Heyer Kamaldeep S, Modi Parth, Morasch Mark D, Matsumura Jon S, Kibbe Melina R, Pearce William H, Resnick Scott A, Eskandari Mark K
Division of Vascular Surgery, Northwestern University Feinberg School of Medicine, 201 E Huron St, Galter 10-105, Chicago, IL 60611, USA.
J Vasc Interv Radiol. 2009 Feb;20(2):173-9. doi: 10.1016/j.jvir.2008.10.032. Epub 2008 Dec 20.
To review several cases of stent-graft infection with respective outcomes to identify clinical presentations and responses to treatment options.
The authors performed a single-center retrospective review of all secondary endograft infections from January 2000 to June 2007. Infections were identified from an institutional database containing all abdominal and thoracic endovascular aneurysm repairs (EVAR and TEVAR) performed at the treating hospital.
From January 2000 to June 2007, 389 EVAR and 105 TEVAR were performed at the treating hospital. Ten endograft infections were identified (five EVAR and five TEVAR). Four infections occurred in grafts placed at outside institutions and six in grafts placed in-house. The in-house prevalence of EVAR and TEVAR infection is 0.26% and 4.77%, respectively. None were placed for a presumed pre-existing mycotic aneurysm. The mean time from the index procedure to the diagnosis of infection was 243.6 days +/- 74.5. Two patients who underwent EVAR presented with a contained rupture, and the remaining eight patients presented with constitutional symptoms and/or abscess formation on imaging studies. Microbiology cultures revealed Propionibacterium species (n = 3), Staphylcoccus species (n = 3), Streptococcus species (n = 2), and Enterobacter cloacae (n = 1). All EVAR patients underwent removal of the infected endograft and reconstruction with extraanatomic bypass (n = 3) or in situ homograft placement (n = 2). During a mean follow-up of more than 1 year, there were no recognized complications or recurrence of infection. Only one of the five TEVAR patients underwent removal and interposition grafting with an antibiotic-impregnated Dacron graft. The remaining four patients were medically managed--one patient survived and was placed in hospice care, two died of mycotic aneurysm rupture, and one died from multiorgan system failure secondary to sepsis.
Graft-related septic complications following EVAR or TEVAR are rare but associated with significant mortality. Several surgical treatment options are available, each potentially equally successful. The effect of prophylactic antibiotic use during subsequent invasive procedures must be solidified.
回顾几例支架型人工血管感染病例及其各自的结局,以确定临床表现和对治疗方案的反应。
作者对2000年1月至2007年6月期间所有继发性人工血管感染进行了单中心回顾性研究。感染是从一个机构数据库中识别出来的,该数据库包含在治疗医院进行的所有腹主动脉和胸主动脉腔内修复术(EVAR和TEVAR)。
2000年1月至2007年6月,治疗医院共进行了389例EVAR和105例TEVAR。共识别出10例人工血管感染(5例EVAR和5例TEVAR)。4例感染发生在外院植入的人工血管,6例发生在本院植入的人工血管。EVAR和TEVAR感染的院内发生率分别为0.26%和4.77%。均非因假定的原有真菌性动脉瘤而植入人工血管。从初次手术到感染诊断的平均时间为243.6天±74.5天。2例行EVAR的患者出现局限性破裂,其余8例患者在影像学检查中表现为全身症状和/或脓肿形成。微生物培养显示丙酸杆菌属(n = 3)、葡萄球菌属(n = 3)、链球菌属(n = 2)和阴沟肠杆菌(n = 1)。所有EVAR患者均接受了感染人工血管移除,并采用解剖外旁路重建(n = 3)或原位同种异体移植(n = 2)。在平均超过1年的随访期间,未发现公认的并发症或感染复发。5例TEVAR患者中只有1例接受了移除并用含抗生素的涤纶人工血管进行了间置移植。其余4例患者接受了药物治疗——1例患者存活并进入临终关怀,2例死于真菌性动脉瘤破裂,1例死于败血症继发的多器官系统衰竭。
EVAR或TEVAR术后与移植物相关的感染性并发症罕见,但死亡率较高。有几种手术治疗方案可供选择,每种方案都可能同样成功。必须明确后续侵入性操作期间预防性使用抗生素的效果。