Low dose contrast media in step-and-shoot coronary angiography with third-generation dual-source computed tomography: feasibility of using 30 mL of contrast media in patients with body surface area <1.7 m2
Original Article

Low dose contrast media in step-and-shoot coronary angiography with third-generation dual-source computed tomography: feasibility of using 30 mL of contrast media in patients with body surface area <1.7 m2

Liang Jin1#, Bing Jie2#, Yiyi Gao1, An’qi Jiang1, Tingwen Weng3, Ming Li1,4

1Radiology Department, Huadong Hospital, affiliated with Fudan University, Shanghai, China; 2Radiology Department, Shanghai Pulmonary Hospital, Affiliated with Tongji University, Shanghai, China; 3Cardiology Department, Huadong Hospital, Affiliated with Fudan University, Shanghai, China; 4Institute of Functional and Molecular Medical Imaging, Fudan University, Shanghai, China

#These authors contributed equally to this work.

Correspondence to: Liang Jin, MD. Radiology Department, Huadong Hospital, affiliated to Fudan University, No.221# West Yan’an Road, JingAn District, Shanghai, China. Email: jin_liang@fudan.edu.cn; Ming Li, MD, PhD. Radiology Department, Huadong Hospital Affiliated to Fudan University, No.221# West Yan’an Road, JingAn District, Shanghai, China; Institute of Functional and Molecular Medical Imaging, Shanghai, China. Email: ming_li@fudan.edu.cn.

Background: Reducing contrast media volume in coronary computed tomography angiography minimizes the risk of adverse events but may compromise diagnostic image quality. We aimed to evaluate coronary computed tomography angiography’s diagnostic image quality while using 30 mL of contrast media in patients with a body surface area <1.7 m2.

Methods: This prospective study included patients who underwent coronary computed tomography angiography from May 2018 to June 2019. The patients were divided into a low-dose group, who received 30 mL of contrast media, and a routine-dose group, who received contrast media based on body weight. Patient characteristics, coronary computed tomography angiography results, and quantitative and qualitative image results were assessed and compared.

Results: In total, 103 patients with a body surface area <1.7 m2 were 53 in the low-dose group and 50 in the routine-dose group. Sex, age, body surface area, body weight, and heart rate were similar between the groups (P>0.05). A contrast media volume of 30±0 mL was used for the low-dose group, and 41.62±4.59 mL was used for the routine-dose group. The low-dose group’s computed tomography values were significantly different from those of the routine-dose group (P<0.05). The radiologists demonstrated agreement regarding diagnostic image quality and accuracy (kappa =0.91 and 0.85, respectively).

Conclusions: Using 30 mL of contrast media for coronary computed tomography angiography in patients with a body surface area <1.7 m2 provided a suitable diagnostic image quality for coronary artery disease diagnosis. Although radiation doses were similar between the groups, the decreased contrast media volume was likely beneficial for the patients.

Keywords: Contrast media; coronary angiography; body surface area; coronary artery disease; computed tomography angiography

Submitted Mar 27, 2020. Accepted for publication Jan 27, 2021.

doi: 10.21037/qims-20-500


Advances in computed tomography (CT) imaging have allowed coronary CT angiography (CCTA) to become a reliable, noninvasive method to assess coronary anatomy, coronary artery disease, and cardiac function (1). Iodinated contrast media (ICM) are extensively used and are indispensable in CCTA and other types of radiologic imaging (2). Optimal vascular attenuation during CCTA is important for obtaining an accurate estimation of the degree of stenosis (3); however, ICM may cause post-contrast acute kidney injury, which is an important consideration in patients at risk of acute hypersensitivity reactions that may occur within 1 hour of injection (2,4). Additionally, an appropriate volume of contrast media (CM) delivered at a specific injection flow rate (IFR) to maintain a constant dose during CT should be used to avoid CM waste and to save costs associated with the fast scan times afforded by modern CT equipment (5). Decreasing both the amount of CM and the injection rate would be advantageous for patients; therefore, the optimal dosage of ICM in CCTA imaging is a topic of ongoing interest (6,7).

The primary challenge related to reduced CM dosage is the effect on diagnostic image quality (DIQ). Lowering the CM dose while maintaining a constant injection duration lowers the IFR, decreasing the iodinated delivery rate (IDR), directly influencing the DIQ of CCTA images (5). Maintaining DIQ within a satisfactory range while using a relatively low dose of ICM has been the subject of many studies (3,8-17). Vascular attenuation during CCTA is influenced by several patient-specific factors, including body mass, blood volume, cardiac output, and factors related to the procedure, such as the administered CM concentration and injection rate (18). Both blood volume and cardiac output are closely correlated with body surface area (BSA) rather than body weight (10,19), and BSA-adapted CM administration protocols have been suggested accordingly (20); however, few studies have administered CM based on the BSA. As previous studies have shown that administration of 40mL of CM to patients with a BSA <1.7 m2, based on a BSA-adapted protocol (19), showed suitable coronary contrast enhancement, we speculated that it might be possible further to decrease the CM volume to below 40 mL. Previous studies have suggested that 30 mL of CM can be used for prospective electrocardiogram (ECG)-triggered high-pitch CCTA (8,14,21), suggesting a low CM volume in high-pitch CCTA imaging may also be feasible. To date, there have been no investigations of low-volume CM administration in patients with a BSA <1.7 m2 who undergo CCTA with the prospective ECG-triggered sequence acquisition scan mode [step-and-shoot (SAS), CCTA]. SAS acquisition has a longer scan time and allows for a higher heart rate (HR) than high-pitch scanning (22,23).

We hypothesized that 30 mL of CM would provide a sufficient DIQ for CCTA images in patients with a BSA <1.7 m2. This study aimed to investigate the effects of 30 mL of CM on the DIQ of SAS CCTA images in patients with a BSA <1.7 m2.


Patient population

A total of 103 patients were prospectively enrolled at our hospital from May 2018 to June 2019. This study was approved by the Ethics Committee of Huadong Hospital (No. 2019K005) and was conducted following the Declaration of Helsinki (1964). Written informed consent was obtained from all patients. The inclusion criteria were as follows: age 18 years or older, clinically suspected coronary heart disease in patients who had undergone CCTA, and a BSA <1.7 m2. The exclusion criteria were as follows: cardiopulmonary insufficiency, renal insufficiency, allergy to CM, prior stent or coronary artery bypass graft, inability to complete breath-holding for 10 s, and a history of using medicine to control HR (Figure 1).

Figure 1 Flow diagram of the patients involved in this study. CCTA, coronary computed tomography angiography; CM, contrast media.

BSA was calculated according to the Stevenson formula: BSA (m2) = 0.0061 × height (cm) + 0.0128 × weight (kg) — 0.1529 (24). The first 53 patients were enrolled in the low-dose (LD) group, and the next 50 participants were enrolled in the routine-dose (RD) group. The LD group received 30 mL of CM and 60 mL of saline at an IFR of 3.5 mL/s; the RD group was administered CM according to their weight (0.7 mL/kg) (11). The IFR of the CM for the RD group was calculated as the volume divided by 10 s, consistent with the IFR of saline. Beta-blockers and nitroglycerin were not administered before scanning.

Image acquisition

A third-generation dual-source CT scanner (Somatom Force, Siemens Healthcare) was used for the CCTA scans. A prospective ECG-triggered sequence acquisition mode, SAS, was used to scan in a cranial-to-caudal direction. The automated anatomical tube current modulation technique with 320 mA (CARE Dose 4DTM, Siemens Healthineers) and automatic tube voltage selection with 100 kV (ATVS, CAREkVTM, Siemens Healthineers) were used. The exposure dose (ECG-pulsing) range was set at 30–80% for the R-R interval. The collimator was 2*(64-96)*0.6 mm, and the gantry rotation time was 0.25 s/rotation. The bolus tracking technique was used for threshold monitoring at the aortic root, with an enhancement threshold of 80 HU and a delay time of 7 s. The slice thickness and image reconstruction interval were both 0.75 mm, and the kernel used was Bv36. Pre-warmed CM [iobitridol, 350 mg iodine (mgI)/mL] was injected using an 18-G closed intravenous catheter system with an Ulrich high-pressure syringe. The IDR was defined as the iodine concentration of CM multiplied by the IFR when injected into the vessel (5).

Quantitative and qualitative analyses

The CT values and standard deviations (SDs) of the luminal segment of the aortic root (AO), proximal left main coronary artery (LMCA-P), middle left anterior descending artery (LAD-M), distal left anterior descending artery (LAD-D), middle left circumflex artery (LCX-M), distal left circumflex artery (LCX-D), proximal right coronary artery (RCA-P), middle right coronary artery (RCA-M), distal right coronary artery (RCA-D), and perivascular adipose tissues (PVAT) were separately measured. The SD of the AO was considered as image noise. The size of the region of interest (ROI) of the AO was set at 90 mm2, and the others at 1 mm2. The following equations were used: signal-to-noise ratio (SNR) = CT value of the ROI/noise; and contrast-to-noise ratio (CNR) = (CT value within the ROI − CT value of the PVAT)/SD of the PVAT.

A quality evaluation was performed by two radiologists (a radiologist with 8 years of experience performing cardiovascular diagnosis and a senior radiologist with more than 15 years of experience). Double-blinded scoring was performed using a scale from 1 to 5: 1, poor opacification insufficient for diagnosis; 2, suboptimal opacification with low diagnostic confidence; 3, acceptable opacification sufficient for diagnosis; 4, good opacification of proximal and distal segments; and 5, excellent opacification of proximal and distal segments. Scores for the RCA, LCA (including LMCA-P, LAD-M, and LAD-D), and LCX were integrated, and subjective scores of ≥3 points were considered sufficient DIQ standard.

Diagnostic accuracy

The presence of stenosis >50% in the three main coronary arteries (LAD, LCX, and RCA) was assessed by the two radiologists mentioned above on a per-segment, per-vessel, and per-patient level using the 16-segment American Heart Association classification. A final consensus read was performed to evaluate the consistency in interpretation between the two observers.

Radiation dose

CCTA radiation dose was recorded, while the radiation doses associated with the scout view, calcium score scan, and the automatic bolus tracking technique were omitted. The dose-length product (DLP) and volume CT dose index (CTDIvol) were automatically provided by the CT scanner. The effective dose was estimated by multiplying the DLP by a factor of 0.014 mSv/(mGy × cm) (8).

Statistical analysis

SPSS 22.0 statistical software (IBM, Armonk, NY) was used for analyses. Quantitative indexes were presented as mean ± SD or as a median (minimum, maximum). The independent samples t-test or Mann-Whitney U test was performed to analyze statistically significant differences between groups. Categorical data were presented as frequencies and percentages and were compared using the chi-squared test. Linear regression analysis was performed to correlate BSA and CT values of all coronary segments in each group. All statistical tests were two-sided, and P values <0.05 were considered statistically significant. Kappa statistics were used to evaluate the consistency of the observers. The kappa values were categorized as follows: <0.20, almost inconsistent; 0.21–0.40, slightly consistent; 0.41–0.60, medium consistency; 0.61–0.80, good consistency; and 0.81–1.00, almost perfect consistency (25).


Patient characteristics are shown in Table 1. The volume (30 mL) and IFR (3.5 mL/s) of CM, volume (60 mL) and IFR (3.5 mL/s) of saline, and IDR (1.23 gI/s) of the LD group were significantly lower than those of the RD group (41.62±4.59 mL, 30 mL, 4.13±0.45 mL/s, and 1.45±0.16 gI/s, respectively; P<0.001).

Table 1
Table 1 Baseline characteristics of patients with a BSA <1.7 m2
Full table

CT values of all measured vessel segments of the LD group were significantly different from those of the RD group (P<0.05). SNR values of the LMCA-P [12.71 (0.57, 64.46)], LAD-D [5.79 (1.59, 15.15)], and LCX-D [7.52 (1.55, 30.98)] were significantly lower in the LD group than in the RD group [21.31 (8.25, 57.80), 9.26 (2.96, 20.74), and 12.19 (4.20, 33.71), respectively]. Inter-rater reliability for the experienced radiologist showed almost perfect scoring consistency for quality (kappa =0.91), and the results of the senior radiologist were used for further analyses. Qualitative analysis of the RCA, LCA, and LCX showed significant differences between groups, but the images showed sufficient DIQ (Table 2).

Table 2
Table 2 Comparison of quantitative and qualitative analyses using CCTA
Full table

To compare the diagnostic accuracy of stenosis between groups, four patients (five main coronary arteries) in the LD group and seven patients (seven main coronary arteries) in the RD group were assessed. As there was good inter-rater reliability between the two radiologists for image accuracy (kappa =0.85), the senior radiologist’s results were used for further analyses.


Despite recent reports that CM risk may be overstated (26), the updated guidelines recommend using the lowest CM dose (27). Previous studies have demonstrated that lower CM volumes and injection speeds reduce the incidence of acute hypersensitivity reactions to non-ionic ICM (4,28). The present study demonstrated that CM volume could be reduced to 30 mL in patients with a relatively low BSA while retaining 100% acceptable DIQ (Figure 2). This is consistent with the findings of previous studies worldwide (3,9-12,14-16,29-32), which have focused on optimizing CM dosage to achieve DIQ with CCTA. Feng et al. (15) demonstrated successful imaging using a total of 28 mL CM (370 mgI/mL) with an IFR of 3.5 mL/s in prospective high-pitch CCTA; therefore, the successful use of 30 mL CM for CCTA imaging should not be surprising. Furthermore, several studies (8,14,21) have demonstrated successful high-pitch CCTA with 30 mL of CM. The study by Feng et al. (15) involved patients with a body mass index (BMI) <26 kg/m2 and achieved an IDR of 1.295 gI/s (370 mgI/mL × 3.5 mL/s). Jia et al. (8) achieved an IDR of 1.2 gI/s (300 mgI/mL × 4 mL/s), while Zhang et al. (21) conducted a study involving 44 patients and achieved an IDR of 1.48 gI/s (370 mgI/mL × 4 mL/s). Furthermore, Wang et al. (14) achieved an IDR of 1.85 gI/s (370 mgI/mL × 5 mL/s). Our study demonstrated the lowest IFR, 3.5 mL/s, and achieved the second-lowest IDR, 1.225 gI/s, without compromising the DIQ. Furthermore, our study is the first to demonstrate that 30 mL of CM for SAS CCTA can result in a satisfactory DIQ, which has not been reported previously for patients with a BSA <1.7 m2. High-pitch CCTA is beneficial as it involves the lowest radiation exposure and has the fastest scan time compared to SAS acquisition; however, SAS acquisition can be performed for patients with a higher HR (<100 bpm) (23), whereas high-pitch CCTA strictly requires an HR of <75 bpm (22).

Figure 2 (A-D) A 67-year-old female patient with chest pain and a body surface area (BSA) of 1.60 m2, body mass index (BMI) of 28.51 kg/m2, 30 mL of contrast media (CM), and a flow rate of 3.5 mL/s. (A) The computed tomography (CT) value of the opening of the coronary sinus was 562 HU. Curved planar reconstruction images of the right coronary artery (B), left anterior descending artery (C), and left circumflex artery (D) are shown. (A1-D1) A 43-year-old male patient with chest pain with a BSA of 1.68 m2, BMI of 28.89 kg/m2, 59.5 mL of CM, and a flow rate of 5.5 mL/s. (A1) The CT value of the opening of the coronary sinus was 503 HU. Curved planar reconstruction images of the right coronary artery (B1), left anterior descending artery (C1), and left circumflex artery (D1) are shown.

Yi et al. designed a study that included 30 patients with a limited BMI (20–25 kg/m2) using 36 mL of CM with an IDR of 1.11 gI/s (370 mgI/mL ×3 mL/s) (9). Qu et al. demonstrated a shortened injection duration with 36.2 mL of CM and an IFR of 4.5±0.71 mL/s (12). Furthermore, Andreini et al. performed CCTA with an ultra-low CM concentration (80 mL bolus) and an IDR of 1.35 gI/s (iodixanol, 270 mgI/mL ×5 mL/s) (16). Therefore, our study demonstrated the lowest CM dose compared to recent studies involving SAS acquisition.

Injection protocols for CCTA involve titration of CM dose based on individual patient characteristics, including adjustments related to patient BSA and blood volume (10,29,30,33). Pazhenkottil et al. adapted a BSA protocol and demonstrated that a significantly lower amount of CM might help prevent contrast-induced nephropathy and its consequences (18,19); however, CM remained in the right heart chambers of patients with a BSA <1.7 m2 when using 40 mL, indicating that CM volume could possibly be reduced even further. In the present study, the CM volume of 40 mL was only reduced by 25% to 30 mL (19); however, this was a great challenge during SAS CCTA imaging, which requires a longer acquisition time compared to high-pitch helical scanning (14,15,17,22). Furthermore, 10 mL of CM with an IFR of 3.5 mL/s was sufficient to maintain vessel enhancement within 3 s, but only if the acquisition time was 3 s longer than that reported in the study by Pazhenkottil et al. (19), whose 40 mL dosage for patients with a BSA <1.7 m2 was unsuccessful. The present study postulated that a further reduction in CM to less than 30 mL could be investigated with decreasing BSA.

HR is another factor that influences both acquisition time and CCTA enhancement (23,33,34). When HR decreases during SAS acquisition—especially when it is <60 bpm—the acquisition time required for the end-diastole phase is longer, increasing the total exposure time (35,36). This makes it difficult to maintain the target blood vessel enhancement with a CM volume of 30 mL. In the study by Pazhenkottil et al., the mean HR of patients who underwent the examination was 56±7 bpm, with a maximum of 74 bpm (19). The higher temporal resolution of the third-generation dual-source CT used in our study (8) allowed for examining patients with an 18.8% higher average HR (69.47±10.78 bpm), with 34% of HRs in the LD group higher than 75 bpm. Zhu et al. reported that an increased HR resulted in increased cardiac output, leading to decreased CM attenuation in the coronary arteries, which was consistent with Tang et al. (37,38) findings. Therefore, BSA-based injection protocols’ ability to provide an appropriate enhancement in higher HR patients is of clinical interest. Our study included 18 patients (34.0%) in the LD group and 21 patients (38.9%) in the RD group with an HR >75 bpm; as the differences between groups were not significant between groups, we assume that this method was successful for patients with an HR >75 bpm.

The body weight-adjusted protocol of the RD group has been used for the LD group in other studies (39-42). All CT values of measured vessel segments in our LD group were lower than those in the RD group, which may be explained by the significantly lower IDR (1.23 gI/s) of the LD group compared with the RD group (1.45 gI/s) and the fact that IDR is the main determinant of vessel contrast enhancement in CCTA (29). Our study demonstrated that the IDR associated with satisfactory DIQ in both groups was lower than 1.5–2.0 gI/s, which is usually recommended for CCTA (29). The SNR and CNR values showed similar image quality between groups, except for the SNR values of the LAD-M, LAD-D, and LCX-D, thus explaining why the CCTA images were reported to have equal DIQ even though the CT values were better in the RD group. The excellent inter-rater reliability for diagnosis of stenosis >50% may also explain why the LD group had comparable diagnostic accuracy compared to the RD group. Using a lower tube voltage (<80 kVp) may have also improved image quality because of the lower average energy closer to the K-edge of iodine (33.2 keV) (5,13). The distribution of tube voltages (Figure 3) showed that >80% of patients in the LD group were scanned using 80 kV with a lower IDR (1.23 gI/s), resulting in better CT, SNR, and CNR values than those reported by Feng et al., who used 28 mL with an IDR of 1.295 gI/s and 70 kV (15). The inverse correlation between CT values and BSA in the LD group showed that CT values of most measured segments decreased when the BSA increased, whereas the RD group had homogeneous CT values (Figure 4), indicating that patients with a BSA <1.7 m2 could still benefit from a personalized protocol based on 30 mL of CM; the smaller the BSA, the lower the volume required (≤30 mL). The inverse correlation between CNR and BSA in the RD group may explain the higher qualitative score of the LD group, as the CNR of the LD group did not decrease with increased BSA.

Figure 3 Distribution of tube voltages of all patients in both groups. LD, low dose; RD, regular dose.
Figure 4 Correlations among computed tomography (CT), signal-to-noise ratio (SNR), and contrast-to-noise ratio (CNR) values and body surface area (BSA) for the two groups. LD, low dose; RD, regular dose.

There were several possible limitations of our patient population. Patients who had undergone a coronary artery bypass graft were excluded because they underwent CCTA with a larger scanning range (usually twice that of patients without a bypass). Patients who were unable to hold their breath for 10 s were also excluded because breathing artifacts worsen the DIQ. Patients who had a history of pharmaceutical HR control were excluded because the present study aimed to investigate SAS acquisition, which allows for higher HR.

Several other limitations existed in this study. As a single-center study, the sample size was small; a larger, multi-center study would provide stronger evidence for these results. The radiation doses for both groups in this study were slightly higher than normal because the range of exposure (ECG-pulsing) was set at 30–80% for the R-R interval; therefore, future research should reduce the exposure time without affecting the conclusions of this study. Furthermore, grouping patients with a BSA <1.7 m2 might not have been sufficiently personalized, and stratification based on BSA could be used in the future to explore the possibility of further contrast dose adjustment through both delivery rate and volume changes. More studies are required to establish whether a BSA-adjusted method might reduce the incidence of contrast-induced adverse events. Finally, the contrast dose associated with a reduced ICM dose and/or injection speed requires further investigation (43,44).


In conclusion, using a CM volume of 30 mL for patients with a BSA <1.7 m2 was appropriate for SAS CCTA with a third-generation dual-source CT and showed suitable DIQ for diagnosis.


Funding: This work was supported by the Youth Medical Talents Medical Imaging Practitioner Program [Grant No. AB83030002019004], the Medical Imaging Key Program of Wise Information Technology of 120, the Health Commission of Shanghai [Grant No. 2018ZHYL0103], the National Natural Science Foundation of China [Grant No. 61976238; Ming Li], and the “Future Star” of famous doctors’ training plan of Fudan University [Ming Li].


Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/qims-20-500). The authors have no conflicts of interest to declare.

Ethical Statement: This study was approved by the Ethics Committee of Huadong Hospital (No. 2019K005) and was conducted in accordance with the Declaration of Helsinki (1964). Written informed consent was obtained from all patients.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Jin L, Jie B, Gao Y, Jiang A, Weng T, Li M. Low dose contrast media in step-and-shoot coronary angiography with third-generation dual-source computed tomography: feasibility of using 30 mL of contrast media in patients with body surface area <1.7 m2. Quant Imaging Med Surg 2021;11(6):2598-2609. doi: 10.21037/qims-20-500