incidental finding

偶然发现
  • 文章类型: Journal Article
    背景:心包积液(PE)的偶然发现对临床护理提出了挑战。PE与恶性病症或严重心脏疾病相关,但也可在健康个体中观察到。这项研究探讨了患病率,决定因素,当然,以及基于人群的队列中PE的预后相关性。
    结果:STAAB(心力衰竭A/B阶段的特征和过程以及进展的决定因素)队列研究招募了维尔茨堡人口的代表性样本,30至79岁。参与者接受了质量控制的经胸超声心动图检查,包括对心包空间的专门评估。在基线纳入的4965名个体中(平均年龄,55±12岁;52%的女性),134(2.7%)表现出偶然诊断的PE(中位直径,2.7毫米;四分位数,2.0-4.1毫米)。在多变量逻辑回归中,较低的体重指数和较高的NT-proBNP(N末端B型利钠肽前体)水平与基线时的PE相关,而炎症,恶性肿瘤,和类风湿疾病没有。在中位时间为34(30-41)个月后参加随访检查的3901名参与者中,在60个人中发现了PE(1.5%;n=18个新PE,n=42持久性PE)。在后续期内,37名参与者死亡,93名参与者报告了新诊断的恶性肿瘤。PE的存在并不能预测全因死亡或新恶性肿瘤的发展。
    结论:在约3%的个体中检测到偶然的PE,与绝大多数测量<10毫米和完全解决。PE与炎症标志物无关,死亡,突发心力衰竭,或者恶性肿瘤。我们的发现证实了当前指南的观点,即无症状个体中的小PE可以被认为是无辜的现象,不需要广泛的短期监测。
    BACKGROUND: The incidental finding of a pericardial effusion (PE) poses a challenge in clinical care. PE is associated with malignant conditions or severe cardiac disease but may also be observed in healthy individuals. This study explored the prevalence, determinants, course, and prognostic relevance of PE in a population-based cohort.
    RESULTS: The STAAB (Characteristics and Course of Heart Failure Stages A/B and Determinants of Progression) cohort study recruited a representative sample of the population of Würzburg, aged 30 to 79 years. Participants underwent quality-controlled transthoracic echocardiography including the dedicated evaluation of the pericardial space. Of 4965 individuals included at baseline (mean age, 55±12 years; 52% women), 134 (2.7%) exhibited an incidentally diagnosed PE (median diameter, 2.7 mm; quartiles, 2.0-4.1 mm). In multivariable logistic regression, lower body mass index and higher NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels were associated with PE at baseline, whereas inflammation, malignancy, and rheumatoid disease were not. Among the 3901 participants attending the follow-up examination after a median time of 34 (30-41) months, PE was found in 60 individuals (1.5%; n=18 new PE, n=42 persistent PE). Within the follow-up period, 37 participants died and 93 participants reported a newly diagnosed malignancy. The presence of PE did not predict all-cause death or the development of new malignancy.
    CONCLUSIONS: Incidental PE was detected in about 3% of individuals, with the vast majority measuring <10 mm and completely resolving. PE was not associated with inflammation markers, death, incident heart failure, or malignancy. Our findings corroborate the view of current guidelines that a small PE in asymptomatic individuals can be considered an innocent phenomenon and does not require extensive short-term monitoring.
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  • 文章类型: Journal Article
    目的:调查偶然发现的发生率和进一步牙科治疗的需求,并分析锥形束计算机断层扫描(CBCT)中视野大小(FOV)和年龄对植入前计划的影响。
    方法:对404个CBCT扫描进行回顾性检查,以了解偶然发现和进一步牙科治疗的需要。对不同年龄(<40岁,40-60年,>60岁)和FOV组(小型,中等,大)。评估了内部检验者和interexaminer协议。
    结果:在82%的扫描中发现了至少一个偶然发现,总共766个。在大FOV的扫描中发现了更多的偶然发现(98%与72%,OR=22.39大vs.小视场,p<0.0001)和>60岁的患者扫描(OR=5.37患者年龄>60岁与<40年,p=0.0003)。由于偶然发现,31%的患者需要进一步的牙科治疗。大FOV的扫描更有可能需要进一步治疗(OR=3.55大vs.小视场,p<0.0001)。部分性脑萎缩症和大FOV被确定为进一步治疗的危险因素(p=0.0003和p<0.0001)。根据偶然发现,患者的进一步转诊被判断为5%。考试者内部和考试者之间的协议非常好(kappa=0.944/0.805)。
    结论:在部分缺牙患者和60岁以上的患者中发现了大量需要进一步牙科治疗的偶然发现。在老年患者的植入前规划中,选择大视场CBCT扫描,包括最近没有做X光检查的牙槽骨区域,帮助检测治疗相关的偶然发现。
    OBJECTIVE: To investigate the prevalence of incidental findings and need for further dental treatment and analyse the influence of size of field-of-view (FOV) and age in cone beam computed tomography (CBCT) for pre-implant planning.
    METHODS: 404 CBCT scans were examined retrospectively for incidental findings and need for further dental treatment. Incidental finding-frequencies and need for further treatment were assessed for different age (< 40 years, 40-60 years, > 60 years) and FOV groups (small, medium, large). Intraexaminer and interexaminer agreements were evaluated.
    RESULTS: In 82% of the scans at least one incidental finding was found, with a total of 766 overall. More incidental findings were found in scans with large FOV (98% vs. 72%, OR = 22.39 large vs. small FOV, p < 0.0001) and in scans of patients > 60 years (OR = 5.37 patient\'s age > 60 years vs. < 40 years, p = 0.0003). Further dental treatment due to incidental findings was needed in 31%. Scans with large FOV were more likely to entail further treatment (OR = 3.55 large vs. small FOV, p < 0.0001). Partial edentulism and large FOV were identified as risk factors for further treatment (p = 0.0003 and p < 0.0001). Further referral of the patient based on incidental findings was judged as indicated in 5%. Intra- and inter-examiner agreements were excellent (kappa = 0.944/0.805).
    CONCLUSIONS: A considerable number of incidental findings with need for further dental treatment was found in partially edentulous patients and in patients > 60 years. In pre-implant planning of elderly patients, the selection of large FOV CBCT scans, including dentoalveolar regions not X-rayed recently, help to detect therapeutically relevant incidental findings.
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  • 文章类型: Journal Article
    进行该研究是为了评估儿童在计算机断层扫描(CT)扫描中偶然发生的鼻旁窦病变的患病率。
    一项非随机回顾性研究是对过去6个月的232例儿科患者进行CT扫描。这些扫描是在0-13岁的不同年龄组中进行评估的,这些年龄组曾因各种其他头颈部相关问题就诊或入院。每次扫描检查所有鼻旁窦的偶然病理发现。使用描述性统计和Fisher精确检验对数据进行分析,以确定变量之间的非随机关联。
    共检查了232名受试者,其中72例(31.03%)有偶然鼻窦病变。在36名受试者中发现了多发性鼻窦病变,28人单窦性受累,其中4例在11岁时没有出现额窦。四名受试者在6-7岁的年龄范围内具有多个鼻窦的病理学以及额窦的发育。
    鼻窦病变在无症状儿童人群中并不罕见,发病率几乎相当于成年人的发病率。早期识别可以帮助诊断不明原因的口面部疼痛,如果儿童容易受到上呼吸道感染及其继发影响,如睡眠呼吸暂停,口腔呼吸器,等。
    谈话P,DeshpandePS,PeneS,etal.小儿计算机断层扫描图像上的鼻旁窦偶然发现:横断面患病率研究。IntJClinPediatrDent2023;16(2):292-294。
    UNASSIGNED: The study was conducted to assess the prevalence of incidental paranasal sinus pathologies in children on computed tomography (CT) scans.
    UNASSIGNED: A nonrandomized retrospective study was done on CT scans of 232 pediatric patients taken in the past 6 months duration. These scans were evaluated in different age groups from 0-13 years who had visited or were admitted to the hospital for various other head and neck-related problems. Each scan was examined for incidental pathologic findings in all the paranasal sinuses. The data were analyzed using descriptive statistics and Fisher\'s exact test to determine non-random associations between variables.
    UNASSIGNED: A total of 232 subjects were examined, amongst which 72 (31.03%) had incidental sinus pathologies. Multiple sinus pathologies were found in 36 subjects, 28 had single sinus involvement, and four showed no development of frontal sinus at the age of 11 years. Four subjects had pathology in multiple sinuses as well as no development of frontal sinus at the age of 6-7 years age range.
    UNASSIGNED: Sinus pathologies are not unusual in the asymptomatic children population, and the incidence is almost equivalent to that of the adult population. Early identification can aid in diagnosing orofacial pain of unknown origin and also if children are susceptible to upper respiratory tract infections and their secondary effects like sleep apnea, mouth breathers, etc.
    UNASSIGNED: Talwade P, Deshpande PS, Pene S, et al. Incidental Paranasal Sinus Findings on Computed Tomography Images of Pediatric Patients: A Cross-sectional Prevalence Study. Int J Clin Pediatr Dent 2023;16(2):292-294.
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  • 文章类型: Journal Article
    背景:缺乏关于放射学孤立综合征(RIS)发生率的大型人群队列研究的数据。我们调查了RIS的发生率和多发性硬化症(MS)的后续风险。
    方法:我们以人群为基础,使用基于数据湖的数字化放射学报告分析的回顾性队列研究.我们在2005-2010年期间(n=102224)使用优化的搜索词筛查了16-70岁人群的所有脑和脊髓MRI,以检测RIS病例。RIS受试者随访至2022年1月。
    结果:根据MAGNIMS2018推荐标准,当包括所有MRI模式时,RIS的累积发生率为0.03%,当仅包括脑MRI时,RIS的累积发生率为0.06%。根据Okuda2009标准,分别为0.03%和0.05%(86%的一致性)。通过使用MAGNIMS,RIS后MS的总体风险相似为32%,通过使用Okuda定义的RIS,为32%。年龄<35.5岁的个体表现出最显着的MS易感性(80%),而那些>35.5岁的人患MS的风险不到10%。在2005-2010年期间,RIS后诊断的MS占人口中MS事件病例的0.8%。
    结论:我们为RIS的发病率及其与MS的关系提供了全人群的背景。与Okuda标准相比,MAGNIMS建议对RIS的检测仅稍敏感。RIS对MS的总体发病率有微妙的影响,然而,年龄在35.5岁以下的个体患MS的风险很大.
    There is an absence of data from large population-based cohort studies on the incidence of radiologically isolated syndrome (RIS). The incidence of RIS and the subsequent risk for multiple sclerosis (MS) were investigated.
    A population-based, retrospective cohort study was conducted using a data-lake-based analysis of digitalized radiology reports. All brain and spinal cord magnetic resonance imaging (MRI) in people aged 16-70 during the years 2005-2010 (n = 102,224) were screened using optimized search terms to detect cases with RIS. The subjects with RIS were followed up until January 2022.
    The cumulative incidence of RIS was 0.03% when all MRI modalities were included and 0.06% when only brain MRI was included according to MAGNIMS 2018 recommendation criteria. With the Okuda 2009 criteria, the respective figures were 0.03% and 0.05% (86% concordance). The overall risk for MS after RIS was similar, 32% by using the MAGNIMS and 32% by using the Okuda definition of RIS. Individuals aged <35.5 years exhibited the most significant predisposition to MS (80%), whilst those >35.5 years had less than 10% risk of MS. MS diagnosed after RIS constituted 0.8% of the incident MS cases in the population during 2005-2010.
    A population-wide context was provided for the incidence of RIS and its relationship to MS. MAGNIMS recommendations were only slightly more sensitive to detect RIS compared to the Okuda criteria. RIS has a subtle effect on the overall incidence of MS, yet the risk for MS in individuals under the age of 35.5 years is substantial.
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  • 文章类型: Journal Article
    未经评估:尽管诊断技术最近有所发展,许多外科医生在手术过程中会遇到意想不到的发现。我们的目标是检查腹部手术中所有IFs的发生率-腹腔镜或腹腔镜-并确定可能的关联。
    UNASSIGNED:本研究是在阿勒颇大学医院外科进行的横断面研究。我们收集了2018-2019年连续两年接受腹部手术的患者数据。
    UNASSIGNED:数据显示,在543例(1.1%)中有6例在腹部手术中发现了偶然的发现,包括对腹膜腔的适当检查,而只有1例包括误诊事件(0.2%)。
    UNASSIGNED:腹部手术中有关IF的流行病学信息对外科医生在各个方面都非常有用,并可以帮助他们为手术和可能遇到的意外病变做好更多准备。我们强烈建议进行更多参与者的进一步研究,因为它们可以提供更广泛的数据。
    UNASSIGNED: Despite the recent development in diagnostic techniques, many surgeons experience unexpected findings during the course of surgery. We aim to examine the incidence of all IFs in abdominal surgery -laparoscopy or laparotomy- and identify possible associations.
    UNASSIGNED: This study is a cross-sectional study conducted in Aleppo University Hospital - Department of Surgery. We collected patients\' data who underwent abdominal surgery during the period of the two-consecutive years 2018-2019.
    UNASSIGNED: The data revealed detection of incidental findings during abdominal surgery -which included proper inspection of peritoneal cavity-in 6 out 543 cases (1.1%), whereas only one case included a misdiagnosis event (0.2%).
    UNASSIGNED: Epidemiological information about IFs in abdominal surgery can be extremely useful for the surgeons on various aspects, and can assist them with being more prepared for the surgery and the possible unexpected lesions that might be encountered. We strongly recommend that further studies with larger numbers of participants are conducted as they can provide more generalizable data.
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  • 文章类型: Journal Article
    这项研究的主要目的是使用国际子宫内膜肿瘤分析(IETA)术语描述无异常子宫出血(AUB)的女性的各种子宫内膜和其他腔内病理的超声特征。次要目的是将我们的发现与发表的关于AUB女性的数据进行比较。
    这是一项前瞻性观察性研究,研究对象是7个妇科超声检查中心之一的女性,从2011年到2018年,对于与AUB无关的适应症。所有患者均使用IETA检查和测量技术进行经阴道超声检查。超声检查作为常规妇科检查或非子宫内膜病理随访的一部分,或者作为不孕症治疗前的一部分,子宫脱垂或卵巢病理。使用IETA术语描述超声发现。超声扫描后进行子宫内膜取样。组织学终点是子宫内膜萎缩,增生性或分泌性子宫内膜,子宫内膜增生无异型,子宫内膜息肉,腔内平滑肌瘤,子宫内膜上皮内瘤变(EIN),子宫内膜癌(EC)和组织不足。我们在没有AUB的女性队列中的发现与在2012年至2015年之间使用相同的IETA检查技术和术语进行经阴道超声检查的AUB女性队列中的发现进行了比较。
    在这项研究(IETA3)中,我们纳入了1,745例无AUB的女性,她们接受了标准化的经阴道超声检查,随后进行了子宫内膜取样并进行组织学诊断(n=1,537)或至少1年的临床和超声随访(n=208).其中,绝经前858例(49.2%),绝经后887例(50.8%)。组织学显示29名(1.7%)女性中存在EC和/或EIN,子宫内膜息肉1028例(58.9%),66例(3.8%)腔内肌瘤,144(8.3%)的增生或分泌变化或无异型增生,子宫内膜萎缩265例(15.2%),组织不足5例(0.3%)。大多数EC或EIN病例(25/29(86.2%))是在绝经后诊断的。EC或EIN患者的平均子宫内膜厚度为11.2mm(95%CI,8.9-13.6mm),平均厚度为2.4毫米(95%可信区间,0.3-4.6毫米),比他们的良性同行。子宫内膜恶性病变的女性表现出非均匀回声(22/29(75.9%))比子宫内膜良性病变的女性(929/1716(54.1%))(差异,+21.8%(95%CI,+4.2%至+39.2%)。在31.0%(9/29)的EC或EIN病例中观察到中度至丰富的血管化(颜色评分3-4),而良性结局的病例为12.8%(220/1716)(差异,+18.2%(95%CI,-0.5%至+36.9%)。24.1%(7/29)的EC或EIN女性与4.0%(68/1716)的良性结局(差异,+20.2%(95%CI,+4.6%至+35.7%)。在EC或EIN(19/29(65.5%))与良性结局(1412/1716(82.3%))的女性中,子宫内膜-肌层交界处的频率较低(差异,-16.8%(95%CI,-34.2%至+0.6%)。在子宫内膜息肉无AUB的女性中,单个优势血管是最常见的血管模式(666/1028(64.8%)).在患有EC的女性中,在有和没有AUB的情况下,子宫内膜通常表现为不均匀的回声,但是子宫内膜平均为8.6mm(95%CI,5.2-12.0mm),血管化程度较低(颜色评分3-4:差异,-26.8%(95%CI,-52.2%至-1.3%)的女性与AUB患者相比。在绝经前和绝经后的女性中,无症状的子宫内膜息肉与子宫内膜变薄有关,它们更频繁地表现出明亮的边缘,规则的子宫内膜-子宫肌层交界处和单个优势血管,而有症状的女性则有息肉,它们的血管化程度较低。
    我们描述了EC的典型超声特征,在没有AUB的女性中使用IETA术语的息肉和其他腔内组织学。我们的发现表明,无症状性息肉或子宫内膜恶性肿瘤的存在可能伴有比有症状的子宫内膜更薄,血管化程度更低的子宫内膜。©2022国际妇产科超声学会。
    The primary aim of this study was to describe the ultrasound features of various endometrial and other intracavitary pathologies in women without abnormal uterine bleeding (AUB) using the International Endometrial Tumor Analysis (IETA) terminology. The secondary aim was to compare our findings with published data on women with AUB.
    This was a prospective observational study of women presenting at one of seven centers specialized in gynecological ultrasonography, from 2011 until 2018, for indications unrelated to AUB. All patients underwent transvaginal ultrasound using the IETA examination and measurement techniques. Ultrasonography was performed as part of routine gynecological examination or follow-up of non-endometrial pathology, or as part of the work-up before undergoing treatment for infertility, uterine prolapse or ovarian pathology. Ultrasound findings were described using the IETA terminology. Endometrial sampling was performed after the ultrasound scan. The histological endpoints were endometrial atrophy, proliferative or secretory endometrium, endometrial hyperplasia without atypia, endometrial polyp, intracavitary leiomyoma, endometrial intraepithelial neoplasia (EIN), endometrial cancer (EC) and insufficient tissue. The findings in our cohort of women without AUB were compared with those in a published cohort of women with AUB who were examined with transvaginal ultrasound between 2012 and 2015 using the same IETA examination technique and terminology.
    In this study (IETA3), we included 1745 women without AUB who underwent a standardized transvaginal ultrasound examination followed by either endometrial sampling with histological diagnosis (n = 1537) or at least 1 year of clinical and ultrasound follow-up (n = 208). Of these, 858 (49.2%) women were premenopausal and 887 (50.8%) were postmenopausal. Histology showed the presence of EC and/or EIN in 29 (1.7%) women, endometrial polyps in 1028 (58.9%), intracavitary myomas in 66 (3.8%), proliferative or secretory changes or hyperplasia without atypia in 144 (8.3%), endometrial atrophy in 265 (15.2%) and insufficient tissue in five (0.3%). Most cases of EC or EIN (25/29 (86.2%)) were diagnosed after menopause. The mean endometrial thickness in women with EC or EIN was 11.2 mm (95% CI, 8.9-13.6 mm), being on average 2.4 mm (95% CI, 0.3-4.6 mm) thicker than their benign counterparts. Women with malignant endometrial pathology manifested more frequently non-uniform echogenicity (22/29 (75.9%)) than did those with benign endometrial pathology (929/1716 (54.1%)) (difference, +21.8% (95% CI, +4.2% to +39.2%)). Moderate to abundant vascularization (color score 3-4) was seen in 31.0% (9/29) of cases with EC or EIN compared with 12.8% (220/1716) of those with a benign outcome (difference, +18.2% (95% CI, -0.5% to +36.9%)). Multiple multifocal vessels were recorded in 24.1% (7/29) women with EC or EIN vs 4.0% (68/1716) of those with a benign outcome (difference, +20.2% (95% CI, +4.6% to +35.7%)). A regular endometrial-myometrial junction was seen less frequently in women with EC or EIN (19/29 (65.5%)) vs those with a benign outcome (1412/1716 (82.3%)) (difference, -16.8% (95% CI, -34.2% to +0.6%)). In women with endometrial polyps without AUB, a single dominant vessel was the most frequent vascular pattern (666/1028 (64.8%)). In women with EC, both in those with and those without AUB, the endometrium usually manifested heterogeneous echogenicity, but the endometrium was on average 8.6 mm (95% CI, 5.2-12.0 mm) thinner and less intensely vascularized (color score 3-4: difference, -26.8% (95% CI, -52.2% to -1.3%)) in women without compared to those with AUB. In both pre- and postmenopausal women, asymptomatic endometrial polyps were associated with a thinner endometrium, and they manifested more frequently a bright edge, a regular endometrial-myometrial junction and a single dominant vessel than did polyps in symptomatic women, and they were less intensely vascularized.
    We describe the typical ultrasound features of EC, polyps and other intracavitary histologies using IETA terminology in women without AUB. Our findings suggest that the presence of asymptomatic polyps or endometrial malignancy may be accompanied by thinner and less intensely vascularized endometria than their symptomatic counterparts. © 2022 International Society of Ultrasound in Obstetrics and Gynecology.
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  • 文章类型: Journal Article
    OBJECTIVE: Arachnoid cysts (ACs) are frequent incidental findings and may be associated with neuropsychiatric symptoms. Usually growth of the ACs with pressure on adjacent brain tissue is regarded as cause of the symptoms. This study was undertaken to identify if and which ACs grow with time.
    METHODS: We used a large database of cranial MRIs for a retrospective analysis.
    RESULTS: During a period of 10 years, we collected 166 ACs of 50 persons, mean observational period was 2.5 years. Among these, only larger cysts at the temporal pole, i.e., Galassi II ACs, grew with a rate of 0.3 ml a year (β = 0.32, SE 0.07, p = 0.003); all other ACs remained constant in size or became smaller. All cysts were clinically silent.
    CONCLUSIONS: Most ACs remain constant in size or become smaller.
    METHODS: This study provides Class III evidence that the majority of arachnoid cysts does not grow.
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  • 文章类型: Journal Article
    OBJECTIVE: Management of incidental findings (IF) remains controversial but highly relevant. Our aim was to assess the frequency, management and psychosocial consequences of IF reporting in a population-based cohort study undergoing whole-body MR imaging.
    METHODS: The study was nested in a prospective cohort from a longitudinal, population-based cohort (KORA-FF4) in southern Germany. All MR obtained on 3 T MR scanner were reviewed by board-certified radiologists regarding clinically relevant IF. A baseline and follow-up questionnaires including PHQ-9 were completed prior to and 6-month after to the scan.
    RESULTS: Of 400 participants (56.3 ± 9.2years, 58 % male) undergoing whole-body MR, IF were found in 22 % of participants (n = 89); most frequently located in the abdominal sequences. In the pre-scan survey, most participants stated as the motivation that they wanted to \"contribute to a scientific purpose\" (91 %), while \"knowing whether I\'m healthy\" was the most frequent motivation reported 6 months post-scan (88 %). The desire for IF reporting increased over time (pre- vs. 6-months-post-scan), also for clinically less important IF (72 % vs. 84 %, p = 0.001). Regarding psychosocial impact, a small portion (3.4 %) reported that awaiting the IF report added \"definitely\" or \"very probably\" additional stress burden. Of participants with reported IF, 56.8 % classified the results as \"very helpful\". In the post-scan survey moderate depression was observed in 3.3 % and severe depression in 1.2 %. This did not differ between participants with and without reported IF.
    CONCLUSIONS: In a cohort with whole-body MR imaging, the prevalence of IF was high. Participants considered reporting of IF highly important and added only minor psychological burden.
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  • 文章类型: Journal Article
    妊娠晚期扫描越来越多地用于尝试防止与胎儿生长异常相关的不良后果。在妊娠晚期生长扫描中发现的意外胎儿畸形很少报道。
    确定在接受常规妊娠晚期生长扫描的妇女中发现的胎儿畸形的发生率和类型。
    这是一项以人口为基础的研究,研究对象是在牛津郡进行为期2年的产前护理的所有单胎妊娠妇女。英国。包括在约会扫描中有可行单胎妊娠的妇女。妇女接受标准的产科护理,包括提供常规约会扫描和三体联合筛查;在18至22周时进行常规异常扫描;在36周时进行常规的妊娠晚期生长扫描。妊娠晚期扫描包括对胎儿表现的评估,羊水,生物测量,脐和大脑中动脉多普勒,但没有进行正式的解剖评估。扫描由经认证的超声医师或临床研究员(n=54)执行,任何可疑的异常都会由一组胎儿医学专家进行评估。我们评估了在此妊娠晚期扫描中首次发现的偶然先天性畸形的频率和类型。所有婴儿在出生后至少随访6个月。
    有15,244名妇女参加常规产前护理。在474(3.1%)胎儿中检测到异常如下:异常扫描前检测到103(21.7%),174(36.7%)在异常扫描,11(2.3%)在异常扫描后和妊娠晚期扫描前,妊娠晚期扫描为43(9.1%),出生后为143(30.2%)。共有13,023名妇女进行了36周的扫描,发现了43例异常,这表明在303人中有1人(95%置信区间,233-432)参加这种扫描的妇女,发现了一个新的畸形。在常规的妊娠晚期扫描中检测到的异常是泌尿道(n=30),中枢神经系统(5),单纯性卵巢囊肿(4),染色体(1),脾囊肿(1),骨骼发育不良(1),皮肤淋巴管瘤(1)。大多数尿路异常是肾盂扩张,57%的病例显示自发消退。
    在对以前做过筛查扫描的女性进行常规的妊娠晚期生长扫描时,在300名女性中大约有1人发现了意外的先天性畸形。
    Third-trimester scans are increasingly used to try to prevent adverse outcomes associated with abnormalities of fetal growth. Unexpected fetal malformations detected at third-trimester growth scans are rarely reported.
    To determine the incidence and type of fetal malformations detected in women attending a routine third-trimester growth scan.
    This was a population-based study of all women with singleton pregnancy attending antenatal care over a 2-year period in Oxfordshire, UK. Women who had a viable singleton pregnancy at dating scan were included. Women had standard obstetrical care including the offer of a routine dating scan and combined screening for trisomies; a routine anomaly scan at 18 to 22 weeks; and a routine third-trimester growth scan at 36 weeks. The third-trimester scan comprises assessment of fetal presentation, amniotic fluid, biometry, umbilical and middle cerebral artery Dopplers, but no formal anatomic assessment is undertaken. Scans are performed by certified sonographers or clinical fellows (n=54), and any suspected abnormalities are evaluated by a team of fetal medicine specialists. We assessed the frequency and type of incidental congenital malformations identified for the first time at this third-trimester scan. All babies were followed-up after birth for a minimum of 6 months.
    There were 15,244 women attending routine antenatal care. Anomalies were detected in 474 (3.1%) fetuses as follows: 103 (21.7%) were detected before the anomaly scan, 174 (36.7%) at the anomaly scan, 11 (2.3%) after the anomaly scan and before the third-trimester scan, 43 (9.1%) at the third-trimester scan and 143 (30.2%) after birth. The 43 abnormalities were found in a total of 13,023 women who had a 36 weeks scan, suggesting that in 1 out of 303 (95% confidence interval, 233-432) women attending such a scan, a new malformation was detected. Anomalies detected at the routine third-trimester scan were of the urinary tract (n=30), central nervous system (5), simple ovarian cysts (4), chromosomal (1), splenic cyst (1), skeletal dysplasia (1), and cutaneous lymphangioma (1). Most urinary tract anomalies were renal pelvic dilatation, which showed spontaneous resolution in 57% of the cases.
    When undertaking a program of routine third-trimester growth scans in women who have had previous screening scans, an unexpected congenital malformation is detected in approximately 1 in 300 women.
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  • 文章类型: Journal Article
    Background: Birth is a traumatic event with molding forces directed to the fetal skull, which may result in intracranial hemorrhages. However, the knowledge on prevalence and risk factors of incidental brain magnetic resonance imaging (MRI) findings in infants is still inconclusive. Methods: The prevalence and nature of incidental MRI findings were assessed in a birth cohort of 175 asymptomatic infants. The role of delivery method as well as other potential risk factors for intracranial hemorrhages were evaluated. The infants underwent 3T MRI at the age of 2-5 weeks, and the neurological status of the infants with an incidental finding was evaluated by a pediatric neurologist. Information on the delivery method, duration of delivery, parity, used anesthesia, oxytocin induction, and Apgar score was gathered to evaluate their association with the prevalence of hemorrhages. Results: Incidental intracranial hemorrhages were detected in 12 infants (6.9%), all following spontaneous or assisted vaginal delivery. Vacuum-assistance was found to be a risk factor for subdural hemorrhages with an odds ratio (OR) of 4.7 (95% CI [1.18; 18.9], p = 0.032). All infants were evaluated to develop normally by their clinical status. Conclusions: Incidental intracranial hemorrhages are relatively common among infants born by vaginal delivery. They are often of little clinical significance within the first years of life and have unlikely consequences for later neurodevelopment either. Despite their benign character, investigators should be prepared to share this information with parents competently as the findings can cause parental anxiety, and especially as the popularity of MRI as a research tool is increasing.
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