Efficacy and safety of propiverine and terazosine combination for one year in male patients with luts and detrusor overactivity


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Sener N. C., Ozturk U., Goktug H. N. G., Gucuk A., NALBANT İ., YEŞİL S., ...Daha Fazla

International Braz J Urol, cilt.39, sa.4, ss.513-518, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 39 Sayı: 4
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1590/s1677-5538.ibju.2013.04.09
  • Dergi Adı: International Braz J Urol
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.513-518
  • Anahtar Kelimeler: Lower Urinary Tract Symptoms, Prostatic Hyperplasia, Urinary Bladder, Overactive, propiverine, URINARY-TRACT SYMPTOMS, BLADDER OUTLET OBSTRUCTION, CONTROLLED-TRIAL, MEN, TOLTERODINE, THERAPY, DOXAZOSIN, PLUS
  • Lokman Hekim Üniversitesi Adresli: Hayır

Özet

Purpose: To evaluate the long term efficacy and safety of the use of propiverine and terazosine combination in patients with LUTS and DO by a placebo controlled study. Materials and Methods: One hundred patients were enrolled in the study. They were randomized into two groups (each group consisted of 50 patients). Terazosine and placebo were administered to the patients in Group 1 and terazosine plus propiverine HCL was administered to Group 2. The patients were evaluated by international prostate symptom score (IPSS), the first four questions of IPSS (IPSS4), the 8th question of IPSS (quality of life-QoL), overactive bladder symptom score questionnaire (OAB-q V8), PSA test, urodynamic studies, post voiding residue (PVR). All patients were followed for one year and were reassessed for comparison. Results: IPSS, IPSS4, OAB symptoms, QoL score, PVR, and Qmax scores of the groups did not differ. After one year treatment, there was significant improvement in IPSS, IPSS4, OAB symptoms, QoL and Qmax values in Group 2. No significant improvement was noted for the same parameters in Group 1. Conclusion: This is the first study to show long term safety and efficacy of anticholinergic therapy for patients with LUTS. In patients with OAB or DO, long term anticholinergic treatment may be regarded as a treatment option.