%0 Journal Article
%T PLACE OF 5¦Á-REDUCTASE IN THE THERAPY FOR BENIGN PROSTATIC HYPERPLASIA
%A C. Novac
%A N. Suditu
%A B. Novac
%A V.D. Radu
%J Jurnalul de Chirurgie
%D 2007
%I University of Medicine and Pharmacy, Iasi
%X Twelve years ago, finasteride, the first 5¦Á-reductase inhibitor, was introduced as drug therapy for benign prostatic hyperplasia, and more recently dutasteride has emerged as an alternative. The efficacy, safety and ability of these 5¦Á-reductase inhibitors to reverse the natural progression of benign prostatic hyperplasia have been convincingly demonstrated and both drugs are now welt established in the medical armamentarium against the disease. Given the multifactorial etiology of benign hyperplasia, the usefulness of 5¦Á-reductase inhibitors in combination with a adrenergic blockers has also been investigated and justified in select patients. Wider applications of 5¦Á-reductase inhibitors are also emerging, though their perhaps most important new role as chemopreventive agents remains unclear.
%K BENIGN PROSTATIC HYPERPLASIA
%K 5¦¡-REDUCTASE INHIBITOR
%U http://www.jurnaluldechirurgie.ro/jurnal/docs/jurnal407/02novac%20HBP.pdf