J Korean Androl Soc.  1993 Jun;11(1):23-27.

Effect of terazosin in symptomatic benign prostatic hyperplasia

Affiliations
  • 1Department of Urology, Yonsei University College of Medicine, Seoul, Korea.

Abstract

We investigate the effectiveness of terazosin in symptomatic benign prostatic hyperplasia (BPH) in 31 evaluable patients. After 2 weeks of treatment, the initial dosage of 2 mg/day was elevated to 4mg/day in 17 randomly chosen patients. At 12 weeks' follow-up, 55% of the patients had > 30% improvement in their symptom scores, and 32% had a > 30% increase in their maximal flow rate. The maximal effect was achieved at 2 weeks, with no further improvement seen threafter in patients who had not already responded. There was no significant difference between the 2-mg and 4-mg doses. We concluded that terazosin is effective in some patients with infravesical obstruction secondary to BPH. Further studies are needed to evaluate the effect of increasing the dose in patients who do not respond to initial low-dose therapy.


MeSH Terms

Follow-Up Studies
Humans
Prostatic Hyperplasia*
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