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The “buddy stent technique” to overcome poor support for cover stent implantation to treat coronary perforation [在治疗冠状动脉穿孔的过程中,采用 "伙伴支架技术 "来克服有盖支架植入过程中的支撑不良问题]。
IF 0.3 Q4 Medicine Pub Date : 2024-07-23 DOI: 10.1016/j.ancard.2024.101784
Alexandre Gautier , Hakim Benamer

An 86-year-old woman was managed for a non-ST-segment elevation myocardial infarction. Coronary angiography revealed significant stenoses at the left anterior descending, left ostial circumflex (LCX), obtuse first marginal, and a Medina 1.0.1 bifurcation lesion at the middle LCX/ second obtuse marginal (OM2). During percutaneous coronary intervention, the rupture of the pre-dilatation balloon was complicated by a type III coronary perforation at the level of the LCX/OM2 bifurcation, leading to cardiac tamponade. Hemodynamics were stabilized by percutaneous pericardial drainage. The placement of a covered stent (BeGraft, Bentley InnoMed), to seal the coronary perforation, was not possible due to its great rigidity and the angulation towards the OM2, even with the use of a guiding catheter extension (Guidezilla, Boston Scientific). To further increase support, we decided to use the flexibility of a regular drug-eluting stent which we implanted from the LCX to the OM2, thereby creating a rail-like path in which the covered stent could then be positioned and deployed successfully, allowing the perforation to be sealed with a good final result. This is what we called the “buddy stent technique”.

一名 86 岁的妇女因非 ST 段抬高型心肌梗死接受治疗。冠状动脉造影显示,左前降支、左侧骨膜环(LCX)、第一钝缘处有明显狭窄,LCX 中段/第二钝缘(OM2)处有 Medina 1.0.1 分叉病变。在经皮冠状动脉介入治疗过程中,LCX/OM2 分叉处的 III 型冠状动脉穿孔导致预扩张球囊破裂,引发心脏填塞。经皮心包引流稳定了血流动力学。由于冠状动脉穿孔处的支架非常坚硬,且向 OM2 成角,即使使用了导引导管延伸器(Guidezilla,波士顿科学公司),也无法放置有盖支架(BeGraft,Bentley InnoMed)封堵冠状动脉穿孔。为了进一步增加支撑力,我们决定利用普通药物洗脱支架的灵活性,将其从 LCX 植入到 OM2,这样就形成了一条类似轨道的路径,覆盖支架就可以在这条路径上成功定位和展开,从而以良好的最终效果封堵穿孔。这就是我们所说的 "伙伴支架技术"。
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引用次数: 0
How to manage an entrapped undeflatable coronary balloon 如何处理被夹住的无法充气的冠状动脉球囊。
IF 0.3 Q4 Medicine Pub Date : 2024-07-23 DOI: 10.1016/j.ancard.2024.101779
Hachem-Ali Haidar , Matthieu Perier , Hakim Benamer

An entrapped undeflatable coronary balloon is a rare complication during percutaneous coronary intervention. It is a complication that can be stressful for the operator, with potentially catastrophic implications for the patient. A fully inflated balloon in the coronaries impedes the blood flow to the distal myocardium and hence causes ischemia, that could jeopardize the hemodynamics of the patients and potentially lead to life-threatening complications.

In this article, we go over the bail-out techniques that have been tried while highlighting the pros and cons of each technique.

无法充气的冠状动脉球囊被夹住是经皮冠状动脉介入治疗过程中一种罕见的并发症。这种并发症会给操作者带来压力,并可能给患者带来灾难性影响。冠状动脉中完全充气的球囊会阻碍远端心肌的血流,从而导致心肌缺血,危及患者的血液动力学,并可能导致危及生命的并发症。在本文中,我们将介绍已尝试过的保外技术,同时强调每种技术的优缺点。
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引用次数: 0
Editorial board / Ours rédaction 编辑部 / Ours rédaction
IF 0.3 Q4 Medicine Pub Date : 2024-06-01 DOI: 10.1016/S0003-3928(24)00051-9
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引用次数: 0
Sommaire 目录
IF 0.3 Q4 Medicine Pub Date : 2024-06-01 DOI: 10.1016/S0003-3928(24)00053-2
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引用次数: 0
Un rare cas de myocardite récurrente révélant un phéochromocytome [一个罕见的复发性心肌炎病例揭示了嗜铬细胞瘤]。
IF 0.3 Q4 Medicine Pub Date : 2024-05-25 DOI: 10.1016/j.ancard.2024.101768
A. Bouamoud, C. Zaim, W. Kerrouani, M. EL Haddioui, K. Bouissou, M. Bouazaze, R. Amri

Pheochromocytoma is a rare neuroendocrine tumor characterized by overproduction of catecholamines. The overproduction of catecholamines leads to cardiac remodeling which manifests in several forms ranging from Takotsubo to dilated cardiomyopathy. Studies suggest that pheochromocytoma-induced cardiomyopathy can take various forms depending on the duration of catecholamine exposure. Myocarditis is a fairly rare presentation of cardiac manifestations of pheochromocytoma which are mainly dominated by Takotsubo and dilated cardiomyopathies.

We report a rare case of recurrent myocarditis in a young 37-year-old patient revealing the diagnosis of adrenal pheochromocytoma.

Through this case and through a review of the literature we will take stock of the epidemiology of cardiac involvement in pheochromocytoma, mainly cardiomyopathies, and we will take stock of the value of diagnosis and early management in improving the prognosis of patients.

嗜铬细胞瘤是一种罕见的神经内分泌肿瘤,其特点是儿茶酚胺过度分泌。儿茶酚胺的过度分泌会导致心脏重塑,表现为从 Takotsubo 到扩张型心肌病等多种形式。研究表明,嗜铬细胞瘤诱发的心肌病可表现为多种形式,具体取决于儿茶酚胺暴露的持续时间。心肌炎是嗜铬细胞瘤心脏表现中相当罕见的一种,主要表现为Takotsubo和扩张型心肌病。我们报告了一例罕见的复发性心肌炎病例,患者 37 岁,诊断为肾上腺嗜铬细胞瘤。通过本病例和文献综述,我们将总结嗜铬细胞瘤累及心脏(主要是心肌病)的流行病学,并总结诊断和早期治疗在改善患者预后方面的价值。
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引用次数: 0
Coronary atherosclerosis among symptomatic patients with zero coronary artery calcium score in computed tomography coronary angiography 在计算机断层扫描冠状动脉造影术中冠状动脉钙化评分为零的无症状患者中存在冠状动脉粥样硬化。
IF 0.3 Q4 Medicine Pub Date : 2024-05-23 DOI: 10.1016/j.ancard.2024.101741
Arun Kadel , Binay Kumar Rauniyar , Sushant Kharel , Keshab Raj Neupane , Dipanker Prajapati , Chandra Mani Adhikari , Nirmal Psd Neupane

Background

Computed tomographic coronary angiography has been recognized as a reliable imaging modality with excellent negative predictive value and a good negative likelihood ratio to exclude coronary artery disease in stable, symptomatic patients with intermediate or high risk. 1) Coronary calcium scoring has been extensively shown to be an invaluable tool to exclude the presence of coronary artery disease in low-risk patients. 2) Our aim was to identify the presence and extent of coronary atherosclerosis in computed tomographic coronary angiography in stable symptomatic patients with a zero Coronary Calcium score.

Results

Three hundred and eighty-three (383) consecutive patients aged ≥ 18 years fulfilling the criteria were enrolled as of January 1, 2021; 165 (43.1%) were male and 218 (56.9%) were female, with a mean age of 57.8 ± 4.9 years and a zero coronary artery calcium score. Two hundred and twenty-six (226) (59.0%) were hypertensive, followed by 125 (32.6%) who were smokers, and 117 (30.5%) who were diabetic. The frequency of atherosclerotic plaque in coronary arteries was 34 (8.9%), with 16 (47.1%) being male and 18 (52.9%) being female. The mean age of patients with atherosclerosis was 54.9 ± 3.3 years; among them, 13 (38.2%) were between the ages of 45 and 54, and 10 (29.4%) were between the ages of 55 and 64. Nineteen (19) (55.9%) were hypertensive, followed by 10 (29.4%) with dyslipidemia. Twenty-three (23) (67.6%) had non-obstructive plaque, and 11 (32.3%) had obstructive plaque. In the subgroup of patients with non-obstructive plaque, 13 (56.5%) were hypertensive, 8 (34.8%) were diabetic, and 16 (69.6%) had single vessel disease, while among patients with obstructive plaque, 6 (54.5%) were hypertensive, 5 (45.5%) were smokers, and all of them had single vessel disease. The most affected artery was the left anterior descending artery.

Conclusion

As the frequency of atherosclerotic plaque in patients with a zero coronary calcium score is relatively high, computed tomographic coronary angiography is indicated in stable, symptomatic patients with a lower likelihood of coronary artery disease.

背景:计算机断层扫描冠状动脉造影已被公认为是一种可靠的成像方式,具有极佳的阴性预测值和良好的阴性似然比,可用于排除病情稳定、无症状的中危或高危患者的冠状动脉疾病。1)冠状动脉钙化评分已被广泛证明是排除低危患者冠状动脉疾病的重要工具。2)我们的目的是在计算机断层扫描冠状动脉造影中确定冠状动脉钙化评分为零的症状稳定患者是否存在冠状动脉粥样硬化及其程度:截至2021年1月1日,共有383名年龄≥18岁、符合标准的连续患者入选,其中男性165人(43.1%),女性218人(56.9%),平均年龄为(57.8±4.9)岁,冠状动脉钙化评分为零。226人(59.0%)患有高血压,125人(32.6%)吸烟,117人(30.5%)患有糖尿病。冠状动脉粥样硬化斑块的患者有 34 人(8.9%),其中男性 16 人(47.1%),女性 18 人(52.9%)。动脉粥样硬化患者的平均年龄为(54.9 ± 3.3)岁,其中 13 人(38.2%)在 45 至 54 岁之间,10 人(29.4%)在 55 至 64 岁之间。19人(55.9%)患有高血压,10人(29.4%)患有血脂异常。23人(67.6%)患有非阻塞性斑块,11人(32.3%)患有阻塞性斑块。在非阻塞性斑块患者分组中,13 人(56.5%)患有高血压,8 人(34.8%)患有糖尿病,16 人(69.6%)患有单血管疾病,而在阻塞性斑块患者中,6 人(54.5%)患有高血压,5 人(45.5%)是吸烟者,他们都患有单血管疾病。受影响最大的动脉是左前降支动脉:结论:由于冠状动脉钙化评分为零的患者出现动脉粥样硬化斑块的频率相对较高,计算机断层扫描冠状动脉造影术适用于病情稳定、无症状且冠状动脉病变可能性较低的患者。
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引用次数: 0
Mort subite de l'adulte : données de 305 cas d'autopsies consécutives en Algérie [成人猝死:阿尔及利亚 305 例连续尸检病例数据]。
IF 0.3 Q4 Medicine Pub Date : 2024-05-17 DOI: 10.1016/j.ancard.2024.101760
Oussama Kerrouche , Houssam Amghar , Hicham Haddad

Background-aims

Sudden death in a young adult who showed no prodrome or complaint during his lifetime is a tragedy. The death often remains unexplained by doctors and is often the subject of a judicial investigation following which an autopsy is ordered. Our study joins several studies around the world, where the results have linked sudden death in adults to a cardiac origin.

Methods

Through a series of 305 autopsies carried out in the forensic medicine department of the Frantz Fanon hospital in the city of Bejaia in Algeria over a period of two years, 57 cases corresponded to unexplained sudden deaths, i.e. an incidence of 3 cases per 100,000 inhabitants per year.

Results

Sudden death was of cardiac origin in 50.8% of cases (N=28). Two epidemiologic profiles emerge in our study: the first is that of a man aged between 50 and 60 years of age, with several deleterious lifestyle habits (in particular smoking) with a cardiovascular history, previously followed by a cardiologist, who died suddenly out-of-hospital, from ischemic heart disease. The second is that of a young adult under 40 years of age, of average build, with no particular medical history, having not previously consulted a cardiologist, who died suddenly of hypertrophic cardiomyopathy.

Conclusions

In many instances, we observed major anatomical lesion, which had not motivated any prior medical consultation either with a general practitioner or with a cardiologist.

背景-目的:青壮年在生前没有任何前兆或症状,却突然死亡,这是一个悲剧。医生往往无法解释其死亡原因,司法调查通常会要求进行尸检。我们的研究与世界各地的多项研究一样,将成人猝死与心脏疾病联系起来:方法:阿尔及利亚贝贾亚市弗朗茨-法农医院法医部在两年内进行了 305 例尸检,其中 57 例为原因不明的猝死,即每年每 10 万居民中有 3 例猝死:结果:50.8%的猝死病例(28 例)源于心脏疾病。在我们的研究中出现了两种流行病学特征:第一种是年龄在 50 岁至 60 岁之间的男性,有多种不良生活习惯(尤其是吸烟),有心血管病史,曾接受过心脏病专家的随访,因缺血性心脏病在院外猝死。第二例是一名 40 岁以下的年轻成年人,中等身材,无特殊病史,此前未就诊于心脏病专家,因肥厚型心肌病猝死:结论:在许多病例中,我们观察到了重大的解剖病变,而这些病变之前并未引起全科医生或心脏病专家的任何诊治。
{"title":"Mort subite de l'adulte : données de 305 cas d'autopsies consécutives en Algérie","authors":"Oussama Kerrouche ,&nbsp;Houssam Amghar ,&nbsp;Hicham Haddad","doi":"10.1016/j.ancard.2024.101760","DOIUrl":"10.1016/j.ancard.2024.101760","url":null,"abstract":"<div><h3>Background-aims</h3><p>Sudden death in a young adult who showed no prodrome or complaint during his lifetime is a tragedy. The death often remains unexplained by doctors and is often the subject of a judicial investigation following which an autopsy is ordered. Our study joins several studies around the world, where the results have linked sudden death in adults to a cardiac origin.</p></div><div><h3>Methods</h3><p>Through a series of 305 autopsies carried out in the forensic medicine department of the Frantz Fanon hospital in the city of Bejaia in Algeria over a period of two years, 57 cases corresponded to unexplained sudden deaths, i.e. an incidence of 3 cases per 100,000 inhabitants per year.</p></div><div><h3>Results</h3><p>Sudden death was of cardiac origin in 50.8% of cases (<em>N</em>=28). Two epidemiologic profiles emerge in our study: the first is that of a man aged between 50 and 60 years of age, with several deleterious lifestyle habits (in particular smoking) with a cardiovascular history, previously followed by a cardiologist, who died suddenly out-of-hospital, from ischemic heart disease. The second is that of a young adult under 40 years of age, of average build, with no particular medical history, having not previously consulted a cardiologist, who died suddenly of hypertrophic cardiomyopathy.</p></div><div><h3>Conclusions</h3><p>In many instances, we observed major anatomical lesion, which had not motivated any prior medical consultation either with a general practitioner or with a cardiologist.</p></div>","PeriodicalId":7899,"journal":{"name":"Annales de cardiologie et d'angeiologie","volume":"73 3","pages":"Article 101760"},"PeriodicalIF":0.3,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140955815","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
Aspirine et prévention de la récidive de la maladie veineuse thromboembolique 阿司匹林与预防血栓栓塞性静脉疾病复发
IF 0.3 Q4 Medicine Pub Date : 2024-05-15 DOI: 10.1016/j.ancard.2024.101761
Raida Ben Salah, Abir Derbel, Imen Chabchoub, Faten Frikha, Sameh Marzouk, Zouhir Bahloul

After a first episode of unprovoked vein thrombosis, the risk of recurrence persists for many years. Long term of anticoagulant therapy prevents the recurrence of vein thrombosis but is associated with a major risk of bleeding.

As platelets play a role in the initiation and propagation of venous thromboembolism as well, antiplatelet agents, may play a role in the treatment and prevention of this disease.

This review summarizes available evidence on effect of aspirin in the prevention of recurrent deep vein thrombosis.

首次无诱因静脉血栓形成后,复发风险会持续多年。由于血小板在静脉血栓栓塞症的发生和传播过程中也扮演着重要角色,因此抗血小板药物可在治疗和预防该疾病方面发挥作用。本综述总结了阿司匹林在预防深静脉血栓复发方面效果的现有证据。
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引用次数: 0
Place de l’électrocardiogramme dans la visite de non-contre-indication à la pratique sportive de compétition entre 12 et 35 ans : enquête auprès des médecins membres de l'Association Guinéenne des Médecins Sportifs 心电图在 12 至 35 岁非竞技体育禁忌症检查中的地位:对几内亚体育医生协会会员医生的调查。
IF 0.3 Q4 Medicine Pub Date : 2024-05-10 DOI: 10.1016/j.ancard.2024.101762
Mamadou Barry , Ibrahima Sory Sylla , Mamadou Dadhi Balde , Mohamed Bangoura , Ibrahima Camara

Introduction

An electrocardiogram (ECG), combined with a well-conducted clinical examination, is more effective than the clinical examination alone in detecting underlying cardiac pathologies in athletes. The aim of this study was to evaluate the use of ECGs by physicians who are members of the Guinean Association of Sports Physicians, during the non-contraindication visit for competitive sports between the ages of 12 and 35.

Methodology

We conducted a web-survey from July 15 to August 15, 2023. A survey form was created on “Google Docs” and pre-tested. It was then broadcast on all the communication networks used by these doctors. The data were secured using “Google Drive” software. Analyses were performed using SPSS version 20 software.

Results

Of the 51 included, 74.51% said they had received at least one training session on ECG interpretation for athletes. All of them either requested or performed an ECG at least once in a while, as part of the check-up for non-contraindication to competitive sport. The ECG was systematic, according to 72.55% of doctors. Three quarters referred to a sports cardiologist in the event of an abnormal ECG, 66.67% to a cardiology resident and 58.82% to a cardiologist. In the absence of an ECG, the presence of functional signs on exertion, the notion of a family history of cardiovascular disease and the presence of at least two cardiovascular risk factors were the main reasons for seeking an opinion.

Conclusion

A resting ECG is carried out almost systematically by doctors who are members of the Guinean Association of Sports Doctors, as part of the check-up for non-contraindication to practising sport.

导言:心电图(ECG)与完善的临床检查相结合,比单独的临床检查更能有效发现运动员潜在的心脏病变。本研究旨在评估几内亚运动医师协会会员医生在对 12 至 35 岁竞技体育运动员进行非禁忌症检查时使用心电图的情况。 方法我们于 2023 年 7 月 15 日至 8 月 15 日进行了一次网络调查。我们在 "谷歌文档 "上创建了调查表,并进行了预先测试。然后在这些医生使用的所有通信网络上进行广播。使用 "Google Drive "软件确保数据安全。结果 在 51 名调查对象中,74.51% 的人表示至少接受过一次关于运动员心电图解读的培训。他们都要求或至少在一段时间内做一次心电图,作为检查是否为竞技体育禁忌症的一部分。72.55%的医生认为心电图检查是系统性的。如果心电图异常,四分之三的医生会转诊给运动心脏病专家,66.67%的医生会转诊给心脏病住院医师,58.82%的医生会转诊给心脏病专家。在没有心电图的情况下,出现劳累时的功能性体征、有心血管疾病家族史以及存在至少两个心血管风险因素是寻求医生意见的主要原因。
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引用次数: 0
Léiomyosarcome portal : une localisation extrêmement rare ! 门静脉良性肉瘤:极其罕见的部位!
IF 0.3 Q4 Medicine Pub Date : 2024-05-08 DOI: 10.1016/j.ancard.2024.101759
Said Adnor, Abderrahmane Ibenyahia, Fadoua Ijim, Mounir Salek, Abdelhamid Maqsoudi, Soukaina Wakrim

Leiomyosarcomas of large vessels are rare. It is a malignant tumour and the vast majority of these tumours arose from the inferior vena cava. We report a rare case of portal vein leiomyosarcoma, in a 56-years-old female patient admitted for chronic abdominal pain with abdominal mass in the right hypochondrium all evolving in a context of deterioration in general condition. We performed an abdominopelvic CT scan and then a MRI with contrast agent which objectified a large tissue mass containing areas of necrosis at the level of the duodeno-pancreatic compartment communicating at a large angle with the portal trunk over its entire length from the hepatic hilum to the spleno-mesenteric confluence responsible for a portal cavernoma downstream. This is associated with multiple secondary nodular tissue hepatic lesions. We also noted a respect for the fatty border separating the mass of the duodenal tract and the head of the pancreas, and also the absence of dilation of the pancreatic ducts making a pancreatic origin unlikely. To eliminate a duodenal origin of the mass we performed an upper digestive endoscopy which came back without any abnormality. An ultrasound-guided trans parietal biopsy of a secondary hepatic lesion was done and the pathological result of which speaks of a secondary hepatic lesion of a leiomyosarcoma.

大血管横纹肌肉瘤非常罕见。它是一种恶性肿瘤,绝大多数来自下腔静脉。我们报告了一例罕见的门静脉横纹肌肉瘤病例,患者是一名 56 岁女性,因慢性腹痛和右下腹肿块入院,全身情况恶化。我们对患者进行了腹盆腔 CT 扫描,然后用造影剂进行了核磁共振成像,结果发现患者的十二指肠-胰腺间隙处有一个巨大的组织肿块,肿块内有多处坏死区,肿块与门静脉主干从肝门到脾门-肠门汇合处全长呈大角度相通,导致门静脉海绵状瘤下行。这与多个继发性肝结节组织病变有关。我们还注意到十二指肠道肿块与胰腺头部之间的脂肪边界,以及胰腺导管没有扩张,因此不太可能是胰腺起源。为了排除十二指肠肿块的来源,我们进行了上消化道内窥镜检查,结果显示没有任何异常。我们在超声引导下对继发性肝脏病变进行了经顶叶活检,病理结果显示继发性肝脏病变为肝癌。
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引用次数: 0
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Annales de cardiologie et d'angeiologie
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