Three-Dimensional Printing Assisted Physician-Modified Fenestrated Endografts for Thoracic Endovascular Aortic Aneurysm Repair in Zone 1

摘要

This protocol describes an approach for repairing aortic arch aneurysms in Zone 1 using physician-modified fenestrated endografts with the assistance of three-dimensional printing.

摘要

Aortic arch aneurysm is a life-threatening cardiovascular disorder that requires timely medical intervention. Aneurysms in Zone 1 typically involve multiple branch arteries, making repair challenging. Open surgical repair often results in significant surgical trauma, massive blood loss, and prolonged operative time. With advancements in endovascular technology, fenestrated/branched thoracic endovascular aortic repair (F/B TEVAR) has been employed for aortic arch repair and branch artery reconstruction. Stent grafts for F/B TEVAR require personalized modification and fabrication based on patient anatomy. Physician-modified fenestrated endografts (PMEGs) offer a feasible approach for personalized aortic arch aneurysm repair in Zone 1. However, fabricating PMEGs demands a thorough understanding of anatomy and extensive experience, making it challenging for most surgeons. To simplify this process, three-dimensional printing is used to assist in precise fenestration. PMEGs guided by three-dimensional printing enhance branch artery patency and reduce post-operative endoleaks following F/B TEVAR. Further follow-up is necessary to assess the long-term benefits and efficacy of this technique.

引言

Aortic aneurysms are common life-threatening aortic diseases that require timely evaluation and therapeutic intervention¹. Aortic arch aneurysms often involve major arterial branches, including the innominate artery, left common carotid artery, and left subclavian artery¹. According to the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines, the aorta is divided into 11 landing zones². Repairing aortic arch aneurysms in Zone 1 requires reconstruction of the aortic arch branch arteries, posing significant anatomical challenges.

The initial approach for aortic arch repair was open surgical repair. DeBakey et al. first successfully repaired an aortic arch aneurysm in 1957³. However, several limitations restrict the application of open surgical repair⁴, including severe surgical trauma, significant blood loss, high complication rates, and prolonged operative duration⁵. With advancements in endovascular technology, thoracic endovascular aortic repair (TEVAR) has been proven effective for treating thoracic aortic aneurysms and dissections^6,7,8. Building on conventional TEVAR, fenestrated/branched thoracic endovascular aortic repair (F/B TEVAR) was developed to address thoracic aortic aneurysms involving branch arteries^9,10. Notably, F/B TEVAR has demonstrated high technical success and acceptable post-operative mortality in patients with post-dissection thoracoabdominal aneurysms^11,12.

F/B TEVAR can restore normal physiological blood flow and achieve high patency rates in branch arteries following thoracic aortic aneurysm repair^13,14. Precise fenestration on the main body stent graft is essential for reconstructing branch arteries. Aortic arch aneurysms in Zone 1 typically involve multiple branch arteries and require stent grafts with triple fenestrations. However, current commercial stents cannot be customized based on individual patient anatomy. Physician-modified fenestrated endografts (PMEGs) offer a viable alternative for personalized treatment of thoracic aortic aneurysms in Zone 1^15,16.

Successful fabrication of PMEGs requires extensive practice and experience, which can be challenging for many surgeons. To simplify the preparation process, this article presents a method for fabricating PMEGs for F/B TEVAR. Three-dimensional (3D) printing was used to achieve precise fenestration on the main body stent graft, followed by the attachment of branch stents in the appropriate orientation. This study reports a case series of 21 patients who underwent F/B TEVAR using PMEGs, providing novel insights into the efficacy and applicability of this technique.

方案

The surgical protocols described here were approved by the ethics committee of Nanjing Drum Tower Hospital, affiliated with Nanjing University Medical School. Written was obtained from the patients participating in this study. The details of the reagents and the equipment used are listed in the Table of Materials.

1. Pre-operative assessment

1. Apply the following inclusion criteria: Patients aged over 18 years; confirmed diagnosis of aortic aneurysms in Zone 1 of the aorta using computed tomography angiography (CTA); no contraindications for F/B TEVAR; informed consent for the surgery.
2. Apply the following exclusion criteria: Patients with other aortic diseases (such as aortic ulcer and dissection); patients with severe concurrent diseases (such as kidney or hepatic failure, uncontrolled diabetes, severe active infections); pregnant women; patients who have undergone aortic arch surgery.
3. Perform pre-operative CTA and reconstruct the aorta to evaluate the position of the aortic aneurysm (Figure 1A,B).
4. Conduct additional examinations, including routine physical examination, blood tests, and urine tests.

2. Preparation of the 3D-printed model

1. Import the original CTA data (DICOM format) of the patient into the 3D reconstruction software.
2. Click on SEGMENT and perform thresholding by defining the maximum and minimum threshold values.
3. Click on Calculate Part to create a 3D preview of the aorta.
4. Click on Edit Masks to optimize the 3D model.
5. Export the 3D model as an STL format file.
6. Import the STL format file into the simulation analysis software.
7. Click on Edit-Select Outliers to delete most of the invalid points.
8. Next, click on Edit-Discontinued Components. Recognize the remaining invalid points using the Separation and Size options, then delete them.
9. Click on Points-Reduce Noise and select Free-form shapes to reduce noisy data.
10. Click on Points-Wrap to generate a 3D model with a polygon wrap.
11. Click on Polygons-Fill Holes-Fill Single to fill holes in the 3D model.
12. Click on Decimate to simplify the model according to curvature.
13. Click on Smooth-Relax/Sandpaper to refine the model surface.
14. Click on Repair-Defeature to further optimize the model.
15. Design fenestrations by clipping branch arteries on the 3D model.
16. Export the final 3D model as an STL format file (Figure 1C).
17. Import the STL format file into a 3D printer and print the 3D model of the aorta using biocompatible clear MED610 materials.
18. Sterilize the model with ethylene oxide to prepare it for modification of the PMEG.

3. Intraoperative fabrication of PMEGs

1. Place the delivery sheath with the main body stent graft into the sterile 3D-printed model before the surgical procedure.
2. Release the main body stent graft inside the 3D-printed model.
3. Mark the fenestrations of branch arteries using a marker pen (Figure 2A).
   NOTE: Place markings between metal edges to prevent interference with stent expansion.
4. Create fenestrations at the marked locations using an electrocautery pen (Figure 2B).
5. Suture metal coils as selection markers at the fenestrations.
6. Constrain the main body stent graft using a guidewire, restricting the diameter to 50%-70% of the original.
   NOTE: Introduce the guidewire through the distal delivery sheath of the stent graft after completing the stent modification. Symmetrically place 4-0 non-absorbable sutures on the posterior aspects of both sides of the fenestration and securely anchor them to the guidewire.
7. Reinstall the prepared PMEG into the delivery sheath of the main body stent.
8. Inflect the PMEG before implantation to facilitate its delivery into the aorta (Figure 2C).

4. Surgical procedure

1. Anesthetize the patient using anesthetic induction agents (propofol 20 mg/mL), analgesics (fentanyl 50 µg/mL), and muscle relaxants (vecuronium 10 mg/mL) administered via intravenous injection (following institutionally approved protocols).
2. Position the patient in the supine position and locate the arteries serving as surgical access points using percutaneous landmarks.
   NOTE: Use femoral arteries as access for the main body stent graft and the left common carotid and brachial arteries as access for the branch stents.
3. Expose the arteries and create access by inserting delivery sheaths.
   NOTE: Use a long delivery sheath (18-20 F) for the main body stent graft and delivery sheaths (4-6 F) for branch stents.
4. Implant a 150 cm guidewire and a 4 F catheter. Perform digital subtraction angiography (DSA) to evaluate the aortic arch aneurysm.
5. Administer systemic heparinization (heparin, 1 mg/kg).
6. Replace the guidewire with a supportive guidewire to facilitate device placement and exchange.
7. Deliver the PMEG to the aortic arch through the femoral artery approach and position it in the planned location (Figure 3A).
8. Slowly release the anterior segment of the main body stent graft while keeping the stent in its constricted state (Figure 3B).
   NOTE: The constricted state allows positional adjustments. Withdrawing the guidewire reliably releases the bilateral sutures, enabling the controlled expansion of the stent graft to align fenestrations with branch arteries.
9. Insert a catheter through each branch artery access. Advance catheters selectively into the respective fenestrations of the innominate artery, left common carotid artery, and left subclavian artery (Figure 3C).
10. Pull out the constraining wire and fully release the main body stent graft.
11. Implant and release branch stents in the innominate artery, left common carotid artery, and left subclavian artery.
12. Dilate expansion balloons at the bridging sites between the main body stent and branch stents.
13. Verify the patency of each branch artery and check for endoleaks using DSA (Figure 3D).
14. Remove catheters, guidewires, and delivery sheaths. Suture the arteries using non-absorbable sutures (6-0 or 7-0).

5. Post-operative monitoring and care

1. Transfer the patient to the post-anesthesia care unit (PACU) or intensive care unit (ICU).
2. Monitor vital signs, including blood pressure, heart rhythm, respiratory function, and blood oxygen saturation.
3. Assess for complications, such as stroke, spinal cord ischemia, and endoleaks.
4. Initiate pain management and rehabilitation care.

结果

Twenty-one patients, aged 35 to 87 years, underwent F/B TEVAR for aortic arch aneurysm repair using PMEGs. Blood flow in all aortic arch branch arteries (innominate artery, left common carotid artery, and left subclavian artery) was restored through triple fenestrations in all cases (Figure 4). The average operative time was 234.3 min ± 70.4 min. Intraoperative blood loss was 150 mL (IQR = 300). The post-operative ICU stay averaged 1.2 ± 2.2 days, while the total hospital stay was 9.0 ± 4.9 ...

讨论

F/B TEVAR is a suitable approach for repairing aortic arch aneurysms in Zone 1, effectively maintaining branch artery patency. Compared with open surgical repair, F/B TEVAR is associated with lower peri-operative morbidity and mortality^15,17. However, endoleaks are likely to occur at fenestration bridging sites post-operatively, potentially requiring reintervention¹⁸. Studies have shown that a greater number of fenestrations increases the ...

材料

本文使用的材料清单

姓名	公司	目录编号	评论
3D 打印机	Stratasys	Eden260VS	用于打印 3D 模型
Ankura TAA 覆膜支架系统	Lifetech	TAA2622B100	用作主体支架移植
生物相容性PolyJet材料	Stratasys	MED610
Fluency Plus血管内支架移植物	Bard外周血管	FEM10100	用作分支支架
Geomagic Wrap软件	OQTON		用于支架植入后血管重塑的模拟分析
GORE DRYSEAL Flex 导引器护套	W.L. Gore &Associates	DSF1065	用作GORE的交货护套
维亚班 内假体	W.L. Gore &合伙人	VBHR051002A	用作分支支架
高扭矩Supra Core外围额外支撑导丝	Abbott	1002703	用作导丝
INFINITI诊断导管	Cordis	SRD6642	用作导管
Lunderquist超硬导丝	COOK MEDICAL	G49228	用作导丝
模拟软件	Materialise		用于进行主动脉
Nester 栓塞线圈	COOK MEDICAL	G47332	用作线圈
PROLENE 聚丙烯缝合线	Johnson&Johnson MedTech	SXPP1B201	用作手术缝合
RADIFOCUS 血管造影导管	Terumo 介入系统	RF-DB1500GM	用作导管
RADIFOCUS 导丝 M	Terumo 介入系统	RF-GA18153M	用作导丝
SurVeil 药物涂层球囊	Abbott	SRV03513504010	用作扩张球囊
V-18 和V-14 ControlWire Guidewire	Boston Scientific Corporation	39216-71822，  46-850	用作导丝
Valiant 胸腔支架移植物与 Captivia 输送系统	Medtronic	VAMF2626C100TU	用作主体支架移植物