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Título
Influence of aspirin therapy in the ulcer associated with chronic venous insufficiency
Año del Documento
2012
Editorial
Universidad de Valladolid. Facultad de Medicina
Descripción
Producción Científica
Documento Fuente
Annals of Vascular Surgery
Abstract
Background: To determine the effect of aspirin on ulcer healing rate in patients with chronic
venous insufficiency, and to establish prognostic factors that influence ulcer evolution.
Methods: Between 2001 and 2005, 78 patients with ulcerated lesions of diameter >2 cm and
associated with chronic venous insufficiency were evaluated in our hospital. Of these, 51 patients
(22 men, 29 women) with mean age of 60 years (range: 36e86) were included in a prospective
randomized trial with a parallel control group. The treatment group received 300 mg of aspirin and
the control group received no drug treatment; in both groups, healing was associated with standard
compression therapy. During follow-up, held weekly in a blinded fashion, there was ulcer
healing as well as cases of recurrence. Results were analyzed by intention-to-treat approach.
Cure rate was estimated using KaplaneMeir survival analysis, and the influence of prognostic
factors was analyzed by applying the Cox proportional hazards model.
Results: In the presence of gradual compression therapy, healing occurred more rapidly in
patients receiving aspirin versus the control subjects (12 weeks in the treated group vs. 22
weeks in the control group), with a 46% reduction in healing time. The main prognostic factor
was estimated initial area of injury (P ¼ 0.032). Age, sex, systemic therapy, and infection
showed little relevance to evolution.
Conclusions: The administration of aspirin daily dose of 300 mg shortens the healing time of
ulcerated lesions in the chronic venous insufficiency (CVI). The main prognostic factor for healing
of venous ulcerated lesions is the initial surface area of the ulcer.
Materias (normalizadas)
Insuficiencia venosa crónica
Aspirina
Úlceras
Revisión por pares
SI
Idioma
eng
Derechos
openAccess
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