1.Clinical Evaluation of SJM Prosthetic Aortic Valve by Doppler Echocardiography: Application of Energy Loss Index (ELI) as a New Index of Aortic Prosthetic Valve Function
Kunihide Nakamura ; Mitsuhiro Yano ; Yoshikazu Yano ; Tomokazu Saitoh ; Katsuhiko Niina ; Kohji Furukawa ; Yusuke Enomoto ; Masanori Nishimura ; Toshio Onitsuka
Japanese Journal of Cardiovascular Surgery 2004;33(2):77-80
Although the pressure gradient (PG) and the effective orifice area (EOA) have been used as indices of prosthetic valve function, these values show correctly neither energy loss, nor increased workload. This study aimed to evaluate the prosthetic valve function using echocardiography and PG, EOA and energy loss index, a new index advocated by Garcia et al. These were calculated for 40 patients with aortic prosthetic valve replacement by SJM valve (19HP, 6 cases; 21mm, 16 cases; 23mm, 14 cases; 25mm, 4 cases). Preoperative and postoperative echocardiographic measurements and their variations were analyzed and compared according to the size of implanted valve. In the comparison before and after aortic valve replacement, left ventricular mass (383±151g vs 288±113g, p<0.01), SV1+RV5 on ECG (5.07±1.73mV vs 3.83±1.5mV, p<0.01), and diastolic left ventricular posterior wall thickness (14.4±3.7mm vs 12.9±2.8mm, p<0.05) decreased significantly after the operation. However, there was no significant difference according to the size of the prosthetic valve in these reduction rates caluculated by (preoperative value-postoperative value)/preoperative value. Small size prosthetic valves were used for patients with small diameter of left ventricular outflow tract (LVOT) (19HP, 18±2mm; 21mm, 21±2mm; 23mm, 23±4mm; 25mm, 27±3mm; p<0.01) and small body surface area (19HP, 1.5±0.2m2; 21mm, 1.5±0.2m2; 23mm, 1.7±0.1m2; 25mm, 1.8±0.1m2; p<0.01) in our study. There was a signifcant difference in EOA (19HP, 1.2±0.4cm2; 21mm, 1.9±0.7cm2; 23mm, 2.2±0.9cm2; 25mm, 3.5±1.1cm2; p<0.01), but not in ELI (19HP, 1.01±0.41cm2/m2; 21mm, 1.87±1.03cm2/m2; 23mm, 1.83±1.09cm2/m2; 25mm, 3.08±1.21cm2/m2; p=0.055) according to the size of the prosthetic valve. Small size prosthetic valves had small EOA, but showed satisfactory valve function in decreasing left ventricular hypertrophy and reducing LVM and ELI of small size was similar to that of large size.
2.The Current Strategy for Managing Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1.
Yusuke NIINA ; Nao FUJIMORI ; Taichi NAKAMURA ; Hisato IGARASHI ; Takamasa OONO ; Kazuhiko NAKAMURA ; Masaki KATO ; Robert T JENSEN ; Tetsuhide ITO ; Ryoichi TAKAYANAGI
Gut and Liver 2012;6(3):287-294
Multiple endocrine neoplasia type 1 (MEN1) is an inherited autosomal dominant disease presenting with pancreatic neuroendocrine tumors (pNETs), parathyroid tumors, or pituitary tumors. Using the PubMed database, we reviewed the literature on information regarding the proper diagnosis and treatment of MEN1-associated pNET. Many cases of MEN1-associated pNET are functioning pNETs. Gastrinomas and insulinomas tend to occur frequently in the duodenum and pancreas, respectively. In addition to diagnostic imaging, the selective arterial secretagogue injection test (SASI test) is useful for localizing functioning pNET. The standard treatment is surgical resection. However, in the case of a functioning pNET, the tumor should first be accurately located using the SASI test before an appropriate surgical method is selected. In cases of a MEN1-associated non-functioning pNET that exceeds 2 cm in diameter, the incidence of distant metastasis is significantly increased, and surgery is recommended. In cases of unresectable pNET, a somatostatin analog has been shown to demonstrate antitumor effects and is considered to be a promising treatment. In addition, molecular-targeted drugs have recently been found to be effective in phase III clinical trials.
Diagnostic Imaging
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Duodenum
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Gastrinoma
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Incidence
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Insulinoma
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Multiple Endocrine Neoplasia
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Multiple Endocrine Neoplasia Type 1
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Neoplasm Metastasis
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Neuroectodermal Tumors, Primitive
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Neuroendocrine Tumors
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Pancreas
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Pituitary Neoplasms
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Somatostatin