Abstract
Objectives
Photon-counting detector computed tomography (PCD-CT) is a promising new technique for CT imaging. The aim of the present study was the in vitro comparison of coil-related artifacts in PCD-CT and conventional energy-integrating detector CT (EID-CT) using a comparable standard brain imaging protocol before and after metal artifact reduction (MAR).
Methods
A nidus-shaped rubber latex, resembling an aneurysm of the cerebral arteries, was filled with neurovascular platinum coils and inserted into a brain imaging phantom. Image acquisition and reconstruction were repeatedly performed for PCD-CT and EID-CT (n = 10, respectively) using a standard brain imaging protocol. Moreover, linear interpolation MAR was performed for PCD-CT and EID-CT images. The degree of artifacts was analyzed quantitatively (standard deviation in a donut-shaped region of interest) and qualitatively (5-point scale analysis).
Results
Quantitative and qualitative analysis demonstrated a lower degree of metal artifacts in the EID-CT images compared to the total-energy PCD-CT images (e.g., 82.99 ± 7.89 Hounsfield units (HU) versus 90.35 ± 6.28 HU; p < 0.001) with no qualitative difference between the high-energy bin PCD-CT images and the EID-CT images (4.18 ± 0.37 and 3.70 ± 0.64; p = 0.575). After MAR, artifacts were more profoundly reduced in the PCD-CT images compared to the EID-CT images in both analyses (e.g., 2.35 ± 0.43 and 3.18 ± 0.34; p < 0.001).
Conclusion
PCD-CT in combination with MAR have the potential to provide an improved option for reduction of coil-related artifacts in cerebral imaging in this in vitro study.
Key Points
• Photon-counting detector CT produces more artifacts compared to energy-integrating detector CT without metal artifact reduction in cerebral in vitro imaging after neurovascular coil-embolization.
• Spectral information of PCD-CT provides the potential for new post-processing techniques, since the coil-related artifacts were lower in PCD-CT images compared to EID-CT images after linear interpolation metal artifact reduction in this in vitro study.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Computed tomography (CT) of the brain is still essential for diagnostics and treatment planning for a large number of brain disorders, for example detection of acute intracranial hemorrhage or ischemic stroke [1,2,3]. Besides the limitations of radiation exposure and insufficient soft tissue contrast, CT imaging may also be impeded by substantial artifacts in patients with metallic implants, in particular imaging after endovascular platinum coil-embolization, e.g., of intracranial aneurysms [4, 5]. Endovascular coil-embolization serves besides neurosurgical clipping as the first-line therapy for the treatment of cerebral aneurysms while both methods bear the low risk of periprocedural hemorrhage [6,7,8]. Since these coil-associated artifacts may cause a limited diagnostic value of subsequent CT recordings, especially for detection of acute cerebral hemorrhage or hypodense ischemic stroke areas surrounding the endovascular platinum coils, as well as the evaluation of aneurysm reperfusion after neurovascular coil-embolization, several acquisition and post-processing techniques have been introduced over the past years to improve image quality and reduce artifacts in clinical use [4, 5, 9,10,11,12,13]. One promising new technique is the photon-counting detector CT (PCD-CT). Compared to the energy-integrating detectors (EID) in currently used clinical CT scanners, this new technology enables the direct conversion of x-ray photons into electronic signals without requiring the intermediate step of converting photons into visible light, as in scintillators. PCD-CT can bring the advantage of a reduced radiation exposure, increased spatial resolution, correction of beam-hardening artifacts, and use of alternative contrast agents while creating opportunities for quantitative imaging [14]. Moreover, PCD-CT inherently provides spectral information which further has the potential of an improved metal artifact reduction (MAR) [15]. To date, there is only a limited number of studies available, investigating metal-related imaging artifacts as well as options for MAR in PCD-CT [15,16,17,18]. Most of these studies focus on orthopedic or dental metallic implants in bone imaging, while so far there is no study available investigating artifacts of endovascular platinum coils in cerebral imaging and compares the potential of both CT techniques for subsequent MAR using the same artifact reduction approach.
The aim of the present study was the systematic assessment of imaging artifacts caused by neurovascular platinum coils as well as the effect of MAR in PCD-CT compared to EID-CT in an experimental in vitro model using a standard brain imaging protocol.
Materials and methods
Preparation of the in vitro model
An experimental in vitro model, resembling an intracranial aneurysm of the cerebral arteries, was specifically designed for investigation of the present study. In brief, a nidus-shaped rubber latex with a diameter of 7 mm was filled with detachable platinum coils which are commonly used for the treatment of cerebral aneurysms in clinical practice using an Excelsior SL-10 microcatheter (Stryker Neurovascular): 1 × 6 mm × 20 cm Target XL 360 Soft coil; 1 × 6 mm × 15 cm Target 360 Soft; 2 × 5 mm × 10 cm Target 360 Soft; 2 × 3 mm × 10 cm Target 360 Ultra; and 1 × 2 mm × 4 cm Target 360 Nano (Stryker Neurovascular; respectively). After preparation, the experimental in vitro model was inserted into a custom-made brain imaging phantom with an average attenuation similar to brain tissue (mean 33.04 ± 0.86 Hounsfield units (HU)) — measured on the EID-CT images, consisting of saline (NaCl 0.9%) mixed with contrast medium (Imeron 300, Bracco Imaging GmbH) [19]. The in vitro model had a fixed placement at the center of the imaging phantom with minimal artificial movement between each scan. However, there was no movement between the corresponding PCT-CD and EID-CT scans to ensure reliable comparability. To reduce a possible influence caused by artificial air bubbles within the in vitro model, we inserted small holes to the natural rubber latex after insertion to the imaging phantom. This procedure ensured that the residual amount of air contained in the in vitro model was replaced by the mixture of saline and contrast medium of the imaging phantom. A schematic illustration of the imaging phantom is provided in Fig. 1.
PCD-CT scanner system and imaging
Image acquisition of all CT images was performed on an experimental prototype whole-body PCD-CT scanner (SOMATOM CounT; Siemens Healthineers) at the German Cancer Research Center (DKFZ). In this CT system, the PCD is integrated in a dual-source system that also houses a conventional EID, while detailed technical information on the used CT scanner have been recently described by Yu et al [20]. For the present study, the Macro imaging mode was used that provides a detector pixel size similar to the EID. Settings for EID- and PCD-CT were similar to the standard brain imaging protocol of our institution. Image acquisition was performed at a tube voltage of 120 kV, as used in clinical routine. For PCD-CT, the low-energy threshold was set at 25 keV and high-energy threshold at 70 keV. Detailed information on the individual acquisition protocols are provided in Table 1. Each ten scans were conducted consecutively for PCD-CT and EID-CT, respectively.
Image reconstruction and post-processing
Image reconstruction of all scans was conducted with the ReconCT prototype software (version 14.0.1.45000; Siemens Healthineers) with a slice thickness of 1 mm and B30f brain imaging kernel. To ensure an adequate comparability between PCD-CT and EID-CT images, a weighted filtered back projection algorithm was used for reconstruction. In addition, PCD-CT scans were reconstructed as total-energy images (25–120 keV), low-energy bin images (25–70 keV), and high-energy bin images (70–120 keV). An overview of the individual reconstruction parameters is demonstrated in Table 1. After image reconstruction, linear interpolation MAR was applied to the total-energy PCD-CT and EID-CT images as described by Kalender et al [21]
Quantitative image analysis
Quantitative image analysis was conducted with the Medical Imaging Interaction Toolkit (MITK; German Cancer Research Center (DKFZ)) [22].
As described previously, a special feature of the MITK software allowed us to place a standardized region of interest (ROI) with a donut-shaped configuration adjacent to and surrounding the center of the in vitro model of each scan [23,24,25]. This procedure allowed us the measurement of the surrounding artifacts while the coils were excluded from the analysis. The inner diameter of the donut-shaped ROI was 9 mm while the outer diameter was 108 mm. To ensure the consideration of artifacts of different positions, three separate ROIs were placed on the three central image slices and the standard deviation (SD) of the CT-values was calculated to assess the degree of artifacts. Manual adjustment of window width (W) and level/center (L) was allowed for an adequate ROI placement. Quantitative analysis was performed for the PCD-CT and EID-CT scans before and after MAR, focusing on the total-energy images of the PCD-CT scans (25–120 keV).
Qualitative image analysis
Qualitative analysis of the degree of coil-related artifacts in PCD-CT and EID-CT scans before and after MAR was performed by two different readers (reader 1 with 4 years and reader 2 with 5 years of experience in diagnostic imaging) on a CENTRICITY PACS 4.0 workstation (GE Healthcare), both blinded to the type of detector and image reconstruction. Moreover, qualitative analysis for PCD-CT scans without MAR was conducted for total-energy images (25–120 keV), low-energy bin images (25–70 keV), and high-energy bin images (70–120 keV) while after MAR we focused on the total-energy PCD-CT images. All images were reviewed in the axial plane with standard brain window settings (W: 80 HU, L: 40 HU) while window adjustment was not allowed. The degree of coil-related artifacts was graded by a 5-point scale: (1) no artifacts, (2) minor artifacts, (3) moderate artifacts, (4) marked artifacts, (5) severe artifacts. To further improve the quality of the image analysis, a second read by both readers was performed after 6 weeks.
Statistics
GraphPad Prism software (version 9.2.0) was used for statistical analysis. Results of the quantitative image analysis are provided as mean SD ± SD while results of the qualitative analysis are shown as mean score ± SD.
To evaluate statistical differences between the individual study groups before and after MAR, the Wilcoxon matched-pairs signed rank test was conducted. Moreover, the Kruskal-Wallis test and Dunn’s test for multiple comparisons using statistical hypothesis testing were performed for qualitative analysis.
Cohen’s κ coefficient was calculated to assess the inter-reader and intra-reader agreement of the qualitative analysis [26]. The κ values were interpreted as follows: ≤ 0.20, no agreement; 0.21–0.39, minimal agreement; 0.40–0.59, weak agreement; 0.60–0.79, moderate agreement; 0.80–0.90, strong agreement; and ≥ 0.90, almost perfect agreement. The level of statistical significance was defined as p < 0.05 [27].
Results
A summary of the results of the quantitative image analysis is provided in Figs. 2 and 3 as well as Tables 2 and 4.
The Wilcoxon matched-pairs signed rank test showed a higher degree of coil-related artifacts for the total-energy PCD-CT images (25–120 keV; 90.35 ± 6.28 HU) compared to the EID-CT images (82.99 ± 7.89 HU) without MAR, using a standardized, donut-shaped ROI on the three central image slices (p < 0.001). After MAR, the artifacts were significantly lower in the total-energy PCD-CT images compared to the EID-CT images in quantitative analysis (p < 0.001).
The results of the qualitative image analysis are summarized in Figs. 2 and 3 as well as Tables 2, 3, and 4.
The Kruskal-Wallis test demonstrated a significant difference between the individual study groups of PCD-CT (total-energy PCD-CT, low-energy bin PCD-CT, and high-energy bin PCD-CT) and EID-CT without MAR (p < 0.001). Moreover, Dunn’s test for multiple comparisons revealed a higher degree of artifacts for the total-energy PCD-CT images (25–120 keV; 4.65 ± 0.40) compared to the high-energy bin PCD-CT images (70–120 keV; 4.18 ± 0.37; p = 0.048) and the EID-CT images (3.70 ± 0.64; p < 0.001) while there was no difference to the low-energy bin PCD-CT images (25–70 keV; 5.00 ± 0.00; p = 0.236), without MAR, respectively. Low-energy bin PCD-CT images (25–70 keV) presented a higher degree of artifacts compared to EID-CT (p < 0.001) while high-energy bin PCD-CT images (70–120 keV) presented a lower degree of artifacts compared to the low-energy bin PCD-CT images (25–70 keV, p < 0.001) and no difference compared to the EID-CT images, without MAR respectively. After MAR, the Wilcoxon matched-pairs signed rank test demonstrated a lower degree of artifacts in the total-energy PCD-CT images compared to the EID-CT images in qualitative analysis (2.35 ± 0.43 and 3.18 ± 0.34; p < 0.001).
Inter-reader and intra-reader reliability showed a strong agreement for the rating of the coil-related artifacts, respectively (inter-reader: κ = 0.816; range: 0.732–0.900; intra-reader: κ = 0.838; range: 0.759–0.918).
Representative images of the PCD-CT and EID-CT scans before and after MAR are demonstrated in Figs. 4 and 5.
Discussion
In this study, a systematic in vitro comparison of a standard brain imaging protocol in PCD-CT versus EID-CT with respect to metal artifacts induced by neurovascular platinum coils was conducted before and after MAR. Results of the quantitative and qualitative analysis demonstrated a higher degree of coil-related artifacts in the total-energy PCD-CT and low-energy bin PCD-CT images compared to the EID-CT images while there was no qualitative difference between the high-energy bin PCD-CT images and the EID-CT images without MAR, respectively. Further qualitative analysis of the PCD-CT scans without MAR revealed the lowest degree of coil-related artifacts for the high-energy bin PCD-CT images and the highest degree for the low-energy bin PCD-CT images while there was no difference between the total-energy PCD-CT and the low-energy bin PCD-CT images. After MAR, the artifacts were significantly lower in the total-energy PCD-CT images compared to the EID-CT images in quantitative and qualitative analysis. Thus, our in vitro findings suggest that the spectral information of the PCD-CT in combination with MAR has the potential to reduce coil-related metal artifacts more profoundly in cerebral imaging compared to EID-CT.
PCD-CT represents a promising new CT technique for clinical routine for various reasons, for example due to a reduction of radiation exposure [14]. To date there are only a limited number of reports available investigating human brain imaging and metal-related artifacts as well as options for MAR in PCD-CT [14,15,16,17,18, 28]. One recently published study by Pourmorteza et al performed an in vivo and in vitro comparison of PCD-CT and EID-CT and reported a greater gray-white matter contrast for the PCD-CT scans compared to conventional CT using a standard brain imaging protocol [28]. Moreover, they described that the image noise for the low-energy bin and the high-energy bin PCD-CT images was higher than that of the total-energy PCD-CT images because each bin contains only a subset of the detected photons. Comparing these image reconstructions, the low-energy bin PCD-CT images provided a good gray-white matter differentiation but were susceptible to beam-hardening while the high-energy bin PCD-CT images were less susceptible to beam-hardening but demonstrated a less adequate differentiation of gray and white matter. For this reason, we focused the quantitative analysis of our in vitro study on the total-energy PCD-CT images with the advantage to enable a more precise comparability between PCD-CT and EID-CT and at the same time having the best relationship between beam-hardening and noise. Furthermore, the degree of coil-related artifacts was assessed with a donut-shaped ROI placed on the three central image slices of the PCD-CT and EID-CT images. Compared to previous artifact-investigating PCD-CT studies which used circular ROIs or threshold-based segmentation for artifact assessment [15,16,17,18], the donut-shaped ROI allowed us to include all surrounding artifacts in a highly standardized procedure without taking the coils into account [23,24,25]. The calculation of the SD of the CT-values ensured that the coil-related artifacts, typically consisting of high- and low-attenuation areas [4, 5], might not be canceled out as it might be for the mean HUs.
Most studies investigating metal-related artifacts in PCD-CT focused on methods for MAR of orthopedic or dental implants [15,16,17,18]. For example, Zhou et al described a substantial decrease in artifacts of orthopedic implants using tin filtration in PCD-CT with a tube voltage of 140 kV [18] while Do et al demonstrated the lowest degree of artifacts of orthopedic implants for images acquired at 140 kV using high-energy bin image reconstruction [16]. Since a tube voltage of 140 kV and tin filtration would prevent a reliable differentiation of the gray and white matter on non-contrast-enhanced cerebral CT images, image acquisition of the present study focused on a tube voltage of 120 kV without tin filtration. Comparing the PCD-CT and EID-CT images, quantitative analysis demonstrated a significantly lower degree of coil-related artifacts for EID-CT without MAR. Similar findings were demonstrated for qualitative analysis with a higher degree of artifacts for the low-energy bin PCD-CT and total-energy PCD-CT images compared to EID-CT, while there was no statistical difference between the EID-CT images and the high-energy bin PCD-CT images without MAR, respectively. These results are in accordance with the findings of Pourmorteza et al [28] and Do et al [16] that the high-energy bin images are less susceptible to metal-related artifacts. A possible reason for this could be that the effective energy of the high-energy bins is greater and thus the attenuation coefficient is significantly smaller in PCD-CT compared to EID-CT. However, the low-energy x-ray photons are primary responsible for the soft tissue contrast. To combine the advantages of the high-energy bin images and the low-energy bin images, further MAR was performed for the total-energy PCD-CT images and compared to the EID-CT images. So far, there is no commercial software for MAR in PCD-CT images available. In order to provide a reliable comparability between the PCD-CT and EID-CT images and due to the limited complexity of the used in vitro model, linear interpolation MAR was applied to both CT image datasets [21]. Further MAR procedures such as the photon-counting normalized metal artifact reduction (PCNMAR) by Byl et al may provide a more reliable MAR for clinical PCD-CT images of higher complexity [15]. However, the PCNMAR was specifically designed for PCD-CT imaging data and therefore not suitable for the present study. The present in vitro results demonstrated that metal artifacts can be reduced more profoundly in the PCD-CT images compared to the EID-CT images in quantitative and qualitative analysis. Thus, the spectral information of the PCD-CT has the potential to provide an improved option for MAR in cerebral CT imaging of patients after endovascular platinum coil-embolization. However, despite reaching statistical significance, the subjective differences between the PCD-CT and EID-CT images after MAR are small and the clinical impact on the advantage of the present findings is unclear. Certainly, there will be no major impact on the detection of large cerebral pathologies, but there may be a minor advantage for the detection of small pathologic lesions, which need to be further investigated in clinical studies.
We acknowledge that this study has several limitations. Since the present study used a brain imaging phantom, the transferability of an in vitro model to the human brain is limited and future in vivo studies are necessary. Moreover, the mixture of contrast medium and saline within the brain imaging phantom may result in a different attenuation depending on the specific energy of the photons used for imaging, which might lead to certain bias in quantitative and qualitative analysis. Due to cost-factors, our model contained only a defined number of neurovascular coils while a variable number of coils might have further influence on the degree of artifacts. Only the CT brain imaging settings of our institution have been applied while other institutions might use different settings. Moreover, only the Macro imaging mode was used for PCD-CT imaging; thus, other available PCD-CT imaging modes might lead to different results. Also the intrinsically available spectral information of PCD-CT has not been exploited in this study.
Conclusion
PCD-CT constitutes a promising new technique for future CT imaging in clinical routine. The results of the present study demonstrated no difference in the degree of platinum coil–related artifacts between the high-energy bin PCD-CT images and the conventional EID-CT images while low-energy bin PCD-CT and total-energy PCD-CT images both showed a higher degree of artifacts, without MAR, respectively. However, linear interpolation MAR was able to reduce the coil-related artifacts in the total-energy PCD-CT images with differences compared to the EID-CT images in both analyses. Thus, PCD-CT in combination with MAR has the potential to provide an improved option for reduction of coil-related artifacts in cerebral imaging in this in vitro study.
Abbreviations
- CT:
-
Computed tomography
- DKFZ:
-
German Cancer Research Center
- EID-CT:
-
Energy-integrating detector CT
- HU:
-
Hounsfield units
- L:
-
Window level/center
- MAR:
-
Metal artifact reduction
- MITK:
-
Medical Imaging Interaction Toolkit
- PCD-CT:
-
Photon-counting detector CT
- PCNMAR:
-
Photon-counting normalized metal artifact reduction
- ROI:
-
Region of interest
- SD:
-
Standard deviation
- W:
-
Window width
References
Birenbaum D, Bancroft LW, Felsberg GJ (2011) Imaging in acute stroke. West J Emerg Med 12:67–76
Parizel PM, Makkat S, Van Miert E, Van Goethem JW, van den Hauwe L, De Schepper AM (2001) Intracranial hemorrhage: principles of CT and MRI interpretation. Eur Radiol 11:1770–1783
Runge VM, Aoki S, Bradley WG Jr et al (2015) Magnetic resonance imaging and computed tomography of the brain-50 years of innovation, with a focus on the future. Invest Radiol 50:551–556
Prell D, Kyriakou Y, Struffert T, Dorfler A, Kalender WA (2010) Metal artifact reduction for clipping and coiling in interventional C-arm CT. AJNR Am J Neuroradiol 31:634–639
Katsura M, Sato J, Akahane M et al (2018) Single-energy metal artifact reduction technique for reducing metallic coil artifacts on post-interventional cerebral CT and CT angiography. Neuroradiology 60:1141–1150
Connolly ES Jr, Rabinstein AA, Carhuapoma JR et al (2012) Guidelines for the management of aneurysmal subarachnoid hemorrhage: a guideline for healthcare professionals from the American Heart Association/american Stroke Association. Stroke 43:1711–1737
Park HK, Horowitz M, Jungreis C et al (2005) Periprocedural morbidity and mortality associated with endovascular treatment of intracranial aneurysms. AJNR Am J Neuroradiol 26:506–514
Darkwah Oppong M, Pierscianek D, Ahmadipour Y et al (2018) Intraoperative aneurysm rupture during microsurgical clipping: risk re-evaluation in the post-international subarachnoid aneurysm trial era. World Neurosurg 119:e349–e356
Katsura M, Sato J, Akahane M, Kunimatsu A, Abe O (2018) Current and novel techniques for metal artifact reduction at CT: practical guide for radiologists. Radiographics 38:450–461
Otsuka T, Nishihori M, Izumi T et al (2021) Streak metal artifact reduction technique in cone beam computed tomography images after endovascular neurosurgery. Neurol Med Chir (Tokyo). https://doi.org/10.2176/nmc.oa.2021-0014
Morsbach F, Bickelhaupt S, Wanner GA, Krauss A, Schmidt B, Alkadhi H (2013) Reduction of metal artifacts from hip prostheses on CT images of the pelvis: value of iterative reconstructions. Radiology 268:237–244
Barrett JF, Keat N (2004) Artifacts in CT: recognition and avoidance. Radiographics 24:1679–1691
Amelung N, Maus V, Behme D et al (2019) Evaluation of an optimized metal artifact reduction algorithm for flat-detector angiography compared to DSA imaging in follow-up after neurovascular procedures. BMC Med Imaging 19:66
Willemink MJ, Persson M, Pourmorteza A, Pelc NJ, Fleischmann D (2018) Photon-counting CT: technical principles and clinical prospects. Radiology 289:293–312
Byl A, Klein L, Sawall S, Heinze S, Schlemmer HP, Kachelriess M (2021) Photon-counting normalized metal artifact reduction (NMAR) in diagnostic CT. Med Phys 48:3572–3582
Do TD, Sawall S, Heinze S et al (2020) A semi-automated quantitative comparison of metal artifact reduction in photon-counting computed tomography by energy-selective thresholding. Sci Rep 10:21099
Lee CL, Park J, Nam S et al (2021) Metal artifact reduction and tumor detection using photon-counting multi-energy computed tomography. PLoS One 16:e0247355
Zhou W, Bartlett DJ, Diehn FE et al (2019) Reduction of metal artifacts and improvement in dose efficiency using photon-counting detector computed tomography and tin filtration. Invest Radiol 54:204–211
Daubner D, Spieth S, Cerhova J, Linn J, Kirchhof K (2016) Measuring ventricular width on cranial computed tomography: feasibility of dose reduction in a custom-made adult phantom. Rofo 188:73–81
Yu Z, Leng S, Jorgensen SM et al (2016) Evaluation of conventional imaging performance in a research whole-body CT system with a photon-counting detector array. Phys Med Biol 61:1572–1595
Kalender WA, Hebel R, Ebersberger J (1987) Reduction of CT artifacts caused by metallic implants. Radiology 164:576–577
Nolden M, Zelzer S, Seitel A et al (2013) The Medical Imaging Interaction Toolkit: challenges and advances : 10 years of open-source development. Int J Comput Assist Radiol Surg 8:607–620
Schmitt N, Floca RO, Paech D et al (2020) Imaging artifacts of liquid embolic agents on conventional CT in an experimental in vitro model. AJNR Am J Neuroradiol. https://doi.org/10.3174/ajnr.A6867
Schmitt N, Floca RO, Paech D et al (2021) Imaging artifacts of nonadhesive liquid embolic agents in conventional and cone-beam CT in a novel in vitro AVM model. Clin Neuroradiol. https://doi.org/10.1007/s00062-021-01013-5
Schmitt N, Weyland CS, Wucherpfennig L et al (2021) The impact of software-based metal artifact reduction on the liquid embolic agent Onyx in cone-beam CT: a systematic in vitro and in vivo study. J Neurointerv Surg. https://doi.org/10.1136/neurintsurg-2021-018018
Cohen J (1960) A coefficient of agreement for nominal scales. Educ Psychol Meas 20:37–46
McHugh ML (2012) Interrater reliability: the kappa statistic. Biochem Med (Zagreb) 22:276–282
Pourmorteza A, Symons R, Reich DS et al (2017) Photon-counting CT of the brain: in vivo human results and image-quality assessment. AJNR Am J Neuroradiol 38:2257–2263
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Guarantor
The scientific guarantor of this publication is Dominik Vollherbst.
Conflict of interest
HUK: declares relationships with Siemens, Philips, Bayer, Boehringer Ingelheim, Astra Zeneca, Merck Sharp Dohme. MB: reports board membership: DSMB Vascular Dynamics; consultancy: Roche, Guerbet, Codman; grants/grants pending: DFG, Hopp Foundation, Novartis, Siemens, Guerbet, Stryker, Covidien; payment for lectures (including service on speakers bureaus): Novartis, Roche, Guerbet, Teva, Bayer, Codman. MAM: has received consulting fees, speaker fees, and travel support outside this work from Codman, Covidien/Medtronic, MicroVention, Phenox, and Stryker. DFV: has received travel support outside this work from MicroVention, Stryker and Cerenovus. HPS is a member of the European Radiology Editorial Board. They have not taken part in the review or selection process of this article. All other authors have nothing to disclosure in regard of this work.
Statistics and biometry
No complex statistical methods were necessary for this paper.
Informed consent
Written informed consent was not necessary due to the in vitro character of the study.
Ethical approval
Institutional review board approval was not required because of the in vitro character of this study.
Methodology
• Prospective
• Experimental
• Multicenter study
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Schmitt, N., Wucherpfennig, L., Rotkopf, L.T. et al. Metal artifacts and artifact reduction of neurovascular coils in photon-counting detector CT versus energy-integrating detector CT — in vitro comparison of a standard brain imaging protocol. Eur Radiol 33, 803–811 (2023). https://doi.org/10.1007/s00330-022-09073-y
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00330-022-09073-y