Central Pseudo-aneurysm Formation following Arterial Closure with a StarClose SE Device

2015-11-08 18:06:12

Category: Interventional Radiology, Region: Upper extremity-Vessels, Plane: Other

Abstract Vascular closure devices are frequently used for hemostasis during endovascular procedures by employing sutures, plug devices (using collagen or hydrogel) or through the use of a metal clip made of nickel and titanium as with the StarClose device. We present a case where a StarClose SE vascular closure device (VCD) was deployed for hemostasis post diagnostic cardiac catheterization and upon repeat access, four days later for coronary intervention, retrograde sheath angiography revealed a pseudo-aneurysm emanating from the center of the StarClose clip. Review of literature indicates StarClose to be safe and effective in achieving hemostasis in majority of endovascular procedures and the incidence of pseudo-aneurysm to be infrequent. Introduction Femoral arterial hemostasis post cardiac catheterization can be achieved through manual compression (MC), mechanical compression or vascular closure devices (VCDs). Although VCDs have been shown to be non-inferior to MC with respect to access site hemostasis and complications, MC is still considered the gold standard for achieving hemostasis [1]. The use of VCDs avoids the need to interrupt anticoagulation, improves patient comfort, provides faster time to ambulation and discharge and reduces healthcare burden by freeing staff resources [2]. In deciding the method of arterial closure, MC versus VCD, one must take into account numerous factors from patient characteristics to the site of arterial puncture to minimize VCD related complications. Keywords access site management, vascular closure devices, pseudo-aneurysm, complications, endovascular procedures, StarClose SE Case Description A 77-year-old man with history of ischemic cardiomyopathy with left ventricular ejection fraction 20-25% and atrial fibrillation was transferred to our hospital post cardiac arrest. He was noted to have positive troponins and was diagnosed with NSTEMI. Anticoagulation was started with a loading dose aspirin 325mg and Plavix 600mg with maintenance dose of 81mg and 75mg respectively, along with intravenous heparin infusion. After stabilization, cardiac catheterization was performed via a right femoral approach, due to limited radial arterial access, revealing multi-vessel coronary artery disease with a syntax score of 16. Hemostasis post-procedure was achieved with a StarClose SE device with no post deployment oozing or delayed hemostasis. He was felt to be at extreme surgical risk and was referred for high-risk percutaneous coronary intervention (PCI). Again, right femoral arterial access was obtained and a 6F sheath was introduced. PCI was performed with the placement of four drug-eluting stents: one in the proximal LAD, a second in the ramus intermedius, and two in the first obtuse marginal. Prior to PCI, retrograde sheath angiography was performed to evaluate the access site for hemostasis and suitability for closure. The femoral arterial cannulation site was noted to be approximately 2 cm cranial to the prior access site closed with the StarClose device (Figure 1A). Retrograde sheath angiography revealed the previously deployed StarClose clip with a 0.5cm pseudo-aneurysm emanating from its center (Figure 1B). As the pseudo-aneurysm was small, the decision was made to achieve hemostasis and to treat the pseudo-aneurysm simultaneously by applying manual pressure for hemostasis. There was no post-compression bleeding, oozing or other post-procedure complications. Discussion The StarClose device (Abbott Vascular Abbott Park, Illinois) is a 4mm circular nitinol clip that is deployed at the arterial puncture site drawing edges of arteriotomy together for closure (Figure 2). Complications associated with the StarClose device as published in trials, case reports and compiled through databases such as the Manufacturer and User Facility Device Experience (MAUDE) collectively include; failure to achieve hemostasis, inability to complete deployment sequence, entrapped deployment device, clip not being deployed, late bleeding or oozing from dermatotomy site, bleeding requiring transfusions, vascular injury requiring repair, ipsilateral lower extremity ischemia, vessel occlusion requiring stenting, re-access catheter entrapment requiring surgical extraction, retroperitoneal hematoma, pseudo-aneurysm, hematoma of >= 6cm and oripsilateral DVT[3,4,5,6,7]. Review of literature indicatesStarClose to be a safe and effective modality in achieving hemostasis when directly compared to MC and other VCDs. Tavris et al, reported StarClose to be one of four VCD’s demonstrating significantly lower bleeding or vascular complications than MC control[8]. Anterograde and retrograde femoral access in more than 1000 consecutive peripheral angioplasty procedures reported the overall hemostasis success rate to be 93.9%, with overall major and minor complications rates to be 0.3% and 5.3% respectively[9]. Williams et al, reported closure of anterograde punctures with StarClose device following infrainguinal endovascular interventions to be successful in 94.6% of 212 patients. The reasons for failure was device failure in 5, obesity was 1, groin scarring in 2 and uncertain cause in 4 patients[10]. Ratnam et el, prospectively compared Starclose with MC and collagen plug based angio-seal device, showing significantly higher number of starclose patients requiring additional manual compression to achieve hemostasis, however the incidence of major complications was lowest with StarClose patients (1.9%) vsangioseal (2.9%) and greatest with MC (3.7%)[11]. Although StarClosemaybe associated with increased post-deployment oozing, it is successfully deployed in majority of the patients and has a lower incidence of major complications in comparison to MC. Pseudo-aneurysm formation post StarClose clip deployment is an extremely infrequent occurrence. The initial multicenter randomized CLIP Study evaluating major and minor complications in 208 diagnostic and 275 interventional patients at 17 centers in U.S reported no pseudo-aneurysms post-procedure[12,13]. The subsequent prospective RISE study, following 171 patients for post-procedure 30-day complications and early time to ambulation with StarClose device in cardiac and peripheral vascular procedures reported only one patient with pseudo-aneurysm formation[14]. A more recent study utilizing the MAUDE database identified 1,118 total complications with StarClose with the complication of pseudo-aneurysm being reported in only 6 patients[4]. The use of anti-platelet agents (aspirin and plavix), anticoagulation, large sheath size ( >8F), age >65 years, obesity, poor post procedural compression, simultaneous artery and vein catheterization, hypertension, peripheral arterial disease, hemodialysis, complex interventions and low or high grade punctures at external iliac or superficial or deep femoral artery level have all been associated to increase the risk of pseudo-aneurysm formation[15]. Therefore, although pseudo-aneurysm is a rare occurrence with StarClose, further risk can be decreased by careful patient selection. Conclusion: The StarClose closure device has a success rate of achieving hemostasis approaching 97%[2]. We present a case report with an interesting radiographic image of a pseudo-aneurysm emanating from the center of the StarClose clip. The small pseudo-aneurysm was successfully treated with manual compression. Pseudo-aneurysm is an infrequent occurrence with StarClose clip device and despite optimal access and closure technique it can still occur.