Diagnostic algorithm

诊断算法
  • 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: Case Reports
    Kerioncelsi(KC),称为头皮癣,是儿童中最常见的皮肤癣菌病。在墨西哥,它在皮肤癣菌中排名第四,频率为4%-10%。KC是头癣(TC)的炎性品种,最常见的病原体是犬小孢子菌和毛癣菌。我们介绍了一名6岁男性被诊断患有KC的临床病例。直接检查用氯唑黑染色,并进行培养,产生负面结果。组织病理学研究显示,毛干内部和周围有孢子和短菌丝。伊曲康唑治疗是基于对小孢子菌的怀疑而开始的。从内窥镜检查的结果。我们提出了一种用于kerioncelsi的诊断和治疗算法。
    Kerion celsi (KC), known as scalp ringworm, is the most common dermatophytosis in children. In Mexico, it ranks fourth among dermatophytoses, with a frequency of 4%-10%. KC is the inflammatory variety of tinea capitis (TC), with the most common causative agents being Microsporum canis and Trichophyton mentagrophytes. We present the clinical case of a six-year-old male diagnosed with KC. Direct examination stained with chlorazol black and cultures were performed, yielding negative results. Histopathological study revealed spores and short hyphae within and surrounding the hair shaft. Treatment with itraconazole was initiated based on suspicion of Microsporum spp. from the trichoscopy findings. We propose a diagnostic and therapeutic algorithm for kerion celsi.
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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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  • 文章类型: Journal Article
    目的:儿童嗜酸性粒细胞增多是临床上常见的难题,通常导致资源和耗时的评估。我们旨在评估来自不同社会经济环境的儿童嗜酸性粒细胞增多的主要病因,并提出诊断算法。
    方法:通过PubMed进行了系统的文献综述,Embase和Cochrane图书馆。纳入2012年1月至2023年6月发表的报告儿童外周嗜酸性粒细胞增多的发病率和病因的研究。比较了来自低收入或高收入国家儿童研究的证据。
    结果:共15项观察性研究,包括3409名儿童,包括在内。嗜酸性粒细胞增多的原因因儿童的起源和嗜酸性粒细胞增多的严重程度而异。在高收入国家的儿童中,过敏性疾病是主要原因,患病率为7.7%-78.2%,而寄生虫病从1.0%到9.1%不等。在低收入国家的儿童中,寄生虫病占主导地位,从17.7%到88.3%,尽管在2.5%-4.8%的病例中发现了过敏性疾病。关于严重性,过敏性疾病是轻度至中度嗜酸性粒细胞增多的主要原因;寄生虫病与中度至重度嗜酸性粒细胞增多有关,而免疫疾病大多见于严重病例。
    结论:我们开发了一种升级诊断算法,该算法考虑了儿童的起源和嗜酸性粒细胞增多的严重程度,并可以优化资源分配。
    OBJECTIVE: Paediatric eosinophilia is a common clinical dilemma, often leading to resource- and time-consuming assessments. We aim to evaluate the main aetiologies of eosinophilia in children from different socioeconomic settings and propose a diagnostic algorithm.
    METHODS: A systematic literature review was conducted through PubMed, Embase and the Cochrane Library. Studies published from January 2012 to June 2023 reporting the incidence and aetiology of peripheral eosinophilia in children were included. Evidence from studies on children originating from low- or high-income countries was compared.
    RESULTS: A total of 15 observational studies, encompassing 3409 children, were included. The causes of eosinophilia varied based on the children\'s origin and the eosinophilia severity. In children from high-income countries, allergic diseases were the leading cause, with a prevalence of 7.7%-78.2%, while parasitosis ranged from 1.0% to 9.1%. In children from low-income countries, parasitosis was predominant, ranging from 17.7% to 88.3%, although allergic diseases were found in 2.5%-4.8% of cases. Concerning severity, allergic diseases were the leading cause of mild-to-moderate eosinophilia; parasitosis was associated with moderate-to-severe eosinophilia, while immunological disorders were mostly found in severe cases.
    CONCLUSIONS: We developed a step-up diagnostic algorithm that considers the child\'s origin and eosinophilia severity and could optimise resource allocation.
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  • 文章类型: Journal Article
    新诊断为肛门直肠畸形(ARM)的新生儿对临床团队提出了独特的挑战。ARM与额外的中线畸形密切相关,例如在VACTERL序列中观察到的那些,包括椎骨,心脏,和肾脏畸形.及时评估是必要的,以确定需要干预的异常情况,并防止过度的压力和延迟治疗。我们利用多学科团队开发了一种算法,指导新诊断为ARM的患者的中线检查。如果出生在或转移到我们的新生儿重症监护病房(NICU),或者在一个月内的临床上看到的。完整成像被定义为超声心动图,肾超声,和脊柱磁共振成像或超声检查在生命的第一个月内。我们比较了三个时期:实施前(2010-2014年),收养期(2015年),和延迟实施(2022年);p≤0.05被认为是显著的。从实施前到延迟实施的完全成像率显著提高(65.2%vs.50.0%vs.97.0%,p=0.0003);在脊柱成像中观察到最大的增长(71.0%vs.90.0%vs.100.0%,p=0.001)。虽然识别出的异常率没有差异,算法的漏诊次数较少(10.0%与47.6%,p=0.05)。我们证明了标准化算法的实施可以显着增加对与ARM新诊断相关的异常的适当筛查,并可以减少延迟诊断。进一步的定性研究将有助于改进和优化算法。
    Neonates with a new diagnosis of anorectal malformation (ARM) present a unique challenge to the clinical team. ARM is strongly associated with additional midline malformations, such as those observed in the VACTERL sequence, including vertebral, cardiac, and renal malformations. Timely assessment is necessary to identify anomalies requiring intervention and to prevent undue stress and delayed treatment. We utilized a multidisciplinary team to develop an algorithm guiding the midline workup of patients newly diagnosed with ARM. Patients were included if born in or transferred to our neonatal intensive care unit (NICU), or if seen in clinic within one month of life. Complete imaging was defined as an echocardiogram, renal ultrasound, and spinal magnetic resonance imaging or ultrasound within the first month of life. We compared three periods: prior to implementation (2010-2014), adoption period (2015), and delayed implementation (2022); p ≤ 0.05 was considered significant. Rates of complete imaging significantly improved from pre-implementation to delayed implementation (65.2% vs. 50.0% vs. 97.0%, p = 0.0003); the most growth was observed in spinal imaging (71.0% vs. 90.0% vs. 100.0%, p = 0.001). While there were no differences in the rates of identified anomalies, there were fewer missed diagnoses with the algorithm (10.0% vs. 47.6%, p = 0.05). We demonstrate that the implementation of a standardized algorithm can significantly increase appropriate screening for anomalies associated with a new diagnosis of ARM and can decrease delayed diagnosis. Further qualitative studies will help to refine and optimize the algorithm moving forward.
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