- Open Access
Cardiovascular imaging in children and adults following Kawasaki disease
Insights into Imaging volume 6, pages697–705(2015)
Kawasaki disease (KD) is a paediatric vasculitis with coronary artery aneurysms (CAA) as its main complication. Two guidelines exist regarding the follow-up of patients after KD, by the American Heart Association and the Japanese Circulation Society. After the acute phase, CAA-negative patients are checked for cardiovascular risk assessment or with ECG and echocardiography until 5 years after the disease. In CAA-positive patients, monitoring includes myocardial perfusion imaging, conventional angiography and CT-angiography. However, the invasive nature and high radiation exposure do not reflect technical advances in cardiovascular imaging. Newer techniques, such as cardiac MRI, are mentioned but not directly implemented in the follow-up. Cardiac MRI can be performed to identify CAA, but also evaluate functional abnormalities, ischemia and previous myocardial infarction including adenosine stress-testing. Low-dose CT angiography can be implemented at a young age when MRI without anaesthesia is not feasible. CT calcium scoring with a very low radiation dose can be useful in risk stratification years after the disease. By incorporating newer imaging techniques, detection of CAA will be improved while reducing radiation burden and potential complications of invasive imaging modalities. Based on the current knowledge, a possible pathway to follow-up patients after KD is introduced.
• Kawasaki disease is a paediatric vasculitis with coronary aneurysms as major complication.
• Current guidelines include invasive, high-radiation modalities not reflecting new technical advances.
• Cardiac MRI can provide information on coronary anatomy as well as cardiac function.
• (Low-dose) CT-angiography and CT calcium score can also provide important information.
• Current guidelines for follow-up of patients with KD need to be revised.
Kawasaki disease (KD) is an acute paediatric vasculitis that mainly affects children younger than 5 years of age. Although the exact cause is still unknown, it is thought to be caused by an infectious agent in genetically predisposed children. This fits with the observed epidemiology of seasonal occurrence throughout the northern hemisphere, the increased incidence in children of Japanese descent, and the established association with specific genetic polymorphisms [1, 2]. In about 25 % of untreated patients, coronary artery aneurysms (CAA) will develop during the acute phase of KD. Since the introduction of high-dose intravenous immunoglobulin as effective treatment, the percentage of CAA has dropped to 5–7 % for patients treated within 10 days after fever onset . For patients not treated within 10 days, the rate of developing aneurysms may be higher .
During CAA formation it is thought that an influx of inflammatory cells leads to dissociation and disruption of the medial and internal elastic lamina layer. Even when the lumen of the artery returns to its normal size, the artery wall remains damaged, although the extent of the damage varies among patients. In one autopsy study, active remodelling of the artery was seen many years after the acute disease in children with aneurysms . The KD-related vasculopathy during follow-up with characteristic myointimal proliferation and/or layering of thrombus can result in progressive stenosis, which may lead to ischemic cardiomyopathy.
Calcification of the damaged artery is progressive after the acute phase of the disease and may develop in coronary arteries with lesions that persist or, although rarely, in transiently dilated arteries when the vessel lumen has normalized . The extensive calcification of the coronary artery wall is typical of the pathology observed in the remodelled lesional wall (Fig. 1).
CAA are diagnosed by echocardiography during the acute or subacute phase of the disease. CAA are traditionally classified according to the definitions of the Japanese Ministry of Health: a luminal diameter of >3 mm in children <5 years of age, >4 mm in children ≥5 years of age, or a diameter 1.5 times the size of an adjacent segment or an irregular lumen in children ≥5 years of age. A giant aneurysm is defined as an aneurysm with an internal diameter of ≥8 mm or a diameter >4 times that of an adjacent segment in children ≥5 years old [7, 8]. However, over the past years it has become clear that z-scores, adjusted for body-surface area, may be a better indicator of any serious enlargement [9, 10]. Using this approach, a z-score of ≥2.5 is considered an aneurysm; a z-score of ≥10 is a giant aneurysm.
It is clear that a 6 mm aneurysm in a 6-month-old child represents a more severely damaged artery than a 6 mm aneurysm in a 6-year old child. As z-scores might differ from the traditional definitions, especially in younger and smaller children, this may alter their (long-term) therapy and monitoring.
It should be emphasized that all patients who develop CAA carry a lifelong increased risk for coronary thrombosis and stenotic coronary lesions that may result in myocardial ischemia, infarction, and sudden death .
There has been much debate about the appropriate way to follow-up on our KD patients, both with and without CAA. Several imaging techniques have been proposed and different guidelines have been published. The aim of this paper was to analyse the existing guidelines regarding the cardiovascular follow-up of patients after KD and to propose a new pathway for follow-up, based on the current knowledge and our own experience.
Among the many issues concerning clinical management of patients with a history of KD, several controversies exist. One of these is the timing and need for long-term follow-up. Two consensus guidelines have been published, one by the American Heart Association (AHA) in 2004, and one by the Japanese Circulation Society (JCS) in 2014 [8, 12]. These guidelines are summarized in Tables 1 and 2, starting at 1 year after the acute disease. In both guidelines, patients are risk-stratified based on the severity of the coronary artery lesions and likelihood of complications, including myocardial ischemia and congestive heart failure.
In children without CAA or with early, transient coronary artery dilatations, the AHA advises echocardiograms at initial diagnosis and 2 and 6–8 weeks later. A repeat echocardiogram at 1 year is considered optional. Subsequently, only periodic assessment and counselling about cardiovascular risk factors are recommended. To evaluate patients without CAA, the JCS advises an ECG and echocardiogram at 1, 2, 6 and 12 months, and a final evaluation at 5 years with an exercise ECG.
For patients diagnosed with persisting CAA after the acute phase, both guidelines advise a more intensive and prolonged follow-up with additional imaging modalities.
In children with small to medium aneurysms, the AHA advises an annual routine follow-up and biennial stress testing with myocardial nuclear perfusion scans. In case of large and/or multiple or complex aneurysms within one artery, the AHA recommends an invasive coronary angiography (CAG) to be performed routinely 6–12 months after the disease onset and repeated if the non-invasive stress test or clinical signs suggest myocardial ischemia.. It should be noted that these guidelines were last revised in 2004 and many aspects of clinical care and imaging have changed during this interval.
The JCS has recently published a revised guideline in which the committee recommends follow-up for patients with small aneurysms at 30 days after the acute illness with an echocardiogram and ECG every 3 months until the dilatation has disappeared. Patients with medium-sized aneurysms should be more intensely evaluated, i.e., every 1–3 months with (exercise) ECG, echocardiography and chest X-ray until dilatation is no longer observed and should undergo MDCT or MR Coronary Angiography (MRCA) every 5 years. This scheme differs from the AHA guidelines.
For those with larger CAA, JCS advises a follow-up in a risk-stratified manner using methods that are largely overlapping the AHA recommendations. There are no specific recommendations for imaging modalities.
There are two main drawbacks to the current guidelines for follow-up imaging of patients with KD.
The invasive nature and high radiation exposure of the advised follow-up modalities do not reflect technical advances in the field of cardiovascular imaging and result in possible complications and unnecessary hazardous radiation exposure.
Coronary aneurysms, especially those more distal in the coronary tree, can be missed by echocardiography, potentially leading to underestimation of disease severity.
For this reason the use of alternative imaging methods should be considered, and we suggest a feasible, accurate, and sustainable follow-up scheme for KD as outlined below.
Cardiac Magnetic Resonance Imaging (CMRI)
CMRI is a robust imaging technique that is being widely adopted by many centres for the evaluation of coronary artery disease. Besides coronary anatomy, CMRI provides clinically relevant information about myocardial ischemia, infarction, inflammation, and function. In experienced centres, cardiac nuclear scintigraphy has been largely abandoned because of low sensitivity and high radiation exposure while being outperformed by CMRI . The current availability of CMRI and expertise to apply CMRI varies greatly across centres.
Using a comprehensive CMRI protocol with adenosine stress testing during the follow-up of 63 children with KD, we showed that CMRI was safe and able to identify coronary artery pathology, signs of ischemia, and previous myocardial infarction . CMRI, including MRCA, compared favourably with echocardiography for the identification of CAA; in six patients CAA were missed by echocardiography and identified by CMRI. Mavrogeni et al. compared coronary MRCA to conventional CAG in 12 patients . The two techniques agreed completely in the detection of aneurysms, and the maximal aneurysm diameters were similar. A larger study from Suzuki et al. compared coronary MRCA in 106 patients with echocardiography and found 28 additional aneurysms with MRCA . When comparing coronary MRCA to conventional CAG in 12 patients with imaging methods <6 months apart, they found no significant difference in arterial diameter using bright blood imaging, although one occlusion of the circumflex artery was only detected by conventional CAG.
Coronary artery evaluation can be easily combined with the assessment of ischemia, infarction, ventricular dimensions, and function within the same procedure, for which CMRI has become the standard .
Based on our experience with CMRI in more than 150 patients with KD, a 2-step CMRI protocol was introduced in 2012. This CMRI is performed on a 1.5-T whole-body MRI scanner equipped with cardiac software. The first step of this CMRI protocol, consisting of MRCA and cardiac function evaluation, is offered routinely during adolescence, when the teenager is able to fully cooperate. An ECG-gated 3D steady-state free precession sequence with T2 and fat saturation prepulses is used to visualize the coronary arteries. If coronary abnormalities have been observed by echocardiography on two or more different occasions, the second-step of our CMRI protocol is also performed in one procedure. If CAA are observed unexpectedly upon the first step of CMRI, a second step will subsequently be performed.
The second step involves the administration of intravenous contrast (0.1 mmol/kg of gadolinium) and adenosine (140 ug/kg/min) to detect myocardial perfusion abnormalities and myocardial scar. Standard, commercially available, CMRI techniques are used with fast single shot T1-weighted gradient echo sequences (e.g., Turbo-FLASH, TFE) for perfusion imaging and segmented inversion recovery sequences for myocardial scar imaging [18, 19].
We introduced this 2-step protocol because perfusion abnormalities and ischemia upon adenosine stress were detected only in patients with persistent CAA.
Based on current data, it is unlikely that patients without CAA will omit develop clinically significant cardiovascular changes from their KD. However, in patients that are children with missed CAA by echocardiography, long-term complications can still occur.
Low-radiation dose CT angiography
Although CMRI is a feasible technique in early adolescence, assessment of younger children with CAA often requires general anaesthesia and is, therefore, less suitable.
ECG-gated multislice CT is an attractive alternative imaging technique for the younger patient. In teenagers with a history of KD, CT-angiography confirmed all aneurysms, stenoses, and occlusions previously demonstrated by invasive CAG . In another study, aneurysms were detected by CT-angiography in young children with a history of KD that had been missed by echocardiography .
Although effective, traditional CT-angiography carries a high radiation exposure, especially harmful for young children. Low-radiation dose CT-angiography with prospective ECG triggering is increasingly available. The use of next generation scanners decreases the radiation burden from a median of 6.9 mSv per scan down to a median of 1 mSv on a 128 dual-source CT scanner . New imaging protocols can be used to reduce the radiation dose for which the use of prospective instead of retrospective ECG-triggering is most important. The use of a single heart beat (high-pitch) protocol has been shown to result in a reduction of the radiation dose requirements even further. On the other hand, studies are conflicting as to whether the image quality is reduced in patients with a relatively high heart rate, hence, in most children [22, 23]. With the use of iterative reconstruction, the image-to-noise ratio can be reduced such that lower tube currents can be used . In children with congenital heart disease, this has already shown to generate qualitatively excellent results, but studies evaluating the coronary arteries in patients following acute KD have not yet been performed .
A recent study in infants and young children with KD showed that low-dose, free-breathing prospective ECG-triggered CT-angiography without the use of beta-blockers diagnosed all CAA detected with ultrasound plus the more distal aneurysms and dilatations . The data acquisition window was set to 40 % of the RR-interval. The effective radiation dose was calculated at 0.32 to 0.40 mSv, depending on the patient’s age. Although this was a small study in 19 patients, it is very promising that good images could be obtained without much radiation exposure and no pre-medication. Apart from replacing invasive CAG in an early stage of follow-up, low-radiation dose CT-angiography can also be used at a later stage to check for the development of stenosis in patients with CAA.
CT calcium scoring
Whereas CMRI is most useful for functional imaging, calcifications can be best picked up by CT imaging. CT calcium scoring, a technique without intravenous contrast, measures calcification in the coronary arteries, which was a strong predictor of coronary events in a large adult cohort of patients without evidence for cardiovascular disease at enrolment . It can be used to detect coronary calcifications that may have been missed by echocardiography or CMRI and is associated with a very low radiation dose of approximately 1 mSv or less with prospective ECG triggering [6, 28].
Although the exact clinical implication of small coronary artery calcifications is still unknown, CT calcium scoring may be useful in risk-stratification of recently identified patients whose aneurysms were missed in the past or not well monitored since the acute phase. In such patients, the aneurysm may have remodelled such that the lumen is of normal internal diameter but the arterial wall is significantly damaged and associated with calcium deposition. These patients are at risk for late stenosis and must be carefully followed. Figure 2 illustrates the different purposes of conventional techniques, CMRI and CT.
All current guidelines are based on the opinion of experts. Evidence-based KD guidelines for cardiovascular assessment of KD patients do not exist. Based on the current knowledge and our own experience regarding different imaging modalities, we herewith suggest a pathway for follow-up in patients with KD into adulthood (Fig. 3). Advantages and disadvantages of the different techniques are outlined in Table 3.
By not performing frequent echocardiography after the acute phase, costs are kept to a minimum. Furthermore, by detecting missed aneurysms or other lesions on CMRI, possible complications such as myocardial infarction can be prevented. It must be stated that this pathway will depend on the available technical quality and experience of a centre with CMRI, which varies across centres.
For patients with CAA, the pathway must be customized depending on the extent of the lesions. For instance, a young child with giant aneurysms and suspected ischemia will require invasive or CT-angiography, as well as MRI under general anaesthesia, repeated regularly as an individual approach, to obtain the best interpretation of CAA and functional stenosis.
In contrast to infants and children, adolescents and adults are able to report cardiac symptoms of ischemia. Asymptomatic adults with aneurysms must be followed for early signs of ischemia upon (stress) echocardiography, but the frequency of additional imaging studies can largely be guided by symptoms. Since echocardiography in general is insensitive for evaluating stenosis, symptomatic adults require other imaging techniques.
In addition to the techniques mentioned above, in a selected group of patients, conventional CAG can be considered when a catheter-based intervention is contemplated. Invasive CAG can be combined with fractional flow reserve to obtain hemodynamic and structural data to help guide therapeutic decisions . These tests for interventional decision-making have not often been reported in KD and are beyond the scope of this article.
Future studies are needed to evaluate the risks and benefits of different cardiovascular imaging modalities and the most appropriate timing of such imaging to optimize care for KD patients. Evidence is lacking about the long-term effects of KD, especially in children without prior evidence of CAA. We might not appreciate late cardiovascular sequelae that may become clinically important later in life. In order to answer these questions, long-term follow-up is required.
In summary, we believe that the current guidelines for follow-up of patients with KD need to be revised. By incorporating new imaging techniques in our guidelines, detection of CAA will be improved, while reducing the radiation burden and potential complications of invasive angiography. This may enable better adherence to the guidelines in clinical practice and improve follow-up of patients into adulthood.
Burns JC, Herzog L, Fabri O et al (2013) Seasonality of Kawasaki disease: a global perspective. PLoS One 8(9), e74529
Onouchi Y (2012) Genetics of Kawasaki disease: what we know and don’t know. Circ J 76(7):1581–1586
Newburger JW, Takahashi M, Beiser AS et al (1991) A single intravenous infusion of gamma globulin as compared with four infusions in the treatment of acute Kawasaki syndrome. N Engl J Med 324(23):1633–1639
Tacke CE, Breunis WB, Pereira RR, Breur JM, Kuipers IM, Kuijpers TW (2014) Five years of Kawasaki disease in the Netherlands: a national surveillance study. Pediatr Infect Dis J 33(8):793–797
Suzuki A, Miyagawa-Tomita S, Komatsu K et al (2000) Active remodeling of the coronary arterial lesions in the late phase of Kawasaki disease: immunohistochemical study. Circulation 101(25):2935–2941
Kahn AM, Budoff MJ, Daniels LB et al (2012) Calcium scoring in patients with a history of Kawasaki disease. JACC Cardiovasc Imaging 5(3):264–272
Research Committee on Kawasaki Disease (1986) Report of the Subcommittee on Standardization of Diagnostic Criteria and Reporting of Coronary Artery Lesions in Kawasaki Disease. Ministry of Health and Welfare, Tokyo
8 Group JCSJW (2014) Guidelines for diagnosis and management of cardiovascular sequelae in Kawasaki disease (JCS 2013). Digest version. Circ J 78(10):2521–2562
McCrindle BW, Li JS, Minich LL et al (2007) Coronary artery involvement in children with Kawasaki disease: risk factors from analysis of serial normalized measurements. Circulation 116(2):174–179
Manlhiot C, Millar K, Golding F, McCrindle BW (2010) Improved classification of coronary artery abnormalities based only on coronary artery z-scores after Kawasaki disease. Pediatr Cardiol 31(2):242–249
Kato H, Sugimura T, Akagi T et al (1996) Long-term consequences of Kawasaki disease. A 10- to 21-year follow-up study of 594 patients. Circulation 94(6):1379–1385
Newburger JW, Takahashi M, Gerber MA et al (2004) Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation 110(17):2747–2771
Lee DC, Simonetti OP, Harris KR et al (2004) Magnetic resonance versus radionuclide pharmacological stress perfusion imaging for flow-limiting stenoses of varying severity. Circulation 110(1):58–65
Tacke CE, Kuipers IM, Groenink M, Spijkerboer AM, Kuijpers TW (2011) Cardiac magnetic resonance imaging for noninvasive assessment of cardiovascular disease during the follow-up of patients with Kawasaki disease. Circ Cardiovasc Imaging 4(6):712–720
Mavrogeni S, Papadopoulos G, Douskou M et al (2004) Magnetic resonance angiography is equivalent to X-ray coronary angiography for the evaluation of coronary arteries in Kawasaki disease. J Am Coll Cardiol 43(4):649–652
Suzuki A, Takemura A, Inaba R, Sonobe T, Tsuchiya K, Korenaga T (2006) Magnetic resonance coronary angiography to evaluate coronary arterial lesions in patients with Kawasaki disease. Cardiol Young 16(6):563–571
Tacke CE, Romeih S, Kuipers IM, Spijkerboer AM, Groenink M, Kuijpers TW (2013) Evaluation of cardiac function by magnetic resonance imaging during the follow-up of patients with Kawasaki disease. Circ Cardiovasc Imaging 6(1):67–73
Takx RA, Blomberg BA, El Aidi H et al (2015) Diagnostic accuracy of stress myocardial perfusion imaging compared to invasive coronary angiography with fractional flow reserve meta-analysis. Circ Cardiovasc Imaging 8(1)
Rajiah P, Desai MY, Kwon D, Flamm SD (2013) MR imaging of myocardial infarction. Radiographics 33(5):1383–1412
Carbone I, Cannata D, Algeri E et al (2011) Adolescent Kawasaki disease: usefulness of 64-slice CT coronary angiography for follow-up investigation. Pediatr Radiol 41(9):1165–1173
Xing Y, Wang H, Yu X, Chen R, Hou Y (2009) Assessment of coronary artery lesions in children with Kawasaki disease: evaluation of MSCT in comparison with 2-D echocardiography. Pediatr Radiol 39(11):1209–1215
Ghoshhajra BB, Lee AM, Engel LC et al (2014) Radiation dose reduction in pediatric cardiac computed tomography: experience from a tertiary medical center. Pediatr Cardiol 35(1):171–179
Neefjes LA, Dharampal AS, Rossi A et al (2011) Image quality and radiation exposure using different low-dose scan protocols in dual-source CT coronary angiography: randomized study. Radiology 261(3):779–786
Naoum C, Blanke P, Leipsic J (2015) Iterative reconstruction in cardiac CT. J Cardiovasc Comput Tomogr 9(4):255–263
Zheng M, Zhao H, Xu J, Wu Y, Li J (2013) Image quality of ultra-low-dose dual-source CT angiography using high-pitch spiral acquisition and iterative reconstruction in young children with congenital heart disease. J Cardiovasc Comput Tomogr 7(6):376–382
Duan Y, Wang X, Cheng Z, Wu D, Wu L (2012) Application of prospective ECG-triggered dual-source CT coronary angiography for infants and children with coronary artery aneurysms due to Kawasaki disease. Br J Radiol 85(1020):e1190–e1197
Detrano R, Guerci AD, Carr JJ et al (2008) Coronary calcium as a predictor of coronary events in four racial or ethnic groups. N Engl J Med 358(13):1336–1345
Gerber TC, Carr JJ, Arai AE et al (2009) Ionizing radiation in cardiac imaging: a science advisory from the American Heart Association Committee on Cardiac Imaging of the Council on Clinical Cardiology and Committee on Cardiovascular Imaging and Intervention of the Council on Cardiovascular Radiology and Intervention. Circulation 119(7):1056–1065
De Bruyne B, Pijls NH, Kalesan B et al (2012) Fractional flow reserve-guided PCI versus medical therapy in stable coronary disease. N Engl J Med 367(11):991–1001
We are grateful to Dr. Hein Verberne (Academic Medical Centre, Amsterdam, The Netherlands) and Chisato Shimizu (University of California, San Diego, USA) for their help with the selection of images.
This work was supported by “Stichting Stinafo”.
About this article
Cite this article
Dietz, S.M., Tacke, C.E., Kuipers, I.M. et al. Cardiovascular imaging in children and adults following Kawasaki disease. Insights Imaging 6, 697–705 (2015). https://doi.org/10.1007/s13244-015-0422-0
- Kawasaki disease
- (Cardiac) MRI
- Coronary aneurysm
- Cardiac imaging