Sirignano Pasqualino, Andreoli Francesco, Gaggiano Andrea, Accarino Giancarlo, Tusini Nicola, Benedetto Filippo, Veroux Pierfrancesco, Silingardi Roberto, Taurino Maurizio, Speziale Francesco
Vascular and Endovascular Surgery Unit, Department of General and Specialistic Surgery, Sant'Andrea Hospital of Rome, Sapienza University of Rome, Roma, Italy.
Department of Vascular Surgery, Ospedale Civile di Baggiovara, Azienda Ospedaliero-Universitaria di Modena, University of Modena and Reggio Emilia, Modena, Italy.
J Endovasc Ther. 2024 Oct 6:15266028241284364. doi: 10.1177/15266028241284364.
To confirm real-world clinical practice results reported with anatomically fixed bifurcated endograft, a physician-initiated study was designed-AFX2-LIVE registry.
From November 2019 to August 2021, investigators enrolled all consecutive patients treated with AFX2 (Endologix Inc., Irvine, CA, USA) endograft. Patients with abdominal aortic aneurysms (AAAs), penetrating aortic ulcers (PAU), and isolated infrarenal aortic dissections were included. Clinical and anatomical data, including baseline, intraoperative, and in-hospital details, as well as follow-up data, were collected in an anonymized prospectively compiled database. The primary endpoint of this study was to evaluate the technical and clinical success of endovascular aortic repair (EVAR) using AFX2 endograft.
A total of 535 patients were enrolled from 43 Italian and Spanish centers and analyzed according to the protocol. Four hundred eighty-nine patients were male (91.4%), with a mean age of 75±8.92 years (range 52-94). Four hundred sixty-six patients (87.1%) were treated for AAA, 49 (9.3%) for PAU, and 20 (3.6%) for isolated abdominal aortic dissection. A proximal extension was needed in 48% of the cases. Assisted technical success was achieved in all but one patient (99.8%). At 30 days follow-up, no AAA-related deaths were recorded, and nine patients (1.6%) required reintervention. At a mean follow-up period of 15.22±13.65 (range 1-53) months, data were available for 479 patients (89.5%). Clinical success was achieved in 98.2% (95% confidence interval [CI]: 96.4-99.1) at 3 months, 93.9% (95% CI: 90.1-96.1) at 1 year, and 74.1% (95% CI: 62.8-82.4) at 4 years follow-up. The estimated freedom from all-cause mortality was 97.7%, 93.4%, 81.6%, 77.5%, and 70.9%, and freedom from AAA-related mortality was 100%, 99.6%, 99.6%, 99.6%, and 97.3% at 3, 12, 24, 36, and 48 months, respectively. Twenty reinterventions (3.7%) were required in 19 patients, of which 3 late open conversions (0.6%) were performed, and 2 AAA-related deaths were observed.
This study demonstrated excellent clinical and technical success rates of EVAR with anatomically fixed endografts, providing valuable insights into real-world clinical outcomes.
The AFX2-LIVE study could have a significant impact by providing robust evidence supporting the effectiveness and safety of EVAR using bifurcated endografts with anatomical fixation in real-world clinical practice, ultimately leading to improved outcomes and enhanced patient care in the management of abdominal aortic pathologies.
为证实解剖固定分叉型腔内移植物所报告的真实世界临床实践结果,设计了一项由医生发起的研究——AFX2-LIVE注册研究。
2019年11月至2021年8月,研究人员纳入了所有连续接受AFX2(美国加利福尼亚州尔湾市Endologix公司)腔内移植物治疗的患者。纳入腹主动脉瘤(AAA)、穿透性主动脉溃疡(PAU)和孤立性肾下腹主动脉夹层患者。临床和解剖学数据,包括基线、术中及住院期间详细信息以及随访数据,均收集于一个匿名的前瞻性汇编数据库中。本研究的主要终点是评估使用AFX2腔内移植物进行血管腔内主动脉修复(EVAR)的技术和临床成功率。
共从43个意大利和西班牙中心纳入535例患者,并按方案进行分析。489例患者为男性(91.4%),平均年龄75±8.92岁(范围52 - 94岁)。466例患者(87.1%)因AAA接受治疗,49例(9.3%)因PAU接受治疗,20例(3.6%)因孤立性腹主动脉夹层接受治疗。48%的病例需要近端延伸。除1例患者外,所有患者均取得了辅助技术成功(99.8%)。在30天随访时,未记录到与AAA相关的死亡病例,9例患者(1.6%)需要再次干预。在平均随访期15.22±13.65(范围1 - 53)个月时,479例患者(占89.5%)有可用数据。在3个月时临床成功率为98.2%(95%置信区间[CI]:96.4 - 99.1),1年时为93.9%(95% CI:90.1 - 96.1),4年随访时为74.1%(95% CI:62.8 - 82.4)。估计全因死亡率的自由度在3、12、24、36和48个月时分别为97.7%、93.4%、81.6%、77.5%和70.9%,与AAA相关死亡率的自由度分别为100%、99.6%、99.6%、99.6%和97.3%。19例患者需要进行20次再次干预(3.7%),其中进行了3次晚期开放转换(0.6%),观察到2例与AAA相关的死亡病例。
本研究表明解剖固定腔内移植物的EVAR具有出色的临床和技术成功率,为真实世界临床结果提供了有价值的见解。
AFX2-LIVE研究可能会产生重大影响提供有力证据,支持在真实世界临床实践中使用解剖固定分叉型腔内移植物进行EVAR的有效性和安全性,最终改善腹主动脉疾病管理的结果并加强患者护理。