Diagnostic algorithm

诊断算法
  • 文章类型: Journal Article
    卵巢癌(OC)是发达国家中最致命的妇科癌症。大多数病例在晚期III-IV期诊断,5年总生存率非常低。几项研究表明,与非使用者相比,激素治疗(HT)使用者的OC风险更高。HT的持续时间延长是统计学上显著的风险因素。糖类抗原或癌抗原125(CA-125)仍然是OC的最佳筛选工具;然而,由于特异性低,其价值有限,导致不必要的干预,手术,和心理伤害。此外,超声解释的变异性凸显了迫切需要开发一种敏感性和特异性更高的单变量指数,以早期诊断HT患者的OC。在这里,我们批判性地回顾了用于检测OC的生物标志物的局限性,旨在提出准确且具有成本效益的诊断比率,消除体重指数的影响。年龄,HT,吸烟,和良性卵巢疾病的测量。许多研究将生物标志物如CA-125、人附睾蛋白4和胸苷激酶1结合到诊断算法中。数据表明,雌激素受体的表达可能具有诊断和预后价值。由于ERβ下调,OC中雌激素受体α(ERα):雌激素受体β(ERβ)的比例明显高于正常组织。CA-125和糖类抗原或癌抗原72-4(CA72-4)的表达与ERα和ERβ呈高度正相关,分别,提出新的比率CA-125:CA72-4可能是监测HT下绝经后妇女的节点。
    Ovarian cancer (OC) is the most lethal gynecological cancer in the developed world. Most cases are diagnosed at late stage III-IV with a very low 5-year overall survival rate. Several studies revealed an elevated risk of OC in users of hormone treatment (HT) compared with non-users. The extended duration of HT is a statistically significant risk factor. Carbohydrate antigen or cancer antigen 125 (CA-125) remains the best screening tool for OC; however, its value is limited due to low specificity, leading to unnecessary interventions, surgeries, and psychological harm. Additionally, the variability of ultrasound interpretation highlights the urgent need to develop a univariate index with higher sensitivity and specificity for early diagnosis of OC in women under HT. Herein we critically review the limitations of biomarkers for the detection of OC aiming to suggest an accurate and cost-effective diagnostic ratio that eliminates the impact of body mass index, age, HT, smoking, and benign ovarian diseases on measurements. Numerous studies combine biomarkers such as CA-125, human epididymis protein 4, and thymidine kinase 1 into diagnostic algorithms. Data suggest that the expression of estrogen receptors may have diagnostic and prognostic value, as the estrogen receptor α (ERα):estrogen receptor β (ERβ) ratio is significantly higher in OC than in normal tissue due to ERβ downregulation. A high positive correlation between expression of CA-125 and carbohydrate antigen or cancer antigen 72 - 4 (CA72-4) with ERα and ERβ, respectively, poses that a novel ratio CA-125:CA72-4 could be nodal for monitoring post-menopausal women under HT.
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  • 文章类型: Journal Article
    肠道超声(IUS)最近已成为不同类型肠道炎症患者的首选成像技术。IUS有很高的灵敏度,特异性,正预测值,诊断克罗恩病或溃疡性结肠炎时的阴性预测值。Further,由于它的非侵袭性,它现在是常规IBD重新评估的首选成像模式,成本效益,可用性(至少在欧洲),和所有年龄组的可重复性。然而,IUS的临床成功需要对执行IUS的医生和技术人员进行IUS培训,并对末端回肠和整个结肠的超声检查结果进行标准化描述.并发症如脓肿形成,瘘管,和狭窄可以通过常规IUS或对比增强超声(CEUS)检测。最近,已经为克罗恩病提出了几种疾病活动评分,术后克罗恩病,成人(包括老年人)和儿童的溃疡性结肠炎。IUS已成功用于随机临床试验,以测量治疗反应。因此,IUS现在在临床决策中起着核心作用。
    Intestinal ultrasound (IUS) has recently become the imaging technique of choice for patients with different types of intestinal inflammation. IUS has a high sensitivity, specificity, positive predictive value, and negative predictive value when diagnosing Crohn\'s disease or ulcerative colitis. Further, it is now the preferred imaging modality for routine IBD reevaluations because of its non-invasiveness, cost-effectiveness, availability (at least in Europe), and reproducibility in all age groups. However, the clinical success of IUS requires IUS training for doctors and technicians who perform IUS with a standardised description of ultrasound findings of the terminal ileum and entire colon. Complications such as abscess formation, fistulae, and stenosis can be detected by either conventional IUS or contrast-enhanced ultrasound (CEUS). Lately, several disease activity scores have been proposed for Crohn\'s disease, postoperative Crohn\'s disease, and ulcerative colitis both in adults (including elderly) and in children. IUS was successfully used in randomised clinical trials in order to measure the treatment response. Therefore, IUS now plays a central role in clinical decision making.
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  • 文章类型: Journal Article
    在评估肝细胞癌(HCC)的患者中,当多相对比增强计算机断层扫描(ceCT)尚无定论时,通常会辅助使用磁共振成像(MRI)。我们调查了增加MRI的临床影响。
    这项单机构回顾性研究包括2016年5月至2023年7月进行的48次MRI扫描(44例患者),原因是在多期ceCT扫描中怀疑HCC。数据包括病史,之前和之后的成像,组织学可用时,以及在多学科小组会议上做出的决定。
    如果肝癌可能复发,63%的MRI扫描诊断为HCC。对于80%的阴性MRI扫描,患者在肝脏可疑区域的中位时间165天内被诊断为HCC.在肝硬化患者可能的新生肝癌的情况下,22%的扫描诊断为HCC,33%的MRI扫描阴性的患者在109天内被诊断为HCC。没有一个非肝硬化患者可能的新生肝癌和阴性的MRI扫描(64%)后来诊断为肝癌。但不确定扫描的3/5是活检中诊断为HCC的患者。
    可疑HCC的多阶段ceCT扫描的二次MRI在排除非肝硬化患者的HCC以及在肝硬化患者和先前HCC患者的非侵入性诊断HCC方面非常有价值。如果MRI结果不确定或阴性,患有肝硬化或先前HCC的患者仍然有很高的HCC风险。
    UNASSIGNED: In patients evaluated for hepatocellular carcinoma (HCC), magnetic resonance imaging (MRI) is often used secondarily when multiphase contrast-enhanced computed tomography (ceCT) is inconclusive. We investigated the clinical impact of adding MRI.
    UNASSIGNED: This single-institution retrospective study included 48 MRI scans (44 patients) conducted from May 2016 to July 2023 due to suspicion of HCC on a multiphase ceCT scan. Data included medical history, preceding and subsequent imaging, histology when available, and decisions made at multidisciplinary team meetings.
    UNASSIGNED: In case of possible HCC recurrence, 63% of the MRI scans were diagnostic of HCC. For 80% of the negative MRI scans, the patients were diagnosed with HCC within a median of 165 days in the suspicious area of the liver. In case of possible de-novo HCC in patients with cirrhosis, 22% of the scans were diagnostic of HCC and 33% of the negative MRI scans were of patients diagnosed with HCC within a median of 109 days. None of the non-cirrhotic patients with possible de-novo HCC and negative MRI scans (64%) were later diagnosed with HCC, but 3/5 of the indeterminate scans were of patients diagnosed with HCC in a biopsy.
    UNASSIGNED: Secondary MRI to a multiphase ceCT scan suspicious of HCC is highly valuable in ruling out HCC in non-cirrhotic patients and in diagnosing HCC non-invasively in cirrhotic patients and patients with prior HCC. Patients with cirrhosis or prior HCC are still at high risk of having HCC if MRI results are inconclusive or negative.
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  • 文章类型: Journal Article
    目标:全球,头颈部肉瘤的治疗途径仍不清楚。2018年,伦敦肉瘤服务(LSS)成立了专门的头颈部肉瘤(HNS)多学科团队(MDT),其明确目标是正式获得诊断方面的超级专家专业知识。HNS的治疗计划和管理。该研究的目的是提供专用HNSMDT的初步结果。
    方法:2018年至2022年期间讨论的所有患者,在HNSMDT中,一项新的组织学证实的HNS诊断纳入研究.人口统计,解剖部位,形态学,MDT建议,治疗细节和结局来自电子病历.
    结果:在HNSMDT中总共讨论了337例患者,其中178例患者被纳入研究,年龄中位数为53岁(范围2-94);67%为软组织肉瘤(STS),33%为骨肉瘤(BS),其中43%和71%是高级的,分别。55%的BS和39%的STS接受了手术。9%的BS和7%的STS接受辅助质子束治疗。中位随访时间为2.16年,12%观察到复发,6%的患者发生远处转移,总生存率为72%。
    结论:HNSMDT为HNS的诊断和多模态管理提供了专业知识。STS更容易被误诊。非典型的影像学特征应触发专家转诊。初次就诊时的适当手术仍然是治疗的主要手段,也是总体生存率的最强预测指标。成立专门针对HNS的专家工作组必须致力于简化肉瘤护理。
    OBJECTIVE: Globally, head & neck sarcoma care pathways remain unclear. In 2018, the London Sarcoma Service (LSS) set up a dedicated head and neck sarcoma (HNS) multidisciplinary team (MDT) with a clear objective to provide formal access to super-specialist expertise in diagnosis, treatment planning and management of HNS. The aim of the study is to provide first results of a dedicated HNS MDT.
    METHODS: All patients discussed between 2018 and 2022, in HNS MDT, with a new histologically confirmed HNS diagnosis were included in the study. Demographics, anatomic site, morphology, MDT recommendation, treatment details and outcomes were obtained from electronic patient records.
    RESULTS: A total of 337 patients were discussed in the HNS MDT of which 178 patients were included in the study, with a median age of 53 years(range 2-94); 67 % were soft tissue sarcomas(STS) and 33 % were bone sarcomas(BS), of which 43 % and 71 % were high grade, respectively. 55 % BS and 39 % STS underwent surgery. 9 % of BS and 7 % of STS received adjuvant Proton Beam therapy. With a median follow-up of 2.16 years, recurrence was observed in 12 %, distant metastasis in 6 % of patients and overall survival was 72 %.
    CONCLUSIONS: The HNS MDT provides expertise on diagnosis and multi-modality management of HNS. STS are more likely to be misdiagnosed. Atypical imaging characteristics should trigger a specialist referral. Adequate surgery at first presentation remains the mainstay of treatment and the strongest prognosticator of overall survival. Formation of an expert working group specific to HNS must work towards streamlining sarcoma care.
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  • 文章类型: English Abstract
    本文讨论了初级卫生保健(PHC)范围内的掌plant皮肤病(PPD)的诊断挑战。这些常见的皮肤状况,在日常实践中遇到,表现出各种各样的症状和形态,使他们的诊断复杂化。它们在病因学上分为感染性炎症,非感染性炎症,和遗传性角膜炎.虽然各种皮肤病可能会影响手掌和脚底,很少有人专门针对这个领域。值得注意的例子包括掌plant脓疱病,汗肿,Pernio红斑,和Bazex综合征.鉴于PHC皮肤科咨询的患病率很高,这篇文章强调了PHC专业人士关于这些条件的知识的重要性。它提出了一种诊断算法,以方便他们的管理和及时转诊。
    This article addresses the diagnostic challenges of palmoplantar dermatoses (PPD) within the scope of Primary Health Care (PHC). These common skin conditions, encountered in daily practice, exhibit a diverse range of symptoms and morphologies, complicating their diagnosis. They are etiologically classified into infectious inflammatory, non-infectious inflammatory, and hereditary keratodermas. While various dermatoses may affect the palms and soles, few are specific to this area. Notable examples include palmoplantar pustulosis, dyshidrosis, erythema pernio, and Bazex syndrome. Given the high prevalence of dermatological consultations in PHC, this article underscores the significance of PHC professionals\' knowledge regarding these conditions. It proposes a diagnostic algorithm to facilitate their management and timely referral.
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  • 文章类型: Journal Article
    随着可用诊断工具的进步,印度的结核病诊断得到了简化。这有助于私人医生“病人优先”的早期诊断方法;然而,成本仍然很高。印度的NTEP建立了结核病诊断网络,这对患者是免费的,并激励私人医生参与。从这一背景出发,设计和实现了一站式结核病诊断解决方案模型,这是在希萨尔区进行的,哈里亚纳邦,允许根据NTEP诊断算法收集和测试来自私人医生的推定结核病患者的标本。在项目期间分析了与私人医生有关的数据子集。还通过使用滚雪球方法采访医生来收集定性数据,以捕获医生对该模型的看法。在从60个设施收集的1159个标本中,在32%的标本中检测到MTB,在7%的标本中检测到利福平抗性。所有标本都通过了诊断算法。接受采访的30名医生对所提供的服务感到满意,并对实施这种“以患者为中心”模式的计划表示赞赏。实施结果表明,需要通过认证过程加强私人诊断,以确保提供高质量的结核病诊断服务。
    TB diagnosis has been simplified in India following advances in available diagnostic tools. This facilitates private doctors\' \"patient first\" approach toward early diagnosis; however, costs remain high. India\'s NTEP established a TB diagnostic network, which is free for patients and incentivizes private doctors to participate. Drawing from this context led to the design and implementation of the One-Stop TB Diagnostic Solution model, which was conducted in the Hisar district, Haryana, allowing specimens from presumptive TB patients from private doctors to be collected and tested as per NTEPs diagnostic algorithm. A subset of data pertaining to private doctors was analyzed for the project period. Qualitative data were also collected by interviewing doctors using a snowball method to capture doctors\' perception about the model. Out of 1159 specimens collected from 60 facilities, MTB was detected in 32% and rifampicin resistance was detected in 7% specimens. All specimens went through the diagnostic algorithm. Thirty doctors interviewed were satisfied with the services offered and were appreciative of the program that implements this \"patient centric\" model. Results from implementation indicate the need to strengthen private diagnostics through a certification process to ensure provision of quality TB diagnostic services.
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  • 文章类型: English Abstract
    BACKGROUND: The reason-related identification of mild cognitive impairment (MCI) in primary care is helpful to treat reversible causes or decelerate progression to dementia by optimal management of existing risk factors. In this process general practitioners are in a key position. The present feasibility study investigated the practicability of a diagnostic algorithm (brain check-up), comprising neuropsychological examinations, differential diagnoses and follow-up measures.
    METHODS: By means of a standardized questionnaire, the utilization and practicability of the brain check-up was surveyed in n = 37 medical practices of general practitioners and internists in Germany.
    RESULTS: The brain check-up was performed by n = 37 physicians in 389 patients (66%). The main barriers to implementation included patients\' fear of facing the results, the professionals\' lack of time, and costs. Overall, 73% of the participants agreed that the brain check-up was practical in everyday treatment. Long waiting times for an appointment with a neurological/psychiatric specialist were perceived as a barrier for optimal care.
    CONCLUSIONS: The structured algorithm is convenient in physician\'s everyday practice and can contribute to identify patients with MCI more easily. Therefore, it appears to be a helpful tool in primary care. To achieve sustainability in everyday use, identified barriers need to be addressed during the implementation phase.
    UNASSIGNED: HINTERGRUND: Die anlassbezogene Identifizierung der leichten kognitiven Störung („mild cognitive impairment“, MCI) in der Primärversorgung ist wichtig, um reversible Ursachen zu behandeln oder das Fortschreiten zu einem demenziellen Syndrom zu verlangsamen. Hierzu wurde die Praxistauglichkeit eines Diagnosealgorithmus, im Weiteren als „Gehirn-Check-up“ bezeichnet, untersucht.
    METHODS: Mittels eines standardisierten Fragebogens wurden das Nutzungsverhalten und die Praxistauglichkeit des Gehirn-Check-up in n = 37 allgemeinmedizinischen und internistischen Arztpraxen in Deutschland erhoben.
    UNASSIGNED: Der Gehirn-Check-up wurde von n = 37 Ärzt:innen bei 389 Personen (66 %) durchgeführt. Zu den Barrieren bezüglich der Durchführung zählten: Angst der Betroffenen vor dem Ergebnis, Zeitmangel des Fachpersonals sowie Kosten. Insgesamt bewerteten 73 % der Teilnehmenden den Gehirn-Check-up im Behandlungsalltag als praxistauglich. Lange Wartezeiten auf einen Termin bei neurologischen/psychiatrischen Fachärzt:innen wurden als Hürde für eine optimale Betreuung genannt.
    UNASSIGNED: Der strukturierte Algorithmus Gehirn-Check-up scheint hilfreich in der Primärversorgung zu sein, da dieser unter Routinebedingungen im hausärztlichen Setting praxistauglich ist und dazu beitragen kann, anlassbezogen Patient:innen mit einer MCI leichter zu identifizieren. Um weitere Barrieren besser adressieren zu können, bedarf es jedoch weiterer Machbarkeitsstudien.
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  • 文章类型: Journal Article
    过敏性肺炎(HP)的诊断标准随时间而变化。我们的目标是将最近的诊断算法应用于一系列诊断为HP的历史患者,以根据当前的诊断标准和所获得的诊断置信度来评估其分布。
    对每个患者应用算法标准。诊断为HP(≥90%),临时高(70-89%)或低置信度(51-69%)或非HP(不太可能)(≤50%);或HP,临时或非HP,如果他们做了肺活检.
    。包括129例患者[平均年龄64±12岁;79例(61.2%)妇女],其中16例(12.4%)是根据高度临床怀疑诊断的。应用算法后,可以评估106例患者(82.2%),其中83例(78.3%)诊断为HP或高置信度。肺活检能够在另外21例患者中建立确定性诊断,在另外9例患者中建立临时诊断[总计,113(87.6%)]。没有严格的HP诊断标准的16例患者诊断可信度低。根据新指南,总共可以避免56例肺活检(64.4%)。
    该算法的应用在H,显着减少所需的肺活检数量。
    UNASSIGNED: The diagnostic criteria for Hypersensitivity pneumonitis (HP) have changed over time. Our aim is to apply a recent diagnostic algorithm to a historical series of patients diagnosed with HP to assess its distribution according to current diagnostic criteria and the diagnostic confidence achieved.
    UNASSIGNED: Application to each patient the algorithm criteria. The diagnosis was HP (≥90%), provisional high (70-89%) or low confidence (51-69%) or non-HP (unlikely) (≤50%); or HP, provisional or non-HP, if they had lung biopsy.
    UNASSIGNED: 129 patients [mean age 64 ± 12 years; 79 (61.2%) women] were included of which 16 (12.4%) were diagnosed on the basis of high clinical suspicion. After applying the algorithm, 106 patients (82.2%) could be evaluated and 83 (78.3%) had a diagnosis of HP or high confidence. Lung biopsy was able to establish a diagnosis of certainty in another 21 patients and a provisional diagnosis in 9 more [total, 113 (87.6%)]. The 16 patients without strict diagnostic criteria for HP had a low confidence diagnosis. A total of 56 lung biopsies (64.4%) could have been avoided according to the new guidelines.
    UNASSIGNED: The application of this algorithm achieves a high diagnostic yield in HP, significantly reducing the number of lung biopsies required.
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  • 文章类型: Journal Article
    尽管结核病在低收入和中等收入国家非常普遍,使用当前的诊断方法仍有数百万例未被发现。为了解决这个问题,研究人员提出了预测规则。
    我们分析了诊断肺结核的现有预测规则,并确定了与该疾病具有中等至高强度关联的因素。
    我们对相关数据库进行了全面搜索(MEDLINE/PubMed,科克伦图书馆,科学直接,全球健康报告,和谷歌学者)截至2022年11月14日。包括开发低收入和中等收入国家成人肺结核诊断算法的研究。两名评审员进行了研究筛选,数据提取,和质量评估。使用诊断准确性研究质量评估-2评估研究质量。我们进行了叙事综合。
    在所选的26篇文章中,只有一半包括人类免疫缺陷病毒阳性患者。在有症状的人类免疫缺陷病毒患者中,影像学检查结果和体重指数是肺结核的有力预测因子,赔率比>4。然而,在人类免疫缺陷病毒阴性个体中,生物标志物显示与该疾病中度相关.在有症状的人类免疫缺陷病毒患者中,C-反应蛋白水平-10mg/L的敏感性和特异性为93%和40%,分别,而一项抗生素试验的特异性为86%,敏感性为43%.在涂片阴性的患者中,抗结核治疗的敏感性为52%,特异性为63%.
    预测因子和诊断算法的性能因患者亚组而异,例如在人类免疫缺陷病毒阳性患者中,射线照相结果,和体重指数是肺结核的有力预测因子。然而,在人类免疫缺陷病毒阴性个体中,生物标志物显示与该疾病中度相关.一些模型已经达到了世界卫生组织的建议。因此,未来应该做更多的工作来加强结核病筛查的预测模型,应该严格开发,考虑到临床工作中人群的异质性。
    UNASSIGNED: Although tuberculosis is highly prevalent in low- and middle-income countries, millions of cases remain undetected using current diagnostic methods. To address this problem, researchers have proposed prediction rules.
    UNASSIGNED: We analyzed existing prediction rules for the diagnosis of pulmonary tuberculosis and identified factors with a moderate to high strength of association with the disease.
    UNASSIGNED: We conducted a comprehensive search of relevant databases (MEDLINE/PubMed, Cochrane Library, Science Direct, Global Health for Reports, and Google Scholar) up to 14 November 2022. Studies that developed diagnostic algorithms for pulmonary tuberculosis in adults from low and middle-income countries were included. Two reviewers performed study screening, data extraction, and quality assessment. The study quality was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2. We performed a narrative synthesis.
    UNASSIGNED: Of the 26 articles selected, only half included human immune deficiency virus-positive patients. In symptomatic human immune deficiency virus patients, radiographic findings and body mass index were strong predictors of pulmonary tuberculosis, with an odds ratio of >4. However, in human immune deficiency virus-negative individuals, the biomarkers showed a moderate association with the disease. In symptomatic human immune deficiency virus patients, a C-reactive protein level ⩾10 mg/L had a sensitivity and specificity of 93% and 40%, respectively, whereas a trial of antibiotics had a specificity of 86% and a sensitivity of 43%. In smear-negative patients, anti-tuberculosis treatment showed a sensitivity of 52% and a specificity of 63%.
    UNASSIGNED: The performance of predictors and diagnostic algorithms differs among patient subgroups, such as in human immune deficiency virus-positive patients, radiographic findings, and body mass index were strong predictors of pulmonary tuberculosis. However, in human immune deficiency virus-negative individuals, the biomarkers showed a moderate association with the disease. A few models have reached the World Health Organization\'s recommendation. Therefore, more work should be done to strengthen the predictive models for tuberculosis screening in the future, and they should be developed rigorously, considering the heterogeneity of the population in clinical work.
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  • 文章类型: Journal Article
    积分理论范式(ITP)有25年的成功治疗膀胱/肠/疼痛症状引起的特定韧带松弛的记录,即使脱垂很小。基于ITP的治疗涉及韧带支撑,可以是非手术或日托手术。需要准确的诊断方案。积分理论诊断系统在门诊环境中执行。它是一个一步一步的“如何”资源的临床医生谁希望学习一种实用的解剖诊断方法,可以快速,准确地确定膀胱/肠/疼痛症状的韧带原因,因此,有可能治愈他们。结构化ITP诊断流程图使用症状来诊断解剖缺陷。它包括4个相关步骤。ITP是整体的,和膀胱,肠,疼痛症状并存。第一步,因此,是建立所有可能的症状转移到诊断算法,这是第二步。因为病人抱怨一个主要症状,其他症状必须通过直接询问来定位,使用诊断算法作为备忘录,或问卷调查来定位膀胱,肠,疼痛症状。第二步:将症状置于3个解剖区域:前区,耻骨尿道韧带(PUL)[压力性尿失禁(SUI)];中间区,主韧带(CL)(横断性膀胱膨出);后区,子宫骶韧带(USL)(子宫脱垂和肠膨出)。第三步是阴道检查以确认由算法预测的三个区域中的韧带损伤(脱垂)。第四步是“模拟操作”(每个阴道特定韧带的机械支持),以验证诊断算法指示的特定韧带,确实导致了这种症状。对于SUI,止血剂在阴道止血剂测试支持PUL在咳嗽时阻止尿液流失;将双壳窥器的下部刀片轻轻插入阴道可以缓解冲动和疼痛。
    The Integral Theory Paradigm (ITP) has a 25-year track record of successfully treating bladder/bowel/pain symptoms caused by laxity in specific ligaments, even when the prolapse is minimal. The ITP-based treatment involves ligament support and can be nonsurgical or daycare surgical. An accurate diagnostic protocol is required. The Integral Theory Diagnostic system is performed in an outpatient setting. It a step-by-step \"how to\" resource for clinicians who wish to learn a practical anatomical diagnostic method which can quickly and accurately identify a ligament cause for bladder/bowel/pain symptoms, and therefore, potentially cure them. The structured ITP diagnosis flow chart uses symptoms to diagnose anatomical defects. It comprises 4 related steps. The ITP is holistic, and bladder, bowel, pain symptoms co-occur. The first step, therefore, is to establish all possible symptoms for transfer to the Diagnostic Algorithm which is the second step. Because patients complain of one main symptom, other symptoms must be located by direct questioning, using the Diagnostic Algorithm as an aide memoire, or a questionnaire to locate bladder, bowel, pain symptoms. Second step: symptoms are placed into 3 anatomical zones: anterior zone, pubourethral ligament (PUL) [stress urinary incontinence (SUI)]; middle zone, cardinal ligament (CL) (transverse defect cystocele); posterior zone, uterosacral ligament (USL) (uterine prolapse and enterocele). The third step is a vaginal examination to confirm the ligament damage (prolapses) in the three zones predicted by the algorithm. The fourth step is \"simulated operations\" (mechanical support of specific ligaments per vaginam) to validate the particular ligament indicated by the diagnostic algorithm, is indeed causing that symptom. For SUI, a hemostat test at midurethra supports PUL vaginally to stop urine loss on coughing; the lower blade of a bivalve speculum gently inserted into the vagina can relieve urge and pain.
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