Early low-molecular-weight heparin administration is associated with shorter time to SARS-CoV-2 swab negativity.


Journal

Antiviral therapy
ISSN: 2040-2058
Titre abrégé: Antivir Ther
Pays: England
ID NLM: 9815705

Informations de publication

Date de publication:
2020
Historique:
accepted: 22 12 2020
pubmed: 29 1 2021
medline: 15 5 2021
entrez: 28 1 2021
Statut: ppublish

Résumé

Antiviral and immune-modulating properties of low-molecular-weight heparin (LMWH) against Coronaviridae have been reported by in vitro studies, but no in vivo evidence is yet available. We sought to know whether the timing of prophylactic doses of LMWH during the course of COVID-19 may affect the time to SARS-CoV-2 nasal-oropharyngeal swab negativization. Retrospective monocentric cross-sectional study on patients requiring sub-intensive ward admission due to first SARS-CoV-2 infection and undergoing early (EH; within 7 days from COVID-19 signs and symptoms onset) versus delayed prophylactic LMWH (DH; after 7 days). SARS-CoV-2 RNA was measured by reverse transcription real-time PCR according to scheduled time points: first swab after 2 weeks from COVID-19 onset, then at 1-week intervals until negativity. Time to SARS-CoV-2 swab negativity was shorter in EH (38 patients) compared with DH (55 patients): 22 versus 37 days (P=0.004). The number of confirmative negative swabs in EH was significantly higher compared with DH at week 2 (21.1% versus 3.6%; P=0.017) and 4 (60.0% versus 19.6%; P<0.001). At univariate, EH differed from DH for several disease severity and clinical management parameters. Nevertheless, after accounting for the differences, Cox regression showed early LMWH administration (hazard ratio [HR] 2.91 [1.51, 5.63]; P=0.002) and higher lymphocytes nadir (HR 1.04 [1.01, 1.08]; P=0.020) as predictors of shorter time to swab negativity. This potential antiviral and/or immune-modulating activity of LMWH needs further in vivo confirmations by randomized controlled trials.

Sections du résumé

BACKGROUND
Antiviral and immune-modulating properties of low-molecular-weight heparin (LMWH) against Coronaviridae have been reported by in vitro studies, but no in vivo evidence is yet available. We sought to know whether the timing of prophylactic doses of LMWH during the course of COVID-19 may affect the time to SARS-CoV-2 nasal-oropharyngeal swab negativization.
METHODS
Retrospective monocentric cross-sectional study on patients requiring sub-intensive ward admission due to first SARS-CoV-2 infection and undergoing early (EH; within 7 days from COVID-19 signs and symptoms onset) versus delayed prophylactic LMWH (DH; after 7 days). SARS-CoV-2 RNA was measured by reverse transcription real-time PCR according to scheduled time points: first swab after 2 weeks from COVID-19 onset, then at 1-week intervals until negativity.
RESULTS
Time to SARS-CoV-2 swab negativity was shorter in EH (38 patients) compared with DH (55 patients): 22 versus 37 days (P=0.004). The number of confirmative negative swabs in EH was significantly higher compared with DH at week 2 (21.1% versus 3.6%; P=0.017) and 4 (60.0% versus 19.6%; P<0.001). At univariate, EH differed from DH for several disease severity and clinical management parameters. Nevertheless, after accounting for the differences, Cox regression showed early LMWH administration (hazard ratio [HR] 2.91 [1.51, 5.63]; P=0.002) and higher lymphocytes nadir (HR 1.04 [1.01, 1.08]; P=0.020) as predictors of shorter time to swab negativity.
CONCLUSIONS
This potential antiviral and/or immune-modulating activity of LMWH needs further in vivo confirmations by randomized controlled trials.

Identifiants

pubmed: 33506810
doi: 10.3851/IMP3377
doi:

Substances chimiques

Antiviral Agents 0
Heparin, Low-Molecular-Weight 0
RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

327-333

Auteurs

Mattia Trunfio (M)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Elena Salvador (E)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Alberto Gaviraghi (A)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Sabrina Audagnotto (S)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Letizia Marinaro (L)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Ilaria Motta (I)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Riccardo Casciaro (R)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Valeria Ghisetti (V)

Microbiology and Molecular Biology Laboratory, "Amedeo di Savoia" Hospital, ASL Città di Turin, Turin, Italy.

Carmen Fava (C)

Department of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.

Stefano Bonora (S)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Giovanni Di Perri (G)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

Andrea Calcagno (A)

Department of Medical Sciences, University of Turin at the Unit of Infectious Diseases, "Amedeo di Savoia" Hospital, Turin, Italy.

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