Kalkat Maninder S, Rahman Ishtiaq, Kotidis Kostas, Davies Ben, Bonser Robert S
Department of Cardiothoracic Surgery, University Hospital Birmingham NHS Trust, Queen Elizabeth Hospital, Birmingham B15 2TH, United Kingdom.
Eur J Cardiothorac Surg. 2007 Aug;32(2):250-4. doi: 10.1016/j.ejcts.2007.04.013. Epub 2007 May 22.
In Marfan's syndrome, there is a paucity of data regarding intervention criteria for surgery of the dissected thoraco-abdominal aorta.
A retrospective analysis of 22 Marfan's patients with distal aortic dissection managed between September 1999 and April 2006 was performed. Serial diameters and linear expansion rates were calculated from imaging studies and the outcome of intervention was analysed.
There were 14/22 male patients (median age 38 years), and 18 had prior aortic surgery. Surgery was recommended in 20 patients and undertaken in 19 (1 died prior to operation). Of the operated patients, 2 presented with rupture, 2 with airway obstruction, 1 with intermittent paraplegia and 14 underwent planned surgery for increased expansion rate or pain. All patients had residual type A or chronic type B dissection. The median aortic dimension at surgery was 6.7 cm (interquartile range (IQR) 5.5-8.2). The preoperative mean expansion rate increased from 0.5 cm/year to 1.7 cm/year (p<0.001), prior to operation. Fifteen patients underwent Crawford Extent II, two underwent Extent I and two underwent Extent III repair. Profound hypothermia and CSF drainage was used in 16 and 18 patients, respectively. There was no early mortality, paraplegia or renal failure. At a median postoperative follow-up of 56 months (range 6-86), the survival of the operated cohort was 90%.
Thoraco-abdominal aortic aneurysm repair in Marfan's syndrome can be performed with good outcomes. Intervention should be based on size or accelerated expansion. Any role of endovascular management needs careful consideration.
在马凡综合征中,关于胸主动脉夹层手术干预标准的数据较少。
对1999年9月至2006年4月间接受治疗的22例马凡综合征合并远端主动脉夹层患者进行回顾性分析。通过影像学研究计算系列直径和线性扩张率,并分析干预结果。
22例患者中有14例男性(中位年龄38岁),18例曾接受主动脉手术。20例患者被建议手术,19例接受了手术(1例在手术前死亡)。在接受手术的患者中,2例出现破裂,2例出现气道梗阻,1例出现间歇性截瘫,14例因扩张率增加或疼痛接受计划性手术。所有患者均有残余A型或慢性B型夹层。手术时主动脉的中位尺寸为6.7 cm(四分位间距(IQR)5.5 - 8.2)。术前平均扩张率在手术前从0.5 cm/年增加到1.7 cm/年(p<0.001)。15例患者接受了克劳福德II型修复,2例接受了I型修复,2例接受了III型修复。16例和18例患者分别采用了深度低温和脑脊液引流。无早期死亡、截瘫或肾衰竭发生。术后中位随访56个月(范围6 - 86个月),手术队列的生存率为90%。
马凡综合征胸主动脉瘤修复手术可取得良好效果。干预应基于尺寸或加速扩张。血管内治疗的任何作用都需要仔细考虑。