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Multidisciplinary approach to prostatitis

机译:前列腺炎的多学科方法

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The modern clinical research on prostatitis started with the work of Stamey and coworkers who developed the basic principles we are still using. They established the segmented culture technique for localizing the infections in the males to the urethra, the bladder, or the prostate and to differentiate the main categories of prostatitis. Such categories with slight modifications are still used according to the NIH classification: acute bacterial prostatitis, chronic bacterial prostatitis, Chronic Pelvic Pain Syndrome (CPPS) and asymptomatic prostatitis. Prostatic inflammation is considered an important factor in influencing both prostatic growth and progression of symptoms of benign prostatic hyperplasia and prostatitis. Chronic inflammationeuroinflammation is a result of a deregulated acute phase response of the innate immune system affecting surrounding neural tissue at molecular, structural and functional levels. Clinical observations suggest that chronic inflammation correlates with chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) and benign prostatic hyperplasia (BPH) and an history of clinical chronic prostatitis significantly increases the odds for prostate cancer. The NIHNIDDK classification based on the use of the microbiological 4- glasses localization test or simplified 2-glasses test, is currently accepted worldwide. The UPOINT system identifies groups of clinicians with homogeneous clinical presentation and is used to recognize phenotypes to be submitted to specific treatments. The UPOINTS algorithm implemented the original UPOINT adding to the urinary domains (U), psycho-social (P), organspecific (O), infection (I), neurological (N), muscle tension and tenderness (T) a further domain related to sexuality (S). In fact sexual dysfunction (erectile, ejaculatory, libido loss) has been described in 46-92% of cases with a high impact on the quality of life of patients with CP/CPPS. Prostatic ultrasound represents the most popular imaging test in the work-up of either acute and chronic prostatitis although no specific hypo-hyperechoic pattern has been clearly associated with chronic bacterial prostatitis and CPPS. Use of a digital-processing software to calculate the extension of prostatic calcification area at ultrasound demonstrated a higher percentage of prostatic calcification in patients with chronic bacterial prostatitis. Multiparametric Magnetic Resonance Imaging (mpMRI) is the current state-of-the art imaging modality in the assessment of patients with prostate cancer although a variety of benign conditions, including inflammation, may mimic prostate cancer and act as confounding factors in the discrimination between neoplastic and non-neoplastic lesions. Bacteria can infect prostate gland by: ascending the urethra, reflux of urine into the prostatic ducts, direct inoculation of bacteria through inserted biopsy needles or hematogenous seeding. Enterobacteriaceae are the predominant pathogens in acute and chronic bacterial prostatitis, but an increasing role of Enterococci has been reported. Many strains of these uropathogens exhibit the ability to form biofilm and multidrug- resistance. Sexually Transmitted Infections (STI) agents, in particular Chlamydia trachomatis and Mycoplasma genitalium, have been also considered as causative pathogens of chronic bacterial prostatitis. On the contrary the effective role in genital diseases of other "genital mycoplasmas" is still a much debated issue. Sexually Transmitted Infections agents should be investigated by molecular methods in both patient and sexual partner. “Next generation” investigations, such as cytokine analysis, cytological typing of immune cells could help stratifying the immune response. Epigenetic dysregulation of inflammatory factors should be investigated according to systemic and compartment-specific signals. The search for biomarkers should also include evaluation of hormonal pathways, as measurement of estrogen levels in semen. Antimicrobials are the first line agents for the treatment of bacterial prostatitis. The success of antimicrobial treatment depends on the antibacterial activity and the pharmacokinetic characteristics of the drug which must reach high concentrations in prostate secretion and prostate tissue. Acute bacterial prostatitis can be a serious infection with a potential risk for urosepsis For iInitial treatment of severely ill patients, intravenous administration of high doses of bactericidal antimicrobials, such as broad-spectrum penicillins, third-generation cephalosporins or fluoroquinolones, is recommended in combination with an aminoglycoside. Use of piperacillin-tazobactam and meropenem is justified in presence of multiresistant gramnegative pathogens. The antibiotic treatment of chronic prostatitis is currently based on the use of fluoroquinolones that, given for 2 to 4 weeks, cured about 70% of men with chronic bacterial prostatitis. For the treatment of Chlamydial prostatitis macrolides were s
机译:前列腺炎的现代临床研究始于Stamey及其同事的工作,他们发展了我们仍在使用的基本原理。他们建立了分段培养技术,将男性的感染定位在尿道,膀胱或前列腺,并区分了前列腺炎的主要类别。根据NIH分类,仍会使用经过轻微修改的此类类别:急性细菌性前列腺炎,慢性细菌性前列腺炎,慢性盆腔疼痛综合征(CPPS)和无症状性前列腺炎。前列腺炎症被认为是影响前列腺生长和良性前列腺增生和前列腺炎症状发展的重要因素。慢性炎症/神经炎症是先天免疫系统在分子,结构和功能水平上影响周围神经组织的急性阶段反应失控的结果。临床观察表明,慢性炎症与慢性前列腺炎/慢性盆腔疼痛综合征(CP / CPPS)和良性前列腺增生(BPH)相关,并且临床慢性前列腺炎的病史显着增加了前列腺癌的几率。目前,基于微生物学的4-杯定位测试或简化的2-杯测试的NIHNIDDK分类已为全球所接受。 UPOINT系统识别具有均一临床表现的临床医生群体,并用于识别要接受特定治疗的表型。 UPOINTS算法实现了原始的UPOINT,在尿路域(U),社会心理(P),器官特异性(O),感染(I),神经系统(N),肌肉张力和触痛(T)上增加了与性(S)。实际上,在46-92%的病例中已经描述了性功能障碍(勃起,射精,性欲减退),对CP / CPPS患者的生活质量产生了重大影响。前列腺超声代表了急性和慢性前列腺炎检查中最受欢迎的影像学检查,尽管没有明确的低回声模式与慢性细菌性前列腺炎和CPPS有明显关系。在慢性细菌性前列腺炎患者中,使用数字处理软件计算前列腺钙化区域的扩展表明,前列腺钙化的百分比更高。多参数磁共振成像(mpMRI)是目前对前列腺癌患者进行评估的最新成像方式,尽管包括炎症在内的多种良性疾病可能会模仿前列腺癌,并成为区分赘生性肿瘤的混杂因素。和非肿瘤性病变。细菌可通过以下方式感染前列腺:上升尿道,尿液回流至前列腺导管,通过插入的活检针或血生性种子直接接种细菌。肠杆菌科是急性和慢性细菌性前列腺炎的主要病原体,但据报道肠球菌的作用越来越大。这些尿毒症的许多菌株表现出形成生物膜和多药耐药性的能力。性传播感染(STI)剂,特别是沙眼衣原体和生殖道支原体,也被认为是慢性细菌性前列腺炎的病原体。相反,其他“生殖支原体”在生殖器疾病中的有效作用仍是一个备受争议的问题。性传播感染剂应通过分子方法对患者和性伴侣进行调查。 “下一代”研究,例如细胞因子分析,免疫细胞的细胞学分型可以帮助分层免疫反应。炎症因子的表观遗传失调应根据全身和区室特异性信号进行研究。寻找生物标志物还应包括评估激素途径,作为精液中雌激素水平的测定。抗菌剂是治疗细菌性前列腺炎的一线药物。抗菌治疗的成功取决于抗菌活性和药物的药代动力学特性,这些特性必须在前列腺分泌物和前列腺组织中达到高浓度。急性细菌性前列腺炎可能是严重的感染,有尿毒症的潜在风险。对于重症患者的初始治疗,建议与大剂量青霉素,第三代头孢菌素或氟喹诺酮类药物一起静脉内给药高剂量的杀菌剂氨基糖苷。在存在多重耐药的革兰氏阴性病原体的情况下,使用哌拉西林-他唑巴坦和美罗培南是合理的。慢性前列腺炎的抗生素治疗目前是基于氟喹诺酮类药物的治疗,给予氟喹诺酮类药物治疗2至4周可治愈约70%的慢性细菌性前列腺炎男性。用于治疗衣原体性前列腺炎的大环内酯类药物

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