right atrium

右心房
  • 文章类型: Case Reports
    异常肺静脉连接伴鼻中隔异常(MSP)是一种罕见的小儿心血管畸形。尽管文献中的报道很少,准确的术前影像学诊断对于选择合适的临床干预措施和确定患病儿童的预后至关重要。
    在这两种情况下,心血管畸形是偶然发现.在第二种情况下,由于肺炎,在胸部X光片上观察到扩大的心脏轮廓,随后通过超声波证实。结合计算机断层扫描血管造影检查,建立了MSP型肺静脉异位连接的诊断。
    全面的影像学检查对于减少误诊和实现MSP型肺静脉异位连接的准确诊断至关重要。MSP型肺静脉异位连接的典型影像学表现包括隔段上缘带缺失或发育不全,鼻中隔最初向左移位,和部分或全部肺静脉引流到解剖右心房。
    UNASSIGNED: Anomalous pulmonary venous connection with malposition of septum primum (MSP) is a rare pediatric cardiovascular malformation. Although reports in the literature are scarce, accurate pre-operative imaging diagnosis is crucial for selecting the appropriate clinical intervention and determining the prognosis for affected children.
    UNASSIGNED: In both case reports, the cardiovascular malformations were incidental findings. In the second case, an enlarged cardiac silhouette was observed on chest x-ray due to pneumonia, which was subsequently confirmed by ultrasound. Combined with computed tomography angiography examination, the diagnosis of MSP-type anomalous pulmonary venous connection was established.
    UNASSIGNED: Comprehensive imaging examinations are essential in reducing misdiagnosis and achieving an accurate diagnosis of MSP-type anomalous pulmonary venous connection. The typical imaging findings for MSP-type anomalous pulmonary venous connection include absence or hypoplasia of the superior limbic band of the septum secundum, leftward displacement of the septum primum, and partial or total pulmonary vein drainage into the anatomical right atrium.
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  • 文章类型: Case Reports
    一名9岁男孩右心房特发性心脏骨化生,伴有右心房Chiari网络和右肺动脉栓塞。这种情况很少见,很容易被误诊。
    我们遇到了一个9岁男孩,右心房直径3.5厘米的肿瘤。术前影像学诊断不能确定肿瘤的性质,和最初的临床怀疑心脏粘液瘤。入院后,进行了心脏切开术以去除异物和肺动脉血栓切除术。
    特发性心脏骨化生相对罕见,在右心房有Chiari网络陪伴的情况更为罕见。由于这种情况下病变的位置和特征,临床上易误诊为心房粘液瘤。无论是特发性骨化生还是粘液瘤,它需要进行手术治疗和病理检查可以很容易地排除粘液瘤的诊断。然而,由于特发性心脏上皮化生在临床工作中很难遇到,文献报道较少,临床医生和病理学家需要查阅更多相关文献.通过多方咨询学会了解和掌握疾病。
    UNASSIGNED: Idiopathic cardiac osseous metaplasia in the right atrium of a 9-year-old boy, accompanied by right atrial Chiari network and right pulmonary artery embolism. This case is rare and can easily be misdiagnosed.
    UNASSIGNED: We encountered a case of a 9-year-old boy with a 3.5 cm diameter neoplasm in the right atrium. Preoperative imaging diagnosis could not determine the nature of the tumor, and the initial clinical suspicion of cardiac myxoma. After admission, a cardiotomy to remove foreign bodies and a pulmonary artery thrombectomy were performed.
    UNASSIGNED: Idiopathic cardiac osseous metaplasia is relatively rare, and it is even rarer to be accompanied by a Chiari network in the right atrium. Due to the location and characteristics of the lesion in this case, it is easy to be misdiagnosed as atrial myxoma in clinical practice. Whether it is idiopathic osseous metaplasia or myxoma, it needs to be performed surgical treatment and pathological examination can easily rule out the diagnosis of myxoma. However, as idiopathic cardiac metaplasia is difficult to encounter in clinical work and there are few reports in the literature, clinicians and pathologists need to consult more relevant literature. Learn to understand and master the disease through multi-party consultation.
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  • 文章类型: Journal Article
    背景:最近的研究表明,右心房(RA)功能是心血管疾病发病率和死亡率的重要预测因子。然而,关于阻塞性睡眠呼吸暂停综合征(OSAS)患者RA相位功能的研究数据很少,尤其是基于左心室的几何形状.所以,我们旨在通过多模式超声心动图评估OSAS患者左心室几何形状对RA分期功能的影响.
    方法:本横断面研究共纳入235例OSAS患者,多导睡眠图,和超声心动图检查。根据左心室质量指数(LVMI)和相对壁厚(RWT)将OSAS患者分为四组:正常几何形状(NG),同心重塑(CR),同心肥大(CH),和偏心肥大(EH)。通过多模态超声心动图方法(二维超声心动图双平面法[2DE];二维斑点追踪超声心动图[2D-STE];和三维超声心动图[3DE])评估RA的相位功能。多元线性回归分析用于确定左心室几何形状与RA相位功能之间的关系。
    结果:RA体积和指数从NG到CR再到EH再到CH增加。收缩期RA总排空分数和RA应变从NG到CR再到EH再到CH降低。舒张早期RA被动排空分数和RA应变类似地降低。舒张后期RA活性排空分数和RA应变也逐渐增加。在根据性别进行调整的分析中,年龄,身体质量指数,收缩压,呼吸暂停低通气指数,LVMI,肺动脉收缩压,和右心室游离壁厚度,CH通过2DE面积-长度法与RA储层和导管功能相关,而CH和EH通过2D-STE和3DE方法与RA储层和导管功能相关。Further,CH通过2DE面积长度法与RA增压泵功能相关,2D-STE,和3DE方法。
    结论:通过多模态超声心动图方法,RA体积和相位功能随左心室几何形状而变化。CH对RA分期功能有明显的负面影响。
    BACKGROUND: Recent studies have shown that right atrial (RA) function are important predictors of cardiovascular morbidity and mortality. However, the study data about RA phasic function in obstructive sleep apnea syndrome (OSAS) patients are scarce, especially based on the left ventricular geometry. So, we aimed to assess the influence of left ventricular geometry on RA phasic function in OSAS patients via a multimodal echocardiographic approach.
    METHODS: Total of 235 OSAS patients were enrolled in this cross-section study and underwent complete clinical, polysomnography, and echocardiography examinations. The OSAS patients were divided into four groups based on left ventricular mass index (LVMI) and relative wall thickness (RWT): normal geometry (NG), concentric remodeling (CR), concentric hypertrophy (CH), and eccentric hypertrophy (EH). RA phasic function was evaluated via multimodal echocardiography approach (two-dimensional echocardiography biplane method [2DE]; two-dimensional speckle-tracking echocardiography [2D-STE]; and three-dimensional echocardiography [3DE]). The multiple linear regression analysis was used to determine the relationship between left ventricular geometry and RA phasic function.
    RESULTS: The RA volume and indices increased from NG to CR to EH to CH. RA total emptying fraction and RA strain during systole decreased from NG to CR to EH to CH. RA passive emptying fraction and RA strain during early diastole similarly decreased. RA active emptying fraction and RA strain during late diastole also gradually increased similarly. In analyses that adjusted for gender, age, body mass index, systolic blood pressure, apnea-hypopnea index, LVMI, systolic pulmonary artery pressure, and right ventricular free wall thickness, CH was associated with RA reservoir and conduit function via 2DE area-length method, whereas CH and EH were associated with RA reservoir and conduit function via 2D-STE and 3DE method. Further, CH was associated with RA booster pump function via 2DE area-length method, 2D-STE, and 3DE method.
    CONCLUSIONS: The RA volumes and phasic function varied with left ventricular geometry via multimodal echocardiography approach. CH had the apparent negative effect on RA phasic function.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    右心房动脉瘤是一种罕见的不明原因的心脏畸形。它通常是无症状的,但偶尔会导致危及生命和严重的并发症。
    我们介绍了一个8岁儿童的右心房动脉瘤,该儿童出现了包括心房动脉瘤破裂在内的并发症,血栓形成,在一个月内反复出现大量心包积液。手术治疗后,患儿预后良好.
    先天性右心房动脉瘤可能表现为右心房广泛扩张或局部扩张,较小的囊状突起。在后一种情况下,仅通过经胸超声心动图进行诊断可能具有挑战性,并且可能需要进行心脏计算机断层扫描血管造影检查以进行明确诊断。对于在一个月内反复出现大量血性心包积液的患者,在超声心动图中没有显示心房扩大,但显示心房壁异常,重要的是要警惕心房动脉瘤破裂的可能性。及时治疗对于防止病情进展至关重要,否则可能导致不良预后。
    UNASSIGNED: The right atrial aneurysm is a rare cardiac malformation of unknown origin. It is typically asymptomatic but can occasionally lead to life-threatening and serious complications.
    UNASSIGNED: We present a case of a right atrial aneurysm in an eight-year-old child who experienced complications including rupture of the atrial aneurysm, thrombosis, and recurrent large pericardial effusions over a one-month period. Following surgical treatment, the child had a favorable prognosis.
    UNASSIGNED: A congenital right atrial aneurysm may manifest as either a widespread enlargement of the right atrium or a localized, smaller sac-like protrusion. In the latter case, diagnosis can be challenging to confirm through transthoracic echocardiography alone, and may require a cardiac computed tomography angiography examination for a definitive diagnosis. For patients experiencing recurrent large volumes of bloody pericardial effusion within one month, and exhibiting no atrial enlargement but showing abnormalities of the atrial wall in echocardiography, it is important to be vigilant about the potential for atrial aneurysm rupture in the heart. Timely treatment is essential to prevent the progression of the condition, which could otherwise result in a poor prognosis.
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  • 文章类型: Journal Article
    右心房(RA)结构和功能评估最近已成为各种心血管疾病中不良事件的强大生物标志物。右心房的定量分析,通常进行容量变化或斑点追踪超声心动图(STE),显著改变了我们对RA功能和重塑的认识。了解超声心动图参考值和RA体积和心肌功能的测量方法是在临床常规中引入RA定量的前提。这篇综述描述了方法论,基于目前对右心房解剖结构和生理功能的了解,通过超声心动图测量RA大小和功能的益处和陷阱,并提供相关心脏病中右心房功能的最新知识。
    Right atrial (RA) structural and functional evaluations have recently emerged as powerful biomarkers for adverse events in various cardiovascular conditions. Quantitative analysis of the right atrium, usually performed with volume changes or speckle-tracking echocardiography (STE), has markedly changed our understanding of RA function and remodeling. Knowledge of reference echocardiographic values and measurement methods of RA volumes and myocardial function is a prerequisite to introduce RA quantitation in the clinical routine. This review describes the methodology, benefits and pitfalls of measuring RA size and function by echocardiography based on the current understanding of right atrial anatomy and physiological function and provides the current knowledge of right atrial function in related cardiac diseases.
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  • 文章类型: Case Reports
    一名患有5期慢性肾脏疾病的46岁女性由于胸中央静脉阻塞(TCVO)和隧道袖口导管阻塞而无法接受血液透析治疗。该患者还出现TCVO症状。当无法进行经皮手术时,我们通过体外循环下的无名右心房旁路移植术解决了阻塞。关于这种手术方法的报道很少。就患者预后而言,这可能是解决这个问题的有效方法。
    A 46-year-old woman with stage 5 chronic kidney disease was unable to undergo hemodialysis treatment due to thoracic central venous obstruction (TCVO) and blockage of the tunneled cuffed catheter. This patient also presented with symptoms of TCVO. When percutaneous procedure was not possible, we resolved the obstruction with the innominate-to-right-atrial bypass grafting technique under extracorporeal circulation. There are few reports on this surgical approach. In terms of patient prognosis, this may be an effective solution to this problem.
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  • 文章类型: Journal Article
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  • 文章类型: Randomized Controlled Trial
    背景:持续性心房颤动(PerAF)通常与右心房(RA)增大有关。我们调查了RA干预对PerAF和RA扩大患者的疗效。
    方法:将PerAF和RA增大的患者随机(1:1)接受辅助RA消融术(LA+RA组,n=60)或单独接受左心房(LA)消融(仅LA组,n=60)。在LA+RA组中,如果LA消融未能终止AF,则进行RA消融。主要终点是无房颤/房性心动过速(AT)复发,在没有抗心律失常药物治疗的单次消融术后12个月。
    结果:在LA+RA组中,40例(67%)患者需要RA消融。LA+RA组的急性房颤终止率高于仅LA组(63.3%vs.36.7%,p=0.003)。在12个月的随访结束时,LA+RA组42例(70%)患者无AF/AT复发,与仅LA组的31(51.7%)相比(对数秩p=0.034;风险比0.549[95%置信区间,0.310-0.974])。LA+RA组的房颤复发率也高于仅LA组(81.7%vs.63.3%,对数秩p=0.019)。两组的不良事件发生率相似(5%vs.3.3%,p=0.648)。
    结论:辅助RA消融术提高了PerAF和RA扩大患者的单次消融术成功率。
    背景:唯一标识符:ChiCTR220056844。
    BACKGROUND: Persistent atrial fibrillation (PerAF) is often associated with right atrial (RA) enlargement. We investigated the efficacy of RA intervention in patients with PerAF and RA enlargement.
    METHODS: Patients with PerAF and RA enlargement were randomised (1:1) to receive adjunctive RA ablation (left atrial [LA] + RA group; n = 60) or to receive LA ablation alone (LA-only group; n = 60). In the LA + RA group, RA ablation was performed if LA ablation failed to terminate AF. The primary end point was freedom from AF/atrial tachycardia (AT) recurrence at 12 months after a single ablation procedure without antiarrhythmic drug therapy.
    RESULTS: In the LA + RA group, 40 patients (67%) required RA ablation. The LA + RA group had a higher rate of acute AF termination than the LA-only group (63.3% vs 36.7%; P = 0.003). At the end of 12-month follow-up, 42 patients (70%) in the LA + RA group were free of AF/AT recurrence, compared with 31 (51.7%) in the LA-only group (log rank P = 0.034; hazard ratio 0.549, 95% confidence interval 0.310-0.974). The rate of freedom from AF recurrence was also higher in the LA + RA group than in the LA-only group (81.7% vs 63.3%; log rank P = 0.019). The 2 groups had similar rates of adverse events (5% vs 3.3%; P = 0.648).
    CONCLUSIONS: Adjunctive RA ablation increased the success rate of a single ablation in patients with PerAF and RA enlargement.
    UNASSIGNED: ChiCTR220056844.
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