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Venous thromboembolism management in Northeast Melbourne: how does it compare to international guidelines and data?
Author(s) -
Lim Hui Y.,
Chua Chong C.,
Tacey Mark,
Sleeman Matthew,
Donnan Geoffrey,
Nandurkar Harshal,
Ho Prahlad
Publication year - 2017
Publication title -
internal medicine journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 70
eISSN - 1445-5994
pISSN - 1444-0903
DOI - 10.1111/imj.13525
Subject(s) - medicine , pulmonary embolism , warfarin , hazard ratio , malignancy , real world data , thrombosis , deep vein , venous thromboembolism , thrombophilia , proportional hazards model , retrospective cohort study , intensive care medicine , pediatrics , emergency medicine , confidence interval , data science , computer science , atrial fibrillation
Background Venous thromboembolism ( VTE ) is a major cause of morbidity and mortality with significant heterogeneity in its management, both within our local practice and in international guidelines. Aims To provide a holistic evaluation of ‘real‐world’ Australian experience in the warfarin era, including how we compare to international guidelines. Methods Retrospective evaluation of VTE from July 2011 to December 2012 at two major hospitals in Melbourne, Australia. These results were compared to recommendations in the international guidelines. Results A total of 752 episodes involving 742 patients was identified. Contrary to international guidelines, an unwarranted heritable thrombophilia screen was performed in 22.0% of patients, amounting to a cost of AU$29 000. The duration of anticoagulation was longer compared to international recommendations, although the overall recurrence (3.2/100 person‐years) and clinically significant bleeding rates (2.4/100 person‐years) were comparable to ‘real‐world’ data. Unprovoked VTE (hazard ratio 2.06; P  = 0.01) was a risk factor for recurrence, and there was no difference in recurrence between major VTE (proximal deep vein thrombosis ( DVT ) and/or pulmonary embolism) and isolated distal DVT (3.02 vs 3.94/100 person‐years; P  = 0.25). Fourteen patients were subsequently diagnosed with malignancy, and patients with recurrent VTE had increased risk of prospective cancer diagnosis (relative risk 6.68; P  < 0.001). Conclusions While our ‘real‐world’ VTE experience during the warfarin era largely correlates with international guidelines, there remains heterogeneity in the management strategies, including excessive thrombophilia screening and longer duration of anticoagulation. This audit highlights the need for national VTE guidelines, as well as prospective auditing of VTE management, in the direct oral anticoagulant era for future comparison.

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