Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36191
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dc.contributor.authorTran H.A.en
dc.contributor.authorMaclachlan K.H.en
dc.contributor.authorChunilal S.D.en
dc.contributor.authorStevens H.P.en
dc.date.accessioned2021-05-14T12:16:06Zen
dc.date.available2021-05-14T12:16:06Zen
dc.date.copyright2019en
dc.date.created20190306en
dc.date.issued2019-03-06en
dc.identifier.citationSeminars in Thrombosis and Hemostasis. 45 (1) (pp 94-99), 2019. Date of Publication: 2019.en
dc.identifier.issn0094-6176en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36191en
dc.description.abstractIn trials assessing venous thromboembolism (VTE) treatment, obese patients are under-represented or excluded. The main objective of this article is to examine the safety of weight-based enoxaparin dosing in obesity, as assessed by anti-factor Xa (anti-Xa) activity, bleeding, and recurrence. A 5-year retrospective audit of patients with acute VTE, weighing > 100 kg, prescribed enoxaparin 1 mg/kg twice daily, with an anti-Xa level 2 to 6 hours post-dose. The primary outcome was anti-Xa levels, and the secondary outcomes were bleeding and recurrence. Results were compared with patients weighing < 100 kg (n = 64), and obese patients prescribed doses < 1 mg/kg (n = 28). One-hundred sixty-six patients weighing > 100 kg with VTE were identified, with 64 excluded for not fulfilling criteria. The remaining 102 patients had a median weight of 130 kg (range: 105-222 kg). The median peak anti-Xa level was 0.93 U/mL, with 56% of levels being in the proposed therapeutic range (0.5-1.0 U/mL), 40% > 1.0 U/mL, and 4% < 0.5 U/mL. The median anti-Xa levels and distribution were not significantly different between patients > 100 kg and patients < 100 kg, while obese patients prescribed < 1 mg/kg were more frequently subtherapeutic (21%). Regardless of weight, the majority of patients with moderate renal impairment (eGFR 30-59 mL/min) had an anti-Xa level > 1.0 U/mL (61%). In the obese patients, there was no major bleeding or recurrence within 30 days. In comparison, patients weighing < 100 kg, despite similar peak anti-Xa levels, had higher rates of bleeding and recurrence. This was likely due to their older age and comorbidities, particularly renal impairment and cancer. These data support weight-based dosing of enoxaparin in obesity with no maximum dose, ensuring therapeutic drug levels, with anti-Xa levels suggested in obese patients with clinical risk factors for bleeding.Copyright © 2019 by Thieme Medical Publishers, Inc.en
dc.languageenen
dc.languageEnglishen
dc.publisherThieme Medical Publishers, Inc. (E-mail: custserv@thieme.com)en
dc.relation.ispartofSeminars in Thrombosis and Hemostasisen
dc.titleWeight-Based Enoxaparin for Venous Thromboembolism in Obesity Gives Similar Anti-Xa Levels to Patients <100 kg, with No Increase in Major Bleeding.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1055/s-0038-1677019en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid30630208 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30630208]en
dc.identifier.source626234909en
dc.identifier.institution(Maclachlan, Stevens, Tran, Chunilal) Department of Clinical Haematology, Monash Medical Centre, Clayton, VIC, Australiaen
dc.description.addressK.H. Maclachlan, Peter MacCallum Cancer Centre, 305 Grattan St, VIC 3000, Australia. E-mail: Kylee.Maclachlan@petermac.orgen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsheparin low-molecular-weight obesity venous thromboembolismen
dc.identifier.authoremailMaclachlan K.H.; Kylee.Maclachlan@petermac.orgen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
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