Literature DB >> 33823560

Treatment-Dose LMWH versus Prophylactic/Intermediate Dose Heparins in High-Risk COVID-19 Inpatients: Rationale and Design of the HEP-COVID Trial.

Mark Goldin1,2, Dimitrios Giannis1, Wassim Diab2, Janice Wang1,2, Sameer Khanijo2, Gulru Sharifova2, Marc Cohen3, Jeet M Lund4, Andrea Mignatti2,5, Eugenia Gianos2,5, Alfonso Tafur6,7, Paul A Lewis8, Kevin Cohoon9, John M Kittelson10, Martin L Lesser1,2, Cristina P Sison1,2, Husneara Rahman1, Kanta Ochani1, William R Hiatt11,12, Rita A Dale11, Victoria E Anderson11, Marc Bonaca11,12, Jonathan L Halperin13, Jeffrey I Weitz14,15,16, Alex C Spyropoulos1,2.   

Abstract

Coronavirus disease-2019 (COVID-19) has been associated with significant risk of venous thromboembolism (VTE), arterial thromboembolism (ATE), and mortality particularly among hospitalized patients with critical illness and elevated D-dimer (Dd) levels. Conflicting data have yet to elucidate optimal thromboprophylaxis dosing. HEP-COVID (NCT04401293) is a phase 3, multicenter, pragmatic, prospective, randomized, pseudo-blinded, active control trial to evaluate efficacy and safety of therapeutic-dose low-molecular-weight heparin (LMWH) versus prophylactic-/intermediate-dose LMWH or unfractionated heparin (UFH) for prevention of a primary efficacy composite outcome of VTE, ATE, and all-cause mortality 30 ± 2 days post-enrollment. Eligible patients have COVID-19 diagnosis by nasal swab or serologic testing, requirement for supplemental oxygen per investigator judgment, and Dd >4 × upper limit of normal (ULN) or sepsis-induced coagulopathy score ≥4. Subjects are randomized to enoxaparin 1 mg/kg subcutaneous (SQ)/two times a day (BID) (creatinine clearance [CrCl] ≥ 30 mL/min) or 0.5 mg/kg (CrCl 15-30 mL/min) versus local institutional prophylactic regimens including (1) UFH up to 22,500 IU (international unit) daily (divided BID or three times a day), (2) enoxaparin 30 and 40 mg SQ QD (once daily) or BID, or (3) dalteparin 2,500 IU or 5,000 IU QD. The principal safety outcome is major bleeding. Events are adjudicated locally. Based on expected 40% relative risk reduction with treatment-dose compared with prophylactic-dose prophylaxis, 308 subjects will be enrolled (assuming 20% drop-out) to achieve 80% power. Distinguishing design features include an enriched population for the composite endpoint anchored on Dd >4 × ULN, stratification by intensive care unit (ICU) versus non-ICU, and the ability to capture asymptomatic proximal deep venous thrombosis via screening ultrasonography prior to discharge. Thieme. All rights reserved.

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Year:  2021        PMID: 33823560     DOI: 10.1055/a-1475-2351

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   6.681


  4 in total

Review 1.  Anticoagulants for people hospitalised with COVID-19.

Authors:  Ronald Lg Flumignan; Vinicius T Civile; Jéssica Dantas de Sá Tinôco; Patricia If Pascoal; Libnah L Areias; Charbel F Matar; Britta Tendal; Virginia Fm Trevisani; Álvaro N Atallah; Luis Cu Nakano
Journal:  Cochrane Database Syst Rev       Date:  2022-03-04

2.  Randomized trials of therapeutic heparin for COVID-19: A meta-analysis.

Authors:  Michelle Sholzberg; Bruno R da Costa; Grace H Tang; Hassan Rahhal; Musaad AlHamzah; Lisa Baumann Kreuziger; Fionnuala Ní Áinle; Mozah Obaid Almarshoodi; Paula D James; David Lillicrap; Marc Carrier; Andrew Beckett; Michael Fralick; Saskia Middeldorp; Agnes Y Y Lee; Kevin E Thorpe; Elnara Márcia Negri; Mary Cushman; Peter Jüni
Journal:  Res Pract Thromb Haemost       Date:  2021-12-17

Review 3.  Tinzaparin-a review of its molecular profile, pharmacology, special properties, and clinical uses.

Authors:  Marina Amerali; Marianna Politou
Journal:  Eur J Clin Pharmacol       Date:  2022-07-23       Impact factor: 3.064

Review 4.  Fundamental and Advanced Therapies, Vaccine Development against SARS-CoV-2.

Authors:  Nikola Hudakova; Simona Hricikova; Amod Kulkarni; Mangesh Bhide; Eva Kontsekova; Dasa Cizkova
Journal:  Pathogens       Date:  2021-05-21
  4 in total

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