Intensity differences before and after Sonazoid administration. A-pre-injection (A-pre) and –post-injection (A-post): 1.3 ± 3.5 dB. B-pre and B-post: 0.9 ± 3.3 dB. The intensity differences for each pair were not significantly different. C-pre and C-post: -33.4 ± 5.1 dB and -22.3 ± 6.8 dB; D-pre and D-post: -36.2 ± 4.8 dB and -22.6 ± 10.7 dB. The differences between C (14.1 ± 5.8 dB) and D (11.5 ± 4.3 dB) were judged significant (P < 0.001)
The ability to prevent, diagnosis and treat cardiac disease has improved over the last two decades due to the remarkable and seemingly exponential advances in imaging technology [1,2,3,4 ]. Ironically, the surprising increases in computing power and software design now at the physician’s disposal have been greatly enhanced by the advent of a relatively uncomplicated and a readily-synthesized molecule, the microbubble. Perfluorobutane microbubbles consist of a macromolecular shell encapsulating a high molecular weight gas  and are typically 1 to 10 µ in diameter. Their small size allows them to be introduced safely into the circulatory system where they enhance ultrasonic wave scattering by blood, thereby providing higher contrast to ultrasound images of the left ventricular myocardial wall. Ultrascanners operating at frequencies < 15 MHz oscillate the microbubbles, which results in increased echo contrast. The vibrating microbubbles also emit harmonic signals that can preferentially enhance the signal-to-noise ratio. In addition to their diagnostic advantages, microbubbles also avoid the use of radiation and are generally more economical to use. Microbubble ultrasound technology has been used to image other organs besides the heart (liver, pancreas, breast and kidney, in particular), and can be used to target drug-delivery vehicles to different organs . Basic biomedical researchers are also benefitting from microbubble reagents for delivering macromolecules, such as plasmid DNAs, into cells .
Two microbubble contrast agents for cardiac echocardiography, OPTISON™ and Definity™, are approved for use in the United States, SonoVue™ is approved in Europe and China, and Levovist in Japan. But OPTISON™ and Definity™ are used for opacification of the left ventricular cavity and endocardial border definition only. Levovist is used for myocardial contrast echocardiography (MCE). Safety problems occurred initially with each agent, but continuing clinical studies overwhelmingly indicated their efficacy and safety [8,9]. More recently, contrast-enhanced ultrasound (CEUS) has been found safe for pediatric use in subjects as young as two years old . Furthermore, at the recent
Because of these findings and our own clinical experience, we have persisted in our studies on perfluorobutane microbubbles for coronary artery disease. However, at the present time, this contrast agent has only been approved for hepatic diseases in Japan . Here, we report our experience with the use of perfluorobutane microbubbles to perform MCE in 66 patients who had undergone coronary angiography. Our data showed that perfluorobutane microbubbles markedly and stably enhance visualization of ischemic myocardial areas due to significant coronary artery stenosis and provided superior images compared with LevovistTM, but with the caveat that imaging parameters require careful optimization.
3. Materials and Methods
Sixty-six patients with a history of coronary angiography (CAG) within the last three months were enrolled in this study, and informed consent was obtained. The study was approved by the clinic’s ethics committee. All procedures were performed in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki) for experiments involving humans. The following aspects of the consent form were explained to the patients: 1) the advantages, benefits, risks and possible side effects of the procedure to them specifically as well as to patients with coronary artery disease in general, 2) the cost of the procedure according to the regulations of the National Health Service, 3) the approximate time of the procedure, and 4) the clinic staff and specialists that would be present during the procedure. In addition, the approval of the ethics committee required that the procedure be performed by a special team that included the following personnel: Dr. R. Kakihara since he was in charge of the study, the nurses and echocardiographers who had experience with MCE, at least one specialist in the use of SonazoidTM from Daiichi Sankyo Co. Ltd, and a mechanical engineer and a technical specialist to operate the Vivid 7 Ultrasound System. All 24 patients enrolled had ≥ 75% significant coronary artery stenosis (significant stenosis). Among them, single vessel disease was present in 11 patients, double vessel disease in 9 and triple vessel disease in 4. No subject had a history of previous myocardial infarction. The following patient data were obtained: age, 69.9±11.4 y/o; body weight, 60.5±12.1 kg; body surface area, 1.61±4.3 m²; blood pressure, 128.6±15.3/ 67.7±9.9 mmHg; heart rate, 65.3±9.0 beats/min; LVEF (by angiography), 60.5±4.3%; LDL-cholesterol, 125.6±38.1 mg/dl; and triglyceride, 193.1±134.1 mg/dl. Six patients were treated for diabetes mellitus by oral medication and their average HbA1c was 6.3±1.5%.
Phase-inversion harmonic ultrasonography was performed using the Vivid 7 Dimension digital ultrasound system, Version 7.0.3 (General Electric Healthcare, Inc., U.S.A.), and a 1.5/4.0 MHz active-matrix array (AMA) probe. The images were analyzed offline using EchoPAC PC Version 108.1.4. Phase inversion harmonic sonography is two phase-inverted but otherwise identical sonographic pulses are transmitted. Summing the returning echoes in a buffer cancels most of the fundamental and odd harmonic echoes and effectively amplifies the second harmonic. 
3.3. The first step
A longitudinal peak systolic strain map (LPSSM) has high diagnostic reliability to detect segmental left ventricular wall abnormalities. [13,14] Thus, an LPSSM was created on any patient with coronary artery disease (CAD) risk factors. When the LPSSM showed abnormal left ventricular segmental wall systolic function, myocardial contrast echocardiography (MCE) was done using Sonazoid™ to confirm whether the dysfunction was due to myocardial ischemia.
3.4. The second step
Any remaining Sonazoid should be stored at room temperature and used within 2 hours.
Because SonazoidTM microbubbles are susceptible to destruction by physical pressure, 2.5 ml were injected over at least 20 sec, not less than the systemic circulation time under the stress of low dose ATP (0.15 mg/kg/min of Adenosine 5- Triphosphate Disodium) Figure 1, Figure 2, Figure 3, Figure 4.
None of the patients experienced adverse affects of this procedure. Each of the 66 patients enrolled in the study had undergone CAG and was diagnosed with significant coronary artery stenosis. Patients were divided into four groups as described above, and myocardial segments perfused by the stenotic and normal vasculatures were examined by ultrasonography before and after Sonazoid administration. The data for one patient (#7) are presented in Figures 5 through Figure 10. Ultrasound images taken before and after Sonazoid administration are shown in 6 Figures, which represent the strain maps and APLAX, AP2ch, AP4ch and SAX-papillary muscle (pm) views, respectively. Figure 5 and Figure 6 show the longitudinal peak systolic strain map and Figure 6 which is superimposed coronary arteries on the map strongly implys this patient experienced no adverse affect and had LAD single vessel disease. Figure 11 shows an angiogram of the left and right coronary arteries. In the left panel, the angiogram (left coronary artery) clearly reveals left anterior descending coronary artery stenosis obstructing 75% of the vessel’s normal diameter. Stenotic regions are indicated by the arrows.In contrast, no involvement of the right coronary artery could be discerned.
The data from 100 myocardial segments (16 patients) perfused by normal coronary arteries and from 283 myocardial segments (50 patients) perfused by stenotic coronary arteries in 66 patients with coronary artery disease were grouped into A, B, C and D as designated above and are summarized in Tables 1 and Table 2. Specifically, the intensity difference between A-pre-injection (A-pre) and A–post-injection (A-post) was 1.3 ± 3.5 dB; the intensity difference between B-pre and B-post was 0.9 ± 3.3 dB. The intensity differences in groups A and B were not significant. For C-pre and C-post, the intensities were -33.4 ± 5.1 dB and -22.3 ± 6.8 dB, respectively; and D-pre and D-post were -36.2 ± 4.8 dB and -22.6 ± 10.7 dB, respectively. The intensity differences in groups C (14.1 ± 5.8 dB) and D (11.5 ± 4.3 dB) were both significant (p < 0.001). By ROC (receiver operating characteristic curve) analysis, intensity differences ≤ 6.3 dB in the AP views could detect ≥ 75% stenosis with a sensitivity of 98%, specificity of 94% and accuracy of 97%. An intensity difference ≤ 5.1 dB in the SAX view could detect ≥ 75% stenosis with a sensitivity of 97%, specificity of 96% and accuracy of 97%. These data indicate the sensitivity, specificity and diagnostic accuracy of MCE using Sonazoid to detect ≥ 75% stenosis.
|A/AP||1.3 ± 3.5 dB (N.S.)|
|B/SAX||0.9 ± 3.3 dB (N.S)|
|C/AP||14.1 ± 5.8 dB (|
|D/SAX||11.5 ± 4.3 dB (|
|AP (Δ ≤ 6.3 dB)||0.98||0.94||0.97|
|SAXpm (Δ ≤ 5.1 dB)||0.97||0.96||0.97|
The intraobserver reproducibility was determined by imaging the same patients after a four-week interval and then calculating Cohen’s kappa (κ= 0.76, p < 0.001). To obtain the four-week interval and then calculating Cohen’s kappa (κ= 0.76, p < 0.001). To obtain the interobserver reproducibility, the same images were evaluated by another echocardiographer who was employed at a different medical institute and had no knowledge of the protocol. The interobserver reproducibility was excellent (κ= 0.98, p < 0.001). These two results indicate that the reproducibly of Sonazoid MCE is sufficient for the use of this agent in the clinical setting.
Remarkable progress has been made over the last decade in medical imaging of the heart and other organs. However, there is still an enormous worldwide mortality and morbidity from coronary artery disease. A major hurdle in overcoming this situation is the inability to make a definite diagnosis of coronary artery stenosis or to screen coronary artery disease easily and inexpensively. Although myocardial ischemia it thought to start from 75% stenosis, patients usually have no symptoms with normal daily activities. When the stenosis is ≥ 90%, patients may become symptomatic with normal daily activities. Presently, CAG is only one diagnostic method, but it is invasive and expensive. Routine preventative cardiac imaging that would be safe (no ionizing radiation or allergenic contrast dyes), highly sensitive, specific and economical would obviously help mitigate this ongoing public health burden.
Echocardiography is one of the areas in which the most exciting advances have been made, and it is especially attractive because it is becoming progressively more miniaturized and can be used in a typical office setting rather than a dedicated imaging center. Current modalities include real-time three-dimensional echocardiography, speckle tracking, contrast echocardiography, intracardiac echocardiography and hand-held echocardiography.
Here, we show that Sonazoid can be successfully used in a local clinical setting and this contrast agent allows the accurate detection of coronary artery stenosis ≥ 75%. This may be accounted for by Sonazoid’s resistance to acoustic pressure and its long half-life compared to other microbubble-based contrast agents . Our patients did not experience adverse effects during or after the procedure. This is likely due to Sonazoid’s intrinsic nontoxicity, but also by the rapid metabolism of microbubbles via the respiratory system. We compared our results with those of other studies [16, 17] and found similar accuracy for the detection of significant (≥ 75%) coronary artery stenosis. Thus, our data argue for continued investigations into its suitability for MCE and ultimate approval for this purpose, especially in view of the limited number of microbubble-based contrast agents now available to cardiologists. In future studies, it will be of great interest to determine whether Sonazoid is capable of detecting less significant degrees of stenosis.
The limitations of this method are the same as the limitations of echocardiography. It is difficult to obtain good B-mode images in patients with a thick subcutaneous fatty layer or emphysematous lung. The reliability of MCE to detect ischemia is clearly dependent on the quality of the B-mode images. Another limitation is the process of making SonazoidTM since the solution is somewhat complex compared with LevovistTM. In addition, the detection of ischemic myocardial areas requires the ability to make and read time-intensity graphs. However, we learned to overcome these limitations after four or five subjects.
This study showed that SonazoidTM has good clinical utility and better diagnostic accuracy to detect significant coronary artery stenosis than other contrast agents. This is because the concentration of SonazoidTM in circulating blood is more stable, and the agent has a longer half-life than other contrast agents.
Comparisons between myocardial regions of affected and normal arteries in these patients before and after SonazoidTM administration under low-dose ATP stress showed that MCE could detect ≥75% stenosis with a sensitivity of 97%, specificity of 96% and accuracy of 97%. An important factor in achieving these results was the optimization of the MI settings. We believe that these data, taken together with patients not experiencing adverse effects during or after the procedure, provide a compelling argument for extending these studies, with the ultimate goal of providing cardiologists a powerful new tool for routine echocardiography.
The ability of this MCE method to identify various degrees of coronary artery stenosis needs to be confirmed in larger, randomized trials. Although conventional echocardiography cannot detect the extent of myocardial tissue ischemia due to coronary artery stenosis, it can detect LV wall systolic dysfunction due to myocardial ischemia by strain mapping. By applying these two methods, we could develop a new and more accurate diagnostic method. The creation of an MCE map along with a strain map might be used to directly diagnose the severity of coronary artery stenosis and extent of the ischemic myocardial area.
The extent of the ischemic myocardial area surely play a more leading and important role as an index more than the severity of coronary artery stenosis to decide the indication of coronary artery intervention.