Pub Date : 2026-02-17DOI: 10.1177/08927790261417886
Amir S Patel, Perry Xu, Kyle Tsai, Alyssa McDonald, Allaa Fadl-Alla, Amy Krambeck
Introduction: Iodinated contrast media (ICM) improves image quality, but there is a subset of patients who can develop life-threatening allergic reactions when exposed. Recent literature has challenged the dogma that prior allergies to contrast or shellfish can predict reactions with intravenous ICM use. It remains unclear if this holds true when used in the urinary tract. This study aims to evaluate patients who are exposed to ICM in their urinary tract and assess if preoperative allergic prophylaxis (PAP) or prior allergy to ICM (a-ICM) can predict severe adverse reactions (SARs).
Methods: This is a single-institution retrospective study of patients who had a ureteroscopy (URS) or percutaneous nephrolithotomy (PCNL) in the last 22 years. Patients with a documented allergy to ICM were divided based on if they received PAP and the procedure performed. Data were obtained through the Northwestern Enterprise Data Warehouse. Postoperative ICU admission and intraoperative epinephrine use in patients with a-ICM are our primary outcome measures as a surrogate for a SAR.
Results: There were 12,020 patients who underwent URS or PCNL with a 0.5% rate of SARs. There is no difference in SAR rate based on a-ICM status (0.4% vs 0.5% [p = 1.00]). Logistic regression shows a similar no significant correlation between SAR and a-ICM (odds ratios [OR]: 0.47; 95% confidence interval [CI]: 0.08-1.57) as well as SAR and PAP (OR: 0.43; 95% CI: 0.15-0.99). American Society of Anesthesiologists score, female sex (OR: 2.69; 95% CI: 1.58-4.74), and length of hospitalization (OR: 1.07; 95% CI: 1.04-1.11) correlated with SAR.
Conclusions: After reviewing data from 22 years of patients undergoing procedures for nephrolithiasis, we found a low rate of severe adverse reactions. Developing a reaction to ICM cannot be predicted based on prior contrast allergies or routinely prevented with PAP.
{"title":"Allergies to Iodinated Contrast Do Not Predict Adverse Reactions with Contrast Use in Genito-Urinary Surgery.","authors":"Amir S Patel, Perry Xu, Kyle Tsai, Alyssa McDonald, Allaa Fadl-Alla, Amy Krambeck","doi":"10.1177/08927790261417886","DOIUrl":"https://doi.org/10.1177/08927790261417886","url":null,"abstract":"<p><strong>Introduction: </strong>Iodinated contrast media (ICM) improves image quality, but there is a subset of patients who can develop life-threatening allergic reactions when exposed. Recent literature has challenged the dogma that prior allergies to contrast or shellfish can predict reactions with intravenous ICM use. It remains unclear if this holds true when used in the urinary tract. This study aims to evaluate patients who are exposed to ICM in their urinary tract and assess if preoperative allergic prophylaxis (PAP) or prior allergy to ICM (a-ICM) can predict severe adverse reactions (SARs).</p><p><strong>Methods: </strong>This is a single-institution retrospective study of patients who had a ureteroscopy (URS) or percutaneous nephrolithotomy (PCNL) in the last 22 years. Patients with a documented allergy to ICM were divided based on if they received PAP and the procedure performed. Data were obtained through the Northwestern Enterprise Data Warehouse. Postoperative ICU admission and intraoperative epinephrine use in patients with a-ICM are our primary outcome measures as a surrogate for a SAR.</p><p><strong>Results: </strong>There were 12,020 patients who underwent URS or PCNL with a 0.5% rate of SARs. There is no difference in SAR rate based on a-ICM status (0.4% <i>vs</i> 0.5% [<i>p</i> = 1.00]). Logistic regression shows a similar no significant correlation between SAR and a-ICM (odds ratios [OR]: 0.47; 95% confidence interval [CI]: 0.08-1.57) as well as SAR and PAP (OR: 0.43; 95% CI: 0.15-0.99). American Society of Anesthesiologists score, female sex (OR: 2.69; 95% CI: 1.58-4.74), and length of hospitalization (OR: 1.07; 95% CI: 1.04-1.11) correlated with SAR.</p><p><strong>Conclusions: </strong>After reviewing data from 22 years of patients undergoing procedures for nephrolithiasis, we found a low rate of severe adverse reactions. Developing a reaction to ICM cannot be predicted based on prior contrast allergies or routinely prevented with PAP.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261417886"},"PeriodicalIF":2.8,"publicationDate":"2026-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146213408","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}
Pub Date : 2026-02-17DOI: 10.1177/08927790251370363
Wajid Memon, Rachana Mehta, Ranjana Sah
{"title":"<i>Letter:</i> Comment on \"The Feasibility and Safety of the Glean Urodynamics System: The Modern Urodynamics System Efficacy Study\".","authors":"Wajid Memon, Rachana Mehta, Ranjana Sah","doi":"10.1177/08927790251370363","DOIUrl":"10.1177/08927790251370363","url":null,"abstract":"","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790251370363"},"PeriodicalIF":2.8,"publicationDate":"2026-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144855402","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}
Pub Date : 2026-02-16DOI: 10.1177/08927790261422977
Peitong Li, Niall M Corcoran, Nathan Lawrentschuk, Dinesh K Agarwal
Objective: To critically appraise the Radius, Exophytic/endophytic, Nearness of tumor to collecting system or sinus, Anterior/posterior, Location relative to polar lines (R.E.N.A.L.), Preoperative Aspects and Dimensions Used for an Anatomical classification (PADUA), and Radius, Position, iNvasion of sinus (RPN) nephrometry systems with respect to their classification of tumor complexity for surgical planning in robot-assisted partial nephrectomy (RAPN) and to compare their statistical validity, methodological rigor, and predictive performance.
Materials and methods: A structured synthesis of published evidence identified large multicenter series, prospective cohorts, and meta-analyses from 2009 to 2025 that evaluated the predictive accuracy, methodological design, and clinical relevance of these systems. Key evaluation domains included statistical validation, anatomical parameter selection, and correlation with surgeon-perceived difficulty in RAPN.
Results: Both the R.E.N.A.L. and PADUA scores were developed using empirically selected parameters and have historically been validated based on their correlation with perioperative outcomes. However, evidence in the literature now shows that such correlations are inconsistent and often clinically irrelevant in RAPN. In contrast, the RPN score was developed using a statistically modeled approach, reflecting the real-world surgical difficulty of RAPN as perceived by experienced robotic surgeons.
Conclusion: Current evidence does not support the continued use of R.E.N.A.L. and PADUA scores as validated tools in RAPN. The RPN score, with its statistically validated, anatomy-based methodology and alignment with surgical difficulty, represents a scientifically superior and clinically practical alternative for standardizing tumor complexity in RAPN.
{"title":"A Critical Appraisal of Nephrometry in Robot-Assisted Partial Nephrectomy: Why the RPN Score Outperforms R.E.N.A.L. and PADUA in the Robotic Era.","authors":"Peitong Li, Niall M Corcoran, Nathan Lawrentschuk, Dinesh K Agarwal","doi":"10.1177/08927790261422977","DOIUrl":"https://doi.org/10.1177/08927790261422977","url":null,"abstract":"<p><strong>Objective: </strong>To critically appraise the Radius, Exophytic/endophytic, Nearness of tumor to collecting system or sinus, Anterior/posterior, Location relative to polar lines (R.E.N.A.L.), Preoperative Aspects and Dimensions Used for an Anatomical classification (PADUA), and Radius, Position, iNvasion of sinus (RPN) nephrometry systems with respect to their classification of tumor complexity for surgical planning in robot-assisted partial nephrectomy (RAPN) and to compare their statistical validity, methodological rigor, and predictive performance.</p><p><strong>Materials and methods: </strong>A structured synthesis of published evidence identified large multicenter series, prospective cohorts, and meta-analyses from 2009 to 2025 that evaluated the predictive accuracy, methodological design, and clinical relevance of these systems. Key evaluation domains included statistical validation, anatomical parameter selection, and correlation with surgeon-perceived difficulty in RAPN.</p><p><strong>Results: </strong>Both the R.E.N.A.L. and PADUA scores were developed using empirically selected parameters and have historically been validated based on their correlation with perioperative outcomes. However, evidence in the literature now shows that such correlations are inconsistent and often clinically irrelevant in RAPN. In contrast, the RPN score was developed using a statistically modeled approach, reflecting the real-world surgical difficulty of RAPN as perceived by experienced robotic surgeons.</p><p><strong>Conclusion: </strong>Current evidence does not support the continued use of R.E.N.A.L. and PADUA scores as validated tools in RAPN. The RPN score, with its statistically validated, anatomy-based methodology and alignment with surgical difficulty, represents a scientifically superior and clinically practical alternative for standardizing tumor complexity in RAPN.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261422977"},"PeriodicalIF":2.8,"publicationDate":"2026-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146202046","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}
Objective: To evaluate the predictability of postoperative complications in patients undergoing supine mini-percutaneous nephrolithotomy (mPNL) using the Estimation of Physiologic Ability and Surgical Stress (E-PASS) scoring system. The study investigated whether the E-PASS scoring system could serve as an objective criterion for identifying patients at high risk of complications. The ultimate goal was to enhance postoperative patient management and minimize complications.
Methods: The data of 224 patients who underwent supine mPNL in our clinic between April 2017 and July 2024 were retrospectively analyzed. Postoperative complications were assessed according to the modified Clavien-Dindo classification.
Results: Postoperative complications were observed in 31 (13.8%) of the 224 patients included in the study. While there were no significant differences between the groups in terms of age, sex, or body mass index, the complication group had a higher American Society of Anesthesiologists score (p = 0.007) and a higher Eastern Cooperative Oncology Group performance score (p = 0.001). Furthermore, the complication group exhibited greater blood loss (p = 0.001) and a longer hospital stay (p = 0.017). Comprehensive risk score (CRS) was identified as an independent predictor of postoperative complications (odds ratio: 7.481, 95% confidence interval: 3.054-18.322; p = 0.001). The area under the curve in the receiver operating characteristic curve analysis for CRS was calculated to be 0.862.
Conclusion: The E-PASS scoring system was found to be successful in predicting complications following supine mPNL. A CRS value exceeding 0.862 was associated with an increased risk of severe complications. Therefore, it is recommended that less invasive surgical options be considered for patients with high CRS values.
{"title":"Predicting Complications in Supine Mini-Percutaneous Nephrolithotomy: The Role of the E-PASS Scoring System.","authors":"Feyzi Sinan Erdal, Sedat Cakmak, Caglar Dizdaroglu, Mucahit Gelmis, Faruk Ozgor","doi":"10.1177/08927790261426074","DOIUrl":"https://doi.org/10.1177/08927790261426074","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the predictability of postoperative complications in patients undergoing supine mini-percutaneous nephrolithotomy (mPNL) using the Estimation of Physiologic Ability and Surgical Stress (E-PASS) scoring system. The study investigated whether the E-PASS scoring system could serve as an objective criterion for identifying patients at high risk of complications. The ultimate goal was to enhance postoperative patient management and minimize complications.</p><p><strong>Methods: </strong>The data of 224 patients who underwent supine mPNL in our clinic between April 2017 and July 2024 were retrospectively analyzed. Postoperative complications were assessed according to the modified Clavien-Dindo classification.</p><p><strong>Results: </strong>Postoperative complications were observed in 31 (13.8%) of the 224 patients included in the study. While there were no significant differences between the groups in terms of age, sex, or body mass index, the complication group had a higher American Society of Anesthesiologists score (<i>p</i> = 0.007) and a higher Eastern Cooperative Oncology Group performance score (<i>p</i> = 0.001). Furthermore, the complication group exhibited greater blood loss (<i>p</i> = 0.001) and a longer hospital stay (<i>p</i> = 0.017). Comprehensive risk score (CRS) was identified as an independent predictor of postoperative complications (odds ratio: 7.481, 95% confidence interval: 3.054-18.322; <i>p</i> = 0.001). The area under the curve in the receiver operating characteristic curve analysis for CRS was calculated to be 0.862.</p><p><strong>Conclusion: </strong>The E-PASS scoring system was found to be successful in predicting complications following supine mPNL. A CRS value exceeding 0.862 was associated with an increased risk of severe complications. Therefore, it is recommended that less invasive surgical options be considered for patients with high CRS values.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261426074"},"PeriodicalIF":2.8,"publicationDate":"2026-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146201717","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}
Pub Date : 2026-02-12DOI: 10.1177/08927790261422982
Mert Hamza Özbilen, Burak Sağmak, Yusuf Enes Kök, Hakan Anıl, Ümit Uysal, Batuhan Ergani, Adem Altunkol, Ergün Alma, Zafer Gökhan Gürbüz
Purpose: To evaluate the effects of renal parenchymal thickness (RPT) and tract length (TL) on the stone-free rate (SFR) and complications in pediatric patients who underwent minimally invasive percutaneous nephrolithotomy (mini-PCNL).
Materials and methods: The data of pediatric age group (<18 years) patients who underwent mini-PCNL between 2017 and 2025 in our clinic, which is a tertiary referral center, were retrieved. Eighty patients were included in this study. SFR was determined using low-dose nonenhanced CT in all patients 1 month after procedure. Stone-free status was defined as the complete absence of stones, and the presence of any stone fragment, regardless of size, was defined as residual stone.
Results: The mean stone diameter was 22.8 mm, and the mean stone burden was 402 mm2. Although 46.3% of the stones were located only in the renal pelvis, 32.5% were staghorn. Mean RPT was 13.6 ± 5.0 mm, TL was 33.0 ± 10.5 mm, and RPT/TL ratio was 0.42 ± 0.13. Complications occurred in 27.5% of the patients. No major (grade 4-5) complications were observed in any patient. After mini-PCNL, stone-free status was achieved in 65% of patients. The mean diameter of residual stone was 3.4 ± 5.9 mm. When comparing patients who were stone free and those with residual stones, RPT (p = 0.059), TL (p = 0.315), and RPT/TL ratio (p = 0.563) were similar between groups. When patients with and without complications were compared, no statistically significant difference was found between the two groups in RPT (p = 0.084), TL (p = 0.589), and RPT/TL ratio (p = 0.723).
Conclusions: Mini-PCNL appears to be an effective and safe surgical technique that can be applied in pediatric patients with kidney stones, regardless of RPT and TL; however, prospective multicenter studies are necessary to confirm our results in a larger number of patients.
{"title":"The Role of Renal Parenchymal Thickness and Tract Length on Mini-Percutaneous Nephrolithotomy Outcomes in Pediatric Patients.","authors":"Mert Hamza Özbilen, Burak Sağmak, Yusuf Enes Kök, Hakan Anıl, Ümit Uysal, Batuhan Ergani, Adem Altunkol, Ergün Alma, Zafer Gökhan Gürbüz","doi":"10.1177/08927790261422982","DOIUrl":"https://doi.org/10.1177/08927790261422982","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the effects of renal parenchymal thickness (RPT) and tract length (TL) on the stone-free rate (SFR) and complications in pediatric patients who underwent minimally invasive percutaneous nephrolithotomy (mini-PCNL).</p><p><strong>Materials and methods: </strong>The data of pediatric age group (<18 years) patients who underwent mini-PCNL between 2017 and 2025 in our clinic, which is a tertiary referral center, were retrieved. Eighty patients were included in this study. SFR was determined using low-dose nonenhanced CT in all patients 1 month after procedure. Stone-free status was defined as the complete absence of stones, and the presence of any stone fragment, regardless of size, was defined as residual stone.</p><p><strong>Results: </strong>The mean stone diameter was 22.8 mm, and the mean stone burden was 402 mm<sup>2</sup>. Although 46.3% of the stones were located only in the renal pelvis, 32.5% were staghorn. Mean RPT was 13.6 ± 5.0 mm, TL was 33.0 ± 10.5 mm, and RPT/TL ratio was 0.42 ± 0.13. Complications occurred in 27.5% of the patients. No major (grade 4-5) complications were observed in any patient. After mini-PCNL, stone-free status was achieved in 65% of patients. The mean diameter of residual stone was 3.4 ± 5.9 mm. When comparing patients who were stone free and those with residual stones, RPT (<i>p</i> = 0.059), TL (<i>p</i> = 0.315), and RPT/TL ratio (<i>p</i> = 0.563) were similar between groups. When patients with and without complications were compared, no statistically significant difference was found between the two groups in RPT (<i>p</i> = 0.084), TL (<i>p</i> = 0.589), and RPT/TL ratio (<i>p</i> = 0.723).</p><p><strong>Conclusions: </strong>Mini-PCNL appears to be an effective and safe surgical technique that can be applied in pediatric patients with kidney stones, regardless of RPT and TL; however, prospective multicenter studies are necessary to confirm our results in a larger number of patients.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261422982"},"PeriodicalIF":2.8,"publicationDate":"2026-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146180138","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}
Pub Date : 2026-02-11DOI: 10.1177/08927790261422980
Rita R Palanjian, Taylor Veschio, Ava A Delu, Sunchin Kim, David T Tzou, Joel T Funk
Introduction: Holmium laser enucleation of the prostate (HoLEP) is a size-independent treatment for benign prostatic hyperplasia (BPH) that has emerged as the gold standard. Pulse-modulated energy delivery, MOSES™ laser technology, optimizes the delivery of energy by reducing energy loss between the laser fiber and tissue. This study aims to compare the operative parameters of HoLEP using MOSES™ 1.0 vs 2.0.
Materials and methods: We prospectively enlisted patients undergoing HoLEP at two sites in a single institution. Patients were assigned to MOSES™ 1.0 or 2.0 by site and remained blinded to laser settings. Primary outcomes were differences in postoperative hemoglobin and enucleation, morcellation and hemostasis times. Secondary outcomes were improvement in International Prostate Symptom Score, maximum urinary flow rate, proportion of prostate enucleated and enucleation efficiency.
Results: Among 236 patients (median age 73 (46-90), 67 (28%) were assigned to the 1.0 group and 169 (72%) to the 2.0 group. Baseline demographics were similar, except higher rates of active anticoagulation in the 2.0 cohort (0 vs 8%, p < 0.03). The 2.0 group had significantly higher hemoglobin on postoperative day 1 (POD1) (1.0: 12.5 vs 2.0: 13.0, p < 0.05). Enucleation (51.0 vs 46.5 minutes) and morcellation (6.0 vs 7.0) were comparable. Hemostasis was 33% faster with the 2.0 (15.0 vs 10.0 minutes, p < 0.001), even when adjusted for prostate volume (p < 0.0001) and anticoagulation status (p = 0.001). Although not statistically different, the 1.0 cohort had higher rate of urinary tract infection (11.9% vs 6.0%), while the 2.0 cohort had more Clavien-Dindo IV complications (0% vs 1.2%) and clot retention (0% vs 1.2%).
Conclusions: Compared with the 1.0, the MOSES™ 2.0 laser demonstrated significantly improved intraoperative hemostasis while maintaining comparable enucleation efficiency. Although POD1 hemoglobin values were higher with the 2.0 system, the difference was small and unlikely clinically meaningful. Secondary postoperative outcomes were also similar between groups. Our findings suggest that the primary advantage of the updated technology lies in enhanced hemostatic performance rather than procedural efficiency.
简介:钬激光前列腺摘除(HoLEP)是一种治疗良性前列腺增生(BPH)的非尺寸治疗方法,已成为金标准。脉冲调制能量输送,MOSES™激光技术,通过减少激光光纤和组织之间的能量损失来优化能量输送。本研究旨在比较使用MOSES™1.0和2.0的HoLEP的操作参数。材料和方法:我们在同一机构的两个地点前瞻性地招募了接受HoLEP的患者。患者按部位被分配到MOSES™1.0或2.0,并对激光设置保持盲视。主要结果是术后血红蛋白和去核、碎裂和止血时间的差异。次要结果为国际前列腺症状评分、最大尿流率、前列腺去核比例和去核效率的改善。结果:236例患者中位年龄73岁(46 ~ 90岁),1.0组67例(28%),2.0组169例(72%)。基线人口统计学相似,除了2.0组的主动抗凝率更高(0比8%,p < 0.03)。2.0组术后第1天血红蛋白明显增高(1.0:12.5 vs 2.0: 13.0, p < 0.05)。去核(51.0 vs 46.5分钟)和分块(6.0 vs 7.0分钟)具有可比性。即使在调整前列腺体积(p < 0.0001)和抗凝状态(p = 0.001)后,2.0组的止血速度也快33% (15.0 vs 10.0分钟,p < 0.001)。虽然无统计学差异,但1.0组尿路感染发生率较高(11.9% vs 6.0%), 2.0组有更多的Clavien-Dindo IV并发症(0% vs 1.2%)和血栓潴留(0% vs 1.2%)。结论:与1.0相比,MOSES™2.0激光术中止血效果明显改善,同时保持相当的去核效率。虽然2.0系统的POD1血红蛋白值较高,但差异很小,不太可能具有临床意义。两组间的术后二次结果也相似。我们的研究结果表明,更新技术的主要优势在于增强止血性能,而不是手术效率。
{"title":"Comparative Outcomes of MOSES<b>™</b> 1.0 Versus 2.0 in Holmium Laser Enucleation of the Prostate Is There Really a Difference?","authors":"Rita R Palanjian, Taylor Veschio, Ava A Delu, Sunchin Kim, David T Tzou, Joel T Funk","doi":"10.1177/08927790261422980","DOIUrl":"https://doi.org/10.1177/08927790261422980","url":null,"abstract":"<p><strong>Introduction: </strong>Holmium laser enucleation of the prostate (HoLEP) is a size-independent treatment for benign prostatic hyperplasia (BPH) that has emerged as the gold standard. Pulse-modulated energy delivery, MOSES™ laser technology, optimizes the delivery of energy by reducing energy loss between the laser fiber and tissue. This study aims to compare the operative parameters of HoLEP using MOSES™ 1.0 <i>vs</i> 2.0.</p><p><strong>Materials and methods: </strong>We prospectively enlisted patients undergoing HoLEP at two sites in a single institution. Patients were assigned to MOSES™ 1.0 or 2.0 by site and remained blinded to laser settings. Primary outcomes were differences in postoperative hemoglobin and enucleation, morcellation and hemostasis times. Secondary outcomes were improvement in International Prostate Symptom Score, maximum urinary flow rate, proportion of prostate enucleated and enucleation efficiency.</p><p><strong>Results: </strong>Among 236 patients (median age 73 (46-90), 67 (28%) were assigned to the 1.0 group and 169 (72%) to the 2.0 group. Baseline demographics were similar, except higher rates of active anticoagulation in the 2.0 cohort (0 <i>vs</i> 8%, <i>p</i> < 0.03). The 2.0 group had significantly higher hemoglobin on postoperative day 1 (POD1) (1.0: 12.5 <i>vs</i> 2.0: 13.0, <i>p</i> < 0.05). Enucleation (51.0 <i>vs</i> 46.5 minutes) and morcellation (6.0 <i>vs</i> 7.0) were comparable. Hemostasis was 33% faster with the 2.0 (15.0 <i>vs</i> 10.0 minutes, <i>p</i> < 0.001), even when adjusted for prostate volume (<i>p</i> < 0.0001) and anticoagulation status (<i>p</i> = 0.001). Although not statistically different, the 1.0 cohort had higher rate of urinary tract infection (11.9% <i>vs</i> 6.0%), while the 2.0 cohort had more Clavien-Dindo IV complications (0% <i>vs</i> 1.2%) and clot retention (0% <i>vs</i> 1.2%).</p><p><strong>Conclusions: </strong>Compared with the 1.0, the MOSES™ 2.0 laser demonstrated significantly improved intraoperative hemostasis while maintaining comparable enucleation efficiency. Although POD1 hemoglobin values were higher with the 2.0 system, the difference was small and unlikely clinically meaningful. Secondary postoperative outcomes were also similar between groups. Our findings suggest that the primary advantage of the updated technology lies in enhanced hemostatic performance rather than procedural efficiency.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261422980"},"PeriodicalIF":2.8,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146165473","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}
Pub Date : 2026-02-11DOI: 10.1177/08927790261420565
Brian R Matlaga, Thomas J Mueller, Brett Johnson, Jay B Page, J Stuart Wolf, Glenn M Preminger, Loren Jones, Ilya Sobol, Karen L Stern, Michael Lipkin, David Cuellar, Kaitlan Cobb, Robert Barsky, Robert Medairos, Charles Marguet, Naren Nimmagadda, Mark White, Michael Levin, Thomas Chi
Purpose: The ASPiration to Improve Renal Calculi Removal Effectiveness study showed steerable ureteroscopic renal evacuation (SURE) with CVAC that significantly reduced residual stone volume at 30 days vs standard ureteroscopy (URS). This report presents 2-year health care consumption and stone events (SE) and their link to residual stone volume and other variables (n = 101 at primary end point; n = 93 at 2 years).
Materials and methods: Logistic regression identified predictors of health care consumption events (HCEs), that is, emergency department visits, hospitalization, surgical retreatment, and SE across the study population. Incidence was compared between the treatment groups with Kaplan-Meier survival analysis.
Results: At 2 years, residual stone volume was significantly associated with both HCEs and SE. For every 100 mm3 increase in residual stone volume, the HCE risk increased by 50% to 54%, and the SE risk increased by 70%. Stone-free rate, the number of residual fragments (RFs), and RF total stone burden (based on diameter) were not predictors. Significantly fewer HCEs occurred in the SURE group (3 vs 20 events, p = 0.0004). Survival analysis confirmed this (4.3% vs 20%, log-rank p = 0.02), with a 73% risk reduction (hazard ratio 0.27, 95% Cl 0.09-0.80, p = 0.02). Fewer SE occurred in the SURE group, although not statistically significant. These subjects also had longer event-free survival.
Conclusion: High-quality volumetric analysis supports evaluation of stone removal therapies, as residual stone volume predicts HCEs and SE. SURE significantly reduces the downstream incidence and risk of HCEs compared with standard URS.
目的:抽吸提高肾结石清除效果的研究表明,与标准输尿管镜(URS)相比,采用CVAC的可操控输尿管镜肾排出术(SURE)在30天内显著减少残留结石体积。本报告介绍了2年的医疗保健消费和结石事件(SE)及其与剩余结石体积和其他变量的联系(n = 101, 2年n = 93)。材料和方法:Logistic回归确定了卫生保健消费事件(HCEs)的预测因素,即急诊就诊、住院、手术再治疗和研究人群中的SE。采用Kaplan-Meier生存分析比较两组间的发病率。结果:2年时,残余结石体积与hce和SE均显著相关。残余结石体积每增加100 mm3, HCE风险增加50% ~ 54%,SE风险增加70%。结石游离率、残留碎片(RF)数量和RF总结石负荷(基于直径)不是预测因子。SURE组hce发生率明显减少(3 vs 20, p = 0.0004)。生存分析证实了这一点(4.3% vs 20%, log-rank p = 0.02),风险降低73%(风险比0.27,95% Cl 0.09-0.80, p = 0.02)。SURE组的SE发生率较低,但无统计学意义。这些受试者也有更长的无事件生存期。结论:高质量的体积分析支持结石去除治疗的评估,因为残余结石体积可以预测hce和SE。与标准URS相比,SURE可显著降低hce的下游发生率和风险。
{"title":"Residual Stone Volume Predicts Health Care Consumption and Stone Events: Analysis of Two-Year Results of the ASPIRE Study.","authors":"Brian R Matlaga, Thomas J Mueller, Brett Johnson, Jay B Page, J Stuart Wolf, Glenn M Preminger, Loren Jones, Ilya Sobol, Karen L Stern, Michael Lipkin, David Cuellar, Kaitlan Cobb, Robert Barsky, Robert Medairos, Charles Marguet, Naren Nimmagadda, Mark White, Michael Levin, Thomas Chi","doi":"10.1177/08927790261420565","DOIUrl":"https://doi.org/10.1177/08927790261420565","url":null,"abstract":"<p><strong>Purpose: </strong>The ASPiration to Improve Renal Calculi Removal Effectiveness study showed steerable ureteroscopic renal evacuation (SURE) with CVAC that significantly reduced residual stone volume at 30 days <i>vs</i> standard ureteroscopy (URS). This report presents 2-year health care consumption and stone events (SE) and their link to residual stone volume and other variables (<i>n</i> = 101 at primary end point; <i>n</i> = 93 at 2 years).</p><p><strong>Materials and methods: </strong>Logistic regression identified predictors of health care consumption events (HCEs), that is, emergency department visits, hospitalization, surgical retreatment, and SE across the study population. Incidence was compared between the treatment groups with Kaplan-Meier survival analysis.</p><p><strong>Results: </strong>At 2 years, residual stone volume was significantly associated with both HCEs and SE. For every 100 mm<sup>3</sup> increase in residual stone volume, the HCE risk increased by 50% to 54%, and the SE risk increased by 70%. Stone-free rate, the number of residual fragments (RFs), and RF total stone burden (based on diameter) were not predictors. Significantly fewer HCEs occurred in the SURE group (3 <i>vs</i> 20 events, <i>p</i> = 0.0004). Survival analysis confirmed this (4.3% <i>vs</i> 20%, log-rank <i>p</i> = 0.02), with a 73% risk reduction (hazard ratio 0.27, 95% Cl 0.09-0.80, <i>p</i> = 0.02). Fewer SE occurred in the SURE group, although not statistically significant. These subjects also had longer event-free survival.</p><p><strong>Conclusion: </strong>High-quality volumetric analysis supports evaluation of stone removal therapies, as residual stone volume predicts HCEs and SE. SURE significantly reduces the downstream incidence and risk of HCEs compared with standard URS.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790261420565"},"PeriodicalIF":2.8,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146165526","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}
Pub Date : 2026-02-10DOI: 10.1177/08927790251394635
Thomas Chi, Camilla Gomes, Brandon Cowan, Nancy L Sehgel, Maggie Lin, Paul Morris, Marshall L Stoller
Purpose: Robotic-assisted urologic stone removal and any potential histopathological effects of this approach have not been well studied. Here we assess safety and user experience of the novel MONARCH™ Platform, Urology, in performing both robotic-assisted ureteroscopy (URS) and percutaneous nephrolithotomy (PCNL) within a preclinical setting, alongside conventional devices.
Materials and methods: Two endourologists conducted six simulated robotic-assisted URS and six robotic-assisted PCNL in a porcine model, comparing these with conventional approaches. The primary objectives were (1) perceived ease of completion as rated by the endourologists using a numerical 1-4 rating scale; (2) occurrence of adverse safety events as determined by the operating endourologists; (3) assessment of contrast extravasation seen on post-operative retrograde pyelogram; and (4) histopathological evaluation of the porcine models' urinary tracts. Mantel-Haenszel chi-square test was used, with p < 0.05 considered significant.
Results: Tasks within URS and PCNL exhibited comparable ease of completion score means (median of all scores 4 in conventional URS and 4 in robot-assisted URS, p = 0.131; 3.17 in conventional PCNL and 4 in robot-assisted PCNL, p = 0.258). No safety events were observed by the endourologist during URS or PCNL procedures for either the robotic-assisted or conventional devices. In post-procedure pyelograms, none of the robotic-assisted cohort had more than minimal contrast extravasation, statistically similar to conventional devices (URS: median [range]; conventional, 0 [0-2] vs. robotic-assisted, 0 [0-1], p = 0.337; and PCNL: conventional, 0 [0-2] vs. robotic-assisted, 0 [0-1], p = 0.379). Blinded pathology assessment demonstrated no biologically significant nor clinically relevant differences between robotic-assisted and conventional devices in any category.
Conclusions: This study demonstrates that the MONARCH™ Platform in Urology has a safety profile comparable with conventional devices and a trend of easier completion of some tasks. This foundational study establishes the feasibility of a single platform to complete both robotic-assisted URS and PCNL, as a new treatment paradigm for urologic stone management.
{"title":"Preclinical Evaluation of the Safety of Robotic-Assisted Ureteroscopy and Guided Percutaneous Nephrolithotomy.","authors":"Thomas Chi, Camilla Gomes, Brandon Cowan, Nancy L Sehgel, Maggie Lin, Paul Morris, Marshall L Stoller","doi":"10.1177/08927790251394635","DOIUrl":"https://doi.org/10.1177/08927790251394635","url":null,"abstract":"<p><strong>Purpose: </strong>Robotic-assisted urologic stone removal and any potential histopathological effects of this approach have not been well studied. Here we assess safety and user experience of the novel MONARCH™ Platform, Urology, in performing both robotic-assisted ureteroscopy (URS) and percutaneous nephrolithotomy (PCNL) within a preclinical setting, alongside conventional devices.</p><p><strong>Materials and methods: </strong>Two endourologists conducted six simulated robotic-assisted URS and six robotic-assisted PCNL in a porcine model, comparing these with conventional approaches. The primary objectives were (1) perceived ease of completion as rated by the endourologists using a numerical 1-4 rating scale; (2) occurrence of adverse safety events as determined by the operating endourologists; (3) assessment of contrast extravasation seen on post-operative retrograde pyelogram; and (4) histopathological evaluation of the porcine models' urinary tracts. Mantel-Haenszel chi-square test was used, with <i>p</i> < 0.05 considered significant.</p><p><strong>Results: </strong>Tasks within URS and PCNL exhibited comparable ease of completion score means (median of all scores 4 in conventional URS and 4 in robot-assisted URS, <i>p</i> = 0.131; 3.17 in conventional PCNL and 4 in robot-assisted PCNL, <i>p</i> = 0.258). No safety events were observed by the endourologist during URS or PCNL procedures for either the robotic-assisted or conventional devices. In post-procedure pyelograms, none of the robotic-assisted cohort had more than minimal contrast extravasation, statistically similar to conventional devices (URS: median [range]; conventional, 0 [0-2] vs. robotic-assisted, 0 [0-1], <i>p</i> = 0.337; and PCNL: conventional, 0 [0-2] vs. robotic-assisted, 0 [0-1], <i>p</i> = 0.379). Blinded pathology assessment demonstrated no biologically significant nor clinically relevant differences between robotic-assisted and conventional devices in any category.</p><p><strong>Conclusions: </strong>This study demonstrates that the MONARCH™ Platform in Urology has a safety profile comparable with conventional devices and a trend of easier completion of some tasks. This foundational study establishes the feasibility of a single platform to complete both robotic-assisted URS and PCNL, as a new treatment paradigm for urologic stone management.</p>","PeriodicalId":15723,"journal":{"name":"Journal of endourology","volume":" ","pages":"8927790251394635"},"PeriodicalIF":2.8,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146157264","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}