Tzinieris Ioannis N, Papaioannou Georgios I, Dragomanovits Spyridon I, Deliargyris Efthymios N
Interventional Cardiology Department, Athens Medical Center, Athens, Greece.
Hellenic J Cardiol. 2007 May-Jun;48(3):127-33.
In this study we report local complication rates in patients undergoing percutaneous coronary intervention (PCI) utilizing a strategy of fluoroscopically guided puncture and preferential use of a closure device based on access site angiography.
We included 201 consecutive PCIs where the initial puncture was fluoroscopically guided using the inferior border of the femoral head as the guiding bony landmark. At the end of each PCI, access site angiography determined whether the deployment of a closure device, specifically the Angioseal device, was anatomically feasible. The access site was evaluated 3 and 24 hours post PCI. All patients were contacted by phone 30 days following the index procedure and questioned about any further incidents following hospital discharge.
Deployment of the Angioseal device was feasible in 76% (153/201) of cases with a success rate over 99% (152/153). In the remaining 48 patients the access site was managed with manual compression, elastic bandage placement and prolonged bed rest. Patients who received the Angioseal device could be mobilized after 6 hours, while the group that was managed with manual compression required overnight bed rest. Local complication rates where very low for the study group as a whole (1.5%) without significant differences associated with the use of the Angioseal device. We did not observe any significant influence of the established risk factors for local complications, such as age, female sex, sheath size, elevated systolic blood pressure or use of glycoprotein IIb/IIIa platelet inhibitors, within our study population.
The appropriate use of the Angioseal is feasible in three quarters of patients undergoing PCI and allows for more rapid mobilization while ensuring very low local complication rates.
在本研究中,我们报告了采用荧光透视引导穿刺策略并根据穿刺部位血管造影优先使用闭合装置的经皮冠状动脉介入治疗(PCI)患者的局部并发症发生率。
我们纳入了201例连续的PCI病例,初始穿刺采用荧光透视引导,以股骨头下缘作为引导骨性标志。在每次PCI结束时,通过穿刺部位血管造影确定闭合装置(特别是Angioseal装置)的植入在解剖学上是否可行。在PCI术后3小时和24小时对穿刺部位进行评估。在索引手术30天后通过电话联系所有患者,询问出院后是否有任何进一步的事件。
在76%(153/201)的病例中,Angioseal装置的植入是可行的,成功率超过99%(152/153)。在其余48例患者中,穿刺部位采用手动压迫、弹性绷带包扎和延长卧床休息进行处理。接受Angioseal装置的患者术后6小时即可活动,而采用手动压迫处理的组需要卧床休息过夜。整个研究组的局部并发症发生率非常低(1.5%),使用Angioseal装置与局部并发症发生率无显著差异。在我们的研究人群中,我们未观察到已确定的局部并发症危险因素(如年龄、女性、鞘管尺寸、收缩压升高或使用糖蛋白IIb/IIIa血小板抑制剂)有任何显著影响。
在四分之三接受PCI的患者中,适当使用Angioseal装置是可行的,可使患者更快活动,同时确保局部并发症发生率非常低。