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"Natural" History of Operated Type A Aortic Dissection. A型主动脉夹层手术的“自然”病史。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2023-11-10 DOI: 10.1055/s-0043-1774415
Gian B Danzi, Alberto Carrozza, Silvia Frattini

We describe the case of a 66-year-old gentleman with a previous replacement of the ascending aorta for an acute Type A aortic dissection who did not attend any scheduled follow-up visit. Seventeen years later, he presented to our institution with severe aortic regurgitation and with a giant aneurysmal dilation of the abdominal aorta.

我们描述了一位66岁的男性患者的病例,他曾因急性a型主动脉夹层接受升主动脉置换术,但没有参加任何预定的随访。17年后,他因严重的主动脉反流和腹主动脉巨大的动脉瘤样扩张来到我们的机构。
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引用次数: 0
Endovascular Repair of Zone 0 Ascending Aortic Pseudoaneurysm: A Case Report. 0 区升主动脉假性动脉瘤的血管内修复术:病例报告。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2024-03-19 DOI: 10.1055/s-0043-1777436
Sarah Halbert, Christian Nagy, Jared Antevil, Shawn Sarin, Gregory Trachiotis

Although open surgery is standard of care for ascending aortic pathology, endovascular approaches can be viable options. We report the case of a 77-year-old man with a 5.7-cm ascending aorta penetrating ulcer. Given his age and clinical profile, the patient underwent Zone 0 thoracic endovascular aortic repair.

虽然开放手术是升主动脉病变的标准治疗方法,但血管内方法也是可行的选择。我们报告了一例患有 5.7 厘米升主动脉穿透性溃疡的 77 岁男性病例。考虑到患者的年龄和临床特征,他接受了 0 区胸腔内主动脉血管修补术。
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引用次数: 0
Secondary Endovascular Conversions for Failed Open Repair. 开放性修复失败的二次血管内转换。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2023-11-10 DOI: 10.1055/s-0043-1774724
Ryan Gouveia E Melo, Paolo Spath, Jan Stana, Carlota F Prendes, Konstantinous Stavroulakis, Barbara Rantner, Maximilian Pichlmaier, Nikolaos Tsilimparis

Late aortic and graft-related complications after open aortic repair are not infrequent and a significant number of them are missed, diagnosed at a very late stage, or present as urgent complications such as aortic rupture or aorto-enteric fistula. Once a late complication is diagnosed and reintervention is necessary, both open and endovascular strategies are possible. Open reintervention is complex and usually associated with very high rates of morbidity and mortality. Endovascular techniques may offer several solutions for these cases, which may be tailored to the patient and specific complication. In this review, we aim to summarize current indications, options, and strategies for endovascular salvage after failed or complicated open surgical repair.

开放式主动脉修复后的晚期主动脉和移植物相关并发症并不罕见,其中相当多的并发症是遗漏的、在非常晚期诊断的,或表现为紧急并发症,如主动脉破裂或主动脉-肠瘘。一旦诊断出晚期并发症并需要再次干预,开放和血管内策略都是可能的。开放性再干预是复杂的,通常与非常高的发病率和死亡率有关。血管内技术可以为这些病例提供几种解决方案,这些方案可以根据患者和特定并发症进行定制。在这篇综述中,我们旨在总结失败或复杂的开放手术修复后血管内挽救的当前适应症、选择和策略。
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引用次数: 0
Contributing Reviewers in 2023. 2023 年的特约评论员。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2024-04-23 DOI: 10.1055/s-0044-1786353
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引用次数: 0
A Rare but Fatal Behçet Variant: The Hughes-Stovin Syndrome-Successful Case Report and New Evidence from Literature Review. 一种罕见但致命的贝赫切特变异体:休斯-斯托文综合征--成功的病例报告和文献综述中的新证据。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2024-03-26 DOI: 10.1055/s-0043-1777994
Andrea Ascoli Marchetti, Lorella Belvivere, Renato Argirò, Barbara Kroegler, Fabio M Oddi, Federico Pennetta, Alice de Giorgi, Stefano Fazzini, Daniele Morosetti, Paola Triggianese, Elisabetta Greco, Arianna D'Antonio, Ilaria Coccia, Manfredi Tesauro, Federica Sangiuolo, Arnaldo Ippoliti

Hughes-Stovin syndrome (HSS) is a rare potentially fatal vasculitis supposedly belonging to the spectrum of Behçet disease without ocular involvement. HSS tends to play by a temporal pattern, starting with thrombosis and followed by formation of pulmonary aneurysms. Since its mortality can reach 25% of cases, early recognition and appropriate therapy represent the major clinical challenges. We describe a rare case of HSS successfully treated via multidisciplinary management by an endovascular approach and immunosuppressive therapy.

休斯-斯托文综合征(HSS)是一种罕见的潜在致命性血管炎,据说属于贝赫切特病(Behçet disease)的一种,但不累及眼部。休斯-斯托文综合征的发病往往具有时间性,首先是血栓形成,然后是肺动脉瘤的形成。由于其死亡率高达 25%,因此早期识别和适当治疗是临床面临的主要挑战。我们描述了一例罕见的 HSS 病例,该病例通过血管内治疗和免疫抑制疗法等多学科治疗获得成功。
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引用次数: 0
Near-Infrared Spectroscopy for Spinal Cord Monitoring-A Roadmap to Translational Research in Aortic Medicine. 近红外光谱用于脊髓监测——主动脉医学转化研究的路线图。
Q3 Medicine Pub Date : 2023-08-01 Epub Date: 2023-11-10 DOI: 10.1055/s-0043-1772774
Konstantin von Aspern, Josephina Haunschild, Jens Garbade, Christian D Etz

Extensive aortic aneurysms represent a unique challenge necessitating interdisciplinary efforts for safe and effective treatment. Despite various adjunctive neuroprotective strategies, ischemic spinal cord injury remains a devastating complication. This article describes the implementation of collateral network near-infrared spectroscopy as the first noninvasive spinal cord monitoring modality in the setting of extensive open and endovascular aortic repair, from early conceptualization to clinical utilization. Potential capabilities and remaining uncertainties based on current evidence are outlined and discussed.

广泛的主动脉瘤是一个独特的挑战,需要跨学科努力进行安全有效的治疗。尽管有各种辅助神经保护策略,缺血性脊髓损伤仍然是一种毁灭性的并发症。本文描述了侧支网络近红外光谱作为第一种无创脊髓监测模式在广泛开放和血管内主动脉修复中的应用,从早期概念化到临床应用。概述并讨论了基于现有证据的潜在能力和剩余的不确定性。
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引用次数: 0
Comparison of Genes Associated with Thoracic and Abdominal Aortic Aneurysms. 胸主动脉瘤和腹主动脉瘤相关基因的比较
Q3 Medicine Pub Date : 2023-06-01 Epub Date: 2023-06-06 DOI: 10.1055/s-0043-57266
Argyrios Gyftopoulos, Bulat A Ziganshin, John A Elefteriades, Cassius I Ochoa Chaar

Aneurysms impacting the ascending thoracic aorta and the abdominal aorta affect patient populations with distinct clinical characteristics. Through a literature review, this paper compares the genetic associations of ascending thoracic aortic aneurysm (ATAA) with abdominal aortic aneurysms (AAA). Genes related to atherosclerosis, lipid metabolism, and tumor development are associated specifically with sporadic AAA, while genes controlling extracellular matrix (ECM) structure, ECM remodeling, and tumor growth factor β function are associated with both AAA and ATAA. Contractile element genes uniquely predispose to ATAA. Aside from known syndromic connective tissue disease and poly-aneurysmal syndromes (Marfan disease, Loeys-Dietz syndrome, and Ehlers-Danlos syndrome), there is only limited genetic overlap between AAA and ATAA. The rapid advances in genotyping and bioinformatics will elucidate further the various pathways associated with the development of aneurysms affecting various parts of the aorta.

影响升胸主动脉和腹主动脉的动脉瘤会影响具有不同临床特征的患者群体。通过文献综述,本文比较了升胸主动脉瘤(ATAA)与腹主动脉瘤(AAA)的遗传关联。与动脉粥样硬化、脂质代谢和肿瘤发生有关的基因与散发性 AAA 特别相关,而控制细胞外基质(ECM)结构、ECM 重塑和肿瘤生长因子 β 功能的基因与 AAA 和 ATAA 都相关。收缩元件基因是导致 ATAA 的独特诱因。除了已知的综合结缔组织病和多动脉瘤综合征(马凡病、Loeys-Dietz 综合征和 Ehlers-Danlos 综合征)外,AAA 和 ATAA 之间的遗传重叠非常有限。基因分型和生物信息学的飞速发展将进一步阐明与影响主动脉各部位动脉瘤发病相关的各种途径。
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引用次数: 0
Frozen Elephant Trunk for Acute Type A Dissection: Is Risk from Procedure or Patient Characteristics? 冷冻象鼻用于急性A型解剖:风险来自手术还是患者特征?
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.1055/s-0043-1768970
R Wilson King, Adam M Carroll, Kelly C Higa, Joseph C Cleveland, Jessica Y Rove, Muhammad Aftab, Thomas Brett Reece

Background:  The initial goal of acute Type A aortic dissection (ATAAD) repair remains to get the patient off the table safely. More extensive repair is being pushed at the index operation with the frozen elephant trunk (FET) operation, but outcomes are suggested to be worse. However, we hypothesize that the risk associated with the FET in ATAAD is from the patient presenting factors rather than the operation itself.

Methods:  A retrospective review of a single institution prospective database from 2015 to 2021 was performed. Two cohorts were created based on the indication for FET: evidence of radiographic malperfusion (n = 44) or clinical malperfusion (n = 31). Data were analyzed for preoperative characteristics, intraoperative characteristics, and postoperative outcomes. Statistical univariate analysis was performed with chi-square analysis and t-tests with significance determined at an alpha level of 0.05.

Results:  Preoperative characteristics were similar in each group, independent of malperfusion markers. The intraoperative characteristics were similar, except the clinical malperfusion group had more packed red blood cells and cryoprecipitate given. The clinical malperfusion group had longer intensive care unit length of stay (p < 0.001), more postoperative strokes (p < 0.001), more reoperations (p <0.0001), and higher mortality rate (p = 0.0003).

Conclusion:  These data suggest that clinical malperfusion increases the risk of major complications and death. However, full arch replacement with FET in the absence of clinical malperfusion does not appear to add risk to the operation for ATAAD. Patients with increased risk of distal degeneration should be considered for more aggressive replacement to avoid subsequent arch replacement.

背景:急性A型主动脉夹层(ATAAD)修复的最初目标仍然是使患者安全下床。更广泛的修复正在推进与冷冻象鼻(FET)手术的索引操作,但结果被认为更差。然而,我们假设与ATAAD中FET相关的风险来自患者的表现因素,而不是手术本身。方法:对2015年至2021年的单一机构前瞻性数据库进行回顾性分析。根据FET的适应症创建了两个队列:影像学灌注不良证据(n = 44)或临床灌注不良证据(n = 31)。对数据进行术前、术中、术后结果分析。统计单变量分析采用卡方分析和t检验,α水平为0.05,具有显著性。结果:各组术前特征相似,不受灌注不良指标影响。术中特征相似,但临床灌注不良组红细胞堆积较多,给予低温沉淀。临床灌注不良组重症监护病房住院时间更长(p p p p = 0.0003)。结论:临床灌注不良增加了主要并发症和死亡的风险。然而,在没有临床灌注不良的情况下,用FET进行全弓置换似乎不会增加ATAAD手术的风险。远端退变风险增加的患者应考虑更积极的置换术,以避免后续的弓置换术。
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引用次数: 0
Reoperation or Aortic Regurgitation Progression after Reimplantation of the Aortic Valve (David's Procedure) Using the Valsalva Graft. Valsalva瓣植入术后再手术或主动脉返流进展。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.1055/s-0043-1768968
Kristina Ma, Emelie Carlestål, Anders Franco-Cereceda, Christian Olsson

Background:  This study aimed to assess predictors of a composite endpoint (reoperation for aortic valve [AV] failure or aortic regurgitation [AR] grade ≥ 2) after reimplantation of the aortic valve (RAV) using the Valsalva graft.

Methods:  From 2012 to 2021, 112 patients underwent RAV in a single center. Clinical and echocardiographic data were collected retrospectively. Cox regression analysis was used to identify predictors of the composite endpoint. Kaplan-Meier methods were used for time-to-event analysis.

Results:  Median (interquartile range) age was 52 years (44, 62). Nineteen patients (17%) were operated for acute Type A aortic dissection, and the remainder for aortic root aneurysm, 60 mm or larger in 12/112 (11%). Thirty-day mortality was 1/112 (1%). During follow-up, four patients (3.6%) were reoperated for AV failure, and another nine patients (8.1%) developed AR grade ≥ 2. Overall estimated freedom from reoperation or AR grade ≥ 2 was 87% (95% confidence interval: 76-93%) at 5 years. Significantly lower estimated 5-year freedom from the composite endpoint was found in cases with simultaneous aortic valve repair (AVr; 77 vs. 90%, p = 0.007) and nearly significant for large (≥ 6 cm) aortic root diameter (82 vs. 87%, p = 0.055). In Cox's analysis, aortic root diameter and simultaneous AVr were independent predictors for the composite endpoint.

Conclusion:  Outcomes (survival, reoperation, freedom from AR grade ≥ 2) with RAV were good up to 11-year follow-up. Larger aortic root diameter and simultaneous AVr were identified as predictors for reoperation or AR grade ≥ 2. Long-term follow-up remains necessary to confirm adequate AV function.

背景:本研究旨在评估使用Valsalva移植物重植术(RAV)后复合终点(主动脉瓣[AV]衰竭或主动脉反流[AR]等级≥2)的预测因素。方法:2012年至2021年,在单个中心接受RAV治疗的112例患者。回顾性收集临床及超声心动图资料。采用Cox回归分析确定复合终点的预测因子。Kaplan-Meier方法用于时间-事件分析。结果:年龄中位数(四分位数间距)为52岁(44,62岁)。急性A型主动脉夹层19例(17%),60 mm及以上主动脉根动脉瘤12/112例(11%)。30天死亡率为1/112(1%)。随访期间,4例(3.6%)患者因房室功能衰竭再次手术,另有9例(8.1%)患者发生≥2级AR。总体估计5年时再手术或AR等级≥2的自由度为87%(95%置信区间:76-93%)。同时主动脉瓣修复(AVr;77比90%,p = 0.007),主动脉根直径大(≥6 cm)的患者几乎显著(82比87%,p = 0.055)。在Cox分析中,主动脉根直径和同时AVr是复合终点的独立预测因子。结论:随访11年,RAV患者的预后(生存、再手术、不再出现≥2级AR)良好。较大的主动脉根直径和同时AVr被认为是再次手术或AR等级≥2的预测因素。长期随访仍有必要确认足够的房室功能。
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引用次数: 0
Redo Aortic Surgery in a Patient with a Large Arachnoid Cyst and Myelodysplasia. 大蛛网膜囊肿伴骨髓增生患者重做主动脉手术1例。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.1055/s-0043-1770959
Syed F Hashmi, Ragheb Traify, Ioannis Dimarakis

A 70-year-old man was referred for redo root and ascending aortic surgery. Preoperative investigations depicted a large arachnoid cyst occupying the left frontotemporal region and myelodysplasia with persistent thrombocytopenia. We describe successful operative management of this patient in the context of such rare intracranial pathology.

一位70岁的男性被推荐做重根和升主动脉手术。术前检查显示一个巨大的蛛网膜囊肿占据左侧额颞区和骨髓发育不良伴持续性血小板减少。我们描述成功的手术管理的情况下,这种罕见的颅内病理这名患者。
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引用次数: 0
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