cystoscopy

膀胱镜检查
  • 文章类型: English Abstract
    In 2022, American Urological Association updated the guideline for the diagnosis and treatment of interstitial cystitis/bladder pain syndrome (IC/BPS). A significant change has been made in treatment recommendations. The updated guideline no longer divided treatments into first-line through sixth-line tiers. Instead, treatment is categorized into behavioral/non-pharmacologic, oral medicines, bladder instillations, procedures, and major surgery. This change emphasizes the heterogeneity of IC/BPS patients and the importance of individualized treatment, overturns traditional unreasonable ideas about hierarchical and progressive treatment, and encourages patients and physicians to make treatment decisions together. At the same time, the panel emphasized the importance of early implementation of cystoscopy in patients suspected of Hunner lesions and warned against the possibility of pentosan polysulfate causing a unique retinal pigmentary maculopathy. Urinary reconstruction surgery was considered to only be used as a last resort for the treatment of IC/BPS, and there is uncertainty about the overall balance between benefits and risks/burdens. The updated guideline provides a new understanding and decision-making basis for the diagnosis and treatment of IC/BPS. However, it should be noted that the clinical characteristics of Chinese patients should be considered in practice and the application of the guideline should be localized.
    2022年美国泌尿外科学会更新了间质性膀胱炎/膀胱疼痛综合征(IC/BPS)的诊断和治疗指南,本次更新在治疗推荐方面做了大幅改动,不再推荐一线至六线治疗,而将目前已有的治疗方案分为五大类,包括行为和非药物治疗、口服药物、膀胱药物灌注、经尿道手术和骶神经调节,以及尿路重建手术。这种改变强调了IC/BPS患者的异质性及个体化治疗的重要性,打破了长期以来层级递进式的治疗观念,并且鼓励患者参与治疗方案的决策。同时,专家委员会强调了IC/BPS病程早期进行膀胱镜检查的重要性,也指出应用戊聚糖多硫酸盐导致视网膜色素性黄斑病的风险,并且认为尿路重建手术仅作为治疗IC/BPS的最后手段,且收益风险比不明确。更新后的指南就IC/BPS的诊断和治疗为医师提供了新的认识和决策依据,但需要注意的是,实践中需考虑中国患者的临床特征,做到指南应用本土化。.
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  • 文章类型: Review
    美国泌尿外科协会(AUA)/泌尿外科肿瘤学会(SUO)指南修正案的目的是为非肌层浸润性膀胱癌(NMIBC)的有效循证治疗策略提供有用的参考。
    2023年,NMIBC指南通过AUA修订过程进行了更新,在该过程中,对新发布的文献进行了审查,并将其整合到先前发布的指南中,以保持货币。该修正案允许纳入自2020年上一次修正案以来发布的其他文献。更新的搜索收集了2019年7月至2023年5月的文献。这篇评论确定了1918年的摘要,其中75人符合纳入标准。如果有足够的证据,证据体被指定为强度等级A(高),B(中等),或C(低)支持Strong,中等,或有条件的建议。在缺乏充分证据的情况下,其他信息作为临床原则和专家意见提供。
    对变异组织学的陈述进行了更新,诊断为膀胱癌后的尿液标志物,膀胱内治疗,BCG维护,增强膀胱镜检查,和未来的方向。酌情对方法和参考部分进行了进一步修订。
    本指南旨在根据现有证据提高临床医生评估和治疗NMIBC患者的能力。未来的研究对于进一步支持或完善这些陈述以改善患者护理至关重要。
    UNASSIGNED: The purpose of this American Urological Association (AUA)/Society of Urologic Oncology (SUO) guideline amendment is to provide a useful reference on the effective evidence-based treatment strategies for non-muscle invasive bladder cancer (NMIBC).
    UNASSIGNED: In 2023, the NMIBC guideline was updated through the AUA amendment process in which newly published literature is reviewed and integrated into previously published guidelines in an effort to maintain currency. The amendment allowed for the incorporation of additional literature released since the previous 2020 amendment. The updated search gathered literature from July 2019 to May 2023. This review identified 1918 abstracts, of which 75 met inclusion criteria.When sufficient evidence existed, the body of evidence was assigned a strength rating of A (high), B (moderate), or C (low) in support of Strong, Moderate, or Conditional Recommendations. In the absence of sufficient evidence, additional information is provided as Clinical Principles and Expert Opinions.
    UNASSIGNED: Updates were made to statements on variant histologies, urine markers after diagnosis of bladder cancer, intravesical therapy, BCG maintenance, enhanced cystoscopy, and future directions. Further revisions were made to the methodology and reference sections as appropriate.
    UNASSIGNED: This guideline seeks to improve clinicians\' ability to evaluate and treat patients with NMIBC based on currently available evidence. Future studies will be essential to further support or refine these statements to improve patient care.
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  • 文章类型: Systematic Review
    背景:血尿可以是宏观的(可见血尿[VH])或微观的(非可见血尿[NVH]),可能是由许多潜在的病因引起的。目前,在血尿的情况下,膀胱镜检查是筛查整个膀胱恶性肿瘤的标准诊断工具.
    目的:本系统评价的目的是确定膀胱镜检查的诊断测试准确性(与其他测试相比,例如,计算机断层扫描,尿液生物标志物,和尿细胞学)用于检测成人膀胱癌。
    方法:根据《Cochrane诊断测试准确性系统评价手册》和用于诊断测试准确性研究的系统评价和荟萃分析(PRISMA)扩展的首选报告项目》对文献进行系统评价。MEDLINE,Embase,科克伦中部,和CochraneCDSR数据库(通过Ovid)在2022年7月13日之前进行了搜索。人群包括患有VH或NVH的患者,没有以前的泌尿系癌症。两名审稿人独立筛选所有文章,搜索检索到的文章的参考列表,并进行数据提取。使用诊断准确性研究质量评估(QUADAS-2)评估偏倚风险。
    结果:总体而言,9项研究纳入了定性分析.与放射学成像相比,9项纳入的试验中有7项涵盖了膀胱镜检查的使用。总的来说,膀胱镜检查的敏感度从87%到100%,特异性从64%到100%,阳性预测值从79%到98%,阴性预测值在98%至100%之间。两项试验比较了增强膀胱镜检查或空气膀胱镜检查与常规膀胱镜检查。常规白光膀胱镜检查的总体敏感性为47%至100%,特异性为93.4%至100%。
    结论:膀胱镜检查在血尿背景下检测膀胱癌的真正准确性尚未得到广泛研究,导致血尿患者的表现数据不一致。与成像模式相比,一些试验前瞻性地评估了膀胱镜检查的诊断性能,确认膀胱镜检查的准确性非常高,超过任何其他影像学检查的诊断价值。
    结果:回顾了在出现血尿(尿中有血)的成人中检测膀胱癌的试验证据。最常用的检查是膀胱镜检查,这仍然是目前诊断膀胱癌的标准。
    BACKGROUND: Haematuria can be macroscopic (visible haematuria [VH]) or microscopic (nonvisible haematuria [NVH]), and may be caused by a number of underlying aetiologies. Currently, in case of haematuria, cystoscopy is the standard diagnostic tool to screen the entire bladder for malignancy.
    OBJECTIVE: The objective of this systematic review is to determine the diagnostic test accuracy of cystoscopy (compared with other tests, eg, computed tomography, urine biomarkers, and urine cytology) for detecting bladder cancer in adults.
    METHODS: A systematic review of the literature was performed according to the Cochrane Handbook for Systematic Reviews of Diagnostic Test Accuracy and Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) extension for diagnostic test accuracy studies\' checklist. The MEDLINE, Embase, Cochrane CENTRAL, and Cochrane CDSR databases (via Ovid) were searched up to July 13, 2022. The population comprises patients presenting with either VH or NVH, without previous urological cancers. Two reviewers independently screened all articles, searched reference lists of retrieved articles, and performed data extraction. The risk of bias was assessed using Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2).
    RESULTS: Overall, nine studies were included in the qualitative analysis. Seven out of nine included trials covered the use of cystoscopy in comparison with radiological imaging. Overall, sensitivity of cystoscopy ranged from 87% to 100%, specificity from 64% to 100%, positive predictive value from 79% to 98%, and negative predictive values between 98% and 100%. Two trials compared enhanced or air cystoscopy versus conventional cystoscopy. Overall sensitivity of conventional white light cystoscopy ranged from 47% to 100% and specificity from 93.4% to 100%.
    CONCLUSIONS: The true accuracy of cystoscopy for the detection of bladder cancer within the context of haematuria has not been studied extensively, resulting in inconsistent data regarding its performance for patients with haematuria. In comparison with imaging modalities, a few trials have prospectively assessed the diagnostic performance of cystoscopy, confirming very high accuracy for cystoscopy, exceeding the diagnostic value of any other imaging test.
    RESULTS: Evidence of tests for detecting bladder cancer in adults presenting with haematuria (blood in urine) was reviewed. The most common test used was cystoscopy, which remains the current standard for diagnosing bladder cancer.
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  • 文章类型: Journal Article
    背景:AUA指南建议对行膀胱镜检查的高危患者进行围手术期抗菌预防。我们试图确定实施简单的质量改进方案是否可以提高指南的合规性。
    方法:作为质量改进计划的一部分,4个简单的变化被纳入我们的办公室膀胱镜检查的实践,包括创建“是/否”检查表以识别高风险患者,泌尿科提供者下的清单审查和电子抗生素订单,立即护士指导单剂量最常见的推荐抗生素给药,以及在程序前超时期间审查检查表和抗生素的使用。我们回顾性比较了干预前3个月和实施后3个月患者的抗生素依从性。收集的数据包括年龄,性别,程序指示,程序类型和高风险状态。
    结果:共307例患者纳入研究(实施前157例,实施后150例)。在干预前组中,120名患者(76.4%)被认为是高风险的,应该给予抗生素预防,虽然只有38人(31.7%)实际收到了。在干预后组中,104名患者(69.3%)被认为是高风险的,应该给予抗生素预防,84人(80.8%)实际收到了。总的来说,这项质量改进举措使适当的抗生素给药增加了49.1%(p<0.0001).
    结论:实施简单的4步质量改进计划导致在办公室膀胱镜检查中使用适当抗生素的显着增加。
    BACKGROUND: AUA guidelines recommend periprocedural antibacterial prophylaxis for high risk patients undergoing in-office cystoscopy. We sought to determine if implementation of a simple quality improvement protocol could increase guideline compliance.
    METHODS: As part of a quality improvement initiative, 4 simple changes were incorporated into our practice for in-office cystoscopy, including creation of a \"yes/no\" checklist to identify high risk patients, checklist review and electronic antibiotics order placed by urology provider, immediate nurse directed administration of single doses of the most common recommended antibiotics, and review of the checklist and antibiotic administration during the preprocedural time-out. We retrospectively compared antibiotic adherence in patients 3 months before and 3 months after implementation of the intervention. Data collected included age, gender, indication for procedure, type of procedure and high risk status.
    RESULTS: A total of 307 patients were included in the study (157 before implementation and 150 after implementation of the protocol). In the pre-intervention group 120 patients (76.4%) were considered high risk and should have been administered antibiotic prophylaxis, although only 38 (31.7%) actually received it. In the post-intervention group 104 patients (69.3%) were considered high risk and should have been given antibiotic prophylaxis, and 84 (80.8%) actually received it. Overall, this quality improvement initiative resulted in a 49.1% increase in appropriate antibiotic administration (p <0.0001).
    CONCLUSIONS: Implementation of a simple 4-step quality improvement initiative resulted in a significant increase in the administration of appropriate antibiotics for in-office cystoscopy.
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  • 文章类型: Journal Article
    背景:我们确定了2011年美国泌尿外科协会(AUA)修订的临床指南前后膀胱镜检查伴水力扩张(CH)的发生率,间质性膀胱炎/膀胱疼痛综合征的诊断和治疗。\"
    方法:在2009年1月至2020年2月期间,在Vizient®临床数据库中确定了诊断为间质性膀胱炎/膀胱疼痛综合征(IC/BPS)的临床接触,其中进行了有或没有水扩张的膀胱镜检查。人口统计学和临床信息,如患者年龄,性别,种族,治疗医师专业,记录了保险类型和医院类型(教学与非教学)。描述性统计,使用Wilcoxon2样本检验和卡方检验来比较变量。根据2011年6月AUA指南,使用中断时间序列分析评估CH率的变化。
    结果:从2009年1月至2020年2月,69,983例患者被确定为IC/BPS诊断,并接受了门诊膀胱镜检查,其中7502(10.7%)为CH。与那些没有接受CH的人相比,接受CH的IC/BPS受试者更年轻,主要是女性,高加索人,有商业保险。在准则之前,在所有医学专业中,CH的基本比率从16.6%上升,每月为0.12%。在指南发布之后,CH率下降了6.8%,每月下降0.07%,直到2020年2月。相对于所有其他医学专业,这种模式在泌尿外科中最为明显。
    结论:接受门诊CH的IC/BPS患者的月平均CH发生率从2011年AUA指南前的近17%下降到2020年初的不到10%。
    BACKGROUND: We determined the rate of cystoscopy with hydrodistention (CH) before and after the 2011 American Urological Association (AUA) amended clinical guideline, \"Diagnosis and Treatment of Interstitial Cystitis/Bladder Pain Syndrome.\"
    METHODS: Clinical encounters with a diagnosis of interstitial cystitis/bladder pain syndrome (IC/BPS) where cystoscopy with and without hydrodistention was performed were identified in the Vizient® Clinical Data Base between January 2009 and February 2020. Demographic and clinical information such as patient age, gender, race, treating physician specialty, insurance type and type of hospital (teaching vs nonteaching) was recorded. Descriptive statistics, Wilcoxon 2-sample test and chi-square test were used to compare variables. An interrupted time series analysis was used to assess the change in CH rate following the June 2011 AUA guideline.
    RESULTS: From January 2009 to February 2020, 69,983 encounters were identified to have an IC/BPS diagnosis and to have undergone outpatient cystoscopy, of which 7,502 (10.7%) were CH. Compared to those not undergoing CH, subjects with IC/BPS undergoing CH were younger, predominantly female, Caucasian and had commercial insurance. Before the guideline, across all medical specialties, the base rate of CH was rising from 16.6% at a rate of 0.12% per month. Following guideline release, the CH rate dropped by 6.8%, declining 0.07% per month until February 2020. This pattern was most pronounced in urology relative to all other medical specialties.
    CONCLUSIONS: The monthly average rate of CH among individuals with IC/BPS undergoing an outpatient CH dropped from nearly 17% before the 2011 AUA guideline to less than 10% in early 2020.
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  • 文章类型: Journal Article
    目的:在全球范围内,对怀疑患有膀胱疼痛综合征/间质性膀胱炎(BPS/IC)的患者常规进行膀胱镜检查。各种准则报告的方法似乎在技术上有所不同,因此有必要审查所有这些技术,以便达成共识。目的是回顾描述BPS/IC患者膀胱镜检查的流行技术的文献,并尝试达成共识。
    方法:全局性间质性膀胱炎,膀胱疼痛协会(GIBS)集体使用关键词系统地回顾文献,“Hunner病变的膀胱镜检查,膀胱疼痛综合征,膀胱疼痛综合征和间质性膀胱炎,Cochrane,和SCOPUS数据库。共研究了3,857篇摘要,其中96篇涉及膀胱镜检查技术的某些部分的文章入围,作为全长文章进行审查。最后,纳入了6篇对膀胱镜检查技术进行描述的文章进行最终列表和比较.该小组继续就BPS/IC的诊断和治疗性膀胱镜检查的逐步技术达成共识。该技术已与先前描述的技术进行了比较,并且可以用作治疗医生的有用实用指南。
    结论:对于BPS/IC患者进行诊断和治疗性膀胱镜检查,有一个统一的标准化技术是很重要的。在本文中已经达成并描述了一种这样的技术的共识。
    Cystoscopy has been routinely performed in patients suspected to be suffering from bladder pain syndrome/interstitial cystitis (BPS/IC) across the globe. The methodology reported by various guidelines appears to have differences in the techniques and hence there is a need for a review of all those techniques in order to arrive at a consensus. The aim was to review the literature describing the prevalent techniques of cystoscopy for patients of BPS/IC and try to evolve a consensus.
    The group the Global Interstitial Cystitis, Bladder Pain Society (GIBS) has worked collectively to systematically review the literature using the key words, \"Cystoscopy in Hunner\'s lesions, bladder pain syndrome, painful bladder syndrome and interstitial cystitis\" in the PubMed, COCHRANE, and SCOPUS databases. A total of 3,857 abstracts were studied and 96 articles referring to some part of technique of cystoscopy were short-listed for review as full-length articles. Finally, six articles with a description of a technique of cystoscopy were included for final tabulation and comparison. The group went on to arrive at a consensus for a stepwise technique of diagnostic and therapeutic cystoscopy in cases of BPS/IC. This technique has been compared with the previously described techniques and may serve to be a useful practical guide for treating physicians.
    It is important to have a uniform standardized technique for performing a diagnostic and therapeutic cystoscopy in patients with BPS/IC. Consensus on one such a technique has been arrived at and described in the present article.
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  • 文章类型: Journal Article
    泌尿外科手术中的外科抗菌预防(SAP)的主要目的是预防菌血症,手术部位感染(SSIs),术后尿路感染(ppUTIs)。缺乏儿科泌尿外科SAP指南。只研究了这个复杂课题的某些方面,而且在手术前使用抗生素预防似乎更经常与机构学派或专家意见有关,而不是与证明最正确和最优选的治疗方法的研究所规定的规则有关。因此,使用RAND/UCLA适当性方法实现的本共识文件的目的是为临床医生提供一系列关于SAP预防菌血症的建议,SSIs,和儿科患者泌尿系统成像和外科手术后的ppUTI。尽管现有的研究很少,专家同意一些与SAP相关的基底概念,用于儿科患者的泌尿外科手术。在进行任何泌尿外科手术之前,必须排除UTI。清洁程序不需要SAP,除了假体装置植入和腹股沟和会阴切口外,SSI风险可能会增加。相比之下,在清洁污染的程序中需要SAP。研究还表明,在小儿疝修补术和睾丸固定术中消除SAP的安全性。为了限制抵抗的出现,必须尽一切努力减少和合理化SAP的抗生素消费。在这方面,增加抗生素管理的使用可能非常有效。
    The main aim of surgical antimicrobial prophylaxis (SAP) in urologic procedures is to prevent bacteraemia, surgical site infections (SSIs), and postoperative urinary tract infections (ppUTIs). Guidelines for SAP in paediatric urology are lacking. Only some aspects of this complex topic have been studied, and the use of antibiotic prophylaxis prior to surgical procedures seems to be more often linked to institutional schools of thought or experts\' opinions than to rules dictated by studies demonstrating the most correct and preferred management. Therefore, the aim of this Consensus document realized using the RAND/UCLA appropriateness method is to provide clinicians with a series of recommendations on SAP for the prevention of bacteraemia, SSIs, and ppUTIs after urologic imaging and surgical procedures in paediatric patients. Despite the few available studies, experts agree on some basilar concepts related to SAP for urologic procedures in paediatric patients. Before any urological procedure is conducted, UTI must be excluded. Clean procedures do not require SAP, with the exception of prosthetic device implantation and groin and perineal incisions where the SSI risk may be increased. In contrast, SAP is needed in clean-contaminated procedures. Studies have also suggested the safety of eliminating SAP in paediatric hernia repair and orchiopexy. To limit the emergence of resistance, every effort to reduce and rationalize antibiotic consumption for SAP must be made. Increased use of antibiotic stewardship can be greatly effective in this regard.
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  • 文章类型: Journal Article
    BACKGROUND: The European Association of Urology (EAU) has released an updated version of the guidelines on non-muscle-invasive bladder cancer (NMIBC).
    OBJECTIVE: To present the 2021 EAU guidelines on NMIBC.
    METHODS: A broad and comprehensive scoping exercise covering all areas of the NMIBC guidelines since the 2020 version was performed. Databases covered by the search included Medline, EMBASE, and the Cochrane Libraries. Previous guidelines were updated, and the level of evidence and grade of recommendation were assigned.
    RESULTS: Tumours staged as Ta, T1 and carcinoma in situ (CIS) are grouped under the heading of NMIBC. Diagnosis depends on cystoscopy and histological evaluation of tissue obtained via transurethral resection of the bladder (TURB) for papillary tumours or via multiple bladder biopsies for CIS. For papillary lesions, a complete TURB is essential for the patient\'s prognosis and correct diagnosis. In cases for which the initial resection is incomplete, there is no muscle in the specimen, or a T1 tumour is detected, a second TURB should be performed within 2-6 wk. The risk of progression may be estimated for individual patients using the 2021 EAU scoring model. On the basis of their individual risk of progression, patients are stratified as having low, intermediate, high, or very high risk, which is pivotal to recommending adjuvant treatment. For patients with tumours presumed to be at low risk and for small papillary recurrences detected more than 1 yr after a previous TURB, one immediate chemotherapy instillation is recommended. Patients with an intermediate-risk tumour should receive 1 yr of full-dose intravesical bacillus Calmette-Guérin (BCG) immunotherapy or instillations of chemotherapy for a maximum of 1 yr. For patients with high-risk tumours, full-dose intravesical BCG for 1-3 yr is indicated. For patients at very high risk of tumour progression, immediate radical cystectomy should be considered. Cystectomy is also recommended for BCG-unresponsive tumours. The extended version of the guidelines is available on the EAU website at https://uroweb.org/guideline/non-muscle-invasive-bladder-cancer/.
    CONCLUSIONS: These abridged EAU guidelines present updated information on the diagnosis and treatment of NMIBC for incorporation into clinical practice.
    UNASSIGNED: The European Association of Urology has released updated guidelines on the classification, risk factors, diagnosis, prognostic factors, and treatment of non-muscle-invasive bladder cancer. The recommendations are based on the literature up to 2020, with emphasis on the highest level of evidence. Classification of patients as having low, intermediate, or and high risk is essential in deciding on suitable treatment. Surgical removal of the bladder should be considered for tumours that do not respond to bacillus Calmette-Guérin (BCG) treatment and tumours with the highest risk of progression.
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  • 文章类型: Journal Article
    表现为微血尿的患者代表具有广泛的泌尿生殖系统恶性肿瘤风险的异质人群。认识到患者特异性特征改变潜在恶性病因的风险,本指南旨在提供个性化诊断测试策略.
    系统评价纳入了2010年1月至2019年2月发表的证据,并进行了最新的文献检索,包括截至2019年12月发表的研究。专家小组编写了基于证据的陈述,陈述类型与证据强度相关,确定性水平,以及小组关于利益和风险/负担之间平衡的判断。
    在单个标本的显微镜评估中,小血尿应定义为每个高倍视野≥3个红细胞。在诊断为妇科或非恶性泌尿生殖系统来源的微血尿患者中,临床医师应在解决妇科或非恶性泌尿生殖系统病因后重复尿液分析.小组为微血尿患者创建了一个风险分类系统,分层为低,中介-,或泌尿生殖系统恶性肿瘤的高风险。风险组是基于包括年龄在内的因素,性别,吸烟和其他尿路上皮癌危险因素,微血尿的程度和持续性,以及之前的肉眼血尿。建议根据患者风险和共同决策进行膀胱镜检查和上尿路成像的诊断评估。声明还告知阴性微血尿评估后的随访。
    微血尿患者应根据其泌尿生殖系统恶性肿瘤的风险进行分类,并采用基于风险的策略进行评估。未来需要高质量的研究来改善这些患者的护理。
    Patients presenting with microhematuria represent a heterogeneous population with a broad spectrum of risk for genitourinary malignancy. Recognizing that patient-specific characteristics modify the risk of underlying malignant etiologies, this guideline sought to provide a personalized diagnostic testing strategy.
    The systematic review incorporated evidence published from January 2010 through February 2019, with an updated literature search to include studies published up to December 2019. Evidence-based statements were developed by the expert Panel, with statement type linked to evidence strength, level of certainty, and the Panel\'s judgment regarding the balance between benefits and risks/burdens.
    Microhematuria should be defined as ≥ 3 red blood cells per high power field on microscopic evaluation of a single specimen. In patients diagnosed with gynecologic or non-malignant genitourinary sources of microhematuria, clinicians should repeat urinalysis following resolution of the gynecologic or non-malignant genitourinary cause. The Panel created a risk classification system for patients with microhematuria, stratified as low-, intermediate-, or high-risk for genitourinary malignancy. Risk groups were based on factors including age, sex, smoking and other urothelial cancer risk factors, degree and persistence of microhematuria, as well as prior gross hematuria. Diagnostic evaluation with cystoscopy and upper tract imaging was recommended according to patient risk and involving shared decision-making. Statements also inform follow-up after a negative microhematuria evaluation.
    Patients with microhematuria should be classified based on their risk of genitourinary malignancy and evaluated with a risk-based strategy. Future high-quality studies are required to improve the care of these patients.
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  • 文章类型: Journal Article
    这项系统评价评估了对非肌肉浸润性膀胱癌(NMIBC)治疗指南的依从性。
    公共的,WebofScience,科克伦图书馆,和Scopus数据库于2019年11月根据系统评价和荟萃分析声明的首选报告项目进行检索。
    15项研究纳入了10,575名NMIBC患者的研究纳入本系统评价。我们发现,在假定低或中等风险的患者中,单次立即膀胱内滴注的依从性为53.0%。在中等风险的人群中,37.1%使用膀胱内卡介苗或化疗,在高危患者中进行第二次经尿道电切术的占43.4%,32.5%,在高危患者中使用辅助膀胱内卡介苗,36.1%的根治性膀胱切除术在高危患者中,82.2%采用膀胱镜检查进行随访。
    NMIBC指南的合规性仍然很低。更好的指南教育和理解是实现高度合规的关键。迫切需要在医生一级提高指南依从性的策略。
    This systematic review assessed compliance to guidelines for the management of nonmuscle-invasive bladder carcinoma (NMIBC).
    The PUBMED, Web of Science, Cochrane Library, and Scopus databases were searched in November 2019 in accordance with the Preferred Reporting Items for Systematic Review and Meta-analysis statement.
    Fifteen studies incorporating a collective total of 10,575 NMIBC patients were eligible for inclusion in this systematic review. We found that the rates of compliance were 53.0% with a single immediate intravesical instillation in patients with presumed low or intermediate risk, 37.1% with intravesical bacillus Calmette-Guerin or chemotherapy in those with intermediate risk, 43.4% with performance of a second transurethral resection in high-risk patients, 32.5% with administration of adjuvant intravesical bacillus Calmette-Guerin in high-risk patients, 36.1% with radical cystectomy in highest-risk patients, and 82.2% with cystoscopy for follow-up.
    Compliance with NMIBC guidelines remains low. Better guideline education and understanding holds the key to achieving high compliance. Strategies to improve guideline compliance at the physician level are urgently required.
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