Objective Benign prostatic hyperplasia (BPH) is a common reproductive organ disease in elderly men. Early adoption of appropriate treatment methods in clinical practice is crucial for the treatment of benign prostatic hyperplasia. This study aimed to compare the therapeutic effects of tamsulosin and alfuzosin on benign prostatic hyperplasia and provide references for clinical rational drug use.
Method A retrospective analysis was conducted on patients with benign prostatic hyperplasia admitted to Yongkang Hospital of Traditional Chinese Medicine from January 2020 to December 2020. The patients in the tamsulosin group received oral tamsulosin hydrochloride sustained-release capsules, while the patients in the alfuzosin group received alfuzosin hydrochloride sustained-release tablets. The international prostate symptom score (IPSS), international erectile function index (IIEF), maximum urinary flow (MFR), bladder residual urine volume (RU), prostate volume (PV), quality of life (SF-36 scale), and treatment effectiveness before and after treatment were compared to evaluate clinical efficacy. Liver function [alanine transferase (ALT), aspartate transferase (AST), total bilirubin], renal function [blood urea nitrogen (BUN) and creatinine (Cr)], prostate tumor markers serum free prostate specific antigen (F-PSA), and serum total prostate specific antigen (T-PSA) before and after treatment were compared to evaluate the safety.
Result 106 patients with benign prostatic hyperplasia were included (55 cases in tamsulosin group and 51 cases in alfuzosin group). Compared to before treatment, IPSS, RU and PV of the patients in the two groups after 6 months, 12 months, and 24 months of treatment were significantly decreased (P<0.05), and the quality of life were significantly increased (P<0.05). Compared with alfuzosin group, patients in tamsulosin group showed a significant decrease in IPSS, Ru and PV after 6 months, 12 months, and 24 months of treatment (P<0.05) and an increase in IIEF, MFR and quality of life (P<0.05). The total effective rate of the Tamsulosin group was significantly higher than that of the alfuzosin group (92.73% vs. 78.43%, P=0.035). There were no significant changes in liver and kidney function and prostate biomarker in both groups before and after treatment (P>0.05), and they were all in the normal range.
Conclusion Both of tamsulosin and alfazosin could effectively improve the symptoms of benign prostatic hyperplasia and the quality of life of patients, with good safety. Furthermore, tamsulosin has a more significant therapeutic effect on patients with benign prostatic hyperplasia.
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