Lupus anticoagulant associates with thrombosis in patients with COVID-19 admitted to intensive care units: A retrospective cohort study.

COVID‐19 critically ill lupus anticoagulant risk factor thrombosis

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 16 05 2022
revised: 22 08 2022
accepted: 24 08 2022
entrez: 30 9 2022
pubmed: 1 10 2022
medline: 1 10 2022
Statut: epublish

Résumé

Thrombosis is a frequent and severe complication in patients with coronavirus disease 2019 (COVID-19) admitted to the intensive care unit (ICU). Lupus anticoagulant (LA) is a strong acquired risk factor for thrombosis in various diseases and is frequently observed in patients with COVID-19. Whether LA is associated with thrombosis in patients with severe COVID-19 is currently unclear. To investigate if LA is associated with thrombosis in critically ill patients with COVID-19. The presence of LA and other antiphospholipid antibodies was assessed in patients with COVID-19 admitted to the ICU. LA was determined with dilute Russell's viper venom time (dRVVT) and LA-sensitive activated partial thromboplastin time (aPTT) reagents. Of 169 patients with COVID-19, 116 (69%) tested positive for at least one antiphospholipid antibody upon admission to the ICU. Forty (24%) patients tested positive for LA; of whom 29 (17%) tested positive with a dRVVT, 19 (11%) tested positive with an LA-sensitive aPTT, and 8 (5%) tested positive on both tests. Fifty-eight (34%) patients developed thrombosis after ICU admission. The odds ratio (OR) for thrombosis in patients with LA based on a dRVVT was 2.5 (95% confidence interval [CI], 1.1-5.7), which increased to 4.5 (95% CI, 1.4-14.3) in patients at or below the median age in this study (64 years). LA positivity based on a dRVVT or LA-sensitive aPTT was only associated with thrombosis in patients aged less than 65 years (OR, 3.8; 95% CI, 1.3-11.4) and disappeared after adjustment for C-reactive protein. Lupus anticoagulant on admission is strongly associated with thrombosis in critically ill patients with COVID-19, especially in patients aged less than 65 years.

Sections du résumé

Background UNASSIGNED
Thrombosis is a frequent and severe complication in patients with coronavirus disease 2019 (COVID-19) admitted to the intensive care unit (ICU). Lupus anticoagulant (LA) is a strong acquired risk factor for thrombosis in various diseases and is frequently observed in patients with COVID-19. Whether LA is associated with thrombosis in patients with severe COVID-19 is currently unclear.
Objective UNASSIGNED
To investigate if LA is associated with thrombosis in critically ill patients with COVID-19.
Patients/Methods UNASSIGNED
The presence of LA and other antiphospholipid antibodies was assessed in patients with COVID-19 admitted to the ICU. LA was determined with dilute Russell's viper venom time (dRVVT) and LA-sensitive activated partial thromboplastin time (aPTT) reagents.
Results UNASSIGNED
Of 169 patients with COVID-19, 116 (69%) tested positive for at least one antiphospholipid antibody upon admission to the ICU. Forty (24%) patients tested positive for LA; of whom 29 (17%) tested positive with a dRVVT, 19 (11%) tested positive with an LA-sensitive aPTT, and 8 (5%) tested positive on both tests. Fifty-eight (34%) patients developed thrombosis after ICU admission. The odds ratio (OR) for thrombosis in patients with LA based on a dRVVT was 2.5 (95% confidence interval [CI], 1.1-5.7), which increased to 4.5 (95% CI, 1.4-14.3) in patients at or below the median age in this study (64 years). LA positivity based on a dRVVT or LA-sensitive aPTT was only associated with thrombosis in patients aged less than 65 years (OR, 3.8; 95% CI, 1.3-11.4) and disappeared after adjustment for C-reactive protein.
Conclusion UNASSIGNED
Lupus anticoagulant on admission is strongly associated with thrombosis in critically ill patients with COVID-19, especially in patients aged less than 65 years.

Identifiants

pubmed: 36178455
doi: 10.1002/rth2.12809
pii: S2475-0379(22)02363-9
pmc: PMC9481876
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12809

Investigateurs

D van de Beek (D)
M C Brouwer (MC)
S de Bruin (S)
M Coppens (M)
N van Es (N)
T F van Haaps (TF)
N P Juffermans (NP)
M C A Muller (MCA)
A P J Vlaar (APJ)
C M P M Hertogh (CMPM)
L M A Heunks (LMA)
J G Hugtenburg (JG)
J van Kooten (J)
E J Nossent (EJ)
Y Smulders (Y)
P R Tuinman (PR)
A Vonk Noordegraaf (A)
M J J H Grootenboers (MJJH)
C van Guldener (C)
M Kant (M)
A Lansbergen (A)
J Faber (J)
G Hajer (G)
A Stemerdink (A)
J van den Akker (J)
R Bierings (R)
H Endeman (H)
M Goeijenbier (M)
N G M Hunfeld (NGM)
E C M van Gorp (ECM)
D A M P J Gommers (DAMPJ)
M P G Koopmans (MPG)
M J H A Kruip (MJHA)
T Kuiken (T)
T Langerak (T)
None Leebeek
M N Lauw (MN)
M P M de Maat (MPM)
D Noack (D)
M S Paats (MS)
M P Raadsen (MP)
B Rockx (B)
C Rokx (C)
C A M Schurink (CAM)
K Tong-Minh (K)
L van den Toorn (L)
C A den Uil (CA)
C Visser (C)
F Boutkourt (F)
T Roest (T)
R A Douma (RA)
L R de Haan (LR)
M Ten Wolde (M)
R H H Bemelmans (RHH)
B Festen (B)
S Stads (S)
C P C de Jager (CPC)
K S Simons (KS)
M L Antoni (ML)
M H Bos (MH)
J L I Burggraaf (JLI)
S C Cannegieter (SC)
H C J Eikenboom (HCJ)
P L den Exter (PL)
J J M Geelhoed (JJM)
M V Huisman (MV)
E de Jonge (E)
F H J Kaptein (FHJ)
F A Klok (FA)
L J M Kroft (LJM)
W M Lijfering (WM)
L Nab (L)
M K Ninaber (MK)
H Putter (H)
S R S Ramai (SRS)
A M da Rocha Rondon (AM)
A H E Roukens (AHE)
M A M Stals (MAM)
H H Versteeg (HH)
H W Vliegen (HW)
B J M van Vlijmen (BJM)
T van de Berg (T)
R Bruggemann (R)
B C T van Bussel (BCT)
H Ten Cate (H)
A Ten Cate-Hoek (A)
T M Hackeng (TM)
Ir Y Henskens (IY)
A Hulshof (A)
M Mulder (M)
R H Olie (RH)
L Schurgers (L)
B Spaetgens (B)
H Spronk (H)
K Winckers (K)
L Nieuwenhuizen (L)
B Franken (B)
I M Schrover (IM)
E G M de Waal (EGM)
A Beishuizen (A)
A Cornet (A)
J Krabbe (J)
K Kramers (K)
J Leentjens (J)
Q de Mast (Q)
S Middeldorp (S)
R E Brouwer (RE)
J L J Ellerbroek (JLJ)
J Tijmensen (J)
M M C Hovens (MMC)
E A N Oostdijk (EAN)
B D Westerhof (BD)
L M Faber (LM)
M van den Biggelaar (M)
J C M Meijers (JCM)
J Voorberg (J)
M E Kevenaar (ME)
Y L Soei (YL)
E J Wils (EJ)
F N Croles (FN)
B de Laat (B)
P W Kamphuisen (PW)
R Vink (R)
T Lisman (T)
K Meijer (K)
Y I G van Tichelaar (YIG)
O L Cremer (OL)
G Geersing (G)
H A H Kaasjager (HAH)
N Kusadasi (N)
A Huisman (A)
C Maas (C)
M Nijkeuter (M)
R E G Schutgens (REG)
Van Creveldkliniek (V)
R T Urbanus (RT)
Van Creveldkliniek (V)
J Westerink (J)
H J Faber (HJ)
S C E Koster (SCE)
P van Montfort (P)
D J L van Twist (DJL)

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).

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Auteurs

Tessa Noordermeer (T)

Center for Benign Hematology, Thrombosis and Haemostasis, Van Creveldkliniek University Medical Center Utrecht, Utrecht University Utrecht The Netherlands.

Roger E G Schutgens (REG)

Center for Benign Hematology, Thrombosis and Haemostasis, Van Creveldkliniek University Medical Center Utrecht, Utrecht University Utrecht The Netherlands.

Chantal Visser (C)

Department of Hematology, Erasmus MC Erasmus University Medical Center Rotterdam Rotterdam The Netherlands.

Emma Rademaker (E)

Julius Center for Health Sciences and Primary Care University Medical Center Utrecht Utrecht The Netherlands.

Moniek P M de Maat (MPM)

Department of Hematology, Erasmus MC Erasmus University Medical Center Rotterdam Rotterdam The Netherlands.

A J Gerard Jansen (AJG)

Department of Hematology, Erasmus MC Erasmus University Medical Center Rotterdam Rotterdam The Netherlands.

Maarten Limper (M)

Department of Rheumatology and Clinical Immunology University Medical Center Utrecht, Utrecht University Utrecht The Netherlands.

Olaf L Cremer (OL)

Intensive Care Center University Medical Center Utrecht Utrecht The Netherlands.

Marieke J H A Kruip (MJHA)

Department of Hematology, Erasmus MC Erasmus University Medical Center Rotterdam Rotterdam The Netherlands.

Henrik Endeman (H)

Department of Intensive Care Medicine, Erasmus MC University Medical Center Rotterdam Rotterdam The Netherlands.

Coen Maas (C)

Central Diagnostic Laboratory University Medical Center Utrecht, Utrecht University Utrecht The Netherlands.

Bas de Laat (B)

Department of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM) Maastricht University, Maastricht, the Netherlands Synapse Research Institute Maastricht The Netherlands.

Rolf T Urbanus (RT)

Center for Benign Hematology, Thrombosis and Haemostasis, Van Creveldkliniek University Medical Center Utrecht, Utrecht University Utrecht The Netherlands.

Classifications MeSH