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| dc.contributor.author | Frost, Freddy | |
| dc.contributor.author | Rivera-Caravaca, José-Miguel | |
| dc.contributor.author | Lip, Gregory-Y-H | |
| dc.date.accessioned | 2026-03-06T14:08:53Z | |
| dc.date.available | 2026-03-06T14:08:53Z | |
| dc.date.issued | 2025-04-05 | |
| dc.identifier.citation | Frost F, Rivera-Caravaca JM, Lip GYH. The use of oral anticoagulation at the time of acute COVID-19 infection and subsequent development of long-COVID/post-acute sequelae of SARS-CoV-2 infection. J Thromb Thrombolysis. 5 de abril de 2025;58(4):585-9. doi:10.1007/s11239-025-03096-0 | |
| dc.identifier.issn | 0929-5305 | |
| dc.identifier.uri | https://sms.carm.es/ricsmur/handle/123456789/24641 | |
| dc.description.abstract | Long COVID (LC) or post-acute sequelae of SARS-CoV-2 infection (PASC) is defined as ongoing, relapsing or new symptoms/conditions persisting after an acute COVID-19 infection. Given the potential role of oral anticoagulants (OAC) in treating thrombotic sequelae of LC/PASC, we investigated whether prevalent OAC use at the time of acute COVID-19 infection was associated with reduced development of LC/PASC. Retrospective cohort study within the TriNetx network. The primary cohort was defined as adults with a confirmed diagnosis of COVID-19. We defined OAC users as those who had received OACs (either direct-acting OACs [DOACs] or vitamin K antagonists [VKA]) in the preceding 3-months and non-users as those without OAC use within the previous 12-months. The primary outcome was a composite of 9 features associated with LC/PASC We identified 38,409 DOAC users, 19,243 VKA users, and 2,329,771 non-OAC users with acute COVID-19 infection. After successful propensity score matching (PSM), we found an increased risk of LC/PASC features in those receiving DOAC compared to non-OAC (HR [95% CI] 1.50 [1.35 to 1.68], p < 0.0001), and in VKA users compared to non-OACs (HR [95% CI] 1.98 [1.78 to 2.20], p < 0.0001), while DOAC users were at reduced risk compared to VKA users (HR [95% CI] 0.71 [0.62 to 0.81], p < 0.0001). We found no evidence that prevalent OAC at the time of acute COVID-19 infection was associated with reduced risk of LC/PASC. Further work is needed to understand whether there is a role for OAC therapy in the management of LC/PASC. | |
| dc.language.iso | eng | |
| dc.publisher | SPRINGER | |
| dc.rights | Atribución/Reconocimiento 4.0 Internacional | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/deed.es | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | COVID-19/complications/diagnosis/blood | |
| dc.subject.mesh | Retrospective Studies | |
| dc.subject.mesh | Anticoagulants/administration & dosage/adverse effects | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Administration, Oral | |
| dc.subject.mesh | Aged | |
| dc.subject.mesh | Post-Acute COVID-19 Syndrome | |
| dc.subject.mesh | SARS-CoV-2 | |
| dc.subject.mesh | COVID-19 Drug Treatment | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Time Factors | |
| dc.subject.mesh | Risk Factors | |
| dc.subject.mesh | Vitamin K/antagonists & inhibitors | |
| dc.subject.mesh | Thrombosis/etiology/prevention & control/diagnosis | |
| dc.title | The use of oral anticoagulation at the time of acute COVID-19 infection and subsequent development of long-COVID/post-acute sequelae of SARS-CoV-2 infection | |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.pmid | 40186701 | |
| dc.relation.publisherversion | https://link.springer.com/10.1007/s11239-025-03096-0 | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dc.identifier.doi | 10.1007/s11239-025-03096-0 | |
| dc.journal.title | Journal of Thrombosis and Thrombolysis | |
| dc.identifier.essn | 1573-742X |