congenital heart disease

先天性心脏病
  • 文章类型: Journal Article
    先天性心脏病(CHD)是当今主要的出生异常之一。CHD儿童面临适应性功能挑战的风险。睡眠困难在CHD儿童中也很常见。的确,睡眠呼吸紊乱,一种常见的睡眠功能障碍,与CHD婴儿死亡率增加相关。本研究检查了适应性功能和睡眠质量之间的关联(即,与健康儿童(n=38)相比,冠心病儿童(n=23)的持续时间和中断)。结果表明,CHD组的平均睡眠时间与总体适应功能之间存在关联r(21)=.57,p=.005,而健康组则没有。CHD小组在概念中表现出较低水平的适应性功能,t(59)=2.12,p=.039,科恩的d=0.53,实用,t(59)=2.22,p=.030,科恩的d=0.55域,和整体自适应功能(即,一般适应性复合)与健康组相比接近统计意义,t(59)=2.00,p=.051,科恩的d=0.51。CHD组还表现出夜间清醒的时间更长,t(56)=2.19,p=.033,科恩的d=0.58,更多的父母-照顾者报告打鼾,χ2(1,N=60)=5.25,p=0.022,V=0.296。需要进一步探索冠心病患者的适应性功能与睡眠质量之间的关系,以指导临床实践指南。
    Congenital heart disease (CHD) is one of today\'s leading birth anomalies. Children with CHD are at risk for adaptive functioning challenges. Sleep difficulties are also common in children with CHD. Indeed, sleep-disordered breathing, a common type of sleep dysfunction, is associated with increased mortality for infants with CHD. The present study examined the associations between adaptive functioning and sleep quality (i.e., duration and disruptions) in children with CHD (n = 23) compared to healthy children (n = 38). Results demonstrated associations between mean hours slept and overall adaptive functioning in the CHD group r(21) = .57, p = .005 but not in the healthy group. The CHD group demonstrated lower levels of adaptive functioning in the Conceptual, t(59) = 2.12, p = .039, Cohen\'s d = 0.53 and Practical, t(59) = 2.22, p = .030, Cohen\'s d = 0.55 domains, and overall adaptive functioning (i.e., General Adaptive Composite) nearing statistical significance in comparison to the healthy group, t(59) = 2.00, p = .051, Cohen\'s d = 0.51. The CHD group also demonstrated greater time awake at night, t(56) = 2.19, p = .033, Cohen\'s d = 0.58 and a greater instance of parent-caregiver reported snoring, χ2 (1, N = 60) = 5.25, p = .022, V = .296 than the healthy group. Further exploration of the association between adaptive functioning and sleep quality in those with CHD is required to inform clinical practice guidelines.
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  • 文章类型: Journal Article
    目前没有关于儿科心脏病学期刊编辑委员会成员(EBM)多样性的数据。
    目的是调查5种儿科心脏病学期刊的编辑委员会,以评估这些委员会在地理上的组成,性别,以及其成员的经济代表性。
    有关EBM的信息直接从2022年2月访问的5个期刊网站上收集。收集了以下数据:实践国家(包括世界银行的地域和收入分类),实践机构,在编辑委员会中的角色,以及个人是否在包括的一个或多个董事会中担任角色。
    总共鉴定出455个EBM。共有369人(81%)为男性。所有主编都是男性,4人来自美国。在北美执业的EBM占所审查编辑委员会的278人(61%)。接下来的大多数EBM在欧洲和中亚进行实践(23%,n=103),东亚和太平洋地区(7%,n=31),中东和北非(4%,n=18),拉丁美洲和加勒比地区(4%,n=16)。撒哈拉以南非洲和南亚不到2%(n=9)。超过90%(n=415)在高收入国家执业。低收入国家没有代表。
    在欧洲和北美以外的国家执业的妇女和儿科心脏病专家在所研究期刊的编辑委员会中的代表性不足。编辑委员会的多样化组成可以为服务不足的地区提供更大的代表性,并鼓励更广泛的调查和研究途径。
    UNASSIGNED: No data currently exist on the diversity of editorial board members (EBMs) of pediatric cardiology journals.
    UNASSIGNED: The objective was to investigate the editorial boards of 5 pediatric cardiology journals to assess the composition of these boards in terms of the geographical, gender, and economic representation of their members.
    UNASSIGNED: Information on EBMs was collected directly from 5 journal websites accessed in February 2022. The following data were collected: country of practice (including World Bank geographical and income classification), institution of practice, role on editorial board, and whether an individual held a role on 1 or more of the boards included.
    UNASSIGNED: A total of 455 EBMs were identified. A total of 369 (81%) were male. All editors-in-chief were male, and 4 were from the United States. EBMs practicing in North America accounted for 278 individuals (61%) of the editorial boards reviewed. The next majority of EBMs are practicing within Europe and Central Asia (23%, n = 103), East Asia and Pacific (7%, n = 31), Middle East and North Africa (4%, n = 18), and Latin America and Caribbean (4%, n = 16). Less than 2% (n = 9) practice in Sub-Saharan Africa and South Asia. Over 90% (n = 415) practice in high-income countries. There was no representation from low-income countries.
    UNASSIGNED: Women and pediatric cardiologists practicing in countries outside of Europe and North America were underrepresented on the editorial boards of the journals studied. Diversifying composition of editorial boards may provide greater representation of underserved areas and encourage broader avenues of investigation and research.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    动脉粥样硬化性疾病是成人先天性心脏病(CHD)发病的重要原因。该组中血脂异常的患病率描述不佳。
    本研究旨在描述成人冠心病患者血脂异常的患病率。
    预期,我们在4个新英格兰门诊先天性心脏病中心的≥18岁成人中进行了门诊筛查研究.对参与者进行了心血管危险因素调查。使用即时脂质分析仪获得非空腹手指样本进行分析。
    186名参与者完成了脂质筛查(中位年龄30[范围18-71]岁,50%女性)。18(10%)有简单的CHD解剖,和63(34%)有复杂的解剖结构。169名受访者中只有15%报告了高胆固醇史。85(46%)参与者符合国家胆固醇教育计划对血脂异常的定义,其中60(32%)。62(34%),和37(20%)具有低高密度脂蛋白胆固醇(HDL-C<40mg/dL),高非HDL-C(≥130mg/dL),和高总胆固醇(TC≥200mg/dL),分别。单纯性CHD患者的TC高于中度和复杂病变患者(平均178.4±48.7vs170.1±35.0vs157.6±34.5mg/dL;P=0.03)。复杂CHD患者的HDL-C低于单纯和中度病变患者(平均44.1±13.5vs46.9±12.5vs49.8±15.3mg/dL;P=0.05)。
    血脂异常在我们的冠心病成人队列中非常普遍,尽管<15%报告了先前的诊断。低HDL-C在复杂的冠心病中更为常见,高TC在单纯性或中度CHD中更为常见。脂质筛查应该是所有冠心病成人预防性健康维护的一部分。
    UNASSIGNED: Atherosclerotic disease is an important cause of morbidity among adults with congenital heart disease (CHD). Prevalence of dyslipidemia in this group is poorly described.
    UNASSIGNED: This study aimed to describe the prevalence of dyslipidemia among adults with CHD.
    UNASSIGNED: A prospective, outpatient screening study was conducted among adults aged ≥18 years at 4 New England ambulatory congenital cardiology centers. Participants were surveyed regarding cardiovascular risk factors. Nonfasting fingerstick samples were obtained for analysis using a point-of-care lipid analyzer.
    UNASSIGNED: Lipid screening was completed on 186 participants (median age 30 [range 18-71] years, 50% female). Eighteen (10%) had simple CHD anatomy, and 63 (34%) had complex anatomy. Only 15% of 169 respondents reported history of high cholesterol. Eighty-five (46%) participants met National Cholesterol Education Program definition of dyslipidemia with 60 (32%), 62 (34%), and 37 (20%) having low high-density lipoprotein cholesterol (HDL-C <40 mg/dL), high non-HDL-C (≥130 mg/dL), and high total cholesterol (TC ≥200 mg/dL), respectively. TC was higher among participants with simple CHD than among those with moderate and complex lesions (mean 178.4 ± 48.7 vs 170.1 ± 35.0 vs 157.6 ± 34.5 mg/dL; P = 0.03). HDL-C was lower among participants with complex CHD than among those with simple and moderate lesions (mean 44.1 ± 13.5 vs 46.9 ± 12.5 vs 49.8 ± 15.3 mg/dL; P = 0.05).
    UNASSIGNED: Dyslipidemia is highly prevalent among our cohort of adults with CHD, despite <15% reporting a prior diagnosis. Low HDL-C was more common in complex CHD, and high TC was more common in simple or moderate CHD. Lipid screening should be part of preventive health maintenance for all adults with CHD.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    当前的大数据时代为临床医生提供了大量新的机会,让他们利用人工智能来优化患有先天性心脏病的儿科和成人患者的护理。目前,在临床诊断中,人工智能的使用严重不足,预后,和先天性心脏病患者的管理。该文件是一项行动呼吁,将描述先天性心脏病中人工智能的现状,审查挑战,讨论机会,并专注于基于人工智能的先心病部署的首要任务。
    The current era of big data offers a wealth of new opportunities for clinicians to leverage artificial intelligence to optimize care for pediatric and adult patients with a congenital heart disease. At present, there is a significant underutilization of artificial intelligence in the clinical setting for the diagnosis, prognosis, and management of congenital heart disease patients. This document is a call to action and will describe the current state of artificial intelligence in congenital heart disease, review challenges, discuss opportunities, and focus on the top priorities of artificial intelligence-based deployment in congenital heart disease.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    随着人们对在医疗实践和研究中使用大型索赔数据库的兴趣日益浓厚,这是有效识别感兴趣疾病患者的有意义和必要的步骤。
    本研究旨在建立一种机器学习(ML)方法,以在大型索赔数据库中识别先天性心脏病(CHD)患者。
    我们利用了1983年至2000年魁北克索赔和住院数据库的数据。该研究包括19,187名患者。其中,使用临床医生开发的算法将3,784名患者标记为真正的CHD患者,并将其手动审核视为黄金标准。为了建立准确的ML授权的自动CHD分类系统,我们评估了ML方法,包括梯度提升决策树,支持向量机,决策树,并将其与正则化逻辑回归进行比较。精确回忆曲线下的面积用作评估度量。使用更新的数据集到2010年对不同的受试者进行外部验证。
    在我们评估的ML方法中,梯度提升决策树引领了识别精确召回曲线下99.3%面积的真正冠心病患者的性能,灵敏度为98.0%,和99.7%的特异性。外部验证返回了有关模型性能的类似统计信息。
    这项研究表明,用于CHD患者识别的繁琐而耗时的临床检查可以被大型索赔数据库中极其高效的ML算法所取代。我们的发现表明,ML方法可用于自动化复杂的算法来识别患有复杂疾病的患者。
    UNASSIGNED: With an increasing interest in using large claims databases in medical practice and research, it is a meaningful and essential step to efficiently identify patients with the disease of interest.
    UNASSIGNED: This study aims to establish a machine learning (ML) approach to identify patients with congenital heart disease (CHD) in large claims databases.
    UNASSIGNED: We harnessed data from the Quebec claims and hospitalization databases from 1983 to 2000. The study included 19,187 patients. Of them, 3,784 were labeled as true CHD patients using a clinician developed algorithm with manual audits considered as the gold standards. To establish an accurate ML-empowered automated CHD classification system, we evaluated ML methods including Gradient Boosting Decision Tree, Support Vector Machine, Decision tree, and compared them to regularized logistic regression. The Area Under the Precision Recall Curve was used as the evaluation metric. External validation was conducted with an updated data set to 2010 with different subjects.
    UNASSIGNED: Among the ML methods we evaluated, Gradient Boosting Decision Tree led the performance in identifying true CHD patients with 99.3% Area Under the Precision Recall Curve, 98.0% for sensitivity, and 99.7% for specificity. External validation returned similar statistics on model performance.
    UNASSIGNED: This study shows that a tedious and time-consuming clinical inspection for CHD patient identification can be replaced by an extremely efficient ML algorithm in large claims database. Our findings demonstrate that ML methods can be used to automate complicated algorithms to identify patients with complex diseases.
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  • 文章类型: Journal Article
    动脉粥样硬化性心血管疾病(ASCVD)对先天性心脏病(CHD)成人心血管死亡的影响尚不清楚。
    本研究的目的是确定成人冠心病患者ASCVD危险因素的患病率和预后意义。我们假设ASCVD危险因素与定义为心力衰竭住院的心血管事件相关,心脏移植,心血管死亡。
    这是一项在梅奥诊所(2003-2019)对冠心病成人进行的回顾性队列研究。排除有冠状动脉疾病(CAD)病史的患者。ASCVD危险因素定义为高血压,高脂血症,糖尿病,肥胖,吸烟,和早熟CAD家族史。
    有5,025例患者没有CAD病史。平均年龄为35(23-45)岁,男性为2,558人(51%)。在5025名患者中,2,382(47%)在基线时具有≥1个ASCVD危险因素,16%的患者在5年内出现了额外的ASCVD危险因素(新发ASCVD风险).基线ASCVD危险因素(风险比1.27,95%置信区间1.06-1.38)和随访期间新发ASCVD危险因素(风险比1.06,95%置信区间1.02-1.11)与心血管事件相关。
    ASCVD因子与成人冠心病患者心血管事件相关。由于改变ASCVD风险的干预措施已被证明可以降低普通人群的心血管死亡,预期此类干预措施也将改善CHD人群的临床结局是合乎逻辑的.
    UNASSIGNED: The effect of atherosclerotic cardiovascular disease (ASCVD) on cardiovascular death in adults with congenital heart disease (CHD) is not well understood.
    UNASSIGNED: The purpose of this study was to determine the prevalence and prognostic implications of ASCVD risk factors in adults with CHD. We hypothesized that ASCVD risk factors were associated with cardiovascular events defined as heart failure hospitalization, heart transplant, and cardiovascular death.
    UNASSIGNED: This is a retrospective cohort study of adults with CHD at the Mayo Clinic (2003-2019). Patients with a history of coronary artery disease (CAD) were excluded. ASCVD risk factors were defined as hypertension, hyperlipidemia, diabetes, obesity, smoking, and family history of premature CAD.
    UNASSIGNED: There were 5,025 patients without a prior history of CAD. The mean age was 35 (23-45) years, and 2,558 (51%) were males. Of 5,025 patients, 2,382 (47%) had ≥1 ASCVD risk factors at baseline, and 16% developed additional ASCVD risk factors within 5 years (new-onset ASCVD risk). ASCVD risk factors at baseline (hazard ratio 1.27, 95% confidence interval 1.06-1.38) and new-onset ASCVD risk factors during follow-up (hazard ratio 1.06, 95% confidence interval 1.02-1.11) were associated with cardiovascular events.
    UNASSIGNED: ASCVD factors were associated with cardiovascular events in adults with CHD. Since interventions that modify ASCVD risk have been shown to decrease cardiovascular death in the general population, it is logical to expect that such interventions would also improve clinical outcomes in the CHD population.
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