Sociedad Americana de Hirudoterapia

Venous thromboembolism management in Northeast Melbourne: how does it compare to international guidelines and data?

Research article published in Internal medicine journal (2017)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Observational studyEnsayos clínicosLim HY et al. · Internal medicine journal, 2017

Abstract

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.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeComparative StudyJournal ArticleMulticenter Study
Indexed MeSH termsAdolescentAdultAgedAged, 80 and overAnticoagulantsData Interpretation, StatisticalDisease ManagementFemaleFollow-Up StudiesHumansInternationalityMale

Resumen

Peer-reviewed clinical and outcomes research relevant to medicinal leech therapy and its biology. Indexed in PubMed and verified against the NCBI record.

Por qué esto importa para la hirudoterapia

Esta auditoría retrospectiva de 752 episodios de venous thromboembolism (VTE) en dos hospitales de Melbourne durante la era de la warfarin encontró que la práctica fue mayoritariamente consistente con las guías internacionales, pero señaló un exceso de cribado de trombofilia y una anticoagulación más prolongada de lo recomendado, vinculando el VTE no provocado y la recurrencia con una mayor tasa de recidiva y un diagnóstico de cáncer posterior. Su relevancia para la hirudoterapia es únicamente como antecedente sobre cómo se maneja el venous thromboembolism y sobre el contexto de anticoagulación en el que se sitúan los antitrombóticos derivados de sanguijuelas; el estudio en sí examina el manejo clínico de la era de la warfarin y no contiene información sobre sanguijuelas ni sobre el secretoma de las mismas. Como advertencia, se trata de una auditoría local de mundo real, no de evidencia intervencional, y no tiene incidencia en la eficacia o seguridad de la hirudoterapia; se incluye para completar el contexto clínico más que como un respaldo directo.

Citación

Venous thromboembolism management in Northeast Melbourne: how does it compare to international guidelines and data?.

Lim HY et al. · Internal medicine journal, 2017

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.