Computed Tomography Angiography
Extracorporeal Membrane Oxygenation
Female
Fibrin Fibrinogen Degradation Products
/ metabolism
Fibrinogen
/ metabolism
Humans
Influenza A Virus, H1N1 Subtype
Influenza A virus
Influenza B virus
Influenza, Human
/ therapy
Intracranial Hemorrhages
/ complications
London
/ epidemiology
Male
Middle Aged
Pulmonary Embolism
/ complications
Retrospective Studies
SARS-CoV-2
State Medicine
Tertiary Care Centers
Ultrasonography, Doppler
Venous Thromboembolism
/ complications
Venous Thrombosis
/ complications
Journal
Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501
Informations de publication
Date de publication:
01 07 2021
01 07 2021
Historique:
pubmed:
17
4
2021
medline:
2
7
2021
entrez:
16
4
2021
Statut:
ppublish
Résumé
Extracorporeal membrane oxygenation is a lifesaving therapy for patients with severe acute respiratory distress syndrome refractory to conventional mechanical ventilation. It is frequently complicated by both thrombosis and hemorrhage. A markedly prothrombotic state associated with high rates of venous thromboembolism has been described in patients with severe acute respiratory syndrome coronavirus 2 (coronavirus disease 2019) infection. These rates have currently not been described during extracorporeal membrane oxygenation in comparison to other viral pneumonias. Retrospective observational study. Single high-volume tertiary critical care department at a university hospital. Patients 16 years old or greater receiving venovenous extracorporeal membrane oxygenation between March 1, 2020, and May 31, 2020, with coronavirus disease 2019 were compared with a cohort of patients with influenza pneumonia between June 1, 2012, and May 31, 2020. None. The rates of venous thromboembolism and hemorrhage were compared in patients with coronavirus disease 2019 against a historic population of patients with influenza pneumonia who required extracorporeal membrane oxygenation. There were 51 patients who received extracorporeal membrane oxygenation due to coronavirus disease 2019 and 80 patients with influenza. At cannulation for extracorporeal membrane oxygenation, 37% of patients with coronavirus disease 2019 compared with 8% of patients with influenza had filling defects on CT pulmonary angiography (p = 0.0001). Catheter-associated deep vein thrombosis shown on ultrasound Doppler after decannulation was present in 53% with coronavirus disease 2019 versus 25% with influenza (p = 0.01). The rates of intracranial hemorrhage at the time of cannulation were 16% with coronavirus disease 2019 and 14% with influenza (p = 0.8). Elevated d-dimer levels were seen in both conditions and were significantly higher in those with pulmonary thromboembolism than those without in coronavirus disease 2019 (p = 0.02). Fibrinogen and C-reactive protein levels were significantly higher in those with coronavirus disease 2019 than influenza (p < 0.01). Significant rates of pulmonary thromboembolism and of catheter-associated deep vein thrombosis were seen in both viral infections but were greater in those requiring the use of extracorporeal membrane oxygenation in coronavirus disease 2019 than for influenza.
Identifiants
pubmed: 33861545
pii: 00003246-202107000-00031
doi: 10.1097/CCM.0000000000004971
doi:
Substances chimiques
Fibrin Fibrinogen Degradation Products
0
fibrin fragment D
0
Fibrinogen
9001-32-5
C-Reactive Protein
9007-41-4
Types de publication
Comparative Study
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e663-e672Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2021 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.
Déclaration de conflit d'intérêts
Dr. Hunt disclosed that she is the Medical Director of Thrombosis UK. Dr. Barrett received research and educational support from Maquet and ALung Incorporated. The remaining authors have disclosed that they do not have any potential conflicts of interest.
Références
Desborough MJR, Doyle AJ, Griffiths A, et al. Image-proven thromboembolism in patients with severe COVID-19 in a tertiary critical care unit in the United Kingdom. Thromb Res. 2020; 193:1–4
Klok FA, Kruip MJHA, van der Meer NJM, et al. Confirmation of the high cumulative incidence of thrombotic complications in critically ill ICU patients with COVID-19: An updated analysis. Thromb Res. 2020; 191:148–150
Thomas W, Varley J, Johnston A, et al. Thrombotic complications of patients admitted to intensive care with COVID-19 at a teaching hospital in the United Kingdom. Thromb Res. 2020; 191:76–77
Nopp S, Moik F, Jilma B, et al. Risk of venous thromboembolism in patients with COVID-19: A systematic review and meta-analysis. Res Pract Thromb Haemost. 2020; 4:1178–1191
Tomashefski JF Jr, Davies P, Boggis C, et al. The pulmonary vascular lesions of the adult respiratory distress syndrome. Am J Pathol. 1983; 112:112–126
Hariri L, Hardin CC. COVID-19, angiogenesis, and ARDS endotypes. N Engl J Med. 2020; 383:182–183
Avnon LS, Munteanu D, Smoliakov A, et al. Thromboembolic events in patients with severe pandemic influenza A/H1N1. Eur J Intern Med. 2015; 26:596–598
Obi AT, Tignanelli CJ, Jacobs BN, et al. Empirical systemic anticoagulation is associated with decreased venous thromboembolism in critically ill influenza A H1N1 acute respiratory distress syndrome patients. J Vasc Surg Venous Lymphat Disord. 2019; 7:317–324
Ackermann M, Verleden SE, Kuehnel M, et al. Pulmonary vascular endothelialitis, thrombosis, and angiogenesis in COVID-19. N Engl J Med. 2020; 383:120–128
Bao L, Deng W, Huang B, et al. The pathogenicity of SARS-CoV-2 in hACE2 transgenic mice. Nature. 2020; 583:830–833
Masi P, Hékimian G, Lejeune M, et al. Systemic inflammatory response syndrome is a major contributor to COVID-19-associated coagulopathy: Insights from a prospective, single-center cohort study. Circulation. 2020; 142:611–614
Schmidt M, Hajage D, Lebreton G, et al.; Groupe de Recherche Clinique en REanimation et Soins intensifs du Patient en Insuffisance Respiratoire aiguE (GRC-RESPIRE) Sorbonne Université; Paris-Sorbonne ECMO-COVID investigators. Extracorporeal membrane oxygenation for severe acute respiratory distress syndrome associated with COVID-19: A retrospective cohort study. Lancet Respir Med. 2020; 8:1121–1131
Mustafa AK, Alexander PJ, Joshi DJ, et al. Extracorporeal membrane oxygenation for patients with COVID-19 in severe respiratory failure. JAMA Surg. 2020; 155:990–992
Doyle AJ, Hunt BJ. Current understanding of how extracorporeal membrane oxygenators activate haemostasis and other blood components. Front Med (Lausanne). 2018; 5:352
Extracorporeal Life Support Organization. ELSO Anticoagulation Guideline (2014). 2014. Available at: https://www.elso.org/Portals/0/Files/elsoanticoagulationguideline8-2014-table-contents.pdf . Accessed July 17, 2020
NICE Guideline [NG 158]. Venous Thromboembolic Diseases: Diagnosis, Management and Thrombophilia Testing. London, United Kingdom, National Institute for Health and Care Excellence. 2020. Available at: https://www.nice.org.uk/guidance/ng158/resources/venous-thromboembolic-diseases-diagnosis-management-and-thrombophilia-testing-pdf-66141847001797 . Accessed July 17, 2020
Burns J, Cooper E, Salt G, et al. Retrospective observational review of percutaneous cannulation for extracorporeal membrane oxygenation. ASAIO J. 2016; 62:325–328
Hunt BJ, Levi M. Re The source of elevated plasma D-dimer levels in COVID-19 infection. Br J Haematol. 2020; 190:e133–e134
NICE Guideline [NG89]. Venous Thromboembolism in Over 16s; Reducing the Risk of Hospital-Acquired Deep Vein Thrombosis or Pulmonary Embolism. London, United Kingdom, National Institute for Health and Care Excellence. 2018. Available at: https://www.nice.org.uk/guidance/ng89/resources/venous-thromboembolism-in-over-16s-reducing-the-risk-of-hospitalacquired-deep-vein-thrombosis-or-pulmonary-embolism-pdf-1837703092165 . Accessed July 17, 2020
Taylor FB Jr, Toh CH, Hoots WK, et al.; Scientific Subcommittee on Disseminated Intravascular Coagulation (DIC) of the International Society on Thrombosis and Haemostasis (ISTH). Towards definition, clinical and laboratory criteria, and a scoring system for disseminated intravascular coagulation. Thromb Haemost. 2001; 86:1327–1330
Combes A, Hajage D, Capellier G, et al.; EOLIA Trial Group, REVA, and ECMONet. Extracorporeal membrane oxygenation for severe acute respiratory distress syndrome. N Engl J Med. 2018; 378:1965–1975
Iba T, Levy JH, Levi M, et al. Coagulopathy of coronavirus disease 2019. Crit Care Med. 2020; 48:1358–1364
Oudit GY, Pfeffer MA. Plasma angiotensin-converting enzyme 2: Novel biomarker in heart failure with implications for COVID-19. Eur Heart J. 2020; 41:1818–1820
Hartley EL, Singh N, Barrett N, et al. Screening pulmonary angiogram and the effect on anticoagulation strategies in severe respiratory failure patients on venovenous extracorporeal membrane oxygenation. J Thromb Haemost. 2020; 18:217–221
Minet C, Lugosi M, Savoye PY, et al. Pulmonary embolism in mechanically ventilated patients requiring computed tomography: Prevalence, risk factors, and outcome. Crit Care Med. 2012; 40:3202–3208
Agarwal PP, Cinti S, Kazerooni EA. Chest radiographic and CT findings in novel swine-origin influenza A (H1N1) virus (S-OIV) infection. AJR Am J Roentgenol. 2009; 193:1488–1493
Walters KA, D’Agnillo F, Sheng ZM, et al. 1918 pandemic influenza virus and Streptococcus pneumoniae co-infection results in activation of coagulation and widespread pulmonary thrombosis in mice and humans. J Pathol. 2016; 238:85–97
Nougier C, Benoit R, Simon M, et al. Hypofibrinolytic state and high thrombin generation may play a major role in SARS-CoV2 associated thrombosis. J Thromb Haemost. 2020; 18:2215–2219
Cooper E, Burns J, Retter A, et al. Prevalence of venous thrombosis following venovenous extracorporeal membrane oxygenation in patients with severe respiratory failure. Crit Care Med. 2015; 43:e581–e584
Menaker J, Tabatabai A, Rector R, et al. Incidence of cannula-associated deep vein thrombosis after veno-venous extracorporeal membrane oxygenation. ASAIO J. 2017; 63:588–591
Fletcher-Sandersjöö A, Thelin EP, Bartek J Jr, et al. Incidence, outcome, and predictors of intracranial hemorrhage in adult patients on extracorporeal membrane oxygenation: A systematic and narrative review. Front Neurol. 2018; 9:548
Lockie CJA, Gillon SA, Barrett NA, et al. Severe respiratory failure, extracorporeal membrane oxygenation, and intracranial hemorrhage. Crit Care Med. 2017; 45:1642–1649
Dutt T, Simcox D, Downey C, et al. Thromboprophylaxis in COVID-19: Anti-FXa-the missing factor? Am J Respir Crit Care Med. 2020; 202:455–457
Yin S, Huang M, Li D, et al. Difference of coagulation features between severe pneumonia induced by SARS-CoV2 and non-SARS-CoV2. J Thromb Thrombolysis. 2020 Apr 3. [online ahead of print]
Tang N, Li D, Wang X, et al. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020; 18:844–847
Arnouk S, Altshuler D, Lewis TC, et al. Evaluation of anti-Xa and activated partial thromboplastin time monitoring of heparin in adult patients receiving extracorporeal membrane oxygenation support. ASAIO J. 2020; 66:300–306