The use of prostate extract preparations in patients after transurethral resection of prostate for its benign hyperplasia

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Abstract

The purpose of the study is to study the efficacy and safety of the prostate extract (GEROFARM LLC, Russia) in the postoperative period in patients after transurethral bipolar resection of the prostate. Materials and methods. The clinical study included 127 men aged 50 to 78 years with grade II benign prostatic hyperplasia (adenoma) who underwent a typical bipolar transurethral resection of the prostate. Patients of the main (n=60) group received tamsulosin 0.4 mg/day for 30 days in the postoperative period in combination with prostate extract 10 mg rectally for 21 days. In the control group (n=67) - tamsulosin 0.4 mg/day for 30 days as monotherapy. To assess the results of treatment, the questionnaire of the international system of total assessment of symptoms in prostate diseases (IPSS) with the definition of quality of life (QoL), the international index of erectile function (IIEF-5) and uroflowmetry were used. The control was carried out in terms of 1 and 3 months after the operation. Results. In the main group, in the observation period of 1 and 3 months after the operation, a decrease in the average IPSS score by 40.2% and 52.9% was revealed, and an improvement in the quality of life by 45% and 64.7%, respectively, was noted. In the control group, at the same time of observation, a decrease in the average IPSS score by 34% and 44.7%, respectively, was revealed, and the quality of life improved by 25.5% and 37.3%, respectively. The increase in the average rate of urination in the main group by the end of 1 and 3 months of treatment was 59.2% and 85.7%, respectively, and in the control group, these figures were 40.5% and 50%. The positive effect of the proposed combination therapy on erectile function in the main group by the end of 1 and 3 months of treatment was 5.2% and 9.2%, respectively, and in the control group, these figures were 2.9% and 5.2%. Discussion. There is a significant decrease in the symptoms of the lower urinary tract in the group of patients who received the drug Prostateks (GEROFARM LLC, Russia). Conclusions. The efficacy results of Prostatex (GEROFARM LLC, Russia) (reduced symptom severity on IPSS (11.7 1.2 ) and QoL (2.3 0.3)) scales are comparable to those of Vitprost® Plus which allows you to evaluate the effectiveness of two drugs equally.

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About the authors

V. N Pavlov

Bashkir State Medical University of the Ministry of Health of Russia

Email: pavlov@bashgmu.ru
Rector, Academician of the Russian Academy of Sciences, MD, Professor, Head of the Department of Urology with the course of IDPO Ufa, Russia

A. A Kazikhinurov

Bashkir State Medical University of the Ministry of Health of Russia

Email: alberturo@maii.ru
MD, Professor of the Department of Urology with the course of IDPO Ufa, Russia

R. A Kazikhinurov

Bashkir State Medical University of the Ministry of Health of Russia

Ph.D., Associate Professor of the Department of Urology with the course of IDPO Ufa, Russia

S. Sh Sabirzyanov

Bashkir State Medical University of the Ministry of Health of Russia

Email: sobir08-97@mail.ru
Clinical resident of the Department of Urology with the course of IDPO Ufa, Russia

Yu. D Saleeva

Bashkir State Medical University of the Ministry of Health of Russia

Email: ygileva@bk.ru
Clinical resident of the Department of Urology with the course of IDPO Ufa, Russia

K. A Kazikhinurova

Bashkir State Medical University of the Ministry of Health of Russia

5th year student Ufa, Russia

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