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在中等收入国家中及时识别和手术矫正马凡综合征主动脉疾病的挑战:一项病例系列研究。

Challenges in prompt identification and surgical correction of Marfan Syndrome aortic disease in a middle-income country: a case series study.

机构信息

Vascular and Endovascular Surgery Research Group, Fundación Cardioinfantil-Instituto de Cardiología, Cra 13B No. 161-85 Torre I Piso 8, Bogotá, 110131, Colombia.

School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.

出版信息

J Cardiothorac Surg. 2024 Jun 7;19(1):323. doi: 10.1186/s13019-024-02793-w.

Abstract

BACKGROUND

Marfan Syndrome is an autosomal dominant disease caused by pathogenetic variants in the FBN1 gene. The progressive dilatation of the aorta and the potential risk of acute aortic syndromes influence the prognosis of these patients. We aim to describe population characteristics, long-term survival, and re-intervention patterns in patients who underwent aortic surgery with a previously confirmed clinical diagnosis of Marfan Syndrome in a middle-income country.

METHODS

A retrospective single-center case series study was conducted. All Marfan Syndrome patients who underwent aortic procedures from 2004 until 2021 were included. Qualitative variables were frequency-presented, while quantitative ones adopted mean ± standard deviation. A subgroup analysis between elective and emergent procedures was conducted. Kaplan-Meier plots depicted cumulative survival and re-intervention-free. Control appointments and government data tracked out-of-hospital mortality.

RESULTS

Fifty patients were identified. The mean age was 38.79 ± 14.41 years, with a male-to-female ratio of 2:1. Common comorbidities included aortic valve regurgitation (66%) and hypertension (50%). Aortic aneurysms were observed in 64% without dissection and 36% with dissection. Surgical procedures comprised elective (52%) and emergent cases (48%). The most common surgery performed was the David procedure (64%), and the Bentall procedure (14%). The in-hospital mortality rate was 4%. Complications included stroke (10%), and acute kidney injury (6%). The average follow-up was 8.88 ± 5.78 years. Survival rates at 5, 10, and 15 years were 89%, 73%, and 68%, respectively. Reintervention rates at 1, 2.5, and 5 years were 10%, 14%, and 17%, respectively. The emergent subgroup was younger (37.58 ± 14.49 years), had the largest number of Stanford A aortic dissections, presented hemodynamic instability (41.67%), and had a higher requirement of reinterventions in the first 5 years of follow-up (p = 0.030).

CONCLUSION

In our study, surveillance programs played a pivotal role in sustaining high survival rates and identifying re-intervention requirements. However, challenges persist, as 48% of the patients required emergent surgery. Despite not affecting survival rates, a greater requirement for reinterventions was observed, emphasizing the necessity of timely diagnosis. Enhanced educational initiatives for healthcare providers and increased patient involvement in follow-up programs are imperative to address these concerns.

摘要

背景

马凡综合征是一种常染色体显性疾病,由 FBN1 基因的致病性变异引起。主动脉的进行性扩张和急性主动脉综合征的潜在风险影响这些患者的预后。我们旨在描述在一个中等收入国家,经先前临床诊断为马凡综合征的患者接受主动脉手术后的人群特征、长期生存率和再干预模式。

方法

进行了一项回顾性单中心病例系列研究。纳入了 2004 年至 2021 年期间接受主动脉手术的所有马凡综合征患者。定性变量采用频率表示,定量变量采用平均值±标准差表示。对择期和紧急手术进行了亚组分析。Kaplan-Meier 图描绘了累积生存率和无再干预生存率。控制就诊和政府数据跟踪院外死亡率。

结果

共确定了 50 名患者。平均年龄为 38.79±14.41 岁,男女比例为 2:1。常见的合并症包括主动脉瓣反流(66%)和高血压(50%)。64%的患者存在主动脉瘤,无夹层,36%的患者存在夹层。手术方式包括择期(52%)和紧急(48%)。最常见的手术是 David 手术(64%)和 Bentall 手术(14%)。住院死亡率为 4%。并发症包括中风(10%)和急性肾损伤(6%)。平均随访时间为 8.88±5.78 年。5、10 和 15 年的生存率分别为 89%、73%和 68%。1、2.5 和 5 年的再干预率分别为 10%、14%和 17%。紧急亚组的患者年龄较小(37.58±14.49 岁),Stanford A 型主动脉夹层数量最多,存在血流动力学不稳定(41.67%),并且在随访的前 5 年需要更多的再干预(p=0.030)。

结论

在我们的研究中,监测计划在维持高生存率和确定再干预需求方面发挥了关键作用。然而,挑战依然存在,因为 48%的患者需要紧急手术。尽管不影响生存率,但观察到需要更多的再干预,这强调了及时诊断的必要性。增强医疗保健提供者的教育计划和增加患者对随访计划的参与对于解决这些问题至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8610/11157853/e65894c6c7df/13019_2024_2793_Fig1_HTML.jpg

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