Intermediate-dose anticoagulation, aspirin, and in-hospital mortality in COVID-19: a propensity score-matched analysis.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
15 Jan 2021
Historique:
pubmed: 21 1 2021
medline: 21 1 2021
entrez: 20 1 2021
Statut: epublish

Résumé

Thrombotic complications occur at high rates in hospitalized patients with COVID-19, yet the impact of intensive antithrombotic therapy on mortality is uncertain. How does in-hospital mortality compare with intermediate- versus prophylactic-dose anticoagulation, and separately with in-hospital aspirin versus no antiplatelet therapy, in treatment of COVID-19? Using data from 2785 hospitalized adult COVID-19 patients, we established two separate, nested cohorts of patients (1) who received intermediate- or prophylactic-dose anticoagulation ("anticoagulation cohort", N = 1624), or (2) who were not on home antiplatelet therapy and received either in-hospital aspirin or no antiplatelet therapy ("aspirin cohort", N = 1956). Propensity score matching utilizing various markers of illness severity and other patient-specific covariates yielded treatment groups with well-balanced covariates in each cohort. The primary outcome was cumulative incidence of in-hospital death. Among propensity score-matched patients in the anticoagulation cohort (N = 382), in a multivariable regression model, intermediate- compared to prophylactic-dose anticoagulation was associated with a significantly lower cumulative incidence of in-hospital death (hazard ratio 0.518 [0.308-0.872]). Among propensity-score matched patients in the aspirin cohort (N = 638), in a multivariable regression model, in-hospital aspirin compared to no antiplatelet therapy was associated with a significantly lower cumulative incidence of in-hospital death (hazard ratio 0.522 [0.336-0.812]). In this propensity score-matched, observational study of COVID-19, intermediate-dose anticoagulation and aspirin were each associated with a lower cumulative incidence of in-hospital death.

Sections du résumé

Background UNASSIGNED
Thrombotic complications occur at high rates in hospitalized patients with COVID-19, yet the impact of intensive antithrombotic therapy on mortality is uncertain.
Research Question UNASSIGNED
How does in-hospital mortality compare with intermediate- versus prophylactic-dose anticoagulation, and separately with in-hospital aspirin versus no antiplatelet therapy, in treatment of COVID-19?
Study Design and Methods UNASSIGNED
Using data from 2785 hospitalized adult COVID-19 patients, we established two separate, nested cohorts of patients (1) who received intermediate- or prophylactic-dose anticoagulation ("anticoagulation cohort", N = 1624), or (2) who were not on home antiplatelet therapy and received either in-hospital aspirin or no antiplatelet therapy ("aspirin cohort", N = 1956). Propensity score matching utilizing various markers of illness severity and other patient-specific covariates yielded treatment groups with well-balanced covariates in each cohort. The primary outcome was cumulative incidence of in-hospital death.
Results UNASSIGNED
Among propensity score-matched patients in the anticoagulation cohort (N = 382), in a multivariable regression model, intermediate- compared to prophylactic-dose anticoagulation was associated with a significantly lower cumulative incidence of in-hospital death (hazard ratio 0.518 [0.308-0.872]). Among propensity-score matched patients in the aspirin cohort (N = 638), in a multivariable regression model, in-hospital aspirin compared to no antiplatelet therapy was associated with a significantly lower cumulative incidence of in-hospital death (hazard ratio 0.522 [0.336-0.812]).
Interpretation UNASSIGNED
In this propensity score-matched, observational study of COVID-19, intermediate-dose anticoagulation and aspirin were each associated with a lower cumulative incidence of in-hospital death.

Identifiants

pubmed: 33469595
doi: 10.1101/2021.01.12.21249577
pmc: PMC7814841
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : F31 HL139116
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL142818
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM136651
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Commentaires et corrections

Type : UpdateIn

Déclaration de conflit d'intérêts

Summary conflict of interest statements: No conflict of interest exists for any author on this manuscript.

Auteurs

Matthew L Meizlish (ML)

Yale School of Medicine, New Haven, CT.

George Goshua (G)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Yiwen Liu (Y)

Dana-Farber Cancer Institute, Boston, MA.

Rebecca Fine (R)

Department of Medicine, Yale School of Medicine, New Haven, CT.

Kejal Amin (K)

Department of Pharmacy, Yale-New Haven Hospital, New Haven, CT.

Eric Chang (E)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Nicholas DeFilippo (N)

Department of Pharmacy, Yale-New Haven Hospital, New Haven, CT.
School of Pharmacy, University of Connecticut, Storrs, CT.

Craig Keating (C)

Joint Data Analytics Team, Yale New Haven Hospital, New Haven, CT.

Yuxin Liu (Y)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Michael Mankbadi (M)

Department of Medicine, Yale School of Medicine, New Haven, CT.

Dayna McManus (D)

Department of Pharmacy, Yale-New Haven Hospital, New Haven, CT.

Stephen Wang (S)

Department of Medicine, Yale School of Medicine, New Haven, CT.

Christina Price (C)

Section of Allergy and Immunology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Robert D Bona (RD)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Cassius Iyad Ochoa Chaar (CIO)

Section of Vascular Surgery, Department of Surgery, Yale School of Medicine, New Haven, CT.

Hyung J Chun (HJ)

Section of Cardiology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Alexander B Pine (AB)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Henry M Rinder (HM)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.
Department of Laboratory Medicine, Yale School of Medicine, New Haven, CT.

Jonathan Siner (J)

Section of Pulmonary and Sleep Medicine, Department of Medicine, Yale School of Medicine, New Haven, CT.

Donna S Neuberg (DS)

Dana-Farber Cancer Institute, Boston, MA.

Kent A Owusu (KA)

Department of Pharmacy, Yale-New Haven Hospital, New Haven, CT.
Clinical Redesign, Yale New Haven Health, New Haven, CT.

Alfred Ian Lee (AI)

Section of Hematology, Department of Medicine, Yale School of Medicine, New Haven, CT.

Classifications MeSH