Gurofsky Rebecca C, Sabharwal Tarun, Manlhiot Cedric, Redington Andrew N, Benson Lee N, Chahal Nita, McCrindle Brian W
Department of Pediatrics, Division of Cardiology, Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, Toronto, Canada.
Catheter Cardiovasc Interv. 2009 May 1;73(6):809-13. doi: 10.1002/ccd.21892.
To determine whether patients with Kawasaki Disease (KD) undergoing percutaneous catheter angiography were at increased risk of arterial complications at the point of arterial access compared to patients with structural heart abnormalities, but normal vessels.
Systemic arterial damage can occur as a result of KD.
Medical histories of all patients with KD undergoing percutaneous catheter angiography at The Hospital for Sick Children between January 1990 and August 2008 were reviewed.
A total of 44 patients with KD underwent 82 catheter procedures. Of these, 3 were associated with important arterial complications (2 males; age: 4 months, 3 and 17 years). All patients who experienced complications had multiple large and/or giant coronary artery aneurysms and two were within 3 months of the acute phase of KD. All patients developed pseudoaneurysms of the femoral artery which had been utilized for catheter access. All pseudoaneurysms were treated with ultrasound-guided thrombin injection and compression, and resolved with no long-term complications. One patient also developed a substantial arteriovenous fistula of the femoral circulation which had to be surgically repaired with no permanent sequela. Odds for arterial complications in patients with KD were 10.4 times greater (95%CI: 3.2-33.8) than that noted for the general pediatric cardiac catheterization population (3.6% vs. 0.4%, P < 0.0001) which indicates higher risk associated with arterial access in patients with KD.
Greater care in obtaining arterial access for angiography is warranted, especially in the first month directly following the acute phase, possibly related to systemic arterial damage associated with KD.
确定与患有结构性心脏异常但血管正常的患者相比,接受经皮导管血管造影术的川崎病(KD)患者在动脉穿刺部位发生动脉并发症的风险是否增加。
KD可导致全身动脉损伤。
回顾了1990年1月至2008年8月在病童医院接受经皮导管血管造影术的所有KD患者的病史。
共有44例KD患者接受了82次导管手术。其中3例发生了严重的动脉并发症(2例男性;年龄分别为4个月、3岁和17岁)。所有发生并发症的患者均有多个大的和/或巨大的冠状动脉瘤,其中2例在KD急性期的3个月内。所有患者均在用于导管穿刺的股动脉处形成了假性动脉瘤。所有假性动脉瘤均采用超声引导下注射凝血酶和压迫治疗,且均已治愈,无长期并发症。1例患者还出现了严重的股循环动静脉瘘,必须进行手术修复,且无永久性后遗症。KD患者发生动脉并发症的几率比一般儿科心脏导管插入术人群高10.4倍(95%可信区间:3.2 - 33.8)(3.6%对0.4%,P < 0.0001),这表明KD患者动脉穿刺相关风险更高。
在进行血管造影的动脉穿刺时需要格外小心,尤其是在急性期后的第一个月,这可能与KD相关的全身动脉损伤有关。