Yoshinori Komazawa
Shimane University
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Publication
Featured researches published by Yoshinori Komazawa.
Journal of Gastroenterology and Hepatology | 2003
Yoshinori Komazawa; Kyoichi Adachi; Takafumi Mihara; Masahiro Ono; Akira Kawamura; Hirofumi Fujishiro; Yoshikazu Kinoshita
Background and Aim: The attenuated antisecretory activity observed during continuous administration of ranitidine has been described as tolerance. However, it remains unclear whether a similar phenomenon occurs with other histamine H2 receptor antagonists (H2RA). We investigated whether tolerance to famotidine, a stronger H2RA than ranitidine, occurs during long‐term administration.
Journal of Gastroenterology and Hepatology | 2003
Kyoichi Adachi; Tomoyuki Hashimoto; Naoharu Hamamoto; Kazuya Hirakawa; Masatoshi Niigaki; Tatsuya Miyake; Hiroyuki Taniura; Masahiro Ono; Takekazu Kaji; Hiroshi Suetsugu; Junko Yagi; Yoshinori Komazawa; Takafumi Mihara; Tomoko Katsube; Hirofumi Fujishiro; Toshihiro Shizuku; Shuzo Hattori; Shun Yamamoto; Yoshikazu Kinoshita
Background and Aim: Rabeprazole has a faster onset of antisecretory activity than omeprazole and lansoprazole. The aim of the present study was to clarify whether there is any difference in the speed of symptom relief in patients with reflux esophagitis following the administration of these three proton pump inhibitors (PPI).
Journal of Gastroenterology and Hepatology | 2006
Hirofumi Fujishiro; Kyoichi Adachi; Tomonori Imaoka; Tomoyuki Hashimoto; Naruaki Kohge; Nobuyuki Moriyama; Hiroshi Suetsugu; Kousaku Kawashima; Yoshinori Komazawa; Norihisa Ishimura; Shunji Ishihara; Yuji Amano; Yoshikazu Kinoshita
Background and Aim: Endoscopic retrograde cholangiopancreatography (ERCP) is a useful diagnostic and therapeutic procedure; however, ERCP occasionally causes post‐ERCP pancreatitis. The administration of gabexate mesilate has been reported to be effective for the prevention for post‐ERCP pancreatitis when given during and after the procedure. The aim of the present study was to investigate the preventive effect of the novel protease inhibitor ulinastatin on post‐ERCP pancreatitis.
Journal of Gastroenterology and Hepatology | 2003
Kyoichi Adachi; Hirofumi Fujishiro; Takafumi Mihara; Yoshinori Komazawa; Yoshikazu Kinoshita
Background and Aim: The sensitivity of the urea breath test (UBT) has been reported to be influenced by the administration of omeprazole, lansoprazole and ranitidine. However, it is unclear whether other H2 receptor antagonists (H2RA), except ranitidine, and rebamipide, a mucosal protective agent, affect UBT sensitivity. The aim of this study is to clarify the effects of lansoprazole, famotidine, roxatidine and rebamipide administration on UBT sensitivity.
Journal of Gastroenterology | 2003
Kyoichi Adachi; Yoshinori Komazawa; Hirofumi Fujishiro; Takafumi Mihara; Masahiro Ono; Mika Yuki; Akira Kawamura; Mohammad Azharul Karim Rumi; Yuji Amano; Yoshikazu Kinoshita
Background. Nocturnal gastric acid breakthrough (NAB) is defined as nocturnal intragastric pH less than 4 for more than 1 h during proton pump inhibitor (PPI) administration. A bedtime dose of an H2 receptor antagonist (H2RA) inhibites NAB, but the efficacy of the H2RA decreases with continuous administration. We carried out the present study to investigate the effect of 14-day H2RA administration on NAB. Methods. Ten male volunteers without Helicobacter pylori infection received four different 14-day regimens of rabeprazole and ranitidine (study a, morning dose of 20 mg rabeprazole; study b, morning dose of 20 mg rabeprazole with a single bedtime dose of 150 mg ranitidine only on the last day; study c, continuous 20 mg morning dose of rabeprazole and 150 mg at bedtime; study d, morning and evening doses of 10 mg rabeprazole). Ambulatory 24-h gastric pH monitoring was conducted on the last day of each regimen. Results. NAB in studies a, b, c, and d was observed in 9, 1, 4, and 4 subjects, respectively, and the longest periods of nocturnal gastric pH at less than 4.0 were 102.5, 14.0, 37.5, and 52.5 min, respectively (study b vs study c, P < 0.05). Conclusions. The continuous inhibitory effect of ranitidine combined with rabeprazole on nocturnal gastric acid secretion declined during 14-day-long administration in H. Pylori-negative subjects. Split dosing of rabeprazole was more effective than the single morning dose for inhibiting nocturnal gastric acid secretion.
Alimentary Pharmacology & Therapeutics | 2004
Tomoo Fujisawa; Kyoichi Adachi; Yoshinori Komazawa; Takafumi Mihara; Takane Azumi; Tomoko Katsube; Koichiro Furuta; Hideaki Kazumori; Yoshikazu Kinoshita
Background : The attenuated anti‐secretory activity of H2 receptor antagonists (H2RA) during continuous administration is referred to as the tolerance phenomenon. However, it is not clarified whether Helicobacter pylori infection affects the occurrence of tolerance to H2RA. It is also not clarified whether the tolerance phenomenon occurs to a new H2RA, lafutidine.
Journal of Gastroenterology and Hepatology | 2006
Kenji Furuta; Kyoichi Adachi; Yoshinori Komazawa; Takafumi Mihara; Masaharu Miki; Takane Azumi; Tomoo Fujisawa; Tomoko Katsube; Yoshikazu Kinoshita
Background and Aim: The attenuated antisecretory activity of H2 receptor antagonists (H2RA) during continuous administration is known as the tolerance phenomenon. The authors recently clarified that presence or absence of Helicobacter pylori infection influences the occurrence of the tolerance phenomenon. The aim of this study was to clarify whether tolerance to H2RA is correlated with attenuation of the inhibitory effect against gastroesophageal acid reflux in patients with gastroesophageal reflux disease (GERD).
Journal of Gastroenterology and Hepatology | 2003
Kyoichi Adachi; Noriyuki Arima; Toshiharu Takashima; Youichi Miyaoka; Mika Yuki; Masahiro Ono; Yoshinori Komazawa; Akira Kawamura; Hirofumi Fujishiro; Shunji Ishihara; Yoshikazu Kinoshita
Background: Helicobacter pylori infection has been reported to correlate with the onset of cardiovascular diseases. However, the relationship between H. pylori infection and the development of arteriosclerosis has not been fully investigated. We performed a cross‐sectional study to clarify the possible role of H. pylori infection in the development of arteriosclerosis.
Journal of Gastroenterology and Hepatology | 2005
Kyoichi Adachi; Yoshinori Komazawa; Takafumi Mihara; Takane Azumi; Tomoo Fujisawa; Tomoko Katsube; Kenji Furuta; Yoshikazu Kinoshita
Background and Aim: H2 histamine receptor antagonists (H2RAs) are widely used in patients with acid‐related diseases, and the onset of antisecretory activity of H2RAs is reported to be faster than that of proton pump inhibitors (PPIs). The aim of this study was to compare the rapidity of onset of antisecretory activity of cimetidine and famotidine when orally administered.
Current Therapeutic Research-clinical and Experimental | 2012
Shino Shimura; Naoharu Hamamoto; Nagisa Yoshino; Yoshinori Kushiyama; Hirofumi Fujishiro; Yoshinori Komazawa; Kenji Furuta; Shunji Ishihara; Kyoichi Adachi; Yoshikazu Kinoshita
BACKGROUND The number of patients who require treatment with proton pump inhibitors (PPIs) is increasing in Japan. One of their adverse effects is diarrhea. OBJECTIVES We investigated the incidence of diarrhea caused by 3 different PPIs: lansoprazole, rabeprazole, and omeprazole. METHODS Patients using PPIs for >1 month were enrolled. Enrolled patients recorded daily stool frequency, stool consistency using the Bristol Stool Scale Form, and impaired quality of life caused by diarrhea for 1 month. Their attending physicians described the types and dosages, and duration of PPI administration, as well as other necessary information. RESULTS A total of 255 patients participated. Mean age of the patients was 70.7 years old. During the 1-month observation period, 3.5% of the patients complained of diarrhea. There was no significant difference for the incidence of diarrhea among the 3 types of PPIs. Furthermore, no correlations between diarrhea and length and dosage of PPI administration were found. CONCLUSIONS The incidence of diarrhea in patients receiving long-term therapy did not differ among 3 different PPIs. ClinicalTrials.gov identifier: UMIN ID 000005300.