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The use of enoxaparin is generally not recommended in patients with end-stage renal disease (ESRD) and undergoing haemodialysis. We describe the administration of high-dose enoxaparin in a haemodialysis patient with heparin resistance and recurrent deep vein thrombosis (DVT) outlining a novel dosing regimen along an innovative method for monitoring antifactor Xa activity. As a last resort of his recurrent DVT, a critically ill intensive care unit patient undergoing dialysis was prescribed high-dose enoxaparin, administered exclusively after dialysis, on dialysis days for a period of 2 months. Antifactor Xa activity was measured 4 hours postadministration with a target range of 0.7-1.2 IU/mL. The patient's DVT demonstrated clinical improvement, antifactor Xa levels were maintained within the therapeutic range and haemoglobin levels remained stable with no signs of bleeding. This case reports the implementation of a high-dose enoxaparin dosing and monitoring strategy in a high-risk patient. However, further studies involving larger patient cohorts are required to validate this approach.
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http://dx.doi.org/10.1136/bcr-2024-262939 | DOI Listing |
BMJ Case Rep
August 2025
Pulmonary and Critical Care Division, Internal Medicine Department, American University of Beirut Medical Center, Beirut, Lebanon
The use of enoxaparin is generally not recommended in patients with end-stage renal disease (ESRD) and undergoing haemodialysis. We describe the administration of high-dose enoxaparin in a haemodialysis patient with heparin resistance and recurrent deep vein thrombosis (DVT) outlining a novel dosing regimen along an innovative method for monitoring antifactor Xa activity. As a last resort of his recurrent DVT, a critically ill intensive care unit patient undergoing dialysis was prescribed high-dose enoxaparin, administered exclusively after dialysis, on dialysis days for a period of 2 months.
View Article and Find Full Text PDFF1000Res
November 2024
Cardiovascular, Mataram University, Mataram, West Nusa Tenggara, 83126, Indonesia.
Background: Acute coronary syndrome (ACS) remains one of the leading causes of death worldwide. Smoking may also increase the risk of developing ACS. The most advantageous therapy is percutaneous coronary intervention.
View Article and Find Full Text PDFCan J Infect Dis Med Microbiol
May 2024
Centre for Occupational and Environmental Health (COEH), Maulana Azad Medical College, New Delhi, India.
Purpose: Since February 2020, the world has been overwhelmed by the SARS-CoV-2 outbreak, and several patients suffered interstitial pneumonia and respiratory failure requiring mechanical ventilation, threatening the capability of healthcare systems to handle this amount of critical cases. Intravenous immunoglobulins (IVIG) possess potential immunomodulatory properties beneficial for COVID-19 patients, yet evidence supporting IVIG as adjunctive therapy remains sparse. This study evaluated the outcomes of adjunctive IVIG with the standard of care (SoC) in moderate-to-severe COVID-19 patients.
View Article and Find Full Text PDFArterioscler Thromb Vasc Biol
July 2024
Thrombosis and Atherosclerosis Research Institute, Hamilton, Ontario, Canada (R.A.M., J.Z., J.C.F., J.I.W.).
Background: Polyphosphate (polyP), a procoagulant released from platelets, activates coagulation via the contact system and modulates cardiomyocyte viability. High-dose intravenous polyP is lethal in mice, presumably because of thrombosis. Previously, we showed that HRG (histidine-rich glycoprotein) binds polyP and attenuates its procoagulant effects.
View Article and Find Full Text PDFTurk Gogus Kalp Damar Cerrahisi Derg
January 2024
Department of Chest Surgery, Necmettin Erbakan University Faculty of Medicine, Konya, Türkiye.
Background: The aim of this study was to investigate the antifibrinolytic and anti-inflammatory effects of hesperidin, tenoxicam and enoxaparin on intrapleural adhesions in an experimental rat model.
Methods: A total of 52 healthy adult male Wistar Albino rats from the same colony were randomly divided into six groups as sham (Group 1), surgical control (Group 2), low-dose hesperidin (Group 3), high-dose hesperidin (Group 4), tenoxicam (Group 5), and enoxaparin (Group 6). All subjects underwent left thoracotomy and except for the sham group, an adhesion model was applied and, postoperatively, the drugs were administered intraperitoneally.