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Prostate cancer incidence and newly diagnosed patient profile in Spain in 2010. [artículo]

Por: Rodríguez Antolín, Alfredo [Urología].
Colaborador(es): Servicio de Urología.
Editor: BJU International 2012Descripción: 110(11B):E701-6.Recursos en línea: Solicitar documento Resumen: What's known on the subject? and What does the study add? Prostate cancer (PCa) accounts for 12% of newly diagnosed cases of cancer in Europe. It is one of the most frequently diagnosed tumours in the developed world. Since the introduction of prostate specific antigen as a test for early detection of PCa, the rate of diagnosis has increased significantly and specific mortality has reduced in most western countries. Most of the data on the incidence of PCa are obtained from population-based cancer registries which frequently do not cover the whole population. This first national hospital-based PCa registry aims not only to estimate the incidence of the disease but to ascertain the clinical profile of newly diagnosed PCa patients, a useful tool for evaluating the impact of the disease and its socio-health management.
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Artículo Artículo PC2247 (Navegar estantería) Disponible

Formato Vancouver:
Cózar JM, Miñana B, Gómez-Veiga F, Rodríguez-Antolín A, Villavicencio H, Cantalapiedra A, et al. Prostate cancer incidence and newly diagnosed patient profile in Spain in 2010.
BJU Int. 2012 Dec;110(11 Pt B):E701-6.

PMID: 22989066

Contiene 24 referencias

What's known on the subject? and What does the study add? Prostate cancer (PCa) accounts for 12% of newly diagnosed cases of cancer in Europe. It is one of the most frequently diagnosed tumours in the developed world. Since the introduction of prostate specific antigen as a test for early detection of PCa, the rate of diagnosis has increased significantly and specific mortality has reduced in most western countries. Most of the data on the incidence of PCa are obtained from population-based cancer registries which frequently do not cover the whole population. This first national hospital-based PCa registry aims not only to estimate the incidence of the disease but to ascertain the clinical profile of newly diagnosed PCa patients, a useful tool for evaluating the impact of the disease and its socio-health management.

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