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Initial experience of the Versius robotic system in robot-assisted radical prostatectomy: a study of 58 cases. Versius机器人系统在机器人辅助根治性前列腺切除术中的初步经验:对58例病例的研究。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-08 DOI: 10.5173/ceju.2023.241
Wojciech Polom, Marcin Matuszewski

Introduction: The study presents the initial outcomes of robot-assisted radical prostatectomies (RARPs) using the Versius robotic system in a urological centre with no prior robotic surgery experience.

Material and methods: A retrospective analysis of 58 RARPs was conducted, including patients' parameters as well as Versius system performance.

Results: The study involved 58 patients (average age 66.9 years). Median preoperative prostate specific antigen (PSA) was 9.8 ng/ml, with 48% having ISUP grade group ≥ 3 on biopsy and 25.8% showing extraprostatic extension on MRI. Median blood loss was 437 ml, with complications (10.3% Clavien-Dindo grade II and 4 grade III cases). One conversion to open surgery occurred (0.58%). Final pathology revealed 46.5% extraprostatic disease, and 25.8% had positive margins. Post-surgery, 96.5% had undetectable PSA at 6 weeks. Continence rates were 89.7% at 6 weeks, increasing to 91.3% at 12 months. Median catheter duration was 7.9 days, and the hospital stay was 4.5 days. Console time averaged 150.9 minutes, with a median operative time of 213 minutes. The Versius system reported medium priority alarms in 24.1% of operations, including 1266 alarms related to robotic arm clashes and 43 instrument swaps. One bedside unit exchange occurred with no console or robotic system failures.

Conclusions: The Versius robotic system can be successfully introduced in a urological centre without prior robotic surgery experience. Our setup and operating room positioning are effective, safe, and reproducible. We encountered and resolved surgical and technical challenges. Further follow-up studies are needed to assess the system's performance.

简介:该研究介绍了在一个没有机器人手术经验的泌尿外科中心使用Versius机器人系统进行机器人辅助前列腺癌根治术(RARP)的初步结果:对58例前列腺癌根治术进行了回顾性分析,包括患者参数和Versius系统性能:研究涉及 58 名患者(平均年龄 66.9 岁)。术前前列腺特异性抗原(PSA)中位数为9.8纳克/毫升,48%的患者活检结果为ISUP分级≥3级,25.8%的患者核磁共振成像显示前列腺外扩展。中位失血量为 437 毫升,出现并发症(10.3% 为 Clavien-Dindo II 级,4 例为 III 级)。有一次转为开放手术(0.58%)。最终病理结果显示,46.5%的患者患有前列腺外疾病,25.8%的患者边缘呈阳性。手术后,96.5%的患者在6周时检测不到PSA。6周时的尿失禁率为89.7%,12个月时增至91.3%。导管持续时间中位数为 7.9 天,住院时间为 4.5 天。控制台时间平均为 150.9 分钟,中位手术时间为 213 分钟。Versius系统在24.1%的手术中报告了中等优先级警报,其中包括1266次机械臂冲突警报和43次器械交换警报。在控制台或机器人系统未发生故障的情况下,发生了一次床旁设备交换:结论:没有机器人手术经验的泌尿外科中心也能成功引进 Versius 机器人系统。我们的设置和手术室定位是有效、安全和可重复的。我们遇到并解决了手术和技术方面的难题。需要进一步的后续研究来评估该系统的性能。
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引用次数: 0
The role of gel-infused translabial ultrasound as a new modality in evaluation of female urethral stricture. 注入凝胶的经皮腔超声波作为一种新模式在评估女性尿道狭窄中的作用。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-31 DOI: 10.5173/ceju.2024.168
Nastaran Mahmoudnejad, Alireza Abrishami, Farzaneh Sharifiaghdas, Ramin Borabadi, Mehdi Dadpour, Amirhossein Nayebzade, Mehdi Khazaei

Introduction: To investigate the role of trans-labial ultrasound study in detection of female urethral stenosis (FUS) compared to former cysto-urethroscopy as the currently available definitive diagnostic modality.

Material and methods: In this cross-sectional study, 60 consecutive patients with bladder outlet obstruction diagnosed by clinical symptoms and urodynamic study, were included from 2019 to 2022. For additional assessment, all these patients underwent gel-Infused trans-labial ultrasound (GITLUS) and cystourethroscopy. Trans-labial real-time ultrasonography was performed following the insertion of 20 ml steady stream viscous jelly into the urethral meatus to assess the length of the urethra and exact location and length of the probable narrowing, as well as the presence of peri-urethral fibrosis (PUF).

Results: In GITLUS evaluation, urethral stricture was found in 27 patients. Mean urethral length and stricture length were 35.63 ±4.78 and 17.04 ±10.59, respectively. All these stenosis were confirmed via cysto-urethroscopy. PUF was found in 20 of 27 patients. In cysto-urethroscopy, urethral stricture was confirmed in 40 patients: 13 in urethral meatus and 27 in other parts or pan-urethra. GITLUS could not reveal urethral stricture in 13 patients with meatal stenosis, confirmed with cystoscopy. GITLUS detected FUS less accurately when it involves pure distal urethra compared to other parts of urethra or pan-urethral stenosis (p value = 0.002).

Conclusions: GITLUS is a safe, non-invasive, and valuable technique for detecting FUS. The location and the length of the stricture and probable peri-urethral fibrosis can be identified by this method. However, in meatal or pure short-length distal urethral strictures, this method should be used with caution.

导言研究经腹腔超声检查在女性尿道狭窄(FUS)检测中的作用,与目前可用的明确诊断方式--前膀胱尿道镜检查相比:在这项横断面研究中,从2019年至2022年连续纳入了60名通过临床症状和尿动力学检查确诊的膀胱出口梗阻患者。为了进行额外评估,所有这些患者都接受了凝胶注入式经唇超声检查(GITLUS)和膀胱尿道镜检查。将20毫升稳定流动的粘稠果冻注入尿道肉腔后,进行经唇实时超声检查,以评估尿道长度、可能狭窄的确切位置和长度,以及是否存在尿道周围纤维化(PUF):结果:在 GITLUS 评估中,27 名患者发现了尿道狭窄。平均尿道长度和狭窄长度分别为(35.63 ± 4.78)和(17.04 ± 10.59)。所有这些狭窄均经膀胱尿道镜检查证实。27 名患者中有 20 人发现了 PUF。在膀胱尿道镜检查中,40 名患者被确诊为尿道狭窄:其中 13 例位于尿道肉腔,27 例位于其他部位或泛尿道。GITLUS 无法发现 13 名尿道肉腔狭窄患者的尿道狭窄,膀胱镜检查证实了这一点。与尿道其他部位或全尿道狭窄相比,当 FUS 涉及纯远端尿道时,GITLUS 检测 FUS 的准确性较低(P 值 = 0.002):GITLUS是一种安全、无创、有价值的FUS检测技术。结论:GITLUS 是一种安全、无创和有价值的 FUS 检测技术,可通过该方法确定狭窄的位置和长度以及可能的尿道周围纤维化。但是,对于肉腔或纯短尿道远端狭窄,应谨慎使用这种方法。
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引用次数: 0
The use of indocyanine green in partial nephrectomy: a systematic review. 吲哚菁绿在肾部分切除术中的应用:系统综述。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-08 DOI: 10.5173/ceju.2023.155
Stamatios Katsimperis, Lazaros Tzelves, Themistoklis Bellos, Ioannis Manolitsis, Panagiotis Mourmouris, Nikolaos Kostakopoulos, Nikolaos Pyrgidis, Bhaskar Somani, Athanasios Papatsoris, Andreas Skolarikos

Introduction: The aim of this review was to assess the outcomes of partial nephrectomy using indocyanine green (ICG) regarding ischemia time, positive surgical margins (PSM), estimated blood loss (EBL) and estimated GFR reduction while also suggesting the optimal dosage scheme.

Material and methods: A systematic review was performed using Medline (PubMed), ClinicalTrials.gov, and Cochrane Library (CENTRAL) databases, in concordance with the PRISMA statement. Studies in English regarding the use of indocyanine green in partial nephrectomy were reviewed. Reviews and meta-analyses, editorials, perspectives, and letters to the editors were excluded.

Results: Individual ICG dose was 5 mg in most of the studies. The mean warm ischemia time (WIT) on each study ranged from 11.6 minutes to 27.2 minutes. The reported eGFR reduction ranged from 0% to 15.47%. Lowest mean EBL rate was 48.2 ml and the highest was 347 ml. Positive surgical margin rates were between 0.3% to 11%.

Conclusions: Indocyanine green seems to be a useful tool in partial nephrectomy as it can assist surgeons in identifying tumor and its related vasculature. Thereby, warm ischemia time can be reduced and, in some cases, selective ischemia can be implemented leading to better renal functional preservation.

简介:本综述旨在评估使用吲哚菁绿(ICG)进行肾部分切除术在缺血时间、手术切缘阳性(PSM)、估计失血量(EBL)和估计 GFR 减少方面的结果,同时提出最佳剂量方案:根据 PRISMA 声明,使用 Medline (PubMed)、ClinicalTrials.gov 和 Cochrane Library (CENTRAL) 数据库进行了系统性综述。综述了有关在肾部分切除术中使用吲哚菁绿的英文研究。结果:结果:大多数研究中 ICG 的单次剂量为 5 毫克。每项研究的平均热缺血时间(WIT)从 11.6 分钟到 27.2 分钟不等。报告的 eGFR 降低率从 0% 到 15.47% 不等。平均 EBL 率最低为 48.2 毫升,最高为 347 毫升。手术切缘阳性率在 0.3% 到 11% 之间:吲哚菁绿似乎是肾部分切除术中的一种有用工具,因为它可以帮助外科医生识别肿瘤及其相关血管。结论:吲哚菁绿似乎是肾部分切除术中非常有用的工具,因为它可以帮助外科医生识别肿瘤及其相关血管,从而减少温热缺血时间,在某些情况下还可以实施选择性缺血,从而更好地保留肾功能。
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引用次数: 0
Efficacy and safety of photoselective vaporization of the prostate using the Greenlight XPS 180W laser and simple prostatectomy for high-volume prostate hypertrophy: a comparative analysis. 使用 Greenlight XPS 180W 激光对前列腺进行光选择性汽化和单纯前列腺切除术治疗高容量前列腺肥大的疗效和安全性:对比分析。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-13 DOI: 10.5173/ceju.2023.191
Hubert Burdziak, Tomasz Syryło, Agnieszka Grabińska, Karol Burdziak, Janusz Ławiński, Monika Tomaka, Henryk Zieliński

Introduction: This study aimed to compare the safety and efficacy of treatment using simple prostatectomy (SP) and using photoselective vaporization of the prostate (PVP) with a 180W GreenLight XPS laser in patients with high-volume prostate hypertrophy.

Material and methods: The study included 120 patients with LUTS symptoms caused by prostatic enlargement of more than 80 ml; 79 patients were treated with SP, while 41 were treated with PVP. The analysis included subjective the International Prostate Symptom Score (IPSS) and Quality of Life (QoL), and objective (Qmax), (Qave), and post-void residual volume (PVR) parameters before treatment and at an average of 38 months after surgical treatment. Early and late adverse effects and length of hospitalisation were assessed. Complication reports were performed according to the modified Clavien-Dindo system.

Results: The analysis independently showed the effectiveness of both methods. Subjective parameters (IPSS, QoL), showed no significant differences. Patients treated with SP scored slightly better on objective parameters (Qmax, Qave, and PVR). Analysis of adverse effects and hospitalisation time were more favourable after PVP.

Conclusions: SP and PVP were found to be comparable and highly effective in treating benign prostatic hyperplasia in terms of IPSS and QoL. Patients treated with the SP method obtained slightly better results of objective parameters such as Qmax, Qave, and PVR. Compared with SP, PVP has a more favourable safety profile.

简介本研究旨在比较对高体积前列腺肥大患者使用单纯前列腺切除术(SP)和使用 180W GreenLight XPS 激光进行前列腺光选择性汽化术(PVP)治疗的安全性和有效性:研究纳入了120名因前列腺增生超过80毫升而出现尿失禁症状的患者,其中79名患者接受了SP治疗,41名患者接受了PVP治疗。分析包括治疗前和手术治疗后平均 38 个月的主观国际前列腺症状评分(IPSS)、生活质量(QoL)、客观(Qmax)、(Qave)和排尿后残余尿量(PVR)参数。对早期和晚期不良反应以及住院时间进行了评估。并发症报告根据修改后的克拉维恩-丁多系统进行:结果:分析结果显示,两种方法均有效。主观参数(IPSS、QoL)无明显差异。接受 SP 治疗的患者在客观参数(Qmax、Qave 和 PVR)上的得分略高。对不良反应和住院时间的分析显示,PVP治疗效果更佳:就 IPSS 和 QoL 而言,SP 和 PVP 在治疗良性前列腺增生方面具有可比性和高效性。采用 SP 方法治疗的患者在 Qmax、Qave 和 PVR 等客观参数方面的效果略好。与 SP 相比,PVP 的安全性更佳。
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引用次数: 0
Transperitoneal single-port robotic Firefly-guided bladder diverticulectomy and simple prostatectomy. 经腹腔单孔萤火虫引导机器人膀胱憩室切除术和单纯前列腺切除术。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-06 DOI: 10.5173/ceju.2023.277
Eugenio Bologna, Antonio Franco, Leslie Claire Licari, Francesco Ditonno, Celeste Manfredi, Jacob T Emerson, Edward E Cherullo, Riccardo Autorino
{"title":"Transperitoneal single-port robotic Firefly-guided bladder diverticulectomy and simple prostatectomy.","authors":"Eugenio Bologna, Antonio Franco, Leslie Claire Licari, Francesco Ditonno, Celeste Manfredi, Jacob T Emerson, Edward E Cherullo, Riccardo Autorino","doi":"10.5173/ceju.2023.277","DOIUrl":"https://doi.org/10.5173/ceju.2023.277","url":null,"abstract":"","PeriodicalId":9744,"journal":{"name":"Central European Journal of Urology","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11032038/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140847148","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}
引用次数: 0
First worldwide report on safety and efficacy of using small 7.5 Fr scope for pediatric ureteroscopy: prospective pilot series from Europe. 全球首份关于使用 7.5 Fr 小镜进行小儿输尿管镜检查的安全性和有效性的报告:来自欧洲的前瞻性试验系列。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-20 DOI: 10.5173/ceju.2023.248
Victoria Jahrreiss, Yesica Quiroz Madarriaga, Anna Bujons Tur, Erika Llorens de Knecht, Stephen Griffin, Bhaskar Somani

Introduction: Although pediatric urolithiasis remains relatively uncommon, its global prevalence is on the rise. Technological advances have led to miniaturization of instruments especially in the form of single use scopes. As the evidence on the use of small single use ureteroscopes in children is scarce, we have conducted a pilot two-center study to analyze the outcomes of pediatric patients treated with the Pusen 7.5 Fr single use scopes at our institutions.

Material and methods: This study included consecutive pediatric patients with urinary stones treated with the small Pusen 7.5 Fr single use ureteroscope. The study was conducted at two large European tertiary endourology centers that specialize in pediatric kidney stone management. Patient data and outcomes were prospectively collected, and analysis was performed regarding patient demographics, stone parameters, as well as stone free rate (SFR), operating time, and complications.

Results: In this pilot study, 26 patients were included with a median age of 12 years (7.0-16.0) and a male to female ratio of 14:12. The mean cumulative stone size was 15.15 mm (SD ±11.1) and multiple stones were present in 9 (34.6%) patients. Pre-operative stent, access sheath and post-operative stent usage was done in 12 (46.2%), 23 (88.5%) and 13 (50%) patients respectively. The median operative time was 47 minutes (IQR: 40.0-63.8). Following the initial procedure 24 (92.3%) patients were stone free, while no intra or postoperative complications were observed.

Conclusions: Our study demonstrates that the use of the small 7.5 single use ureteroscope is safe and efficient for the treatment of urinary stones in pediatric patients with high stone-free rates and no complications noted in our series. While this might become a standard of care in future, to confirm and validate our findings further studies with larger cohorts are warranted.

导言:尽管小儿泌尿系统结石仍相对少见,但其全球发病率却在不断上升。技术的进步导致了器械的微型化,尤其是一次性使用的尿道镜。由于在儿童中使用小型一次性输尿管镜的证据很少,我们在两个中心开展了一项试验性研究,以分析本机构使用 Pusen 7.5 Fr 一次性输尿管镜治疗儿童患者的效果:这项研究包括使用小型 Pusen 7.5 Fr 单用输尿管镜治疗的连续小儿泌尿系结石患者。这项研究在欧洲两家专门从事儿科肾结石治疗的大型三级内镜中心进行。前瞻性地收集了患者数据和结果,并对患者人口统计学、结石参数、无结石率(SFR)、手术时间和并发症进行了分析:在这项试点研究中,共纳入了26名患者,中位年龄为12岁(7.0-16.0),男女比例为14:12。平均累积结石大小为 15.15 毫米(标准差 ±11.1),9 名患者(34.6%)存在多发性结石。12例(46.2%)、23例(88.5%)和13例(50%)患者分别在术前使用了支架、入路鞘和术后使用了支架。手术时间中位数为 47 分钟(IQR:40.0-63.8)。首次手术后,24 名(92.3%)患者无结石,术中和术后未发现并发症:我们的研究表明,使用小型 7.5 单次使用输尿管镜治疗儿科患者的泌尿系结石安全有效,无结石率高,且无并发症。虽然这可能会成为未来的护理标准,但为了证实和验证我们的研究结果,有必要进行更大规模的研究。
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引用次数: 0
Assessment of the incidence and risk factors of postoperative urosepsis in patients undergoing ureteroscopic lithotripsy. 评估输尿管镜碎石术患者术后尿毒症的发生率和风险因素。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-08 DOI: 10.5173/ceju.2023.167
Krystian Kaczmarek, Marta Jankowska, Jakub Kalembkiewicz, Jakub Kienitz, Ositadima Chukwu, Artur Lemiński, Marcin Słojewski

Introduction: Ureteroscopic lithotripsy (URSL) is an approved, minimally invasive, low-risk procedure for urolithiasis treatment. However, some patients may develop urinary tract infection (UTI) post-procedure, eventually leading to urosepsis. Determining the predictors of infection after URSL would help identify patients at a high risk of urosepsis, thereby enabling the early implementation of effective treatment. Therefore, we aimed to establish the incidence and predictors of urosepsis after URSL.

Material and methods: We assessed 231 patients who underwent URSL using a holmium laser. The incidence of urosepsis during the 30-day post-treatment period was analysed, and potential predictors of urosepsis, including patient characteristics and individual clinical factors, were examined.

Results: Statistical analysis revealed that 16.88% of patients had a confirmed positive urine culture before the procedure. Post-procedure urosepsis occurred in 4.76% of patients. Univariable analysis revealed that 3 factors were significantly associated with the risk of postoperative urosepsis: double-J stent insertion before URSL, pre-operative positive urine culture, and MDR pathogen found preoperatively. In multivariable analysis, only positive urine culture remained significantly associated with the risk of urosepsis after URSL.

Conclusions: Patients with positive urine culture before URSL are at significantly higher risk of urosepsis in the postoperative period. Hence, urine culture should be routinely performed before planned endoscopic urolithiasis treatment.

导言:输尿管镜碎石术(URSL)是一种已获批准的治疗尿路结石的微创、低风险手术。然而,一些患者可能会在手术后出现尿路感染(UTI),最终导致尿毒症。确定尿路结石手术后感染的预测因素将有助于识别尿毒症高风险患者,从而及早实施有效治疗。因此,我们旨在确定尿道上皮内切开术后尿道炎的发生率和预测因素:我们评估了 231 名使用钬激光进行尿路结石手术的患者。分析了治疗后 30 天内尿道炎的发生率,并研究了尿道炎的潜在预测因素,包括患者特征和个体临床因素:统计分析显示,16.88%的患者在手术前尿培养呈阳性。4.76%的患者在手术后出现尿毒症。单变量分析显示,有三个因素与术后尿毒症的风险显著相关:尿道支架植入术前插入双 J 支架、术前尿培养阳性、术前发现 MDR 病原。在多变量分析中,只有尿培养阳性仍与尿道上皮内切开术后尿路败血症的风险显著相关:结论:尿道上裂前尿培养阳性的患者术后发生尿毒症的风险明显更高。因此,在计划进行内镜下尿路结石治疗前,应常规进行尿培养。
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引用次数: 0
Evolving types of pudendal neuromodulation for lower urinary tract dysfunction. 用于治疗下尿路功能障碍的不断演变的阴部神经调控类型。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-06 DOI: 10.5173/ceju.2023.86
Stefano Parodi, Harry J Kendall, Carlo Terrone, John Pfa Heesakkers

Introduction: Sacral neuromodulation and posterior tibial nerve stimulation for lower urinary tract dysfunction (LUTD) and overactive bladder yield good and reliable results. However, neuromodulation research is continuously evolving because there is still need for more patient-friendly treatment options in the therapeutic management of LUTD. Pudendal neuromodulation (PNM) has been emerging as a promising alternative treatment option for the last few decades. The aim of this study is to review the current state of the art of PNM.

Material and methods: A wide literature search was conducted in the field of PNM using Medline through the PubMed database and Elsevier using the Scopus database; a critical review of the results was then carried out. PNM has been studied in its various possible aspects: percutaneous PNM, transrectal/transvaginal PNM, and both percutaneous and transcutaneous dorsal genital nerve stimulation.

Results: Each technique was found to result in promising improvements in different clinical outcomes, with some trials reporting even better results than sacral neuromodulation.

Conclusions: As a result of a comparison between the various PNM techniques with both sacral neuromodulation and posterior tibial nerve stimulation, we think that PNM should be seen as seriously promising, and we believe it will expand the treatment options for overactive bladder. Even though several studies accordingly showed PNM to be safe and effective, a systematic review and meta-analysis were not feasible. PNM in its various techniques is a promising treatment for LUTD. Nevertheless, further research is needed to include it in treatment algorithms.

简介:骶神经调控和胫后神经刺激治疗下尿路功能障碍(LUTD)和膀胱过度活动症取得了良好可靠的效果。然而,神经调控研究仍在不断发展,因为在下尿路功能障碍的治疗过程中,仍需要更多方便患者的治疗方案。在过去的几十年中,耻骨神经调控(PNM)已成为一种前景广阔的替代治疗方案。本研究的目的是回顾 PNM 的技术现状:通过 PubMed 数据库的 Medline 和 Scopus 数据库的 Elsevier 对 PNM 领域的文献进行了广泛的搜索;然后对搜索结果进行了严格的审查。PNM 的研究涉及各个方面:经皮 PNM、经直肠/经阴道 PNM 以及经皮和经皮生殖器背神经刺激:结果:每种技术都有望改善不同的临床结果,有些试验报告的结果甚至优于骶神经调控技术:通过对各种膀胱过度活动症治疗技术与骶神经调控术和胫后神经刺激术的比较,我们认为膀胱过度活动症治疗技术前景广阔,相信它将扩大膀胱过度活动症的治疗范围。尽管有多项研究显示 PNM 安全有效,但进行系统回顾和荟萃分析并不可行。各种技术的 PNM 是治疗膀胱过度活动症的一种很有前景的方法。不过,要将其纳入治疗算法,还需要进一步的研究。
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引用次数: 0
Heavy as a rock or light as dust: a comparison between the perceived workload for extracorporeal shockwave lithotripsy, ureterorenoscopy and percutaneous nephrolithotomy. 重如磐石还是轻如尘埃:体外冲击波碎石术、输尿管镜检查和经皮肾镜碎石术的工作量比较。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-26 DOI: 10.5173/ceju.2023.214
Michaël Mel Henderickx, Nora Hendriks, A Carolien Bouma-Houwert, Joyce Baard, Guido M Kamphuis, Hugo W Schuil, Harrie P Beerlage, D Martijn de Bruin

Introduction: There are three common treatment options for kidney stones: extracorporeal shockwave lithotripsy (ESWL), ureterorenoscopy (URS) and percutaneous nephrolithotomy (PNL). The choice of treatment is based on stone- and patient-related characteristics. However, some stones are eligible for several approaches and the decision is made based on patient and urologist's preferences. This study evaluates which approach has the highest workload.

Material and methods: Between March and August 2022, five members of the Amsterdam Endourology Research Group collected data from 22 ESWL, 31 URS and 22 PNL procedures. After each procedure, the SURG-TLX questionnaire was completed by the surgeon to evaluate workload. Six dimensions were scored for each procedure, including: mental demands, physical demands, temporal demands, task complexity, situational stress, and distractions. The total workload, and the median for each dimension, was calculated and compared for the three treatments.

Results: ESWL scored significantly lower than URS for mental demands, physical demands, temporal demands, situational stress, distraction and total workload. However, task complexity did not differ significantly between the two techniques. Compared with PNL, ESWL scored significantly lower for all dimensions. Finally, PNL received significantly higher scores for mental demands, physical demands, temporal demands, situational stress, distractions and total workload than URS. Only task complexity showed no significant difference between both groups.

Conclusions: Urologists perceive the highest workload during PNL, followed by URS and finally ESWL. A follow-up study is needed to identify stressors that increase perceived workload with the purpose to address these variables and as final objective to improve urologists' workload, patient safety and treatment outcomes.

导言:肾结石有三种常见的治疗方法:体外冲击波碎石(ESWL)、输尿管镜检查(URS)和经皮肾镜碎石术(PNL)。治疗方法的选择取决于结石和患者的相关特征。不过,有些结石可采用多种方法治疗,因此要根据患者和泌尿科医生的喜好来决定。本研究评估了哪种方法的工作量最大:2022 年 3 月至 8 月间,阿姆斯特丹腔内泌尿学研究小组的五名成员收集了 22 例 ESWL、31 例 URS 和 22 例 PNL 手术的数据。每次手术后,外科医生都要填写 SURG-TLX 问卷,以评估工作量。每项手术都有六个方面的评分,包括:精神需求、体力需求、时间需求、任务复杂性、情境压力和分心。计算并比较了三种治疗方法的总工作量和每个维度的中位数:结果:ESWL 在精神需求、体力需求、时间需求、情境压力、分心和总工作量方面的得分明显低于 URS。然而,两种技术的任务复杂性并无明显差异。与 PNL 相比,ESWL 在所有方面的得分都明显较低。最后,PNL 在心理需求、生理需求、时间需求、情境压力、注意力分散和总工作量方面的得分都明显高于 URS。只有任务复杂性在两组之间没有明显差异:结论:泌尿科医生在 PNL 过程中的工作量最大,其次是 URS,最后是 ESWL。需要进行后续研究,以确定增加感知工作量的压力因素,从而解决这些变量,并将改善泌尿科医生的工作量、患者安全和治疗效果作为最终目标。
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引用次数: 0
Efficacy of combination therapy tadalafil plus tamsulosin in ureteral stents-related symptoms relief. 他达拉非加坦索罗辛联合疗法对缓解输尿管支架相关症状的疗效。
IF 1.2 Q3 Medicine Pub Date : 2024-01-01 Epub Date: 2023-11-20 DOI: 10.5173/ceju.2023.66
Ihor Komisarenko, Oleg Banyra, Oleg Nikitin, Yaroslav Klymenko, Mykola Chaplia, Andrii Borzhievskyy

Introduction: Ureteral stents-related symptoms (USRs) are the common complications of ureteral stenting. Tamsulosin a selective alpha-1 blocker and Tadalafil a PDE-5 inhibitor are one of drugs have been used for USRs relief. In this study we aimed to evaluate the effectiveness and safety of combination therapy Tamsulosin+Tadalafil for treating USRs comparing it with the efficacy of either Tamsulosin or Tadalafil monotherapies.

Material and methods: 279 patients with indwelled unilateral ureteral stents were randomized to Tamsulosin 0.4 mg + Tadalafil 5 mg once a day (Group 1, n = 67), Tamsulosin 0.4 mg once a day (Group 2, n = 71), Tadalafil 5 mg once a day (Group 3, n = 69) and Placebo once a day (Group 4, n = 72). USRs severity was registered and calculated by using the Ureteral Symptoms Score Questionnaire (USSQ) at the 14th day of treatment. Side-effects and total analgesic use were recorded and compared.

Results: At the endpoint in patients with unilateral ureteral stents the combination therapy Tamsulosin + Tadalafil led to statistically lower intensity of urinary symptoms comparing with Tamsulosin (15.2 ±4.3 vs 21.8±3.6, p = 0.0003) or Tadalafil (15.2 ±4.3 vs 20.6 ±2.8, p = 0.0004) monotherapy. All groups of treatment demonstrated significant relief of USRs comparing with Placebo mostly beneficial in the combined therapy group. Body pain and analgesic need in Group 1 was lower than in Groups 2, 3 or 4. Side-effects were registered rarely without statistical differences in frequency between groups.

Conclusions: Combination therapy with Tamsulosin + Tadalafil is an effective and safe option that achieves the statistically more significant relief of USRs comparing with Tadalafil or Tamsulosin monotherapies.

导言:输尿管支架相关症状(USRs)是输尿管支架植入术的常见并发症。选择性α-1受体阻滞剂坦索罗辛(Tamsulosin)和PDE-5抑制剂他达拉非(Tadalafil)是缓解输尿管支架相关症状的药物之一。本研究旨在评估坦索罗辛+他达拉非联合疗法治疗 USR 的有效性和安全性,并与坦索罗辛或他达拉非单一疗法的疗效进行比较。材料和方法:279 名单侧留置输尿管支架的患者被随机分为坦索罗辛 0.4 毫克+他达拉非 5 毫克每天一次(第 1 组,n = 67)、坦索罗辛 0.4 毫克每天一次(第 2 组,n = 71)、他达拉非 5 毫克每天一次(第 3 组,n = 69)和安慰剂每天一次(第 4 组,n = 72)。在治疗的第14天,使用输尿管症状评分问卷(USSQ)登记并计算USRs的严重程度。对副作用和镇痛剂总用量进行了记录和比较:结果:在单侧输尿管支架患者的终点,坦索罗辛+他达拉非联合疗法与坦索罗辛(15.2 ±4.3 vs 21.8±3.6,p = 0.0003)或他达拉非(15.2 ±4.3 vs 20.6 ±2.8,p = 0.0004)单药疗法相比,排尿症状强度明显降低。与安慰剂相比,所有治疗组的 USR 均有明显缓解,其中以联合治疗组最为明显。第 1 组的身体疼痛和镇痛需求低于第 2、3 或 4 组。副作用极少,组间频率无统计学差异:结论:与他达拉非或坦索罗辛单一疗法相比,坦索罗辛+他达拉非联合疗法是一种有效而安全的选择,能在统计学上更显著地缓解USR。
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Central European Journal of Urology
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