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[A complete atrioventricular block during exertion]. [运动时完全性房室传导阻滞]。
A Medeiros, P Iturralde, F Millán, L Colín, F Cruz, J A González Hermosillo, A Méndez

Exercise-induced atrioventricular (AV) block in patients with normal electrocardiogram at rest is uncommon. We report the clinical features of two patients with AV block during treadmill test. The first patient was a woman of 54 years of age with presyncope on exercise. She developed complete AV block during exercise testing without evidence of ischemic myocardial disease. Electrophysiologic study documented distal AV block. The second patient was a man 31 years old who developed angina and third-degree AV block with depression of ST segment during treadmill test. Myocardial perfusion study suggested ischemic heart disease. He received anti-ischemic drugs with improvement of symptoms. A control exercise testing demonstrated normal AV conduction and electrophysiologic study was normal. In the first case, exercise AV block was probably due to abnormal His Purkinje conduction system refractoriness to autonomic modulation, while in second case AV block was secondary to ischemic heart disease. Third-degree AV block at exercise can be present in patients without conduction system abnormalities at rest. Exercise-induced infra-Hisian AV block must be treated with pacing until ischemic heart disease has been ruled out.

在静息时心电图正常的患者中,运动引起的房室传导阻滞并不常见。我们报告两例在跑步机试验中出现房室传导阻滞的患者的临床特征。第一位患者是一位54岁的女性,在运动中出现了晕厥前症。她在运动试验中出现完全的房室传导阻滞,没有缺血性心肌疾病的证据。电生理检查证实远端房室传导阻滞。第二例患者为31岁男性,在跑步机试验中出现心绞痛和三度房室传导阻滞并ST段下降。心肌灌注研究提示缺血性心脏病。他接受了抗缺血药物治疗,症状有所改善。对照运动试验显示房室传导正常,电生理检查正常。在第一种情况下,运动性房室传导阻滞可能是由于His浦肯野传导系统异常对自主神经调节的难耐,而在第二种情况下,房室传导阻滞是继发于缺血性心脏病。运动时三度房室传导阻滞可出现在静止时无传导系统异常的患者。在排除缺血性心脏病之前,必须采用起搏治疗运动引起的下hisian房室传导阻滞。
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引用次数: 0
[Surgical complications and mortality in octogenarian patients undergoing revascularization surgery]. [八旬老人行血运重建术患者的手术并发症及死亡率]。
A Palao Mendoza, C Kúsulas Zerón, J A Palomo Villada

Unlabelled: Our objective was to identify preoperative, operative and postoperative factors associated with complications and mortality in patients equal to or greater than 70 years of age with coronary artery disease treated with coronary bypass surgery. From january 1990 to june 1994 of those that underwent 37 coronary artery bypass surgery. 32 were men (86.5%) and five women (13.5%). History of cardiovascular disease, diabetes mellitus, systemic arterial hypertension, pulmonary disease, hypercholesterolemia, renal function, and severity of coronary artery disease were considered. Also analysed were aortic clamp and cardiopulmonary bypass time, number and type of grafts. Use of intraaortic balloon counterpulsation, inotropic drugs, ventilatory support, hemorrhage, infection, renal and liver failure, neurological, rhythm and conduction abnormalities and myocardial ischemia were also considered. Identified risk factors: diabetes mellitus, (p = 0.028), ejection fraction < 30% (p = 0.023), ventricular wall motion abnormalities (p < 0.05), aortic clamp > 60 minutes (p = 0.026), cardiopulmonary bypass < 120 minutes (p = 0.022), reverse saphenous vein grafts (p = 0.014), prolonged ventilatory support, inotropic drugs and intraaortic balloon counterpulsation.

Conclusions: Surgery should be reserved for patients with at least three vessel or left main coronary artery disease or proximal lesion of the left anterior descending artery with severe ischemia, deteriorated myocardial function and angina with no response to medical treatment; age of the patient is not a contraindication.

未标记:我们的目的是确定术前、手术和术后与冠状动脉搭桥手术治疗的年龄等于或大于70岁的冠状动脉疾病患者并发症和死亡率相关的因素。从1990年1月到1994年6月进行了37次冠状动脉搭桥手术。男性32人(86.5%),女性5人(13.5%)。考虑心血管病史、糖尿病、全身性动脉高血压、肺病、高胆固醇血症、肾功能和冠状动脉疾病严重程度。同时分析了主动脉夹夹和体外循环的时间、移植物的数量和类型。使用主动脉内球囊反搏、肌力药物、通气支持、出血、感染、肾和肝衰竭、神经、节律和传导异常以及心肌缺血也被考虑在内。确定的危险因素:糖尿病(p = 0.028),射血分数< 30% (p = 0.023),心室壁运动异常(p < 0.05),主动脉夹持> 60分钟(p = 0.026),体外循环< 120分钟(p = 0.022),反向隐静脉移植(p = 0.014),延长通气支持,肌力药物和主动脉球囊反搏。结论:至少有三支血管或左主干病变或左前降支近端病变,且严重缺血、心肌功能恶化、心绞痛,药物治疗无效的患者应保留手术;患者的年龄不是禁忌。
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引用次数: 0
[Bicentennial of the death of Lazzaro Spallanzani, pioneer of cardiovascular and respiratory physiology]. [心血管和呼吸生理学先驱拉扎罗·斯帕兰扎尼逝世200周年]。
A de Micheli
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引用次数: 0
[Persistent common trunk. Anatamopathological study of 25 specimen]. [持久的公共主干。]25例标本的解剖病理研究[j]。
L Muñoz Castellanos, M Kuri Nivón, C A Vázquez Antona

In order to inform the pathologic features and their associated anomalies twenty five hearts with common trunk were studied with the segmental sequential system. An anatomico-embryological correlation was made to understand the pathological complex of this malformation. The results were: type I truncus (96%), infundibular ventricular septal defect (96%), displastic truncal valve (28%), ventriculo infundibular fold (92%), left coronary artery arising from the posterior wall of the truncus (75%), right coronary artery arising from their anterior wall (96%), coronary arteries arising from opposite Valsalva sinuses in the tetracuspid valves; the biventricular conection of the truncus was balanced in 60%, prevailing on the right (16%) or on the left (16%) ventricles. Among the associated anomalies there were right aortic arch, interruption of the aortic arch, anomalous origin of the left subclavian artery, vascular ring, aneurysm of the sinus of Valsalva, and absence of the left branch of the pulmonary artery. Developmentally common trunk is explained as a failure of truncoconal septation in the embryonic heart; a migration arrest of neural crest cells is implicated in the Di George syndrome. Knowledge of the anatomic features of common trunk and their associated anomalies, provides the morphological basis to interpret correctly the clinical diagnostic imagenology.

为了解其病理特征及相关异常,采用节段序贯系统对25例有主干的心脏进行了研究。解剖-胚胎学相关性是为了了解这种畸形的病理复杂性。结果:I型干(96%),室间隔缺损(96%),截断瓣发育不全(28%),室间隔褶(92%),左冠状动脉起源于干后壁(75%),右冠状动脉起源于前壁(96%),冠状动脉起源于四尖瓣对侧Valsalva窦;双心室主干连接平衡的比例为60%,主要分布在右心室(16%)或左心室(16%)。相关异常包括右主动脉弓、主动脉弓中断、左锁骨下动脉起源异常、血管环、Valsalva窦动脉瘤、肺动脉左支缺失。发育上的共同干被解释为胚胎心脏的干隔分离失败;神经嵴细胞的迁移阻滞与Di George综合征有关。了解共干的解剖特征及其相关异常,为正确解释临床诊断影像学提供形态学依据。
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引用次数: 0
[New strategies for the classification and treatment of acute ischemic coronary syndromes. A proposal]. 急性缺血性冠状动脉综合征的分类和治疗新策略。建议)。
C Jerjes-Sanchez Díaz, A Garza-Ruiz, P Gutiérrez-Fajardo, G Villareal Coindreau
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引用次数: 0
[Medical-surgical management of left heart valve prosthesis dysfunction due to obstruction. Eleven year's experience]. 左心瓣膜梗阻功能障碍的内科-外科治疗。11年的经验]。
J S Valencia Sánchez, R Arriaga Nava, A Martínez Enríquez, J Navarro Robles, J A Palomo Villada

Unlabelled: We report the surgical-medical experience in left side mechanic prosthesis cardiac valve dysfunction. From January 1986 to June 1997 we included 108 consecutive patients (pts), 24 were men and 84 women, mean age 45 years, they underwent 114 surgical procedures, 104 in mitral and 10 in aortic position.

Results: The dysfunction was due to obstruction in fixed disc in 107 pts and intermitent in 7 pts. The pathological findings were thrombosis in 92 pts, pannus in 9 pts and both in 13 pts. The time interval between valve replacement and dysfunction was from 1 to 247 months, mean 53.8 +/- 56.7. Seventy five percent of patients received inadequate anticoagulant therapy, the mean INR was 2.06 +/- 0.79. In 76% of patients the functional class was III or IV NYHA. The diagnosis was made by clinical and echocardiographic findings in 96% of patients. The surgical procedures included valve replacement in 103, and toilette in 11 pts. The time of extracorporeal circulation in patients who died us survival patients were (159.9 +/- 108.95 vs 87.32 +/- 27.53 min) and aortic cross-clamp (64.8 +/- 20.69 vs 48.28 +/- 23.71 min) respectively (p < 0.001). The overall mortality was 12 pts (10.5%), all in functional class III or IV NYHA (p < 0.05), five patients died during surgical procedure. In conclusion the diagnosis must be established clinically as well as by echocardiography. The risk factors associated with mortality were pulmonary edema, shock, delayed surgery, surgical time prolonged and functional class III or IV NYHA.

未标记:我们报告左侧机械假体心脏瓣膜功能障碍的外科医疗经验。从1986年1月至1997年6月,我们纳入了108例患者,其中男性24例,女性84例,平均年龄45岁,接受了114例手术,其中二尖瓣104例,主动脉10例。结果:固定椎间盘梗阻者107例,间歇性者7例。病理表现为血栓92例,静脉血栓9例,两者均有13例。瓣膜置换术与功能障碍之间的时间间隔为1 ~ 247个月,平均53.8 +/- 56.7。75%的患者接受了不充分的抗凝治疗,平均INR为2.06±0.79。76%的患者功能等级为III级或IV级NYHA。96%的患者通过临床和超声心动图诊断。手术包括103例瓣膜置换术,11例洗漱。死亡患者体外循环时间和存活患者体外循环时间分别为(159.9 +/- 108.95 vs 87.32 +/- 27.53 min)和(64.8 +/- 20.69 vs 48.28 +/- 23.71 min) (p < 0.001)。总死亡率为12例(10.5%),均为功能性III或IV级NYHA (p < 0.05), 5例患者在手术过程中死亡。总之,诊断必须建立临床和超声心动图。与死亡率相关的危险因素是肺水肿、休克、手术延迟、手术时间延长和NYHA功能为III或IV级。
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引用次数: 0
[Translumbar coronary angiography and aortography in a patient with Takayasu's arteritis]. 【经腰冠状动脉造影及主动脉造影1例Takayasu动脉炎】。
S Tovar Blanco, R Ernesto Marenco, M A Peña Duque, J Luna Guerra, J Vázquez Sánchez, M A Martínez Ríos

Since its introduction by Dos Santos in 1929, arterial angiography by translumbar percutaneous approach has suffered some transformations. Nowadays it has been replaced by other percutaneous approaches and it is indicated only when these routes of access have failed due to aortoiliac or subclavian arteries obstruction. This report presents a patient with Takayasu's Arteritis with severe peripheral arterial obstruction and unstable angina, who underwent coronary arteriography and aortography by translumbar approach. A review of this technique is made.

自1929年Dos Santos引入经腰经皮动脉血管造影术以来,动脉血管造影术经历了一些变化。如今,它已被其他经皮入路所取代,只有当这些途径由于髂主动脉或锁骨下动脉阻塞而失败时才适用。本文报告一例伴有严重外周动脉阻塞和不稳定型心绞痛的Takayasu动脉炎患者,行冠状动脉造影和经腰椎入路主动脉造影。本文对该技术进行了综述。
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引用次数: 0
[Cardiology review. Molecular and genetic aspects of cardiopathies]. [心脏病审查。心脏病的分子和遗传方面]。
D Jay
{"title":"[Cardiology review. Molecular and genetic aspects of cardiopathies].","authors":"D Jay","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75556,"journal":{"name":"Archivos del Instituto de Cardiologia de Mexico","volume":"69 2","pages":"157-62"},"PeriodicalIF":0.0,"publicationDate":"1999-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21341326","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
[The benefit of a coronary stent in the reduction of major cardiac complications in acute coronary syndromes]. [冠状动脉支架在减少急性冠状动脉综合征的主要心脏并发症中的益处]。
M A Martínez-Ríos, G Eid-Lidt, J Luna Guerra, R Villavicencio Fernández, E Ban Hayashi, J Gaspar Hernández, M A Peña Duque

To assess the incidence of in-hospital major adverse cardiac events (MACE), we analyzed 694 procedures in 613 consecutive patients during one year period. Patient population included 550 (79.2%) patients with unstable angina, 43 (6.2%) with stable angina and 101 (14.5%) with acute myocardial infarction. Elective percutaneous transluminal coronary angioplasty (PTCA) was performed in 593 (85.4%) patients, rescue PTCA in 7 (1%), and primary PTCA in 94 (13.5%). Angiographic lesion morphology was as follows: type A 30%; type B 58%; type C 12%. We compared patient population who received stent with PTCA-balloon only. Technical success was 95% and clinical success was achieved in 80% of the cases. Overall mortality was 1% in the stent group and 3% in the conventional PTCA. The incidence of MACE was 4% and 15.1% in the stent and angioplasty balloon groups respectively. We found a dramatic impact on reduction of the incidence of acute complications in the groups with stenting for unstable angina (p = 0.0001) and acute myocardial infarction (p = 0.0001). The major clinical advantage of stenting over balloon angioplasty was a lower need for repeated procedures.

为了评估院内主要心脏不良事件(MACE)的发生率,我们分析了613例连续患者一年内的694例手术。其中不稳定型心绞痛550例(79.2%),稳定型心绞痛43例(6.2%),急性心肌梗死101例(14.5%)。593例(85.4%)患者行择期经皮腔内冠状动脉成形术(PTCA),救救性PTCA 7例(1%),原发性PTCA 94例(13.5%)。血管造影病变形态如下:A型占30%;B型58%;C型12%。我们比较了接受支架和ptca球囊的患者。技术成功率为95%,临床成功率为80%。支架组的总死亡率为1%,传统PTCA组的总死亡率为3%。支架组MACE发生率为4%,球囊组MACE发生率为15.1%。我们发现支架置入治疗不稳定心绞痛组(p = 0.0001)和急性心肌梗死组(p = 0.0001)对降低急性并发症发生率有显著影响。与球囊血管成形术相比,支架置入术的主要临床优势是不需要重复手术。
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引用次数: 0
Interruption of the aortic arch in adults. 成人主动脉弓中断。
A Rangel, E Chávez, I Espinosa

The interruption of the aortic arch is a rare cardiac congenital disease; such patients may occasionally survive to adulthood without surgery. The associated intracardiac malformations may modify survival. Our aim is to report three young adults (18-19 years of age) with interruption of the aortic arch. Two had type C, and the other had type B with subpulmonic ventricular septal defect and pulmonary valve insufficiency. We review 106 cases collected from the medical literature into 3 groups: 1) the whole group of patients; 2) patients with isolated interruption of the aortic arch, and 3) patients with interruption of the aortic arch associated with ventricular septal defect. In the whole group we found 18 cases of interruption of the aortic arch type A, and 25 cases of interruption of the aortic arch type B; 37 cases of isolated interruption of the aortic arch and 43 cases associated with ventricular septal defect. Fifty percent of the patients died before 15 days of life (0.042 years). According to the cumulative frequency graphic, only 5% of the patients survived beyond the age of 5 years. We found no information to relate patient's survival rate and anatomic type of the interruption of the aortic arch. From adolescence, the survival of the patients with interruption of the aortic arch associated to septal ventricular defect was 7%, and a 14% survival was found in patients with isolated interruption of the aortic arch. No statistical difference was found between the means of the ages of these two groups (P > 0.25).

主动脉弓中断是一种罕见的心脏先天性疾病;这样的病人偶尔可以不做手术存活到成年。相关的心内畸形可能影响生存率。我们的目的是报告三名年轻人(18-19岁)主动脉弓中断。2例为C型,1例为B型,合并肺动脉下室间隔缺损和肺动脉瓣功能不全。我们从医学文献中收集106例病例,将其分为3组:1)整组患者;2)孤立性主动脉弓中断患者,3)主动脉弓中断合并室间隔缺损患者。全组A型主动脉弓中断18例,B型主动脉弓中断25例;孤立性主动脉弓中断37例,合并室间隔缺损43例。50%的患者在15天(0.042岁)前死亡。根据累积频率图,只有5%的患者存活超过5年。我们没有发现患者存活率与主动脉弓中断的解剖类型相关的信息。从青春期开始,主动脉弓中断与室间隔缺损相关的患者的生存率为7%,而孤立性主动脉弓中断患者的生存率为14%。两组患者年龄均值比较,差异无统计学意义(P > 0.25)。
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引用次数: 0
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Archivos del Instituto de Cardiologia de Mexico
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