Coagulation Influencing Liberation from Respiratory Support in Patients with Coronavirus Disease 2019: A Retrospective, Observational Study
Background: Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill...
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Published in | Journal of Nippon Medical School Vol. 89; no. 5; pp. 479 - 486 |
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25.10.2022
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Abstract | Background: Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill patients with COVID-19 by combining the results of rotational thromboelastometry (ROTEM) with standard laboratory tests. Methods: This single-center, retrospective, observational study included 31 consecutive adult patients with COVID-19 who were admitted to the intensive care unit (ICU) and who required respiratory support between April 2021 and August 2021. We divided the patients into two groups according to the liberation from respiratory support and analyzed the differences between the groups. Results: There were 20 patients in the liberation group and 11 in the non-liberation group. There were no significant differences in the overt disseminated intravascular coagulation scores or abnormal counts in the ROTEM parameters at admission between groups, although there was a significant difference in the highest score in the ICU. The Sequential Organ Failure Assessment and sepsis-induced coagulopathy scores were significantly different between both groups at admission and at the time when the highest values were reported during the ICU stay. Conclusions: High sepsis-induced coagulopathy scores at admission to the ICU were found to be useful predictors of difficulties in the liberation from respiratory support in patients with severe COVID-19. However, increased overt disseminated intravascular coagulation scores and abnormal counts in the ROTEM parameters during the ICU stay were associated with difficulties in the liberation from respiratory support. |
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AbstractList | Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill patients with COVID-19 by combining the results of rotational thromboelastometry (ROTEM) with standard laboratory tests.BACKGROUNDPatients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill patients with COVID-19 by combining the results of rotational thromboelastometry (ROTEM) with standard laboratory tests.This single-center, retrospective, observational study included 31 consecutive adult patients with COVID-19 who were admitted to the intensive care unit (ICU) and who required respiratory support between April 2021 and August 2021. We divided the patients into two groups according to the liberation from respiratory support and analyzed the differences between the groups.METHODSThis single-center, retrospective, observational study included 31 consecutive adult patients with COVID-19 who were admitted to the intensive care unit (ICU) and who required respiratory support between April 2021 and August 2021. We divided the patients into two groups according to the liberation from respiratory support and analyzed the differences between the groups.There were 20 patients in the liberation group and 11 in the non-liberation group. There were no significant differences in the overt disseminated intravascular coagulation scores or abnormal counts in the ROTEM parameters at admission between groups, although there was a significant difference in the highest score in the ICU. The Sequential Organ Failure Assessment and sepsis-induced coagulopathy scores were significantly different between both groups at admission and at the time when the highest values were reported during the ICU stay.RESULTSThere were 20 patients in the liberation group and 11 in the non-liberation group. There were no significant differences in the overt disseminated intravascular coagulation scores or abnormal counts in the ROTEM parameters at admission between groups, although there was a significant difference in the highest score in the ICU. The Sequential Organ Failure Assessment and sepsis-induced coagulopathy scores were significantly different between both groups at admission and at the time when the highest values were reported during the ICU stay.High sepsis-induced coagulopathy scores at admission to the ICU were found to be useful predictors of difficulties in the liberation from respiratory support in patients with severe COVID-19. However, increased overt disseminated intravascular coagulation scores and abnormal counts in the ROTEM parameters during the ICU stay were associated with difficulties in the liberation from respiratory support.CONCLUSIONSHigh sepsis-induced coagulopathy scores at admission to the ICU were found to be useful predictors of difficulties in the liberation from respiratory support in patients with severe COVID-19. However, increased overt disseminated intravascular coagulation scores and abnormal counts in the ROTEM parameters during the ICU stay were associated with difficulties in the liberation from respiratory support. Background: Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill patients with COVID-19 by combining the results of rotational thromboelastometry (ROTEM) with standard laboratory tests. Methods: This single-center, retrospective, observational study included 31 consecutive adult patients with COVID-19 who were admitted to the intensive care unit (ICU) and who required respiratory support between April 2021 and August 2021. We divided the patients into two groups according to the liberation from respiratory support and analyzed the differences between the groups. Results: There were 20 patients in the liberation group and 11 in the non-liberation group. There were no significant differences in the overt disseminated intravascular coagulation scores or abnormal counts in the ROTEM parameters at admission between groups, although there was a significant difference in the highest score in the ICU. The Sequential Organ Failure Assessment and sepsis-induced coagulopathy scores were significantly different between both groups at admission and at the time when the highest values were reported during the ICU stay. Conclusions: High sepsis-induced coagulopathy scores at admission to the ICU were found to be useful predictors of difficulties in the liberation from respiratory support in patients with severe COVID-19. However, increased overt disseminated intravascular coagulation scores and abnormal counts in the ROTEM parameters during the ICU stay were associated with difficulties in the liberation from respiratory support. Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation abnormalities at admission and during the course of hospitalization can predict the liberation from respiratory support in critically ill patients with COVID-19 by combining the results of rotational thromboelastometry (ROTEM) with standard laboratory tests. This single-center, retrospective, observational study included 31 consecutive adult patients with COVID-19 who were admitted to the intensive care unit (ICU) and who required respiratory support between April 2021 and August 2021. We divided the patients into two groups according to the liberation from respiratory support and analyzed the differences between the groups. There were 20 patients in the liberation group and 11 in the non-liberation group. There were no significant differences in the overt disseminated intravascular coagulation scores or abnormal counts in the ROTEM parameters at admission between groups, although there was a significant difference in the highest score in the ICU. The Sequential Organ Failure Assessment and sepsis-induced coagulopathy scores were significantly different between both groups at admission and at the time when the highest values were reported during the ICU stay. High sepsis-induced coagulopathy scores at admission to the ICU were found to be useful predictors of difficulties in the liberation from respiratory support in patients with severe COVID-19. However, increased overt disseminated intravascular coagulation scores and abnormal counts in the ROTEM parameters during the ICU stay were associated with difficulties in the liberation from respiratory support. |
ArticleNumber | JNMS.2022_89-506 |
Author | Nakayama, Kento Sakamoto, Yuichiro Sasaki, Akira Sakurai, Ryota Asahi, Miho Goto, Taku Mori, Kosuke Narumi, Shogo Matsuoka, Ayaka Koami, Hiroyuki Miike, Toru Miyazaki, Mariko Yamazaki, Hirotaka Shinada, Kota Yoshitake, Kunimasa Koba, Mayuko |
Author_xml | – sequence: 1 fullname: Asahi, Miho organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Narumi, Shogo organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Nakayama, Kento organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Koami, Hiroyuki organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Yamazaki, Hirotaka organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Koba, Mayuko organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Shinada, Kota organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Sakurai, Ryota organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Sasaki, Akira organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Mori, Kosuke organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Matsuoka, Ayaka organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Miyazaki, Mariko organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Sakamoto, Yuichiro organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Miike, Toru organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Goto, Taku organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University – sequence: 1 fullname: Yoshitake, Kunimasa organization: Department of Emergency and Critical Care Medicine, Faculty of Medicine, Saga University |
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Cites_doi | 10.2147/RMHP.S268238 10.1186/cc13721 10.1016/j.rppneu.2011.06.015 10.1016/j.mayocp.2020.10.031 10.1111/jth.14768 10.1007/BF01709751 10.1097/00003246-198510000-00009 10.1097/MBC.0000000000000755 10.1080/09537104.2021.1881949 10.3390/jcm10081740 10.1177/08850666211020281 10.1161/01.ATV.0000046238.23903.FC 10.1055/s-0040-1712155 10.1016/S1474-4422(14)70120-6 10.1055/s-0037-1616068 10.35772/ghm.2020.01044 10.1136/bmjopen-2017-017046 10.1016/j.surg.2009.06.054 10.1001/jamainternmed.2020.3539 10.1007/s00134-020-06088-1 10.1002/ajh.23599 10.4097/kja.20327 10.1111/jth.14810 10.1177/0885066618773679 10.1016/j.cca.2020.03.022 |
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References | 11. Mann KG, Butenas S, Brummel K. The dynamics of thrombin formation. Arterioscler Thromb Vasc Biol. 2003;23 (1):17-25. 14. Bareille M, Hardy M, Douxfils J, et al. Viscoelastometric testing to assess hemostasis of COVID-19: a systematic review. J Clin Med. 2021;10 (8):1740. 23. Kong R, Hutchinson N, Görlinger K. Hyper- and hypocoagulability in COVID-19 as assessed by thromboelastometry -two case reports. Korean J Anesthesiol. 2021;74 (4):350-4. 22. Teasdale G, Maas A, Lecky F, Manley G, Stocchetti N, Murray G. The Glasgow Coma Scale at 40 years: standing the test of time. Lancet Neurol. 2014;13 (8):844-54. 9. Long X, Zhang Z, Zou W, et al. Coagulopathy of patients with COVID-19 is associated with infectious and inflammatory markers. Risk Manag Healthc Policy. 2020;13:1965-75. 24. Mitrovic M, Sabljic N, Cvetkovic Z, et al. Rotational thromboelastometry (ROTEM) profiling of COVID-19 patients. Platelets. 2021;32 (5):690-6. 26. Iba T, Nisio MD, Levy JH, Kitamura N, Thachil J. New criteria for sepsis-induced coagulopathy (SIC) following the revised sepsis definition: a retrospective analysis of a nationwide survey. BMJ Open. 2017;7 (9):e017046. 6. Lippi G, Plebani M, Henry BM. Thrombocytopenia is associated with severe coronavirus disease 2019 (COVID-19) infections: a meta-analysis. Clin Chim Acta. 2020;506:145-8. 8. Taylor FB Jr, Toh CH, Hoots WK, Wada H, Levi M. 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 (5):1327-30. 21. Matic I, Titlic M, Dikanovic M, Jurjevic M, Jukic I, Tonkic A. Effects of APACHE II score on mechanical ventilation; prediction and outcome. Acta Anaesthesiol Belg. 2007;58 (3):177-83. 3. Lippi G, Sanchis-Gomar F, Favaloro EJ, Lavie CJ, Henry BM. Coronavirus disease 2019-associated coagulopathy. Mayo Clin Proc. 2021;96 (1):203-17. 12. Kashuk JL, Moore EE, Sabel A, et al. Rapid thrombelastography (r-TEG) identifies hypercoagulability and predicts thromboembolic events in surgical patients. Surgery. 2009;146 (4):764-72;discussion 772-4. 27. Iba T, Arakawa M, Di Nisio M, et al. Newly proposed sepsis-induced coagulopathy precedes International Society on Thrombosis and Haemostasis overt-disseminated intravascular coagulation and predicts high mortality. J Intensive Care Med. 2020;35 (7):643-9. 20. Ionescu F, Zimmer MS, Petrescu I, et al. Extubation failure in critically ill COVID-19 patients: risk factors and impact on in-hospital mortality. J Intensive Care Med. 2021;36 (9):1018-24. 25. Gnanapandithan K, Agarwal R, Aggarwal AN, Gupta D. Weaning by gradual pressure support (PS) reduction without an initial spontaneous breathing trial (SBT) versus PS-supported SBT: a pilot study. Rev Port Pneumol. 2011;17 (6):244-52. 15. Ministry of Health, Labour and Welfare. Clinical Management of Patients with COVID-19 version 4.2 [Internet]. 2021 Feb 19 [cited 2022 Feb 1]. Available from: https://www.mhlw.go.jp/content/000742297.pdf 7. Ding R, Wang Z, Lin Y, Liu B, Zhang Z, Ma X. Comparison of a new criteria for sepsis-induced coagulopathy and International Society on Thrombosis and Haemostasis disseminated intravascular coagulation score in critically ill patients with sepsis 3.0: a retrospective study. Blood Coagul Fibrinolysis. 2018;29 (6):551-8. 1. Joly BS, Siguret V, Veyradier A. Understanding pathophysiology of hemostasis disorders in critically ill patients with COVID-19. Intensive Care Med. 2020;46 (8):1603-6. 4. Thachil J, Srivastava A. SARS-2 coronavirus-associated hemostatic lung abnormality in COVID-19: is it pulmonary thrombosis or pulmonary embolism? Semin Thromb Hemost. 2020;46 (7):777-80. 5. Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020;18 (4):844-7. 2. Thachil J, Tang N, Gando S, et al. ISTH interim guidance on recognition and management of coagulopathy in COVID-19. J Thromb Haemost. 2020;18 (5):102-6. 19. Grasselli G, Greco M, Zanella A, et al. Risk factors associated with mortality among patients with COVID-19 in intensive care units in Lombardy, Italy. JAMA Intern Med. 2020;180 (10):1345-55. 18. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med. 1985;13 (10):818-29. 17. Vincent JL, Moreno R, Takala J, et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. 1996;22 (7):707-10. 13. Müller MC, Meijers JC, Vroom MB, Juffermans NP. Utility of thromboelastography and/or thromboelastometry in adults with sepsis: a systematic review. Crit Care. 2014;18 (1):R30. 10. Whiting D, DiNardo JA. TEG and ROTEM: technology and clinical applications. Am J Hematol. 2014;89 (2):228-32. 16. Sato R, Ishikane M, Kinoshita N, et al. A new challenge of unfractionated heparin anticoagulation treatment for moderate to severe COVID-19 in Japan. Glob Health Med. 2020;2 (3):190-2. 22 23 24 25 26 27 10 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 21 |
References_xml | – reference: 17. Vincent JL, Moreno R, Takala J, et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. 1996;22 (7):707-10. – reference: 9. Long X, Zhang Z, Zou W, et al. Coagulopathy of patients with COVID-19 is associated with infectious and inflammatory markers. Risk Manag Healthc Policy. 2020;13:1965-75. – reference: 21. Matic I, Titlic M, Dikanovic M, Jurjevic M, Jukic I, Tonkic A. Effects of APACHE II score on mechanical ventilation; prediction and outcome. Acta Anaesthesiol Belg. 2007;58 (3):177-83. – reference: 27. Iba T, Arakawa M, Di Nisio M, et al. Newly proposed sepsis-induced coagulopathy precedes International Society on Thrombosis and Haemostasis overt-disseminated intravascular coagulation and predicts high mortality. J Intensive Care Med. 2020;35 (7):643-9. – reference: 4. Thachil J, Srivastava A. SARS-2 coronavirus-associated hemostatic lung abnormality in COVID-19: is it pulmonary thrombosis or pulmonary embolism? Semin Thromb Hemost. 2020;46 (7):777-80. – reference: 18. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med. 1985;13 (10):818-29. – reference: 16. Sato R, Ishikane M, Kinoshita N, et al. A new challenge of unfractionated heparin anticoagulation treatment for moderate to severe COVID-19 in Japan. Glob Health Med. 2020;2 (3):190-2. – reference: 13. Müller MC, Meijers JC, Vroom MB, Juffermans NP. Utility of thromboelastography and/or thromboelastometry in adults with sepsis: a systematic review. Crit Care. 2014;18 (1):R30. – reference: 10. Whiting D, DiNardo JA. TEG and ROTEM: technology and clinical applications. Am J Hematol. 2014;89 (2):228-32. – reference: 23. Kong R, Hutchinson N, Görlinger K. Hyper- and hypocoagulability in COVID-19 as assessed by thromboelastometry -two case reports. Korean J Anesthesiol. 2021;74 (4):350-4. – reference: 7. Ding R, Wang Z, Lin Y, Liu B, Zhang Z, Ma X. Comparison of a new criteria for sepsis-induced coagulopathy and International Society on Thrombosis and Haemostasis disseminated intravascular coagulation score in critically ill patients with sepsis 3.0: a retrospective study. Blood Coagul Fibrinolysis. 2018;29 (6):551-8. – reference: 2. Thachil J, Tang N, Gando S, et al. ISTH interim guidance on recognition and management of coagulopathy in COVID-19. J Thromb Haemost. 2020;18 (5):102-6. – reference: 15. Ministry of Health, Labour and Welfare. Clinical Management of Patients with COVID-19 version 4.2 [Internet]. 2021 Feb 19 [cited 2022 Feb 1]. Available from: https://www.mhlw.go.jp/content/000742297.pdf – reference: 3. Lippi G, Sanchis-Gomar F, Favaloro EJ, Lavie CJ, Henry BM. Coronavirus disease 2019-associated coagulopathy. Mayo Clin Proc. 2021;96 (1):203-17. – reference: 26. Iba T, Nisio MD, Levy JH, Kitamura N, Thachil J. New criteria for sepsis-induced coagulopathy (SIC) following the revised sepsis definition: a retrospective analysis of a nationwide survey. BMJ Open. 2017;7 (9):e017046. – reference: 19. Grasselli G, Greco M, Zanella A, et al. Risk factors associated with mortality among patients with COVID-19 in intensive care units in Lombardy, Italy. JAMA Intern Med. 2020;180 (10):1345-55. – reference: 14. Bareille M, Hardy M, Douxfils J, et al. Viscoelastometric testing to assess hemostasis of COVID-19: a systematic review. J Clin Med. 2021;10 (8):1740. – reference: 22. Teasdale G, Maas A, Lecky F, Manley G, Stocchetti N, Murray G. The Glasgow Coma Scale at 40 years: standing the test of time. Lancet Neurol. 2014;13 (8):844-54. – reference: 25. Gnanapandithan K, Agarwal R, Aggarwal AN, Gupta D. Weaning by gradual pressure support (PS) reduction without an initial spontaneous breathing trial (SBT) versus PS-supported SBT: a pilot study. Rev Port Pneumol. 2011;17 (6):244-52. – reference: 6. Lippi G, Plebani M, Henry BM. Thrombocytopenia is associated with severe coronavirus disease 2019 (COVID-19) infections: a meta-analysis. Clin Chim Acta. 2020;506:145-8. – reference: 12. Kashuk JL, Moore EE, Sabel A, et al. Rapid thrombelastography (r-TEG) identifies hypercoagulability and predicts thromboembolic events in surgical patients. Surgery. 2009;146 (4):764-72;discussion 772-4. – reference: 1. Joly BS, Siguret V, Veyradier A. Understanding pathophysiology of hemostasis disorders in critically ill patients with COVID-19. Intensive Care Med. 2020;46 (8):1603-6. – reference: 20. Ionescu F, Zimmer MS, Petrescu I, et al. Extubation failure in critically ill COVID-19 patients: risk factors and impact on in-hospital mortality. J Intensive Care Med. 2021;36 (9):1018-24. – reference: 8. Taylor FB Jr, Toh CH, Hoots WK, Wada H, Levi M. 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 (5):1327-30. – reference: 5. Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020;18 (4):844-7. – reference: 11. Mann KG, Butenas S, Brummel K. The dynamics of thrombin formation. Arterioscler Thromb Vasc Biol. 2003;23 (1):17-25. – reference: 24. Mitrovic M, Sabljic N, Cvetkovic Z, et al. Rotational thromboelastometry (ROTEM) profiling of COVID-19 patients. Platelets. 2021;32 (5):690-6. – ident: 9 doi: 10.2147/RMHP.S268238 – ident: 13 doi: 10.1186/cc13721 – ident: 25 doi: 10.1016/j.rppneu.2011.06.015 – ident: 3 doi: 10.1016/j.mayocp.2020.10.031 – ident: 5 doi: 10.1111/jth.14768 – ident: 17 doi: 10.1007/BF01709751 – ident: 18 doi: 10.1097/00003246-198510000-00009 – ident: 7 doi: 10.1097/MBC.0000000000000755 – ident: 24 doi: 10.1080/09537104.2021.1881949 – ident: 14 doi: 10.3390/jcm10081740 – ident: 20 doi: 10.1177/08850666211020281 – ident: 11 doi: 10.1161/01.ATV.0000046238.23903.FC – ident: 4 doi: 10.1055/s-0040-1712155 – ident: 22 doi: 10.1016/S1474-4422(14)70120-6 – ident: 8 doi: 10.1055/s-0037-1616068 – ident: 16 doi: 10.35772/ghm.2020.01044 – ident: 26 doi: 10.1136/bmjopen-2017-017046 – ident: 12 doi: 10.1016/j.surg.2009.06.054 – ident: 19 doi: 10.1001/jamainternmed.2020.3539 – ident: 1 doi: 10.1007/s00134-020-06088-1 – ident: 10 doi: 10.1002/ajh.23599 – ident: 15 – ident: 23 doi: 10.4097/kja.20327 – ident: 2 doi: 10.1111/jth.14810 – ident: 21 – ident: 27 doi: 10.1177/0885066618773679 – ident: 6 doi: 10.1016/j.cca.2020.03.022 |
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Snippet | Background: Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether... Patients with coronavirus disease 2019 (COVID-19) occasionally develop respiratory failure and coagulopathy. We aimed to determine whether coagulation... |
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SubjectTerms | COVID-19 intensive care units respiratory insufficiency |
Title | Coagulation Influencing Liberation from Respiratory Support in Patients with Coronavirus Disease 2019: A Retrospective, Observational Study |
URI | https://www.jstage.jst.go.jp/article/jnms/89/5/89_JNMS.2022_89-506/_article/-char/en https://www.ncbi.nlm.nih.gov/pubmed/35644549 https://www.proquest.com/docview/2672316808 |
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ispartofPNX | Journal of Nippon Medical School, 2022/10/25, Vol.89(5), pp.479-486 |
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