Abstract:The sexuality and the management of benign prostatic hyperplasia (BPH) with alfuzosin (SAMBA) trial evaluated the effect of alfuzosin on sexual function in men treated for BPH using two sexual function scales: male sexual health questionnaire (MSHQ) and international index of erectile function (IIEF-15). A total of 148 patients with BPH were treated with alfuzosin for 24 weeks. The patients were followed at baseline, 4, 12 and 24 weeks after medication with alfuzosin. MSHQ was collected at every visit, whereas… Show more
“…A major limitation of the current study was the high incompletion rate of MSHQ questionnaire (44%) at week 24, which might have contributed to the lack of a significant difference observed in the primary endpoint. Nevertheless, overall our results are in line with those of the similarly designed SAMBA trial, in which 83% of patients were evaluable in the final analysis [15].…”
Section: Discussionsupporting
confidence: 90%
“…The results of the current study are in line with those of the similarly designed 24‐week SAMBA trial, conducted in 148 Korean patients aged ≥50 years with BPH [15]. Patients enrolled in these two studies had similar baseline characteristics: mean age (59.4 vs. 57.8 years in the Korean SAMBA trial), total IPSS (17.3 vs. 17.4, respectively), and bother score (3.8 vs. 3.9, respectively) [15]. In both studies, an improvement in urinary symptoms with alfuzosin 10 mg once daily was paralleled by significant improvements in ejaculatory function.…”
Section: Discussionsupporting
confidence: 86%
“…Furthermore, these improvements, as measured by the MSHQ, were correlated with IIEF‐5. While the onset of action of alfuzosin was not evaluated in Korean patients [15], the current study demonstrated significant improvements in IPSS total scores following 1 week of treatment.…”
Section: Discussionmentioning
confidence: 57%
“…The improvement in erectile function remained significant when the cut‐off score of IIEF‐5 ≤ 11 (moderate to severe ED) and ≤16 (mild to severe ED) was used. The benefits of alfuzosin 10 mg once daily on sexual function have also been confirmed in a number of other studies [12,15,31,32]. The improvement in sexual function was particularly evident in men with severe LUTS or a severe bother score at baseline [12].…”
Section: Discussionmentioning
confidence: 61%
“…The Male Sexual Health Questionnaire (MSHQ) is a newly developed questionnaire which allows a detailed and accurate evaluation of male sexual function [8]. It has recently been utilized to assess sexual dysfunction in Korean and Thai patients enrolled in the Sexuality and the Management of BPH with Alfuzosin (SAMBA) trial [15,16]. To the best of our knowledge, the present study is the first study to assess the effect of alfuzosin 10 mg once daily on sexual function in Taiwanese patients, utilizing the MSHQ and International Index of Erectile Function—five‐item (IIEF‐5), and to confirm its efficacy and safety profile.…”
To assess the effect of alfuzosin (XATRAL) 10 mg once daily on sexual function in men with moderate to severe lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH), patients with suggestive symptomatic BPH, an International Prostate Symptom Score (IPSS) >8 (range of scores, 0-35), and sexual attempts at least once per month were enrolled. All patients received alfuzosin 10 mg once daily for 24 weeks and were asked to complete the IPSS test and Male Sexual Health Questionnaire at weeks 0 (baseline), 1, 4, 12, and 24. Other assessments included the International Index of Erectile Function-five-item version (range of scores: 5-25), as well as onset of action and peak urinary flow rate (Q(max)). From September 2006 to May 2008, 279 patients were enrolled from nine centers in Taiwan. At 24 weeks, alfuzosin effectively improved LUTS and quality of life, as demonstrated by a reduction in the IPSS total score (17.3 vs. 9.9, p < 0.001) and the IPSS bother score (3.8 vs. 2.5, p < 0.001). The majority (85%) of patients perceived an improvement of urinary symptoms within 1 month of administration. In patients with an International Index of Erectile Function-five-item version score of ≤16, alfuzosin significantly improved erectile disorder and satisfaction subscores at each time point (p ≤ 0.02). Prolonged-release alfuzosin effectively improved LUTS, quality of life, erectile function, and sexual satisfaction in men with BPH and mild to severe erectile dysfunction. Alfuzosin is an effective treatment option for the management of patients with BPH/LUTS and concomitant sexual dysfunction.
“…A major limitation of the current study was the high incompletion rate of MSHQ questionnaire (44%) at week 24, which might have contributed to the lack of a significant difference observed in the primary endpoint. Nevertheless, overall our results are in line with those of the similarly designed SAMBA trial, in which 83% of patients were evaluable in the final analysis [15].…”
Section: Discussionsupporting
confidence: 90%
“…The results of the current study are in line with those of the similarly designed 24‐week SAMBA trial, conducted in 148 Korean patients aged ≥50 years with BPH [15]. Patients enrolled in these two studies had similar baseline characteristics: mean age (59.4 vs. 57.8 years in the Korean SAMBA trial), total IPSS (17.3 vs. 17.4, respectively), and bother score (3.8 vs. 3.9, respectively) [15]. In both studies, an improvement in urinary symptoms with alfuzosin 10 mg once daily was paralleled by significant improvements in ejaculatory function.…”
Section: Discussionsupporting
confidence: 86%
“…Furthermore, these improvements, as measured by the MSHQ, were correlated with IIEF‐5. While the onset of action of alfuzosin was not evaluated in Korean patients [15], the current study demonstrated significant improvements in IPSS total scores following 1 week of treatment.…”
Section: Discussionmentioning
confidence: 57%
“…The improvement in erectile function remained significant when the cut‐off score of IIEF‐5 ≤ 11 (moderate to severe ED) and ≤16 (mild to severe ED) was used. The benefits of alfuzosin 10 mg once daily on sexual function have also been confirmed in a number of other studies [12,15,31,32]. The improvement in sexual function was particularly evident in men with severe LUTS or a severe bother score at baseline [12].…”
Section: Discussionmentioning
confidence: 61%
“…The Male Sexual Health Questionnaire (MSHQ) is a newly developed questionnaire which allows a detailed and accurate evaluation of male sexual function [8]. It has recently been utilized to assess sexual dysfunction in Korean and Thai patients enrolled in the Sexuality and the Management of BPH with Alfuzosin (SAMBA) trial [15,16]. To the best of our knowledge, the present study is the first study to assess the effect of alfuzosin 10 mg once daily on sexual function in Taiwanese patients, utilizing the MSHQ and International Index of Erectile Function—five‐item (IIEF‐5), and to confirm its efficacy and safety profile.…”
To assess the effect of alfuzosin (XATRAL) 10 mg once daily on sexual function in men with moderate to severe lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH), patients with suggestive symptomatic BPH, an International Prostate Symptom Score (IPSS) >8 (range of scores, 0-35), and sexual attempts at least once per month were enrolled. All patients received alfuzosin 10 mg once daily for 24 weeks and were asked to complete the IPSS test and Male Sexual Health Questionnaire at weeks 0 (baseline), 1, 4, 12, and 24. Other assessments included the International Index of Erectile Function-five-item version (range of scores: 5-25), as well as onset of action and peak urinary flow rate (Q(max)). From September 2006 to May 2008, 279 patients were enrolled from nine centers in Taiwan. At 24 weeks, alfuzosin effectively improved LUTS and quality of life, as demonstrated by a reduction in the IPSS total score (17.3 vs. 9.9, p < 0.001) and the IPSS bother score (3.8 vs. 2.5, p < 0.001). The majority (85%) of patients perceived an improvement of urinary symptoms within 1 month of administration. In patients with an International Index of Erectile Function-five-item version score of ≤16, alfuzosin significantly improved erectile disorder and satisfaction subscores at each time point (p ≤ 0.02). Prolonged-release alfuzosin effectively improved LUTS, quality of life, erectile function, and sexual satisfaction in men with BPH and mild to severe erectile dysfunction. Alfuzosin is an effective treatment option for the management of patients with BPH/LUTS and concomitant sexual dysfunction.
A water-soluble chitosan derivative namely, N-(2-hydroxy) propyl-3-trimethylammonium chitosan chloride (HTCC) was synthesized by the reaction of chitosan with glycidyltrimethyl ammonium chloride in a neutral aqueous condition and solution blended with polyacrylonitrile (PAN) in an organic solvent. Polymeric films were made by casting, and they were dyed with an acid dye, a basic dye, and mixture of them. Results obtained from differential scanning calorimetry, scanning electron microscopy, and dyeing show that these polymers are immiscible even at low percentage of HTCC (lower than 20%). However, at higher ratio, the phase separation takes place.Fibers obtained from this blend system by wet-spinning technique show a good mechanical properties and increasing the amount of HTCC causes an increment in the mechanical strength of the fibers up to 20% of HTCC and beyond that due to phase separation mechanical strength reduces. Blending PAN with HTCC improves the dyeing behavior of the films and fibers.
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