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Featured researches published by Masataka Hayashi.


American Journal of Cardiology | 1988

F-18 deoxyglucose and stress N-13 ammonia positron emission tomography in anterior wall healed myocardial infarction

Tetsuro Fudo; Hirofumi Kambara; Tetsuo Hashimoto; Masataka Hayashi; Ryuji Nohara; Nagara Tamaki; Yoshiharu Yonekura; Michio Senda; Junji Konishi; Chuichi Kawai

To evaluate myocardial blood flow and glucose utilization, N-13 ammonia (NH3) and F-18 deoxyglucose positron emission tomography scanning was performed in 22 patients with previous anterior wall myocardial infarction, using a high-resolution, multi-slice, whole-body scanner. The N-13 ammonia study was performed at rest and after exercise. The F-18 deoxyglucose study was performed at rest after fasting greater than 5 hours. The N-13 ammonia study revealed a hypoperfused area in 19 of the 22 patients (86%), that corresponded to the infarcted regions as diagnosed by electrocardiography, coronary arteriography and left ventriculography (21 patients). The hypoperfused areas expanded after exercise in 16 of 22 patients (73%). F-18 deoxyglucose uptake was observed in these hypoperfused areas, especially in patients with hypokinetic wall motion on left ventriculography and in exercise-induced hypoperfused areas. However, positron emission tomography demonstrated diffuse uptake of F-18 deoxyglucose in 3 of 8 patients with dyskinetic wall motion. Thus, metabolically active myocardium in infarcted areas or periinfarct ischemia can be visualized with F-18 deoxyglucose and stress N-13 ammonia studies.


Journal of the American College of Cardiology | 1988

Non-Q wave versus Q wave myocardial infarction: regional myocardial metabolism and blood flow assessed by positron emission tomography

Tetsuo Hashimoto; Hirofumi Kambara; Tetsuro Fudo; Masataka Hayashi; Shunichi Tamaki; Shingo Tokunaga; Nagara Tamaki; Yoshiharu Yonekura; Junji Konishi; Chuichi Kawai

This study compared regional myocardial blood flow at rest and during supine exercise as well as regional myocardial glucose utilization in the fasting condition in 22 patients, 11 with antecedent non-Q wave and 11 with antecedent Q wave infarction. With use of N-13 (nitrogen-13) ammonia and F-18 (fluorine-18) deoxyglucose as tracers of blood flow and exogenous glucose utilization and positron emission tomography, hypoperfused areas were noted at rest and during exercise in all 11 patients (100%) with Q wave infarction. Among the 11 patients with non-Q wave infarction such areas were noted in only 5 (45%) at rest and in 8 (73%) during exercise. Furthermore, segmentally enhanced F-18 deoxyglucose uptake corresponding to the infarcted areas (identified electrocardiographically) was seen in 10 (91%) of the 11 patients with non-Q wave infarction but in only 4 (36%) of the 11 patients with Q wave infarction (p less than 0.01). In conclusion, segmental F-18 deoxyglucose uptake as a possible sign of myocardial viability was seen more frequently in non-Q wave than in Q wave infarction and, importantly, regionally enhanced F-18 deoxyglucose uptake occurred even in the absence of segmental rest or exercise blood flow abnormalities, or both, in 5 (45%) of 11 patients with non-Q wave infarction.


American Journal of Cardiology | 1989

Increased fluorine-18 deoxyglucose uptake after percutaneous transluminal coronary angioplasty in recently infarcted myocardium.

Tetsuo Hashimoto; Hirofumi Kambara; Tetsuro Fudo; Ryuji Nohara; Masataka Hayashi; Yoshiki Takatsu; Nagara Tamaki; Junji Konishi; Chuichi Kawai

Abstract Positron emission tomography (PET) allows the noninvasive assessment of relative myocardial perfusion and glucose utilization in humans. 1 Relative myocardial perfusion is assessed with nitrogen-13 ammonia and relative glucose utilization is assessed with the glucose analog fluorine-18 deoxyglucose. Using this technique, we will describe 2 patients whose infarcted areas revealed new fluorine-18 deoxyglucose uptake many weeks after successful percutaneous transluminal coronary angioplasty (PTCA).


Cardiovascular Drugs and Therapy | 1990

Effects of Nifedipine on Cardiac Function in Patients with Coronary Artery Disease Evaluated with Ambulatory Radionuclide Monitoring

Hirofumi Kambara; Ishtiaque H. Mohiuddin; Nagara Tamaki; Tetsuo Fudo; Masataka Hayashi; Ryuji Nohara; Junji Konishi; Chuuichi Kawai

SummaryThe effects of nifedipine on left ventricular function were evaluated in 17 patients with coronary artery disease with an ambulatory radionuclide detector (VEST). Hemodynamic data were recorded continuously at rest and during upringht bicycle ergometer exercise before and 30 minutes after 10 mg of oral nifedipine administration. The heart rate increased and the resting systolic blood pressure decreased significantly with nifedipine. The end-diastolic and end-systolic volumes during exercise were significantly reduced and EF increased during exercise after nifedipine administration. These salutary hemodynamic responses of nifedipine appear to be beneficial for patients with effort angina pectoris.


Archive | 1990

Direct Measurement of Aortic and Vena Caval Flow to Evaluate the Effect of Vasodilators in Experimental Acute mitral regurgitation

Hitoshi Tanio; Toshiaki Kumada; Yasuki Kihara; Shunichi Miyazaki; Masataka Hayashi; Yoshihiro Himura; Masashi Kanbayashi; Wataru Hayashida; Yasuyuki Nakamura; Chuichi Kawai

To evaluate the effect of bunazosin hydrochloride (Bz), a newly developed α1-blocker, on arterial and venous blood flow and on left ventricular function in acute left heart failure, we produced acute mitral regurgitation in seven open chest anesthetized dogs by transmyocardial chordal sectioning. With the administration of Bz (1μg/kg/min for 5 minutes intravenously) or nitroprusside (Np: 1.7 μg/kg/min for 3 to 5 minutes intravenously), the mean aortic pressure and systemic vascular resistance (SVR) decreased to the same levels. With Np, cardiac output (CO) did not change (from 1.80±0.72 to 1.87±0.80 L/min; NS), and mean inferior vena caval blood flow (IVCF) decreased by 5.5% (from 1.25±0.40 to 1.19±0.40 L/min; p < 0.01.). With Bz, CO increased significantly from 1.83±0.46 to 1.98±0.72 L/min (p < 0.05), and IVCF also increased significantly from 1.09 + 0.34 L/min to 1.18 + 0.33 L/min (p < 0.01). This suggests that Bz decreases SVR to the same level as Np, but the vasodilatory effect of Bz on the venous system is smaller than that of Np. We conclude that Bz is useful in treating heart failure where cardiac output must be augmented, while maintaining venous return.


Japanese Circulation Journal-english Edition | 1991

Hemodynamic efficacy of E-1020 in comparison with dopamine on acute mitral regurgitation in anesthetized dogs.

Hitoshi Tanio; Toshiaki Kumada; Masataka Hayashi; Yoshihiro Himura; Yasuyuki Nakamura; Chuichi Kawai


Japanese Circulation Journal-english Edition | 1990

Cardiac Sports Rehabilitation for Patients with Ischemic Heart Disease

Ryuji Nohara; Hirofumi Kambara; Ishtiaque H. Mohiuddin; Shinji Ono; Kazumi Okuda; Shigeru Makita; Hiroshi Hamazaki; Kouichi Aoto; Masatsugu Shimomura; Masataka Hayashi; Tetsuro Fudou; Shunichi Tamaki; Yukisono Suzuki; Shigeru Kubo; Minoru Ito; Chuichi Kawai


Japanese Circulation Journal-english Edition | 1989

Silent myocardial ischemia in patients with myocardial infarction: evaluation with positron emission computed tomography.

Hirofumi Kambara; Tetsuro Fudo; Tetsuo Hashimoto; Masataka Hayashi; Chuichi Kawai; Nagara Tamaki; K. Yamashita; Yoshiharu Yonekura; Junji Konishi


Japanese Circulation Journal-english Edition | 1991

Evaluation and clinical use of early washout ratio of thallium-201 in normal and ischemic myocardium after dipyridamole-induced vasodilation using ring-type emission computed tomography.

Masataka Hayashi; Hirofumi Kambara; Ryuji Nohara; Tetsuro Fudo; Tetsuo Hashimoto; Chuichi Kawai; Nagara Tamaki; Yoshiharu Yonekura; Junji Konishi


Shinzo | 1989

Evaluation of myocardial viability in infarcted regions: using positron emission computed tomography

Tetsuro Fudo; Hirofumi Kambara; Tetsuo Hashimoto; Masataka Hayashi; Ishtiaque H. Mohiuddin; Nagara Tamaki; Yoshiharu Yonekura; Keiji Yamashita; Junji Konishi; Chuichi Kawai

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Chuichi Kawai

Takeda Pharmaceutical Company

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