CHD

CHD
  • 文章类型: Case Reports
    我们报告了一个罕见的病例报告,即完全异常肺静脉回流到上腔静脉口底部的右心房,没有静脉窦缺损。在situsitus中,没有垂直静脉或后肺静脉汇合。
    We report an uncommon case report of total anomalous pulmonary venous returns into the right atrium at the base of the superior caval vein\'s ostium without a sinus venosus defect, in situs solitus, without vertical vein or a posterior pulmonary venous confluence.
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  • 文章类型: Journal Article
    目的:坏死性小肠结肠炎与肠道菌群改变有关,剖腹产与新生儿肠道微生物组失衡有关。我们旨在研究分娩方式(阴道或剖腹产)和胎龄在冠心病足月新生儿(≥37周)坏死性小肠结肠炎发展中的作用。
    方法:病例对照研究。我们研究了所有在新生儿(≤28日龄)期间接受心脏手术的CHD新生儿,2007年至2017年。完全正确,60例坏死性小肠结肠炎患者(按出生年份和先天性心脏病类型)与180例对照(1:3比例)相匹配。多变量条件逻辑回归用于评估研究问题。
    结果:在患有冠心病的足月新生儿中,坏死性小肠结肠炎的总患病率为6.3%。患有左心室流出道病变或单心室病变的新生儿占55%(n=33)。62%(n=37)的病例处于改良的Bell\s2期或以上的坏死性小肠结肠炎分类。在多变量建模中,出生时的胎龄与坏死性小肠结肠炎的发展无关[调整后的每周比值比增加,95%置信区间:1.20(0.90-1.60)]。剖腹产分娩(与阴道分娩相比)与坏死性小肠结肠炎的发展密切相关[调整比值比(95%置信区间):2.64(1.31-5.29)]。我们未能确定术前肠内营养与坏死性小肠结肠炎之间的关联。
    结论:这项研究表明,通过剖腹产出生的危重CHD新生儿发生坏死性小肠结肠炎的风险很高。鉴于CHD新生儿中剖腹产计划分娩的患病率很高,因此此信息很重要。
    OBJECTIVE: Necrotising enterocolitis is linked with altered intestinal microbiota, and caesarean birth is associated with imbalance of newborn intestinal microbiome. We aimed to investigate the role of delivery mode (vaginal or caesarean) and gestational age in the development of necrotising enterocolitis among term-born neonates (≥ 37 weeks) with CHD.
    METHODS: Case-control study. We studied all newborns with CHD who underwent cardiac surgery during the neonatal (≤ 28 days of age) period, between 2007 and 2017. Totally, 60 cases of necrotising enterocolitis were matched (by year of birth and type of congenital heart lesion) with 180 controls (1:3 ratio). Multivariable conditional logistic regression was used to assess the study question.
    RESULTS: The overall prevalence of necrotising enterocolitis was 6.3% in term-born newborns with CHD. Neonates with a left-ventricular outflow tract lesion or single ventricle lesion accounted for 55% (n = 33) of cases. 62% (n = 37) cases were in the modified Bell\'s stage 2 or more for necrotising enterocolitis classification. In multivariable modelling, gestational age at birth was not associated with the development of necrotising enterocolitis [adjusted odds ratio per week increase, 95% confidence interval: 1.20 (0.90-1.60)]. Birth by caesarean delivery (compared to vaginal) was strongly associated with development of necrotising enterocolitis [adjusted odds ratio (95% confidence interval): 2.64 (1.31-5.29)]. We failed to identify an association between preoperative enteral nutrition and necrotising enterocolitis.
    CONCLUSIONS: This study showed a high risk of necrotising enterocolitis in newborns with critical CHD born via caesarean. This information is important given the high prevalence of planned birth by caesarean in newborns with CHD.
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  • 文章类型: Case Reports
    肺动脉闭锁和室间隔缺损合并主肺侧支动脉是一个极其复杂的,异质,和罕见的异常。如果没有任何干预或治疗,这组患者可能无法生存到成年。尽管对新生儿诊断的患者进行手术管理,婴儿,或者童年早期很清楚,在成年期诊断的患者的治疗仍然是一个重大问题。术前临床状况,成像方法,和操作发现可能有助于规划最合适的管理。在这里,我们报道了1例肺动脉闭锁和室间隔缺损伴主要主肺侧支动脉的独特病例,直到18岁时仍无症状.
    Pulmonary atresia and ventricular septal defect with major aortopulmonary collateral arteries is an extremely complex, heterogeneous, and rare anomaly. This group of patients may not be able to survive until adulthood without any interventions or treatment. Although surgical management of patients diagnosed in newborn, infant, or early childhood is clear, treatment of patients diagnosed in adulthood still remains a significant problem. The pre-operative clinical status, imaging methods, and operative findings might be helpful for planning the most appropriate management. Herein, we report a unique case of pulmonary atresia and ventricular septal defect with major aortopulmonary collateral arteries who remained asymptomatic until the age of 18 years.
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  • 文章类型: Case Reports
    具有破骨细胞样巨细胞的未分化癌(UCOGC)是一种罕见的癌症变体,具有独特的放射学和病理学特征。据报道,这种不寻常的癌症存在于各种器官中,胰腺是最常见的解剖部位。胰腺的UCOGC具有相对惰性的临床行为,应与普通的胰胆管腺癌区分开。本文介绍了第一例UCOGC,涉及胆总管(CBD)和肝总管(CHD)的整个节段,而没有延伸到胰腺组织。熟悉它的临床,尽管发生了异常位置,但放射学和病理学特征可以帮助建立准确的诊断。
    Undifferentiated carcinoma with osteoclast-like giant cells (UCOGC) is a rare variant of carcinoma with unique radiological and pathological features. This unusual carcinoma has been reported in a variety of organs and pancreas is the most frequently involved anatomical site. UCOGC of pancreas attains a relatively indolent clinical behavior and should be distinguished from ordinary pancreatobiliary adenocarcinoma. This paper presents the first case of UCOGC involving the entire segment of common bile duct (CBD) and common hepatic duct (CHD) without extending to the pancreatic tissue. Getting familiar with its clinical, radiological and pathological characters can help establish accurate diagnosis despite the occurrence of an unusual location.
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  • 文章类型: Case Reports
    我们介绍了一例CHD新生儿可能与垂直COVID-19传播相关的小儿炎症性多系统综合征。在轻度主动脉瓣狭窄的背景下诊断出心肌炎和室上性心动过速以及肝损伤和肾衰竭;该患者成功接受了免疫调节治疗。由于儿科炎症多系统综合征会影响心脏,我们可以认为,血液动力学不显著CHD的新生儿发生致死结局的风险较高.与早期诊断和管理有关的问题需要解决。
    We present a case of possible vertical COVID-19 transmission-related paediatric inflammatory multisystem syndrome in a neonate with CHD. Myocarditis and supraventricular tachycardia along with hepatic injury and renal failure were diagnosed on a background of mild aortic valve stenosis; the patient was successfully treated with immunomodulation. Since paediatric inflammatory multisystem syndrome can affect the heart, we could consider neonates with haemodynamically insignificant CHD to be at a higher risk of fatal outcomes. Issues related to early diagnosis and management need to be addressed.
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  • 文章类型: Case Reports
    先天性左心室憩室是一种罕见的心脏畸形,它可能与坎特雷尔的五联和其他心脏缺陷有关。然而,在完全Cantrell综合征中,没有任何其他心脏缺陷的孤立性心室憩室非常罕见。我们描述了一名6岁的男性患者,患有完全的Cantrell综合征,并伴有孤立的左心室憩室。
    The congenital left ventricular diverticulum is a rare cardiac malformation, and it may associate with Cantrell\'s Pentalogy with other cardiac defects. However, isolated ventricular diverticulum without any other cardiac defect in complete Cantrell\'s syndrome is very rare. We describe a 6-year-old male patient with a complete Cantrell\'s syndrome with isolated left ventricular diverticulum.
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  • 文章类型: Journal Article
    我们报告了2例急性低血压患儿在静脉注射阿奇霉素后,失代偿性心力衰竭.在我们报告的每个案例中,阿奇霉素被用于治疗可能的支原体心肌炎。在这份报告中,我们的目的是将低血压描述为静脉注射阿奇霉素的一种可能罕见的不良反应,并鼓励在心功能不全患者中谨慎使用.
    We report two cases of acute hypotension after intravenous azithromycin administration in children with acute, decompensated heart failure. In each of our reported cases, azithromycin was being used to treat possible Mycoplasma myocarditis. In this report, we aim to describe hypotension as a potentially rare adverse reaction to intravenous azithromycin and encourage judicious use in patients with cardiac dysfunction.
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  • 文章类型: Journal Article
    冠心病,全球死亡的主要原因,空气污染可能会加剧或加剧,给患者带来很高的负担。迄今为止,有限的研究估计了中国短期暴露于空气污染与CHD疾病负担之间的关系,结果不一致。因此,我们旨在评估环境PM污染物对CHD和特定CHD住院的短期影响和负担.
    在四川省9个城市的82个监测站测量了PM10和PM2.5,2017-2018年中国。基于时间分层的案例交叉设计,评估了短期暴露于颗粒物(PM)污染对冠心病(CHD)住院患者的影响.同时,估计了由于环境PM污染导致的CHD相关负担。
    共有104,779例冠心病记录来自这9个城市的153家医院。在四川省,PM污染对CHD和特定CHD的住院人数(HAs)有显着影响。PM10和PM2.5的10μg/m3增加与0.46%(95%CI:0.08,0.84%)相关,在lag7时,CHD的HAs分别增加0.57%(95%CI:0.05,1.09%)。空气污染物对健康的影响按年龄相当,季节和性别,显示老年人(≥65岁)和寒冷季节更容易受到环境空气污染的影响,而特定性别的影响是积极的,但不是决定性的。以世界卫生组织的空气质量准则为参考,冠心病的HAs总数分别为1784例和2847例,可归因于PM10和PM2.5。从2017年到2018年,超过PM10和PM2.5的总医疗费用分别为42.04和6725万元人民币。
    这项研究表明,短期暴露于空气污染物与四川省冠心病的HAs增加有关,这可能对当地环境改善和政策参考产生影响。
    Coronary heart disease (CHD), the leading cause of death globally, might be developed or exacerbated by air pollution, resulting high burden to patients. To date, limited studies have estimated the relations between short-term exposure to air pollution and CHD disease burden in China, with inconsistent results. Hence, we aimed to estimate the short-term impact and burden of ambient PM pollutants on hospitalizations of CHD and specific CHD.
    PM10 and PM2.5 were measured at 82 monitoring stations in 9 cities in Sichuan Province, China during 2017-2018. Based on the time-stratified case-crossover design, the effects of short-term exposure to particle matter (PM) pollution on coronary heart disease (CHD) hospital admissions were estimated. Meanwhile, the linked burden of CHD owing to ambient PM pollution were estimated.
    A total of 104,779 CHD records were derived from 153 hospitals from these 9 cities. There were significant effects of PM pollution on hospital admissions (HAs) for CHD and specific CHD in Sichuan Province. A 10 μg/m3 increase of PM10 and PM2.5 was linked with a 0.46% (95% CI: 0.08, 0.84%), and 0.57% (95% CI: 0.05, 1.09%) increments in HAs for CHD at lag7, respectively. The health effects of air pollutants were comparable modified by age, season and gender, showing old (≥ 65 years) and in cold season being more vulnerable to the effects of ambient air pollution, while gender-specific effects is positive but not conclusive. Involving the WHO\'s air quality guidelines as the reference, 1784 and 2847 total cases of HAs for CHD could be attributable to PM10 and PM2.5, separately. The total medical cost that could be attributable to exceeding PM10 and PM2.5 were 42.04 and 67.25 million CNY from 2017 to 2018, respectively.
    This study suggested that the short-term exposure to air pollutants were associated with increased HAs for CHD in Sichuan Province, which could be implications for local environment improvement and policy reference.
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  • 文章类型: Journal Article
    本地设备感染是一种严重的并发症,尤其是新生儿。完整的设备移除是治疗心脏设备感染的黄金标准;然而,在选定的情况下,可以采用替代策略。我们描述了一个14天大的新生儿的案例,体重2.5kg,曾接受心外膜双腔起搏器植入治疗先天性完全性房室传导阻滞的患者。发生器袋在腹直肌下方的上腹部区域中创建。植入后六天,发现口袋感染;血培养和经食管超声心动图正常。由于新生儿的体重较低,以及在远离感染区域的地方寻找新的舒适地点来容纳发电机的可能性有限,我们选择了保守的策略。我们成功应用了抗生素联合治疗,真空辅助伤口闭合系统(KCI,德国)40天,然后在不移除装置的情况下从右侧转移皮瓣。在一年的随访中,没有局部或全身感染迹象。
    UNASSIGNED: Local device infection is a serious complication, especially in neonates. Complete device removal is the gold standard treatment for cardiac device infection; however, in selected cases alternative strategies could be adopted. We describe a case of a 14-day-old neonate, weighing 2.5kg, who had undergone epicardial double chamber pacemaker implantation for a congenital complete atrioventricular block. The generator pocket was created in the epigastric area below the rectus abdominis. At six days after implantation, pocket infection was found; blood cultures and the transoesophageal echocardiogram were normal. Due to the low weight of the neonate, and the limited possibility of finding a new comfortable site for housing the generator far from the infected area, we opted for a conservative strategy. We successfully applied a combination of antibiotic therapy, a vacuum-assisted wound closure system (KCI, Germany) for 40 days, and then skin transfer flap from the right flank without device removal. At one-year follow-up there were no local or systemic signs of infection.
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  • 文章类型: Journal Article
    The left atrial appendage congenital aneurysm is an extremely rare heart defect. The entity can remain asymptomatic for a long time; however, it may lead to life-threatening morbidity or death.
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