Article Text

Original research
Clinical and economic impact of extracardiac lesions on coronary CT angiography
  1. Andrew Kelion1,
  2. Nikant Sabharwal1,
  3. David Holdsworth1,
  4. Sam Dawkins1,
  5. Heiko Peschl2,
  6. Anny Sykes3,
  7. Yaver Bashir1
  1. 1 Department of Cardiology, Oxford University Hospitals NHS Foundation Trust, Oxford, Oxfordshire, UK
  2. 2 Department of Radiology, Oxford University Hospitals NHS Foundation Trust, Oxford, Oxfordshire, UK
  3. 3 Department of Respiratory Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, Oxfordshire, UK
  1. Correspondence to Dr Andrew Kelion, Department of Cardiology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK; andrew.kelion{at}


Objective When reporting coronary CT angiography (CCTA), extracardiac structures are routinely assessed, usually on a wide field-of-view (FOV) reconstruction. We performed a retrospective observational cross-sectional study to investigate the impact of incidental extracardiac abnormalities on resource utilisation and treatment, and cost-effectiveness.

Methods All patients undergoing CCTA at a single institution between January 2012 and March 2020 were identified. The indication for CCTA was chest pain or dyspnoea in >90%. Patients with ≥1 significant extracardiac findings were selected. Clinical follow-up, investigations and treatment were documented, and costs were calculated.

Results 4340 patients underwent CCTA; 717 extracardiac abnormalities were identified in 687 individuals (15.8%; age 62±12 years; male 336, 49%). The abnormality was already known in 162 (23.6%). Lung nodules and cysts were the most common abnormalities (296, 43.1%). Clinical and/or imaging follow-up was pursued in 292 patients (42.5%). Treatment was required by 14 patients (0.3% of the entire population), including lung resection for adenocarcinoma in six (0.1%). All but two abnormalities (both adenocarcinomas) were identifiable on the limited cardiac FOV. The cost of reporting (£20) and follow-up (£33) of extracardiac abnormalities was £53 per patient. The cost per discounted quality-adjusted life year was £23 930, increasing to £46 674 for reporting the wide FOV rather than the cardiac FOV alone.

Conclusions Extracardiac abnormalities are common on CCTA, but identification and follow-up are costly. The few requiring treatment are usually identifiable without review of the wide FOV. The way in which CCTAs are scrutinised for extracardiac abnormalities in a resource-limited healthcare system should be questioned.

  • multidetector computed tomography
  • coronary artery disease
  • health care economics and organizations

Data availability statement

Data are available on reasonable request.

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Coronary CT angiography (CCTA) is increasingly the first-line investigation for patients presenting with angina.1 To analyse the coronary arteries, tomograms are reconstructed using a relatively tight field of view (FOV) encompassing the heart. However, because the X-ray beam has traversed the entire width of the chest, it is easy to reconstruct an additional wide FOV dataset. This allows a more extensive assessment of extracardiac structures (especially the lungs) that were not of primary interest to the referrer. Incidental findings are common,2–12 and review of the available reconstructions for extracardiac abnormalities is routine in radiology departments in many countries, increasing the time required to report CCTA. When cardiac findings have been reported by a cardiologist, this may necessitate a separate read by a radiologist.

Although incidental extracardiac abnormalities—typically lung nodules—are frequently seen on CCTA,2–12 only a minority will ultimately require specific treatment with the potential for prognostic benefit. To achieve this, a large proportion will be subjected to further imaging—often requiring additional radiation exposure—and clinical follow-up. This generates patient anxiety, risk and healthcare expense. We performed a retrospective observational cross-sectional study of patients undergoing CCTA in our tertiary cardiac centre over a period of >8 years. We quantified the burden of clinical and imaging follow-up triggered by incidental extracardiac abnormalities, in relation to the proportion that subsequently required specific treatment. The cost-effectiveness of scrutinising CCTA studies for extracardiac abnormalities was also considered.

Materials and methods


We identified all patients undergoing clinically indicated gated cardiovascular CT studies between January 2012 and March 2020 from our Computerised Radiology Information System. Patients in whom craniocaudal coverage was extended above the carina or below the diaphragm were excluded (figure 1). This was a retrospective observational study in patients who had undergone clinical scans, so written informed consent and ethical committee approval were not obtained. Patients and the public were not involved in the design, conduct, reporting or dissemination plans of our research.

Figure 1

Study flow chart. TAVI, transcatheter aortic valve implantation.

CT imaging and reporting

The indication for CCTA was chest pain or dyspnoea in >90% of cases. Scans were performed using several General Electric 64-detector and 256-detector scanners and a Canon Aquilion One 320-detector scanner. Best-phase cardiac reconstructions were reviewed and reported by experienced imaging cardiologists (>90%) or radiologists. A wide FOV dataset was reconstructed for all patients and was reported by a radiologist. Cardiac and extracardiac findings were combined into a single clinical report.


Reports were scrutinised to identify patients with ≥1 potentially significant non-cardiovascular findings. Patients with abnormalities that were stated to be of no clinical importance by the reporting radiologist were not included. The Computerised Radiology Information System and Electronic Patient Record were interrogated for each patient to establish what additional investigations, clinical follow-up and treatment resulted directly from the identification of each extracardiac abnormality. For patients undergoing follow-up, both the cardiac FOV and wide FOV were reviewed (by author AK) to see if the extracardiac abnormality was clearly identifiable on the former.

Follow-up of each abnormality was at the discretion of the referring clinician, informed by the advice of the reporting radiologist. During the 8-year period covered by the study, both the British Thoracic Society (2015) and the Fleischner Society (2017) published updated guidelines for the follow-up of lung nodules.13 14 We compared the prevalence and rate of follow-up of lung nodules during periods before, between and after publication of the two documents.


Costs for investigations and outpatient clinics were the NHS tariffs for the year 2019–2020 (online supplemental table 1).15 The reporting tariff for a CT scan of one area (£20) was used to reflect our usual practice of extracardiac reporting by a radiologist following cardiac reporting by a cardiologist. A cost of £20 was allocated for any discussion at a multidisciplinary meeting. We included only costs accruing up to the point of discharge from follow-up or initiation of treatment. The cost of treatment itself, whether surgical or medical, was not included: had patients not had their extracardiac lesion detected on CCTA, we assumed that they would have required similar treatment at a later (symptomatic) stage.

Supplemental material

Clinical benefit of early detection of lung cancer

We anticipated that the main health gain of extracardiac reporting would arise from identification of lung cancer at an early stage. In the context of CT screening programmes, Whynes16 has described a method for estimating this benefit (online supplemental methods). The UK’s National Institute for Health and Care Excellence (NICE) requires that health gains be expressed as quality-adjusted life years (QALYs), discounted at the same interest rate as that used for discounting costs (3.5% per annum).17 Applying this to real-life data from the UK Lung Cancer Screening pilot trial yields an average gain per cancer identified of 1.6 QALYs discounted.18

Statistical analysis

Continuous variables are expressed as mean±SD if normally distributed, or median (25th–75th centile) otherwise. A χ2 test was used to compare the prevalence and rate of follow-up of lung nodules during the three consecutive time periods.


Range of extracardiac abnormalities

Between January 2012 and March 2020, 5329 gated cardiovascular CT studies were performed (figure 1). Nine hundred and eighty-nine involved extended craniocaudal coverage and were excluded. Among the remaining 4340, 717 significant extracardiac abnormalities were identified in 687 patients (15.8%; mean age 62±12 years; male 336, 49%) (table 1). Lung nodules and cysts constituted the largest category and were found in 296 patients (43.1%; 41.3% of total lesions). Appearances suggestive of subclinical lung infection and interstitial lung disease were also frequent.

Table 1

Findings in 687 patients with ≥1 extracardiac abnormality


The clinical courses of the 687 patients are shown in table 2. Information was unavailable for 16 patients who were out of area. In 162 patients (23.6%), the extracardiac abnormality was known from previous imaging. Further follow-up was triggered in nine of these, but none of them subsequently required any alteration in treatment. Of 509 patients with previously unknown findings, clinical and/or imaging follow-up was pursued in 283 (55.6%). Follow-up remains ongoing in 30 patients (25 with lung nodules), with a median duration to November 2021 of 27 (23-36) months. Patients with lung nodules (210/252, 83.3%) or findings suggestive of interstitial lung disease (28/47, 59.6%) were more likely to undergo follow-up and/or treatment than those with other findings (61/227, 26.9%).

Table 2

Clinical outcome in 687 patients with ≥1 extracardiac abnormality

In 231 of the 292 patients who underwent follow-up, both the cardiac FOV and wide FOV reconstructions were accessible for review from the radiology Picture Archiving and Communication System. The extracardiac abnormality was clearly visible on the cardiac FOV in 130 (56.3%). One hundred and seventy of the patients were followed for lung nodules or cysts, and the lesion was clearly visible on the cardiac FOV in 82 (48.2%).

The prevalence of reported lung nodules was similar during the time periods 2012–2015, 2016–2017 and 2018–2020 (table 3). There was no significant difference in the proportions of nodules undergoing follow-up or leading to resection for lung cancer.

Table 3

Temporal trends in reported prevalence and rate of follow-up of previously unknown lung nodules

Changes in treatment

Treatment was changed in 14 patients (0.3% of the entire population) after identification of an extracardiac finding and its subsequent follow-up (examples in figure 2). Eight patients with lung nodules underwent video-assisted thoracoscopic surgical (VATS) lung resection, all within 9 months of CCTA: six for carcinoma, one for a typical carcinoid and one for an inflammatory myofibroblastic tumour. All of the carcinomas were adenocarcinomas, only one of whom (16.7%) was known to have smoked. The smallest was 13 mm on the index CCTA. One patient with lung nodules was diagnosed with classic Hodgkin’s disease and received chemotherapy. Four patients with newly diagnosed interstitial lung disease received medical therapy: all of these were dyspnoeic at the time and had deteriorating pulmonary function tests. One patient with dyspnoea had segmental pulmonary emboli and was anticoagulated. All but two of the treated lesions (both adenocarcinomas) were clearly visible on the cardiac FOV as well as on the wide FOV images.

Figure 2

Four example cases where an extracardiac abnormality seen on CCTA led to a change in treatment. All images are transaxial tomograms from the cardiac (limited FOV) reconstruction. Top left: adeno-squamous carcinoma; a 30 mm spiculated cavitating mass is seen in the left upper lobe (white arrow). Top right: idiopathic pulmonary fibrosis; reticulation is seen peripherally (black arrows) and more densely in the anterior left lower lobe along the oblique fissure, with a small focal area of opacification (white arrow). Bottom left: Hodgkin’s disease; enlarged mediastinal and subcarinal lymph nodes are seen (white arrows). Bottom right: emboli in right lower lobe segmental pulmonary arteries (white arrows).

In three other patients, follow-up imaging for an extracardiac abnormality seen on CCTA identified a previously occult and unrelated lesion requiring treatment. (1) CT follow-up for atelectasis revealed new and progressive multifocal ground glass opacification, which resolved on stopping amiodarone. (2) CT follow-up for possible interstitial lung disease identified a large left renal cell carcinoma, which was resected. (3) CT follow-up for a lung nodule demonstrated multiple lytic bone lesions due to multiple myeloma, which was treated with chemotherapy.

Costs and cost-effectiveness of follow-up

Table 4 shows the total numbers and costs of additional appointments and diagnostic procedures attended by the 292 patients following extracardiac findings. Further CT scans, chiefly non-contrast scans of the chest, were the most common downstream investigation (490), and the majority were performed in patients with lung nodules (414, 84.5%). The majority of patients completing follow-up for previously unknown lung nodules required only one subsequent chest CT (104/183, 56.8%).

Table 4

Additional appointments and diagnostic procedures attended by patients followed as a result of one or more extracardiac finding on CCTA

The cost of reporting the wide FOV in all 4340 patients (£20 per patient) was £86 800. The cost of consequent clinical and imaging follow-up was £142 928 (£33 per patient), making a total of £229 728 (£53 per patient). For those with lung nodules, the cost of follow-up was £113 743: £537 per patient followed. The total health gain from identification of the six carcinomas was 9.6 discounted QALYs, implying a cost per discounted QALY of £23 930.

Compared with inspection of the cardiac FOV alone, separate examination of the wide FOV in all patients cost £86 800 for initial reporting plus an estimated £62 558 for follow-up of additional abnormalities, making a total of £149 358 (£34 per patient). Given that only two of the resected lung carcinomas were identifiable on the wide FOV alone, the cost per discounted QALY was £46 674.


This is one of the largest studies to have investigated the prevalence of extracardiac abnormalities on CCTA (online supplemental table 2).2–12 We have focused on the need for a change in treatment as the most meaningful indication of a clinically ‘significant’ lesion. Importantly, we have considered the downstream costs and cost-effectiveness associated with detection of extracardiac abnormalities.

In 2016, NICE recommended CCTA as the first-line investigation for patients with angina of recent onset.1 In response, the British Society of Cardiovascular Imaging/CT estimated that full implementation would require a sevenfold increase in CCTA activity.19 The Royal College of Radiologists has calculated ‘a current estimated shortage of 1939 consultant radiologists, equivalent to a third (33%) of the workforce’ in the UK.20 The shortfall is likely to be amplified in the aftermath of the COVID-19 pandemic. Detailed reporting of extracardiac findings in every patient undergoing CCTA is time consuming and generates downstream testing and follow-up. This expenditure of limited resources can only be justified if it leads to cost-effective benefits for patients.

Burden of extracardiac findings

In our large series, 16% of patients had ≥1 significant extracardiac abnormality on CCTA, of which 43% (7% of the overall population) were lung nodules or cysts with the potential to represent cancer. While this burden of extracardiac findings is significant, it is lower than that found in most previous studies where values up to 70% have been quoted (online supplemental table 2).2–12 The discrepancy may be due to the varying threshold of radiologists for reporting borderline abnormalities. Moreover, in some previous studies extracardiac vascular findings (eg, aortic abnormalities) were included among the noncardiac abnormalities.

Lung cancers undergoing resection

In our study, treatment was ultimately changed in 14 patients (0.3%), of whom six patients (0.1%) underwent VATS lung resection of an adenocarcinoma: this is typical of the prevalence of lung cancer reported in previous studies (online supplemental table 2).2–12 All six patients had a large nodule on the index CCTA (≥13 mm), and all underwent lung resection within 9 months of initial detection, rather than after prolonged CT follow-up. It should be noted that 25 patients with lung nodules remain under follow-up, and it is possible that one or more of these will ultimately require cancer surgery.

Previous studies have suggested that only a minority of lung nodules visible on the wide FOV reconstruction can be identified on the cardiac reconstruction.2 6 Kim et al 7 used an imaging protocol that included a full chest CT following CCTA in a group of 11 654 patients. Of 36 lesions seen on the full chest CT that turned out to be lung cancer, 19 (53%) were visible on the wide cardiac FOV. Of these only four (21%) were detectable on the limited cardiac FOV. In contrast, we found that four of the six (66.7%) resected lung cancers were clearly visible on the limited cardiac reconstruction. The discrepancy may reflect interdepartmental differences in the rigour with which the lungs are excluded from the limited ‘cardiac’ reconstruction. It could also reflect differences in patient population or the play of chance, given the relatively small numbers of cancers.

Reporting lung nodules as a screening exercise

Asymptomatic lung nodules identified on a wide FOV reconstruction are equivalent to those discovered by deliberate screening. In response to the positive results of the National Lung Screening Trial (NLST) in the USA,21 the Society of Cardiovascular CT (SCCT) has suggested that the wide FOV dataset should be routinely reconstructed and reported following CCTA in patients meeting the inclusion criteria for that study: age 55–74 years, ≥30 pack years of smoking.22 An Australian prospective survey of 229 CCTA patients calculated that only 6% would fall into that category.23 In NLST, only 36% of lung cancers were adenocarcinomas,21 whereas in our cohort they all were. This predominance of adenocarcinomas is consistent with previous studies in CCTA patients.7 Of the various types of lung cancer, adenocarcinomas show the weakest association with smoking,24 and indeed only one of our six cancer patients is known to have smoked and might have been included in NLST. Therefore, the data provide little support for the SCCT’s approach to selective lung cancer screening in CCTA patients.

Other pathologies receiving treatment

Eight patients with non-carcinomatous abnormalities received treatment, and all were clearly identifiable on the cardiac FOV. The prognostic value of presymptomatic detection is questionable in this group. Typical low-grade bronchial carcinoids and inflammatory myofibroblastic tumours are slow growing with little or no tendency to metastasise.25 26 For Hodgkin’s disease, cure rates remain high even at an advanced stage, with little difference between stages III and IV.27 In the four patients with interstitial lung disease, treatment was initiated for progressive dyspnoea with deteriorating pulmonary function tests. There is no evidence that early detection would have improved prognosis.28 The patient with segmental pulmonary emboli was being investigated as an outpatient for stable rather than acute dyspnoea, and any prognostic benefit of earlier anticoagulation in this setting is hard to quantify. Important non-cardiac diagnoses requiring treatment were made in a further three patients during imaging follow-up for an unrelated finding. Such indirectly identified lesions cannot reasonably be used as an argument for reporting extracardiac findings in CCTA.

Direct and downstream costs of reporting extracardiac findings and cost-effectiveness

Few previous studies have quantified the downstream costs of noncardiac findings on CCTA (online supplemental table 2). Machaalany et al 3 estimated a cost of Canadian $60 per patient (£36 at current exchange rates), Bendix et al 8 58 euro per patient (£50) and Williams et al 10 £10 per patient. In our larger study, the cost of clinical and imaging follow-up was £33 per patient. None of the previous studies considered the resource implications of the initial extracardiac reporting, which we estimate adds a further £20 to the cost of each study in our practice. We recognise that this is controversial: a radiologist reporting extracardiac alongside cardiac findings does so seamlessly, and the additional time required may be modest (although not negligible). However, given the national shortage of radiologists in the UK, we would argue that future growth of CCTA will depend on cardiologists. Assigning a reasonable cost for separate radiological review of the wide FOV reflects this reality.

Neither Machaalany nor Williams considered the impact of extracardiac diagnoses on treatment or its likely benefit,3 10 and hence they calculated costs but not cost-effectiveness. Bendix calculated a cost ‘per life saved’ of 40 190 euro (£34 307)8 but used the questionable assumption that surgery for lung cancer was straightforwardly curative. Goehler et al 29 calculated a much larger cost per QALY of $154 700 (£115 319). Using lower UK costs and a higher estimate of prognostic benefit per cancer, we calculated a cost per discounted QALY of £23 930. This lies above the £20 000 threshold below which NICE would routinely consider an intervention to be cost-effective for the NHS.17 However, if reporting the wide FOV reconstruction is analysed as a stand-alone procedure, the cost per discounted QALY is even higher at £46 674. Our findings and conclusions may not be straightforwardly applicable to other healthcare systems. Setting aside the variable costs of clinical and imaging follow-up, in more litigious countries a missed lung cancer could result in a costly lawsuit, which we have not considered in our calculations.

During the 8-year period covered by this study, guidelines were published that might have reduced the proportion of lung nodules undergoing follow-up.13 14 However, we found no evidence of a change in the prevalence of ‘significant’ lung nodules being reported or the proportion undergoing follow-up. It is therefore unlikely that the cost-effectiveness of extracardiac reporting has improved with time in our population.

Identification of unexpected noncardiac findings on CCTA has additional non-financial costs that are harder to quantify. Radiation exposure from downstream imaging has carcinogenic potential that cannot be ignored given the low prevalence of cancers being sought. Moreover, significant psychological distress may be caused to patients by unexpected extracardiac findings—which might represent cancer—and the need for ongoing follow-up.30


Extracardiac findings are common on CCTA and generate a substantial burden of expensive clinical and imaging follow-up. However, subsequent changes in treatment are uncommon and, in our series, usually occurred in patients with lesions that were clearly visible on the cardiac reconstruction without recourse to the wide FOV. We conclude that formal review of the wide FOV dataset may represent a poor use of a radiologist’s time, and an argument can be made that its reconstruction should be avoided unless clinically indicated. A quick examination of the cardiac reconstruction for extracardiac lesions by the cardiac reporter might suffice to identify the most clinically relevant lesions.

Key messages

What is already known on this subject?

  • Incidental extracardiac abnormalities are commonly identified on coronary CT angiography (CCTA). Some of these lesions, for example, potentially malignant lung nodules, may have prognostic implications. Their identification often triggers clinical and imaging follow-up, but few studies have attempted to quantify this relative to the proportion that subsequently require specific treatment. The overall cost-effectiveness of scrutinising CCTA studies for extracardiac abnormalities is poorly defined.

What might this study add?

  • Significant extracardiac abnormalities are identified on 16% of CCTA studies, and clinical and imaging follow-up is pursued in 43% of these. Specific changes in treatment are uncommon (0.3% of all scans), and 86% of these patients have obvious lesions on the limited field-of-view (FOV) cardiac reconstruction, with no need for a wide FOV reconstruction (that maximises lung coverage). The overall cost-effectiveness of detailed scrutiny of CCTA studies for extracardiac abnormalities is questionable: £23 930 per discounted quality-adjusted life year, increasing to £46 674 for reporting the wide FOV in addition to the cardiac FOV.

How might this impact on clinical practice?

  • Routine reconstruction and careful examination of the wide FOV dataset could be discontinued. A quick check of extracardiac structures visible on the cardiac reconstruction would suffice to identify the most clinically relevant lesions.

Data availability statement

Data are available on reasonable request.

Ethics statements

Patient consent for publication

Ethics approval

This is a retrospective observational study of anonymised patients undergoing normal clinical management and hence was exempt from ethical committee approval. Retrospective study of patients undergoing routine clinical care.


Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.


  • Contributors All authors have provided significant contributions to the manuscript. Study design: AK and YB. Data collection, analysis and interpretation: AK, NS, DH, SD and HP. Writing: AK. Review and editing: AK, NS, DH, SD, HP, AS and YB. Guarantor: AK.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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