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REC: CardioClinics最新文献

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Cor triatriatum sinistrum in adulthood: A case report 成年后心房三裂1例
Q4 Medicine Pub Date : 2025-07-01 DOI: 10.1016/j.rccl.2024.11.002
Margarida Cabral , Luís Graça Santos , Catarina Ruivo , João Morais
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引用次数: 0
Índice de autores 作者索引
Q4 Medicine Pub Date : 2025-05-01 DOI: 10.1016/S2605-1532(25)00108-6
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引用次数: 0
Comité Organizador, Comité Científico y Junta Directiva 组织委员会、科学委员会和理事会
Q4 Medicine Pub Date : 2025-05-01 DOI: 10.1016/S2605-1532(25)00106-2
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引用次数: 0
Comunicaciones 通信
Q4 Medicine Pub Date : 2025-05-01 DOI: 10.1016/S2605-1532(25)00107-4
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引用次数: 0
La impresión tridimensional a partir de la ecografía transtorácica en las cardiopatías congénitas 在先天性心脏病中使用经口超声进行三维打印
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2025.01.006
Rocío García-Orta , Miguel Morales García , Eduardo Moreno Escobar
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引用次数: 0
Creatina, el suplemento de moda en deportistas, ¿útil en insuficiencia cardiaca? 肌酸,运动员的时尚补充剂,对心力衰竭有用吗?
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2025.01.004
Dámaris Carballeira Puentes , David Dobarro , María Melendo-Viu
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引用次数: 0
Impacto del síndrome de deleción 22q11.2 en la mortalidad de los pacientes pediátricos con defectos conotruncales corregidos 22q11.2缺失综合征对矫正锥管缺陷的儿科患者死亡率的影响
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2024.12.003
Carlos Alcántara Noguez , Alejandra Contreras-Ramos , Maria Esther Lazcano Melo , Karen Janeth Zúñiga Sánchez , Sergio Ruiz , Patricia Romero Cárdenas , Alejandro Bolio Cerdán , Juan Manuel Vera Canelo

Introduction and objectives

The 22q11.2 deletion syndrome (22q11.2 DS), known as DiGeorge syndrome, is phenotypically associated with conotruncal heart defects. The aim of this review was to evaluate mortality in pediatric patients with corrected conotruncal defects.

Methods

A literature search was conducted in the databases PubMed, ScienceDirect, Google Scholar, and Redalyc databases, covering the last 10 years. Original articles with pediatric population diagnosed with 22q11.2 DS and conotruncal congenital heart defects were included. A statistical analysis of 5 studies was performed, evaluating the odds ratio (OR), 95% confidence intervals (95%CI), and statistical significance using the chi-square test for each exposure variable. The ROBINS-E tool was used to assess the risk of bias.

Results

A total of 18 articles were collected, including a total population of 10 993 patients (3225 with 22q11.2 DS). The most frequent cardiac defect was tetralogy of Fallot (n = 655). The most common intraoperative complications were arrhythmias, and the most common postoperative complications were infections. Mortality in patients with 22q11.2 DS was assessed. The OR was 0.74 (95%CI, 0.38-1.45; P = .38). Heterogeneity test yielded an I2 = 66%.

Conclusions

22q11.2 DS is not associated with post-surgical mortality in patients treated for conotruncal congenital heart defects.
22q11.2缺失综合征(22q11.2 DS),又称DiGeorge综合征,在表型上与圆锥状心脏缺陷相关。这篇综述的目的是评估小儿患者的死亡率矫正圆锥锥体缺陷。方法采用PubMed、ScienceDirect、谷歌Scholar和Redalyc数据库进行近10年的文献检索。纳入了诊断为22q11.2 DS和圆锥截形先天性心脏缺陷的儿科人群的原创文章。对5项研究进行统计分析,对每个暴露变量使用卡方检验评估比值比(OR)、95%置信区间(95% ci)和统计学显著性。使用ROBINS-E工具评估偏倚风险。结果共收集文献18篇,共纳入患者10 993例(3225例,22q11.2 DS)。最常见的心脏缺陷是法洛四联症(n = 655)。术中最常见的并发症是心律失常,术后最常见的并发症是感染。评估22q11.2 DS患者的死亡率。OR为0.74 (95%CI, 0.38-1.45;p = .38)。结论22q11.2 DS与圆锥状先天性心脏缺损患者术后死亡率无相关性。
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引用次数: 0
Pheochromocytoma as a trigger of miocarditis in arrhythmogenic cardiomyopathy 嗜铬细胞瘤是诱发心律失常性心肌病的心肌炎的一个因素
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2024.10.009
Jon Zubiaur , Víctor Fernández Lobo , Gonzalo Martín Gorria , Luis Javier Ruiz Guerrero
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引用次数: 0
REC: CardioClinics 2024 REC:心脏诊所2024
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2025.01.003
Sergio Raposeiras-Roubín , Elena Díaz-Peláez , Victoria Cañadas-Godoy
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引用次数: 0
Calcificación caseosa del anillo mitral: ¿una entidad benigna? 二尖瓣钙化:良性实体?
Q4 Medicine Pub Date : 2025-04-01 DOI: 10.1016/j.rccl.2024.10.002
Andoni Fernández González, Amaia Martínez León, Betel Olaizola Balboa
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引用次数: 0
期刊
REC: CardioClinics
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