Heart Aneurysm

心脏动脉瘤
  • 文章类型: Journal Article
    目的:在本研究中,我们探讨了急性心肌梗死(AMI)后室壁瘤发展的决定因素,从而促使及时干预,提高患者预后。
    方法:在本回顾性队列分析中,我们评估了常州市第一人民医院收治的297例AMI患者。本研究的结构如下。全面的基线数据收集包括血液学评估,心电图,超声心动图,入院时冠状动脉造影。AMI后3个月内,心脏超声检查用于检测室壁瘤的发展.采用单变量和多变量逻辑回归分析来确定室壁瘤形成的决定因素。随后,建立了AMI后室壁瘤的预测模型.此外,使用ROC曲线评价该模型的诊断效能.
    结果:在我们对291例AMI患者的分析中,年龄范围为32-91岁,247人为男性(84.9%)。在为期3个月的观察期结束时,该队列分为两个子集:278例无室壁瘤患者和13例有明显室壁瘤患者。室壁瘤亚组的区别特征是年龄明显较高的值,B型利钠肽(BNP),左心房(LA),左心室舒张末期内径(LEVDD),左心室收缩末期直径(LVEWD),E波速度(E),左心房容积(LAV),E/A比(E/A),E/E比(E/E),相邻四根导线升高的心电图(4个ST段抬高),和前壁心肌梗死(AWMI)相比,它们的对应物(p<0.05)。在奇异的预测因素中,总胆固醇(TC)成为心室动脉瘤发展的最重要预测因子,表现出0.704的AUC。然而,在构建一个融合性别的多因素模型时,TC,相邻四导联的ST段抬高,和前壁梗塞,它的诊断能力:明显超过了独立TC,产生的AUC为0.883(z=-9.405,p=0.000),而不是0.704。多变量预测模型包括性别,总胆固醇,4个相邻导线的ST抬高,前壁心肌梗死,多因素预测模型显示出比单因素指标TC更好的诊断效能(AUC:0.883vs.0.704,z=-9.405,p=0.000),它还提高了正确重新分类AMI患者室壁瘤发生的预测能力,NRI=28.42%(95%CI:6.29-50.55%;p=0.012)。决策曲线分析表明,使用组合模型具有正的净收益。
    结论:血脂联合心电图模型可用于预测心肌梗死后室壁瘤的形成,旨在优化和调整治疗策略。
    OBJECTIVE: In this study, we explored the determinants of ventricular aneurysm development following acute myocardial infarction (AMI), thereby prompting timely interventions to enhance patient prognosis.
    METHODS: In this retrospective cohort analysis, we evaluated 297 AMI patients admitted to the First People\'s Hospital of Changzhou. The study was structured as follows. Comprehensive baseline data collection included hematological evaluations, ECG, echocardiography, and coronary angiography upon admission. Within 3 months post-AMI, cardiac ultrasounds were administered to detect ventricular aneurysm development. Univariate and multivariate logistic regression analysis were employed to pinpoint the determinants of ventricular aneurysm formation. Subsequently, a predictive model was formulated for ventricular aneurysm post-AMI. Moreover, the diagnostic efficacy of this model was appraised using the ROC curves.
    RESULTS: In our analysis of 291 AMI patients, spanning an age range of 32-91 years, 247 were male (84.9%). At the conclusion of a 3-month observational period, the cohort bifurcated into two subsets: 278 patients without ventricular aneurysm and 13 with evident ventricular aneurysm. Distinguishing features of the ventricular aneurysm subgroup were markedly higher values for age, B-type natriuretic peptide(BNP), Left atrium(LA), Left ventricular end-diastolic dimension (LEVDD), left ventricular end systolic diameter (LVEWD), E-wave velocity (E), Left atrial volume (LAV), E/A ratio (E/A), E/e ratio (E/e), ECG with elevated adjacent four leads(4 ST-Elevation), and anterior wall myocardial infarction(AWMI) compared to their counterparts (p < 0.05). Among the singular predictive factors, total cholesterol (TC) emerged as the most significant predictor for ventricular aneurysm development, exhibiting an AUC of 0.704. However, upon crafting a multifactorial model that incorporated gender, TC, an elevated ST-segment in adjacent four leads, and anterior wall infarction, its diagnostic capability: notably surpassed that of the standalone TC, yielding an AUC of 0.883 (z = -9.405, p = 0.000) as opposed to 0.704. Multivariate predictive model included gender, total cholesterol, ST elevation in 4 adjacent leads, anterior myocardial infarction, the multivariate predictive model showed better diagnostic efficacy than single factor index TC (AUC: 0. 883 vs. 0.704,z =-9.405, p = 0.000), it also improved predictive power for correctly reclassifying ventricular aneurysm occurrence in patients with AMI, NRI = 28.42% (95% CI: 6.29-50.55%; p = 0.012). Decision curve analysis showed that the use of combination model had a positive net benefit.
    CONCLUSIONS: Lipid combined with ECG model after myocardial infarction could be used to predict the formation of ventricular aneurysm and aimed to optimize and adjust treatment strategies.
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  • 文章类型: Case Reports
    先天性心室动脉瘤(CVA)是罕见的心脏异常,主要在黑人人群中有所描述。它们的特征是通常位于基底和顶端段的运动异常的心室突出。尽管诊断通常是偶然的,并且大多数患者无症状,危及生命的事件,如持续性室性心律失常,CVA破裂,心力衰竭并不少见。然而,目前尚无标准化治疗,保守治疗和手术治疗均有良好的结局.我们报告了两名年轻的非洲黑人患者的病例,这些患者有巨大的症状性CVA病变,他们通过心室修复技术成功进行了手术修复。2例均因胸痛和呼吸困难而接受咨询。胸部X线及经胸多普勒超声心动图提示诊断。胸部血管造影和胸部磁共振成像证实了诊断。两名患者均接受了成功的手术。本病例报告旨在重新审视这种罕见病理的诊断和治疗方法。在我们的专业环境中。
    Congenital ventricular aneurysms (CVA) are rare cardiac anomalies that have been predominantly described in the Black population. They are characterized by an akinetic ventricular protrusion that is commonly located at the basal and apical segments. Although the diagnosis is often incidental and the majority of patients are asymptomatic, life-threatening events such as persistent ventricular arrhythmias, CVA rupture, and heart failure are not uncommon. However, no standardized therapy is currently available and good outcomes have been reported with both conservative and surgical management. We report the cases of two young Black African patients with huge symptomatic CVA lesions who underwent successful surgical repair with a ventricular restoration technique. Both cases were consulted for chest pain and dyspnea. Chest X-ray and transthoracic Doppler echocardiography suggested the diagnosis. Thoracic angioscanner and thoracic magnetic resonance imaging confirmed the diagnosis. Both patients underwent successful surgery. This case report aims to revisit the diagnostic and therapeutic approach to this rare pathology, in our professional environment.
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  • 文章类型: Case Reports
    主动脉根部假性动脉瘤是主动脉瓣置换术后的破坏性并发症,死亡率很高。解剖室间隔动脉瘤是主动脉根部假性动脉瘤的一种罕见变种,这几乎没有报道。多模态成像对其诊断和鉴别诊断具有重要价值。
    Aortic root pseudoaneurysm is a devastating complication post aortic valve replacement with a high mortality rate. And dissecting aneurysm into the interventricular septum is a rare variant of aortic root pseudoaneurysm, which is scarcely reported. Multimodal imaging is of great value in its diagnosis and differential diagnosis.
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  • 文章类型: Case Reports
    背景:二尖瓣-主动脉瓣间纤维性假性动脉瘤(PMAIF)是感染性心内膜炎或主动脉瓣手术的罕见并发症。建议手术治疗,但保守治疗的长期随访仍不清楚.
    方法:对一名主动脉瓣置换术6年后出现PMAIF的患者进行了33年的随访。患者出现呼吸困难到我们中心,超声心动图显示射血分数为20%,PMAIF为7×10mm。尽管被建议接受手术,患者因担心手术结局而拒绝治疗.因此,开始保守治疗,密切观察,但不进行手术.在33年的随访期间,患者未出现任何不良健康影响.
    结论:当诊断为PMAIF时,应考虑手术干预。然而,在手术不适用的情况下,保守的管理可能会导致长期生存,基于此和文献中的类似病例报告。
    BACKGROUND: Pseudoaneurysm of the mitral-aortic intervalvular fibrosa (PMAIF) is a rare complication of infective endocarditis or aortic valve surgery. Surgical treatment is suggested, but the long-term follow-up of conservative management remains unclear.
    METHODS: A 33-year follow-up of a patient who developed PMAIF six years after aortic valve replacement is reported. The patient presented to our center with dyspnea, and the echocardiography revealed an ejection fraction of 20% and a PMAIF measuring 7 × 10 mm. Despite being advised to undergo surgery, the patient declined due to fear of surgical outcomes. Consequently, conservative treatment with close observation but without surgery was initiated. During the 33-year follow-up period, the patient did not experience any adverse health effects.
    CONCLUSIONS: Surgical intervention should be considered whenever the PMAIF is diagnosed. However, in any case that the surgery was not applicable, conservative management might lead to long-term survival, based on this and similar case reports in the literature.
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  • 文章类型: Case Reports
    我们描述了一名22岁女性的超声心动图特征,该女性患有膜室间隔(AMVS)的巨大动脉瘤。经胸超声心动图(TTE)和经食管超声心动图(TEE)均显示主动脉瓣环明显扩张和严重的主动脉瓣反流。检测到巨大的动脉瘤,从大型膜性室间隔缺损(MVSD)延伸到主动脉根前表面。对比增强CT和三维CT显示,位于主动脉根部下方并连接到左心室流出道(LVOT)的巨大动脉瘤。经手术及术后病理检查确诊。
    We describe the echocardiographic features of a 22-year-old female with a giant aneurysm of membranous ventricular septum (AMVS). Both transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE) demonstrated significant dilatation of the aortic annulus and severe aortic regurgitation. A giant aneurysm was detected extending from a large membranous ventricular septal defect (MVSD) to the anterior surface of the aortic root. Contrast-enhanced CT and three-dimensional CT revealed a giant aneurysm located below the aortic root and connected to the left ventricular outflow tract (LVOT). The diagnosis was confirmed by surgery and postoperative pathological examination.
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  • 文章类型: Journal Article
    目的:目的:评估康复潜力,在疗养院阶段,景观疗法在梗塞后心脏硬化(PC)并发慢性梗塞后心脏动脉瘤(CPCA)患者的复杂康复治疗中的有效性和安全性。
    方法:材料和方法:我们检查了62例PC并发CCPA患者,年龄38至65岁。患者被随机分为两组:第一组在城市接受“渐进步态”身体活动方案,和第二组-在疗养院的康复部门。Survey,六分钟步行测试,心电图,超声心动图,进行冠状动脉造影。
    结果:结果:第二组患者在6分钟内的平均步行距离从301.00±17.00增加到467.00±32.00m(p<0.05)。只有第2组患者在3周的复杂康复过程中,体重指数从23.70±1.60降低到18.90±1.50,小腿肌肉的直径从33.90±2.30cm显着增加到38.10±3.10cm(p<0.05)。第二组射血分数为51.00±4.50%,第一组为44.70±3.60%(p<0.05),伴随着第2组患者的心力衰竭功能等级的降低。
    结论:结论:景观疗法在疗养院阶段复杂PC患者的复杂康复治疗中的康复潜力取决于患者心肌收缩力和身体耐力的显着改善,提高生活质量。
    OBJECTIVE: Aim: To evaluate the rehabilitation potential, effectiveness and safety of landscape therapy in the complex rehabilitation treatment of patients with post-infarction cardiosclerosis (PC) complicated by chronic post-infarction cardiac aneurysm (CPCA) at the sanatorium stage.
    METHODS: Materials and Methods: We examined 62 patients with PC complicated by CPCA aged 38 to 65 years. Patients were randomized into two groups: the 1st group was undergoing the \"Progressive gait\" physical activity protocol in the city, and the 2nd group - in the rehabilitation department in a sanatorium. Survey, six-minute walk test, electrocardiography, echocardiography, coronary angiography were performed.
    RESULTS: Results: The average distance that 2nd group patients walked in 6 minutes increased from 301.00 ±17.00 to 467.00 ±32.00 m (p<0.05). Only in patients of 2nd group during 3 weeks of complex rehabilitation there was a decrease in body mass index from 23.70 ±1.60 to 18.90 ±1.50 and the diameter of the calf muscle significantly increased from 33.90 ±2.30 cm to 38.10 ±3.10 cm (p < 0.05). Ejection fraction in the 2nd group was 51.00 ±4.50% compared to the 1st group - 44.70 ±3.60% (p < 0.05), which was accompanied by a decrease in the functional class of heart failure in patients of the 2nd group.
    CONCLUSIONS: Conclusions: The rehabilitation potential of landscape therapy in the complex rehabilitation treatment of patients with complicated PC at the sanatorium stage is determined by a significant improvement in myocardial contractility and physical endurance of patients, and improving the quality of life.
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  • 文章类型: Case Reports
    背景:左心耳动脉瘤是一种罕见的心脏肿块,只有少数病例报告。通常没有特定的症状。和一些病人去看医生的症状。
    方法:一名20岁男性患者到我院就诊,在另一家医院经医学评估发现心包囊肿2年。“在我们医院诊所进行的心脏超声检查提示左心室侧壁和前侧壁有一个囊性暗区,与心包囊肿和轻度二尖瓣反流一致。经过进一步的相关检查并排除禁忌症,左心耳动脉瘤切除术是在全身麻醉和心脏跳动的体外循环下进行的.术后病理结果确定:(左心耳)纤维囊壁样组织,局灶性上皮为扁平上皮,符合良性囊肿.
    结论:左心耳动脉瘤是罕见且隐匿的。它们通常是在医学评估期间偶然发现的。如果位置不好或体积太大,然后是压迫症状或心律失常,会出现血栓形成和其他伴随症状。手术切除是目前唯一有效的治疗左心耳动脉瘤的方法。
    BACKGROUND: Left atrial appendage aneurysm is a rare cardiac mass, with only a few cases reported. There are usually no specific symptoms, and a few patients visit the doctor with symptoms.
    METHODS: A 20-year-old male presented to our hospital with a \"pericardial cyst found by medical evaluation in another hospital for 2 years.\" Cardiac ultrasound performed at clinics of our hospital suggested a cystic dark area in the left ventricular lateral wall and the anterior lateral wall, consistent with a pericardial cyst and mild mitral regurgitation. After further relevant examinations and ruling out contraindications, an excision of the left atrial appendage aneurysm was performed under general anesthesia and cardiopulmonary bypass with beating-heart. The postoperative pathological results identified that: (left atrial appendage) fibrocystic wall-like tissue with a focal lining of the flat epithelium, consistent with a benign cyst.
    CONCLUSIONS: Left atrial appendage aneurysms are rare and insidious. They are usually found by chance during medical evaluations. If the location is not good or the volume is too large, then compression symptoms or arrhythmia, thrombosis and other concomitant symptoms will occur. Surgical resection is presently the only effective radical cure for a left atrial appendage aneurysm.
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  • 文章类型: Case Reports
    左心室动脉瘤是由薄的心肌壁描绘的外袋,更常在左心室心尖遇到,很少有运动障碍或运动障碍。除了冠状动脉疾病,病因可能具有挑战性。我们报告了一例30岁的男性,该男性患有孤立的心尖左心室动脉瘤,并在超声心动图上伴有明显的小梁。
    Left ventricular aneurysms are outpouchings delineated by a thin myocardial wall, more frequently encountered at the apex of the left ventricle, which is seldom dyskinetic or akinetic. Apart from coronary artery disease, the etiology can be challenging. We report the case of a 30-year-old man with an isolated apical left ventricular aneurysm associated with prominent trabeculations on echocardiography.
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  • 文章类型: Case Reports
    一名55岁的男子在胃肠道出血后1个月出现呼吸急促恶化,被送往急诊科。他有充血性心力衰竭,心电图提示缺血性心脏病受累.超声心动图显示室间隔缺损并发下后壁左心室动脉瘤。开始保守治疗,但入院第3天发生血流动力学塌陷,冠状动脉造影显示右侧第4冠状动脉后降支血管重建性病变.随后,他的血液动力学状态继续恶化,即使使用ImpellaCP®心脏泵,因此进行了室间隔缺损补片闭合和左心室动脉瘤缝合。他的病情有所改善,他在入院第23天出院,并且在手术后6个月内没有再次入院。室间隔缺损的血流动力学管理需要减少后负荷的装置,临床医生应注意消化道出血后发生心肌梗死的风险。
    A 55-year-old man presented to the emergency department with worsening shortness of breath 1 month after a gastrointestinal bleed. He had congestive heart failure, and an electrocardiogram suggested ischemic heart disease involvement. Echocardiography revealed a ventricular septal defect complicated by a left ventricular aneurysm in the inferior-posterior wall. Conservative treatment was started, but hemodynamic collapse occurred on the third day of admission and coronary angiography revealed a revascularizing lesion in the right fourth posterior descending coronary artery. Subsequently, his hemodynamic status continued to deteriorate, even with an Impella CP® heart pump, so ventricular septal defect patch closure and left ventricular aneurysm suture were performed. His condition improved and he was discharged on day 23 of admission and was not readmitted within 6 months after the procedure. Hemodynamic management of ventricular septal defects requires devices that reduce afterload, and clinicians should be aware of the risk of myocardial infarction after gastrointestinal bleeding.
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  • 文章类型: Case Reports
    二尖瓣下左心室动脉瘤是一种罕见的疾病。这是左心室壁的先天性外袋,总是发生在二尖瓣后小叶附近。二尖瓣下动脉瘤(SMA)通常被报道为心肌缺血(MI)的结果,风湿性心脏病,结核病,和感染性心内膜炎.然而,在印度很少有先天性SMA的病例报道。它通常表现为心力衰竭的症状。我们报告了一名27岁的印度年轻人中罕见的先天性SMA病例,并通过跨动脉瘤方法成功进行了治疗。
    UNASSIGNED: A sub-mitral left ventricular aneurysm is a rare condition. It is a congenital outpouching of the left ventricular wall, invariably occurring adjacent to the posterior mitral leaflet. Sub-mitral aneurysm (SMA) has usually been reported as a consequence of myocardial ischemia (MI), rheumatic heart disease, tuberculosis, and infective endocarditis. Nevertheless, there have been few case reports of congenital SMA in India. It usually presents with symptoms of heart failure. We report a rare case of congenital SMA in a 27-year-old young Indian and its successful management through a trans-aneurysmal approach.
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