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1.
Transplant Proc ; 36(2 Suppl): 461S-464S, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15041388

ABSTRACT

We investigated the clinical benefits of cyclosporine microemulsion preconcentrate (CyA-MEPC; Neoral) in 16 de novo renal transplant recipients. The dose of CyA-MEPC was managed from AUC(0-4h), with serial target values of AUC(0-4h) at 5000-->4000-->3000-->2000 ng. hr/mL. The frequency of acute rejection episodes was 25%. The decreased renal function reached a low value of 12.5%, and creatinine was stable. Therefore, setting the target AUC(0-4h) value in the early phase at 5000 ng.hr/mL is an effective strategy to prevent acute rejection episodes. The single dose of Neoral given immediately after the renal transplant was 6 mg/kg (making a daily dose of 12 mg/kg). Thereafter, the dose-normalized AUC(0-4h) was set at a constant value to 4 weeks posttransplant. At week 4, the single dose was decreased to 4 mg/kg twice daily (a daily dose of 8 mg/kg). From these studies a daily dose of 12 mg/kg is suggested to be the appropriate amount for the first dose immediately after transplant. The renal biopsy performed at 6 months posttransplant showed neither cyclosporine-induced renal impairments, nor findings of chronic rejection, suggesting that 2000 ng.hr/mL is an appropriate target AUC(0-4h) value in the maintenance phase. These results suggest that it is possible to set the target value of C2 monitoring in the maintenance phase to a value slightly lower than that proposed from other studies.


Subject(s)
Cyclosporine/pharmacokinetics , Cyclosporine/therapeutic use , Intestinal Absorption/physiology , Kidney Transplantation/immunology , Mycophenolic Acid/analogs & derivatives , Adult , Area Under Curve , Cyclosporine/administration & dosage , Cyclosporine/blood , Drug Therapy, Combination , Female , Graft Rejection/epidemiology , Graft Rejection/prevention & control , Humans , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/pharmacokinetics , Immunosuppressive Agents/therapeutic use , Kidney Transplantation/physiology , Male , Mycophenolic Acid/therapeutic use , Postoperative Period , Time Factors
4.
J Hepatobiliary Pancreat Surg ; 7(2): 183-7, 2000.
Article in English | MEDLINE | ID: mdl-10982611

ABSTRACT

Distal pancreatectomy with resection of the celiac axis can increase resectability of carcinoma of the body and tail of the pancreas. We performed reconstruction of the hepatic artery to avoid complications caused by a decrease in hepatic arterial flow. We carried out distal pancreatectomy with resection of the celiac axis for carcinoma of the body and tail of the pancreas in four patients. When pulsation in the proper hepatic artery was weak after occlusion of the celiac axis, we performed reconstruction of the hepatic artery, using the splenic artery, which had been taken beforehand from the resected specimen. In two patients, we performed reconstruction of the hepatic artery. These two patients underwent reconstruction of the portal vein combined with prolonged clamping of the portal vein. Levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were elevated just after the operation, but recovered to normal levels within 10 days. No complications related to hepatic ischemia were observed. These results suggested that reconstruction of the hepatic artery allowed us to safely perform distal pancreatectomy with resection of the celiac axis for carcinoma of the body and tail of the pancreas.


Subject(s)
Carcinoma/surgery , Hepatic Artery/surgery , Pancreatectomy/methods , Pancreatic Neoplasms/surgery , Plastic Surgery Procedures/methods , Aged , Carcinoma/diagnosis , Carcinoma/mortality , Celiac Artery/surgery , Female , Hepatic Artery/pathology , Humans , Male , Middle Aged , Pancreas/blood supply , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/mortality , Prognosis , Survival Rate , Treatment Outcome
5.
Jpn J Clin Oncol ; 29(5): 256-60, 1999 May.
Article in English | MEDLINE | ID: mdl-10379338

ABSTRACT

We successfully fabricated a large maxillofacial prosthesis for replacement of a total mandibular defect resulting from surgical failure to reconstruct the mandible. Although a number of reports have described procedures for fabricating midfacial prostheses, there is little information on prostheses to compensate for total loss of the mandible. A 54-year-old woman was referred to the Dentistry and Oral Surgery Division of the National Cancer Center Hospital with total loss of the mandible and the surrounding facial soft tissue. The facial prosthesis we used to treat this patient is unique in that it is adequately retained without the use of extraoral implants and conventional adhesives. This prosthesis is retained by the bilateral auricles and the remaining upper front teeth. We present details of the design of this large silicone maxillofacial prosthesis, with which we successfully rehabilitated the patient.


Subject(s)
Mandible/surgery , Mandibular Diseases/surgery , Maxillofacial Prosthesis Implantation/methods , Maxillofacial Prosthesis , Osteoradionecrosis/surgery , Plastic Surgery Procedures , Female , Humans , Mandibular Diseases/etiology , Middle Aged , Osteoradionecrosis/etiology , Tongue Neoplasms/radiotherapy , Tongue Neoplasms/surgery
7.
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