Arrhythmia

心律失常
  • 文章类型: Journal Article
    探讨二丁酰腺苷环磷酸钙(dbcAMP-Ca)联合美托洛尔治疗老年心力衰竭合并心律失常的疗效和安全性。
    在2021年2月至2023年4月期间,我院共纳入102例心力衰竭合并心律失常的老年患者。由不参与研究的独立人员将入选患者名单输入随机数据库,并通过SAS9.4软件生成随机分配序列。然后,将102例老年患者分为对照组(n=51)和实验组(n=51)。对照组患者给予美托洛尔,初始剂量为6.25mg/d,逐渐增加至目标剂量25mg/d。实验组患者在对照组治疗的基础上,每天一次静脉滴注40mgdbcAMP-Ca。两组均治疗4周。对临床治疗的有效反应率(达到显着效果的病例数和达到某些效果的病例数除以该组中的总病例数)被定义为主要结果指标。次要指标包括心功能,心率变异性,锻炼能力,血液流变学,心肌损伤指标,炎症指标,以及不良反应的发生。
    实验组临床治疗有效率高于对照组(94.12%[48/51]vs.78.43%[40/51],P<0.05)。治疗后,实验组左心室舒张末期和收缩末期尺寸(LVEDD和LVESD)和室间隔厚度(IVS)均低于对照组,实验组左室射血分数(LVEF)和每搏输出量(SV)均高于对照组(P<0.05)。在治疗后的心率变异性方面,所有正常到正常间隔的标准偏差/所有正常到正常间隔的平均值(SDNN/SDANN),NN50在正常到正常间隔总数中的百分比(PNN50%),试验组相邻正常与正常间期之间的差异均方根/连续R-R间期的均方根差异(RMSSD)均高于对照组(P<0.05)。在治疗后的运动能力方面,实验组受试者在6min步行试验中的距离大于对照组(P<0.05)。在治疗后的血液流变学指标方面,血小板聚集率(PAgT),纤维蛋白原(FIB),红细胞沉降率(ESR),实验组全血黏度(ηb)低于对照组(P<0.05)。治疗后的心肌损伤指标,实验组血清N末端脑钠肽前体(NT-proBNP)和肌钙蛋白I(cTnI)水平低于对照组,实验组胰岛素样生长因子1(IGF-1)和心肌营养素1(CT-1)水平高于对照组(P<0.05)。在治疗后的炎症指标方面,白细胞介素-6(IL-6)的水平,高敏C反应蛋白(hs-CRP),实验组肿瘤坏死因子-α(TNF-α)水平低于对照组(P<0.05)。试验组不良反应发生率(9.80%)与对照组(7.84%)比较,差异无统计学意义(P>0.05)。
    除美托洛尔外,使用dbcAMP-Ca可有效改善心功能,心率变异性,和运动耐力,同时抑制老年心力衰竭合并心律失常患者的炎症反应,用药安全性高。与单独使用美托洛尔相比,联合用药显示出更好的安全性和治疗效果。
    UNASSIGNED: To explore the effect and safety of calcium dibutyryl adenosine cyclophosphate (dbcAMP-Ca) combined with metoprolol in the treatment of older adults with heart failure combined with arrhythmia.
    UNASSIGNED: A total of 102 elderly patients with heart failure combined with arrhythmia were enrolled in our hospital between February 2021 and April 2023. The list of patients enrolled was entered into a random database by independent staffs not involved in the study and random assignment sequences were generated by the SAS9.4 software. Then, the 102 elderly patients were divided into a control group ( n=51) and an experimental group ( n=51). Patients in the control group were given metoprolol at an initial dose of 6.25 mg/d, which was gradually increased to the target dose of 25 mg/d. Patients in the experimental group were given 40 mg of dbcAMP-Ca once a day via intravenous drip in addition to the treatment given to the control group. Both groups were treated for 4 weeks. The rate of effective response to clinical treatment (the number of cases achieving significant effects and those achieving some effects divided by the total number of cases in the group) was defined as the main outcome index. Secondary indexes included cardiac function, heart rate variability, exercise ability, hemorheology, myocardial injury indexes, inflammatory indexes, and the occurrence of adverse reactions.
    UNASSIGNED: The rate of effective response to clinical treatment was higher in the experimental group than that in the control group (94.12% [48/51] vs. 78.43% [40/51], P<0.05). After treatment, the left ventricular end-diastolic and end-systolic dimensions (LVEDD and LVESD) and the interventricular septal thickness (IVS) were lower in the experimental group than those in the control group, while the left ventricular ejection fraction (LVEF) and the stroke volume (SV) were higher in the experimental group than those in the control group ( P<0.05). In terms of heart rate variability after treatment, the standard deviation of all the normal-to-normal intervals/the average of all the normal-to-normal intervals (SDNN/SDANN), the percentage of NN50 in the total number of normal-to-normal intervals (PNN50%), and the root mean square of the differences between adjacent normal-to-normal intervals/root mean square differences of successive R-R intervals (RMSSD) were higher in the experimental group than those in the control group ( P<0.05). In terms of exercise capacity after treatment, the subjects in the experimental group covered more distance in the 6-min walk test than those in the control group did ( P<0.05). In terms of the hemorheology indexes after treatment, the levels of platelet aggregation rate (PAgT), fibrinogen (FIB), erythrocyte sedimentation rate (ESR), and whole blood viscosity (ηb) were lower in the experimental group than those in the control group ( P<0.05). In terms of the myocardial injury indexes after treatment, the levels of serum N-terminal pro-brain natriuretic peptide (NT-pro BNP) and cardiac troponin I (cTnI) were lower in the experimental group than those in the control group, while the levels of insulin-like growth factor 1 (IGF-1) and cardiotrophin 1 (CT-1) were higher in the experimental group than those in the control group ( P<0.05). In terms of the inflammatory indexes after treatment, the levels of interleukin-6 (IL-6), high-sensitive C-reactive protein (hs-CRP), and tumor necrosis factor-α (TNF-α) were lower in the experimental group than those in the control group ( P<0.05). The incidence of adverse reactions in the experimental group (9.80%) and that in the control group (7.84%) were comparable ( P>0.05).
    UNASSIGNED: The use of dbcAMP-Ca in addition to metoprolol can effectively improve cardiac function, heart rate variability, and exercise tolerance, while inhibiting inflammatory response in elderly patients with heart failure combined with arrhythmia, with high medication safety. The combination medication shows better safety and therapeutic effects than those of metoprolol used alone.
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  • 文章类型: Journal Article
    抗磷脂综合征(APS)是一种以动脉或静脉血栓形成为特征的全身性自身免疫综合征,妊娠并发症和血小板减少症。本研究旨在探讨北京大学人民医院患者APS与心房颤动(AF)的关系。进行单中心回顾性研究。病例为心脏病专家诊断为房颤的住院患者,而对照组患者未出现心脏病。研究结果表明,在多变量逻辑回归中,APS,抗心磷脂抗体(aCL)阳性和抗β-2-糖蛋白抗体(抗β2GPI)阳性是房颤的独立危险因素。APS,aCL阳性和抗β2GPI阳性在AF患者和非AF患者之间有统计学差异。接下来的研究需要阐明APS和AF之间的潜在联系。
    Antiphospholipid syndrome (APS) is a systemic autoimmune syndrome characterized by arterial or venous thrombosis, pregnancy complications and thrombocytopenia. The aim of this study is to investigate the association between APS and atrial fibrillation (AF) among patients in Peking University People\'s Hospital. A single center retrospective study was conducted. Cases were hospitalized patients diagnosed with AF by a cardiologist while the control group patients did not exhibit cardiac diseases. The results of the study revealed that in multivariable logistic regression, APS, anticardiolipin antibody (aCL) positivity and anti-beta-2-glycoprotein antibody (anti-β2GPI) positivity are independent risk factors of AF. APS, aCL positivity and anti-β 2GPI positivity are statistically different between AF patients and non-AF patients. Forthcoming studies are needed to clarify the potential link between APS and AF.
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  • 文章类型: Journal Article
    心律失常治疗是一项临床挑战,需要更安全和更有效的治疗方法。最近的研究强调了围联的作用,富含电压门控钠通道的插层圆盘纳米结构域,包括Nav1.5和β1亚基,毗邻间隙连接。这些发现提供了对心脏动作电位传导的见解。一种19个氨基酸的SCN1B(β1/β1B)模拟肽,βadp1,破坏VGSCβ亚基介导的心脏附着性,诱导心律失常性变化。我们旨在探索βadp1的机制,并开发影响β1介导的粘附的新型SCN1B模拟肽。在新生大鼠心肌细胞中使用膜片钳测定法和β1表达细胞中的电细胞底物阻抗传感(ECIS),我们观察到βadp1维持抑制作用长达5小时。基于βadp1羧基末端的较短肽(LQLEED)模拟了这种抑制作用,而含有重复LQLEED序列的二聚体肽在较长时间的过程中矛盾地促进细胞间粘附。此外,我们发现这些肽与β1调节的膜内蛋白水解(RIP)之间存在联系,RIP是影响基因转录的信号通路,包括VGSC亚基。βadp1在48h内连续增加RIP,而二聚体激动剂急剧增强RIP长达6小时。在DAPT的存在下,一种RIP抑制剂,βadp1对ECIS测量的细胞间粘附的影响降低,提示RIP与肽的抑制作用之间的关系。总之,据报道,新型SCN1B(β1/β1B)模拟肽具有调节细胞间VGSCβ1介导的粘附的潜力,可能通过β1RIP。这些发现为开发针对外周的抗心律失常药物提供了途径。
    Cardiac arrhythmia treatment is a clinical challenge necessitating safer and more effective therapies. Recent studies have highlighted the role of the perinexus, an intercalated disc nanodomain enriched in voltage-gated sodium channels including both Nav1.5 and β1 subunits, adjacent to gap junctions. These findings offer insights into action potential conduction in the heart. A 19-amino acid SCN1B (β1/β1B) mimetic peptide, βadp1, disrupts VGSC beta subunit-mediated adhesion in cardiac perinexii, inducing arrhythmogenic changes. We aimed to explore βadp1\'s mechanism and develop novel SCN1B mimetic peptides affecting β1-mediated adhesion. Using patch clamp assays in neonatal rat cardiomyocytes and electric cell substrate impedance sensing (ECIS) in β1-expressing cells, we observed βadp1 maintained inhibitory effects for up to 5 h. A shorter peptide (LQLEED) based on the carboxyl-terminus of βadp1 mimicked this inhibitory effect, while dimeric peptides containing repeated LQLEED sequences paradoxically promoted intercellular adhesion over longer time courses. Moreover, we found a link between these peptides and β1-regulated intramembrane proteolysis (RIP) - a signaling pathway effecting gene transcription including that of VGSC subunits. βadp1 increased RIP continuously over 48 h, while dimeric agonists acutely boosted RIP for up to 6 h. In the presence of DAPT, an RIP inhibitor, βadp1\'s effects on ECIS-measured intercellular adhesion was reduced, suggesting a relationship between RIP and the peptide\'s inhibitory action. In conclusion, novel SCN1B (β1/β1B) mimetic peptides are reported with the potential to modulate intercellular VGSC β1-mediated adhesion, potentially through β1 RIP. These findings suggest a path towards the development of anti-arrhythmic drugs targeting the perinexus.
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  • 文章类型: Journal Article
    小儿肥厚型心肌病(HCM)患者的运动压力测试(EST)在大型异质性队列中尚未得到很好的描述。
    本研究的目的是确定EST在小儿HCM中的临床应用。
    这是对2000年1月1日至2019年1月1日期间患有EST的21岁以下HCM患者的回顾性单中心分析。临床,人口特征,和EST数据进行了分析,在研究期间或事件发生之前,使用具有主要结局的受试者的最后一个EST。主要复合终点包括心脏死亡,移植,或需要植入心脏复律除颤器的心律失常。使用Cox比例风险模型进行结果分析。
    该研究队列包括140名患者,52%具有公认的遗传变异。由于安全问题,有2项测试中止(ST段变化,心室异位)。首次EST的中位年龄为13.6岁。百分之九十的患者使用周期测功进行了测试,44%的患者服用β受体阻滞剂。峰值耗氧量中位数为37.1mL/kg/min(IQR:12.5mL/kg/min)或预测的81.2%,平均无氧阈值为21.8mL(IQR:8.3mL),峰值功率中位数为2.6±1.1W/kg,预测值为73.7%。44%的患者在EST期间出现异位,8%的人对运动有异常的血压反应。12例患者达到终点。任何程度的异位的存在都是复合终点的预测因子(风险比:5.8;95%CI:1.3-26.7)。
    EST对某些患有HCM的儿科患者具有临床有用性。EST的异位性是心脏死亡的危险因素,心脏移植,和心律失常需要植入式心脏复律除颤器。
    UNASSIGNED: Exercise stress testing (EST) in pediatric hypertrophic cardiomyopathy (HCM) patients has not well described in a large heterogenous cohort.
    UNASSIGNED: The objective of the study was to determine the clinical utility of EST in pediatric HCM.
    UNASSIGNED: This was a retrospective single-center analysis of HCM patients younger than 21 years who had EST between January 1, 2000, and January 1, 2019. Clinical, demographic characteristics, and EST data were analyzed, using the last EST during the study or prior to the event in subjects with a primary outcome. The primary composite endpoint included cardiac death, transplant, or arrhythmia requiring implantable cardioverter-defibrillator placement. Outcome analysis was performed using Cox proportional hazard modeling.
    UNASSIGNED: The study cohort included 140 patients, 52% with a recognized genetic variant. There were 2 tests aborted due to safety concerns (ST-segment changes, ventricular ectopy). The median age at first EST was 13.6 years. Ninety percent of patients were tested using cycle ergometry, and 44% were on a beta-blocker. The median peak oxygen consumption was 37.1 mL/kg/min (IQR: 12.5 mL/kg/min) or 81.2% predicted, the mean anaerobic threshold was 21.8 Ml (IQR: 8.3 mL), and the median peak power was 2.6 ± 1.1 W/kg or 73.7% predicted. Ectopy during EST was seen in 44% of patients, and 8% had an abnormal blood pressure response to exercise. The endpoint was reached in 12 patients. The presence of any degree of ectopy was a predictor of the composite endpoint (hazard ratio: 5.8; 95% CI: 1.3-26.7).
    UNASSIGNED: EST is clinically useful in select pediatric patients with HCM. Ectopy on EST is a risk factor for cardiac death, cardiac transplant, and arrhythmias requiring implantable cardioverter-defibrillator.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    心律失常的全球发病率和患病率不断增加。然而,潜在心律失常发生的确切机制和有效治疗的最佳措施仍未完全了解。血红素加氧酶的可诱导形式,被称为血红素加氧酶-1(HO-1),被认为是能够发挥抗炎和抗凋亡作用的有效抗氧化剂分子。最近的研究表明,HO-1通过减轻心脏重塑在预防心律失常中起作用。包括电气改造,离子重塑,和结构重塑。这篇综述旨在巩固目前有关HO-1参与心律失常的知识,并阐明其潜在的作用机制。
    The global incidence and prevalence of arrhythmias are continuously increasing. However, the precise mechanisms of underlying arrhythmogenesis and the optimal measures for effective treatment remain incompletely understood. The inducible form of heme oxygenase, known as heme oxygenase-1 (HO-1), is recognized as a potent antioxidant molecule capable of exerting anti-inflammatory and anti-apoptotic effects. Recent research indicates that HO-1 plays a role in preventing arrhythmias by mitigating cardiac remodeling, including electrical remodeling, ion remodeling, and structural remodeling. This review aimed to consolidate current knowledge regarding the involvement of HO-1 in arrhythmias and elucidate its underlying mechanisms of action.
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  • 文章类型: Journal Article
    目的:本研究旨在解决使用心电图(ECG)进行不平衡心跳分类的挑战。在这个提出的新颖的深度学习方法中,重点是准确识别以ECG数据显着失衡为特征的少数群体。&#xD;&#xD;方法:我们提出了一种通过动态少数群体偏置批量加权损失函数增强的特征融合神经网络。该网络包括三个专门的分支:完整的ECG数据分支,用于全面查看ECG信号,本地QRS波分支,用于QRS波群的详细特征,和R波信息分支分析R波特征。该结构被设计为提取ECG数据的不同方面。动态损失函数优先考虑少数类,同时保持对多数类的识别,在不改变原始数据分布的情况下调整网络的学习重点。一起,这种融合结构和自适应损失函数显著提高了网络区分各种心跳类别的能力,提高了少数民族阶级识别的准确性。&#xD;&#xD;主要结果:所提出的方法在MIT-BIH数据集中展示了平衡的性能,尤其是少数民族。在患者内部范式下,准确性,灵敏度,特异性,室上性异位搏动的阳性预测值(PPV)为99.63%,93.62%,99.81%,92.98%,分别,融合节拍为99.76%,85.56%,99.87%,和84.16%,分别。在患者间范式下,这些指标是96.56%,89.16%,96.84%,室上性异位搏动为51.99%,和96.10%,77.06%,96.25%,和13.92%的融合节拍,分别。&#xD;&#xD;意义:该方法有效地解决了ECG数据集中的类不平衡。通过利用不同的ECG信号信息和新颖的损失函数,这种方法为心脏疾病的诊断和治疗提供了有希望的工具. .
    OBJECTIVE: This study aims to address the challenges of imbalanced heartbeat classification using electrocardiogram (ECG). In this proposed novel deep-learning method, the focus is on accurately identifying minority classes in conditions characterized by significant imbalances in ECG data. Approach: We propose a Feature Fusion Neural Network enhanced by a Dynamic Minority-Biased Batch Weighting Loss Function. This network comprises three specialized branches: the Complete ECG Data Branch for a comprehensive view of ECG signals, the Local QRS Wave Branch for detailed features of the QRS complex, and the R Wave Information Branch to analyze R wave characteristics. This structure is designed to extract diverse aspects of ECG data. The dynamic loss function prioritizes minority classes while maintaining the recognition of majority classes, adjusting the network\'s learning focus without altering the original data distribution. Together, this fusion structure and adaptive loss function significantly improve the network\'s ability to distinguish between various heartbeat classes, enhancing the accuracy of minority class identification. Main Results: The proposed method demonstrated balanced performance within the MIT-BIH dataset, especially for minority classes. Under the intra-patient paradigm, the accuracy, sensitivity, specificity, and positive predictive value (PPV) for Supraventricular ectopic beat were 99.63%, 93.62%, 99.81%, and 92.98%, respectively, and for Fusion beat were 99.76%, 85.56%, 99.87%, and 84.16%, respectively. Under the inter-patient paradigm, these metrics were 96.56%, 89.16%, 96.84%, and 51.99% for Supraventricular ectopic beat, and 96.10%, 77.06%, 96.25%, and 13.92% for Fusion beat, respectively. Significance: This method effectively addresses the class imbalance in ECG datasets. By leveraging diverse ECG signal information and a novel loss function, this approach offers a promising tool for aiding in the diagnosis and treatment of cardiac conditions. .
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  • 文章类型: Journal Article
    背景:兰地洛,具有短半衰期(2.4-4分钟)的高心脏选择性药物,通常用作灌注器或推注应用来治疗心动过速性心律失常。一些小型研究表明,先前口服β受体阻滞剂的使用会导致对静脉β受体阻滞剂的有效反应。方法:这项研究调查了在患有急性心动过速性心律失常的重症监护患者中,先前的慢性口服β受体阻滞剂(Lβ)或先前没有慢性口服β受体阻滞剂(L-)的摄入是否会影响静脉推注剂量兰地洛尔的反应。结果:分析了30例患者(67[55-72]年)的疗效,10人(33.3%)和20人(66.7%)没有口服β受体阻滞剂治疗。14例患者的心律失常被诊断为心动过速性心房颤动,非流体依赖性,室上性心动过速16例。成功控制心率(Lβ4与L-7,p=1.00)和节律控制(Lβ3与L-6,p=1.00)在两组之间没有显着差异。在推注给药前后比较,两组均显示心率显着降低,两组间无显著差异(Lβ-26/minvs.L--33/min,p=0.528)。口服β受体阻滞剂治疗也不影响兰地洛尔推注后平均动脉血压的变化(Lβ-5mmHg与L--4mmHg,p=0.761)。结论:先前长期摄入β受体阻滞剂既不会影响推动剂量兰地洛尔在心率或心律控制中的有效性,也不会影响兰地洛尔推注前后心率或平均动脉血压的差异。
    Background: Landiolol, a highly cardioselective agent with a short half-life (2.4-4 min), is commonly used as a perfusor or bolus application to treat tachycardic arrhythmia. Some small studies suggest that prior oral β-blocker use results in a less effective response to intravenous β-blockers. Methods: This study investigated whether prior chronic oral β-blocker (Lβ) or no prior chronic oral β-blocker (L-) intake influences the response to intravenous push-dose Landiolol in intensive care patients with acute tachycardic arrhythmia. Results: The effects in 30 patients (67 [55-72] years) were analyzed, 10 (33.3%) with and 20 (66.7%) without prior oral β-blocker therapy. Arrhythmias were diagnosed as tachycardic atrial fibrillation in 14 patients and regular, non-fluid-dependent, supraventricular tachycardia in 16 cases. Successful heart rate control (Lβ 4 vs. L- 7, p = 1.00) and rhythm control (Lβ 3 vs. L- 6, p = 1.00) did not significantly differ between the two groups. Both groups showed a significant decrease in heart rate when comparing before and after the bolus administration, without significant differences between the two groups (Lβ -26/min vs. L- -33/min, p = 0.528). Oral β-blocker therapy also did not influence the change in mean arterial blood pressure after Landiolol bolus administration (Lβ -5 mmHg vs. L- -4 mmHg, p = 0.761). Conclusions: A prior chronic intake of β-blockers neither affected the effectiveness of push-dose Landiolol in heart rate or rhythm control nor impacted the difference in heart rate or mean arterial blood pressure before and after the Landiolol boli.
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  • 文章类型: Journal Article
    背景:输血依赖性β地中海贫血(TDβT)的现代治疗方法使患者在没有铁过载的情况下达到了较高的预期寿命。尽管生存有所改善,心房颤动(AF)已成为相关问题。TDβT的AF病理生理学和特征与普通人群不同。心外膜脂肪组织(EAT)可能起作用,但尚未探讨其与TDβT患者AF的关系。方法:单中心,横断面研究,连续招募TDβT患者。磁共振评估心外膜脂肪组织(EAT)。研究了有和没有房颤史的患者的特征。分析与房颤患病率相关的独立因素。结果:共纳入116例患者。所有患者均接受常规螯合治疗。房颤患病率为29.3%(34/116)。有和没有AF的患者之间的心脏T2*和肝脏铁浓度没有差异。房颤患者左心房EAT厚度明显增高,右心房和右心室(5.0vs.4.0mm,p<0.01,4.4vs.4.0,p=0.02和5.0与4.3,p=0.04)。房颤患者年龄较大,(53vs.49年,p<0.01),更多甲状腺功能减退(44.1vs.20.7%,p=0.01),肺动脉高压(23.5vs.2.4%p<0.01),脾切除术(88.2vs.64.6%,p=0.01),右心房和左心房容积较高(61vs.40和74vs.43mL,两者p<0.01)。在多变量分析中,甲状腺功能减退,左心房容积和左心房EAT与房颤独立相关(比值比分别为9.95,1.09和1.91).结论:在TDβT患者的当代队列中,用常规的螯合疗法治疗,房颤的患病率与铁超负荷无关.EAT与房颤独立相关。
    Background: Modern treatments for transfusion-dependent β-thalassemia (TDβT) have allowed patients to reach high life expectancy with no iron overload. Despite survival improvement, atrial fibrillation (AF) has emerged as a relevant issue. AF pathophysiology and characteristics in TDβT are different than in the general population. Epicardial adipose tissue (EAT) may play a role but its relationship with AF in patients with TDβT has not been explored. Methods: A monocentric, cross-sectional study, enrolling consecutive patients with TDβT. Epicardial adipose tissue (EAT) was evaluated at magnetic resonance. Characteristics of patients with and without history of AF were investigated. Factors independently associated with AF prevalence were analyzed. Results: A total of 116 patients were enrolled. All patients were treated with regular chelation therapy. The prevalence of AF was 29.3% (34/116). Cardiac T2* and liver iron concentration were no different between patients with and without AF. EAT thickness was significantly higher in patients with AF at left atrium, right atrium and right ventricle (5.0 vs. 4.0 mm, p < 0.01, 4.4 vs. 4.0, p = 0.02 and 5.0 vs. 4.3, p = 0.04). Patients with AF presented with older age, (53 vs. 49 years, p < 0.01), more hypothyroidism (44.1 vs. 20.7%, p = 0.01), pulmonary hypertension (23.5 vs. 2.4% p < 0.01), splenectomy (88.2 vs. 64.6%, p = 0.01), higher right and left atrial volume (61 vs. 40 and 74 vs. 43 mL, both p < 0.01). At multivariable analysis, hypothyroidism, left atrial volume and left atrial EAT were independently associated with AF (odds ratio 9.95, 1.09 and 1.91, respectively). Conclusions: In a contemporary cohort of patients with TDβT, treated with regular chelation therapy, prevalence of AF was unrelated to iron overload. EAT was independently associated with AF.
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  • 文章类型: Journal Article
    尽管严重急性呼吸衰竭是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的发病和死亡的主要原因,这种病毒感染会导致一些人的心血管疾病。该病毒的心脏效应包括心肌炎,心包炎,心律失常,冠状动脉瘤和心肌病,并可导致心源性休克和多系统器官衰竭。
    这篇综述总结了SARS-CoV-2在儿科人群中的心脏表现。我们对与急性冠状病毒病2019(COVID-19)感染相关的心血管疾病进行了范围审查,儿童多系统炎症综合征(MIS-C),和mRNACOVID-19疫苗。还检查了儿科运动员的特殊考虑因素,并在COVID-19感染后重返赛场。
    出现急性COVID-19的儿童应进行心功能不全筛查,并获得全面的病史。在心律失常的任何体征/症状后,应考虑进一步的心血管评估。低心输出量,和/或心肌心包炎。严重急性COVID-19入院的患者应进行连续心脏监测。实验室测试,如临床所示,包括肌钙蛋白和B型利钠肽或N末端前脑利钠肽的测试。超声心动图与应变评估和/或心脏磁共振成像应考虑评估舒张和收缩功能障碍。冠状动脉解剖学,心包和心肌.对于MIS-C患者,静脉注射免疫球蛋白和糖皮质激素联合治疗是安全和潜在的疾病改变.MIS-C的治疗靶向超免疫应答。支持性护理,包括机械支撑,在某些情况下是需要的。
    心血管疾病是SARS-CoV-2感染的一个显著特征。大多数婴儿,患有COVID-19心脏病的儿童和青少年完全康复,没有持续的心功能障碍。然而,需要进行长期研究和进一步研究,以评估SARS-CoV-2变种的心血管风险,并了解COVID-19导致心功能不全的病理生理学.
    UNASSIGNED: Although severe acute respiratory failure is the primary cause of morbidity and mortality in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, this viral infection leads to cardiovascular disease in some individuals. Cardiac effects of the virus include myocarditis, pericarditis, arrhythmias, coronary aneurysms and cardiomyopathy, and can result in cardiogenic shock and multisystem organ failure.
    UNASSIGNED: This review summarises cardiac manifesta-tions of SARS-CoV-2 in the paediatric population. We performed a scoping review of cardiovascular disease associated with acute coronavirus disease 2019 (COVID-19) infection, multisystem inflammatory syndrome in children (MIS-C), and mRNA COVID-19 vaccines. Also examined are special considerations for paediatric athletes and return to play following COVID-19 infection.
    UNASSIGNED: Children presenting with acute COVID-19 should be screened for cardiac dysfunction and a thorough history should be obtained. Further cardiovascular evaluation should be considered following any signs/symptoms of arrhythmias, low cardiac output, and/or myopericarditis. Patients admitted with severe acute COVID-19 should be monitored with continuous cardiac monitoring. Laboratory testing, as clinically indicated, includes tests for troponin and B-type natriuretic peptide or N-terminal pro-brain natriuretic peptide. Echocardiography with strain evaluation and/or cardiac magnetic resonance imaging should be considered to evaluate diastolic and systolic dysfunction, coronary anatomy, the pericardium and the myocardium. For patients with MIS-C, combination therapy with intravenous immunoglobulin and glucocorticoid therapy is safe and potentially disease altering. Treatment of MIS-C targets the hyperimmune response. Supportive care, including mechanical support, is needed in some cases.
    UNASSIGNED: Cardiovascular disease is a striking feature of SARS-CoV-2 infection. Most infants, children and adolescents with COVID-19 cardiac disease fully recover with no lasting cardiac dysfunction. However, long-term studies and further research are needed to assess cardiovascular risk with variants of SARS-CoV-2 and to understand the pathophysiology of cardiac dysfunction with COVID-19.
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