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Intensive-Dose Tinzaparin in Hospitalized COVID-19 Patients: The INTERACT Study

Title: Intensive-Dose Tinzaparin in Hospitalized COVID-19 Patients: The INTERACT Study
Authors: Karolina Akinosoglou; Christos Savopoulos; Abraham Pouliakis; Charalampos Triantafyllidis; Eleftherios Markatis; Foteini Golemi; Angelos Liontos; Charikleia Vadala; Ilias C. Papanikolaou; Vasiliki Dimakopoulou; Panagiotis Xarras; Katerina Varela; Georgia Kaiafa; Athanasios Mitsianis; Anastasia Chatzistamati; Efthalia Randou; Spyridon Savvanis; Maria Pavlaki; Georgios Efraimidis; Vasileios Samaras; Dimitrios Papazoglou; Alexandra Konstantinidou; Periklis Panagopoulos; Haralampos Milionis; on behalf of the INTERACT Study Group
Source: Viruses, Vol 14, Iss 4, p 767 (2022)
Publisher Information: MDPI AG
Publication Year: 2022
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: COVID-19; SARS-CoV-2; coronavirus; thrombosis; thromboprophylaxis; low molecular weight heparins; Microbiology; QR1-502
Description: (1) Background: It is well-established that coronavirus disease-2019 (COVID-19) is highly pro-inflammatory, leading to activation of the coagulation cascade. COVID-19-induced hypercoagulability is associated with adverse outcomes and mortality. Current guidelines recommend that hospitalized COVID-19 patients should receive pharmacological prophylaxis against venous thromboembolism (VTE). (2) INTERACT is a retrospective, phase IV, observational cohort study aiming to evaluate the overall clinical effectiveness and safety of a higher than conventionally used prophylactic dose of anticoagulation with tinzaparin administered for VTE prevention in non-critically ill COVID-19 patients with moderate disease severity. (3) Results: A total of 705 patients from 13 hospitals in Greece participated in the study (55% men, median age 62 years). Anticoagulation with tinzaparin was initiated immediately after admission. A full therapeutic dose was received by 36.3% of the participants (mean ± SD 166 ± 33 IU/Kgr/day) and the remaining patients (63.9%) received an intermediate dose (mean ± SD 114 ± 22 IU/Kgr/day). The median treatment duration was 13 days (Q1–Q3: 8–20 days). During the study (April 2020 to November 2021), 14 thrombotic events (2.0%) were diagnosed (i.e., three cases of pulmonary embolism (PE) and 11 cases of deep venous thrombosis, DVT). Four bleeding events were recorded (0.6%). In-hospital death occurred in 12 patients (1.7%). Thrombosis was associated with increasing age (median: 74.5 years, Q1–Q3: 62–79, for patients with thrombosis vs. 61.9 years, Q1–Q3: 49–72, p = 0.0149), increased D-dimer levels for all three evaluation time points (at admission: 2490, Q1–Q3: 1580–6480 vs. 700, Q1–Q3: 400–1475, p < 0.0001), one week ± two days after admission (3510, Q1–Q3: 1458–9500 vs. 619, Q1–Q3: 352–1054.5, p < 0.0001), as well as upon discharge (1618.5, Q1–Q3: 1010–2255 vs. 500, Q1–Q3: 294–918, p < 0.0001). Clinical and laboratory improvement was affirmed by decreasing D-dimer and CRP levels, increasing ...
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1999-4915/14/4/767; https://doaj.org/toc/1999-4915; https://doaj.org/article/06414aafebc44487a76dfbbed0e1d437
DOI: 10.3390/v14040767
Availability: https://doi.org/10.3390/v14040767; https://doaj.org/article/06414aafebc44487a76dfbbed0e1d437
Accession Number: edsbas.7BC8C48A
Database: BASE