Michele Scialpi, Eugenio Martorana, Pietro Scialpi, Alfredo D'Andrea, Francesco Maria Mancioli, Marcello Mignogna, Aldo Di Blasi, Fabio Trippa
Prostate specific antigen (PSA) remains the most used test to assess the response after therapies including the radiation therapy (RT). Apparent diffusion coefficient (ADC) derived from the conventional diffusionweighted imaging (DWI), as a part of noncontrast or biparametric MRI (bpMRI) (T2-weighted and DWI), offers diagnostic accuracy and cancer detection rate equivalent to that of multiparametric MRI. Cellular changes induced by RT can be quali-qualitatively demonstrated as early as 3months after RT as an increase in the signal intensity of the tumor on the ADC map. ADC, in association with PSA, represents a potential biomarker imaging for evaluating treatment efficacy in PCa both during and shortly after RT.
{"title":"MRI apparent diffusion coefficient (ADC): A biomarker for prostate cancer after radiation therapy.","authors":"Michele Scialpi, Eugenio Martorana, Pietro Scialpi, Alfredo D'Andrea, Francesco Maria Mancioli, Marcello Mignogna, Aldo Di Blasi, Fabio Trippa","doi":"10.5152/tud.2021.21274","DOIUrl":"https://doi.org/10.5152/tud.2021.21274","url":null,"abstract":"<p><p>Prostate specific antigen (PSA) remains the most used test to assess the response after therapies including the radiation therapy (RT). Apparent diffusion coefficient (ADC) derived from the conventional diffusionweighted imaging (DWI), as a part of noncontrast or biparametric MRI (bpMRI) (T2-weighted and DWI), offers diagnostic accuracy and cancer detection rate equivalent to that of multiparametric MRI. Cellular changes induced by RT can be quali-qualitatively demonstrated as early as 3months after RT as an increase in the signal intensity of the tumor on the ADC map. ADC, in association with PSA, represents a potential biomarker imaging for evaluating treatment efficacy in PCa both during and shortly after RT.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"448-451"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612745/pdf/tju-47-6-448.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39586393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dwi Nanda Satriyo Arif Wibowo, Doddy Moesbadianto Soebadi, Mohammad Ayodhia Soebadi
In recent years, several studies have reported promising results of Yohimbine as a natural supplement for erectile dysfunction (ED). However, several studies suggested that the aphrodisiac effects of the extract were only a placebo or due to the increase in peripheral vascular congestion. In contrast, other studies reported that it could provide excellent curative effects on organic impotence. We aimed to review the efficacy of Yohimbine as a pharmacological treatment for ED and performed a comprehensive systematic search of published articles in PubMed and Science Direct databases for eligible randomized controlled trials comparing Yohimbine to placebo or no treatment for ED patients. A total of eight studies out of 543 studies were included in this review. Both Yohimbine alone (odds ratio [OR] ¼ 2.08, 95% CI 1.30-3.32, P ¼ .002) and combined (OR ¼ 6.35, 95% CI 3.01-13.41, P < .001) showed a significantly greater probability of erectile function improvement compared to the placebo group (OR ¼ 2.87, 95% CI 1.94-4.25, P < .001). Yohimbine alone did not show a significant difference in the rate of improved sexual function (P ¼ .07); however, the pooled results of both subgroups indicated a higher rate of improved sexual function (OR ¼ 2.65, 95% CI 1.43-4.92, P ¼ .002). Sole administration of Yohimbine and its combination with other supplements can improve the erectile function in ED patients. However, it is not able to improve the sexual function if not combined with other treatments.
{"title":"Yohimbine as a treatment for erectile dysfunction: A systematic review and meta-analysis.","authors":"Dwi Nanda Satriyo Arif Wibowo, Doddy Moesbadianto Soebadi, Mohammad Ayodhia Soebadi","doi":"10.5152/tud.2021.21206","DOIUrl":"10.5152/tud.2021.21206","url":null,"abstract":"<p><p>In recent years, several studies have reported promising results of Yohimbine as a natural supplement for erectile dysfunction (ED). However, several studies suggested that the aphrodisiac effects of the extract were only a placebo or due to the increase in peripheral vascular congestion. In contrast, other studies reported that it could provide excellent curative effects on organic impotence. We aimed to review the efficacy of Yohimbine as a pharmacological treatment for ED and performed a comprehensive systematic search of published articles in PubMed and Science Direct databases for eligible randomized controlled trials comparing Yohimbine to placebo or no treatment for ED patients. A total of eight studies out of 543 studies were included in this review. Both Yohimbine alone (odds ratio [OR] ¼ 2.08, 95% CI 1.30-3.32, P ¼ .002) and combined (OR ¼ 6.35, 95% CI 3.01-13.41, P < .001) showed a significantly greater probability of erectile function improvement compared to the placebo group (OR ¼ 2.87, 95% CI 1.94-4.25, P < .001). Yohimbine alone did not show a significant difference in the rate of improved sexual function (P ¼ .07); however, the pooled results of both subgroups indicated a higher rate of improved sexual function (OR ¼ 2.65, 95% CI 1.43-4.92, P ¼ .002). Sole administration of Yohimbine and its combination with other supplements can improve the erectile function in ED patients. However, it is not able to improve the sexual function if not combined with other treatments.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"482-488"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612744/pdf/tju-47-6-482.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888406","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: To investigate an adapted enhanced recovery after surgery (ERAS) protocol in adult augmentation cystoplasty (AC).
Material and methods: A total of 33 consecutive cases with a history of refractory idiopathic detrusor overactivity (IDO) or neurogenic bladder (NGB) with low capacity, poor compliance, high sustained detrusor pressure, and whose previous therapeutic methods had failed were enrolled. The adapted ERAS fasting8 hours, high protein, low carbohydrate diet, antibiotics, did not use narcotics as much as possible during anesthesia, acetaminophen, early nasogastric tube removal, neostigmine injection postoperation, metoclopramide, early oral diet, and mobilization were applied, and morbidity and hospital stay duration were analyzed.
Results: Twenty-two patients had IDO, and the remained cases were NGB or had low bladder capacity or compliance. The mean age of patients in the IDO group was higher than in NGB cases (P ¼ .020). Following the adapted ERAS protocol implementation, more than two-third of patients returned to a regular diet on the second day postoperation in both groups. The mean (SD) hospital stay duration was 7.7 (1.5) days. Postoperative fasting time was 8.8 6 3. 7 hours, and bowel function was returned 1 day postoperation in 82% of patients. Only 33.3% of adults need postprocedure acetaminophen for 2 days, and in 11 cases, it prescribed for 1 day. All subjects except paraplegic patients had early mobilization 1 day postoperation.
Conclusion: Our findings revealed that adapted ERAS protocol could be safe and effective in adult AC. It accompanied by few complications, reduced intestinal motility problems, and a short length of hospital stay.
{"title":"An adapted enhanced recovery protocol for adult augmentation cystoplasty in limited sources countries: A pilot clinical trial.","authors":"Elham Jahantabi, Farzin Soleimanzadeh, Hanieh Salehi-Pourmehr, Mahsa Zehi Saadat, Maryam Nouri, Sakineh Hajebrahimi","doi":"10.5152/tud.2021.21108","DOIUrl":"https://doi.org/10.5152/tud.2021.21108","url":null,"abstract":"<p><strong>Objective: </strong>To investigate an adapted enhanced recovery after surgery (ERAS) protocol in adult augmentation cystoplasty (AC).</p><p><strong>Material and methods: </strong>A total of 33 consecutive cases with a history of refractory idiopathic detrusor overactivity (IDO) or neurogenic bladder (NGB) with low capacity, poor compliance, high sustained detrusor pressure, and whose previous therapeutic methods had failed were enrolled. The adapted ERAS fasting8 hours, high protein, low carbohydrate diet, antibiotics, did not use narcotics as much as possible during anesthesia, acetaminophen, early nasogastric tube removal, neostigmine injection postoperation, metoclopramide, early oral diet, and mobilization were applied, and morbidity and hospital stay duration were analyzed.</p><p><strong>Results: </strong>Twenty-two patients had IDO, and the remained cases were NGB or had low bladder capacity or compliance. The mean age of patients in the IDO group was higher than in NGB cases (P ¼ .020). Following the adapted ERAS protocol implementation, more than two-third of patients returned to a regular diet on the second day postoperation in both groups. The mean (SD) hospital stay duration was 7.7 (1.5) days. Postoperative fasting time was 8.8 6 3. 7 hours, and bowel function was returned 1 day postoperation in 82% of patients. Only 33.3% of adults need postprocedure acetaminophen for 2 days, and in 11 cases, it prescribed for 1 day. All subjects except paraplegic patients had early mobilization 1 day postoperation.</p><p><strong>Conclusion: </strong>Our findings revealed that adapted ERAS protocol could be safe and effective in adult AC. It accompanied by few complications, reduced intestinal motility problems, and a short length of hospital stay.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"509-517"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/97/c0/tju-47-6-509.PMC9612747.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888410","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: The protective effect of androgen deprivation therapy (ADT) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel hypothesis. ADT may protect patients with prostate cancer through the inhibition of androgen receptor-dependent transmembrane serine protease type 2. We analyzed the role of ADT on SARS-CoV-2 infection risk and disease severity.
Material and methods: Between August 2020 and June 2021, patients with prostate cancer were included in our study. Patients were divided into two groups as men receiving ADT or not. Patients' characteristics such as prostate cancer grade and stage, comorbidities, SARS-CoV-2 infection status, and infection severity were assessed. SARS-CoV-2-infected close relatives and patients' compliance with the precautions against SARSCoV- 2 were also analyzed.
Results: A total of 365 patients, 138 (37.8%) with ADT and 227 (62.2%) without ADT, were included in our analysis. Patients with ADT were older (71.8 vs 66.9 years, P ¼ .001) and had a higher rate of chronic obstructive pulmonary disease (11.6% vs 5.7%, P ¼ .044). Patients receiving ADT were more often locally advanced and metastatic (80.4% vs 32.6%, P ¼ .001). SARS-CoV-2 infection rates were statistically similar between patients who received and did not receive ADT (9.4% vs 13.2%, P ¼ .275, respectively). There was no significant difference between two groups in terms of hospitalization rates (2.9% vs 0.9%, P ¼ .205). In multivariate analysis, the presence of SARS-CoV-2-infected close relatives and precautions score were only independent predictors for both risk of SARS-CoV-2 infection and infection severity.
Conclusion: We could not find any effect of ADT on risk and severity of SARS-CoV-2 infection. SARSCoV- 2 infection and hospitalization rates were similar between patients with and without ADT.
目的:雄激素剥夺治疗(ADT)对严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的保护作用是一个新的假设。ADT可能通过抑制雄激素受体依赖性跨膜丝氨酸蛋白酶2型来保护前列腺癌患者。我们分析了ADT在SARS-CoV-2感染风险和疾病严重程度中的作用。材料和方法:2020年8月至2021年6月期间,前列腺癌患者纳入我们的研究。患者分为男性和未接受ADT治疗两组。评估患者的特征,如前列腺癌分级和分期、合并症、SARS-CoV-2感染状况、感染严重程度等。分析了sars - cov -2感染的近亲属和患者对sars - cov -2预防措施的依从性。结果:共纳入365例患者,其中ADT患者138例(37.8%),非ADT患者227例(62.2%)。ADT患者年龄较大(71.8岁vs 66.9岁,P < 0.001),慢性阻塞性肺疾病发生率较高(11.6% vs 5.7%, P < 0.044)。接受ADT治疗的患者多为局部晚期和转移性患者(80.4% vs 32.6%, P < 0.001)。接受ADT治疗和未接受ADT治疗的患者的SARS-CoV-2感染率在统计学上相似(分别为9.4%和13.2%,P = 0.275)。两组住院率差异无统计学意义(2.9% vs 0.9%, P < 0.05)。在多因素分析中,近亲属感染SARS-CoV-2和预防措施评分仅是SARS-CoV-2感染风险和感染严重程度的独立预测因子。结论:未发现ADT对SARS-CoV-2感染风险和严重程度有影响。ADT患者和非ADT患者的SARSCoV- 2感染和住院率相似。
{"title":"The clinical impact of androgen deprivation therapy on SARS-CoV-2 infection rates and disease severity.","authors":"Özgür Kazan, Meftun Çulpan, Özgür Efiloğlu, Gökhan Atiş, Asıf Yildirim","doi":"10.5152/tud.2021.21278","DOIUrl":"https://doi.org/10.5152/tud.2021.21278","url":null,"abstract":"<p><strong>Objective: </strong>The protective effect of androgen deprivation therapy (ADT) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel hypothesis. ADT may protect patients with prostate cancer through the inhibition of androgen receptor-dependent transmembrane serine protease type 2. We analyzed the role of ADT on SARS-CoV-2 infection risk and disease severity.</p><p><strong>Material and methods: </strong>Between August 2020 and June 2021, patients with prostate cancer were included in our study. Patients were divided into two groups as men receiving ADT or not. Patients' characteristics such as prostate cancer grade and stage, comorbidities, SARS-CoV-2 infection status, and infection severity were assessed. SARS-CoV-2-infected close relatives and patients' compliance with the precautions against SARSCoV- 2 were also analyzed.</p><p><strong>Results: </strong>A total of 365 patients, 138 (37.8%) with ADT and 227 (62.2%) without ADT, were included in our analysis. Patients with ADT were older (71.8 vs 66.9 years, P ¼ .001) and had a higher rate of chronic obstructive pulmonary disease (11.6% vs 5.7%, P ¼ .044). Patients receiving ADT were more often locally advanced and metastatic (80.4% vs 32.6%, P ¼ .001). SARS-CoV-2 infection rates were statistically similar between patients who received and did not receive ADT (9.4% vs 13.2%, P ¼ .275, respectively). There was no significant difference between two groups in terms of hospitalization rates (2.9% vs 0.9%, P ¼ .205). In multivariate analysis, the presence of SARS-CoV-2-infected close relatives and precautions score were only independent predictors for both risk of SARS-CoV-2 infection and infection severity.</p><p><strong>Conclusion: </strong>We could not find any effect of ADT on risk and severity of SARS-CoV-2 infection. SARSCoV- 2 infection and hospitalization rates were similar between patients with and without ADT.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"495-500"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e5/f6/tju-47-6-495.PMC9612749.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888408","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Elif Gezginci, Derya Suluhan, Mehmet Bahadir Caliskan
Objective: Distraction is a nonpharmacological method commonly used during painful procedures in children. However, there are a few studies investigating the effectiveness of active distraction on pain and anxiety in children during circumcision. The purpose of this study was to evaluate the effectiveness of tablet-based interactive distraction on pain and anxiety in children during circumcision.
Material and methods: To evaluate how tablet distraction could improve children's outcomes during circumcision, a single-center, nonblinded, randomized controlled, parallel group trial research design was employed. In this study, 35 children were included in tablet distraction group, which have a control group (n ¼ 35). The primary outcome measure was the Numeric Rating Scale for pain. Secondary outcome measure was the State- Trait Anxiety Scale for Children, and other outcome variables were physiological parameters and satisfaction levels.
Results: During and after the surgical procedure, pain scores (P < .001, P < .001, respectively) and pulse rates (P < .001, P < .001, respectively) were significantly lower in the tablet distraction group, whereas O2 saturation was higher than the control group (P < .001, P < .001, respectively). After the procedure, the anxiety scores were significantly lower in the tablet distraction group (P < .001), whereas the satisfaction scores were higher than control group (P < .001).
Conclusion: This study concluded that the use of tablet distraction during circumcision has a positive effect on children's pain, anxiety, satisfaction levels, and physiological parameters.
目的:分散注意力是儿童疼痛过程中常用的一种非药物治疗方法。然而,有一些研究调查了主动分心对包皮环切术中儿童疼痛和焦虑的有效性。本研究的目的是评估基于片剂的交互式分心对包皮环切术中儿童疼痛和焦虑的有效性。材料和方法:为了评估平板分心如何改善包皮环切术中儿童的预后,采用单中心、非盲、随机对照、平行组试验研究设计。本研究将35名儿童纳入平板电脑分心组,并设对照组(n / 35)。主要结果测量是疼痛的数值评定量表。次要结果测量是儿童状态-特质焦虑量表,其他结果变量是生理参数和满意度。结果:术中、术后,撑开片组疼痛评分(P < 0.001, P < 0.001)、脉搏率(P < 0.001, P < 0.001)明显低于对照组,血氧饱和度明显高于对照组(P < 0.001, P < 0.001)。术后,平板分心组焦虑得分显著低于对照组(P < 0.001),满意度得分显著高于对照组(P < 0.001)。结论:本研究认为,包皮环切术中使用分散药片对儿童的疼痛、焦虑、满意度和生理参数有积极影响。
{"title":"Is tablet-based interactive distraction effective on pain and anxiety during circumcision in children? A randomized controlled trial.","authors":"Elif Gezginci, Derya Suluhan, Mehmet Bahadir Caliskan","doi":"10.5152/tud.2021.21228","DOIUrl":"https://doi.org/10.5152/tud.2021.21228","url":null,"abstract":"<p><strong>Objective: </strong>Distraction is a nonpharmacological method commonly used during painful procedures in children. However, there are a few studies investigating the effectiveness of active distraction on pain and anxiety in children during circumcision. The purpose of this study was to evaluate the effectiveness of tablet-based interactive distraction on pain and anxiety in children during circumcision.</p><p><strong>Material and methods: </strong>To evaluate how tablet distraction could improve children's outcomes during circumcision, a single-center, nonblinded, randomized controlled, parallel group trial research design was employed. In this study, 35 children were included in tablet distraction group, which have a control group (n ¼ 35). The primary outcome measure was the Numeric Rating Scale for pain. Secondary outcome measure was the State- Trait Anxiety Scale for Children, and other outcome variables were physiological parameters and satisfaction levels.</p><p><strong>Results: </strong>During and after the surgical procedure, pain scores (P < .001, P < .001, respectively) and pulse rates (P < .001, P < .001, respectively) were significantly lower in the tablet distraction group, whereas O2 saturation was higher than the control group (P < .001, P < .001, respectively). After the procedure, the anxiety scores were significantly lower in the tablet distraction group (P < .001), whereas the satisfaction scores were higher than control group (P < .001).</p><p><strong>Conclusion: </strong>This study concluded that the use of tablet distraction during circumcision has a positive effect on children's pain, anxiety, satisfaction levels, and physiological parameters.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"518-525"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/1e/99/tju-47-6-518.PMC9612746.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Giorgio Bozzini, Lorenzo Berti, Matteo Maltagliati, Carmine Sciorio, Maria Chiara Sighinolfi, Salvatore Micali, Javier Romero Otero, Carlo Buizza, Bernardo Rocco
Endoscopic enucleation of the prostate (EEP) techniques for the treatment of benign prostatic hyperplasia (BPH) have become increasingly popular among urologists over the past 23 years. Despite the energy source employed, the aim of all these procedures is to endoscopically remove the prostatic lobes by enucleating them from the prostate surgical capsule. The reasons for which EEP has gained popularity among urologists are the reduction in complications and hospital stay compared to endoscopic gold standard Transurethral Resection of the Prostate (TURP), but especially the possibility to treat large prostates, allowing to abandon open simple prostatectomy (OP) and to avoid the burden related to open surgery. Holmium laser enucleation of the prostate (HoLEP) sets the basic principles of all EEP techniques in 1998 and has become the treatment of reference for BPH. Since then, various lasers have been developed and applied to prostatic enucleation. The thulium laser has a slightly shorter wavelength compared to the holmium laser and a continuous wave output, which increase vaporization and reduce penetration depth. These features make it ideal for prostatic enucleation. A vapoenucleating technique called Thulium Laser Vapoenucleation of the Prostate was presented in 2009, followed by a blunt enucleating technique called Thulium Laser Enucleation of the Prostate in 2010. These techniques have become alternatives to HoLEP and TURP; however, the amount of literature and randomized controlled trials available are inferior compared to HoLEP. The aim of th describe, and discuss current evidence on thulium enucleating techniques.
{"title":"Current evidence of ThuLEP for BPH: A review of literature.","authors":"Giorgio Bozzini, Lorenzo Berti, Matteo Maltagliati, Carmine Sciorio, Maria Chiara Sighinolfi, Salvatore Micali, Javier Romero Otero, Carlo Buizza, Bernardo Rocco","doi":"10.5152/tud.2021.21170","DOIUrl":"https://doi.org/10.5152/tud.2021.21170","url":null,"abstract":"<p><p>Endoscopic enucleation of the prostate (EEP) techniques for the treatment of benign prostatic hyperplasia (BPH) have become increasingly popular among urologists over the past 23 years. Despite the energy source employed, the aim of all these procedures is to endoscopically remove the prostatic lobes by enucleating them from the prostate surgical capsule. The reasons for which EEP has gained popularity among urologists are the reduction in complications and hospital stay compared to endoscopic gold standard Transurethral Resection of the Prostate (TURP), but especially the possibility to treat large prostates, allowing to abandon open simple prostatectomy (OP) and to avoid the burden related to open surgery. Holmium laser enucleation of the prostate (HoLEP) sets the basic principles of all EEP techniques in 1998 and has become the treatment of reference for BPH. Since then, various lasers have been developed and applied to prostatic enucleation. The thulium laser has a slightly shorter wavelength compared to the holmium laser and a continuous wave output, which increase vaporization and reduce penetration depth. These features make it ideal for prostatic enucleation. A vapoenucleating technique called Thulium Laser Vapoenucleation of the Prostate was presented in 2009, followed by a blunt enucleating technique called Thulium Laser Enucleation of the Prostate in 2010. These techniques have become alternatives to HoLEP and TURP; however, the amount of literature and randomized controlled trials available are inferior compared to HoLEP. The aim of th describe, and discuss current evidence on thulium enucleating techniques.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"461-469"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/44/be/tju-47-6-461.PMC9612748.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39586395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andrea Cocci, Alessia Celeste Bocchino, Gianmartin Cito, Antonello De Lisa, Giorgio Ivan Russo, Arturo Lo Giudice, Francesco Sessa, Lorenzo Viola, Luca Cindolo, Bhaskar K Somani, Giampaolo Siena
The aim of this study was to review the available literature on the efficacy and safety of the Rezum system for the treatment of symptomatic benign prostatic hyperplasia (BPH). A revision of literature up to January 2021 was carried out. Medline, Scopus, Web of Science, and PubMed archives were screened to identify all the relevant studies investigating the role of Rezum in the treatment of BPH. Randomized controlled trial (RCT), retrospective, prospective, observational, and comparative studies were included. Finally, 17 studies were included, five of which reporting data of a double blind Rezum RCT. Overall, 1,451 patients underwent Rezum procedure. All the studies performed a minimum of 3 months follow-up. Preoperatively, the mean International Prostate Symptom Score (IPSS) score was 19.8, mean Qmax was 9.2mL s1, and mean PVR was 142 cc. At 3 months after surgery, the mean IPSS score was 1.5, mean Qmax was 13.7mL s1, and mean PVR was 74 cc. Six studies investigated sexual function, most of them using the International Index of Erectile Function (IIEF)-5 questionnaire and a few also the Male Sexual Health Questionnaire (MSHQ). Preoperative mean IIEF-5 score was 18.5, and the mean MSHQ score was 7.4. At the 3 months follow-up, the mean IIEF-5 score was 16.4, and the mean MSHQ score was 9.62. None of the studies reported intraoperative complications. Rezum system is a novel minimally invasive treatment for symptomatic BPH using transurethral water vapor thermal energy. It represents a cost-effective and safe procedure with durable relief of lower urinary tract symptom, preservation of sexual function, low complications rate, and short recovery time.
本研究的目的是回顾有关Rezum系统治疗症状性良性前列腺增生(BPH)的有效性和安全性的现有文献。对截至2021年1月的文献进行了修订。对Medline、Scopus、Web of Science和PubMed档案进行筛选,以确定所有调查Rezum在治疗BPH中的作用的相关研究。包括随机对照试验(RCT)、回顾性、前瞻性、观察性和比较研究。最后,纳入了17项研究,其中5项报告了双盲Rezum RCT的数据。总的来说,1451名患者接受了Rezum手术。所有的研究都进行了至少3个月的随访。术前国际前列腺症状评分(IPSS)平均评分为19.8分,平均Qmax为9.2mL s1,平均PVR为142 cc,术后3个月IPSS平均评分为1.5分,平均Qmax为13.7mL s1,平均PVR为74 cc。6项研究对性功能进行了调查,多数采用国际勃起功能指数(IIEF)-5问卷,少数采用男性性健康问卷(MSHQ)。术前IIEF-5平均评分为18.5,MSHQ平均评分为7.4。随访3个月时,IIEF-5平均评分为16.4分,MSHQ平均评分为9.62分。没有研究报告术中并发症。Rezum系统是一种利用经尿道水蒸汽热能治疗BPH症状的新型微创疗法。它是一种经济有效且安全的手术,持久缓解下尿路症状,保留性功能,并发症发生率低,恢复时间短。
{"title":"Role of Rezum in the treatment of benign prostate hyperplasia: A review of the literature.","authors":"Andrea Cocci, Alessia Celeste Bocchino, Gianmartin Cito, Antonello De Lisa, Giorgio Ivan Russo, Arturo Lo Giudice, Francesco Sessa, Lorenzo Viola, Luca Cindolo, Bhaskar K Somani, Giampaolo Siena","doi":"10.5152/tud.2021.21128","DOIUrl":"https://doi.org/10.5152/tud.2021.21128","url":null,"abstract":"<p><p>The aim of this study was to review the available literature on the efficacy and safety of the Rezum system for the treatment of symptomatic benign prostatic hyperplasia (BPH). A revision of literature up to January 2021 was carried out. Medline, Scopus, Web of Science, and PubMed archives were screened to identify all the relevant studies investigating the role of Rezum in the treatment of BPH. Randomized controlled trial (RCT), retrospective, prospective, observational, and comparative studies were included. Finally, 17 studies were included, five of which reporting data of a double blind Rezum RCT. Overall, 1,451 patients underwent Rezum procedure. All the studies performed a minimum of 3 months follow-up. Preoperatively, the mean International Prostate Symptom Score (IPSS) score was 19.8, mean Qmax was 9.2mL s1, and mean PVR was 142 cc. At 3 months after surgery, the mean IPSS score was 1.5, mean Qmax was 13.7mL s1, and mean PVR was 74 cc. Six studies investigated sexual function, most of them using the International Index of Erectile Function (IIEF)-5 questionnaire and a few also the Male Sexual Health Questionnaire (MSHQ). Preoperative mean IIEF-5 score was 18.5, and the mean MSHQ score was 7.4. At the 3 months follow-up, the mean IIEF-5 score was 16.4, and the mean MSHQ score was 9.62. None of the studies reported intraoperative complications. Rezum system is a novel minimally invasive treatment for symptomatic BPH using transurethral water vapor thermal energy. It represents a cost-effective and safe procedure with durable relief of lower urinary tract symptom, preservation of sexual function, low complications rate, and short recovery time.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"452-460"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e6/51/tju-47-6-452.PMC9612750.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39586394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cristian Fiori, Sabrina De Cillis, Gabriele Volpi, Enrico Checcucci, Giovanni Cattaneo, Juliette Meziere, Matteo Manfredi, Michele Di Dio, Daniele Amparore, Francesco Porpiglia
In the last few years, new technologies have been developed to treat benign prostatic hyperplasia (BPH) in order to offer valid surgical alternatives to transurethral resection of the prostate with lower complications and hospitalization while maintaining satisfactory functional results. Among these new approaches, transurethral implantation of first- and second-generation temporary implantable nitinol device (TIND and iTIND, respectively) (Medi-TateVR ; Medi-Tate Ltd., Or Akiva, Israel) has been proposed. The aim of this work is to describe the surgical technique and to perform a systematic review of the available literature on follow-up of functional outcomes. A systematic research of the available literature on this topic was performed via Medline, Embase, and Cochrane databases in April 2021. Current evidence regarding the implantation of iTIND to treat BPH-related lower urinary tract symptoms (LUTSs) is still limited. Seven studies have been found. Only one randomized controlled trial has been published reporting short-term follow-up of implantation of iTIND versus sham procedure. All the studies reported that both procedures are safe, effective, and well-tolerated. Moreover, such treatment seems to not affect patient's sexual and ejaculatory functions. In conclusions, current clinical evidence suggests that temporary implantation of iTIND is a valid option for the minimally invasive surgical treatment of BPH-related LUTS. Further studies are required in order to confirm the functional results, especially over a long-term follow-up.
{"title":"iTIND for BPH: Technique and procedural outcomes: A narrative review of current literature.","authors":"Cristian Fiori, Sabrina De Cillis, Gabriele Volpi, Enrico Checcucci, Giovanni Cattaneo, Juliette Meziere, Matteo Manfredi, Michele Di Dio, Daniele Amparore, Francesco Porpiglia","doi":"10.5152/tud.2021.21145","DOIUrl":"https://doi.org/10.5152/tud.2021.21145","url":null,"abstract":"<p><p>In the last few years, new technologies have been developed to treat benign prostatic hyperplasia (BPH) in order to offer valid surgical alternatives to transurethral resection of the prostate with lower complications and hospitalization while maintaining satisfactory functional results. Among these new approaches, transurethral implantation of first- and second-generation temporary implantable nitinol device (TIND and iTIND, respectively) (Medi-TateVR ; Medi-Tate Ltd., Or Akiva, Israel) has been proposed. The aim of this work is to describe the surgical technique and to perform a systematic review of the available literature on follow-up of functional outcomes. A systematic research of the available literature on this topic was performed via Medline, Embase, and Cochrane databases in April 2021. Current evidence regarding the implantation of iTIND to treat BPH-related lower urinary tract symptoms (LUTSs) is still limited. Seven studies have been found. Only one randomized controlled trial has been published reporting short-term follow-up of implantation of iTIND versus sham procedure. All the studies reported that both procedures are safe, effective, and well-tolerated. Moreover, such treatment seems to not affect patient's sexual and ejaculatory functions. In conclusions, current clinical evidence suggests that temporary implantation of iTIND is a valid option for the minimally invasive surgical treatment of BPH-related LUTS. Further studies are required in order to confirm the functional results, especially over a long-term follow-up.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"470-481"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/68/48/tju-47-6-470.PMC9612743.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tetuka Bagus Laksita, Yudhistira Pradnyan Kloping, Lukman Hakim, Fikri Rizaldi
Objective: This study aimed to translate the IIEF-5 questionnaire into Indonesian and perform a validity and reliability assessment of the translated instrument.
Material and methods: A methodological study on 106 male outpatients, recruited consecutively, was carried out in a tertiary hospital in Surabaya, East Java from January to March 2020. This study was conducted in two stages: translation and validation. Two independent sworn translators performed a forward and backward translation of the first draft. The final version was synthesized by a team of experts comprised two urologists and another sworn translator. The validity of the questionnaire is determined through a Pearson correlation analysis. Cronbach's a internal consistency measurement was used to assess its reliability. Interrater reliability between the patient and the physician was measured using the Cohen's j coefficient.
Results: Pearson's "r" value is significantly higher than the critical value table and indicates a high to a very high level of validity based on Guilford's interpretation (r ¼ 0.70-1.00). A good internal consistency is shown by the Cronbach's a coefficient value (a ¼ 0.828). An almost perfect agreement between the patient's results and the assessment made by the physicians is shown by the Cohen's j coefficient value (j ¼ 0.879, P < .001).
Conclusion: The Indonesian IIEF-5 is a valid and reliable patient-reported outcome measure for evaluating erectile dysfunction in the literate middle-aged and older adult male population in Indonesia.
{"title":"Translation validity and reliability of the Indonesian version of the 5-item International Index of Erectile Function (IIEF-5).","authors":"Tetuka Bagus Laksita, Yudhistira Pradnyan Kloping, Lukman Hakim, Fikri Rizaldi","doi":"10.5152/tud.2021.21185","DOIUrl":"10.5152/tud.2021.21185","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to translate the IIEF-5 questionnaire into Indonesian and perform a validity and reliability assessment of the translated instrument.</p><p><strong>Material and methods: </strong>A methodological study on 106 male outpatients, recruited consecutively, was carried out in a tertiary hospital in Surabaya, East Java from January to March 2020. This study was conducted in two stages: translation and validation. Two independent sworn translators performed a forward and backward translation of the first draft. The final version was synthesized by a team of experts comprised two urologists and another sworn translator. The validity of the questionnaire is determined through a Pearson correlation analysis. Cronbach's a internal consistency measurement was used to assess its reliability. Interrater reliability between the patient and the physician was measured using the Cohen's j coefficient.</p><p><strong>Results: </strong>Pearson's \"r\" value is significantly higher than the critical value table and indicates a high to a very high level of validity based on Guilford's interpretation (r ¼ 0.70-1.00). A good internal consistency is shown by the Cronbach's a coefficient value (a ¼ 0.828). An almost perfect agreement between the patient's results and the assessment made by the physicians is shown by the Cohen's j coefficient value (j ¼ 0.879, P < .001).</p><p><strong>Conclusion: </strong>The Indonesian IIEF-5 is a valid and reliable patient-reported outcome measure for evaluating erectile dysfunction in the literate middle-aged and older adult male population in Indonesia.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"489-494"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3f/93/tju-47-6-489.PMC9612751.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Muhammed Arif İbis, Selahittin Cayan, Zafer Tokatli, İrfan Orhan, Ramazan Ascı, Fatih Kocamanoglu, Erdem Akbay, Onder Yaman
Objective: The aim of this study is to show the surgical trend over the past 14 years using the data from five major centers in Turkey with accumulated experience in benign prostatic hyperplasia (BPH) surgery.
Material and methods: This study included 94,954 patients with low urinary tract symptoms (LUTSs) secondary to BPH. By using electronic databases, we identified 7,163 patients who underwent BPH surgery, including monopolar transurethral prostate resection (M-TURP), bipolar transurethral prostate resection (BTURP), transurethral incision of the prostate (TUIP), open prostatectomy (OP), and holmium laser enucleation of the prostate (HoLEP) from 2006 to 2019. The years were grouped as 2006-2010, 2011-2015, and 2016-2019.
Results: The total number of outpatient treatments for BPH increased by 72.9% from 5,379 in 2006 to 9,302 in 2019. Until 2019, the annual number of surgeries increased from 375 to 937 (increasing 150%). All surgical approaches for BPH, except TUIP, were most frequently performed between the ages of 60 and 69. The rate of surgery including M-TURP, B-TURP, and TUIP was statistically different between 2006 and 2010, 2011 and 2015, and 2016 and 2019 (P < .001), except OP (P ¼ .071). The highest increase was observed in HoLEP in the first half of the 2010s compared to the second half of the 2010s. The rate of M-TURP decreased from 77.9% to 17.9% from 2016 to 2019.
Conclusion: With the aging population, the number of patients diagnosed and treated with BPH is increasing. B-TURP as a resection technique and HoLEP as an enucleation technique replace M-TURP. Healthcare services and government spending should be organized according to these data.
{"title":"Trends in benign prostatic hyperplasia surgery over the years: A multicenter 14-year retrospective study.","authors":"Muhammed Arif İbis, Selahittin Cayan, Zafer Tokatli, İrfan Orhan, Ramazan Ascı, Fatih Kocamanoglu, Erdem Akbay, Onder Yaman","doi":"10.5152/tud.2021.21262","DOIUrl":"https://doi.org/10.5152/tud.2021.21262","url":null,"abstract":"<p><strong>Objective: </strong>The aim of this study is to show the surgical trend over the past 14 years using the data from five major centers in Turkey with accumulated experience in benign prostatic hyperplasia (BPH) surgery.</p><p><strong>Material and methods: </strong>This study included 94,954 patients with low urinary tract symptoms (LUTSs) secondary to BPH. By using electronic databases, we identified 7,163 patients who underwent BPH surgery, including monopolar transurethral prostate resection (M-TURP), bipolar transurethral prostate resection (BTURP), transurethral incision of the prostate (TUIP), open prostatectomy (OP), and holmium laser enucleation of the prostate (HoLEP) from 2006 to 2019. The years were grouped as 2006-2010, 2011-2015, and 2016-2019.</p><p><strong>Results: </strong>The total number of outpatient treatments for BPH increased by 72.9% from 5,379 in 2006 to 9,302 in 2019. Until 2019, the annual number of surgeries increased from 375 to 937 (increasing 150%). All surgical approaches for BPH, except TUIP, were most frequently performed between the ages of 60 and 69. The rate of surgery including M-TURP, B-TURP, and TUIP was statistically different between 2006 and 2010, 2011 and 2015, and 2016 and 2019 (P < .001), except OP (P ¼ .071). The highest increase was observed in HoLEP in the first half of the 2010s compared to the second half of the 2010s. The rate of M-TURP decreased from 77.9% to 17.9% from 2016 to 2019.</p><p><strong>Conclusion: </strong>With the aging population, the number of patients diagnosed and treated with BPH is increasing. B-TURP as a resection technique and HoLEP as an enucleation technique replace M-TURP. Healthcare services and government spending should be organized according to these data.</p>","PeriodicalId":23366,"journal":{"name":"Turkish journal of urology","volume":"47 6","pages":"501-508"},"PeriodicalIF":1.3,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8f/5f/tju-47-6-501.PMC9612752.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39888409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}