Bleeding risk by intensity of anticoagulation in critically ill patients with COVID-19: A retrospective cohort study.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
06 2021
Historique:
received: 16 02 2021
accepted: 23 03 2021
pubmed: 29 3 2021
medline: 3 6 2021
entrez: 28 3 2021
Statut: ppublish

Résumé

Studies report hypercoagulability in coronavirus disease 2019 (COVID-19), leading many institutions to escalate anticoagulation intensity for thrombosis prophylaxis. To determine the bleeding risk with various intensities of anticoagulation in critically ill patients with COVID-19 compared with other respiratory viral illnesses (ORVI). This retrospective cohort study compared the incidence of major bleeding in patients admitted to an intensive care unit (ICU) within a single health system with COVID-19 versus ORVI. In the COVID-19 cohort, we assessed the effect of anticoagulation intensity received on ICU admission on bleeding risk. We performed a secondary analysis with anticoagulation intensity as a time-varying covariate to reflect dose changes after ICU admission. Four hundred and forty-three and 387 patients were included in the COVID-19 and ORVI cohorts, respectively. The hazard ratio of major bleeding for the COVID-19 cohort relative to the ORVI cohort was 1.26 (95% confidence interval [CI]: 0.86-1.86). In COVID-19 patients, an inverse-probability treatment weighted model found therapeutic-intensity anticoagulation on ICU admission had an adjusted hazard ratio of bleeding of 1.55 (95% CI: 0.88-2.73) compared with standard prophylactic-intensity anticoagulation. However, when anticoagulation was assessed as a time-varying covariate and adjusted for other risk factors for bleeding, the adjusted hazard ratio for bleeding on therapeutic-intensity anticoagulation compared with standard thromboprophylaxis was 2.59 (95% CI: 1.20-5.57). Critically ill patients with COVID-19 had a similar bleeding risk as ORVI patients. When accounting for changes in anticoagulation that occurred in COVID-19 patients, therapeutic-intensity anticoagulation was associated with a greater risk of major bleeding compared with standard thromboprophylaxis.

Sections du résumé

BACKGROUND
Studies report hypercoagulability in coronavirus disease 2019 (COVID-19), leading many institutions to escalate anticoagulation intensity for thrombosis prophylaxis.
OBJECTIVE
To determine the bleeding risk with various intensities of anticoagulation in critically ill patients with COVID-19 compared with other respiratory viral illnesses (ORVI).
PATIENTS/METHODS
This retrospective cohort study compared the incidence of major bleeding in patients admitted to an intensive care unit (ICU) within a single health system with COVID-19 versus ORVI. In the COVID-19 cohort, we assessed the effect of anticoagulation intensity received on ICU admission on bleeding risk. We performed a secondary analysis with anticoagulation intensity as a time-varying covariate to reflect dose changes after ICU admission.
RESULTS
Four hundred and forty-three and 387 patients were included in the COVID-19 and ORVI cohorts, respectively. The hazard ratio of major bleeding for the COVID-19 cohort relative to the ORVI cohort was 1.26 (95% confidence interval [CI]: 0.86-1.86). In COVID-19 patients, an inverse-probability treatment weighted model found therapeutic-intensity anticoagulation on ICU admission had an adjusted hazard ratio of bleeding of 1.55 (95% CI: 0.88-2.73) compared with standard prophylactic-intensity anticoagulation. However, when anticoagulation was assessed as a time-varying covariate and adjusted for other risk factors for bleeding, the adjusted hazard ratio for bleeding on therapeutic-intensity anticoagulation compared with standard thromboprophylaxis was 2.59 (95% CI: 1.20-5.57).
CONCLUSIONS
Critically ill patients with COVID-19 had a similar bleeding risk as ORVI patients. When accounting for changes in anticoagulation that occurred in COVID-19 patients, therapeutic-intensity anticoagulation was associated with a greater risk of major bleeding compared with standard thromboprophylaxis.

Identifiants

pubmed: 33774903
doi: 10.1111/jth.15310
pmc: PMC8250316
pii: S1538-7836(22)00789-9
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1533-1545

Subventions

Organisme : Hemostasis and Thrombosis Research Society
ID : Mentored Research Award supported by Sanofi Genzym
Organisme : Penn Cardiovascular Disease Fellowship Innovation Fund

Informations de copyright

© 2021 International Society on Thrombosis and Haemostasis.

Références

Lancet Respir Med. 2021 Mar;9(3):251-259
pubmed: 33341155
N Engl J Med. 2020 Jul 9;383(2):120-128
pubmed: 32437596
J Am Coll Cardiol. 2020 Oct 20;76(16):1815-1826
pubmed: 32860872
Blood Adv. 2021 Feb 9;5(3):872-888
pubmed: 33560401
J Thromb Haemost. 2020 Oct;18(10):2629-2635
pubmed: 32692874
Blood. 2020 Jun 4;135(23):2033-2040
pubmed: 32339221
J Thromb Haemost. 2020 May;18(5):1023-1026
pubmed: 32338827
Intensive Care Med. 2020 Jun;46(6):1089-1098
pubmed: 32367170
JAMA Netw Open. 2020 May 1;3(5):e2010182
pubmed: 32459353
Lancet Infect Dis. 2020 Aug;20(8):e192-e197
pubmed: 32539990
J Thromb Haemost. 2020 Aug;18(8):1995-2002
pubmed: 32369666
Thromb Res. 2020 Jul;191:145-147
pubmed: 32291094
Lancet Respir Med. 2020 Nov;8(11):1121-1131
pubmed: 32798468
Res Pract Thromb Haemost. 2020 Aug 19;4(6):969-983
pubmed: 32838111
Chest. 2021 Mar;159(3):1182-1196
pubmed: 33217420
N Engl J Med. 2011 Apr 7;364(14):1305-14
pubmed: 21417952
Blood Adv. 2018 Nov 27;2(22):3198-3225
pubmed: 30482763
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
Thromb Res. 2020 Jul;191:148-150
pubmed: 32381264
Ann Intern Med. 2021 May;174(5):622-632
pubmed: 33493012
Crit Care. 2020 Jun 2;24(1):275
pubmed: 32487122
Thromb Res. 2020 Dec;196:355-358
pubmed: 32977136
Intensive Care Med. 2013 Dec;39(12):2135-43
pubmed: 23942857
Chest. 2011 Jan;139(1):69-79
pubmed: 20453069
N Engl J Med. 2021 Aug 26;385(9):777-789
pubmed: 34351722
J Thromb Thrombolysis. 2020 Jul;50(1):72-81
pubmed: 32440883
J Biomed Inform. 2019 Jul;95:103208
pubmed: 31078660
Thromb Res. 2020 Dec;196:483-485
pubmed: 33091700
Eur Heart J. 2016 Apr 7;37(14):1104-1112
pubmed: 26547224
Circulation. 2020 Jul 14;142(2):184-186
pubmed: 32330083
Am Heart J. 2021 Jan;231:93-95
pubmed: 33181067
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354
Blood. 2020 Jul 23;136(4):489-500
pubmed: 32492712

Auteurs

Rim Halaby (R)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Adam Cuker (A)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Jennifer Yui (J)

Division of Hematology, Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.

Andrew Matthews (A)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Ella Ishaaya (E)

Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.

Elizabeth Traxler (E)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Christopher Domenico (C)

Department of Pharmacy, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

Tara Cooper (T)

Department of Pharmacy, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

Ann Tierney (A)

Department of Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Pardis Niami (P)

Department of Pharmacy, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

Nathalie van der Rijst (N)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Srinath Adusumalli (S)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Jacob Gutsche (J)

Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Jay Giri (J)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Steven Pugliese (S)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Todd E H Hecht (TEH)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Allyson M Pishko (AM)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH