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Journal of Korean Neurosurgical Society > Volume 68(6); 2025 > Article
Tian, Yu, Long, Shi, Ma, Li, Duan, Ran, and Li: High-Resolution C-arm Computed Tomography for Evaluation of Stent Expansion and Apposition after Intracranial Stent Implantation

Abstract

Objective

C-arm computed tomography (CT) has always played an important role in neurointerventional surgery, in this study, we aimed to investigate the value of high-resolution C-arm CT in evaluating stent expansion and apposition in carotid arteries of Guangxi Bama piglets.

Methods

Twenty-four stents were implanted in the carotid arteries of 24 Guangxi Bama piglets. High-resolution C-arm CT was performed to evaluate stent expansion and the quality of processed images, followed by three-dimensional digital subtraction angiography (3D-DSA). The DSA and high-resolution C-arm CT images were transmitted to a postprocessing workstation for image reconstruction (dual-volume reconstruction method). High-resolution C-arm CT reconstructed images after diluted contrast agent injection (diluted contrast method) were also acquired. In addition to assessing radiation exposure, the accuracy of stent apposition assessment by the two methods was compared, using intravascular ultrasound as the reference standard. Adverse events during and within 24 hours after the procedure were recorded.

Results

One stent was incompletely expanded, while the remaining 23 stents were fully expanded without disruption. The image quality of high-resolution CT was grade I in most cases (n=22/24). Both methods clearly demonstrated stent apposition with a consistency of 100%. However, the dual-volume reconstruction method was associated with significantly higher radiation exposure (p<0.001). Mild-to-moderate vasospasm occurred in four piglets when the diluted contrast method was used. Overall, no serious complications occurred in this study.

Conclusion

High-resolution C-arm CT enables clear microstructure visualization and can be used in combination with different postprocessing techniques to accurately assess the apposition of intracranial stents.

INTRODUCTION

Over the years, intracranial metal stents have been widely used for interventional treatment of atherosclerotic stenosis and stent-assisted embolization of intracranial aneurysms [3,4]. However, the visibility of implanted intracranial stents under ordinary fluoroscopy can be limited despite radioopaque markers on the proximal and distal stent ends. Kinking, incomplete expansion or poor apposition of the stent may occur in severely tortuous blood vessels or stenosed vessels with calcified plaques, resulting in complications such as acute stent thrombosis, perforator vessel occlusion, and prolonged stent endothelialization time [2,22]. The past decade has witnessed several innovations in digital subtraction angiography (DSA) equipment and scanning and postprocessing technologies that have facilitated the progress of neurointerventional therapy. In this regard, high-resolution C-arm computed tomography (CT) provides a clear visualization of the internal structure of lesions [14]. However, few studies have explored the safety and accuracy of stent apposition assessment by high-resolution C-arm CT combined with different post-scan processing techniques [5,18,20]. In this study, we aimed to determine the safety and efficacy of the combination of high-resolution C-arm CT with different postprocessing methods when evaluating the success of intracranial stent implantation in Guangxi Bama piglets.

MATERIALS AND METHODS

The Ethical Committee of The First Affiliated Hospital of Zhengzhou University, authorized this study (grant number : 2022-KY-0911).

Experimental animals

Twenty-four Guangxi Bama piglets (weight, 13.9-24.5 kg; age, 3-4 months) were purchased from Henan Chunying Biotechnology Co., Ltd. (license No. SCXK; Zhengzhou, China). All animals were housed and fed at the experimental animal center before and after the operation.

Main reagents and instruments

Drugs for anesthesia

Atropine (batch no. 62103222; Huayuan Zhongsheng Pharmaceutical Co., Ltd., Hebei, China), xylazine hydrochloride (batch No. 070031777; Dunhua Shengda Animal Medicine Co., Ltd., Jilin, China), sevoflurane (batch No. 20052131; Shanghai Hengrui Pharmaceutical Co., Ltd., Shanghai, China), and midazolam (batch No. H10980025; Nhwa Pharma. Corporation, Jiangsu, China).

Intraoperative contrast agent

The intraoperative contrast agent was UNIVERSUM 370 (batch No. KTOBOLV; Bayer, Whippany, NJ, USA).

Instruments used during operation

Hydrophilic guidewire; pigtail catheter, vertebral arteriography catheter, and 6 F guiding catheter (Cordis, Fremont, CA, USA); 0.014-inch micro-guidewire (Synchro 14; Stryker, Fremont, CA, USA); Neuroform EZ (Easy Deployment) stent (Stryker); Enterprise stent (Cordis); Apollo stent (MicroPort Medical, Shanghai, China); Tubridge flow diverter (FD) stent (MicroPort Medical, Shanghai, China); and DSA equipment (Artis Zeego; Siemens, Erlangen, Germany).

Stent placement

All experimental pigs were given dual antiplatelet therapy (aspirin 300 mg/day and clopidogrel 75 mg/day) 5 days before surgery and fasted for 12 hours before the operation. After the pigs were anesthetized (intramuscular injection of 0.5 mg atropine, 0.1 mL/kg xylazine hydrochloride and 0.1 mg/kg midazolam for induction, and sevoflurane for maintenance), they were immobilized in the supine position. The right femoral artery was punctured using the Seldinger method, and a 6 F arterial sheath was inserted. A 5 F pigtail catheter and a vertebral artery catheter were introduced through the sheath for angiography of the aortic arch (injection rate of 10 mL/s, total amount of 15 mL) and bilateral common carotid arteries (injection rate of 4 mL/s, total amount of 6 mL). A 6 F guiding catheter was placed at the origin of the left common carotid artery, and a stent delivery catheter (XT-27 microcatheter, Neuroform EZ stent [10]); Selecplus microcatheter, Enterprise stent [17]; T-track microcatheter, Tubridge FD [11] or delivery device (Apollo stent [21]) was inserted, with the distal end positioned at the origin of the left external carotid artery. After confirming the correct position of the delivery catheter/device, the stents were released. A detailed description of the release process is available in the literature.

High-resolution C-arm CT scan and postprocessing

The DSA equipment used was a C-arm angiography system capable of CT scanning (C-arm CT; Artis Zeego) with a high-resolution scanning function. Image postprocessing was conducted using its postprocessing workstation (Syngo Workplace, InStudio 3D; Siemens).
Immediately after stent placement, high-resolution C-arm CT (Dyna micro-CT) of the stented area was performed for imaging reconstruction of the stent and surrounding blood vessels. The scanning procedure was conducted as previously described in the literature [14,23]. The reconstructed images were obtained by the dual-volume and diluted contrast medium methods as follows : 1) dual-volume reconstruction method : after stent placement, a three-dimensional (3D)-DSA scan of the left or right common carotid artery was performed with the following scanning parameters : 70 kV voltage, 0.36 mGy/Fr, 48 cm field of view, and 260° rotation angle. Images were acquired while 12 mL of undiluted contrast agent was continuously injected at 2.0 mL/s through the catheter for 6 seconds; the image acquisition delay time was 1 second. The imaging data were transmitted to the DSA postprocessing workstation. The streak metal artifact removal technology (SMART) algorithm was applied to the high-resolution C-arm CT images to obtain a reconstructed image of the stent without any metal artifacts. Finally, the imaging fusion application Syngo DualVolume was used to merge the 3D-DSA image of the blood vessels and the high-resolution metal artifact-free image of the stent to generate a dual-volume 3D fusion reconstructed image. And 2) diluted contrast medium method : high-resolution C-arm CT scan was performed of the stented area during continuous injection of diluted contrast agent into the left common carotid artery through the catheter (rate, 2 mL/s; total volume, 44 mL); the injection time was 20 seconds and the image acquisition delay time was 2 seconds. The scanning parameters were 109 kV voltage, 22 cm maximum field of view, and 200° rotation angle. The data were transferred to the 3D workstation, and the volumetric images were reconstructed to obtain stent images with a resolution of 512×512×512 (Fig. 1).
Different postprocessing techniques (maximum density projection and advanced volume rendering technique, and so on) were used to dynamically observe the relationship between the stent and vessel wall from multiple angles and evaluate stent apposition in reconstructed images from the above two postprocessing methods.

Intravascular ultrasound (IVUS)

After high-resolution C-arm CT scanning, IVUS (model H749393222CC0; Boston Scientific, San Jose, CA, USA) was performed. The IVUS procedure was conducted as previously reported [19]. A Synchro-14 micro guidewire (Styker) was first introduced through the stent lumen distal to the normal external carotid artery, then an IVUS catheter was passed along the micro-guidewire, and the automatic pullback device was used, at a speed of 1 mm/s. IVUS images recorded included the segment within 5 mm of the lesion.

Evaluation of the quality of stent reconstruction images and assessment of stent expansion

The quality of stent reconstruction images was evaluated independently by two experienced neurointerventionists; points of disagreement were resolved by discussion to reach a consensus. The quality of the images was graded according to the high-resolution C-arm CT image quality evaluation standard [5,13] as follows : grade I (overall outline and mesh of the stent clearly visible; only small metal artifacts); grade II (outline of the stent visible, but significantly lower clarity than grade I; stent mesh indistinguishable; mild to moderate metal artifacts present); or grade III (stent blurred, with details indistinguishable and only general outline visible; large metal artifacts present). Multidirectional rotated stent reconstruction images were obtained to observe whether the stent was partially expanded or twisted or if there was any strut breakage.

Evaluation of stent apposition

The accuracy of the dual-volume reconstruction method and the low-concentration contrast agent method for assessing stent apposition was evaluated with IVUS as the reference standard. Stent apposition was scored on a scale of 0 to 1 based on criteria reported by Kato et al. [6], with 0 points indicating complete apposition and 1 point indicating incomplete apposition. Malappositions were classified as type I (stent with proximal or distal malapposition), type II (stent with partial “crescent” malapposition), or type III (incomplete opening of long segment or local distortion).

Radiation dose and safety

The radiation dose (reference air karma [AK] and dose-area product [DAP]) for each method and the incidence of serious complications (e.g., emboli shedding, vascular dissection) during scanning were recorded. Moreover, we assessed the incidence of serious complications such as internal thrombosis and hemorrhage within 24 hours of the procedure.

Statistical analysis

Statistical analysis was performed using SPSS ver. 26.0 (IBM Corp., Armonk, NY, USA). Measurement data were expressed as mean±standard deviation. Interobserver agreement in image quality assessments was evaluated using quadratically weighted Cohen’s kappa (κ) statistics with 95% confidence intervals (CIs), with interpretation thresholds defined by Landis and Koch criteria : κ=0.81-1.00 (near-perfect agreement), 0.61-0.80 (substantial agreement). Stent apposition evaluation data were analyzed by the chi-square or Fisher exact test. A p-value <0.05 was considered statistically significant.

RESULTS

Surgical results

A total of 24 intracranial stents (six each of Neuroform EZ, Enterprise, Apollo, and Tubridge FD) were successfully implanted in the left carotid arteries of 24 experimental piglets, with a technical success rate was 100%. For the dual-volume reconstruction method, the scanning process was divided into two steps (DSA and high-resolution C-arm CT imaging) separated by a long interval, and slight head movements led to difficulties in merging the high-resolution images in three piglets in our study. In such circumstances, a second high-resolution C-arm CT scan was performed for merging and reconstruction.

Evaluation of image reconstruction quality and observation of stent opening and apposition

The quality of the reconstructed images was grade I in 22/24 cases and grade II in 2/24 cases (Figs. 2-4). Interobserver agreement for image quality grading, as assessed independently by two neurointerventional radiologists (Dr. X with 15 years and Dr. Y with 12 years of clinical experience), was substantial, with a Cohen’s κ of 0.78 (95% CI, 0.56-0.99). Multidirectional observation of the reconstructed images showed incomplete expansion of the distal end of a Neuroform EZ stent. The remaining 23 stents were completely expanded without local mechanical disruption or rupture.
In all cases, the dual-volume reconstruction and the diluted contrast medium methods enabled clear visualization of stent apposition. Poor apposition of the distal end of the Neuroform EZ stent was observed in one case (type I malapposition, score 1 point). Good apposition was observed for the remaining 23 stents. The consistency rate between the two methods was 100%.

Radiation exposure dose statistics

A total of 24 5s-DSA scans and 48 high-resolution C-arm CT scans (with contrast agent injection [n=24] or without contrast agent injection [n=24]) were performed in this study. The radiation dose (reference AK and DAP) for each method and stent is shown in Tables 1 and 2. The radiation dose exposure was significantly higher for double volume reconstruction than for the diluted contrast medium method (p<0.001).

Complications

When the diluted contrast agent method was used, mild vasospasm occurred in four piglets. No serious intra-procedural complications were observed, such as vascular dissection and thrombosis. No complications such as intracerebral hemorrhage, stent thrombosis, or puncture site bleeding occurred in any of the pigs within 24 hours after the procedure.

DISCUSSION

It is well-established that early 3D C-arm CT used flat-panel (FD) detectors. After replacing the image intensifier with a flat-panel detector, it was found that the ordinary DSA system could acquire CT-like images through a C-arm rotation scan. In its early stages, this technique was termed flat-panel detector CT or FD-CT. C-arm CT models currently available include the Xper-CT (Philips, Best, Netherlands) and the Dyna-CT (Siemens), while high-resolution C-arm CT models available include the Vaso-CT (Philips) and the Dyna micro-CT (Siemens). The C-arm CT is mainly used for head, neck, chest, and abdominal scanning, while high-resolution C-arm CT is indicated for scanning implanted intracranial stent and coil, providing significantly better spatial resolution. Current evidence suggests that high-resolution C-arm CT combined with metal artifact removal technology significantly reduces the metal artifacts of stents or spring coils during neuro intervention and markedly improves image quality [14]. Commercial metal artifact reduction (MAR) algorithms for spiral CT, including iterative reconstruction (e.g., iMAR) and projection interpolation techniques, have demonstrated artifact reduction rates of 22.5% to 47.3% in hip prostheses, with optimal soft-tissue performance (artifact attenuation up to 41.2% reduction in Hounsfield units [HU]) [9]. However, these techniques exhibit suboptimal efficacy in neurointerventional C-arm CT applications. This limitation arises from inherent challenges posed by 1) high-density embolization coils (attenuation >3000 HU) and 2) submillimeter-scale stent struts (strut thickness : 0.06-0.08 mm), both of which exceed the corrective capacity of conventional MAR systems optimized for orthopedic implants with bulkier metallic components (typical density <2500 HU). Compared to other MAR algorithms, the high-resolution DynaCT Micro (Siemens Healthineers, Erlangen, Germany) incorporates the SMART reconstruction algorithm by utilizing a non-binned acquisition mode, optimized exposure parameters (tube voltage : 109 kVp; tube current : 1.8 mAs/frame), and a reduced field-of-view (FOV; 12×12 cm2). This method achieves an isotropic spatial resolution of 0.15 mm, as confirmed by phantom studies, representing a 65.1% improvement over the baseline resolution of 0.43 mm achieved with other MAR algorithms [5]. A previous in vitro study demonstrated that high-resolution C-arm CT could provide a more detailed display of intracranial stents [13]. To the best of our knowledge, few studies have hitherto assessed the dose of radiation received by patients during the scanning process or the accuracy and safety of various techniques for assessing stent apposition [5,18,20].
Current evidence suggests that high-resolution C-arm CT exhibits a better performance than traditional C-arm CT for displaying different types of intracranial stents during stent-assisted aneurysm embolization and can thus help reduce the long-term recurrence rate of aneurysms and the incidence of complications [5,14]. Consistent with the literature, we found that high-resolution CT yielded clear reconstruction images of the implanted stents, with grade I quality in most cases (22/24). Indeed, a good image quality helps identify problems such as incomplete expansion, distortion, dislocation, or stent fracture during stent release. In a study where high-resolution C-arm CT was used to assess Willis covered stent placement, twisting at the “inverted V” tip of one laser-engraved stent and stent tip embedding in the vessel wall were observed and could not be detected on conventional C-arm CT and fluoroscopy [1].
The diluted contrast medium method is relatively accurate and commonly used for evaluating implanted intracranial stents, especially intracranial dense-mesh stents. However, this technique has certain limitations since the DSA technicians need to reconfigure the low-concentration contrast medium and replace the high-pressure syringe barrel, which prolongs the procedure time. At the same time, the high flow rate and prolonged injection duration (22-25 seconds) of contrast medium through a catheter into the artery increases the risk of vasospasm and dissection. Li et al. [12] reported a case of arterial dissection at the tip of the angiography catheter when the diluted contrast medium method was used following Tubridge FD implantation and treated by placement of two Neuroform EZ stents. In our experiment, mild vasospasm at the tip of the angiographic catheter was observed in four piglets using our approach, highlighting the need for extra caution when performing this technique. Moreover, the tip of the angiographic catheter should not touch the wall to avoid damage induced by the high-speed jet of contrast.
In this study, we found excellent consistency between the dual-volume reconstruction and the diluted contrast medium methods for evaluating stent apposition evaluation, although lower radiation exposure and contrast agent dose were associated with the diluted contrast medium method. It should be pointed out that the dual-volume reconstruction method has strict requirements regarding the body posture during the two scans since even slight displacement can lead to the mismatch of merged images and result in false-positive results for stent malapposition. In addition, the quality of the processed images obtained by the dual-volume reconstruction method is determined by the postprocessing staff’s expertise and patience. In recent years, the high-resolution C-arm CT scanning technique (Vaso-CT) has emerged, requiring an injection of a small amount (9.6 mL) of undiluted contrast agent, with the flow rate adjusted to allow dilution by the blood flow [7]. This technique can provide images with resolution comparable to the diluted contrast medium method and improve the efficiency of high-resolution flat-panel CT for assessment of FD stent apposition.
The quality of imaging yielded by the diluted contrast medium method is related to the C-arm CT device’s physical parameters and the contrast agent’s concentration. Excessively high or low concentrations affect the assessment of the relationship between the stent and the vessel wall. In such cases, the procedure may be repeated. It should also be borne in mind that the concentrations of contrast agents used for high-resolution scanning largely depend on the clinical experience of the operator and the angiography device. The concentration of contrast agents tends to be 10-25% on Siemens devices [5,8] and 10-20% on Philips devices [18,20]. The contrast agent concentrations and injection times required to achieve optimal visualization of the stent, vessel lumen, and vessel wall on different angiography devices must be determined in future studies.
It should be noted that, due to significant differences in vascular anatomy between the experimental animals and humans (average vessel diameter ratio of 1 : 2.8), as well as variability in radiation beam angles during surgery (standard deviation up to 12.7°) caused by positioning challenges, we did not directly compare the absolute radiation doses between the dual-volume reconstruction and the diluted contrast medium methods. Instead, we measured the additional radiation dose relative to the standard surgical procedure. Our experimental data indicate that the dual-volume reconstruction method incurs an approximately 26% higher additional radiation dose than the diluted contrast medium method (Table 1). Nevertheless, this extra dose provides valuable guidance for clinicians when selecting imaging techniques (Table 2). Specifically, the 26% increase is primarily due to : 1) increased X-ray tube loading during the dual-phase acquisition and 2) the additional fluoroscopy time required for 3D-DSA.
While based on an animal model, the multiplanar reconstruction capability of high-resolution C-arm CT effectively overcomes limitations inherent to conventional 2D fluoroscopy, demonstrating superior performance in evaluating stent apposition within calcified vascular segments (simulating diabetic/hypertensive vasculopathy). Furthermore, the technique shows broad applicability for assessing complex vascular pathologies encountered clinically, including atherosclerotic plaque-induced stenosis and congenital tortuosity.
Our research has been extended to human cohorts with protocol optimization [15]. Given the anatomical disparities between Bama minipigs and humans (vascular diameter : 2.8±0.3 mm vs. 4.1±0.5 mm; p<0.001), dual injection protocols were implemented [16] : dual-volume reconstruction : undiluted contrast (5 mL/s; total 14 mL) and low-concentration protocol : 12% hyperosmolar (iopromide 370 mg I/mL) or 16% iso-osmolar (iodixanol 320 mg I/mL) contrast at 3.0 mL/s (total 66 mL over 20 seconds acquisition).
Some limitations were found in the present study. The sample size was small, with only 24 experimental animals and the findings of this study are inherently linked to the imaging parameters of the Artis Zeego system. Furthermore, it should be emphasized that although our study systematically evaluated stent expansion morphology and wall apposition using high-resolution C-arm CT, the study protocol did not include the next-generation Pipeline Flex FD (Ev3, Plymouth, MN, USA). Since this advanced device was not yet integrated into our institution’s clinical practice at the time of the experiments, our findings primarily apply to the technical assessment of conventional stents and current flow-diverter platforms. To address this evidence gap, we plan to conduct a prospective, multicenter registry study with independent, blinded DSA core laboratory readings, comparing three categories of devices—1) conventional stents/first-generation FDs; 2) FRED/Pipeline Flex FD; and 3) FRED Jr/FRED X—using standardized protocols. This study will focus on evaluating stent apposition relative to aneurysm morphological parameters (e.g., dome-to-neck ratio, vessel angulation at the aneurysm neck) and its impact on long-term aneurysm occlusion. Future studies should prioritize multicenter comparisons of imaging equipment, standardized postprocessing protocols, systematic animal cohort validations, and confirmatory, hypothesis-driven clinical trials to ensure reproducibility and generalizability of results across biological scales and clinical contexts.

CONCLUSION

High-resolution C-arm CT enables clear visualization of the microstructure and expansion of intracranial stents. When combined with different postprocessing techniques, the degree of stent apposition can be clearly assessed. However, the advantages and disadvantages of each postprocessing technique should be considered before implementation during clinical practice.

Notes

Conflicts of interest

No potential conflict of interest relevant to this article was reported.

Informed consent

This type of study does not require informed consent.

Author contributions

Conceptualization : TL, QT, SY; Data curation : QT, SY, SL; Formal analysis : QT, SY, CS; Funding acquisition : TL; Methodology : TL, QT, SY, YR; Project administration : TL, JM, ZL, XD; Visualization : QT, SY, TL, YR; Writing - original draft : QT, SY; Writing - review & editing : QT, SY, TL

Data sharing

None

Preprint

None

Acknowledgements

This work was supported by the National Natural Science Foundation of China (81801806); Henan Province Health Science and Technology Innovation Outstanding Young and middle-aged talents training program (YXKC2022029); and Henan Province Medical Science and Technology Tackling Program Provincial Ministry Youth Project (KYDZ2020120441).

The authors gratefully acknowledge the technical support from Ms. Ge Jiajia and Ms. Qiu Yi of the R&D Department at Siemens AG.

Fig. 1.
Workflow optimization for diluted contrast medium method. QA : quality assessment, DICOM : digital imaging and communications in medicine, WW : window width, WL : window level.
jkns-2024-0223f1.jpg
Fig. 2.
High-resolution C-arm computed tomography (CT) technology combined with various postprocessing reconstruction techniques to evaluate the degree of opening and apposition of Lvis stent. A : Ultrasound-guided puncture of the right femoral artery in a Guangxi Bama piglet after endotracheal intubation under general anesthesia. B : Lvis 4.5×30 mm stent placed in the left carotid artery (black arrows). C : High-resolution C-arm CT showing that the stent is fully opened with grade I image quality. D and E : Good stent apposition visualized by the diluted contrast medium method (score 0). F and G : Dual-volume reconstruction method combined with maximum intensity projection postprocessing shows good stent apposition (score 0). H and I : Good stent apposition visualized by the dual-volume reconstruction method combined with the volume rendering postprocessing technique (score 0). J : Intravascular ultrasound image shows full expansion and good apposition of the stent. The thin white arrows indicate the outline of the stent, and the thick white arrows indicate the tunica intima and media of the blood vessel.
jkns-2024-0223f2.jpg
Fig. 3.
Visualization of the degree of opening and apposition by high-resolution C-arm computed tomography (CT) combined with various postprocessing reconstruction techniques during Enterprise stent implantation. A : Two-dimensional (2D)-digital subtraction angiography (DSA) for the right carotid artery in a Guangxi Bama piglet. B : Enterprise 4.0×23 mm stent inserted into the right carotid artery (black arrows). C : High-resolution C-arm CT showing that the stent is fully opened with grade I image quality. D and E : Good stent apposition visualized by the diluted contrast medium method (score 0). F and G : Good stent apposition visualized by the dual-volume reconstruction method combined with maximum intensity projection postprocessing (score 0). H and I : Dual-volume reconstruction method combined with postprocessing by the volume rendering technique shows good apposition of the stent (score 0). J : Full expansion and good apposition of the stent visible on intravascular ultrasound imaging. The thin white arrows indicate the outline of the stent, and the thick white arrows indicate the tunica intima and media of the blood vessel.
jkns-2024-0223f3.jpg
Fig. 4.
High-resolution C-arm computed tomography (CT) combined with various postprocessing reconstruction techniques to evaluate the degree of opening and apposition of the Neuroform EZ stent. A : Two-dimensional (2D)-digital subtraction angiography (DSA) for the left carotid artery in a Guangxi Bama piglet. B : Neuroform 4.5×30 mm stent inserted into the left carotid artery. Black arrows indicate the proximal and distal ends of the stent. C : Incomplete expansion and twisting at the distal end of the stent (white arrow) visualized by high-resolution C-arm CT with grade I image quality. D : Full expansion and good apposition of the proximal end of the stent, but poor apposition at the distal end (type I malapposition) visualized by the diluted contrast medium method (score 1). E : Complete expansion and good apposition of the proximal end of the stent, but there is poor apposition of the distal end of the stent (white arrow) (type I malapposition) by the dual-volume reconstruction method (score 1). F : Poor apposition of the distal end of the stent visible on intravascular ultrasound imaging (thin white arrow indicates the outline of the stent, thick white arrow indicates the tunica intima and media of blood vessel).
jkns-2024-0223f4.jpg
Table 1.
Radiation dose (reference AK and DAP) for each method
Method Average dose of AK (mGy) p-value Average dose of DAP (µGy/m2) p-value
Dual-volume reconstruction method 107.82±5.49 <0.001 901.23±40.21 <0.001
Diluted contrast method 102.58±5.15 712.69±35.83

Values are presented as mean±standard deviation. AK : air kerma, DAP : dose-area product

Table 2.
Radiation dose (reference AK and DAP) for each stent
Stent Dual-volume reconstruction method
Diluted contrast method
5sDSA head
20sDCT head micro
20sDCT head micro
AK (mGy) DAP (µGy/m2) AK (mGy) DAP (µGy/m2) AK (mGy) DAP (µGy/2)
Neuroform EZ* 6.20 194.40 94.00 655.02 101.00 699.74
Neuroform EZ 6.00 185.74 100.00 692.04 109.00 754.45
Neuroform EZ 6.40 200.73 107.00 746.62 109.00 761.27
Neuroform EZ§ 6.20 194.33 102.00 706.23 100.00 696.17
Neuroform EZ 5.90 184.84 108.00 759.83 113.00 782.72
Neuroform EZ 6.50 210.47 97.00 672.61 99.00 689.91
Enterprise* 6.10 189.56 104.00 715.80 105.00 723.83
Enterprise 6.30 198.21 106.00 738.07 97.00 670.82
Enterprise 5.80 182.77 95.00 661.08 112.00 780.34
Enterprise§ 6.00 186.71 100.00 693.10 101.00 702.01
Enterprise 6.20 195.11 98.00 678.62 95.00 652.08
Enterprise 6.90 238.06 107.00 750.07 99.00 691.21
Apollo* 6.20 196.43 94.00 656.83 100.00 695.01
Apollo 6.40 199.70 104.00 717.09 109.00 752.65
Apollo 6.10 190.05 110.00 765.07 104.00 713.07
Apollo§ 6.00 187.85 102.00 708.32 96.00 667.65
Apollo 5.70 176.87 100.00 695.09 103.00 710.06
Apollo 5.90 186.91 101.00 700.87 102.00 707.49
Tubridge FD* 6.10 191.70 112.00 787.90 110.00 770.49
Tubridge FD 5.50 164.82 107.00 742.75 100.00 702.61
Tubridge FD 6.80 227.44 90.00 640.73 101.00 705.37
Tubridge FD§ 6.40 201.13 104.00 720.67 99.00 693.08
Tubridge FD 6.10 189.45 97.00 669.73 100.00 697.81
Tubridge FD 5.90 183.41 101.00 699.48 98.00 684.77

* No. 1.

No. 2.

No. 3.

§ No. 4.

No. 5.

No. 6.

AK : air kerma, DAP : dose-area product, DSA : digital subtraction angiography, DCT : dynamic collimation technology, EZ : Easy Deployment, FD : flow diverter

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