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[First experience with the Visus MG optical videoendoscopic urethral catheter for safe bladder drainage in various urethral injuries]. 【Visus MG光学内镜尿道导管用于各种尿道损伤安全膀胱引流的首次经验】。
Q4 Medicine Pub Date : 2025-09-01
A Yandiev S, A Gazimiev M, V Protoshchak V, G Karpushchenko E, N Akopyan G, V Chinenov D, V Shpot E, M Rapoport L, V Glybochko P
<p><strong>Introduction: </strong>Despite the widespread use of bladder catheterization in both inpatient and outpatient practice, the procedure carries a risk of serious complications, including urethral trauma, strictures, and the development of false passages. According to published data, their incidence ranges from 10.2% to 17.7%. The most common causes of unsuccessful bladder catheterization are anatomical or pathological changes in the urethra, as well as insufficient experience of medical personnel. Repeated attempts at catheterization increase the risk of iatrogenic injuries. In military medicine and emergency care, the problem is aggravated by the high frequency of urethral trauma. Despite the availability of alternative imaging techniques (ultrasound, retrograde urethrography), the choice of the optimal drainage method remains unresolved, particularly in settings with limited access to advanced endoscopic equipment.</p><p><strong>Aim: </strong>To evaluate the efficiency and safety of the Visus MG optical urethral catheter with a portable endoscopic system (PES) in various types of urethral injuries.</p><p><strong>Materials and methods: </strong>A prospective study was conducted at the Institute of Urology and Reproductive Health, Sechenov University, and at the S.M. Kirov Military Medical Academy. Eighty-five patients were included (60 and 25 from each institution, respectively). The efficacy and safety of bladder catheterization using the Visus MG optical urethral catheter with PES were assessed after unsuccessful attempts at standard catheterization, and in some cases without prior standard attempts. Indications included acute urinary retention, urethral trauma (combat or iatrogenic), preoperative drainage, and approximation of urethral edges before urethroplasty. The optical catheter provided visual control of urethral passage and enabled successful drainage in the presence of anatomical obstructions.</p><p><strong>Results: </strong>Patient age ranged from 20 to 86 years (mean: 59.8). The mean prostate volume among non-prostatectomy patients was 33.7 cc, most often between 20-39 cc (42.1%). Bladder catheterization was performed primarily in the operating room (43.5%) or in procedure rooms (37.6%), most commonly under local anesthesia (61.2%). Ahistory of prior urological procedures was documented in 70% of patients. The use of the Visus MG optical urethral catheter with PES achieved successful bladder drainage in 96.5% of cases (82/85) without complications. The main causes of failed standard catheterization were strictures, urethral trauma, and other obstructive conditions.</p><p><strong>Conclusion: </strong>The Visus MG optical urethral catheter with a PES enabled safe and effective bladder drainage in 96.5% of patients after failed standard bladder catheterization. The method is minimally invasive, provides direct visual control, and reduces the risk of false passages and urethral injury. It may serve as an alternative to cystosco
导读:尽管膀胱导尿术在住院和门诊都得到了广泛的应用,但该手术存在严重并发症的风险,包括尿道创伤、狭窄和假通道的形成。根据公布的数据,其发病率从10.2%到17.7%不等。膀胱导尿不成功的最常见原因是尿道的解剖或病理改变,以及医务人员经验不足。反复尝试置管会增加医源性损伤的风险。在军事医学和急诊护理中,尿道创伤的高频率加剧了这个问题。尽管有可替代的成像技术(超声、逆行尿道造影),但最佳引流方法的选择仍未解决,特别是在使用先进内窥镜设备有限的情况下。目的:评价Visus MG光学导尿管与便携式内镜系统(PES)在不同类型尿道损伤中的有效性和安全性。材料和方法:在谢切诺夫大学泌尿外科和生殖健康研究所和S.M.基洛夫军事医学院进行了一项前瞻性研究。85名患者被纳入(每家机构分别为60名和25名)。使用Visus MG光学导尿管与PES进行膀胱导尿的有效性和安全性在标准导尿失败后进行评估,在一些没有事先进行标准导尿尝试的情况下。适应症包括急性尿潴留,尿道外伤(战斗或医源性),术前引流,尿道成形术前尿道边缘逼近。光学导尿管提供了对尿道通道的视觉控制,并在存在解剖障碍的情况下成功引流。结果:患者年龄20 ~ 86岁,平均59.8岁。非前列腺切除术患者的平均前列腺体积为33.7 cc,大多数在20-39 cc之间(42.1%)。膀胱导尿主要在手术室(43.5%)或手术室(37.6%)进行,最常见的是在局麻下(61.2%)。70%的患者有泌尿外科手术史。Visus MG光学导尿管与PES联合使用,96.5%的病例(82/85)膀胱引流成功,无并发症。标准置管失败的主要原因是尿道狭窄、尿道外伤和其他梗阻性疾病。结论:Visus MG光学导尿管加PES可使96.5%的患者在标准膀胱置管失败后安全有效地进行膀胱引流。该方法是微创的,提供直接的视觉控制,并减少了假通道和尿道损伤的风险。在使用全套内窥镜设备受限的情况下,它可以作为膀胱镜检查的替代方法。
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引用次数: 0
[The role of transmission microscopy in assessing morphometric changes in spermatozoa of fertile and infertile men who have had COVID-19]. [透射显微镜在评估患有COVID-19的可育和不育男性精子形态变化中的作用]。
Q4 Medicine Pub Date : 2025-09-01
O Prokop Ya, S Ibishev Kh, A Pogozhaeva M, A Sinelnik E, I Kogan M

Introduction: As COVID-19-induced disorders wreak havoc on populations worldwide, attention to the rehabilitation of the consequences has focused mainly on vital organ systems (lungs, kidneys, and heart) that are vulnerable to the initial viral attack and contribute to the development of acute pathology associated with this disease. However, we should not lose sight of the fact that COVID-19 affects any cells in the body that express ACE2, including human sperm.

Materials and methods: The results of transmission electron microscopy of the ejaculate of 157 men were analyzed. They were divided into four groups: Group I - 49 patients with idiopathic infertility who had COVID-19, Group II - 42 patients with idiopathic infertility who did not have COVID-19 during the study, Group III - 39 fertile men who had COVID-19, Group IV - 27 fertile men who did not have COVID-19.

Objective: To study the role of sperm mitochondrial dysfunction in the development of male infertility associated with COVID-19.

Results: According to transmission microscopy of the ejaculate, men who brought COVID-19 have severe sperm disorders, such as mitochondrial dysfunction and the presence of residual cytoplasm, which were more often recorded in infertile patients, compared to fertile men.

Conclusions: COVID-19 impairs male reproductive potential and may impair male fertility.

导览:随着covid -19引发的疾病对全世界人口造成严重破坏,对后果恢复的关注主要集中在重要器官系统(肺、肾脏和心脏)上,这些系统易受最初病毒攻击的影响,并导致与该疾病相关的急性病理的发展。但是,我们不能忽视的事实是,COVID-19会影响包括人类精子在内的身体中表达ACE2的任何细胞。材料与方法:对157例男性射精的透射电镜结果进行分析。他们被分为四组:第一组- 49例患有COVID-19的特发性不育症患者,第二组- 42例在研究期间未患COVID-19的特发性不育症患者,第三组- 39例患有COVID-19的育龄男性,第四组- 27例未患COVID-19的育龄男性。目的:探讨精子线粒体功能障碍在COVID-19男性不育发生中的作用。结果:射精透射显微镜显示,携带COVID-19的男性存在严重的精子障碍,如线粒体功能障碍和细胞质残留,与有生育能力的男性相比,不育患者更常记录到这些障碍。结论:COVID-19损害男性生殖潜力,可能损害男性生育能力。
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引用次数: 0
[Pain syndrome in urology: features of classification and pathogenetic aspects]. 泌尿科疼痛综合征:分类和发病特点。
Q4 Medicine Pub Date : 2025-09-01
A Plekhanova O, Yu Pushkar D

Key aspects of pain syndrome in urology, including its classification, pathogenesis, and current treatment approaches, are discussed in the article. Special attention is given to the phenomenon of chronic pelvic pain, defined as persistent pain lasting at least three months, accompanied by dysfunction of the genitourinary system and emotional disorders. The main pathogenetic mechanisms underlying pain syndrome determine its complex multisystem nature, which requires a comprehensive approach to both diagnosis and treatment. Various etiologies of urologic chronic pain syndrome are described. Particular emphasis is given on urological causes such as bacterial cystitis and interstitial cystitis/bladder pain syndrome (IC/BPS). Clinical phenotypes of IC/BPS are discussed, along with individualized treatment approaches for each phenotype. The impact of pain syndrome in bacterial cystitis on quality of life and the role of phenazopyridine in pain relief are also highlighted. The importance of an interdisciplinary approach and the combination of different therapeutic methods to achieve good outcomes in the management of pain syndrome is emphasized.

泌尿科疼痛综合征的主要方面,包括其分类、发病机制和目前的治疗方法,在文章中进行了讨论。特别注意慢性盆腔疼痛的现象,定义为持续疼痛持续至少三个月,伴有泌尿生殖系统功能障碍和情绪障碍。疼痛综合征的主要发病机制决定了其复杂的多系统性质,需要综合诊断和治疗。泌尿系统慢性疼痛综合征的各种病因被描述。特别强调泌尿系统的原因,如细菌性膀胱炎和间质性膀胱炎/膀胱疼痛综合征(IC/BPS)。讨论了IC/BPS的临床表型,以及针对每种表型的个性化治疗方法。细菌性膀胱炎疼痛综合征对生活质量的影响以及非那吡啶在缓解疼痛中的作用也得到了强调。强调了跨学科方法和不同治疗方法相结合的重要性,以实现疼痛综合征管理的良好结果。
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引用次数: 0
[Effect of controlled normobaric hypoxia on the subjective state of patients with chronic prostatitis]. 可控常压缺氧对慢性前列腺炎患者主观状态的影响
Q4 Medicine Pub Date : 2025-09-01
A Miziev I, Kh Makhov M, Kh Sabanchieva Zh, A Shiritova L, M Gataova I

Introduction: Unlike other physiotherapy methods, hypoxic therapy has virtually no history of use in urology. We considered it important to evaluate the physiological mechanisms underlying its therapeutic effects in urological patients.

Aim: To assess the efficacy of normobaric interval hypoxic training as an innovative approach to the correction of psychophysiological disorders in patients with chronic prostatitis.

Materials and methods: The study included 36 men divided into three groups. Group 1 (n=12) received standard drug therapy plus 10 sessions of interval normobaric hypoxic training under a "hypoxia-normoxia" regimen (13% O2). Group 2 (n=12) received standard drug therapy plus 10 sessions under a "hypoxia-hyperoxia" regimen (31% O2). Group 3 (n=12) served as the control, receiving drug therapy only. Sessions were carried out weekly, consisting of 5 cycles of 5 minutes each. The effect of hypoxic therapy on patients subjective state was assessed using an asthenic symptom questionnaire before treatment and during the 1st, 5th, and 10th sessions.

Results: The most pronounced positive trends in the dynamics of asthenic symptoms were observed in the "hypoxia-hyperoxia" group: the average total number of complaints decreased almost threefold, while the average severity of complaints decreased by more than twofold. More modest positive changes were noted in the "hypoxia-normoxia" group, where the total number of complaints decreased by less than twofold, and the average severity decreased by about 20%. It should be emphasized that in both groups undergoing hypoxic therapy, highly significant differences were registered across all studied parameters compared with baseline. In the control group, during the same follow-up period, differences compared with baseline were insignificant. The above findings may demonstrate the insufficient efficiency of conventional measures in patients with chronic prostatitis in addressing asthenic and autonomic disorders, which are commonly observed in patients with this condition.

Conclusion: Interval hypoxic training, especially under the "hypoxia-hyperoxia" regimen, effectively reduces asthenic symptoms in patients with chronic prostatitis. This method is recommended as an adjunct to standard therapy to improve quality of life and psychoemotional status. The study supports the potential of hypoxic therapy in urology as a novel non-pharmacological approach with emphasis on psychosomatic aspects of men with chronic prostatitis.

与其他物理治疗方法不同,缺氧治疗在泌尿外科几乎没有使用的历史。我们认为重要的是评估其在泌尿科患者治疗效果的生理机制。目的:探讨常压间歇低氧训练对慢性前列腺炎患者心理生理障碍的治疗效果。材料与方法:研究对象36名男性,分为三组。第1组(n=12)接受标准药物治疗加10次间歇常压低氧训练,采用“低氧-常氧”方案(13% O2)。第二组(n=12)接受标准药物治疗加上10个疗程的“低氧-高氧”方案(31%氧气)。第三组(n=12)为对照组,仅接受药物治疗。每周进行5次,每次5分钟。采用治疗前、治疗第1、5、10期衰弱症状问卷评估低氧治疗对患者主观状态的影响。结果:在“缺氧-高氧”组中观察到衰弱症状动态的最明显的积极趋势:平均总投诉数量减少了近三倍,而平均投诉严重程度减少了两倍以上。在“缺氧-正常缺氧”组中发现了更温和的积极变化,其中投诉总数减少了不到两倍,平均严重程度下降了约20%。需要强调的是,在接受缺氧治疗的两组中,与基线相比,所有研究参数都有高度显著的差异。对照组在相同随访期内,与基线比较差异不显著。上述结果可能表明,在慢性前列腺炎患者中,常规措施在解决乏力和自主神经紊乱方面的效率不足,这些症状在慢性前列腺炎患者中很常见。结论:间歇低氧训练,特别是“低氧-高氧”方案下的低氧训练,可有效减轻慢性前列腺炎患者的乏力症状。该方法被推荐作为标准治疗的辅助手段,以改善生活质量和心理情绪状态。该研究支持低氧治疗在泌尿外科作为一种新的非药物方法的潜力,强调慢性前列腺炎患者的心身方面。
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引用次数: 0
[Uncomplicated urinary tract infections: preserving first-line antimicrobial agents in the updated guidelines]. [无并发症尿路感染:在更新的指南中保留一线抗菌药物]。
Q4 Medicine Pub Date : 2025-09-01
V Zaitsev A, A Khodyreva L, B Kolontarev K, N Bernikov A

Antimicrobial resistance (AMR) poses a global public health threat and may result in serious economic consequences. Although the treatment regimens for uncomplicated urinary tract infections (UTIs) have remained largely unchanged, they require continuous monitoring due to increasing antimicrobial resistance. The most recent updates of clinical guidelines for the management of uncomplicated UTIs did not revise the list of first-line antibiotics, since no new oral agents are currently available. Single-dose fosfomycin administration has been shown to be as safe and effective as other antibiotics in the treatment of uncomplicated UTIs in women. Fosfomycin therefore remains an adequate empirical treatment option. However, ongoing surveillance of regional antimicrobial resistance is essential to ensure the rational selection of antibiotics for empirical therapy.

抗菌素耐药性(AMR)对全球公共卫生构成威胁,并可能导致严重的经济后果。尽管无并发症尿路感染(uti)的治疗方案基本保持不变,但由于抗菌素耐药性增加,需要持续监测。最近更新的非复杂性尿路感染管理临床指南没有修订一线抗生素清单,因为目前没有新的口服药物可用。单剂量磷霉素已被证明与其他抗生素在治疗女性非复杂性尿路感染方面一样安全有效。因此,磷霉素仍然是一种适当的经验性治疗选择。然而,持续监测区域抗菌素耐药性对于确保合理选择抗生素进行经验性治疗至关重要。
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引用次数: 0
[The relationship between bacteria and kidney stones of different compositions in patients with urolithiasis]. [细菌与尿石症患者不同成分肾结石的关系]。
Q4 Medicine Pub Date : 2025-09-01
N Khotko D, I Khotko A, B Bucharskaya A, V Polukonova N, M Popkov V, I Tarasenko A, R Altynbaev R, I M Al-Jazaeri M, A Kozlov D

Urolithiasis is one of the most prevalent urological disorders and remains among the leading urinary tract diseases worldwide. The risk of developing urolithiasis is influenced by a wide range of factors, and its global prevalence continues to rise, particularly in both developed and developing countries. A deeper understanding of its etiology, including the contribution of bacteria, is of paramount importance, as microorganisms may contribute to recurrent stone formation. This review summarizes current evidence supporting bacterial involvement in urolithiasis. Particular attention is given to the potential role of microorganisms in the pathogenesis of so-called non-infectious stones, as well as to the complex interplay between stone formation and urinary tract infection. The aim of this article is to integrate available data on the association between bacteria and urinary stones, with a focus on the pathophysiology of stone formation and the urinary microbiome in calculi of different chemical compositions.

尿石症是最常见的泌尿系统疾病之一,也是世界范围内主要的泌尿系统疾病之一。患尿石症的风险受到多种因素的影响,其全球患病率持续上升,特别是在发达国家和发展中国家。更深入地了解其病因,包括细菌的作用,是至关重要的,因为微生物可能有助于复发性结石的形成。本文综述了目前支持细菌参与尿石症的证据。特别关注微生物在所谓的非感染性结石发病机制中的潜在作用,以及结石形成和尿路感染之间复杂的相互作用。本文的目的是整合有关细菌与尿路结石之间关系的现有数据,重点关注结石形成的病理生理和不同化学成分的结石中的尿微生物组。
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引用次数: 0
[Antibacterial drug fortiazinon for the treatment of complicated and chronic urinary tract infections]. 【抗菌药物福替嗪农治疗复杂慢性尿路感染】。
Q4 Medicine Pub Date : 2025-09-01
Yu Pushkar D, B Beloborodov V, A Zigangirova N, L Gintsburg A

Introduction: The relevance of complicated urinary tract infections (cUTIs) is determined by their high prevalence, recurrent course, and the frequent resistance of pathogens to standard antibacterial regimens. Therefore, the clinical evaluation of new antimicrobial agents (fortiazinon) is one of the promising directions for improving the treatment of cUTIs.

Materials and methods: A prospective, multicenter, randomized, placebo-controlled clinical trial was carried out in two groups of patients with cUTIs who received either a combination of cefepime with fortiazinon or cefepime with placebo. Cefepime 1 g was administered intravenously or intramuscularly every 12 hours; fortiazinon 600 mg (2 tablets of 300 mg) or placebo (2 tablets) was administered orally every 12 hours immediately after cefepime. The treatment duration was 7 days, with the possibility of extension up to 14 days at the discretion of investigators. A total of 357 patients were included: 180 received cefepime + fortiazinon, 177 received cefepime + placebo. The primary endpoint was the proportion of patients with clinical and microbiological cure at day 21 after completion of treatment. Secondary endpoints included clinical efficacy in subgroups (MITT, mMITT, CE), pathogen eradication in microbiologically confirmed cUTIs, and recurrence rates at days 60 and 90 after therapy.

Results: The primary endpoint was achieved in 136/180 (75.6%) of patients treated with cefepime/fortiazinon and in 90/177 (50.8%) of those treated with cefepime/placebo (difference: 24.7%; 97.5% CI: -14.7; two-sided ANOVA test). Analysis of secondary endpoints revealed significant advantages in clinical cure rates: MITT by 21.7%, mMITT by 21.5%, CE by 18.8%, and pathogen eradication by 13.2%. During follow-up, recurrence rates were significantly lower in the fortiazinon group compared with placebo: at day 60 the rates were 1.1% and 16.0%, and at day 90 they were 2.8% and 21.7%, respectively. Adverse events occurred in 37 (20.6%) patients receiving fortiazinon and in 26 (14.7%) patients in the placebo group (difference was insignificant). The most frequent adverse events were sleep disturbances, elevated alanine aminotransferase activity, and increased serum bilirubin. All adverse events were mild, did not require treatment, and did not lead to discontinuation of therapy.

Conclusion: Cefepime/fortiazinon was significantly superior to cefepime/placebo in the treatment of complicated urinary tract infections and in the prevention of recurrence during follow-up.

导读:复杂性尿路感染(cUTIs)的相关性是由其高患病率、复发过程和病原体对标准抗菌方案的频繁耐药性决定的。因此,新型抗菌药物(fortiazinon)的临床评价是改善cUTIs治疗的有希望的方向之一。材料和方法:一项前瞻性、多中心、随机、安慰剂对照的临床试验在两组cUTIs患者中进行,这些患者接受头孢吡肟联合福地嗪农或头孢吡肟联合安慰剂治疗。头孢吡肟每12小时静脉或肌肉注射1 g;头孢吡肟后每隔12小时口服福替嗪农600毫克(每组300毫克2片)或安慰剂2片。治疗持续时间为7天,根据研究人员的判断可能延长至14天。共纳入357例患者:180例接受头孢吡肟+福地嗪农治疗,177例接受头孢吡肟+安慰剂治疗。主要终点是在完成治疗后第21天临床和微生物治愈的患者比例。次要终点包括亚组(MITT, mMITT, CE)的临床疗效,微生物学证实的cUTIs的病原体根除,以及治疗后60天和90天的复发率。结果:使用头孢吡肟/福地嗪酮治疗的136/180(75.6%)患者达到了主要终点,使用头孢吡肟/安慰剂治疗的90/177(50.8%)患者达到了主要终点(差异:24.7%;97.5% CI: -14.7;双侧方差分析检验)。次要终点分析显示临床治愈率有显著优势:MITT为21.7%,mMITT为21.5%,CE为18.8%,病原体根除为13.2%。在随访期间,与安慰剂组相比,fortizinon组的复发率显著降低:第60天的复发率分别为1.1%和16.0%,第90天的复发率分别为2.8%和21.7%。福替嗪农组不良事件发生率为37例(20.6%),安慰剂组为26例(14.7%)(差异无统计学意义)。最常见的不良事件是睡眠障碍、谷丙转氨酶活性升高和血清胆红素升高。所有不良事件都是轻微的,不需要治疗,也没有导致停止治疗。结论:头孢吡肟/福地嗪农在治疗并发症性尿路感染及预防随访复发方面明显优于头孢吡肟/安慰剂。
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引用次数: 0
[Comparative analysis of biomechanical properties of grafts and intact tunica albuginea in experiment]. [实验中移植物与完整白膜生物力学性能的比较分析]。
Q4 Medicine Pub Date : 2025-09-01
V Kotov S, M Sokolov N, A Yapina A, G YusufovA, M TitkovaS, I Klimenko E, P Raksha A, V AnurovM

Introduction: Existing treatment methods for Peyronies Disease (PD) aim to restore the normal biomechanical functions of the tunica albuginea (TA); however, current data on biomechanical changes in PD, as well as on the biomechanical properties of native human TA, are extremely limited. The aim of our study was to evaluate the biomechanical properties of intact TA and the materials most commonly used for its replacement.

Materials and methods: Samples of the TA were collected from 9 male cadavers aged 20 to 65 years. Rectangular sections of the TA were excised from the dorsal surface of the corpora cavernosa. Fixation of the specimens in formalin was not performed, as this could affect the biomechanical properties of the tissue. Prepared samples were divided into longitudinal and transverse fragments. Pericardial grafts (allograft from cadaveric pericardium; xenograft from bovine pericardium) were prepared similarly. The obtained tissue fragments were subjected to mechanical testing. All tensile tests were conducted using a single-column universal material testing machine, the TA.XTplus Texture Analyzer (Stable Micro Systems Ltd., UK). Interactive stress-strain curves were used for result analysis. The following parameters were determined: stress, strength, strain, sample thickness. The obtained data were subjected to statistical analysis.

Results: Analysis of the obtained data revealed that the stress and strength of longitudinal fragments of TA were statistically significantly higher (p=0,0004 and p=0,0008; Tukeys test) than those for the transverse fragments. This indicates that human TA is anisotropic. Correlation analysis showed a negative correlation between the patient age and the strength (r=-0,49; p<0,05; Spearmans rank correlation). Additionally, a negative correlation was found between the patients age and the thickness of their tunica albuginea (r=-0,56; p<0,05 according to Spearmans test). When comparing human TA with grafts from bovine and human pericardium, it was found that the strength and thickness calculated for human tunica albuginea were statistically significantly higher (p=0,0001; Tukeys test) than those for the grafts.

Conclusions: Human and bovine pericardium grafts significantly differ from healthy TA in terms of stress, elastic modulus, strength, and thickness, which may impact the outcomes of surgical treatment for patients with PD.

现有的治疗方法旨在恢复白膜(TA)的正常生物力学功能;然而,目前关于PD的生物力学变化以及原生人类TA的生物力学特性的数据非常有限。我们研究的目的是评估完整TA和最常用的替代材料的生物力学特性。材料与方法:采集9具20 ~ 65岁男性尸体TA标本。从海绵体背表面切除TA的矩形切片。标本未在福尔马林中固定,因为这可能影响组织的生物力学特性。制备的样品分为纵向和横向碎片。心包移植物(尸体心包同种异体移植物和牛心包异体移植物)的制备方法相似。获得的组织碎片进行力学测试。所有拉伸试验均使用单柱万能材料试验机TA进行。XTplus纹理分析仪(英国Stable Micro Systems Ltd.)。采用交互应力-应变曲线进行结果分析。测定了以下参数:应力、强度、应变、试样厚度。对获得的数据进行统计分析。结果:对获得的数据进行分析,TA纵向碎片的应力和强度显著高于横向碎片(p=0,0004和p=0,0008; Tukeys检验)。这表明人类TA具有各向异性。相关分析显示患者年龄与强度呈负相关(r=-0,49)。结论:人和牛心包膜移植物在应力、弹性模量、强度和厚度方面与健康TA存在显著差异,这可能影响PD患者手术治疗的结果。
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引用次数: 0
[Resolution of the Expert Council]. [专家理事会决议]。
Q4 Medicine Pub Date : 2025-09-01
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引用次数: 0
[Recurrence of urothelial bladder cancer in the upper urinary tract after radical cystectomy: is there prevention and what are the treatment options?] 上尿路尿路上皮性膀胱癌根治性膀胱切除术后复发:是否有预防和治疗方案?]
Q4 Medicine Pub Date : 2025-09-01
V Perlin D, O Shmanev A, N Shamkhalov Sh, P Zipunnikov V

Radical cystectomy is recognized as the gold standard in the management of muscle-invasive bladder cancer. However, despite its definitive nature, recurrences of urothelial carcinoma in the upper urinary tract remain an important cause of morbidity and mortality during long-term follow-up. The prognosis of such recurrences is generally poor, largely due to delayed diagnosis. This article presents three clinical cases of upper urinary tract recurrence detected 16-24 months after radical cystectomy. Successful treatment was achieved with radical nephroureterectomy including excision of the adjacent intestinal segment. These cases highlight the effectiveness of this surgical approach for upper tract recurrences following radical cystectomy and emphasize the need to establish criteria to determine whether urothelial tumors in the upper urinary tract represent true recurrences of bladder cancer or previously undiagnosed primary lesions. Further studies are required to develop algorithms for the early detection and management of this relatively rare pattern of disease progression.

根治性膀胱切除术被认为是治疗肌肉浸润性膀胱癌的金标准。然而,尽管具有明确的性质,在长期随访中,上尿路尿路上皮癌的复发仍然是发病率和死亡率的重要原因。这种复发的预后通常很差,主要是由于诊断延迟。本文报告三例膀胱根治术后16-24个月发现上尿路复发的临床病例。成功的治疗取得根治性肾输尿管切除术,包括切除邻近的肠段。这些病例强调了这种手术方法对根治性膀胱切除术后上尿路复发的有效性,并强调需要建立标准来确定上尿路的尿路上皮肿瘤是否代表膀胱癌的真正复发或以前未诊断的原发病变。需要进一步的研究来开发早期发现和管理这种相对罕见的疾病进展模式的算法。
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引用次数: 0
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