Benign prostate hyperplasia

良性前列腺增生
  • 文章类型: Journal Article
    我们调查了与SGLT2(钠-葡萄糖协同转运蛋白-2)抑制剂相关的UTI和复杂UTI的风险,强调老年男性排尿功能障碍的风险较高。
    利用药物警戒病例-病例设计,我们分析了1967年至2022年期间男性患者的VigiBase报告.Vigibase是一个全面的全球药物安全数据库。不相称性分析,它比较了特定药物与其他药物报告的不良事件的频率,使用报告比值比(ROR)和经验贝叶斯估计(EBE)进行。年龄在65岁时分层,作为男性排尿功能障碍易感性增加的阈值。进行敏感性分析以比较SGLT2抑制剂与其他糖尿病药物以及2013年至2022年。
    有484个UTI(ROR6.75[95%CI:6.17-7.39];EBE6.78)和165个复杂UTI(ROR8.09[95%CI:6.94-9.43];EBE8.60)。在65岁以下的男性中,有178个UTI(ROR6.82[95%CI:5.88-7.91];EBE6.99)和65个复杂UTI(ROR7.30[95%CI:5.71-9.32];EBE7.90)。在65岁及以上的男性中,我们发现153个UTI(ROR5.11[95%CI:4.35-5.99];EBE5.44)和59个复杂UTI(ROR8.79[95%CI:6.79-11.37];EBE9.60)。敏感性分析始终显示出显著的信号。
    这项研究表明,服用SGLT2抑制剂的男性尿路感染和复杂尿路感染的风险升高,在可能患有良性前列腺增生相关排尿功能障碍的老年男性中,复杂UTI的风险更为明显。这些发现强调了在处方SGLT2抑制剂时需要一种平衡的方法,特别是在可能更容易感染UTI的人群中。
    UNASSIGNED: We investigated the risk of UTIs and complex UTIs associated with SGLT2 (sodium-glucose cotransporter-2) inhibitors in men, emphasizing older men at higher risk for voiding dysfunction.
    UNASSIGNED: Utilizing a pharmacovigilance case-noncase design, we analyzed VigiBase reports from 1967 to 2022 among male patients. VigiBase is a comprehensive global database for drug safety. Disproportionality analysis, which compares the frequency of reported adverse events for specific drugs against other drugs, was conducted using reporting odds ratio (ROR) and empirical Bayes estimator (EBE). Age was stratified at 65 years as a threshold for increased susceptibility to male voiding dysfunctions. Sensitivity analyses were performed to compare SGLT2 inhibitor with other diabetes medications and years 2013 to 2022.
    UNASSIGNED: There were 484 UTIs (ROR 6.75 [95% CI: 6.17-7.39]; EBE 6.78) and 165 complex UTIs (ROR 8.09 [95% CI: 6.94-9.43]; EBE 8.60). In men under 65, there were 178 UTIs (ROR 6.82 [95% CI: 5.88-7.91]; EBE 6.99) and 65 complex UTIs (ROR 7.30 [95% CI: 5.71-9.32]; EBE 7.90). In men 65 and over, we found 153 UTIs (ROR 5.11 [95% CI: 4.35-5.99]; EBE 5.44) and 59 complex UTIs (ROR 8.79 [95% CI: 6.79-11.37]; EBE 9.60). Sensitivity analyses consistently showed significant signals.
    UNASSIGNED: This study suggests an elevated risk for both UTIs and complex UTIs in men taking SGLT2 inhibitors, with a more pronounced risk for complex UTI in older men who may have benign prostatic hyperplasia-related voiding dysfunction. These findings highlight the need for a balanced approach in prescribing SGLT2 inhibitors, particularly in populations potentially more susceptible to UTIs.
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  • 文章类型: Journal Article
    背景:鲁比(FR),一种具有药用价值的食品,用于中药(TCM)治疗各种肾脏相关问题,比如阳痿,遗精,和尿频。在中国,它也经常用于生产各种功能食品。
    目的:本研究的目的是评估FR二萜苷对RWPE-1上皮细胞(RWPE-1)的治疗作用,人类正常前列腺上皮细胞,良性前列腺增生(BPH)大鼠,两者都暴露于二氢睾酮(DHT)和丙酸睾酮(TP),分别,并研究其作用机制。
    方法:通过药物亲和响应靶标稳定性结合质谱(DARTS/MS)筛选能够稳定结合某些二萜苷的靶标蛋白。DHT诱导的RWPE-1细胞用于检测药物活性。皮下注射TP诱导大鼠BPH。将来自FR(FDS)的二萜糖苷提取物口服给药28天。采用酶联免疫吸附试验(ELISA)检测大鼠血清和前列腺组织中DHT水平,并分析细胞增殖和上皮间质转化(EMT),前列腺特异性抗原(PSA)的蛋白表达,雄激素受体(AR),类固醇5α-还原酶2型(SRD5A2),增殖细胞核抗原(PCNA),S100钙结合蛋白A2(S100A2),转化生长因子-β1(TGF-β1),E-cadherin,波形蛋白,Smad4通过蛋白质印迹(WB)测定,免疫组织化学(IHC),或免疫荧光(IF)。
    结果:FDS降低DHT诱导的RWPE-1细胞的增殖。显著抑制大鼠前列腺肿大;降低血清和前列腺组织中DHT水平;抑制AR蛋白表达,PSA,PCNA,S100A2,TGF-β1,E-cadherin,和Smad4;并增加E-cadherin的蛋白表达。
    结论:本研究首次报道从FR分离的二萜苷在细胞水平上抑制BPH,通过雄激素信号通路调节前列腺细胞的增殖,并通过S100A2介导的TGF-β/Smad信号通路阻止前列腺中的EMT。这些结果表明FDS是BPH的有希望的多靶点治疗。
    BACKGROUND: Fructus Rubi (FR), a food material with medicinal value, is used in traditional Chinese medicine (TCM) for treatment of various kidney-related problems, such as impotence, spermatorrhea, and frequent urination. It is also frequently used to produce diverse functional foods in China.
    OBJECTIVE: The purpose of this research was to assess the therapeutic effects of FR diterpene glycosides on RWPE-1 epithelial cell (RWPE-1), a human normal prostatic epithelial cell, and benign prostate hyperplasia (BPH) rats, both of which had been exposed to dihydrotestosterone (DHT) and testosterone propionate (TP), respectively, and to investigate the mechanism of action.
    METHODS: Target proteins that could stably bind to certain diterpene glycosides were screened through drug affinity responsive target stability combined with mass spectrometry (DARTS/MS). DHT-induced RWPE-1 cells were used to detect drug activity. TP was subcutaneously injected to induce BPH in rats. The extract of diterpene glycosides from FR (FDS) was orally administered for 28 days. The DHT levels in the serum and prostate tissue of the rats were measured through enzyme-linked immunosorbent assay (ELISA), and to analyze cell proliferation and epithelial-mesenchymal transition (EMT), the protein expression of prostate-specific antigen (PSA), androgen receptor (AR), steroid 5α-reductase type 2 (SRD5A2), proliferating cell nuclear antigen (PCNA), S100 calcium-binding protein A2 (S100A2), transforming growth factor-β1 (TGF-β1), E-cadherin, vimentin, and Smad4 was determined through western blotting (WB), immunohistochemistry (IHC), or immunofluorescence (IF).
    RESULTS: FDS reduced the proliferation of DHT-induced RWPE-1 cells. It also significantly inhibited rat prostate enlargement; decreased DHT levels in the serum and prostate tissue; inhibited the protein expression of AR, PSA, PCNA, S100A2, TGF-β1, E-cadherin, and Smad4; and increased the protein expression of E-cadherin.
    CONCLUSIONS: The present study is the first to report that diterpene glycosides isolated from FR inhibited BPH at the cellular level, regulated the proliferation of prostate cells through the androgen signaling pathway, and prevented EMT in the prostate through the S100A2-mediated TGF-β/Smad signaling pathway. These results indicate that FDS is a promising multitarget therapy for BPH.
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  • 文章类型: Journal Article
    较新的药物和设备,以及更好地了解现有治疗方法的益处和局限性,扩大了肺病患者的治疗选择。治疗进展导致哮喘患者的预后改善,慢性阻塞性肺疾病,间质性肺病,肺动脉高压,囊性纤维化.在这些异质性疾病组中,可用治疗的风险和益处是变化很大的。定义新疗法的作用需要对这些疾病的理解和整体治疗方法。本节除了将重点放在这些疾病的新疗法外,还将回顾一般治疗方法。.
    Newer medications and devices, as well as greater understanding of the benefits and limitations of existing treatments, have led to expanded treatment options for patients with lung disease. Treatment advances have led to improved outcomes for patients with asthma, chronic obstructive pulmonary disease, interstitial lung disease, pulmonary hypertension, and cystic fibrosis. The risks and benefits of available treatments are substantially variable within these heterogeneous disease groups. Defining the role of newer therapies mandates both an understanding of these disorders and overall treatment approaches. This section will review general treatment approaches in addition to focusing on newer therapies for these conditions..
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  • 文章类型: Case Reports
    目的:前列腺间质肉瘤是极其罕见的侵袭性恶性肿瘤,占所有类型前列腺癌的不到1%。它经常被误诊为其他下尿路症状(LUTS)问题。
    方法:我们提供一例45岁男性抱怨LUTS问题的病例报告。患者还患有厌食症和体重减轻。他最初被诊断为良性前列腺增生(BPH)。患者进行了经尿道前列腺电切术(TURP)以减轻投诉,但症状恶化并复发。组织病理学检查结果证实前列腺间质肉瘤(T4N0M0)。使用MRI进一步检查患者,然后进行根治性前列腺切除术。
    结论:前列腺间质肉瘤的发病率非常低,最常表现为阻塞性LUTS症状。这可以模拟其他疾病,如BPH或其他类型的前列腺癌。因此,临床医生需要高度怀疑患有复发性LUTS的患者。
    结论:前列腺间质肉瘤的诊断是一种具有挑战性的疾病实体,需要进行组织病理学检查。需要对前列腺间质肉瘤进行及时准确的诊断,以获得更好的预后。
    OBJECTIVE: Prostate stromal sarcoma is extremely rare and aggressive malignancy accounting for less than 1 % of all type of prostate cancers. It is frequently misdiagnosed from other lower urinary tract symptoms (LUTS) problems.
    METHODS: We present a case report of 45-year-old male complaining with LUTS problems. Patient also suffers anorexia and weight loss. He was first diagnosed with benign prostate hyperplasia (BPH). Patients had done transurethral resection of prostate (TURP) to alleviate the complaint, but the symptoms worsened and recurred. Histopathological examination findings confirmed prostate stromal sarcoma (T4N0M0). Patient was further examined using MRI and then radical prostatectomy procedure was performed.
    CONCLUSIONS: Incidence of prostate stromal sarcoma is very low and most commonly presents with obstructive LUTS symptoms. This could mimic other disease such as BPH or other type of prostate cancer. Therefore, clinicians require a high suspicion in patient with recurrent LUTS.
    CONCLUSIONS: Prostate stromal sarcoma diagnosis is a challenging disease entity that necessitates histopathology examination. Timely and accurate diagnosis of prostate stromal sarcoma is needed to achieve better outcome and prognosis for the patients.
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  • 文章类型: Journal Article
    目的:确认CYP17A1基因是否调节导致MetS-BPH的T/E比值。
    方法:824名男性,47-88岁,通过连续的常规体检计划和长期门诊筛查被招募到这项研究中。几个参数,包括CYP17A1基因的SNPs,总睾酮,雌二醇,并获得每个参与者的总睾酮与雌二醇的比率(T/E)。根据BPH的诊断,MetS,还有MetS-BPH,参与者分为BPH和非BPH组,MetS和非MetS组,以及MetS-BPH和非MetS-BPH组。使用单向方差分析评估获得的参数值,学生t检验,卡方检验,和逻辑回归分析。
    结果:CYP17A1基因的SNP,包括rs743572基因型(GG,GA,和AA),rs3781287基因型(GG,GT,TT),和rs4919686基因型(CC,CA,和AA),出现在每个小组中。只有rs743572的GG基因型与BPH独立相关(OR=5.868,95%CI:3.363-7.974,P<0.001),MetS(OR=7.228,95%CI:3.925-11.331,P<0.001),和MetS-BPH(OR=3.417,95%CI:1.783-5.266,P<0.001)。在rs743572基因型GG人群中,T/E比值降低是BPH的独立危险因素(OR=839.756,95%CI:36.978-1334.263,P=0.001),MetS(OR=376.988,95%CI:12.980-488.976,P<0.003),和MetS-BPH(OR=388.236,95%CI:24.869-495.363,P=0.003)。
    结论:CYP17A1基因rs743572调节T/E比值降低的GG基因型可能是MetS-BPH人群的独立危险因素。
    背景:ChiCTR2200057632\“回顾性注册\”。
    2022年3月15日“追溯注册”。
    OBJECTIVE: To confirm if the CYP17A1 gene regulates the ratio of T/E leading to MetS-BPH.
    METHODS: 824 men, aged 47-88 years, were recruited into this study through consecutive routine physical examination programs and long-term outpatient screening. Several parameters, including SNPs of CYP17A1 gene, total testosterone, estradiol, and the ratio of total testosterone to estradiol (T/E) were obtained for each participant. Based on the diagnosis of BPH, MetS, and MetS-BPH, the participants were divided into BPH and non-BPH groups, MetS and non-MetS groups, and MetS-BPH and non-MetS-BPH groups. Values of the obtained parameters were evaluated using one-way analysis of variance, Student\'s t-test, Chi-squared test, and logistic regression analysis.
    RESULTS: SNPs of the CYP17A1 gene, including the rs743572 genotypes (GG, GA, and AA), rs3781287 genotypes (GG, GT, TT), and rs4919686 genotypes (CC, CA, and AA), were present in every group. Only the GG genotype of rs743572 was independently associated with BPH (OR = 5.868, 95% CI: 3.363-7.974, P < 0.001), MetS (OR = 7.228, 95% CI: 3.925-11.331, P < 0.001), and MetS-BPH (OR = 3.417, 95% CI: 1.783-5.266, P < 0.001) after adjusting for age. In the population of genotype GG of rs743572, the decrease in T/E ratio was an independent risk factor for BPH (OR = 839.756, 95% CI: 36.978-1334.263, P = 0.001), MetS (OR = 376.988, 95% CI: 12.980-488.976, P < 0.003), and MetS-BPH (OR = 388.236, 95% CI: 24.869-495.363, P = 0.003).
    CONCLUSIONS: The GG genotype of rs743572 in CYP17A1 gene regulating the decrease of T/E ratio can be an independent risk factor for MetS-BPH populations.
    BACKGROUND: ChiCTR2200057632 \"retrospectively registered\".
    UNASSIGNED: March 15, 2022 \"retrospectively registered\".
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  • 文章类型: Journal Article
    背景:最近的研究表明,5α-还原酶抑制剂(5ARIs)治疗良性前列腺增生(BPH)会导致视网膜解剖结构异常改变。
    目的:比较接受5ARIs或坦索罗辛治疗的BPH患者年龄相关性黄斑变性(AMD)的发生率。
    方法:回顾性,使用新用户和主动比较器设计的基于人群的队列研究。
    方法:一般人群。
    方法:患有BPH的男性,2010年至2018年新接受5ARIs或坦索罗辛。
    方法:数据来自台湾国家健康保险研究数据库。我们使用Cox比例风险模型,倾向评分(PS)匹配,基于意向治疗分析来确定事件AMD的风险。敏感性分析包括处理后的方法和基于加权的PS方法。我们还分别报告了接受非那雄胺和度他雄胺的患者发生AMD的风险,以确定不同5ARI之间的风险差异。
    结果:我们包括13.5865ARIs使用者(平均年龄:69岁)和54.344坦索罗辛使用者(平均年龄:68.37岁)。经过3.7年的平均随访,5ARIs和坦索罗辛使用者发生AMD的风险无差异[风险比(HR):1.06;95%置信区间(95%CI):0.98-1.15],敏感性分析结果相似。然而,接受度他雄胺治疗的患者发生年龄相关性黄斑变性的风险增加[HR:1.13;95%CI:1.02-1.25],但不是那些接受非那雄胺[HR:0.99;95%CI:0.87-1.12],在亚组分析中。
    结论:我们发现在BPH患者中,5ARIs和坦索罗辛的AMD发病率没有差异。然而,AMD的风险状况在度他雄胺和非那雄胺之间略有不同,表明雄激素抑制的效力是与AMD发病相关的因素。
    BACKGROUND: Recent studies suggest that 5α-reductase inhibitors (5ARIs) for benign prostate hyperplasia (BPH) result in abnormal retinal anatomical alteration.
    OBJECTIVE: To compare age-related macular degeneration (AMD) incidence in BPH patients receiving 5ARIs or tamsulosin.
    METHODS: Retrospective, population-based cohort study using new-user and active-comparator design.
    METHODS: General population.
    METHODS: Males with BPH, newly receiving 5ARIs or tamsulosin from 2010 to 2018.
    METHODS: Data were extracted from Taiwan\'s National Health Insurance Research Database. We used Cox proportional hazards model with 1:4 propensity score (PS) matching, based on intention-to-treat analysis to determine the risk of incident AMD. Sensitivity analyses included an as-treated approach and weighting-based PS methods. We also separately reported the risks of incident AMD in patients receiving finasteride and dutasteride to determine risk differences among different 5ARIs.
    RESULTS: We included 13 586 5ARIs users (mean age: 69 years) and 54 344 tamsulosin users (mean age: 68.37 years). After a mean follow-up of 3.7 years, no differences were observed in the risk of incident AMD between 5ARIs and tamsulosin users [hazard ratio (HR): 1.06; 95% confidence intervals (95% CI): 0.98-1.15], with similar results from sensitivity analyses. However, increased risk of incident age-related macular degeneration was observed in patients receiving dutasteride [HR: 1.13; 95% CI: 1.02-1.25], but not in those receiving finasteride [HR: 0.99; 95% CI: 0.87-1.12], in the subgroup analyses.
    CONCLUSIONS: We found no difference between 5ARIs and tamsulosin regarding the incidence of AMD in BPH patients. However, the risk profiles for AMD differed slightly between dutasteride and finasteride, suggesting that the potency of androgen inhibition is a factor related to AMD incidence.
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  • 文章类型: Journal Article
    组织碎石术是一种非侵入性聚焦超声治疗,可机械地分割组织以产生明确定义的病变。在先前治疗良性前列腺增生(BPH)的临床试点试验中,组织切片未导致症状的一致客观改善,可能是因为该组织的纤维化和机械韧性。在这项研究中,我们的目的是确定通过不同的组织学方式使BPH组织匀浆所需的剂量,包括沸腾组织切片(BH)和空化组织切片(CH)。开发了一种通过熵(HLQE)分析进行组织学损伤量化的方法,并将其用于量化各个治疗的损伤面积。这些数据与每个参数设置和剂量治疗前后通过超声剪切波弹性成像测量的机械刚度变化相关。定性评估和定量测量对应于组织学观察到的完全病变的时间点。对于BH治疗,完整的病变发生>=30s治疗时间,相应的最大刚度降低为-90.9±7.2(s.d.)%。高脉冲重复频率(PRF)CH在288s时实现了与BH相似的降低(-91.6±6.0(s.d.)%),在剂量>=144s时,低PRFCH的刚度降低(-82.1±5.1(s.d.)%)。受试者工作特征曲线分析显示,僵硬度降低>~75%与组织学观察到的完整病变呈正相关,并且可以提供替代度量来跟踪治疗进展。
    Histotripsy is a noninvasive focused ultrasound therapy that mechanically fractionates tissue to create well-defined lesions. In a previous clinical pilot trial to treat benign prostatic hyperplasia (BPH), histotripsy did not result in consistent objective improvements in symptoms, potentially because of the fibrotic and mechanically tough nature of this tissue. In this study, we aimed to identify the dosage required to homogenize BPH tissue by different histotripsy modalities, including boiling histotripsy (BH) and cavitation histotripsy (CH). A method for histotripsy lesion quantification via entropy (HLQE) analysis was developed and utilized to quantify lesion area of the respective treatments. These data were correlated to changes in mechanical stiffness measured by ultrasound shear-wave elastography before and after treatment with each parameter set and dose. Time points corresponding to histologically observed complete lesions were qualitatively evaluated and quantitatively measured. For the BH treatment, complete lesions occurred with >=30s treatment time, with a corresponding maximum reduction in stiffness of -90.9±7.2(s.d.)%. High pulse repetition frequency (PRF) CH achieved a similar reduction to that of BH at 288s (-91.6±6.0(s.d.)%), and low-PRF CH achieved a (-82.1±5.1(s.d.)%) reduction in stiffness at dose >=144s. Receiver operating characteristic curve analysis showed that a >~75% reduction in stiffness positively correlated with complete lesions observed histologically, and can provide an alternative metric to track treatment progression.
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  • 文章类型: Journal Article
    良性前列腺增生是男性最常见的疾病之一,50多岁的患病率为50%,80多岁的患病率为80%,主要是用慢性药物治疗。这项研究的目的是分析2008年至2021年向HALMED报告的良性前列腺增生(BPH)治疗药物的不良反应(ADR)。克罗地亚的ADR报告数据来自VigiFlow国家数据库,克罗地亚的BPH药物使用数据来自HALMED的药物利用报告。在观察期间,每种BPH药物的报告数量,报告总数,报告的ADR的严重性,患者年龄和性别,记者的类型,并对大多数报告的ADR进行了分析。结果显示,共收到438份ADR报告,其中45.95%的坦索罗辛作为BPH最常用的药物。在所有报告中,84%是非严重的,男性报告了96%,45岁以上的患者报告了82%。最常报告的不良反应与BPH药物的已知安全性一致。药剂师是BPH药物ADR的最常见(47%)报告者,而33%是由医生报告的。对报告的ADR的分析表明,最常报告的ADR与BPH药物的已知安全性一致。然而,鉴于该疾病的患病率和BPH药物的使用程度,可以说,报告的数量可能会更高(即,34份报告/年)。报告药品不良反应是必要的,以更好地了解药物在授权后期间的安全性。通过提高医疗保健专业人员的认识,可以收集更多关于药物安全使用的信息。
    Benign prostatic hyperplasia is one of the most common diseases in men, with a prevalence rate of 50% in their 50s to 80% in their 80s, and is mostly treated with chronic drug therapy. The aim of this study was to analyze adverse drug reactions (ADR) to drugs used in benign prostate hyperplasia (BPH) treatment reported to HALMED from 2008 to 2021. Data on ADR reports in Croatia were obtained from the VigiFlow national database and on the use of drugs for BPH in Croatia from Drug Utilization Reports from HALMED. In the observed period, the number of reports on each BPH drug, total number of reports, seriousness of reported ADR, patient age and sex, type of reporter, and most reported ADRs were analyzed. Results showed that 438 ADR reports were received, of which 45.95% on tamsulosin as the most frequently used drug for BPH. Of all reports, 84% were non-serious, 96% were reported in men and 82% in patients older than 45 years. The most frequently reported ADRs were consistent with the known safety profile of BPH drugs. Pharmacists were the most common (47%) reporters of ADRs for BPH drugs, while 33% were reported by physicians. Analysis of the reported ADRs showed that most frequently reported ones were in line with the known safety profile of BPH drugs. However, given the prevalence of the disease and the extent of the use of BPH drugs, it could be argued that the number of reports could be higher (i.e., 34 reports/year). Reporting on ADRs is necessary to better understand the safety profile of drugs in the post-authorization period, and more information on the safe use of medicines could be collected by raising awareness of healthcare professionals.
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  • 文章类型: Case Reports
    良性前列腺增生是导致老年男性泌尿症状的常见病。有时会导致前列腺源性血尿,由于增大的腺体的血管分布增加。如果这种类型的血尿严重且保守措施难以治疗,可能会危及生命.前列腺动脉栓塞术(PAE)是传统外科手术的微创替代疗法,特别是有合并症和手术禁忌症的患者。我们介绍了一例79岁男性,患有难治性前列腺源性血尿(RHPO),多种合并症,左上肢和双下肢明显畸形。患者经右桡动脉接受PAE治疗,介入放射学中较不常见的方法。手术成功,血尿完全消退,没有并发症。该报告强调了适应复杂患者治疗的重要性,并表明PAE在这种情况下可以安全有效。
    Benign prostatic hyperplasia is a common condition causing urinary symptoms in older men. It can sometimes lead to hematuria of prostatic origin, due to increased vascularity of the enlarged gland. If this type of hematuria is severe and refractory to conservative measures, it can be life-threatening. Prostatic artery embolization (PAE) serves as a minimally invasive alternative to traditional surgical interventions, particularly in patients with comorbidities and contraindications to surgery. We present a case of a 79-year-old male with refractory hematuria of prostatic origin (RHPO), multiple comorbidities, and significant deformities of the left upper and both lower limbs. The patient was treated with PAE via the right radial artery, a less common approach in interventional radiology. The procedure was successful and led to a complete resolution of hematuria, with no complications. This report highlights the importance of adapting treatment for complex patients and shows that PAE can be safe and effective in such cases.
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  • 文章类型: Journal Article
    良性前列腺增生(BPH)显著影响男性的健康和生活质量,其患病率随着年龄的增长而上升。这篇综述严格审查了BPH药物干预措施的成本效益,以优化患者预后和医疗保健资源利用。
    这篇综述探讨了成本效益分析(CEA)与临床实践的整合,平衡BPH管理的临床疗效与经济效益。我们进行了批判性文献检索,包括最近关于BPH治疗的经济评估的研究,专注于药物治疗,如α-受体阻滞剂和5-α还原酶抑制剂。此外,我们讨论了CEA的概念,并评估了药物和解和避免多重用药对最佳BPH治疗的作用。
    成本效益分析对于评估BPH治疗至关重要,有证据表明,转向手术干预可能会带来更大的长期经济效益。然而,这些模型必须谨慎应用,考虑临床证据和患者偏好,以确保公平和以患者为中心的医疗保健。
    UNASSIGNED: Benign Prostate Hyperplasia (BPH) significantly impacts men\'s health and quality of life, with its prevalence rising with age. This review critically examines the cost-effectiveness of pharmacological interventions for BPH to optimize patient outcomes and healthcare resource utilization.
    UNASSIGNED: This review explores the integration of cost-effectiveness analysis (CEA) into clinical practice, balancing clinical efficacy with economic efficiency in BPH management. We performed a critical literature search, including recent studies on the economic evaluation of BPH treatments, focusing on pharmacotherapies such as alpha-blockers and 5-alpha reductase inhibitors. Additionally, we discussed the concept of CEA and evaluated the role of medicinal reconciliation and the avoidance of polypharmacy in favor of optimal BPH treatment.
    UNASSIGNED: Cost-effectiveness analysis is crucial for evaluating BPH treatments, with evidence suggesting a shift towards surgical interventions may offer greater long-term economic benefits. However, these models must be applied cautiously, considering clinical evidence and patient preferences to ensure equitable and patient-centric healthcare.
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