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Factors Associated with a Higher Risk of Conversion from Radiation-Free Percutaneous Nephrolithotomy (PCNL) to Fluoroscopy-Guided Percutaneous Nephrolithotomy. 无辐射经皮肾镜取石术(PCNL)转换为透视引导下经皮肾镜取石术的高风险相关因素
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2026-02-06 DOI: 10.1177/08927790251405794
Noah Swärd, Anthony Galvez, Riley Hull, Joseph Girgiss, Jonathan Katz, Jake L Roberts, Tyler Sheetz, Luke K Griffiths, Martin Ugander, Roger L Sur

Introduction and objective: Percutaneous nephrolithotomy percutaneous nephrostomy (PCNL) is a minimally invasive procedure for kidney stone removal traditionally guided by fluoroscopy. This study aimed to evaluate the feasibility and outcomes of radiation-free PCNL using ultrasonography alone compared with standard fluoroscopy-guided PCNL.

Methods: A total of 63 PCNL cases were eligible for radiation-free PCNL, but 27 were excluded (intraoperatively aborted, ureteroscopy performed instead, preoperative complex anatomy). Of the remaining 36 cases eligible for radiation-free PCNL, 11 were converted intraoperatively to fluoroscopic-based PCNL. Postoperative computed tomography (CT) imaging was available for only 16 of the 25 radiation-free PCNL cases and 4 of the 11 converted cases. We designated these 16 prospective radiation-free PCNL cases (2024-2025) as Group A. For comparison purposes, we identified a historical case-matched cohort of 150 PCNLs. Of these, 67 were excluded (similar reasons), leaving 83 retrospective fluoroscopy-guided PCNL cases (2022-2024) called Group B. A subset of Group A cases was converted from radiation-free intraoperatively to fluoroscopy and were designated as Group C. The primary outcome was stone-free rate (SFR), assessed postoperatively by noncontrast CT (2-3 mm slices). Secondary outcomes included estimated blood loss, complication rates (Clavien-Dindo), and postoperative stone events.

Results: The median preoperative stone burden was 35 mm in Group A and 27 mm in Groups B and C [p = 0.3]. SFR (Grade A) was comparable across Groups A, B, and C [38%, 30%, and 25%, respectively (p = 0.8)]. No differences were observed in complications or secondary outcomes.

Conclusions: Radiation-free PCNL is feasible and yields comparable outcomes to standard fluoroscopy-guided PCNL, offering a promising method to reduce radiation exposure without compromising surgical success. However, we identified a consistent theme of poor visualization that prompted conversion to fluoroscopy for some of the cases. Innovation directed toward improving tool echogenicity is key to diffusing this technique.

简介和目的:经皮肾镜取石术(PCNL)是一种微创的肾结石取出术,传统上由透视引导。本研究旨在评价超声单独治疗无辐射PCNL与标准透视引导下PCNL的可行性和效果。方法:63例PCNL符合无放射线PCNL条件,27例被排除(术中流产、行输尿管镜检查、术前复杂解剖)。在其余36例符合无辐射PCNL条件的病例中,11例术中转为基于透视的PCNL。25例无放疗的PCNL病例中,仅有16例和11例转化病例中的4例可获得术后计算机断层扫描(CT)。我们将这16例前瞻性无辐射PCNL病例(2024-2025)指定为a组。为了进行比较,我们确定了150例PCNL的历史病例匹配队列。其中67例被排除(原因类似),留下83例回顾性透视引导下的PCNL病例(2022-2024)称为b组。A组病例的一部分从术中无放疗转为透视,称为c组。主要结果是无结石率(SFR),术后通过非对比CT (2-3 mm切片)评估。次要结局包括估计的出血量、并发症发生率(Clavien-Dindo)和术后结石事件。结果:A组术前结石负荷中位数为35 mm, B、C组术前结石负荷中位数为27 mm [p = 0.3]。SFR (A级)在A、B和C组之间具有可比性[分别为38%、30%和25% (p = 0.8)]。在并发症或次要结局方面没有观察到差异。结论:无辐射PCNL是可行的,其结果与标准透视引导下的PCNL相当,是一种在不影响手术成功的情况下减少辐射暴露的有希望的方法。然而,我们发现了一个一致的主题,即视觉不良,促使一些病例改用透视检查。旨在提高工具回声性的创新是推广该技术的关键。
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引用次数: 0
Suction-Assisted Miniaturized Percutaneous Nephrolithotomy Outcomes in Anomalous Kidneys: A Multicenter Prospective Study-An EAU-Endourology Collaboration. 吸痰辅助微型经皮肾镜取石术治疗异常肾的结果:一项多中心前瞻性研究-一项eau -肾盂内腔合作研究。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2026-02-06 DOI: 10.1177/08927790251392896
Vineet Gauhar, Ee Jean Lim, Bhaskar Kumar Somani, Jaisukh Kalathia, Edgar Beltrán-Suárez, Gadzhiev Nariman, Mahmoud Laymon, Kremena Petkova, Esteban Acuna, Mohamed Amine Lakmichi, Khi Yung Fong, Marek Zawadzki, Nitesh Kumar, Amish Mehta, Roy Zen Sing Teng, Gopal Ramdas Tak, Alexey G Martov, Marcos Cepeda, Vigen Malkhasyan, Arun Chawla, Daniele Castellani, Thomas R W Herrmann, Steffi Kar Kei Yuen

Background: Renal stones in anomalous kidneys pose surgical challenges due to altered anatomy. Miniaturized percutaneous nephrolithotomy (mini-PCNL) reduces morbidity, but concerns remain about stone-free rates (SFRs) and infection. Suction-assisted mini-PCNL (SM-PCNL) enhances fragment removal and controls intrarenal pressure, but its role in anomalous kidneys is unclear.

Objective: To evaluate perioperative outcomes of SM-PCNL in anomalous kidneys in a multicenter, real-world study and assess variations based on positioning, lithotripsy modality, and renal anomalies.

Methodology: This prospective study across 15 centers (January-December 2024) included 287 adults undergoing SM-PCNL for renal stones in anomalous kidneys. Patients with normal anatomy, non-suction PCNL, or incomplete data were excluded. SFR was assessed via a 30-day non-contrast CT: 100% stone-free (Grade A), residual fragments ≤4 mm (Grade B), or >4 mm/multiple (Grade C, requiring reintervention).

Results: Malrotation (65.5%) was the most common anomaly, followed by duplex systems (25.1%), horseshoe kidneys (8.4%), and ectopic kidneys (1.0%). Median stone size was 1.7 cm. Supine positioning was used in 54.4%. Lithotripsy was performed with holmium laser (50.9%), thulium fiber laser (11.1%), or pneumatic lithotripsy (26.1%). Intraoperative clearance was 95.4%. At 30 days, 93.4% achieved Grade A, 5.6% Grade B, and 1.0% required reintervention. Complications were low; 0.7% had sepsis requiring intensive care unit admission. No transfusions or pleural injuries occurred.

Conclusion: SM-PCNL using 18F suction sheaths with laser in a single stage achieved 93.4% complete SFR with negligible complications and minimal reintervention.

背景:由于解剖结构的改变,异常肾脏的肾结石给手术带来了挑战。小型化经皮肾镜取石术(mini-PCNL)降低了发病率,但对无结石率(SFRs)和感染的担忧仍然存在。吸吸辅助的迷你pcnl (SM-PCNL)增强碎片去除和控制肾内压,但其在异常肾脏中的作用尚不清楚。目的:在一项多中心、真实世界的研究中评估异常肾脏SM-PCNL的围手术期结果,并评估基于定位、碎石方式和肾脏异常的变化。方法:这项前瞻性研究跨越15个中心(2024年1月至12月),包括287名成年人接受异常肾脏肾结石的SM-PCNL。排除解剖正常、非抽吸PCNL或资料不完整的患者。通过30天的非对比CT评估SFR: 100%无结石(a级),残留碎片≤4mm (B级),或> 4mm /倍(C级,需要再次干预)。结果:旋转不良(65.5%)是最常见的异常,其次是双肾(25.1%)、马蹄肾(8.4%)和异位肾(1.0%)。中位结石大小为1.7 cm。54.4%的患者采用仰卧位。采用钬激光碎石(50.9%)、铥光纤激光碎石(11.1%)、气动碎石(26.1%)。术中清除率为95.4%。30天后,93.4%达到A级,5.6%达到B级,1.0%需要再次干预。并发症低;0.7%的脓毒症患者需要入住重症监护病房。未发生输血或胸膜损伤。结论:SM-PCNL采用18F吸套配合激光,一期完成SFR 93.4%,并发症极少,再干预最少。
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引用次数: 0
HugoTM RAS vs Da Vinci® Xi Robot-Assisted Partial Nephrectomy: First Propensity Score-Matched Comparison of Perioperative and Functional Outcomes. HugoTM RAS与Da Vinci®Xi机器人辅助部分肾切除术:围手术期和功能结果的首次倾向评分匹配比较
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2026-01-14 DOI: 10.1177/08927790251412815
Francesco Prata, Riccardo Mastroianni, Giuseppe Simone, Francesco Tedesco, Umberto Anceschi, Alberto Ragusa, Angelo Civitella, Aldo Brassetti, Alfredo Maria Bove, Andrea Iannuzzi, Alfredo Travino, Alessandro De Giuseppe, Marco Fantozzi, Mariavittoria Vescovo, Simone D'Annunzio, Mariaconsiglia Ferriero, Rocco Simone Flammia, Salvatore Guaglianone, Leonardo Misuraca, Flavia Proietti, Gabriele Tuderti, Costantino Leonardo, Giuseppe Perrone, Roberto Mario Scarpa, Rocco Papalia

Purpose: To report the first multicentric comparison between Hugo™ robot-assisted surgery/system (RAS) and Da Vinci® Xi for robot-assisted partial nephrectomy (RAPN).

Methods: Between October 2022 and March 2024, a total of 258 patients underwent off-clamp RAPN (Hugo RAS = 52 patients, and Da Vinci = 206 patients). Da Vinci and Hugo cases were matched in a 1:1 ratio using propensity score matching (PSM), adjusting for the Radius Exophytic Nearness Anterior Location score and renorrhaphy technique. Trifecta was defined as the coexistence of negative surgical margin status, no Clavien-Dindo grade ≥ 3 complications, and ≤ 30% estimated glomerular filtration rate (eGFR) reduction at discharge.

Results: After 1:1 PSM, two comparable populations of 52 patients each were selected. No intraoperative blood transfusion occurred in any group. The Hugo cohort displayed a higher rate of postoperative transfusions (7.7% vs 0%, p = 0.04). Nevertheless, perioperative complications were comparable (p = 0.32). The median length of stay (LOS) was shorter in the Da Vinci group (2 days vs 3 days, p < 0.001), as for median eGFR at discharge (74.5 mL/min/1.73m2 vs 87.3 mL/min/1.73m2, p = 0.03). No significant difference in positive surgical margins was shown between the two groups (p = 0.08). Finally, a comparable Trifecta rate was achieved for both platforms (88.5% in the Hugo RAS group and 90.4% in the Da Vinci group, p = 0.75).

Conclusions: Despite the hierarchical role of Da Vinci in the robotic surgical landscape, RAPN can be safely carried out with the new Hugo RAS System, with satisfactory perioperative surgical outcomes comparable to the Da Vinci Xi System.

目的:报道Hugo™机器人辅助手术/系统(RAS)与Da Vinci®Xi在机器人辅助部分肾切除术(RAPN)中的首次多中心比较。方法:2022年10月至2024年3月,共258例患者接受了脱钳RAPN (Hugo RAS = 52例,Da Vinci = 206例)。Da Vinci和Hugo病例采用倾向评分匹配(PSM)按1:1比例匹配,调整桡骨外植性近前位评分和再缝合技术。三氟替尼的定义是:伴有手术切界阴性状态,无Clavien-Dindo分级≥3级并发症,出院时估计肾小球滤过率(eGFR)降低≤30%。结果:1:1 PSM后,选择了两个可比较的人群,每个人群52例患者。两组均未发生术中输血。Hugo队列显示出更高的术后输血率(7.7% vs 0%, p = 0.04)。然而,围手术期并发症具有可比性(p = 0.32)。达芬奇组的中位住院时间(LOS)较短(2天vs 3天,p < 0.001),而出院时的中位eGFR (74.5 mL/min/1.73m2 vs 87.3 mL/min/1.73m2, p = 0.03)。两组间阳性切缘差异无统计学意义(p = 0.08)。最后,两种治疗平台的triecta发生率相当(Hugo RAS组为88.5%,Da Vinci组为90.4%,p = 0.75)。结论:尽管达芬奇在机器人手术领域具有等级作用,但新的Hugo RAS系统可以安全地进行RAPN,其围手术期手术效果与达芬奇Xi系统相当。
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引用次数: 0
Feasibility and Safety of Holmium Laser Enucleation of the Prostate for Small to Medium Volumes Under Local Anesthesia with the Schelin Catheter and Sedoanalgesia: Results from a Single-Center Pilot Study. 在Schelin导管和sedo镇痛下局部麻醉下钬激光前列腺切除术的可行性和安全性:一项单中心试点研究的结果。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2026-01-15 DOI: 10.1177/08927790251414138
Gianna Pace, Daniele Romagnoli, Alessandro Del Rosso, Stefano Vidiri, Orest Xhafka, Gianluca Brunetti

Introduction: This study aimed to evaluate the feasibility and safety of patients undergoing holmium laser enucleation of prostate (HoLEP), under transurethral intraprostatic anesthesia (TUIA) using Schelin Catheter (SC) and sedoanalgesia.

Materials and methods: We retrospectively analyzed data of patients affected by benign prostatic obstruction candidate to HoLEP under TUIA using SC, from November 2023 to May 2024.

Results: A total of 50 patients were enrolled, median age 67 years; 14% were ASA ≥ 3, 2% and 22% had anticoagulation and antiplatelet drug therapy; 60% received alpha blockers, and 22% had both alpha blockers and 5α-reductase inhibitors; and 18% with an indwelling catheter. Preoperative median International Prostate Symptom Score (IPSS) and IPSS-quality of life (IPSS-QoL) were 16 (IQR: 11-21) and 4 (IQR: 4-6), median Qmax 10 mL/sec (IQR 3-19), median postvoid residual (PVR) 79 mL (IQR: 0-500). The median prostate volume was 50 mL (IQR 41-70 cc). Median preoperative Prostate Specific Antigen (PSA) was 1,70 (IQR 1,1-2,95). A prostate volume ≥ 80 mL was present in 10% of patients. The median enucleation time was 13,6 minutes (IQR 11,15-21,45) and the median morcellation time was 8,3 minutes (IQR 4,2-10,8). The median enucleated weight was 33 g (IQR 19,50-50). Median pain numeric rating scale before surgical procedure, at SC insertion, during enucleation, during morcellation, 2-hours postoperatively, on day 1 and 2 were 1 (0-3), 5 (2-6), 5 (3-7), 7 (5-10), 2 (1-4), 2 (1-4), and 3 (2-6). During enucleation, 10% required to start the target-controlled infusion with propofol. During morcellation, a half needs to get started propofol administration. The catheter was removed within 2 days in 100% of patients, and all were discharged within 48 hours. IPSS, IPSS-QoL, Qmax, and PVR showed significant improvement at 3 months.

Conclusions: TUIA with sedoanalgesia in HoLEP of small/medium prostate volume offers good pain control, preserving the significant improvement of postoperative outcomes.

前言:本研究旨在评价经尿道前列腺内麻醉(TUIA)下使用Schelin导管(SC)和sedo镇痛的钬激光前列腺摘除(HoLEP)患者的可行性和安全性。材料和方法:我们回顾性分析了2023年11月至2024年5月在TUIA下使用SC的良性前列腺阻塞候选HoLEP患者的资料。结果:共纳入50例患者,中位年龄67岁;ASA≥3.2的占14%,接受抗凝和抗血小板药物治疗的占2%,接受抗凝和抗血小板药物治疗的占22%;60%接受α受体阻滞剂治疗,22%同时接受α受体阻滞剂和5α-还原酶抑制剂治疗;18%的患者采用留置导尿管。术前国际前列腺症状评分中位数(IPSS)和生活质量中位数(IPSS- qol)分别为16 (IQR: 11-21)和4 (IQR: 4-6), Qmax中位数为10 mL/sec (IQR: 3-19),空隙后残留中位数(PVR)为79 mL (IQR: 0-500)。前列腺体积中位数为50 mL (IQR 41-70 cc)。术前前列腺特异性抗原(PSA)中位数为1,70 (IQR 1,1-2,95)。10%的患者前列腺体积≥80ml。中位去核时间为13.6分钟(IQR 11,15-21,45),中位分块时间为8.3分钟(IQR 4,2-10,8)。中位去核重量为33 g (IQR 19,50-50)。手术前、SC插入时、去核时、分拆时、术后2小时、第1天和第2天的中位疼痛数值评定量表分别为1(0-3)、5(2-6)、5(3-7)、7(5-10)、2(1-4)、2(1-4)和3(2-6)。在去核过程中,10%需要开始靶控输注异丙酚。分拆过程中,病人需要开始注射异丙酚。100%患者2天内拔管,48小时内全部出院。IPSS、IPSS- qol、Qmax和PVR在3个月时均有显著改善。结论:中、小前列腺体积HoLEP的TUIA联合sedo镇痛具有良好的疼痛控制,保留了术后疗效的显著改善。
{"title":"Feasibility and Safety of Holmium Laser Enucleation of the Prostate for Small to Medium Volumes Under Local Anesthesia with the Schelin Catheter and Sedoanalgesia: Results from a Single-Center Pilot Study.","authors":"Gianna Pace, Daniele Romagnoli, Alessandro Del Rosso, Stefano Vidiri, Orest Xhafka, Gianluca Brunetti","doi":"10.1177/08927790251414138","DOIUrl":"https://doi.org/10.1177/08927790251414138","url":null,"abstract":"<p><strong>Introduction: </strong>This study aimed to evaluate the feasibility and safety of patients undergoing holmium laser enucleation of prostate (HoLEP), under transurethral intraprostatic anesthesia (TUIA) using Schelin Catheter (SC) and sedoanalgesia.</p><p><strong>Materials and methods: </strong>We retrospectively analyzed data of patients affected by benign prostatic obstruction candidate to HoLEP under TUIA using SC, from November 2023 to May 2024.</p><p><strong>Results: </strong>A total of 50 patients were enrolled, median age 67 years; 14% were ASA ≥ 3, 2% and 22% had anticoagulation and antiplatelet drug therapy; 60% received alpha blockers, and 22% had both alpha blockers and 5α-reductase inhibitors; and 18% with an indwelling catheter. Preoperative median International Prostate Symptom Score (IPSS) and IPSS-quality of life (IPSS-QoL) were 16 (IQR: 11-21) and 4 (IQR: 4-6), median Qmax 10 mL/sec (IQR 3-19), median postvoid residual (PVR) 79 mL (IQR: 0-500). The median prostate volume was 50 mL (IQR 41-70 cc). Median preoperative Prostate Specific Antigen (PSA) was 1,70 (IQR 1,1-2,95). A prostate volume ≥ 80 mL was present in 10% of patients. The median enucleation time was 13,6 minutes (IQR 11,15-21,45) and the median morcellation time was 8,3 minutes (IQR 4,2-10,8). The median enucleated weight was 33 g (IQR 19,50-50). Median pain numeric rating scale before surgical procedure, at SC insertion, during enucleation, during morcellation, 2-hours postoperatively, on day 1 and 2 were 1 (0-3), 5 (2-6), 5 (3-7), 7 (5-10), 2 (1-4), 2 (1-4), and 3 (2-6). During enucleation, 10% required to start the target-controlled infusion with propofol. During morcellation, a half needs to get started propofol administration. The catheter was removed within 2 days in 100% of patients, and all were discharged within 48 hours. IPSS, IPSS-QoL, Qmax, and PVR showed significant improvement at 3 months.</p><p><strong>Conclusions: </strong>TUIA with sedoanalgesia in HoLEP of small/medium prostate volume offers good pain control, preserving the significant improvement of postoperative outcomes.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":"40 2","pages":"212-218"},"PeriodicalIF":2.8,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146201758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Outcomes of Prophylactic Ureteral Catheterization for Ureteral Identification During Non-Urologic Surgery. 非泌尿外科手术中输尿管鉴别预防性输尿管导尿的效果。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2025-10-29 DOI: 10.1177/08927790251390880
Luke Drew, Daniel Jhang, Kirulus Amin, Jersey-Kate Castillo, Ala'a Farkouh, Evan Seibly, Antoin Douglawi, Martin Hofmann, Forrest Jellison, Brian Hu, D Duane Baldwin, Herbert Ruckle, Muhannad Alsyouf

Introduction: Prophylactic ureteral catheterization (PUC) is routinely performed during non-urologic procedures to avoid iatrogenic ureteral injury. However, evidence of its benefit is conflicting, as data suggest that the rate of ureteral injury is unchanged and there is lack of data reporting associated complications. The purpose of this study was to evaluate the outcomes of routine PUC in non-urologic surgeries.

Methods: All consecutive patients who underwent PUC during non-urologic procedures between January 2019 and March 2024 were reviewed. Demographic, clinical, and perioperative characteristics, including ureteral injury rates, were reviewed. Complications within 90 days were divided into low-grade (urinary tract infection [UTI], gross hematuria, and flank pain) and high-grade (new or worsening hydronephrosis and need for nephrostomy or indwelling stent). Logistic regression was performed to identify predictors of PUC-related complications.

Results: Among 233 patients, 63.5% were female. Median age and body mass index were 57 years and 28, respectively. Patient history included neoadjuvant chemotherapy in 54 (23%), pelvic radiation in 43 (18%), and pelvic surgery in 119 (51%). Surgery types included colorectal (75.1%), gynecological (14.2%), or both (10.7%). A total of 101 urologic complications affected 43% of patients, including UTI (22.3%), gross hematuria (24.4%), flank pain (10.7%), new/worsening hydronephrosis (9.9%), and need for nephrostomy tube/stent (1.3%). Intraoperative ureteral injury rate was 3.9%. On multivariate analysis, prior pelvic radiation was significantly associated with the occurrence of high-grade complications (odds ratio 3.29, 95% CI 1.04, 10.43).

Conclusion: PUC during non-urologic procedures is associated with a small but significant risk of urologic complications and does not eliminate the risk of ureteral injury. Prior pelvic radiation is a significant risk factor for PUC-related complications.

导读:预防性输尿管置管术(PUC)在非泌尿外科手术中常规进行,以避免医源性输尿管损伤。然而,其益处的证据是相互矛盾的,因为数据表明输尿管损伤率不变,缺乏相关并发症的数据报告。本研究的目的是评估常规PUC在非泌尿外科手术中的效果。方法:回顾2019年1月至2024年3月期间所有在非泌尿外科手术中连续接受PUC的患者。回顾了人口统计学、临床和围手术期特征,包括输尿管损伤率。90天内的并发症分为低级别(尿路感染[UTI]、肉眼血尿、侧腹疼痛)和高级别(新发或恶化的肾积水,需要肾造口或留置支架)。采用逻辑回归来确定前列腺癌相关并发症的预测因素。结果:233例患者中,女性占63.5%。中位年龄和体重指数分别为57岁和28岁。患者病史包括新辅助化疗54例(23%),盆腔放疗43例(18%),盆腔手术119例(51%)。手术类型包括结直肠(75.1%)、妇科(14.2%)或两者兼而有之(10.7%)。共有101个泌尿系统并发症影响了43%的患者,包括尿路感染(22.3%)、血尿(24.4%)、侧腹疼痛(10.7%)、新发/恶化的肾积水(9.9%)和需要肾造口管/支架(1.3%)。术中输尿管损伤率为3.9%。在多变量分析中,既往盆腔放疗与高级别并发症的发生显著相关(优势比3.29,95% CI 1.04, 10.43)。结论:非泌尿外科手术期间PUC与泌尿外科并发症的风险小但显著相关,并不能消除输尿管损伤的风险。既往盆腔放疗是前列腺癌相关并发症的重要危险因素。
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引用次数: 0
Development and Validation of Predictive Models for Trifecta Achievement in Robot-Assisted Partial Nephrectomy for Renal Hilar Tumors: Preliminary Application of the Modified R.E.N.A.L. Score. 机器人辅助肾门部肿瘤部分切除三联片疗效预测模型的建立与验证:改良R.E.N.A.L.评分的初步应用。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-02-01 Epub Date: 2026-01-23 DOI: 10.1177/08927790251408826
Yuyang Yuan, Lizhi Zhou, Jiaqing Yang, Fuchun Zheng, Xinchang Zou, Xiaoqiang Liu, Luyao Chen, Jieping Hu, Bin Fu

Objective: To develop an interpretable machine learning (ML) model for predicting surgical outcomes in renal hilar tumors and propose a hilar-specific anatomical nephrometry scoring system.

Methods: A total of 414 patients with renal hilar tumors who underwent robot-assisted partial nephrectomy (RAPN) were included in this study, comprising 304 patients from the First Affiliated Hospital of Nanchang University and 110 patients from the Second Affiliated Hospital of Nanchang University, which served as the external validation cohort. To identify predictors of trifecta achievement, we used least absolute shrinkage and selection operator regression and the Boruta algorithm, followed by multivariate logistic regression to identify independent factors. Five ML models were developed and evaluated using receiver operating characteristic curves, calibration plots, decision curve analysis, and precision-recall curves. The generalizability of the model was further validated in external cohort. Finally, we used SHapley Additive exPlanations (SHAP) to interpret the contribution of each predictor and enhance the model's explainability. Furthermore, based on anatomical features identified through logistic regression, we developed a modified nephrometry scoring system and compared its risk stratification performance with the traditional R.E.N.A.L. (i.e., Radius, Exophytic or endophytic, Nearness, Anterior or posterior, and Location) scoring system.

Results: Among the 304 patients in the primary cohort, 168 achieved trifecta outcomes. Eight variables were incorporated into the predictive model, with logistic regression model ultimately being selected as the optimal predictive model. It showed robust predictive performance in internal and external validation. SHAP methods identified surgeon, classification of hilar tumor, and radius as the three most significant predictive variables. Compared with the traditional R.E.N.A.L. score, the modified R.E.N.A.L. score demonstrated superior stratification ability for operation time, change in serum creatinine, change in estimated glomerular filtration rate, and trifecta achievement.

Conclusion: The interpretable ML model accurately predicts trifecta in RAPN for hilar tumors. The modified R.E.N.A.L. score provides refined anatomical stratification and facilitates individualized surgical planning.

目的:建立一个可解释的机器学习(ML)模型来预测肾门部肿瘤的手术结果,并提出一种肾门特异性解剖肾测量评分系统。方法:本研究共纳入414例行机器人辅助部分肾切除术(RAPN)的肾门部肿瘤患者,其中南昌大学第一附属医院304例,南昌大学第二附属医院110例作为外部验证队列。为了确定三连成功的预测因素,我们使用了最小绝对收缩、选择算子回归和Boruta算法,然后使用多元逻辑回归来确定独立因素。开发了五种ML模型,并使用受试者工作特征曲线、校准图、决策曲线分析和精确召回率曲线对其进行了评估。在外部队列中进一步验证了模型的泛化性。最后,我们使用SHapley加性解释(SHAP)来解释每个预测因子的贡献,并增强模型的可解释性。此外,基于通过逻辑回归确定的解剖特征,我们开发了一种改进的肾测量评分系统,并将其风险分层性能与传统的R.E.N.A.L.评分系统(即半径、外生或内生、邻近、前或后、位置)进行比较。结果:在主要队列的304例患者中,168例达到了三合一结局。将8个变量纳入预测模型,最终选择logistic回归模型作为最优预测模型。在内部和外部验证中显示出稳健的预测性能。SHAP方法确定外科医生、肺门肿瘤分类和桡骨为三个最重要的预测变量。与传统的R.E.N.A.L.评分相比,改进的R.E.N.A.L.评分在手术时间、血清肌酐变化、肾小球滤过率估计变化和三合一评分方面表现出更强的分层能力。结论:可解释的ML模型能准确预测肺门肿瘤RAPN的三征。改良后的R.E.N.A.L.评分提供了精细的解剖分层,便于个体化手术计划。
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引用次数: 0
Novel Bilateral Ureteral Occlusion with Modified Expandable Metal Stents to Achieve Complete but Reversible Urinary Diversion. 新型双侧输尿管阻塞与改良的可扩张金属支架实现完全但可逆的尿分流。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-14 DOI: 10.1177/08927790251394381
Stefanie M Croghan, Nnaemeka Eli, Angus Luk, Christoph Schregel, Matthew Shaw, Rob Williams, Alistair Rogers

Urologists face a significant challenge when presented with cases in which complete, yet reversible, urinary diversion is desirable. With multidisciplinary collaboration, we have used a novel technique involving the antegrade deployment of distally-ligated covered metal (Allium®) ureteral stents, achieving ureteral occlusion and complete urinary diversion via nephrostomy tubes. We have used this technique, with good early results, in complex cases, including that of a young male patient with complex pelvic injuries after polytrauma and a female patient with a malignant vesicovaginal fistula, neither of whom were candidates for definitive surgical reconstruction or diversion at the time of treatment. We describe our experience, which we believe may be of interest to urologists and interventional radiologists managing similarly challenging cases.

泌尿科医生面临着一个重大的挑战,当提出的情况下,完全,但可逆的,尿转移是可取的。通过多学科合作,我们采用了一种新技术,包括顺行部署远端结膜金属(Allium®)输尿管支架,通过肾造口管实现输尿管阻塞和完全尿分流。我们已经在复杂的病例中使用了这种技术,并取得了良好的早期效果,包括一名年轻的男性患者在多发创伤后出现复杂的骨盆损伤,以及一名患有恶性膀胱阴道瘘的女性患者,这两名患者在治疗时都不适合进行最终的手术重建或转移。我们描述了我们的经验,我们相信泌尿科医生和介入放射科医生可能会对处理类似具有挑战性的病例感兴趣。
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引用次数: 0
High-Power Retrograde Intrarenal Surgery Holmium Laser Lithotripsy for Kidney Stones Larger Than 20 mm. 大于20mm肾结石的高功率逆行肾内手术钬激光碎石。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-01-01 Epub Date: 2025-12-24 DOI: 10.1177/08927790251388465
Orel Hemo, Asaf Shvero, Dorit E Zilberman, Zohar A Dotan, Nir Kleinmann

Purpose: Percutaneous nephrolithotomy (PCNL) is the gold standard for treating kidney stones >20 mm because of its superior stone-free rates (SFR). However, high-power holmium lasers may challenge this standard. This study evaluates the feasibility, safety, and efficacy of high-power holmium laser retrograde intrarenal surgery (RIRS) for the treatment of kidney stones >20 mm.

Methods: We conducted a retrospective analysis of patients with kidney stones >20 mm treated with either 80W- or 120 W holmium laser RIRS between January 2020 and August 2024. Clinical, intraoperative, and postoperative data were collected. Outcomes included SFR, operative time, complications, and hospital stay. Comparisons between the older-generation (80 W) and newer-generation (120 W) systems were performed using the Mann-Whitney U test and chi-square test, and multivariable analyses identified predictors of non-stone-free status.

Results: A total of 118 patients were included: 31 in the older-generation (80 W) group and 87 in the newer-generation (120 W) group. RIRS using the newer-generation 120 W laser was associated with a shorter operative time (66 vs 79 minutes, p < 0.001) and higher SFR at 5 weeks (82.7% vs 58.1%, p = 0.006), 6 months (92% vs 64.5%, p < 0.001), and 1 year (96.5% vs 83.8%, p = 0.016) postoperative evaluations. Complication rates did not differ significantly between groups (5.7% vs 3.2%, p = 0.208). In multivariable analysis, the use of older-generation 80 W laser was an independent predictor of non-stone-free status at both the first (OR 4.4, p = 0.004) and second (OR 8.8, p = 0.001) follow-up visits.

Conclusions: Treatment of renal stones larger than 2 cm with the newer-generation 120 W Ho:YAG laser is effective, with higher SFR rate and shorter operative time, compared to the older-generation 80 W Ho:YAG laser.

目的:经皮肾镜取石术(PCNL)因其具有较高的无结石率(SFR)而成为治疗直径20毫米肾结石的金标准。然而,高功率钬激光器可能会挑战这一标准。本研究评估高功率钬激光逆行肾内手术(RIRS)治疗肾结石bb0 ~ 20mm的可行性、安全性和有效性。方法:我们对2020年1月至2024年8月期间接受80W或120w钬激光RIRS治疗的肾结石患者进行了回顾性分析。收集临床、术中、术后资料。结果包括SFR、手术时间、并发症和住院时间。使用Mann-Whitney U检验和卡方检验对老一代(80 W)和新一代(120 W)系统进行比较,并通过多变量分析确定非结石状态的预测因子。结果:共纳入118例患者:老一代(80 W)组31例,新一代(120 W)组87例。使用新一代120w激光的RIRS在术后5周(82.7% vs 58.1%, p = 0.006)、6个月(92% vs 64.5%, p < 0.001)和1年(96.5% vs 83.8%, p = 0.016)的评估中与较短的手术时间(66 vs 79分钟,p < 0.001)和较高的SFR相关。两组间并发症发生率无显著差异(5.7% vs 3.2%, p = 0.208)。在多变量分析中,使用老一代80 W激光是第一次(OR 4.4, p = 0.004)和第二次(OR 8.8, p = 0.001)随访时非结石状态的独立预测因子。结论:与老一代80 W Ho:YAG激光相比,新一代120 W Ho:YAG激光治疗大于2 cm的肾结石具有更高的SFR率和更短的手术时间。
{"title":"High-Power Retrograde Intrarenal Surgery Holmium Laser Lithotripsy for Kidney Stones Larger Than 20 mm.","authors":"Orel Hemo, Asaf Shvero, Dorit E Zilberman, Zohar A Dotan, Nir Kleinmann","doi":"10.1177/08927790251388465","DOIUrl":"10.1177/08927790251388465","url":null,"abstract":"<p><strong>Purpose: </strong>Percutaneous nephrolithotomy (PCNL) is the gold standard for treating kidney stones >20 mm because of its superior stone-free rates (SFR). However, high-power holmium lasers may challenge this standard. This study evaluates the feasibility, safety, and efficacy of high-power holmium laser retrograde intrarenal surgery (RIRS) for the treatment of kidney stones >20 mm.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of patients with kidney stones >20 mm treated with either 80W- or 120 W holmium laser RIRS between January 2020 and August 2024. Clinical, intraoperative, and postoperative data were collected. Outcomes included SFR, operative time, complications, and hospital stay. Comparisons between the older-generation (80 W) and newer-generation (120 W) systems were performed using the Mann-Whitney <i>U</i> test and chi-square test, and multivariable analyses identified predictors of non-stone-free status.</p><p><strong>Results: </strong>A total of 118 patients were included: 31 in the older-generation (80 W) group and 87 in the newer-generation (120 W) group. RIRS using the newer-generation 120 W laser was associated with a shorter operative time (66 <i>vs</i> 79 minutes, <i>p</i> < 0.001) and higher SFR at 5 weeks (82.7% <i>vs</i> 58.1%, p = 0.006), 6 months (92% <i>vs</i> 64.5%, <i>p</i> < 0.001), and 1 year (96.5% <i>vs</i> 83.8%, <i>p</i> = 0.016) postoperative evaluations. Complication rates did not differ significantly between groups (5.7% <i>vs</i> 3.2%, <i>p</i> = 0.208). In multivariable analysis, the use of older-generation 80 W laser was an independent predictor of non-stone-free status at both the first (OR 4.4, <i>p</i> = 0.004) and second (OR 8.8, <i>p</i> = 0.001) follow-up visits.</p><p><strong>Conclusions: </strong>Treatment of renal stones larger than 2 cm with the newer-generation 120 W Ho:YAG laser is effective, with higher SFR rate and shorter operative time, compared to the older-generation 80 W Ho:YAG laser.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"1-8"},"PeriodicalIF":2.8,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Comparison of Real-World Utility and Video Quality in Commercially Available Single-Use Ureteroscopes. 市面上可买到的一次性输尿管镜的实际效用和视频质量的比较。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-05 DOI: 10.1177/08927790251390908
Raviraj Rege, Stephen Hassig, Shreya Patel, Scott Quarrier, Nitin Sharma, Rajat Jain

Introduction: Single-use (SU) flexible ureteroscopes have been widely adopted as standard-of-care. However, there are few head-to-head studies comparing SU scopes in real-world clinical scenarios. Further complicating these comparisons is the fast pace of incremental improvement and evolution of SU scopes. We compared usability and video quality for SU ureteroscopes in a real-world clinical scenario to provide information for prospective users.

Methods: Nine SU and one reusable ureteroscope were compared (Boston Scientific LithoVue, LithoVue Elite, Cook Ascend, Dornier Axis, OTU WiScope, Pusen Uscope, Becton Dickinson Aptra, Richard Wolf digital ureteroscope, Storz Flex-XC1, Olympus URF-V2). First, faculty and residents performed ureteroscopy and reviewed scopes with the University of Wisconsin Flexible Ureteroscopy Evaluation Instrument (image quality, deflection, control, irrigation, access, working channel, and satisfaction; 1-5 scale). Second, using a novel video quality evaluation instrument, blinded reviewers rated resolution, contrast, color, sharpness, glare, depth perception, distortion, and overall quality on a 1-5 scale. Multivariate analysis of variance and analysis of variance analyses were conducted.

Results: 167 hands-on and 162 video evaluations were completed. Internal consistency was demonstrated (Cronbach's α > 0.90 for all cases).Hands-on Evaluation:Flex-XC1 and LithoVue Elite had the highest image quality (p < 0.05). Ascend had superior ureteroscopic access (p < 0.05). Uscope ranked lowest in image quality, working channel function, and satisfaction (p < 0.05). LithoVue Elite and Ascend had the highest satisfaction scores (4.64, 4.60, p < 0.05).Video-Based Evaluation:Flex-XC1 and URF-V2 had the highest resolution, contrast, and overall quality (p < 0.05). Flex-XC1 led in color and sharpness (p < 0.05), while Uscope was rated poorly for image resolution, contrast, sharpness, and overall image quality (p < 0.05).

Conclusions: This study is the largest head-to-head comparison to date, providing real-world data for urologists who are prospective purchasers and users of SU ureteroscopes. In the hands-on evaluation, users preferred Cook Ascend, Boston Scientific LithoVue Elite, and Storz Flex-XC1. The Flex-XC1 was rated higher in most categories in video quality evaluation.

简介:一次性(SU)柔性输尿管镜已被广泛采用作为标准护理。然而,很少有在真实临床场景中比较超声内镜的正面研究。进一步使这些比较复杂化的是SU范围的快速增量改进和演变。我们比较了SU输尿管镜在真实临床场景中的可用性和视频质量,为潜在用户提供信息。方法:比较9台SU输尿管镜和1台可重复使用输尿管镜(Boston Scientific LithoVue、LithoVue Elite、Cook Ascend、Dornier Axis、OTU WiScope、Pusen Uscope、Becton Dickinson Aptra、Richard Wolf数字输尿管镜、Storz Flex-XC1、Olympus URF-V2)。首先,教师和住院医生进行输尿管镜检查,并使用威斯康星大学软性输尿管镜评估仪检查范围(图像质量、偏移、控制、灌溉、通道、工作通道和满意度;1-5分)。其次,使用一种新颖的视频质量评估工具,盲法评论者对分辨率、对比度、色彩、清晰度、眩光、深度感知、失真和整体质量进行1-5级评分。进行多变量方差分析和方差分析。结果:完成167个动手评估和162个视频评估。内部一致性证明(所有病例的Cronbach α > 0.90)。实践评价:Flex-XC1和LithoVue Elite成像质量最高(p < 0.05)。Ascend有输尿管镜上通路(p < 0.05)。Uscope在图像质量、工作通道功能和满意度方面排名最低(p < 0.05)。满意度分别为4.64分、4.60分,p < 0.05。基于视频的评价:Flex-XC1和URF-V2具有最高的分辨率、对比度和整体质量(p < 0.05)。Flex-XC1在色彩和清晰度方面领先(p < 0.05),而Uscope在图像分辨率、对比度、清晰度和整体图像质量方面被评为较差(p < 0.05)。结论:这项研究是迄今为止最大的头对头比较,为泌尿科医生提供了真实的数据,他们是SU输尿管镜的潜在购买者和使用者。在实际评估中,用户更喜欢Cook Ascend、Boston Scientific LithoVue Elite和Storz Flex-XC1。Flex-XC1在视频质量评估的大多数类别中都获得了更高的评级。
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引用次数: 0
The Role of Holmium Laser Enucleation of the Prostate in Reducing the Risk of Bladder Cancer Recurrence and Progression. 钬激光前列腺摘除在降低膀胱癌复发和进展风险中的作用。
IF 2.8 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2026-01-01 Epub Date: 2025-11-07 DOI: 10.1177/08927790251390869
Angelo Porreca, Filippo Marino, Davide De Marchi, Marco Giampaoli, Francesca Simonetti, Gian Maria Busetto, Antonio Amodeo, Paolo Corsi, Francesco Claps, Alessandro Crestani, Daniele D'Agostino, Daniele Romagnoli, Pier Paolo Prontera, Luca Di Gianfrancesco

Background: Bladder outlet obstruction (BOO) and urinary retention were recognized contributing factors to bladder cancer (BCa) recurrence and progression due to prolonged urothelial exposure to carcinogens, chronic inflammation, and incomplete bladder emptying. Holmium laser enucleation of prostate (HoLEP) is a minimally invasive and highly effective procedure that completely removes obstructive prostatic tissue, thus resolving BOO. To explore the HoLEP impact on BCa recurrence and progression by improving voiding dynamics and reducing post-void residual (PVR).

Materials and methods: We carried out a retrospective case-control study, based on a multicenter prospectively maintained database, on 100 consecutive male patients (cases) with a first diagnosis of non-muscle-invasive bladder cancer, with BOO and urinary retention and treated with HoLEP (in case of at least 3-months of timor-free status). The cases were compared with 200 patients (controls) with same baseline characteristics but not treated with HoLEP. We evaluated PVR, International Prostatic Symptoms Score-IPSS, BCa recurrence and progression rates. The t-Test, χ2-test, logistic correlations, multivariate analysis were applied to evaluate the association between the BOO resolution and urinary retention by HoLEP and BCa recurrence and progression.

Results: Patients treated with HoLEP showed a significant PVR reduction compared with controls (p < 0.01). The HoLEP group demonstrated statistically significant improvements in IPSS scores, indicating better urinary symptom control. The rates of recurrence and progression were significantly lower in the HoLEP-treated group (p < 0.01). Multivariate analysis identified the BOO resolution by HoLEP as an independent predictor of reduced BCa recurrence (odds ratio 0.65, 95% CI 0.45-0.85, p < 0.001). The control group exhibited persistently elevated PVR and higher rates of BCa recurrence and progression.

Conclusions: Urinary retention could represent a prognostic factor of treatment response, and its active treatment by HoLEP should be considered as an important therapeutic step in the clinical management of patients with BCa.

背景:由于尿路上皮长期暴露于致癌物、慢性炎症和膀胱排空不完全,膀胱出口梗阻(BOO)和尿潴留被认为是膀胱癌(BCa)复发和进展的重要因素。钬激光前列腺摘除(HoLEP)是一种微创、高效的手术,可以完全切除阻塞性前列腺组织,从而解决BOO。目的探讨HoLEP通过改善排尿动力学和减少排尿后残留(PVR)对BCa复发和进展的影响。材料和方法:我们基于一个多中心前瞻性维护的数据库,对100例首次诊断为非肌肉侵袭性膀胱癌,伴有BOO和尿潴留并接受HoLEP治疗的连续男性患者(至少3个月无timor状态的情况下)进行了回顾性病例对照研究。这些病例与200例基线特征相同但未接受HoLEP治疗的患者(对照组)进行比较。我们评估了PVR、国际前列腺症状评分- ipss、BCa复发率和进展率。采用t检验、χ2检验、logistic相关、多因素分析评价HoLEP治疗后尿潴留与BCa复发和进展之间的相关性。结果:与对照组相比,HoLEP治疗组PVR明显降低(p < 0.01)。HoLEP组在IPSS评分上有统计学上的显著改善,表明泌尿症状得到了更好的控制。holep治疗组的复发率和进展率明显低于对照组(p < 0.01)。多变量分析表明,HoLEP的BOO分辨率是减少BCa复发的独立预测因子(优势比0.65,95% CI 0.45-0.85, p < 0.001)。对照组患者PVR持续升高,BCa复发和进展率较高。结论:尿潴留可能是影响治疗效果的一个预后因素,在BCa患者的临床管理中,应将HoLEP积极治疗作为重要的治疗步骤。
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引用次数: 0
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Journal of endourology
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