Evaluation of intermittent tamsulosin in treating symptomatic patients with benign prostatic hyperplasia.

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Urology Annals Pub Date : 2023-01-01 Epub Date: 2022-11-08 DOI:10.4103/ua.ua_143_21
Mohamed G Soliman, Mohammed R Al-Ghadeer, Hasan R Al-Shabaan, Amer H Al-Hamrani, Hussain Adil AlGhadeer
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Abstract

Purpose: The purpose of this study is to evaluate and assess the effect of intermittent tamsulosin treatment as a trial to increase the drug safety (in terms of reducing the drug side effects, particularly retrograde ejaculation) while maintaining the effect in reducing the symptoms and assess its impact on the patients' quality of life.

Materials and methods: Patients who enrolled in this study were suffering from lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH) and were using 0.4 mg tamsulosin daily to relieve their symptoms but complained of ejaculatory problems. A baseline assessment involves medical history and evaluation of ejaculatory function abdominopelvic ultrasound, postvoid residual volume (PVR) estimation, the International Prostate Symptom Score (IPSS), quality of life assessed using global satisfaction, vital signs, physical examination including digital rectal examination, and renal function. During the study, patients consented to take 0.4 mg tamsulosin intermittently every other day and to proceed with their sexual activities on the days they did not take the drug in. Baseline assessment was repeated and recorded after 3 months from starting the treatment. The adverse effects and compliance were analyzed in all patients.

Results: Twenty-five patients had a mean baseline IPSS of 6.6 ± 1 and baseline PVR of 87.6 ± 15.1 ml. At the 3rd month, the mean PVR was 100.4 ± 15.1 ml and the mean IPSS was 7.3 ± 1.1. Moreover, 20 out of the total number of 25 patients (80%) reported improvement in their ejaculation. All our 20 patients who showed improvement in their ejaculatory function are either satisfied or very satisfied (4 or 5), in regard to the global satisfaction rate.

Conclusion: Intermittent tamsulosin therapy (0.4 mg/every other day) is well-tolerated and shows a potential advantage in recovery in patients who suffer from LUTS/BPH and complaining from abnormal ejaculation, especially absent ejaculate. Although there was a significant change in PVR and IPSS after using intermittent tamsulosin therapy. Most patients show a higher overall satisfaction with the treatment compared to the standard dose (0.4 mg/daily). A study on a larger scale is still needed to confirm our results.

Abstract Image

Abstract Image

间歇性坦洛新治疗有症状的良性前列腺增生症的疗效评价。
目的:本研究的目的是评估和评估间歇性坦洛新治疗的效果,作为一项试验,以提高药物安全性(减少药物副作用,特别是逆行射精),同时保持减少症状的效果,并评估其对患者生活质量的影响。材料和方法:参与本研究的患者因良性前列腺增生(BPH)而出现下尿路症状(LUTS),每天使用0.4mg坦洛新缓解症状,但抱怨射精问题。基线评估包括病史和射精功能评估-腹盆超声、排尿后残余容量(PVR)估计、国际前列腺症状评分(IPSS)、使用总体满意度评估的生活质量、生命体征、体检(包括直肠指检)和肾功能。在研究过程中,患者同意每隔一天间歇性服用0.4mg坦索罗辛,并在未服用该药物的日子继续进行性活动。在开始治疗3个月后,重复并记录基线评估。分析所有患者的不良反应和依从性。结果:25例患者的平均基线IPSS为6.6±1,基线PVR为87.6±15.1 ml。第3个月时,平均PVR为100.4±15.1 ml,平均IPSS为7.3±1.1。此外,在总共25名患者中,有20名(80%)报告他们的射精情况有所改善。就总体满意度而言,我们所有20名射精功能改善的患者要么满意,要么非常满意(4或5)。结论:坦洛新间歇治疗(0.4mg/每隔一天)耐受性良好,对LUTS/BHP患者和抱怨射精异常,尤其是无射精的患者具有潜在的康复优势。尽管使用坦索罗辛间歇性治疗后PVR和IPSS有显著变化。与标准剂量(0.4mg/天)相比,大多数患者对治疗的总体满意度更高。仍然需要进行更大规模的研究来证实我们的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Urology Annals
Urology Annals UROLOGY & NEPHROLOGY-
CiteScore
1.20
自引率
0.00%
发文量
59
审稿时长
31 weeks
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