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Postvasectomy Semen Analysis Compliance With Utilization of a Mail-In Semen Analysis Kit. 利用邮寄精液分析套件进行输精管切除术后精液分析的合规性。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-02 DOI: 10.1097/JU.0000000000004185
Catherine Gu, Andre Belarmino, Stacey A Kenfield, Daniel Nolte, Daniel Civello, James F Smith, Stanton Honig, Akanksha Mehta, Nahid Punjani, Lori B Lerner

Purpose: The AUA recommends postvasectomy semen analysis (PVSA) to verify successful vasectomy. However there remains poor patient compliance. We sought to assess whether mail-in PVSA improves patient compliance across a wide range of practice types.

Materials and methods: Prospective data were collected on all men who received a Fellow PVSA kit between April 2021 and August 2023 in a nationwide cohort. Date of kit activation, practice type, clinic zip code, and date of kit accession/processing at the lab were collected. Compliance rates for each practice area were reported. χ2 tests of independence, logistic regression models, and multivariable logistic analysis were performed to assess the impact of relevant variables.

Results: Overall compliance across all practice areas was 69% following an 18-week period of observation (n = 16,105) and 82% (n = 6687) following a 40-week period. Compliance rates were highest and similar for small urology practices (<5 providers), including Veterans Affairs practices, ranging from 76% to 82% at 18 weeks to 85% to 87% at 40 weeks. Large urology practices had slightly lower compliance rates with 66% at 18 weeks to 80% at 40 weeks. The univariable logistic regression model demonstrated that patients in small urology practices have a 63% greater odds of 26-week compliance, on average, compared to those who receive care in large urology practices (odds ratio 1.63, 95% CI 1.48-1.79).

Conclusions: Fellow's mail-in PVSA offers improved PVSA compliance over previously published data. Improved compliance is seen across all practice types. Despite these successes, there is significant room for improvement to achieve 100% compliance.

目的:美国泌尿外科协会建议进行输精管结扎术后精液分析(PVSA),以验证输精管结扎术是否成功。然而,患者的依从性仍然很差。我们试图评估邮寄 PVSA 是否能提高各种类型患者的依从性:我们在全国范围内收集了 2021 年 4 月至 2023 年 8 月期间收到 Fellow PVSA 套件的所有男性的前瞻性数据。收集了试剂盒激活日期、诊所类型、诊所邮政编码以及试剂盒进入实验室/处理的日期。报告了各执业地区的合格率。为评估相关变量的影响,进行了独立性卡方检验、逻辑回归模型和多变量逻辑分析:经过 18 周的观察(n = 16105)和 40 周的观察(n = 6687),所有业务领域的总体合规率分别为 69%和 82%。小型泌尿科诊所的依从率最高,且相差无几(结论:与之前公布的数据相比,Fellow 的邮寄 PVSA 提高了 PVSA 的依从性。所有实践类型的依从性都有所提高。尽管取得了这些成功,但要实现 100% 的依从性还有很大的改进空间。
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引用次数: 0
Generative Artificial Intelligence Platform for Automating Social Media Posts From Urology Journal Articles: A Cross-Sectional Study and Randomized Assessment. 从泌尿学期刊论文中自动生成社交媒体帖子的人工智能平台:一项横断面研究和随机评估
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-14 DOI: 10.1097/JU.0000000000004199
Lorenzo Storino Ramacciotti, Francesco Cei, Jacob S Hershenhouse, Daniel Mokhtar, Severin Rodler, Karanvir Gill, David Strauss, Luis G Medina, Jie Cai, Andre Luis Abreu, Mihir M Desai, Rene Sotelo, Inderbir S Gill, Giovanni E Cacciamani

Purpose: This cross-sectional study assessed a generative artificial intelligence platform to automate the creation of accurate, appropriate, and compelling social media (SoMe) posts from urological journal articles.

Materials and methods: One hundred SoMe posts from the top 3 journals in urology X (formerly Twitter) profiles were collected from August 2022 to October 2023. A freeware generative pre-trained transformer (GPT) tool was developed to autogenerate SoMe posts, which included title summarization, key findings, pertinent emojis, hashtags, and digital object identifier links to the article. Three physicians independently evaluated GPT-generated posts for achieving tetrafecta of accuracy and appropriateness criteria. Fifteen scenarios were created from 5 randomly selected posts from each journal. Each scenario contained both the original and the GPT-generated post for the same article. Five questions were formulated to investigate the posts' likability, shareability, engagement, understandability, and comprehensiveness. The paired posts were then randomized and presented to blinded academic authors and general public through Amazon Mechanical Turk (AMT) responders for preference evaluation.

Results: Median time for post autogeneration was 10.2 seconds (interquartile range 8.5-12.5). Of the 150 rated GPT-generated posts, 115 (76.6%) met the correctness tetrafecta: 144 (96%) accurately summarized the title, 147 (98%) accurately presented the articles' main findings, 131 (87.3%) appropriately used emojis, and 138 (92%) appropriately used hashtags. A total of 258 academic urologists and 493 AMT responders answered the surveys, wherein the GPT-generated posts consistently outperformed the original journals' posts for both academicians and AMT responders (P < .05).

Conclusions: Generative artificial intelligence can automate the creation of SoMe posts from urology journal abstracts that are both accurate and preferable by the academic community and general public.

目的:本横断面研究评估了一个生成式人工智能平台,该平台可根据泌尿外科期刊论文自动创建准确、适当且引人注目的社交媒体(SoMe)帖子:从 2022 年 8 月到 2023 年 10 月,收集了来自泌尿学 X(Twitter)前 3 名期刊的 100 篇 SoMe 帖子。开发了一个免费 GPT 工具,用于自动生成 SoMe 帖子,其中包括标题摘要、主要发现、相关表情符号、标签和文章的 DOI 链接。三位医生对 GPT 生成的帖子进行独立评估,看其是否符合准确性和适当性的四项标准。从每份期刊中随机抽取 5 篇文章,创建了 15 个场景。每个情景都包含同一篇文章的原始帖子和 GPT 生成的帖子。我们设计了五个问题来考察文章的可喜爱性、可分享性、可参与性、可理解性和全面性。然后将配对后的文章进行随机化,并通过亚马逊机械特克(AMT)应答器向盲人学术作者和普通大众展示,以进行偏好评价:帖子自动生成的时间中位数(IQR)为 10.2 秒(8.5-12.5)。在 GPT 生成的 150 篇评分帖子中,115 篇(76.6%)符合正确性四项标准:144 篇(96%)准确概括了标题,147 篇(98%)准确介绍了文章的主要发现,131 篇(87.3%)恰当使用了表情符号和标签 138 篇(92%)。共有 258 名泌尿科学者和 493 名 AMT 答复者回答了调查,其中 GPT 生成的帖子在学者和 AMT 答复者中的表现始终优于原始期刊帖子(P < .05):生成式人工智能可以自动根据泌尿外科期刊摘要创建 SoMe 帖子,这些帖子既准确又受到学术界和公众的青睐。
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引用次数: 0
Editorial Comment. 编辑评论。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-22 DOI: 10.1097/JU.0000000000004192
Nathan M Shaw
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引用次数: 0
Editorial Comment. 编辑评论。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-22 DOI: 10.1097/JU.0000000000004201
Hasan Jhaveri, Rasheed Gbadegesin
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引用次数: 0
Imaging. 成像
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-07-25 DOI: 10.1097/JU.0000000000004140
Cary Siegel
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引用次数: 0
PD52-08 Adherence to Intracavernosal Injection Relative to Prescriber Choices and Patient Income: Erratum. PD52-08 坚持椎管内注射与处方选择和患者收入的关系:勘误。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-11-08 DOI: 10.1097/JU.0000000000004235
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引用次数: 0
A Multi-Institutional Study of Magnetic Resonance/Ultrasound Fusion-Guided Nanoparticle-Directed Focal Therapy for Prostate Ablation. MR/US 融合引导的纳米粒子前列腺消融病灶疗法的多机构研究。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-03 DOI: 10.1097/JU.0000000000004222
Steven E Canfield, Arvin K George, Joshua S Jue, Sara C Lewis, Matthew S Davenport, Varaha S Tammisetti, Mahir Maruf, Leonardo D Borregalaes, Yara Kadria-Vili, Jon A Schwartz, Jennifer West, Naomi J Halas, Ardeshir R Rastinehad

Purpose: Focal therapy aims to provide a durable oncologic treatment option for men with prostate cancer (PCa), while preserving their quality of life. Most focal therapy modalities rely on the direct tissue effect, resulting in a possible nontargeted approach to ablation. Here, we report the results of the first human feasibility trial utilizing nanoparticle-directed focal photothermal ablation for PCa.

Materials and methods: A prospective, open-label, single-arm, multicenter study of men with localized PCa in Gleason Grade Group 1 to 3 was conducted. Men received a single infusion of gold nanoparticles (AuroShells), followed by magnetic resonance (MR)/ultrasound (US) fusion-guided laser excitation of the target tissue to induce photothermal ablation. MRI was used to assess the effectiveness of prostate tissue ablation at 48 to 96 hours, 3 months, and 12 months post treatment. At 3 months, a targeted fusion biopsy of the lesion(s) was conducted. At 12 months, a targeted fusion biopsy and standard templated biopsy were performed. Treatment success was determined based on a negative MR/US fusion biopsy outcome within the treated area.

Results: Forty-six men were enrolled in the study, and 44 men with 45 lesions completed nanoparticle infusion and laser treatment. Baseline mean PSA levels were 9.5 ng/mL, with a statistically significant decrease of 5.9 ng/mL at 3 months and 4.7 ng/mL at 12 months (P < .0001). The oncologic success rates at 3 and 12 months resulted in 29 (66%) and 32 (73%) of 44 patients, respectively, being successfully treated, confirmed with negative MR/US fusion biopsies within the ablation zone. Among Gleason Grade Group, maximum lesion diameter on MRI, prostate volume, and Prostate Imaging Reporting and Data System scoring, the maximum lesion diameter was significantly associated with the odds of treatment failure at 12 months (P = .046).

Conclusions: Nanoparticle-directed focal laser ablation of neoplastic prostate tissue resulted in 73% of patients with successful treatment at 12 months post treatment, confirmed by negative MR/US fusion biopsy of the treated lesion and a systematic biopsy.

Clinical trial registration no.: 02680535.

简介病灶治疗旨在为前列腺癌(PCa)患者提供一种持久的肿瘤治疗方案,同时保证他们的生活质量。大多数病灶治疗模式都依赖于直接组织效应,这可能导致一种非靶向消融方法。在此,我们报告了利用纳米粒子引导的病灶光热消融治疗 PCa 的首个人体可行性试验的结果:一项前瞻性开放标签、单臂多中心研究针对患有局部 PCa 的男性进行,患者的 Gleason 等级组(GGG)为 1 至 3。男性患者接受一次金纳米粒子(AuroShells)输注,然后在 MR/US 融合引导下用激光激发靶组织,诱导光热消融。核磁共振成像用于评估治疗后 48 至 96 小时、3 个月和 12 个月的前列腺组织消融效果。3 个月时,对病灶进行靶向融合活检。12 个月时,进行靶向融合活检和标准模板活检。治疗成功与否取决于治疗区域内的 MR/US 融合活检结果是否为阴性:46名男性参加了这项研究,44名男性的45个病灶完成了纳米颗粒输注和激光治疗。基线PSA平均水平为9.5纳克/毫升,3个月时下降了5.9纳克/毫升,12个月时下降了4.7纳克/毫升(P < .0001)。根据 3 个月和 12 个月的肿瘤学成功率,44 例患者中分别有 29 例(66%)和 32 例(73%)治疗成功,消融区内的 MR/US 融合活检结果均为阴性。在GGG、MRI最大病灶直径(MLD)、前列腺体积和PI-RADS评分中,MLD与12个月时治疗失败的几率显著相关(P = .046):结论:对前列腺肿瘤组织进行纳米粒子定向病灶激光消融术可使73%的患者在治疗后12个月时获得成功治疗,治疗病灶的MR/US融合活检和系统活检结果均为阴性。
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引用次数: 0
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study. 探索儿童日间尿失禁的遗传风险:全基因组关联研究
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-02 DOI: 10.1097/JU.0000000000004187
Anders Breinbjerg, Cecilie Siggaard Jørgensen, G Bragi Walters, Jakob Grove, Thomas D Als, Konstantinos Kamperis, Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg, Clara Albiñana, Bjarni J Vilhjálmsson, Viðar Ö Eðvarðsson, Hreinn Stefánsson, Preben B Mortensen, Esben Agerbo, Thomas Werge, Anders Børglum, Ditte Demontis, Kári Stefánsson, Søren Rittig, Jane Hvarregaard Christensen

Purpose: Childhood incontinence is stigmatized and underprioritized, and a basic understanding of its pathogenesis is missing. Our goal was to identify risk-conferring genetic variants in daytime urinary incontinence (DUI).

Materials and methods: We conducted a genome-wide association study in the Danish iPSYCH2015 cohort. Cases (3024) were identified through DUI diagnosis codes and redeemed prescriptions for DUI medication in individuals aged 5 to 20 years. Controls (30,240), selected from the same sample, were matched to cases on sex and psychiatric diagnoses, if any, and down-sampled to a 1:10 case:control ratio. Replication was performed in the Icelandic deCODE cohort (5475 cases/287,773 controls). Single-nucleotide polymorphism heritability was calculated using the genome-based restricted maximum likelihood method. Cross-trait genetic correlation was estimated using linkage disequilibrium score regression. Polygenic risk scores generated with LDpred2-auto and BOLT-LMM were assessed for association.

Results: Variants on chromosome 6 (rs12210989, odds ratio [OR] 1.24, 95% CI 1.17-1.32, P = 3.21 × 10-12) and 20 (rs4809801, OR 1.18, 95% CI 1.11-1.25, P = 3.66 × 10-8) reached genome-wide significance and implicated the PRDM13 and RIPOR3 genes. Chromosome 6 findings were replicated (P = .024, OR 1.09, 95% CI 1.01-1.16). Liability scale heritability ranged from 10.20% (95% CI 6.40%-14.00%) to 15.30% (95% CI 9.66%-20.94%). DUI and nocturnal enuresis showed positive genetic correlation (rg = 1.28 ± 0.38, P = .0007). DUI was associated with attention-deficit/hyperactivity disorder (OR 1.098, 95% CI 1.046-1.152, P < .0001) and BMI (OR 1.129, 95% CI 1.081-1.178, P < .0001) polygenic risk.

Conclusions: Common genetic variants contribute to the risk of childhood DUI, and genes important in neuronal development and detrusor smooth muscle activity were implicated. These findings may help guide identification of new treatment targets.

目的:儿童尿失禁是一种耻辱,未得到足够重视,对其发病机制也缺乏基本了解。我们的目标是确定日间尿失禁(DUI)的风险诱导基因变异:我们在丹麦 iPSYCH2015 队列中开展了一项全基因组关联研究。病例(3024 例)是通过 5 至 20 岁儿童的白天尿失禁诊断代码和赎回的白天尿失禁药物处方确定的。对照组(30,240 人)从同一样本中选出,与病例的性别和精神诊断(如有)相匹配,并按病例与对照组 1:10 的比例向下取样。在冰岛 deCODE 队列(5475 例病例/287773 例对照)中进行了复制。采用基于基因组的限制性最大似然法计算单核苷酸多态性遗传率。跨性状遗传相关性采用连锁不平衡得分回归法进行估算。利用 LDpred2-auto 和 BOLT-LMM 生成的多基因风险评分对关联性进行了评估:结果:6 号染色体(rs12210989,OR = 1.24 [95% CI:1.17-1.32],P = 3.21 × 10-12)和 20 号染色体(rs4809801,OR = 1.18 [95% CI:1.11-1.25],P = 3.66 × 10-8)上的变异达到全基因组显著性,与 PRDM13 和 RIPOR3 基因有关。6 号染色体的研究结果得到了重复(P = 0.024,OR = 1.09 [95% CI:1.01-1.16])。责任量表遗传率从 10.20% (95% CI: 6.40%-14.00%) 到 15.30% (95% CI: 9.66%-20.94%) 不等。DUI和夜遗尿显示出正遗传相关性(rg = 1.28 ± 0.38,P = .0007)。DUI与注意力缺陷/多动障碍(OR = 1.098 [95% CI: 1.046-1.152],P < .0001)和体重指数(OR = 1.129 [95% CI: 1.081-1.178],P < .0001)多基因风险相关:结论:常见的基因变异会导致儿童酒后驾车的风险,其中牵涉到神经元发育和逼尿肌平滑肌活动的重要基因。这些发现可能有助于确定新的治疗目标。
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引用次数: 0
Editorial Comment. 编辑评论。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-08-23 DOI: 10.1097/JU.0000000000004212
Celestia S Higano, Heather Cheng
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引用次数: 0
Editorial Comment. 编辑评论。
IF 5.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-12 DOI: 10.1097/JU.0000000000004234
Samuel Tremblay, Abhinav Sidana
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引用次数: 0
期刊
Journal of Urology
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