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[Obstructive sleep apnea in cardiology clinical practice. Epidemiology, diagnosis, and treatment. Observational, cross-sectional, retrospective study]. [心脏病学临床实践中的阻塞性睡眠呼吸暂停。流行病学、诊断和治疗。观察性、横断面、回顾性研究]。
Pub Date : 2024-02-02 DOI: 10.24875/ACM.23000078
Jorge Nara-Sauceda, Mario Moreno-Pacheco, Jesica Patiño-García

Objective: To determine the clinical-epidemiological characteristics, diagnostic feasibility of home respiratory polygraphy and treatment of patients with suspected obstructive sleep apnea (OSA) at cardiovascular risk.

Methods: An observational, cross-sectional, descriptive study was conducted in patients seen in a cardiology outpatient service with suspected OSA, from January 2015 to December 2019. The information was obtained from medical records, and a descriptive statistical analysis was applied to this information.

Results: 138 files were reviewed; only 8% of the home respiratory polygraphs were discarded, because they did not meet the required quality standards. It was demonstrated that 89% suffered from OSA, 60% moderate to severe; in men after 50 years of age. The main cardiovascular risk factors was hypertension (89%). The most prevalent heart disease was hypertension (52%). Cardiovascular pharmacological treatment was improved in 82% of the cases. Cardiac rehabilitation in 30%, noninvasive mechanical ventilation 41%, fixed modality 33%, and self-adjustable 9%, all with telemetry.

Conclusions: The prevalence and severity of OSA is higher in the presence of risk or established cardiovascular disease. In the presence of clinical suspicion, it is feasible to confirm the diagnosis with home respiratory poligrafy due to the level of precision and the lower infrastructure required. Greater involvement of the cardiologist in the diagnosis and treatment of this disorder is necessary due to the significant risk of cardiovascular disease it represents.

目的确定具有心血管风险的疑似阻塞性睡眠呼吸暂停(OSA)患者的临床流行病学特征、家庭呼吸聚光仪的诊断可行性和治疗方法:2015年1月至2019年12月,对在心脏病学门诊就诊的疑似OSA患者进行了一项观察性、横断面、描述性研究。信息来自病历,并对这些信息进行了描述性统计分析:审查了138份档案;只有8%的家庭呼吸测谎仪因不符合规定的质量标准而被放弃。结果表明,89%的人患有 OSA,60%为中度至重度;男性多在 50 岁以后。主要的心血管风险因素是高血压(89%)。最常见的心脏病是高血压(52%)。82%的病例的心血管药物治疗得到了改善。心脏康复治疗占 30%,无创机械通气占 41%,固定模式占 33%,自我调节占 9%,所有治疗均采用遥测技术:结论:存在心血管疾病风险或已确诊心血管疾病时,OSA 的患病率和严重程度更高。在有临床怀疑的情况下,使用家用呼吸监测仪确诊是可行的,因为其精确度高,所需的基础设施较少。由于这种疾病具有很大的心血管疾病风险,因此有必要让心脏病专家更多地参与这种疾病的诊断和治疗。
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引用次数: 0
[Interventionism in congenital heart disease in Chiapas. The history after thousand cases performed]. [恰帕斯州先天性心脏病的介入治疗。千例手术后的历史]。
Pub Date : 2024-02-01 DOI: 10.24875/ACM.23000170
Roberto Mijangos-Vázquez, Rogelio Hernández-Reyes

Background: Congenital heart disease is the most common birth defect and the leading cause of childhood mortality in high-income countries. In these countries, the prognosis for a child born with congenital heart disease is excellent, with over 90% achieving adulthood. However, in the low and lower-middle-income countries, as ours, the outlook is starkly different. In Chiapas, because of the progress of the hemodynamics program, more and more types of congenital heart diseases are susceptible to being treated by cardiac catheterization.

Objective: To show the global experience of the interventionism in congenital heart diseases in Chiapas from its inception to recent days.

Method: Through a retrospective study from April 2016 to June 2023, we reviewed the electronic files of the total of patients who underwent cardiac catheterism during the same period of time.

Results: A total of 1000 procedures were performed, 581 in female patients, with a median age of 4 years (1 day to 77 years). Of the total procedures, 115 (11.5%) were diagnostic catheterizations and 885 (88.5%) were interventional.

Conclusions: Cardiac catheterization in pediatrics in Chiapas has displaced cardiac surgery in a large percentage, and the results that have been obtained are undoubtedly encouraging, which already represents a decentralization in the care of congenital heart diseases in our country.

背景:先天性心脏病是最常见的出生缺陷,也是高收入国家儿童死亡的主要原因。在这些国家,先天性心脏病患儿的预后非常好,90% 以上的患儿都能长大成人。然而,在我国这样的中低收入国家,前景却截然不同。在恰帕斯州,由于血液动力学项目的进展,越来越多类型的先天性心脏病可以通过心导管手术进行治疗:展示恰帕斯州先天性心脏病介入治疗从开始到近期的全球经验:通过对 2016 年 4 月至 2023 年 6 月的回顾性研究,我们查阅了同期接受心导管手术的所有患者的电子档案:共进行了 1000 例手术,其中 581 例为女性患者,中位年龄为 4 岁(1 天至 77 岁)。在所有手术中,115 例(11.5%)为诊断性心导管手术,885 例(88.5%)为介入性手术:恰帕斯州儿科心导管手术在很大程度上取代了心脏外科手术,所取得的成果无疑是令人鼓舞的,这已经代表了我国先天性心脏病治疗的分散化。
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引用次数: 0
[Position statement for improvement in reperfusion of ST-elevation myocardial infarction in Latin America]. [关于改善拉丁美洲 ST 段抬高型心肌梗死再灌注的立场声明]。
Pub Date : 2024-01-16 DOI: 10.24875/ACM.23000045
Juan P Costabel, Miguel Quintana, Joaquín Perea, Pablo Lamelas, Alfonsina Candiello, Patricio Sanhueza, Alexandra Arias-Mendoza, Iván Saavedra, Alex Rivera-Toquica, Marildes L de Castro, Manuel Álvarez-Gaviria, Jorge Belardi, Ángel Cequier, Álvaro Sosa-Liprandi, Ricardo Villarreal

The treatment of ST-segment elevation myocardial infarction has barriers depending on the geographic region. Primary coronary angioplasty is the treatment of choice, if it is performed on time and by experienced operators. However, when it is not available, the administration of fibrinolysis and referral for rescue angioplasty, in case of negative reperfusion, is the best strategy. In the same way, coronary angioplasty, as part of a pharmacoinvasive strategy, is the best alternative when there is positive reperfusion. The development of infarct treatment networks increases the number of patients reperfused within the recommended times and improves outcomes. In Latin America, national myocardial infarction treatment programs should focus on improving outcomes, and long-term success depends on working toward defined goals and enhancing functionality, therefore programs should develop capacity to measure their performance. The following document discusses all of these alternatives and suggests opportunities for improvement.

ST 段抬高型心肌梗死的治疗因地域不同而存在障碍。原发性冠状动脉血管成形术是首选的治疗方法,但必须由经验丰富的操作人员及时实施。但是,如果不能及时进行冠状动脉成形术,最好的办法是进行纤维蛋白溶解术,并在再灌注不良的情况下转诊进行抢救性血管成形术。同样,作为药物介入策略的一部分,冠状动脉血管成形术也是再灌注阳性情况下的最佳选择。心梗治疗网络的发展增加了在建议时间内再灌注的患者人数,并改善了治疗效果。在拉丁美洲,国家心肌梗死治疗计划应将重点放在改善预后上,长期的成功取决于努力实现既定目标和增强功能,因此计划应发展衡量其绩效的能力。以下文件讨论了所有这些替代方案,并提出了改进建议。
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引用次数: 0
Eugenio Flamand Rodríguez, in memoriam. Eugenio Flamand Rodríguez, in memoriam.
Pub Date : 2024-01-01 DOI: 10.24875/ACM.23000257
Alejandro Martín-Trenor
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引用次数: 0
Successful endovascular treatment of aortic arch aneurysm in a pediatric patient. 成功用血管内治疗一名儿童主动脉弓动脉瘤。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.22000272
Isabel C Sánchez-Escobar, Silvia J Galvis-Blanco, Luis H Díaz-Medina, Rafael Correa-Velásquez, Rafael Lince-Varela

Background: Ascending aortic aneurysms are rare pathologies in childhood, especially in the absence of previous diseases such as Marfan syndrome.

Objective: Present the possibility of successful endovascular management of large vessel aneurysms, using stents and microcatheters with embolization of the aneurysm sac.

Method: We present the case of a previously healthy ten-year-old patient, in whom a pseudoaneurysm was documented between the origin of the left common carotid artery and left subclavian artery, successfully managed endovascularly, initially with a stent covering the neck of the aneurysm to remodel it and later with embolization of the aneurysm sac using a microcatheter.

Results: Aneurysms of large vessels, such common carotid artery and subclavian artery, are at risk of rupture with devastating complications; endovascular management is considered a minimally invasive management option, with favorable results.

Conclusion: The endovascular management of large vessel aneurysms using stents and microcatheters with embolization of the aneurysmal sac is a novel management option that achieves successful results.

背景:升主动脉瘤是儿童期罕见的病症,尤其是在没有马凡综合征等既往疾病的情况下:介绍使用支架和微导管栓塞动脉瘤囊,成功进行大血管动脉瘤血管内治疗的可能性:我们介绍了一例 10 岁健康患者的病例,该患者左侧颈总动脉和左锁骨下动脉之间有一个假性动脉瘤,通过血管内治疗获得成功,最初使用支架覆盖动脉瘤颈部使其重塑,后来使用微导管对动脉瘤囊进行栓塞:结果:颈总动脉和锁骨下动脉等大血管动脉瘤有破裂的风险,会带来破坏性并发症;血管内治疗被认为是一种微创治疗方案,效果良好:结论:使用支架和微导管对大血管动脉瘤进行血管内治疗,并对动脉瘤囊进行栓塞,是一种新型的治疗方法,能取得成功的结果。
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引用次数: 0
A rare presentation of Takotsubo syndrome and transient dilated cardiomyopathy due to severe hypocalcemia. 严重低钙血症导致的高钙综合征和一过性扩张型心肌病的罕见病例。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.23000248
Alejandro Ezquerra-Osorio, David A Brenes-Castro, Ramón Espinosa-Soto, Jorge L Vargas-Estrada, Rodrigo Cue-Sierra, Alexandra Arias-Mendoza, Diego Araiza-Garaygordobil
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引用次数: 0
Pompe disease: a lesson to learn. 庞贝氏症:一个教训。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.23000139
Claudia A Pavón-Flores, Leonardo Rivera-Rodríguez, Juan E Calderón-Colmenero
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引用次数: 0
Surgical strategies in Ebstein anomaly: 28 years' experience in a pediatric hospital. 埃布斯坦畸形的手术策略:一家儿科医院 28 年的经验。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.23000203
Mariela Mouratian, Claudia Villalba, Agustina Ramos, Fernando Diez-Mori, M ª Victoria Lafuente, Erica Stelmaszewski, Carla Pasinato, Juliana Medina, Marisa Di Santo, Pablo García-Delucis

Objectives: Ebstein's anomaly is a congenital defect characterized by a lack of delamination and apical displacement of the tricuspid valve, tricuspid insufficiency, right atrial enlargement, and ventricular dysfunction. To analyze the results and evolution of the different surgical strategies, data were collected from 45 patients operated on during 1990-2018. Twenty-six patients were included with a median age at initial surgery of 11.3 years (range: 13 days-18.6 years).

Method: Procedures were plastic 10 patients (38%), cone technique reconstruction 11 (42%), and replacement 5 (19%). Additional interventions were required in 7 patients: cavo-pulmonary anastomosis 4 and Cox-maze 4. Nine patients (34.6%) required reoperation due to severe tricuspid insufficiency. Six had previous plastic, two bioprothesis, and one, cone.

Results: Overall mortality was 11.5% (3) at a median of 10.1 years post-surgery (range: 5.7-10.12) associated with arrhythmias (p = 0.05), right (p = 0.008), left (p = 0.0001) ventricular dysfunction and reoperations (p = 0.03). None were previous conus. Median follow-up was 6.5 years (range: 1-29.1). Ninety-one-point-six percent were in functional class I/II and 79.2% in sinus rhythm.

Conclusions: The results of the different classic techniques were similar, although not free of complications and reoperations. Cone reconstruction proved to be effective, with low surgical mortality, less need for reoperations, and durability in the medium term.

目的:埃布斯坦氏畸形是一种先天性缺陷,其特征是三尖瓣缺乏分层和顶端移位、三尖瓣关闭不全、右心房增大和心室功能障碍。为了分析不同手术策略的结果和演变,我们收集了1990-2018年间接受手术的45名患者的数据。纳入的 26 名患者初次手术的中位年龄为 11.3 岁(范围:13 天-18.6 岁):方法:10 名患者接受了整形手术(38%),11 名患者接受了锥体技术重建手术(42%),5 名患者接受了置换手术(19%)。7名患者需要进行额外干预:腔肺吻合术4人,Cox-maze术4人。9名患者(34.6%)因严重三尖瓣关闭不全而需要再次手术。其中六人曾接受过整形手术,两人接受过生物修复术,一人接受过锥切术:总死亡率为 11.5%(3 例),中位数为术后 10.1 年(范围:5.7-10.12),与心律失常(p = 0.05)、右室(p = 0.008)、左室(p = 0.0001)功能障碍和再次手术(p = 0.03)有关。没有人曾接受过锥切手术。中位随访时间为 6.5 年(范围:1-29.1 年)。91.66%的患者功能分级为I/II级,79.2%为窦性心律:结论:不同经典技术的效果相似,但并非没有并发症和再手术。锥体重建被证明是有效的,手术死亡率低,再次手术的需求较少,中期效果持久。
{"title":"Surgical strategies in Ebstein anomaly: 28 years' experience in a pediatric hospital.","authors":"Mariela Mouratian, Claudia Villalba, Agustina Ramos, Fernando Diez-Mori, M ª Victoria Lafuente, Erica Stelmaszewski, Carla Pasinato, Juliana Medina, Marisa Di Santo, Pablo García-Delucis","doi":"10.24875/ACM.23000203","DOIUrl":"10.24875/ACM.23000203","url":null,"abstract":"<p><strong>Objectives: </strong>Ebstein's anomaly is a congenital defect characterized by a lack of delamination and apical displacement of the tricuspid valve, tricuspid insufficiency, right atrial enlargement, and ventricular dysfunction. To analyze the results and evolution of the different surgical strategies, data were collected from 45 patients operated on during 1990-2018. Twenty-six patients were included with a median age at initial surgery of 11.3 years (range: 13 days-18.6 years).</p><p><strong>Method: </strong>Procedures were plastic 10 patients (38%), cone technique reconstruction 11 (42%), and replacement 5 (19%). Additional interventions were required in 7 patients: cavo-pulmonary anastomosis 4 and Cox-maze 4. Nine patients (34.6%) required reoperation due to severe tricuspid insufficiency. Six had previous plastic, two bioprothesis, and one, cone.</p><p><strong>Results: </strong>Overall mortality was 11.5% (3) at a median of 10.1 years post-surgery (range: 5.7-10.12) associated with arrhythmias (p = 0.05), right (p = 0.008), left (p = 0.0001) ventricular dysfunction and reoperations (p = 0.03). None were previous conus. Median follow-up was 6.5 years (range: 1-29.1). Ninety-one-point-six percent were in functional class I/II and 79.2% in sinus rhythm.</p><p><strong>Conclusions: </strong>The results of the different classic techniques were similar, although not free of complications and reoperations. Cone reconstruction proved to be effective, with low surgical mortality, less need for reoperations, and durability in the medium term.</p>","PeriodicalId":93885,"journal":{"name":"Archivos de cardiologia de Mexico","volume":"94 4","pages":"403-411"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142735363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mechanical and electrical uncoupling: the role of cardiac magnetic resonance imaging in arrhythmogenic cardiomyopathy. Proof of concept. 机械和电气解偶联:心脏磁共振成像在心律失常性心肌病中的作用。概念验证。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.23000199
Jorge A Ortega-Hernández, Mario R García-Arias, Jardiel Argüello-Bolaños, Manlio F Márquez-Murillo, Rodrigo Gopar-Nieto, Ángel A Priego-Ranero, Daniel Sierra-Lara-Martínez

Objectives: Arrhythmogenic cardiomyopathy (ACM) is a complex cardiac disorder associated with ventricular arrhythmias. Understanding the relationship between mechanical uncoupling and cardiac structural changes in ACM patients is crucial for improved risk stratification and management.

Methods: In this study, we enrolled 25 ACM patients (median age 34 years, 72% men) based on the 2019 Modified Task Force and Padua criteria. Patients were categorized by the presence or absence of clinically relevant ventricular tachycardia (crVT), necessitating emergency interventions. Right ventricular-arterial coupling (VAC) was assessed using echocardiography. Low-rank regression splines were employed to model left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) in relation to VAC.

Results: Positive associations were observed between VAC and LVEF (ρ = 0.472, p = 0.023), RVEF (ρ = 0.522, p = 0.038), and right ventricular (RV) indexed stroke volume (ρ = 0.79, p < 0.001). Patients with crVT exhibited correlations with RV shortening, reduced RVEF (39.6 vs. 32.2%, p = 0.025), increased left ventricular (LV) mass (38.99 vs. 45.55, p = 0.045), and LV end-diastolic volume (LVEDV) (56.99 vs. 68.15 mL/m2, p = 0.045). Positive associations for VAC were noted with LVEDV (p = 0.039) and LV mass (p = 0.039), while negative correlations were observed with RVEF by CMR (p = 0.023) and RV shortening by echocardiography (p = 0.026).

Conclusions: Our findings underscore the significance of right VAC in ACM, demonstrating correlations with RV and LVEF, RV stroke volume, and clinically relevant arrhythmias. Insights into RVEF, LV mass, and end-diastolic volume provide valuable contributions to the understanding of ACM pathophysiology and may inform risk assessment strategies.

目的:致心律失常性心肌病(ACM)是一种与室性心律失常相关的复杂心脏疾病。了解 ACM 患者的机械解偶联与心脏结构变化之间的关系对于改善风险分层和管理至关重要:在这项研究中,我们根据 2019 年修订的特别工作组和帕多瓦标准招募了 25 名 ACM 患者(中位年龄 34 岁,72% 为男性)。患者根据是否存在需要紧急干预的临床相关性室速(crVT)进行分类。右心室-动脉耦合(VAC)通过超声心动图进行评估。采用低秩回归样条建立左室射血分数(LVEF)和右室射血分数(RVEF)与 VAC 的关系模型:结果:VAC与左室射血分数(LVEF)(ρ = 0.472,p = 0.023)、右室射血分数(RVEF)(ρ = 0.522,p = 0.038)和右室(RV)指数搏出量(ρ = 0.79,p < 0.001)之间呈正相关。crVT患者与RV缩短、RVEF降低(39.6 vs. 32.2%,p = 0.025)、左室(LV)质量增加(38.99 vs. 45.55,p = 0.045)和左室舒张末期容积(LVEDV)(56.99 vs. 68.15 mL/m2,p = 0.045)相关。VAC 与 LVEDV(p = 0.039)和 LV 质量(p = 0.039)呈正相关,而与 CMR 的 RVEF(p = 0.023)和超声心动图的 RV 缩短(p = 0.026)呈负相关:我们的研究结果强调了右 VAC 在 ACM 中的重要性,显示出与 RV 和 LVEF、RV 搏出量以及临床相关心律失常的相关性。对 RVEF、左心室质量和舒张末期容积的深入了解为了解 ACM 病理生理学做出了宝贵贡献,并可为风险评估策略提供参考。
{"title":"Mechanical and electrical uncoupling: the role of cardiac magnetic resonance imaging in arrhythmogenic cardiomyopathy. Proof of concept.","authors":"Jorge A Ortega-Hernández, Mario R García-Arias, Jardiel Argüello-Bolaños, Manlio F Márquez-Murillo, Rodrigo Gopar-Nieto, Ángel A Priego-Ranero, Daniel Sierra-Lara-Martínez","doi":"10.24875/ACM.23000199","DOIUrl":"10.24875/ACM.23000199","url":null,"abstract":"<p><strong>Objectives: </strong>Arrhythmogenic cardiomyopathy (ACM) is a complex cardiac disorder associated with ventricular arrhythmias. Understanding the relationship between mechanical uncoupling and cardiac structural changes in ACM patients is crucial for improved risk stratification and management.</p><p><strong>Methods: </strong>In this study, we enrolled 25 ACM patients (median age 34 years, 72% men) based on the 2019 Modified Task Force and Padua criteria. Patients were categorized by the presence or absence of clinically relevant ventricular tachycardia (crVT), necessitating emergency interventions. Right ventricular-arterial coupling (VAC) was assessed using echocardiography. Low-rank regression splines were employed to model left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) in relation to VAC.</p><p><strong>Results: </strong>Positive associations were observed between VAC and LVEF (ρ = 0.472, p = 0.023), RVEF (ρ = 0.522, p = 0.038), and right ventricular (RV) indexed stroke volume (ρ = 0.79, p < 0.001). Patients with crVT exhibited correlations with RV shortening, reduced RVEF (39.6 vs. 32.2%, p = 0.025), increased left ventricular (LV) mass (38.99 vs. 45.55, p = 0.045), and LV end-diastolic volume (LVEDV) (56.99 vs. 68.15 mL/m<sup>2</sup>, p = 0.045). Positive associations for VAC were noted with LVEDV (p = 0.039) and LV mass (p = 0.039), while negative correlations were observed with RVEF by CMR (p = 0.023) and RV shortening by echocardiography (p = 0.026).</p><p><strong>Conclusions: </strong>Our findings underscore the significance of right VAC in ACM, demonstrating correlations with RV and LVEF, RV stroke volume, and clinically relevant arrhythmias. Insights into RVEF, LV mass, and end-diastolic volume provide valuable contributions to the understanding of ACM pathophysiology and may inform risk assessment strategies.</p>","PeriodicalId":93885,"journal":{"name":"Archivos de cardiologia de Mexico","volume":"94 3","pages":"269-275"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11259420/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141728435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Contrast echocardiogram for diagnosis to pulmonary arterio-venous fistulas in hepato-pulmonary syndrome. 用于诊断肝肺综合征肺动静脉瘘的对比超声心动图。
Pub Date : 2024-01-01 DOI: 10.24875/ACM.22000260
Jesús De Rubens-Figueroa, Joanna Granda-Jiménez, Alfonso Hoyos-Apodaca, Flora Zárate-Mondragón
{"title":"Contrast echocardiogram for diagnosis to pulmonary arterio-venous fistulas in hepato-pulmonary syndrome.","authors":"Jesús De Rubens-Figueroa, Joanna Granda-Jiménez, Alfonso Hoyos-Apodaca, Flora Zárate-Mondragón","doi":"10.24875/ACM.22000260","DOIUrl":"10.24875/ACM.22000260","url":null,"abstract":"","PeriodicalId":93885,"journal":{"name":"Archivos de cardiologia de Mexico","volume":"94 1","pages":"107-110"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11160529/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140178138","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Archivos de cardiologia de Mexico
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