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Ultra-Microangiography for Evaluating Crohn's Disease Activity in Pediatric Patients: A Prospective Study. 超微血管造影评价儿童克罗恩病活动性的前瞻性研究
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-03-13 DOI: 10.1055/a-2771-2690
Ying Wang, Haixia Feng, Li Wei, Rui Cheng, Yunlin Huang, Shiwen Wang, Yueyang Guan, Ying Wang, Kassa Darge, Yi Dong, Wei Cai

To investigate the role of ultra-microangiography (UMA) in evaluating Crohn's disease (CD) activity in pediatric patients.Pediatric patients diagnosed with CD were included in this prospective study. A Resona A20 ultrasound machine (Mindray Medical Systems, China) was used for all patients. The semiquantitative scores of color Doppler flow imaging (CDFI) and UMA on the thickest segments of bowel walls were assessed according to the Limberg score. The Pediatric Crohn's Disease Activity Index (PCDAI) was the reference standard to evaluate CD activity. ROC analysis was performed to compare the diagnostic efficiency of Limberg scores between CDFI and UMA.Sixty pediatric CD patients were included and divided into three groups according to PCDAI: Group 1, inactive CD (n = 37); Group 2, mild CD (n = 13); and Group 3, moderate to severe CD (n = 10). By UMA, significant differences in Limberg scores were found between Groups 1 and 3 (P < 0.001), Groups 2 and 3 (P = 0.044), and Groups 1 and 2 (P = 0.029). The combined AUROC of B-mode ultrasound (BMUS) features and UMA features in pediatric CD activity evaluation was 0.934, with sensitivity of 87.0% and specificity of 94.6%, which was significantly higher than that of the combined BMUS features and CDFI (P = 0.048).By sensitively depicting the low velocity blood flow signals and displaying microvascular morphologies of the bowel wall, UMA is an effective noninvasive imaging method enabling semiquantitative evaluation of the activity of CD in pediatric patients.

目的:探讨超微血管造影(UMA)在评价小儿克罗恩病(CD)活动性中的作用。材料和方法:在这项前瞻性研究中,诊断为乳糜泻的儿科患者被纳入研究对象。所有患者均使用Resona A20超声机(迈瑞医疗系统,中国)。采用Limberg评分法对肠壁最厚段彩色多普勒血流成像(CDFI)和UMA进行半定量评分。儿童克罗恩病活动性指数(PCDAI)是评价CD活动性的参考标准。采用ROC分析比较CDFI和UMA的Limberg评分的诊断效率。结果:纳入60例儿科CD患者,根据PCDAI分为3组:1组,非活动性CD (n = 37);2组,轻度CD (n = 13);第三组为中度至重度CD (n = 10)。经UMA分析,1组与3组、2组与3组、1组与2组的Limberg评分差异均有统计学意义(P < 0.001), P = 0.044, P = 0.029。b超(BMUS)特征与UMA特征联合评价小儿CD活动性的AUROC为0.934,敏感性87.0%,特异性94.6%,显著高于BMUS特征与CDFI联合评价(P = 0.048)。结论:UMA通过灵敏地描绘低速血流信号和显示肠壁微血管形态,是一种有效的无创成像方法,可以半定量评估儿科患者CD的活动性。
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引用次数: 0
Late-onset ventriculoatrial shunt infection presenting as a cervical mass: the key role of ultrasound. 迟发性脑室房分流感染表现为宫颈肿块:超声的关键作用。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-03-10 DOI: 10.1055/a-2831-9529
Lukas Schmutzler, Marcel Kloppenburg, Ljilja Bektic-Tadic, Julia Klingenschmid, Benedikt Hofauer

n/a.

N/A。
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引用次数: 0
Diagnostic value of inguinal ultrasound for predicting histological lymph node status in vulvar cancer. 腹股沟超声对预测外阴癌组织淋巴结状况的诊断价值。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-03-09 DOI: 10.1055/a-2830-7606
Steffi Hartmann, Nicolas Wenk, Ellen Mann, Toralf Reimer, Sarah Fröhlich, Anne Urban, Manja Woelter, Gesche Schultek, Bernd Gerber
<p><strong>Purpose: </strong>As part of pre-therapeutic diagnostics for vulvar cancer, the assessment of inguinal lymph node status should be conducted. The diagnostic value of structured inguinal sonography for predicting the histological lymph node status in patients with vulvar cancer should be determined.</p><p><strong>Materials and methods: </strong>All patients diagnosed with vulvar cancer and scheduled for surgical removal of inguinal lymph nodes were included in the prospective unicentric cohort study from March 2023 to May 2025. Preoperatively, an inguinal ultrasound was performed according to the Vulvar International Tumor Analysis (VITA) protocol. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were determined. These were compared with the retrospectively collected results of an inguinal ultrasound, which was not performed according to the VITA protocol, in patients who had undergone surgery between January 2016 and February 2023.</p><p><strong>Results: </strong>Lymph node sonography performed according to the VITA protocol, followed by inguinofemoral surgery, was conducted in 74 groins. Lymph node metastases could be identified with a sensitivity of 64.3%, a specificity of 78.3%, a PPV of 40.9%, and an NPV of 90.4%. In 92 groin surgeries in patients without application of the VITA protocol, a sensitivity of 56.3%, a specificity of 89.5%, a PPV of 52.9%, and an NPV of 90.7% were determined, which did not differ significantly from the VITA cohort (p > 0.05).</p><p><strong>Conclusions: </strong>Overall, even after the introduction of a structured examination protocol specifically designed for vulvar cancer, inguinofemoral sonography did not demonstrate higher accuracy in determining the histological lymph node status. Ziel: Im Rahmen der prätherapeutischen Diagnostik beim Vulvakarzinom soll eine Beurteilung der Leistenlymphknoten durchgeführt werden. Ziel der aktuellen Untersuchung ist die Bestimmung des diagnostischen Wertes einer strukturierten inguinalen Sonographie für die Vorhersage des histologischen Lymphknotenstatus bei Patientinnen mit Vulvakarzinom.</p><p><strong>Material und methoden: </strong>Patientinnen mit Erstdiagnose eines Vulvakarzinoms, bei denen eine operative Entfernung der Leistenlymphknoten zwischen März 2023 und Mai 2025 geplant war, wurden in die prospektive unizentrische Studienkohorte aufgenommen. Präoperativ wurde eine inguinale Sonographie gemäß dem Vulvar International Tumor Analysis (VITA)-Protokoll durchgeführt. Es wurden Sensitivität, Spezifität, positiver prädiktiver Wert (PPV) und negativer prädiktiver Wert (NPV) bestimmt. Diese wurden mit den retrospektiv erhobenen Ergebnissen der inguinalen Sonographie zwischen Januar 2016 und Februar 2023 ohne Anwendung des VITA-Protokolls verglichen. Ergebnisse: Für die inguinale Sonographie nach VITA-Protokoll wurde bei 74 Leisten ein metastastischer Befall der Lymphknoten mit einer Sensitivität von 64,3%, einer Spezif
目的:腹股沟淋巴结状态评估是外阴癌治疗前诊断的一部分。腹股沟结构化超声在预测外阴癌患者组织学淋巴结状态方面的诊断价值有待确定。材料和方法:2023年3月至2025年5月,所有诊断为外阴癌并计划手术切除腹股沟淋巴结的患者纳入前瞻性单中心队列研究。术前,根据外阴国际肿瘤分析(VITA)方案进行腹股沟超声检查。测定敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。将这些结果与回顾性收集的腹股沟超声结果进行比较,这些结果不是根据VITA方案进行的,是在2016年1月至2023年2月期间接受手术的患者。结果:根据VITA方案行淋巴结超声检查,然后进行腹股沟手术,74例腹股沟。淋巴结转移的敏感性为64.3%,特异性为78.3%,PPV为40.9%,NPV为90.4%。在92例未应用VITA方案的腹股沟手术中,敏感性为56.3%,特异性为89.5%,PPV为52.9%,NPV为90.7%,与VITA队列无显著差异(p < 0.05)。结论:总体而言,即使引入了专门为外阴癌设计的结构化检查方案,腹股沟超声检查在确定组织学淋巴结状态方面也没有更高的准确性。Ziel:我是Rahmen der prätherapeutischen诊断性疾病(Vulvakarzinom)。[2] [1] [1] [2] [1] [2] [3] [1] [3] [4] [3] [4] [4] [4] [4] [4]材料和方法:患者与外阴病变的临床诊断,患者与外阴病变的手术诊断,患者与外阴病变的诊断,患者与外阴病变的诊断,患者与外阴病变的诊断,患者与外阴病变的诊断,患者与外阴病变的诊断,患者与外阴病变的诊断,患者与外阴病变的诊断。Präoperativ wurde eine腹股沟超声gemäß dem外阴国际肿瘤分析(VITA)-方案durchgefhrt。对Sensitivität, Spezifität,正的prädiktiver Wert (PPV)和负的prädiktiver Wert (NPV)的最佳估计。在2016年1月至2023年2月期间,对糖尿病患者的腹股沟超声检查结果进行回顾性分析。检查结果:腹股沟超声检查:VITA-Protokoll wurde bei 74 Leisten转移性淋巴瘤Befall der Lymphknoten mitiner Sensitivität von 64,3%, einer Spezifität von 78,3%, einem PPV von 40,9%, einem NPV von 90,4%。 r 92 leistbei Patientinnen ohne Anwendung der vita - kriteren wurden eine Sensitivität von 56,3 %, eine Spezifität von 89,5 %, eine PPV von 52,9 %, eine NPV von 90,7 %, ermittelt, die sich -显著性von der VITA-Kohorte unterschieden (p >0,05)。schluu ßfolgerungen: Die inguinofemorale超声检查zeigte nach einfinfhrung eines speziell f r das Vulvakarzinom entwickelten strukturierten untersuchungprotokolls keine höhere Genauigkeit beder Bestimmung des histologischen淋巴结状态。
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引用次数: 0
Transthoracic echocardiography - the new AWMF S2k guidelines establish uniform standards. 经胸超声心动图-新的AWMF S2k指南建立了统一的标准。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-19 DOI: 10.1055/a-2751-9217
Jan Knierim
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引用次数: 0
Transthoracic echocardiography Guidelines of the German Society for Ultrasound in Medicine, German Cardiac Society, German Society of Anesthesiology and Intensive Care Medicine, German Society of Internal Medicine, Professional Association of German Internists, and the German Association of Cardiologists in Private Practice (Association of Scientific Medical Societies in Germany, S2k LL85-004, 9/1/20. 德国医学超声学会、德国心脏学会、德国麻醉学和重症监护医学学会、德国内科医学会、德国内科医师专业协会和德国私人执业心脏病专家协会(德国科学医学学会协会,S2k LL85-004, 20年9月1日)的经胸超声心动图指南。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-19 DOI: 10.1055/a-2775-3065
Jan Knierim, Henrik Ten Freyhaus, Harry Magunia, Sebastian Kruck, Matthias Göpfert, Norbert Smetak, Constantin S von Kaisenberg, Caroline Morbach, Sebastian Ewen, Frank Flachskampf

Echocardiography is the most commonly used imaging method for evaluating the heart. It plays a central role in the cardiology routine and in acute and emergency situations, and is an essential component of the medical decision-making process. In spite of its high clinical relevance, national recommendations standardizing the examination procedure, equipment settings, and image documentation have been lacking. The present guidelines were created by the German Society for Ultrasound in Medicine and the German Cardiac Society in coordination with the German Society of Anesthesiology and Intensive Care Medicine, German Society of Internal Medicine, Professional Association of German Internists, and the German Association of Cardiologists in Private Practice. The recommendations were formulated in consensus, published as draft guidelines, and finalized by the participating professional associations after evaluation of the feedback. The document meets the criteria for S2k guidelines in accordance with the Association of Scientific Medical Societies in Germany and defines binding standards for performing transthoracic echocardiography. The guidelines define which images and measurements are required to ensure valid and reproducible findings. The main recommendations relate to device settings, image acquisition, the minimum dataset to be acquired, and the definition of focused cardiac ultrasound (FoCUS). The complete long version of the guidelines is available on the website of the Association of Scientific Medical Societies in Germany. NOTE : The short version of this guideline is being published simultaneously in the journals Ultraschall in der Medizin - European Journal of Ultrasound and Die Kardiologie.

超声心动图是评估心脏最常用的成像方法。它在心脏病常规和急性和紧急情况下起着核心作用,是医疗决策过程的重要组成部分。尽管其具有很高的临床相关性,但缺乏标准化检查程序,设备设置和图像文件的国家建议。目前的指南是由德国医学超声学会和德国心脏学会与德国麻醉学和重症监护医学学会、德国内科医学会、德国内科医生专业协会和德国私人执业心脏病专家协会协调制定的。这些建议是以协商一致方式拟订的,作为准则草案出版,并由参与的专业协会在评价反馈意见后最后确定。该文件符合德国科学医学学会协会的S2k指南标准,并定义了执行经胸超声心动图的约束性标准。该指南定义了需要哪些图像和测量来确保有效和可重复的发现。主要建议涉及设备设置、图像采集、要获取的最小数据集和聚焦心脏超声(FoCUS)的定义。指南的完整长版本可在德国科学医学学会协会的网站上找到。注:本指南的简短版本同时发表在Ultraschall in der Medizin -欧洲超声杂志和Die cardiologie杂志上。
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引用次数: 0
Evaluation of image quality in five different handheld ultrasound devices and analysis of various impact factors. 五种不同手持式超声设备图像质量评价及影响因素分析。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-14 DOI: 10.1055/a-2809-7627
Antje Naas, Julian Kober, Tönnis Trittler, Richard Nauber, Edgar Manfred Gustav Dorausch, Nicole Kampfrath, Franz Brinkmann, Maia Arsova, Julia Husman, Robert Langanke, Stefan Sulk, Katja Matthes, Tina Gabriel, Andreas Teufel, Patrick Behrendt, Antoaneta Markova, Martin Franck, Christian Jenssen, Daniel Merkel, Valentin Blank, Thomas Karlas, Marcus Seeger, Marius Andreas Eckart, Lukas Poralla, Malte Lehmann, Jonas Staudacher, Matthias Ziesch, Julia Aland, Lueder Herzog, Angelika Herzog, Christian Jürgensen, Gerhard Paul Fettweis, Jochen Hampe, Moritz Herzog
<p><strong>Purpose: </strong>Handheld ultrasound (HHUS) devices are increasingly used in clinical practice due to their portability and cost-effectiveness. However, HHUS image quality remains variable, and a standardized expert-based evaluation protocol is lacking. This study compares the image quality of B-mode recordings of five HHUS models with a high-end reference system (HEUS) using a blinded assessment to identify differences, covariates, offering a standardized evaluation framework.</p><p><strong>Materials and methods: </strong>In this blinded, multi-center study, video sequences of the liver, pancreas, and sigmoid colon were recorded in ten volunteers using five HHUS devices - Vscan Air, Butterfly iQ+, Philips Lumify, Clarius C3, and Clarius C3 HD3 - and one HEUS (GE Logiq E10). 22 physicians with many years of abdominal ultrasound experience rated blinded clips for five image quality parameters.</p><p><strong>Results: </strong>The HEUS consistently received the highest ratings. Image quality differed significantly between HHUS devices. Clarius systems showed the smallest deviation from the reference, followed by Vscan Air and Philips Lumify. All image parameters significantly correlated with the overall impression, without a single dominant factor. The patients´ BMI had no relevant influence. Examiner experience was less impactful than device familiarity and personal preference.</p><p><strong>Conclusion: </strong>The image quality of HEUS remained superior to all tested HHUS devices. Further subdivision of image quality aspects did not provide additional information. Furthermore, we could not identify significant covariates in our setup. These findings could justify simplified setups with reduced questionnaires and requirements for examiners. Zielsetzung: Portable Ultraschallsysteme (HHUS) finden aufgrund ihrer Mobilität und Kosteneffizienz zunehmend Anwendung in der Praxis. Ihre Bildqualität ist jedoch variabel und ein standardisiertes, expertenbasiertes Bewertungsprotokoll fehlt bislang. Ziel dieser Studie ist der Vergleich von fünf HHUS-Modellen gegenüber einem High-End-Referenzsystem (HEUS) in einem verblindeten Design sowie die Analyse relevanter Kovariablen, die zur Entwicklung eines standardisierten Bewertungsverfahrens beitragen können.</p><p><strong>Material und methoden: </strong>In dieser multizentrischen, verblindeten Studie wurden Videos von Leber, Pankreas und Sigma bei 10 Probanden mit fünf HHUS-Geräten (Vscan Air, Butterfly iQ+, Philips Lumify, Clarius C3 und C3 HD3) sowie einem HEUS (Ge Logiq E10) aufgezeichnet. 22 Experten mit langjähriger Ultraschallerfahrung bewerteten die verblindeten Videos nach verschiedenen Kriterien zur Bildqualität. Ergebnisse: Das HEUS erzielte die besten Bewertungen, die HHUS unterschieden sich signifikant. Clarius-Systeme wichen am wenigsten vom HEUS ab, gefolgt von Vscan Air und Philips Lumify. Alle Bildparameter korrelierten signifikant mit dem Gesamteindruck, ohne dass ein dominanter Param
目的:手持式超声(HHUS)设备由于其便携性和成本效益越来越多地用于临床实践。然而,hus图像质量仍然是可变的,并且缺乏标准化的基于专家的评估方案。本研究采用盲法评估方法,将五种hus模型的b模式记录图像质量与高端参考系统(HEUS)进行比较,以确定差异和协变量,从而提供标准化的评估框架。材料和方法:在这项盲法、多中心研究中,10名志愿者使用五种hus设备(Vscan Air、Butterfly iQ+、Philips Lumify、Clarius C3和Clarius C3 HD3)和一种HEUS (GE Logiq E10)记录肝脏、胰腺和乙状结肠的视频序列。22名具有多年腹部超声经验的医生对5个图像质量参数进行盲夹评分。结果:HEUS始终获得最高的评分。不同hus设备的图像质量差异显著。Clarius系统与参考值的偏差最小,其次是Vscan Air和Philips Lumify。所有图像参数与整体印象显著相关,没有单一的主导因素。患者的BMI无相关影响。审查员经验的影响小于设备熟悉度和个人偏好。结论:HEUS的图像质量仍优于所有测试的hus设备。进一步细分图像质量方面没有提供额外的信息。此外,我们无法在我们的设置中识别显著的协变量。这些发现可以证明通过减少调查问卷和对审查员的要求来简化设置是合理的。[j]:便携式超声检测系统(HHUS)的研究进展[j] . Mobilität和Kosteneffizienz . zunememeh . Anwendung。在这里,Bildqualität是jedoch变量,在标准变量中,经验的基础是bewertungsprotocol。Ziel dieser studieist der Vergleich von f nf hhs - modellen gegen ber einem High-End-Referenzsystem (HEUS) in einem verblindeen Design sowie die Analyse关联度变量,die zur Entwicklung eines standardisierten Bewertungsverfahrens beitragen können。材料和方法:In dieser multizentrischen, verblindeten studewurden Videos von Leber, Pankreas and Sigma bei 10 Probanden mit f nf HHUS-Geräten (Vscan Air, Butterfly iQ+, Philips Lumify, Clarius C3和C3 HD3) sowie einem HEUS (Ge Logiq E10) aufgezeichnet。22 Experten mit langjähriger Ultraschallerfahrung bewerteten die verblindeten Videos nach verschiedenen Kriterien zur Bildqualität。艾滋病:艾滋病是一种严重的疾病,艾滋病是一种严重的疾病。Clarius-Systeme由HEUS ab, gefolt von Vscan Air和Philips Lumify等公司组成。参数识别率显著高于参数识别率,参数识别率显著高于参数识别率。BMI指数与流感相关。Die Erfahrung der Gutachter war weniger entscheidend也Gerätevertrautheit和persönliche Präferenz。死亡Bildqualität des hus war allen getesteten hus berlegen。Eine weitere Unterteilung in inzelne aspete der Bildqualität lieferte keine zusätzlichen Informationen。将其与相关的可变量进行了识别,得到了 die Etablierung vereinfachter Bewertungsprotokolle mit reduzierten Fragebögen spricht。
{"title":"Evaluation of image quality in five different handheld ultrasound devices and analysis of various impact factors.","authors":"Antje Naas, Julian Kober, Tönnis Trittler, Richard Nauber, Edgar Manfred Gustav Dorausch, Nicole Kampfrath, Franz Brinkmann, Maia Arsova, Julia Husman, Robert Langanke, Stefan Sulk, Katja Matthes, Tina Gabriel, Andreas Teufel, Patrick Behrendt, Antoaneta Markova, Martin Franck, Christian Jenssen, Daniel Merkel, Valentin Blank, Thomas Karlas, Marcus Seeger, Marius Andreas Eckart, Lukas Poralla, Malte Lehmann, Jonas Staudacher, Matthias Ziesch, Julia Aland, Lueder Herzog, Angelika Herzog, Christian Jürgensen, Gerhard Paul Fettweis, Jochen Hampe, Moritz Herzog","doi":"10.1055/a-2809-7627","DOIUrl":"https://doi.org/10.1055/a-2809-7627","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;Handheld ultrasound (HHUS) devices are increasingly used in clinical practice due to their portability and cost-effectiveness. However, HHUS image quality remains variable, and a standardized expert-based evaluation protocol is lacking. This study compares the image quality of B-mode recordings of five HHUS models with a high-end reference system (HEUS) using a blinded assessment to identify differences, covariates, offering a standardized evaluation framework.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Materials and methods: &lt;/strong&gt;In this blinded, multi-center study, video sequences of the liver, pancreas, and sigmoid colon were recorded in ten volunteers using five HHUS devices - Vscan Air, Butterfly iQ+, Philips Lumify, Clarius C3, and Clarius C3 HD3 - and one HEUS (GE Logiq E10). 22 physicians with many years of abdominal ultrasound experience rated blinded clips for five image quality parameters.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The HEUS consistently received the highest ratings. Image quality differed significantly between HHUS devices. Clarius systems showed the smallest deviation from the reference, followed by Vscan Air and Philips Lumify. All image parameters significantly correlated with the overall impression, without a single dominant factor. The patients´ BMI had no relevant influence. Examiner experience was less impactful than device familiarity and personal preference.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;The image quality of HEUS remained superior to all tested HHUS devices. Further subdivision of image quality aspects did not provide additional information. Furthermore, we could not identify significant covariates in our setup. These findings could justify simplified setups with reduced questionnaires and requirements for examiners. Zielsetzung: Portable Ultraschallsysteme (HHUS) finden aufgrund ihrer Mobilität und Kosteneffizienz zunehmend Anwendung in der Praxis. Ihre Bildqualität ist jedoch variabel und ein standardisiertes, expertenbasiertes Bewertungsprotokoll fehlt bislang. Ziel dieser Studie ist der Vergleich von fünf HHUS-Modellen gegenüber einem High-End-Referenzsystem (HEUS) in einem verblindeten Design sowie die Analyse relevanter Kovariablen, die zur Entwicklung eines standardisierten Bewertungsverfahrens beitragen können.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Material und methoden: &lt;/strong&gt;In dieser multizentrischen, verblindeten Studie wurden Videos von Leber, Pankreas und Sigma bei 10 Probanden mit fünf HHUS-Geräten (Vscan Air, Butterfly iQ+, Philips Lumify, Clarius C3 und C3 HD3) sowie einem HEUS (Ge Logiq E10) aufgezeichnet. 22 Experten mit langjähriger Ultraschallerfahrung bewerteten die verblindeten Videos nach verschiedenen Kriterien zur Bildqualität. Ergebnisse: Das HEUS erzielte die besten Bewertungen, die HHUS unterschieden sich signifikant. Clarius-Systeme wichen am wenigsten vom HEUS ab, gefolgt von Vscan Air und Philips Lumify. Alle Bildparameter korrelierten signifikant mit dem Gesamteindruck, ohne dass ein dominanter Param","PeriodicalId":49400,"journal":{"name":"Ultraschall in Der Medizin","volume":" ","pages":""},"PeriodicalIF":2.9,"publicationDate":"2026-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146198008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Causes and outcomes of prenatally unexplained fetal anemia. 产前不明原因胎儿贫血的原因和结局。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-11 DOI: 10.1055/a-2773-2240
Saja Anabusi, Charles Litwin, Greg Ryan, David Chitayat, Shiri Shinar

Despite advances in diagnostic approaches, fetal anemia of unknown etiology continues to be observed in rare cases. This study aimed to assess the incidence of unexplained fetal anemia and to evaluate the associated perinatal outcomes.We conducted an observational retrospective cohort study of all fetuses that underwent fetal blood sampling (FBS) due to an MCA-PSV>1.5 MoM at a tertiary center between 2007 and 2024. Fetuses were included if they had moderate or severe anemia defined as a hemoglobin (Hgb) deviation of more than 20g/L below a gestational age adjusted mean, with a negative anemia workup. Prenatal and postnatal outcomes were obtained.Among 376 fetuses that underwent fetal blood sampling for anemia, 361 (96%) had an identified cause, while 15 (4%) had moderate to severe anemia of unknown etiology. Seven fetuses presented with non-immune hydrops and eight with other major structural anomalies not typically associated with anemia. Eleven (73%) of the 15 fetuses with unexplained anemia had thrombocytopenia, with platelets below 100000/µL in 8 cases and below 50000/µL in 6 cases. Seven cases (47%) resulted in perinatal death. Rare causes of anemia were elucidated in only 5 cases (33%) postnatally despite extensive investigations.Unexplained fetal anemia is uncommon and is associated with poor neonatal outcomes warranting close pre- and postnatal surveillance.

目的:尽管诊断方法的进步,不明原因的胎儿贫血仍在罕见的情况下观察到。本研究旨在评估不明原因胎儿贫血的发生率,并评估相关的围产期结局。材料和方法:我们进行了一项观察性回顾性队列研究,对2007年至2024年间在三级中心因MCA PSV>1.5 MoM而接受胎儿血液采样(FBS)的所有胎儿进行了研究。如果胎儿患有中度或重度贫血,定义为血红蛋白(Hgb)偏差比胎龄调整后的平均值低20 g/L以上,并且贫血检查为阴性。获得产前和产后结果。结果:在376例接受贫血胎儿血液采样的胎儿中,361例(96%)有明确的病因,15例(4%)有病因不明的中度至重度贫血。7例胎儿表现为非免疫性水肿,8例胎儿表现为与贫血无关的其他主要结构异常。15例不明原因性贫血胎儿中有11例(73%)存在血小板减少症,血小板低于10万/µL 8例,低于5万/µL 6例。7例(47%)导致围产期死亡。尽管进行了广泛的调查,但产后贫血的罕见原因仅在5例(33%)中得到阐明。结论:不明原因的胎儿贫血是罕见的,并与新生儿预后不良相关,需要密切的产前和产后监测。
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引用次数: 0
Aortic pulsatile diameter changes in fetuses with growth restriction. 胎儿生长受限时主动脉搏动直径的变化。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-10 DOI: 10.1055/a-2782-7679
Markus Gonser, Ladina Vonzun, Nicole Ochsenbein-Kölble
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引用次数: 0
Protocol-Based Management of Severe Fetomaternal Hemorrhage (1.6 g/dL Hb) Allowing Term Vaginal Delivery. 基于方案的严重胎母出血处理(1.6 g/dL Hb)允许阴道分娩。
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-10 DOI: 10.1055/a-2771-2784
Alex Horky, Eva Nolof, Stephan Spahn, Ammar Al Naimi, Franz Bahlmann
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引用次数: 0
Fertility and Obstetric and Clinical Outcomes following Embolization Management of Symptomatic Pregnancy-Related Arteriovenous Malformations: Two Decades of Follow-up from a Tertiary Medical Center. 栓塞治疗症状性妊娠相关动静脉畸形后的生育、产科和临床结果:来自三级医疗中心的二十年随访
IF 2.9 3区 医学 Q1 ACOUSTICS Pub Date : 2026-02-10 DOI: 10.1055/a-2782-1776
Perry Eliassi Revivo, Marina Pekar-Zlotin, Ron Maymon, Alexei Cherniavsky, Zalman Itzhakov, Tal Fligelman, Tal Rafaeli Yehudai, Yair Shiber, Yaniv Stollero, Yael Tal Bliman, Zvi Vaknin

To evaluate fertility and obstetric and clinical outcomes following uterine artery embolization (UAE) for pregnancy-related symptomatic uterine arteriovenous malformations (AVMs).A retrospective case analysis was conducted at a single tertiary care center and included women diagnosed with symptomatic post-pregnancy uterine AVMs treated between January 2000 and April 2023. Clinical data, management strategies, and follow-up outcomes were extracted from institutional records. A follow-up phone survey was conducted to assess fertility and obstetric outcomes.Forty women with symptomatic uterine AVMs were identified. All presented with vaginal bleeding, the sole symptom in 35 cases (87.5%). Most (31/40, 77.5%) presented at the emergency department within 24 hours. Thirty-eight women (95%) required one UAE; no hysterectomies were performed. Twelve women (30%) experienced massive bleeding requiring transfusion. Of 35 women who responded to the fertility survey, 22 (62.8%) desired a future pregnancy. Of these, 20 (90.9%) achieved pregnancy, with 17 (85%) delivering at term. The median time to conception was under 6 weeks, and 65% conceived within 12 months. Ten women (50%) had multiple successful pregnancies; one had 5 consecutive pregnancies. Regarding post-UAE pregnancies, 4 women (23.5%) experienced abnormal placentation, but no AVM recurrences were reported.In this cohort, UAE for AVMs is highly effective and fertility-sparing, with most women conceiving and delivering successfully. Obstetric risks remain notable, underscoring the need for larger studies to confirm these findings and assess long-term risks.

评估子宫动脉栓塞治疗妊娠相关症状性子宫动静脉畸形(AVMs)后的生育能力、产科和临床结果。回顾性病例分析在单一三级保健中心进行,包括2000年1月至2023年4月期间治疗的诊断为有症状的妊娠后子宫静脉畸形的妇女。临床数据、管理策略和随访结果从机构记录中提取。进行了一项后续电话调查,以评估生育和产科结果。40名有症状性子宫静脉畸形的妇女被确定。35例(87.5%)以阴道出血为唯一症状。大多数患者(31/40,77.5%)在24小时内就诊。38名妇女(95%)需要一个阿联酋;未行子宫切除术。12名妇女(30%)出现大出血,需要输血。在35名接受生育调查的女性中,有22名(62.8%)希望将来怀孕。其中20例(90.9%)成功怀孕,17例(85%)足月分娩。平均受孕时间不到6周,65%在12个月内受孕。10名妇女(50%)多次成功怀孕;其中一名连续怀孕5次。在阿联酋妊娠后,4名妇女(23.5%)经历了异常胎盘,但没有AVM复发的报道。在这个队列中,avm的阿联酋是非常有效的,生育节约,大多数妇女怀孕和分娩成功。产科风险仍然显著,强调需要更大规模的研究来证实这些发现并评估长期风险。
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引用次数: 0
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Ultraschall in Der Medizin
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