Hironori Nemoto
Saitama Medical University
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Featured researches published by Hironori Nemoto.
Blood Purification | 2001
Hironori Nemoto; Hidetomo Nakamoto; Hirokazu Okada; Souichi Sugahara; Kenshi Moriwaki; Mitsuru Arai; Yoshihiko Kanno; Hiromichi Suzuki
Background: Sepsis and septic shock are still major causes of morbidity and mortality in spite of the availability of powerful and broadly active antibiotics. Methods: A prospective, open and randomized trial of the effect of immobilized polymyxin fibers (PMX-F) on the survival of patients with sepsis throughout a follow-up period of 28 days or until discharge, if earlier, was carried out. Ninety-eight patients were included who met at least 4 of the criteria for systemic inflammatory response syndrome due to infection. The patients were classified into three groups based on their Acute Physiology and Chronic Health Evaluation (APACHE) II score. Results: The overall survival rate was significantly improved by using PMX-F compared to the control group (41 vs. 11%) (p = 0.002). In patients with an APACHE II score less than 20, treatment with PMX-F was shown to improve outcome (65 vs. 19%) (p = 0.01). In cases of more severe sepsis with an APACHE II score of 20–29, PMX-F still maintained efficacy in improving outcome (40 vs. 11%) (p = 0.04). However, PMX-F treatment did not improve the survival rate in patients with an APACHE II score of greater than 30 (survival rate 7 vs. 0%) (p = 0.59). Conclusion: From these results, it is concluded that treatment with PMX-F in patients with sepsis is effective and prolongs the survival rate when applied at an early stage of sepsis. However, in severe sepsis, this therapy does not improve the survival rate.
Clinical and Experimental Nephrology | 2003
Yoshihiko Kanno; Martje Witt; Hirokazu Okada; Hironori Nemoto; Soichi Sugahara; Hidetomo Nakamoto; Hiromichi Suzuki
AbstractBackground. No satisfactory treatment exists for IgA nephropathy (IgAN), especially in patients with severe histologic damage. Several trials using steroids combined with other therapies such as warfarin have demonstrated unremarkable results. We investigated the renoprotective effects of warfarin and steroids in IgAN patients with crescent formation. Methods. Fifteen Japanese patients with IgAN were followed for up to 3 years. Crescent formation was recognized in over half of their glomeruli from renal biopsy specimens. Treatments consisted of either 0.5 mg/kg per day of prednisolone, or warfarin monotherapy. Blood pressure was controlled with long-acting calcium channel blockers and alpha-beta blockers. Serum creatinine and urinary protein excretion were evaluated at least every 2 months for 36 months. Results. Ten of the 15 patients completed the study. The serum creatinine levels had increased in both groups by 3 years, but significantly more so in the group treated with warfarin. However, they were not significantly different between the two groups as measured at the beginning and end of the study. Blood pressure for all patients in the study was maintained below 130/85 mmHg. Excluded from the study were 5 patients who experienced either peptic ulcers (n = 2, steroid group) or bleeding problems (n = 3, warfarin group). Conclusions. These results suggest that corticosteroid therapy may assist in preventing deterioration of renal function in patients with IgAN accompanied by crescent formation. However, further study would be required to decide its usefulness.
Journal of Artificial Organs | 2003
Yoshihiko Kanno; Hironori Nemoto; Hidetomo Nakamoto; Hirokazu Okada; Soichi Sugahara; Koichiro Nishidome; Yoshihisa Yamashita; Hiromichi Suzuki
The objective of this study was to analyze retrospectively the efficacy of polymyxin-B immobilized fiber (PMX-F) alone and in combination with continuous venovenous hemofiltration (CHF) on the prognosis of critically ill patients with sepsis using a retrospective chart review in a university hospital in Japan. A cohort of 246 patients meeting the criteria of sepsis, septic shock, or both, according to the American College of Chest Physicians/Society of Critical Care Medicine (ACCP/ACCM) Consensus Conference, were examined in this study. From these patients, 48 were selected who were found to have definitive causative bacteria and whose primary diseases were clearly identified. According to the charts, two major primary diseases were identified: one related to cardiovascular disease and the other to gastrointestinal disease. Other diseases were excluded from this study because of the small numbers of patients in categories such as malignant, hematological, genitourinary, and other diseases. Furthermore, patients who had levels of serum creatinine above 2.0 mg/dl were excluded. The prevalence of diabetes mellitus (up to 63%) was very high in both groups. There were no significant differences between the two groups in age or the Apache II scores at the start of hemoperfusion treatment; however, the gender ratio varied: 72% of the cardiovascular group were male, compared to 46% of the gastrointestinal group. The causative bacteria were markedly different between the two groups. For half of the gastrointestinal group the causative bacterium was Escherichia coli, while for half of the cardiovascular group the causative bacterium was Pseudomonas aeruginosa.The survival rate differed significantly between the two groups. The patients in the cardiovascular group survived longer than those in the gastrointestinal group. Moreover, for the patients with cardiovascular disease, there was no significant difference in the survival rate between treatment with PMX-F alone and with PMX-F and CHF in combination. In contrast, for the patients with gastrointestinal disease, there was a significant difference between treatment with PMX-F alone and with PMX-F and CHF in combination. When a patient with sepsis or septic shock is treated with hemoperfusion, the decision as to whether PMX-F should be given alone or in combination with CHF might be determined on the basis of the primary disease of the patient.
Blood Purification | 2001
Scott J. Hines; Caitlin E. Carroll; Hironori Nemoto; Hidetomo Nakamoto; Hirokazu Okada; Souichi Sugahara; Kenshi Moriwaki; Mitsuru Arai; Yoshihiko Kanno; Hiromichi Suzuki; Toshio Yamada; Takashi Akiba; Sei Sasaki; Fabio Galetta; Adamasco Cupisti; Ferdinando Franzoni; Ester Morelli; Raffaele Caprioli; Paolo Rindi; Giuliano Barsotti; Maria P. Varela; Paul L. Kimmel; Terry M. Phillips; Gary J. Mishkin; Susie Q. Lew; Juan P. Bosch; Guillaume Jean; Bernard Charra; Charles Chazot; Jean-Claude Terrat
May 30 to June 1, 2001, London
Therapeutic Apheresis | 2002
Hiromichi Suzuki; Hironori Nemoto; Hidetomo Nakamoto; Hirokazu Okada; Soichi Sugahara; Yoshihiko Kanno; Kenshi Moriwaki
Advances in peritoneal dialysis. Conference on Peritoneal Dialysis | 2003
Koji Tomori; Hidetomo Nakamoto; Syuhei Kotaki; Yuji Ishida; Hiroshi Takane; Hironori Nemoto; Yoshihiko Kanno; Soichi Sugahara; Hirokazu Okada; Hiromichi Suzuki
Hypertension Research | 2000
Hiromichi Suzuki; Hidetomo Nakamoto; Hironori Nemoto; Souichi Sugahara; Hirokazu Okada
Hypertension Research | 1999
Hidetomo Nakamoto; Hironori Nemoto; Souichi Sugahara; Hirokazu Okada; Hiromichi Suzuki
Blood Purification | 2001
Scott J. Hines; Caitlin E. Carroll; Hironori Nemoto; Hidetomo Nakamoto; Hirokazu Okada; Souichi Sugahara; Kenshi Moriwaki; Mitsuru Arai; Yoshihiko Kanno; Hiromichi Suzuki; Toshio Yamada; Takashi Akiba; Sei Sasaki; Fabio Galetta; Adamasco Cupisti; Ferdinando Franzoni; Ester Morelli; Raffaele Caprioli; Paolo Rindi; Giuliano Barsotti; Maria P. Varela; Paul L. Kimmel; Terry M. Phillips; Gary J. Mishkin; Susie Q. Lew; Juan P. Bosch; Guillaume Jean; Bernard Charra; Charles Chazot; Jean-Claude Terrat
Hemodialysis International | 2004
Souichi Sugahara; Hiromichi Suzuki; Hirokazu Okada; Hidetomo Nakamoto; Hironori Nemoto; Yoshihiko Kanno