Mid-Term Clinical and Morphological Outcomes after Thoracic Endovascular Aortic Repair for Complicated Type B Aortic Dissection

Research Article

Thromb Haemost Res. 2020; 4(3): 1047.

Mid-Term Clinical and Morphological Outcomes after Thoracic Endovascular Aortic Repair for Complicated Type B Aortic Dissection

Zakarya Ahmed, Hesong Zeng*, Saddam Shaiea, Xingwei He and Chang Xu

Department of Cardiology, Huazhong University of Science & Technology, China

*Corresponding author: Hesong Zeng, Department of Cardiovascular Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

Received: May 18, 2020; Accepted: May 28, 2020; Published: June 04, 2020

Abstract

Background: Complicated type B aortic dissections require surgery or Thoracic Endovascular Aortic Repair (TEVAR). In this study, we sought to explore the early and mid-term clinical efficacy of TEVAR treatment for Stanford complicated type B aortic dissection.

Methods: From January 2012 to October 2017, the medical records and the aortic imaging data of 172 consecutive patients treated by TEVAR were retrospectively reviewed for statistical analysis. Aortic remodeling was evaluated based on the preoperative and one-year postoperative followed-up aortic CTA scan results. We analyzed the diameters of the total aortic lumens, True and False lumens diameter and the thrombosis status at different five levels along the descending aorta.

Results: The primary technical success rate was 97%, and the clinical success rate was 94.8%. At 1-year of aortic CTA follow-up after TEVAR, the true lumen diameter at the stented descending thoracic aorta increased significantly, the false lumen diameter significantly reduced. The remodeling process was stable with mild changes of true lumen increase and false lumen reduction at the unstented distal part of the descending thoracic and the abdominal aorta.

Conclusion: This study confirmed that TEVAR treatment for complicated type B aortic dissection has a low mortality rate of mid-term follow-up outcomes. TEVAR stabilize the size of the aorta and precipitate in FL thrombosis. However, FL in the Abdominal aorta still patented and must be carefully observed from further long-term events incidence.

Keywords: Type B; Aortic dissection; Remodeling; Endovascular; Repair

Introduction

Aortic dissection is a critical cardiovascular disease related to high mortality and morbidity rates1. In Stanford TBAD, the dissection is known to involve the level beneath the LSA until the distal regions of the aorta, which does not involve the aortic arch or the ascending aorta. Usually classified as acute subacute or chronic phases, depending on the onset of symptoms. Another essential classification of TBAD based on the presence or absence of complications, which allows us to distinguish between complicated and uncomplicated TBAD. It is important for the estimation of in-hospital death in CTBAD patients which rated nearby 50%, compared to only 10% in un-CTBAD patients. Classically the definition of the acute complications are marked as aortic rupture, refractory pain, despite the persistence of uncontrolled hypertension with adequate medical treatment, rapidly increases in the mean aortic diameter more than 0.5cm per year, or aortic enlargement more than 5.5cm, acute hoarseness, signs of Malperfusion such as visceral or limb ischemia, and acute renal failure. However, some of these terms required further clarification. Complications such as Aortic rupture into the pleural cavity will result in an immediate large amount of hemothorax, leading to severe hypovolemic shock and death.

In 1999, Dake et al. study was the first clinical trial described the medical use of implanted stent-grafts for the management of the aortic aneurysm patients who expected as a high risk for open surgery management [1,2]. At present, this technology has been increasingly applied to CTBAD due to a favorable result when compared to standard open surgery. Closure of the primary entry tear may promote the formation of thrombus in the FL, leading to the degradation and re-expansion changes in the TL, these late effect changes are known as aortic remodeling.

Probably it can prevent the late degenerations of the aneurysm or rupture of the dissected aortic segment; as it was detected earlier in 20 to 50% of patients who applied OMT [3,4]. There were numerous clinical trials reported the remodelling process of the aorta after TEVAR treatment [5-7].

The aortic remodeling changes, and its effectiveness in preventing late aortic events still not fully described. Therefore, our study retrospectively analyzed the aortic database of CTBAD patients who underwent TEVAR treatment, to seek out the main characteristics and the beneficial effects of the aortic remodeling after TEVAR treatment.

Methods

Study design and patients

The current study was approved by the institutional review board of our hospital, in the Declaration of Helsinki, and compliance with the Health Insurance eligible and responsibility Act regulations. The Institutional Review Board conceded the requirement for distinct patients’ consent. The aortic database and the medical record of 172 patients who underwent TEVAR treatment for CTBAD (DeBakey 3b aortic dissection) Between January 2012, and October 2017 were the target group of this retrospective study. The CTBAD was previously defined as any occurrence the following symptoms or signs: relapsed or refractory pain, Malperfusion, aortic rupture, abnormal neurological signs, shock, refractory hypertension, and early aortic dilation or expansion, either at the presentation time or during the hospitalization stay [8-10]. All patients underwent de-novo stenting for the proximal thoracic descending aorta. All patients were being confirmed with the diagnosis of CTBAD by the preoperational thoracoabdominal aorta CTA (Discovery CT750 HD; GE Healthcare, Milwaukee, WI, USA). We excluded the patients who were managed by open surgery due to the aortic condition as they were not appropriate for TEVAR treatment.

TEVAR procedure details

In this study, 141 (82%) patients underwent TEVAR treatment in the acute setting of CTBAD (<14 days of the onset of the symptoms), while 31 (18%) patients were in the sub-acute stage (≥14 days and ≤90 days). The endograft-systems delivery performed via the femoral artery in most cases, only in 7 (4.2%) cases performed through the iliac artery. In all patients, TEVAR procedure completed under the guidance of the Digital Subtraction Angiography (DSA) imaging systems (Allura XpraFD10, Philips Medical Systems Inc., Best, The Netherlands; GE Healthcare Innova IGS 530, BUC CEDEX, France.).

The mean implanted endograft-stents diameter was 31.52±2.33 (ranged between 28 and 40mm), mean length was 164.74±22.65 (ranged between 80 and 200) mm. All endograft-stents were oversized by 5% to 10% according to the decision made by the operators.

The operations conducted under local anesthesia were 143 (83.1%) cases and general anesthesia in 29 (16.9%) cases. The endograftstents brands were Valiant TM stents (n=85 (49.4%) (Medtronic Endovascular, Santa Rosa, California, USA), Relay (n= 39 (22.7%) (Bolton Medical, Sunrise Florida, USA), Hercules TM stent (n=42 (24.4%) (MicroPort Scientific Corporation, Shanghai, China), E-Vita Thoracic (n=4 (2.3%) (JOTEC, Hechingen, Germany), Hemasheild (n=1 (0.6%) (German Healthcare Export Group, Germany), and Lifetech Scientific (n=1 (0.6), (Lifetech Scientific (Shenzhen) Co., Ltd. China). Details of TEVAR endograft brands are listed in Table 1.