Kenichi Iseki
Asahikawa Medical College
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Featured researches published by Kenichi Iseki.
Internal Medicine | 2016
Satomi Okano; Masaya Sugimoto; Masashi Takase; Kenichi Iseki; Aya Kajihama; Hiroshi Azuma
Protein-losing enteropathy (PLE) is a rare and life-threatening complication that occurs after the Fontan procedure. We herein report the case of an 11-year-old Japanese boy who developed PLE six times after undergoing the Fontan procedure. High-dose spironolactone therapy has been effective for 2 years. His high level of serum aldosterone decreased to a nearly normal range and spironolactone may have a diuretic and anti-inflammatory potential.
SpringerPlus | 2014
Tsunehisa Nagamori; Hideharu Oka; Shin Koyano; Hironori Takahashi; Junichi Oki; Yuko Sato; Koichi Murono; Kenichi Iseki; Ryou Takeguchi; Takahiro Takeda; Masayuki Sato; Rika Sugai; Hiroyuki Kitamura; Hiroki Kajino; Yurika Miura; Toru Ishioka; Hiroshi Azuma
ObjectiveTo evaluate the parameters associated with significant gastrointestinal (GI) involvement in Henoch-Schönlein Purpura (HSP), and construct a scoring system for the identification of patients at high risk of gross blood in stools.Study designData for HSP patients hospitalized at each of seven institutes were retrospectively analyzed. Patients were divided into four groups according to the consequent severity of GI involvement. Identification of laboratory parameters at the time of admission were then used to differentiate the groups, and a scoring system to predict gross intestinal bleeding was constructed. Prognostic efficiency, correlation with the subsequent duration of abdominal pain, and association with manifestations excluding abdominal pain were also analyzed.ResultsAn analysis of variance (ANOVA) test showed significant intergroup differences in white blood cell (WBC) count, neutrophil count, serum albumin, potassium, plasma D-dimer and coagulation factor XIII activity. A scoring system consisting of these parameters showed a good prognostic value for gross intestinal bleeding in a receiver operating characteristic (ROC) analysis, and a cut-off value of 4 points showed a sensitivity of 90.0% and specificity of 80.6%. The score was also correlated with the duration of abdominal pain after admission. A significantly higher score (s) was observed in patients presenting with nephritis, although the predictive value was poor.ConclusionA scoring system consisting of generally available parameters was of use in predicting severe GI involvement in HSP patients. Although further study is needed, initial therapy in accordance with disease activity may be taken into consideration using this scoring system.
Journal of Clinical Virology | 2012
Tsunehisa Nagamori; Shin Koyano; Yoko Asai; Fumikatsu Nohara; Toshio Okamoto; Ken Nagaya; Tokitsugi Hayashi; Yurika Miura; Naoya Tsuda; Kenichi Iseki; Hiroshi Azuma
BACKGROUND Disseminated neonatal herpes simplex virus (HSV) infection causes a typical systemic inflammatory response syndrome and has a high mortality rate. However, the validity of anti-inflammatory intervention against this condition remains unknown. OBJECTIVES We sought to demonstrate the sequential changes in the pathophysiology of disseminated neonatal HSV infections. STUDY DESIGN The HSV serum copy number as well as high-mobility group box 1 (HMGB1) and cytochrome c concentrations, which predict the severity and mortality rate of sepsis, were sequentially evaluated in a patient with disseminated neonatal HSV infection caused by HSV-2. RESULTS As the patient presented with evidence of hyper-inflammation and severe illness, we empirically undertook anti-inflammatory intervention that included the administration of prednisolone, high-dose immunoglobulin, and blood exchange therapy in addition to high-dose acyclovir (ACV) therapy. The patient survived without significant neurological sequela. We found that (1) the serum concentrations of both HMGB1 and cytochrome c were extremely high, (2) temporal increases in these biomarkers were observed after admission, and (3) interestingly, the increase in HMGB1 level preceded that of cytochrome c. These results suggested that the pathophysiology of this condition changed sequentially in a dramatic manner, and the timing of our anti-inflammatory intervention was prior to the transition of pathological status from hyper-inflammation to massive apoptosis. CONCLUSIONS Anti-inflammatory intervention may only be effective if it is undertaken during the early phase of disseminated neonatal HSV infections.
Pediatrics | 1983
Hajime Yoshioka; Kenichi Iseki; Kozo Fujita
Bifidobacteria and Microflora | 1991
Yoshioka H; Fujita K; Hiroshi Sakata; Koichi Murono; Kenichi Iseki
JAMA Pediatrics | 1983
Kozo Fujita; Kenichi Iseki; Hajime Yoshioka; Toru Sasaki; Takako Ando; Masayuki Nakamura
The Journal of Antibiotics | 1989
Fujii R; Meguro H; Arimasu O; Shiraishi H; Toshiaki Abe; Yoshioka H; Hiroshi Sakata; Kenichi Iseki; Yoji Takahashi; Koichi Murono; Yoshinori Wagatsuma; Akira Watanabe; Masahito Koshinami; Masaru Yokoyama; Shigeru Kimura; Mikio Minamitani; Kei Hachimori; Hiroshi Hayakawa; Yukishige Yanagawa; Haruo Ichihashi; Hiroshi Hirosawa; Yasuko Ishikawa; Shintaro Takahashi; Hiroo Matsuda; Susumu Nakazawa; Hajime Satou; Kenji Niino; Akira Narita; Makoto Hori; Toyonaga Y
Japanese Journal of Infectious Diseases | 2013
Kazuki Okajima; Kenichi Iseki; Shin Koyano; Atsushi Kato; Hiroshi Azuma
JAMA Pediatrics | 1985
Kozo Fujita; Kenichi Iseki; Hiroshi Azuma; Hajime Yoshioka; Toshihiro Onozawa
The Journal of Antibiotics | 1993
Fujii R; Yoshioka H; Okuno A; Fujita K; Murono K; Maruyama S; Hiroshi Sakata; Kenichi Iseki; Wagatsuma Y; Fukushima N