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自发性孤立性腹腔干或肠系膜上动脉夹层患者的危险因素分析及治疗结果

Risk factor analysis and treatment outcome of patients with spontaneous isolated celiac axis or superior mesenteric artery dissection.

作者信息

Hau Siew Fung, Chan Yiu Che, Cheung Grace C, Cheng Stephen W

机构信息

Division of Vascular and Endovascular Surgery, Department of Surgery, University of Hong Kong Medical Center, Queen Mary Hospital, Hong Kong Special Administration Region, China.

Division of Vascular and Endovascular Surgery, Department of Surgery, University of Hong Kong Medical Center, Queen Mary Hospital, Hong Kong Special Administration Region, China.

出版信息

J Vasc Surg. 2023 Jan;77(1):150-157. doi: 10.1016/j.jvs.2022.08.036. Epub 2022 Sep 7.

Abstract

BACKGROUND

Spontaneous isolated mesenteric artery (celiac axis or superior mesenteric artery [SMA]) dissection (IMAD) is a rare clinical entity. The aim of the present study was to examine the patient demographics, comorbidities, clinical and radiologic features, management, and prognosis and to identify the risk factors predictive of symptoms.

METHODS

We performed a single-center, retrospective review from November 2005 to November 2021 of prospectively collected data from patients with a diagnosis of IMAD. The clinical data and radiologic images were reviewed, and statistical analysis was performed to compare the symptomatic and asymptomatic groups.

RESULTS

A total of 78 patients were identified. Of the 78 patients, 24 (31%) had had celiac dissections, 51 (65%) had had SMA dissections, and 3 (4%) had had both celiac and SMA dissections. The mean age was 57.7 years (range, 36-84 years), with a male predominance (86%). More than one half (55%) of the patients had had hypertension. In addition, 29 patients (37%) were symptomatic, and 24 (31%) had been admitted to the hospital. The symptomatic patients with celiac axis dissections were more likely to have thrombosis (P = .02), significant stenosis (P = .01) or branch extension (P = .02). The symptomatic patients with SMA dissections were more likely to have a smaller artery diameter (P = .07), a longer dissection length (P = .05), thrombosis (P < .001), significant stenosis (P < .001), or branch extension (P = .003). The symptomatic patients were more likely to have been treated with antiplatelet or anticoagulant therapy (P < .001). Only three patients had undergone an intervention. Seven patients (9%) had died of unrelated causes. The Kaplan-Meier survival analysis showed a 5-year survival rate of 96% and 10-year survival rate of 91%.

CONCLUSIONS

IMAD is an uncommon disease entity with a risk of visceral ischemia. Nonetheless, most of these patients can be treated conservatively with medication, with only a small minority requiring emergency surgery.

摘要

背景

自发性孤立性肠系膜动脉(腹腔干或肠系膜上动脉[SMA])夹层(IMAD)是一种罕见的临床病症。本研究的目的是检查患者的人口统计学特征、合并症、临床和影像学特征、治疗及预后情况,并确定症状的预测风险因素。

方法

我们对2005年11月至2021年11月期间前瞻性收集的诊断为IMAD患者的数据进行了单中心回顾性研究。回顾了临床数据和影像学图像,并进行统计分析以比较有症状组和无症状组。

结果

共识别出78例患者。在这78例患者中,24例(31%)发生了腹腔干夹层,51例(65%)发生了SMA夹层,3例(4%)同时发生了腹腔干和SMA夹层。平均年龄为57.7岁(范围36 - 84岁),男性占优势(86%)。超过一半(55%)的患者患有高血压。此外,29例患者(37%)有症状,24例(31%)曾住院治疗。腹腔干夹层的有症状患者更易发生血栓形成(P = 0.02)、严重狭窄(P = 0.01)或分支受累(P = 0.02)。SMA夹层的有症状患者更易出现动脉直径较小(P = 0.07)、夹层长度较长(P = 0.05)、血栓形成(P < 0.001)、严重狭窄(P < 0.001)或分支受累(P = 0.003)。有症状患者更可能接受抗血小板或抗凝治疗(P < 0.001)。仅3例患者接受了干预治疗。7例患者(9%)死于无关原因。Kaplan-Meier生存分析显示5年生存率为96%,10年生存率为91%。

结论

IMAD是一种罕见的疾病,存在内脏缺血风险。尽管如此,这些患者中的大多数可以通过药物进行保守治疗,只有少数患者需要急诊手术。

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