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Clinical characterization of patients with cardiac amyloidosis in a referral center of Colombia. 哥伦比亚一家转诊中心的心脏淀粉样变性患者的临床特征。
Pub Date : 2024-08-01 DOI: 10.24875/ACM.23000236
Paola Ortiz, Camilo A Polania-Sandoval, Juliana Gaviria-Villegas, Claudia Gutiérrez-Villamil, Clarena Zuluaga-Arbeláez, Víctor Marin-Oyaga, María J Rodríguez-González

Objective: The objective of the study is to describe the characteristics of our first cohort of amyloidosis in a Latin America cardiovascular reference center in Colombia.

Methods: This is a historic cohort study and data were taken from the electronic records of the Fundación Cardioinfantil-Instituto de cardiología; adult patients with a diagnosis of cardiac amyloidosis were included and a descriptive analysis was presented.

Results: A total of 31 patients with amyloidosis were included. 17 were Transthyretin Amyloidosis (ATTR) subtype and 14 were AL subtype. An overall mortality of 25% was found. The mean age at diagnosis was 74 years, male sex predominant. More frequent comorbidities were hypertension and atrial fibrillation. The most frequent clinical presentation was congestive heart failure (75%), with mildly reduced ejection fraction (41.94%), followed by reduced ejection fraction (32.26%), and preserved ejection fraction (25.81%). In the ATTR subtype, a reduced ejection fraction was found at 41.18% and a mildly reduced ejection fraction at 35.29%.

Conclusion: These results provide information on the most frequent type of amyloidosis and the late timing to diagnose in our historic cohort study, we present some of the baseline characteristics and most frequent approaches to diagnose Cardiac Amyloidosis that represents all challenges in clinical practice. Improvements are needed in the diagnosis and early treatment of these patients.

研究目的本研究旨在描述哥伦比亚拉丁美洲心血管病参考资料中心第一批淀粉样变性患者的特征:这是一项历史性队列研究,数据来自于 Fundación Cardioinfantil-Instituto de cardiología 的电子记录;研究纳入了诊断为心脏淀粉样变性的成年患者,并进行了描述性分析:结果:共纳入31名淀粉样变性患者。结果:共纳入31例淀粉样变性患者,其中17例为转甲状腺素淀粉样变性(ATTR)亚型,14例为AL亚型。总死亡率为 25%。确诊时的平均年龄为74岁,男性居多。更常见的合并症是高血压和心房颤动。最常见的临床表现是充血性心力衰竭(75%),射血分数轻度降低(41.94%),其次是射血分数降低(32.26%)和射血分数保留(25.81%)。在 ATTR 亚型中,发现射血分数减低的占 41.18%,射血分数轻度减低的占 35.29%:这些结果提供了有关淀粉样变性最常见类型的信息,以及在我们的历史性队列研究中诊断出淀粉样变性的较晚时间,我们介绍了一些基线特征和诊断心脏淀粉样变性的最常见方法,这些都代表了临床实践中的所有挑战。我们需要改进对这些患者的诊断和早期治疗。
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引用次数: 0
Multimodality imaging approach in light chain (AL) cardiac amyloidosis: a case report. 轻链(AL)心脏淀粉样变性的多模式成像方法:病例报告。
Pub Date : 2024-07-29 DOI: 10.24875/ACM.24000027
Alexis Zambrano-Zambrano, Arturo M Ruiz-Beltrán, Alejandro I Rojas-Arriaga, Pamela Ramírez-Rangel, Augusto Pupiales-Dávila, Marco A Ponce-Gallegos
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引用次数: 0
Management of supravalvular aortic stenosis with the Doty technique, in a South American pediatric center. 南美一家儿科中心采用 Doty 技术治疗主动脉瓣上狭窄。
Pub Date : 2024-07-29 DOI: 10.24875/ACM.24000089
Eliana B Yagual-Gutiérrez, Isabel M Freire-Barrezueta, Mercedes C Hernandez-Duarte, Isabel J Calero-Solis, David F Maldonado-González, Darwin E Zhune-Villagran

Supravalvular aortic stenosis (SVAS) is a congenital malformation associated with Williams-Beuren syndrome. It is characterized by severe stenosis of the sinotubular junction. The smooth muscle layer is thickened due to an alteration of the Elastin gene. The treatment is surgical and there are several techniques to relieve obstruction which range from the single-patch technique to the replacement of all three aortic sinuses with three patches. However, the optimal technique is still unclear. The objective of this article is to carry out a bibliographic review of surgical techniques for SVAS and the description of the application of the Doty technique for a 4-year-old infant at the Roberto Gilbert Elizalde Hospital.

主动脉瓣上狭窄(SVAS)是一种与威廉姆斯-伯伦综合征有关的先天性畸形。其特点是窦管交界处严重狭窄。由于弹性蛋白基因的改变,平滑肌层增厚。治疗方法是外科手术,有几种缓解阻塞的技术,从单补片技术到用三个补片置换全部三个主动脉窦。然而,最佳技术仍不明确。本文旨在对 SVAS 的手术技术进行文献综述,并介绍罗伯托-吉尔伯特-埃利萨尔德医院对一名 4 岁婴儿应用 Doty 技术的情况。
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引用次数: 0
The Ottoman empire sword: a variant of partial anomalous pulmonary veins connections. 奥斯曼帝国之剑:部分异常肺静脉连接的变种。
Pub Date : 2024-07-29 DOI: 10.24875/ACM.24000029
Karla A Pupiales-Dávila, Vincenzo Arenas-Fabbri, Edgar García-Cruz, Pamela Ramirez-Rangel
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引用次数: 0
Mexican Registry of Cardiomyopathies: baseline data, diagnostic strategies, and treatment approaches in Mexico. 墨西哥心肌病登记处:墨西哥的基线数据、诊断策略和治疗方法。
Pub Date : 2024-07-29 DOI: 10.24875/ACM.24000033
Guillermo A Llamas-Esperón, Enrique A Berrios-Bárcenas, Jorge E Cossío-Aranda, Sylvia Salmun-Nehmad, Rahab A Morales Flores, Maria C Escalante-Seyffert, Jorge Leal-Cavazos, Eufracino Sandoval-Rodríguez, Eduardo Pamplona-Ávila, Enrique Sánchez-Hiza, Liliana E Ramos-Villalobos, Luisa F Aguilera-Mora, Mario A Benavides-González, Carlos D Carrillo, Guillermo Llamas-Delgado, Jonathan H Zaldívar-Zurita, Norberto Matadamas-Hernández

Objectives: The study aimed to know the clinical, demographic, diagnostic, and treatments characteristics in patients with cardiomyopathies in Mexico.

Methods: The Mexican Registry of Cardiomyopathies (REMEMI) is an observational, prospective and national study of patients with cardiomyopathies, which includes: Dilated cardiomyopathy (DCM), hypertrophic cardiomyopathy (HCM), restrictive cardiomyopathy (RCM) and arrhythmogenic cardiomyopathy of the right ventricle (ARVC).

Results: A total of 1026 patients from most states of the Mexican Republic (19) were included, with 494 corresponding to DCM, 490 to HCM, 35 to RCM, and seven to ARVC. We found significant differences between the various cardiomyopathy phenotypes (p < 0.05) in the coexistence with diabetes, use of implantable defibrillator, presence of ventricular tachycardia, and NYHA functional class ≥ 1. There were no significant differences in age and predominant gender between each one. When analyzing by phenotype, we found that patients with HCM have limited use of diagnostic methods considered indispensable, such as cardiac magnetic resonance, Holter monitoring, and genetic testing in patients and their relatives.

Conclusion: Seeking contemporary information through observational registries in Mexico is a valuable opportunity to understand the characteristics of the methods used in the study and treatment of diseases such as cardiomyopathies by Mexican physicians. It can provide information for the implementation of management guidelines and strategies to disseminate findings to improve healthcare in our country.

研究目的研究旨在了解墨西哥心肌病患者的临床、人口统计学、诊断和治疗特点:墨西哥心肌病登记处(REMEMI)是一项针对心肌病患者的全国性前瞻性观察研究,其中包括结果:来自墨西哥大部分地区的 1026 名心肌病患者接受了该研究,其中包括:扩张型心肌病 (DCM)、肥厚型心肌病 (HCM)、限制型心肌病 (RCM) 和右心室致心律失常性心肌病 (ARVC):共纳入了来自墨西哥共和国大部分州(19 个州)的 1026 名患者,其中 494 人患有 DCM,490 人患有 HCM,35 人患有 RCM,7 人患有 ARVC。我们发现,各种心肌病表型在合并糖尿病、使用植入式除颤器、室性心动过速和 NYHA 功能分级≥ 1 等方面存在明显差异(p < 0.05)。不同患者的年龄和主要性别无明显差异。通过表型分析,我们发现 HCM 患者对心脏磁共振、Holter 监测、患者及其亲属基因检测等不可或缺的诊断方法的使用有限:通过墨西哥的观察性登记寻求当代信息,是了解墨西哥医生在研究和治疗心肌病等疾病时所用方法特点的宝贵机会。它可以为实施管理指南和传播研究结果的战略提供信息,从而改善我国的医疗保健。
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引用次数: 0
Look before you leap! - A case report of left main dissection causing myocardial infarction. 看清楚再跳- 左主干夹层导致心肌梗死的病例报告。
Pub Date : 2024-07-26 DOI: 10.24875/ACM.23000269
Sriram Veeraraghavan, Bharath R Kidambi
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引用次数: 0
[COVID-19 in patients with pre-existing cardiovascular disease: a series of cases during the fourth epidemiologic wave in Mexico City]. [原有心血管疾病患者中的 COVID-19:墨西哥城第四次流行病学浪潮中的一系列病例]。
Pub Date : 2024-07-26 DOI: 10.24875/ACM.23000259
Celso A Mendoza-González, Neftalí E Antonio-Villa, Mireya B Contreras-Alanis, María F Fernández-Sandoval, Jimena Castillo-Macías, Daniel E Sandoval-Colin, Jacobo S Vera-Chávez, Víctor A Quiroz-Martínez, Karina Del Valle-Zamora

Objective: SARS-CoV-2 infection induces an immune response that causes excessive inflammation damaging cardiac tissue and vascular endothelium. The objective of this study is to review a series of cases of hospitalized patients with pre-existing cardiac disease to describe the clinical behavior and highlight the low frequency of morbidity and mortality.

Method: Retrospective study of 17 patients with a confirmed diagnosis of COVID-19 by polymerase chain reaction test or antigen test, a history of cardiovascular disease with or without comorbidities, and a history of at least one dose of the vaccine for COVID-19, during the period between December 30, 2021 and March 17, 2022 at the Ignacio Chávez National Institute of Cardiology in Mexico City.

Results: The most frequent cardiac pathology was acute myocardial infarction (31.25%) and the most common arrhythmia was atrial fibrillation (25%). The median number of days of hospital stay was 10 days (interquartile range: 4-14). Regarding the outcomes, 94% of the patients were discharged due to clinical improvement, and only one patient died during his hospitalization.

Conclusions: It is crucial to continue investigating SARS-CoV-2 effects in patients pre-existing heart disease and in those with persistent symptoms after infection. This will allow the development of more effective strategies for the treatment and prevention of cardiovascular complications associated with COVID-19.

目的SARS-CoV-2 感染会诱发免疫反应,导致过度炎症,损害心脏组织和血管内皮。本研究的目的是回顾一系列已患心脏病的住院患者的病例,以描述其临床表现,并强调其发病率和死亡率较低:回顾性研究:2021年12月30日至2022年3月17日期间,墨西哥城伊格纳西奥-查韦斯国家心脏病研究所对17名通过聚合酶链式反应检测或抗原检测确诊为COVID-19、有或无合并心血管疾病病史、至少接种过一剂COVID-19疫苗的患者进行研究:最常见的心脏病是急性心肌梗塞(31.25%),最常见的心律失常是心房颤动(25%)。住院天数中位数为 10 天(四分位数间距:4-14 天)。就结果而言,94%的患者因临床好转而出院,只有一名患者在住院期间死亡:结论:继续研究 SARS-CoV-2 对原有心脏病患者和感染后症状持续存在的患者的影响至关重要。结论:继续研究 SARS-CoV-2 对原有心脏病患者和感染后症状持续存在的患者的影响至关重要,这将有助于制定更有效的策略来治疗和预防与 COVID-19 相关的心血管并发症。
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引用次数: 0
[Survival after receiving advanced cardiopulmonary resuscitation and associated factors in children over 1 month in a hospital in Mexico]. [墨西哥一家医院 1 个月以上儿童接受高级心肺复苏术后的存活率及相关因素]。
Pub Date : 2024-07-26 DOI: 10.24875/ACM.23000186
Ruth Y Ramos-Gutiérrez, Nancy Acuña-Chávez, Daniel López-Aguilera, Juan C Lona-Reyes
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引用次数: 0
[Giant cardiac rhabdomyoma: an atypical cause of ST-segment elevation in the newborn]. [巨型心脏横纹肌瘤:新生儿 ST 段抬高的非典型原因]。
Pub Date : 2024-07-18 DOI: 10.24875/ACM.23000195
Martín Negreira-Caamaño, Laura Acero-García de la Santa, Daniel Salvo-Chabuel, María Arántzazu-González-Marín
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引用次数: 0
[Aneurysms and coronary artery fistula after endomyocardial biopsy in a patient with a heart transplant. Angiographic and clinical evolution. Report of a case.] [心脏移植患者心内膜活检后出现动脉瘤和冠状动脉瘘。血管造影和临床演变。病例报告]
Pub Date : 2024-07-09 DOI: 10.24875/ACM.24000036
Pedro D Díaz-Sarasa, Herón G Méndez-Sánchez, Guering Eid-Lidt
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引用次数: 0
期刊
Archivos de cardiologia de Mexico
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