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Pregnancy-related cardiovascular conditions and outcomes in a United States Medicaid population 美国医疗补助人群的妊娠相关心血管疾病和结局
Pub Date : 2022-04-13 DOI: 10.1136/heartjnl-2021-320684
S. Marschner, A. von Huben, S. Zaman, H. Reynolds, V. W. Lee, P. Choudhary, L. Mehta, C. Chow
Objective This study aims to examine the incidence of pregnancy-related cardiometabolic conditions and severe cardiovascular outcomes, and their relationship in US Medicaid-funded women. Methods Medicaid is a government-sponsored health insurance programme for low-income families in the USA. We report the incidence of pregnancy-related cardiometabolic conditions (hypertensive disorders and diabetes in, or complicated by, pregnancy) and severe cardiovascular outcomes (myocardial infarction, stroke, acute heart failure, cardiomyopathy, cardiac arrest, ventricular fibrillation, ventricular tachycardia, aortic dissection/aneurysm and peripheral vascular disease) among Medicaid-funded women with a birth (International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) diagnosis code O80 or O82) over the period January 2015–June 2019, from the states of Georgia, Ohio and Indiana. In this cross-sectional cohort, we examined the relationship between pregnancy-related cardiometabolic conditions and severe cardiovascular outcomes from pregnancy through to 60 days after birth using multivariable models. Results Among 74 510 women, mean age 26.4 years (SD 5.5), the incidence per 1000 births of pregnancy-related cardiometabolic conditions was 224.3 (95% CI 221.3 to 227.3). The incidence per 1000 births of severe cardiovascular conditions was 10.8 (95% CI 10.1 to 11.6). Women with pregnancy-related cardiometabolic conditions were at greater risk of having a severe cardiovascular condition with an age-adjusted OR of 3.1 (95% CI 2.7 to 3.5). Conclusion This US cohort of Medicaid-funded women have a high incidence of severe cardiovascular conditions during pregnancy. Cardiometabolic conditions of pregnancy conferred threefold higher odds of severe cardiovascular outcomes.
目的本研究旨在探讨美国医疗补助妇女妊娠相关心脏代谢疾病和严重心血管结局的发生率及其关系。方法医疗补助是美国政府资助的一项针对低收入家庭的医疗保险计划。我们报告了在接受医疗补助的分娩妇女中与妊娠相关的心脏代谢疾病(妊娠期高血压疾病和糖尿病或妊娠并发症)和严重心血管结局(心肌梗死、中风、急性心力衰竭、心肌病、心脏骤停、心室颤动、室性心动过速、主动脉夹层/动脉瘤和外周血管疾病)的发生率(《国际疾病分类》第十版)。2015年1月至2019年6月期间的临床修改(ICD-10-CM)诊断代码O80或O82,来自乔治亚州、俄亥俄州和印第安纳州。在这个横断面队列中,我们使用多变量模型检查了妊娠相关的心脏代谢状况与妊娠至出生后60天严重心血管结局之间的关系。结果在74510名女性中,平均年龄26.4岁(SD 5.5),每1000个新生儿中与妊娠相关的心脏代谢疾病的发生率为224.3 (95% CI 221.3至227.3)。每1000个新生儿中严重心血管疾病的发生率为10.8 (95% CI 10.1 - 11.6)。患有妊娠相关心脏代谢疾病的妇女患严重心血管疾病的风险更高,经年龄调整的OR为3.1 (95% CI为2.7至3.5)。结论:美国医疗补助女性在怀孕期间严重心血管疾病的发生率很高。妊娠期间的心脏代谢状况使发生严重心血管疾病的几率增加了三倍。
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引用次数: 6
Coronary vasospasm and future percutaneous coronary intervention: relax 冠状动脉血管痉挛与未来经皮冠状动脉介入治疗:放松
Pub Date : 2022-04-12 DOI: 10.1136/heartjnl-2022-320974
M. McDermott, R. Bing
A clinical diagnosis of suspected angina that is accompanied by non- obstructive epicardial coronary artery disease is not uncommon, as evidenced by results from contemporary registries and trials of anatomical testing in chest pain. The basket labelled as angina with non-obstructive coronary artery disease (ANOCA—the clinical syndrome that may or may not accompany ischaemia with non- obstructive coronary artery disease (INOCA)) contains heterogeneous patho-physiological entities which vary in clinical presentation and adjunctive investigation findings. 1 One distinct entry in this field is vasospastic angina, a dynamic phenomenon with characteristic symptoms that differ from those induced by fixed epicardial coronary artery stenoses. Although the seminal case series which provided the eponymous nomen-clature for this clinical syndrome was published well before many (probably most) readers of Heart were born, attempts to codify and standardise defini-tions for vasospastic angina have only recently been promulgated. 2 The syndrome is seen in only a small propor-tion of patients with chest pain, with correspondingly limited sections in current guidelines. 3 4 The diagnostic process can be difficult and the clinical course uncertain. The latter is salient, events. 5
疑似心绞痛并伴有非阻塞性心外膜冠状动脉疾病的临床诊断并不罕见,当代胸痛解剖试验的结果证明了这一点。标记为心绞痛合并非阻塞性冠状动脉疾病(anoca -可能或可能不伴有缺血性非阻塞性冠状动脉疾病(INOCA)的临床综合征)的篮子包含异质性的病理生理实体,其临床表现和辅助调查结果各不相同。1血管痉挛性心绞痛是该领域的一个独特的切入点,它是一种动态现象,其特征症状不同于固定心外膜冠状动脉狭窄引起的心绞痛。尽管在许多(可能是大多数)《心脏》杂志的读者出生之前,为这种临床综合征提供同名命名的开创性病例系列就已经出版了,但对血管痉挛性心绞痛的定义进行编纂和标准化的尝试直到最近才被公布。2该综合征仅见于一小部分胸痛患者,在现行指南中相应的分级也有限。诊断过程可能很困难,临床病程也不确定。后者是突出的事件。5
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引用次数: 1
Cardiac resynchronisation therapy with or without a defibrillator: individualising device prescription 心脏再同步治疗有或没有除颤器:个体化设备处方
Pub Date : 2022-04-11 DOI: 10.1136/heartjnl-2022-320909
S. Straw, W. Mullens, K. Witte
Cardiac resynchronisation therapydefibrillators (CRTD) would seem the obvious choice for patients with heart failure with reduced ejection fraction, given implantable cardioverter defibrillators (ICD) reduce the risk of sudden cardiac death in this population. However, despite decades of discussion, COMPANION (Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure) remains the only trial to include both CRTD and CRTpacemakers (CRTP) in which outcomes between the two approaches were similar.
心脏再同步除颤器(CRTD)似乎是射血分数降低的心力衰竭患者的明显选择,因为植入式心律转复除颤器(ICD)可以降低这类人群心源性猝死的风险。然而,尽管经过了几十年的讨论,COMPANION(心脏衰竭的药物治疗、起搏和除颤的比较)仍然是唯一一项同时纳入CRTD和CRTpacemakers (CRTP)的试验,两种方法的结果相似。
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引用次数: 2
Clinical outcomes in spontaneous coronary artery dissection 自发性冠状动脉夹层的临床结果
Pub Date : 2022-04-11 DOI: 10.1136/heartjnl-2022-320830
M. García-Guimarães, M. Masotti, R. Sanz-Ruiz, F. Macaya, G. Roura, J. Nogales, H. Tizón-Marcos, Maite Velázquez-Martín, G. Veiga, X. Flores-Ríos, Omar Abdul-Jawad Altisent, M. Jiménez-Kockar, S. Camacho-Freire, J. Moreu, S. Ojeda, S. Santos-Martínez, A. Sanz-García, D. del Val, T. Bastante, F. Alfonso
Objective Spontaneous coronary artery dissection (SCAD) is an infrequent cause of acute coronary syndrome. Our aim was to assess adverse events at follow-up from a nationwide prospective cohort. Methods The Spanish Registry on SCAD (SR-SCAD) included patients from 34 hospitals. All coronary angiograms were analysed by two experts. Those cases with doubts regarding the diagnosis of SCAD were excluded. The angiographic SCAD classification by Saw et al was followed. Major adverse cardiovascular and cerebrovascular event (MACCE) was predefined as composite of death, myocardial infarction, unplanned revascularisation, SCAD recurrence or stroke. All events were assigned by a Clinical Events Committee. Results After corelab evaluation, 389 patients were included. Most patients were women (88%); median age 53 years (IQR 47–60). Most patients presented as non-ST-segment-elevation myocardial infarction (54%). A type 2 intramural haematoma (IMH) was the most frequent angiographic pattern (61%). A conservative initial management was selected in 78% of patients. At a median time of follow-up of 29 months (IQR 17–38), 46 patients (13%) presented MACCE, mainly driven by reinfarctions (7.6%) and unplanned revascularisations (6.2%). Previous history of hypothyroidism (HR 3.79; p<0.001), proximal vessel involvement (HR 2.69; p=0.009), type 2 IMH (HR 2.12; p=0.037) and dual antiplatelet therapy (DAPT) at discharge (HR 2.18; p=0.042) were independent predictors of MACCE. Conclusions In this large prospective cohort of patients with SCAD, prognosis was overall favourable, with events mainly driven by reinfarctions or unplanned revascularisations. History of hypothyroidism, proximal vessel involvement, type 2 IMH and DAPT at discharge were associated with MACCE. Trial registration number NCT03607981.
目的自发性冠状动脉夹层(SCAD)是急性冠状动脉综合征的罕见病因。我们的目的是评估全国前瞻性队列随访时的不良事件。方法西班牙SCAD登记处(SR-SCAD)包括来自34家医院的患者。两位专家对所有冠状动脉造影照片进行了分析。那些对SCAD的诊断有疑问的病例被排除在外。遵循Saw等人的血管造影SCAD分类。主要心脑血管不良事件(MACCE)被预先定义为死亡、心肌梗死、计划外血运重建、SCAD复发或中风的复合事件。所有事件均由临床事件委员会指定。结果经corelab评估,共纳入389例患者。大多数患者为女性(88%);中位年龄53岁(IQR 47-60)。大多数患者表现为非ST段抬高型心肌梗死(54%)。2型壁内血肿(IMH)是最常见的血管造影模式(61%)。78%的患者选择了保守的初始治疗。中位随访时间为29个月(IQR 17-38),46名患者(13%)出现MACCE,主要由再梗死(7.6%)和计划外血运重建(6.2%)引起。既往甲状腺功能减退史(HR 3.79;p<0.001)、近端血管受累史(HR 2.69;p=0.009),2型IMH(HR 2.12;p=0.037)和出院时双重抗血小板治疗(DAPT)(HR 2.18;p=0.042)是MACCE的独立预测因素。结论在这个庞大的SCAD患者前瞻性队列中,预后总体良好,事件主要由再梗死或计划外血运重建引起。甲状腺功能减退史、近端血管受累、2型IMH和出院时DAPT与MACCE相关。试验注册号NCT03607981。
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引用次数: 12
Predicting outcome after cardiac resynchronisation therapy defibrillator implantation: the cardiac resynchronisation therapy defibrillator Futility score 心脏再同步治疗除颤器植入后预测结果:心脏再同步疗法除颤器Futility评分
Pub Date : 2022-04-11 DOI: 10.1136/heartjnl-2021-320532
B. Maille, A. Bodin, A. Bisson, J. Herbert, B. Pierre, N. Clementy, Victor Klein, F. Franceschi, J. Deharo, L. Fauchier
Background Risk-benefit for cardiac resynchronisation therapy (CRT) defibrillator (CRT-D) over CRT pacemaker remains a matter of debate. We aimed to identify patients with a poor outcome within 1 year of CRT-D implantation, and to develop a CRT-D Futility score. Methods Based on an administrative hospital-discharge database, all consecutive patients treated with prophylactic CRT-D implantation in France (2010–2019) were included. A prediction model was derived and validated for 1-year all-cause death after CRT-D implantation (considered as futility) by using split-sample validation. Results Among 23 029 patients (mean age 68±10 years; 4873 (21.2%) women), 7016 deaths were recorded (yearly incidence rate 7.2%), of which 1604 (22.8%) occurred within 1 year of CRT-D implantation. In the derivation cohort (n=11 514), the final logistic regression model included—as main predictors of futility—older age, diabetes, mitral regurgitation, aortic stenosis, history of hospitalisation with heart failure, history of pulmonary oedema, atrial fibrillation, renal disease, liver disease, undernutrition and anaemia. Area under the curve for the CRT-D Futility score was 0.716 (95% CI: 0.698 to 0.734) in the derivation cohort and 0.692 (0.673 to 0.710) in the validation cohort. The Hosmer-Lemeshow test had a p-value of 0.57 suggesting accurate calibration. The CRT-D Futility score outperformed the Goldenberg and EAARN scores for identifying futility. Based on the CRT-D Futility score, 15.9% of these patients were categorised at high risk (predicted futility of 16.6%). Conclusions The CRT-D Futility score, established from a large nationwide cohort of patients treated with CRT-D, may be a relevant tool for optimising healthcare decision-making.
背景心脏再同步治疗(CRT)除颤器(CRT-D)相对于CRT起搏器的风险效益仍然存在争议。我们的目标是在1 CRT-D植入的年份,并制定CRT-D功能评分。方法基于行政出院数据库,纳入法国(2010-2019年)所有接受预防性CRT-D植入治疗的连续患者。通过分样本验证,推导并验证了CRT-D植入后1年全因死亡的预测模型(被认为是徒劳的)。结果23 029名患者(平均年龄68±10岁;4873名(21.2%)女性),记录了7016例死亡(年发病率7.2%),其中1604例(22.8%)发生在 CRT-D植入年份。在衍生队列中(n=11 514),最终的逻辑回归模型包括——作为无效的主要预测因素——老年、糖尿病、二尖瓣反流、主动脉狭窄、心力衰竭住院史、肺水肿史、心房颤动史、肾病、肝病、营养不良和贫血。CRT-D无效性评分的曲线下面积在推导队列中为0.716(95%置信区间:0.698至0.734),在验证队列中为0.692(0.673至0.710)。Hosmer-Lemeshow检验的p值为0.57,表明校准准确。CRT-D无效性得分在识别无效性方面优于Goldenberg和EAARN得分。根据CRT-D无效性评分,15.9%的患者被归类为高危患者(预测无效性为16.6%)。
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引用次数: 3
Getting the best from the Heart Team: guidance for cardiac multidisciplinary meetings 从心脏团队获得最佳效果:心脏多学科会议指南
Pub Date : 2022-04-08 DOI: 10.1136/heartjnl-2021-320510
A. Archbold, E. Akowuah, A. Banning, A. Baumbach, P. Braidley, G. Cooper, S. Kendall, P. MacCarthy, P. O'Kane, N. O'Keeffe, B. Shah, Victoria Watt, S. Ray
The purpose of this document is to update the existing joint British Societies recommendations on multidisciplinary meetings (MDMs) published in 2015 to reflect changes in practice. We aim to provide guidance on the structure and function of MDMs which should be taking place in every cardiac surgical centre. Out of scope are MDMs that do not require the routine presence of a cardiac surgeon such as electrophysiology MDMs and those which are not provided in every centre, such as complex aortic surgery.
本文件旨在更新2015年发布的英国学会关于多学科会议(MDM)的现有联合建议,以反映实践中的变化。我们的目标是为MDM的结构和功能提供指导,这应该在每个心脏外科中心进行。不需要心脏外科医生常规在场的MDM(如电生理MDM)和并非每个中心都提供的MDM,如复杂的主动脉手术。
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引用次数: 15
British Societies' recommendations for Heart Team multidisciplinary meetings: broadly relevant principles with anticipated regional differences in process 英国学会对心脏团队多学科会议的建议:具有广泛相关性的原则,预计过程中存在区域差异
Pub Date : 2022-04-08 DOI: 10.1136/heartjnl-2021-320775
B. Lindman, K. Goel
The concept of a Heart Team approach to evaluating patients with cardiovascular disease was fuelled by the Synergy between PCI with Taxus and Cardiac Surgery (SYNTAX) trial for severe coronary artery disease and the Placement of Aortic Transcatheter Valves (PARTNER) trial for aortic stenosis (AS). 2 It was subsequently included as a recommended practice in guidelines for the management of patients with coronary artery disease and AS. Unpacking the rationale, purpose, composition, process and work of the Heart Team has been an evolving process that is being increasingly applied to additional cardiovascular diseases. Professor Ray and working group colleagues provide a consensus statement which outlines guidance from the British Societies regarding the multidisciplinary meetings of the Heart Team to address myocardial revascularisation; aortic, mitral and tricuspid valve disease; and endocarditis (figure 1).
心脏团队方法评估心血管疾病患者的概念是由PCI与Taxus和心脏外科(SYNTAX)试验对严重冠状动脉疾病的协同作用和主动脉瓣狭窄(AS)的放置主动脉导管瓣膜(PARTNER)试验推动的。2随后,它被纳入冠状动脉疾病和as患者管理指南的推荐做法。解开心脏团队的基本原理、目的、组成、流程和工作是一个不断发展的过程,越来越多地应用于其他心血管疾病。Ray教授和工作组同事提供了一份共识声明,其中概述了英国学会关于心脏团队多学科会议的指导,以解决心肌血运重建问题;主动脉瓣、二尖瓣和三尖瓣疾病;心内膜炎(图1)。
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引用次数: 1
Heartbeat: hypertension risk is higher when obesity onset occurs earlier in adult life 心跳:成年期肥胖越早,患高血压的风险越高
Pub Date : 2022-04-07 DOI: 10.1136/heartjnl-2022-321152
C. Otto
The risk of hypertension is higher in adults with an increased body mass index but there is little data on whether weight gain at a younger age is more detrimental than weight gain later in life. In order to address the impact of age of onset of overweight on the subsequent risk of hypertension, Li and colleagues compared 4742 subjects with newonset overweight to 4742 age and sexmatched normal weight controls in an ongoing communitybased prospective cohort in China with a mean followup interval of 5 years. After multivariable adjustment, they observed a stepwise increase in risk of hypertension in younger adults (particularly those less than age 40 years) with no significantly increased risk for those with onset of overweight at age 60 years or older (figure 1). In an editorial, Wong comments on the strengths of this study—large sample size, serial measurements, robustness of the data—but also points out the limitations—mostly men (68%), a single occupational class (a mining company), hypertension diagnosis based on a single measurement and lack of outcome data. Wong concludes that ‘These data suggest that prevention efforts aimed at the reduction or delay of overweight and obesity in younger individuals, may significantly impact the onset of hypertension in later life. Whether such an intervention significantly impacts the onset of cardiovascular disease and its related adverse outcomes requires future study.’ In studies based on costs and healthcare delivery in the USA, mitral transcatheter edgetoedge repair (TEER) appears to be costeffective for patients with heart failure with reduced ejection fraction (HFrEF) and severe secondary mitral regurgitation. In this issue of Heart, Cohen and colleagues examined whether mitral TEER in HFrEF patients with severe secondary MR would be costeffective in the NHS healthcare system. Overall, TEER reduced the rate of heart failure hospitalisations and improved survival (figure 2), but costs of TEER were higher than guidelinerecommended medical therapy (GRMT). Even so, the incremental costeffectiveness ratio was
体重指数增加的成年人患高血压的风险更高,但很少有数据表明年轻时的体重增加是否比晚年的体重增加更有害。为了解决超重发病年龄对随后高血压风险的影响,李及其同事在中国进行的基于社区的前瞻性队列中,将4742名新发超重受试者与4742名年龄和性别匹配的正常体重对照者进行了比较,平均随访间隔为5年。经过多变量调整后,他们观察到年轻人(尤其是40岁以下的人)患高血压的风险逐步增加,而60岁或以上超重人群的风险没有显著增加(图1)。在一篇社论中,Wong评论了这项研究的优势——大样本量、连续测量、数据的稳健性——但也指出了局限性——主要是男性(68%)、单一职业类别(矿业公司)、基于单一测量的高血压诊断以及缺乏结果数据。Wong总结道:“这些数据表明,旨在减少或延缓年轻人超重和肥胖的预防措施可能会对晚年高血压的发病产生重大影响。这种干预措施是否会显著影响心血管疾病的发作及其相关的不良后果,需要未来的研究。”在美国基于成本和医疗服务的研究中,二尖瓣经导管边缘修复术(TEER)似乎对射血分数降低(HFrEF)和严重继发性二尖瓣反流的心力衰竭患者具有成本效益。在这期《心脏》杂志上,Cohen及其同事研究了在NHS医疗系统中,患有严重继发性MR的HFrEF患者的二尖瓣TEER是否具有成本效益。总体而言,TEER降低了心力衰竭住院率并提高了生存率(图2),但TEER的成本高于指南推荐的药物治疗(GRMT)。即便如此,增量成本效益比
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引用次数: 1
A strange heart 一颗奇怪的心
Pub Date : 2022-04-07 DOI: 10.1136/heartjnl-2021-320677
Marinha Silva, Vitor Hugo Pereira, Alexandra Sousa
24 Coronel R, Casini S, Koopmann TT, et al. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study. Circulation 2005;112:2769–77. 25 Blok M, Boukens BJ. Mechanisms of arrhythmias in the Brugada syndrome. Int J Mol Sci 2020;21:7051–20. 26 Hoogendijk MGet al. The Brugada ECG pattern a marker of channelopathy, structural heart disease, or neither? Toward a unifying mechanism of the Brugada syndrome. Circ. Arrhythmia Electrophysiol 2010;3:283–90. 27 Catalano O, Antonaci S, Moro G, et al. Magnetic resonance investigations in Brugada syndrome reveal unexpectedly high rate of structural abnormalities. Eur Heart J 2009;30:2241–8. 28 Nademanee K, Raju H, de Noronha SV, et al. Fibrosis, connexin43, and conduction abnormalities in the Brugada syndrome. J Am Coll Cardiol 2015;66:1976–86. 29 Andorin A, Behr ER, Denjoy I, et al. Impact of clinical and genetic findings on the management of young patients with Brugada syndrome. Heart Rhythm 2016;13:1274–82. 30 Michowitz Y, Milman A, SarquellaBrugada G, et al. Feverrelated arrhythmic events in the multicenter survey on arrhythmic events in Brugada syndrome. Heart Rhythm 2018;15:1394–401. 31 Chung FP, Raharjo SB, Lin YJ, et al. A novel method to enhance phenotype, epicardial functional substrates, and ventricular tachyarrhythmias in Brugada syndrome. Heart Rhythm 2017;14:508–17. 32 Ikeda T, Abe A, Yusu S, et al. The full stomach test as a novel diagnostic technique for identifying patients at risk of Brugada syndrome. J Cardiovasc Electrophysiol 2006;17:602–7. 33 Miyazaki T, Mitamura H, Miyoshi S, et al. Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome. J Am Coll Cardiol 1996;27:1061–70. 34 Jons C, Gollob MH. Brugada syndrome: Let’s talk about sex. Heart Rhythm 2018;15:1466–7. 35 Sacher F, Probst V, Maury P, et al. Outcome after implantation of a cardioverterdefibrillator in patients with Brugada syndrome: a multicenter studypart 2. Circulation 2013;128:1739–47. 36 Raju H, Papadakis M, Govindan M, et al. Low prevalence of risk markers in cases of sudden death due to Brugada syndrome relevance to risk stratification in Brugada syndrome. J Am Coll Cardiol 2011;57:2340–5. 37 Sroubek J, Probst V, Mazzanti A, et al. Programmed ventricular stimulation for risk stratification in the Brugada syndrome: a pooled analysis. Circulation 2016;133:622–30. 38 Honarbakhsh S, Providencia R, Lambiase PD. Risk stratification in Brugada syndrome: current status and emerging approaches. Arrhythm Electrophysiol Rev 2018;7:79. 39 Meregalli PG, Tan HL, Probst V, et al. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in lossoffunction sodium channelopathies. Heart Rhythm 2009;6:341–8. 40 AlKhatib SMet al. 2017 AHA/ACC/HRS guideline for management of patients with ventricular arrhythmias and the prevention of sudden cardiac
[24]王晓东,王晓东,王晓东,等。Brugada综合征临床症状患者的右心室纤维化和传导延迟:电生理、遗传、组织病理学和计算研究发行量2005;112:2769 - 77。布肯斯街M座25号。Brugada综合征心律失常的发生机制。中国生物医学工程学报(英文版);2020;21(1):591 - 591。Brugada心电图模式是通道病变、结构性心脏病的标志,还是两者都不是?探讨Brugada综合征的统一机制。中国心律失常电生理杂志2010;3:283-90。[27]李建军,李建军,李建军,等。Brugada综合征的磁共振检查显示出乎意料的高结构异常率。[J] .中华医学杂志,2009;30(3):391 - 391。[28]王晓明,王晓明,王晓明,等。Brugada综合征的纤维化、连接蛋白43和传导异常。[J]中华医学杂志,2015;16(6):396 - 396。[29]刘建军,刘建军,李建军,等。临床和遗传学结果对年轻Brugada综合征患者治疗的影响。心脏节律2016;13:1274-82。[30]张建军,张建军,张建军,等。Brugada综合征心律失常多中心调查中的发热相关心律失常心脏节律2018;15:1394-401。[31]钟凤凤,李建平,林玉军,等。一种增强Brugada综合征表型、心外膜功能底物和室性心动过速的新方法。心脏节律2017;14:508-17。[32]李建军,李建军,李建军,等。全胃试验作为一种新的诊断技术,用于识别有Brugada综合征风险的患者。[J]中华心血管病杂志,2006;17(6):591 - 591。[33]王晓明,王晓明,王晓明,等。Brugada综合征患者ST段抬高的自主和抗心律失常药物调节。[J]中华医学杂志1996;27:1061-70。34 . jon C, Gollob MH. Brugada综合征:让我们来谈谈性。心脏节律2018;15:14 . 66 - 7。[35]李建军,李建军,李建军,等。Brugada综合征患者植入心律转复除颤器后的预后:一项多中心研究(2)发行量2013;128:1739-47。[6]王晓明,王晓明,王晓明,等。Brugada综合征猝死病例中危险标志物的低流行率与Brugada综合征的风险分层相关[J]中华医学杂志,2011;37(5):544 - 544。[3]张建军,张建军,张建军,等。程序性心室刺激对Brugada综合征风险分层的影响:一项汇总分析。发行量2016;133:622-30。[38]刘建军,刘建军,刘建军,等。Brugada综合征的风险分层:现状和新兴方法。心律失常电生理学报,2018;7:79。[39]李建平,陈海燕,李建平,等。SCN5A突变类型决定了钠通道病丧失功能的临床严重程度和传导减慢程度。心脏节律2009;6:341-8。2017 AHA/ACC/HRS室性心律失常患者的管理和心脏性猝死的预防指南。发行量2018;138:e272 - 391。[4]李建平,李建平,李建平。使用多基因风险评分预测钠通道阻断和Brugada综合征的心电反应。[J] .中华医学杂志,2019;39(4):391 - 391。[4]张建军,张建军,张建军,等。Brugada综合征患者一级预防临床风险评分模型(BRUGADARISK)中华医学杂志(英文版);2021;7:210-22。[43]李建军,刘建军,刘建军,等。Brugada综合征患者心源性猝死预测评分的稳健性和相关性[J] .中国生物医学工程学报(英文版);2009;32(2):391 - 391。[4]吴琦,波西马,王晓明,等。SARSCoV2、covid - 19和遗传性心律失常综合征。心脏节律2020;17:14 . 56 - 62。[45]李建平,王志强,王志强,等。HRS/EHRA/APHRS关于遗传性原发性心律失常综合征患者诊断和管理的专家共识声明:HRS、EHRA和APHRS于2013年5月批准,ACCF、AHA、PACES和AEPC于2013年6月批准。心脏节律2013;10:193263。[46]王尔德,王尔德,王尔德,等。Brugada综合征晕厥:患病率,临床意义,以及从历史上区分心律失常和非心律失常原因的线索。心律2015;12:367-75。[4]刘建军,刘建军,刘建军。2018 ESC晕厥诊断和治疗指南。欧洲心脏杂志2018;39。[8]李建军,李建军,李建军,等。Brugada综合征儿童和青少年的植入式心律转复除颤器。[J]中国医学杂志,2018;31(1):1 - 4。[4]王晓明,王晓明,王晓明,等。无法获得奎尼丁治疗的情况将变得更糟。中华医学杂志,2013;32(2):355。[5]王晓明,王晓明,王晓明,等。连续135例Brugada综合征患者的电底物消除。心律失常电生理学报,2017;10:1-13。
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引用次数: 0
Inherited and modifiable factors need to be identified in young patients with atrioventricular block 需要确定年轻房室传导阻滞患者的遗传因素和可改变因素
Pub Date : 2022-04-05 DOI: 10.1136/heartjnl-2022-320841
E. Roseboom, A. Maass
Atrioventricular block (AVB) is among the leading diagnoses requiring pacemaker implantation. The incidence of this cardiac conduction disorder increases with age: from the UK Biobank, a community-dwelling cohort of approximately half a million participants, conduction disorders were far more present in those ≥65 years of age versus under the age of 55 (55/10.000 vs 11/10.000, respectively). 1 AVB is defined as delayed or interrupted impulse conduction and can be caused by anatomical or func-tional disorders of the conduction system. An extrinsic or physiological AVB can be secondary to increased parasympathetic tone, and is often self- limiting and does not require therapy. Intrinsic or pathological AVB is subdivided into suprahisian and infrahisian, the being predominantly benign and the requiring is referred The main is the conduction elder
房室传导阻滞(AVB)是需要植入起搏器的主要诊断之一。这种心脏传导障碍的发病率随着年龄的增长而增加:来自英国生物银行,一个大约50万参与者的社区居住队列,传导障碍在≥65岁的人群中比55岁以下的人群更常见(分别为55/ 10,000和11/ 10,000)。AVB被定义为脉冲传导延迟或中断,可由传导系统的解剖或功能障碍引起。外源性或生理性AVB可继发于副交感神经张力增加,通常是自限性的,不需要治疗。内源性或病理性AVB又分为上肌和下肌,以良性为主,以传导性为主
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引用次数: 1
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British Heart Journal
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