Takako Sasai
Dokkyo University
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Featured researches published by Takako Sasai.
The American Journal of Gastroenterology | 1998
Takako Sasai; Hideyuki Hiraishi; Yasunaga Suzuki; Hironori Masuyama; Motoo Ishida; Akira Terano
Several nonsurgical approaches to the treatment of postradiation proctitis have been described, but no effective conservative treatment has yet been established. As an alternative to the usual treatment, three cases of chronic postradiation proctitis with hemorrhage were successfully treated with oral administration of sucralfate, with resultant decreased bleeding in long term follow-up period. Oral sucralfate may provide a novel approach to the treatment of intractable postradiation proctitis.
Digestion | 2015
Hironori Masuyama; Naoto Yoshitake; Takako Sasai; Tetsuya Nakamura; Atsushi Masuyama; Toru Zuiki; Kentaro Kurashina; Mitsuyo Mieda; Keijiro Sunada; Hironori Yamamoto; Kazutomo Togashi; Akira Terano; Hideyuki Hiraishi
Background: The relationship between Helicobacter pylori infection and gastric cancer has been demonstrated, and the risk of gastric cancer occurrence is known to increase with the progression of atrophic changes associated with chronic gastritis. Endoscopic evaluation of the degree and extent of atrophy of the gastric mucosa is a simple and very important means of identifying a group at high risk for gastric cancer. This study aimed to clarify the carcinogenic risk in relation to the degree of atrophy. Methods: A total of 27,777 patients (272 with early gastric cancer and 135 with advanced gastric cancer) were included in this study. Endoscopically evaluated atrophy of the gastric mucosa was classified as C-0 to O-3 according to the Kimura and Takemoto classification system. Results: The cancer detection rate in relation to the degree of gastric mucosal atrophy was 0.04% (2/4,183 patients) for C-0, 0% (0/4,506) for C-1, 0.25% (9/3,660) for C-2, 0.71% (21/2,960) for C-3, 1.32% (75/5,684) for O-1, 3.70% (140/3,780) for O-2 and 5.33% (160/3,004) for O-3. As to the proportions of differentiated and undifferentiated cancers, the latter were relatively frequent in the C-0 to C-2 groups, but differentiated cancers became predominant as atrophy progressed. On the other hand, the number of both differentiated and undifferentiated cancers detected increased as gastric mucosal atrophy progressed. In addition, open-type atrophy was found in 29 (96.7%) of 30 patients with synchronous multiple gastric cancers and in all 20 patients with metachronous multiple gastric cancers. Conclusion: Endoscopic evaluation of gastric mucosal atrophy can provide a simple and reliable predictive index for both current and future carcinogenic risk.
Alimentary Pharmacology & Therapeutics | 2000
Y. Mitobe; Hideyuki Hiraishi; Takako Sasai; Tadahito Shimada; Akira Terano
Background: Helicobacter pylori‐associated inflammation leads to exposure of the gastric epithelium to reactive oxygen species (ROS) generated in the gastric mucosa. In some pathological conditions, such as those induced by nonsteroidal anti‐inflammatory drugs, the gastric mucosa may become more susceptible to ROS.
Gastrointestinal Endoscopy | 1998
Kaori Sakata; Motoo Ishida; Hideyuki Hiraishi; Takako Sasai; Naomi Watanabe; Yasunaga Suzuki; Hironori Masuyama; Akira Terano
Lancet 1996;347:975. 10. Salmeron M, Desplaces N, Lavergne A, Houdart R. Campylobacter-like organisms and acute purulent gastritis. Lancet 1986;2:975-6. 11. Mitchell JD, Mitchell HM, Tobias V. Acute Helicobacter infection in an infant, associated with gastric ulceration and serological evidence of intra-familial transmission. Am J Gastroenterol 1992;87:382-6. 12. Frommer DJ, Carrick J, Lee A, Hazell S. Acute presentation of Campylobacter pylori gastritis. Am J Gastroenterol 1988; 83:1168-71. 13. Rocha GA, Queiroz DMM, Mendes EN, Barbosa AJA, Lima GF Jr, Oliveira CA. Helicobacter pylori acute gastritis: histological, endoscopical, clinical, and therapeutic features. Am J Gastroentrol 1991;86:1592-5. 14. Xiang Z, Censini S, Bayeli PF, Telford JL, Figura N, Rappuoli R, et al. Analysis of expression of CagA and VacA virulence factors in 43 strains of Helicobacter pylori reveals that clinical isolates can be divided into two major types and that CagA is not necessary for expression of the vacuolating cytotoxin. Infect Immun 1995;63:94-8. 15. Tummuru MKR, Cover TL, Blaser MJ. Cloning and expression of a high-molecular-mass major antigens of Helicobacter pylori: evidence of linkage to cytotoxin production. Infect Immun 1993;61:1799-809. 16. Fujimoto S, Marshall B, Blaser M. PCR-based restriction fragment length polymorphism typing of Helicobacter pylori. J Clin Microbiol 1994;32:331-4. 17. Katz D, Siegal HI. Erosive gastritis and acute gastrointestinal mucosal lesions. In: Glass GBJ, editor. Progress in gastroenterology. Vol 1. New York: Grune and Siralton; 1968. p. 67-96. 18. Laine L, Cominelli F, Sloane R, Casini-Raggi V, MarinSorensen M, Weinstein WM. Interaction of NSAIDs and Helicobacter pylori on gastrointestinal injury and prostaglandin production: a controlled double-blind trial. Aliment Pharmacol Ther 1995;9:127-35. 19. Graham DY, Alpert LC, Smith JL, Yoshimura HH. Iatrogenic Campylobacter pylori infection is a cause of epidemic achlorhydia. Am J Gastroenterol 1988;83:974-80. 20. Langenberg W, Rauws EAJ, Oudbier JH, Tytgat GNJ. Patient-to-patient transmission of Campylobacter pylori infection by fiberoptic gastroduodenoscopy and biopsy. J Infect Dis 1990;161:507-11. 21. Sugiyama T, Naka H, Yabana T, Awakawa T, Furuyama S, Kawauchi H, et al. Is Helicobacter pylori infection responsible for postendoscopic acute gastric mucosal lesions? Eur J Gastroenterol Hepatol 1992;4(Suppl 1):S93-6. 22. Miyaji H, Kohli Y, Azuma T, Ito S, Hirai M, Ito Y, et al. Endoscopic cross-infection with Helicobacter pylori [letter]. Lancet 1995;345:464. 23. Matysiak-Budnik T, Briet F, Heyman M, Megraud F. Laboratory-acquired Helicobacter pylori infection. Lancet 1995;346:1489-90. 24. Ghiara P, Marchetti M, Blaser MJ, Tummuru MKR, Cover TL, Segal ED, et al. Role of the Helicobacter pylori virulence factors vacuolating cytotoxin, CagA, and urease in a mouse model of disease. Infect Immun 1995;63:4154-60.
Gastrointestinal Endoscopy | 2000
Yoshihito Watanabe; Hideyuki Hiraishi; Yasunaga Suzuki; Kazuhiro Sakuma; Takako Sasai; Takeshi Oinuma; Kazunari Kanke; Hidetaka Watanabe; Motoo Ishida; Hironori Masuyama; Tadahito Shimada; Akira Terano
Background: Endoscopic variceal banding ligation (EVL) and sclerotherapy (EVS) have been used to prevent variceal hemorrhage. However, the rate of recurrence of esophageal varices after EVL or EVS is considerably high. Argon plasma coagulation (APC) is a new modality of electrosurgery to apply high frequency electric current into tissue to cause defined thermal effects. This study was conducted to determine whether APC is beneficial for eradication of residual esophageal varices after EVL or EIS. Methods: Cirrhotic patients with endoscopically assessed high-risk esophageal varices but no history of bleeding underwent EVL or EIS to reduce the risk of hemorrhage. When the size of varices was reduced 1 week later, the entire esophageal mucosae 4-5 cm proximal to the esophagogastric junction was coagulated with one session of APC in a total of 15 patients.APC was performed with the use of argon source APC300 and high frequency generator ICC 200 (ERBE, Germany). Follow-up endoscopy was performed 7 days and 1 month after the initial procedure and thereafter every 3 months, to check for recurrent/residual esophageal varices and its complications. Results: Ten to 14 days after APC, ulcerations with white coating were noted in all cases, whereas varices were completely eradicated. One month after APC, while the varices remained eradicated, coagulated esophageal mucosae became whitish and the ulcerations were nearly completely healed. During the course, no patients complained of dysphagia or retrosternal pain. Furthermore, neither development of gastric varices nor aggravation of portal hypertensive gastropathy was observed endoscopically. No serious complication such as bleeding necessitating endoscopic therapy and perforation or stricture of the esophagus was encountered. Over a maximum follow-up period of 5 months, neither recurrence of nor hemorrhage from esophageal varices was observed. Conclusions: APC ablation of residual esophageal varices in patients who have undergone prior EVL or EIS is safe and may be a novel approach to eradicate esophageal varices. It requires a long term follow-up of the eradicated varices to further evaluate its efficacy.
World Journal of Gastroenterology | 2018
Koh Fukushi; Keiichi Tominaga; Kazunori Nagashima; Akira Kanamori; Naoya Izawa; Mimari Kanazawa; Takako Sasai; Hideyuki Hiraishi
AIM To determine the clinical characteristics of elderly patients of hemorrhagic gastroduodenal ulcer on low-dose aspirin (LDA) therapy. METHODS A total of 1105 patients with hemorrhagic gastroduodenal ulcer treated in our hospital between January 2000 and March 2016 were grouped by age and drugs used, and these groups were compared in several factors. These groups were compared in terms of length of hospital stay, presence/absence of hemoglobin (Hb) decrease, presence/absence of blood transfusion, Forrest I, percentage of Helicobacter pylori infection, presence/absence of underlying disease, and percentage of severe cases. RESULTS The percentage of blood transfusion (62.6% vs 47.7 %, P < 0.001), Hb decrease (53.8% vs 40.8%, P < 0.001), and the length of hospital stay (23.5 d vs 16.7 d, P < 0.001) were significantly greater in those on drug therapy. The percentage of blood transfusion (65.3% vs 47.8%, P < 0.001), Hb decrease (54.2% vs 42.1%, P < 0.001), and length of hospital stay (23.3 d vs 17.5 d, P < 0.001) were significantly greater in the elderly. In comparison with the LDA monotherapy group, the percentage of severe cases was significantly higher in the LDA combination therapy group when elderly patients were concerned (16.1% vs 34.0%, P = 0.030). Meanwhile, among those on LDA monotherapy, there was no significant difference between elderly and non-elderly (16.1% vs 16.0%, P = 0.985). CONCLUSION A combination of LDA with antithrombotic drugs or non-steroidal anti-inflammatory drugs (NSAIDs) contributes to aggravation. And advanced age is not an aggravating factor when LDA monotherapy is used.
Journal of Gastroenterology and Hepatology | 2018
Kazunori Nagashima; Keiichi Tominaga; Koh Fukushi; Akira Kanamori; Takako Sasai; Hideyuki Hiraishi
Gastrointestinal hemorrhage occurs frequently. We reviewed the tendency of occurrence of bleeding gastric and duodenal ulcers and their association with antithrombotic therapy before and after the widespread use of Evidence‐Based Clinical Practice Guidelines for Peptic Ulcer 2009 (1st edition), which was published to improve treatment outcomes and prevent peptic ulcers.
Internal Medicine | 2018
Hitoshi Kino; Masakazu Nakano; Akira Kanamori; Tsunehiro Suzuki; Yoshihito Kaneko; Chieko Tsuchida; Kouhei Tsuchida; Keiichi Tominaga; Takako Sasai; Hidetsugu Yamagishi; Hideyuki Hiraishi
A 78-year-old man underwent endoscopic submucosal dissection (ESD) for early gastric adenocarcinoma twice in 2009 and 2014. Between the procedures, he successfully completed Helicobacter pylori eradication therapy. In May 2015, upper endoscopy screening showed two elevated lesions on the gastric fundus, and en bloc resection by ESD was performed. We histopathologically diagnosed the patient to have gastric adenocarcinoma of the fundic gland type. In this case, the two lesions of gastric adenocarcinoma of the fundic gland type multifocally developed after ESD for metachronous gastric tubular adenocarcinoma. Furthermore, they appeared in the gastric fundus, where atrophy had been improved due to eradication therapy.
World Journal of Gastroenterology | 2017
Chieko Tsuchida; Naoto Yoshitake; Hitoshi Kino; Yoshihito Kaneko; Masakazu Nakano; Kohei Tsuchida; Keiichi Tominaga; Takako Sasai; Hironori Masuyama; Hidetsugu Yamagishi; Hideyuki Hiraishi
AIM To evaluate the usefulness of total colonoscopy (TCS) for patients undergoing gastric endoscopic submucosal dissection (ESD) and to assess risk factors for colorectal neoplasms. METHODS Of the 263 patients who underwent ESD at our department between May 2010 and December 2013, 172 patients undergoing TCS during a one-year period before and after ESD were targeted. After excluding patients with a history of surgery or endoscopic therapy for colorectal neoplasms, 158 patients were analyzed. Of the 868 asymptomatic patients who underwent TCS during the same period because of positive fecal immunochemical test (FIT) results, 158 patients with no history of either surgery or endoscopic therapy for colorectal neoplasms who were matched for age and sex served as the control group for comparison. RESULTS TCS revealed adenoma less than 10 mm in 53 patients (33.6%), advanced adenoma in 17 (10.8%), early colorectal cancer in 5 (3.2%), and advanced colorectal cancer in 4 (2.5%). When the presence or absence of adenoma less than 10 mm, advanced adenoma, and colorectal cancer and the number of adenomas were compared between patients undergoing ESD and FIT-positive patients, there were no statistically significant differences in any of the parameters assessed. The patients undergoing ESD appeared to have the same risk of colorectal neoplasms as the FIT-positive patients. Colorectal neoplasms were clearly more common in men than in women (P = 0.031). Advanced adenoma and cancer were significantly more frequent in patients with at least two of the following conditions: hypertension, dyslipidemia, and diabetes mellitus (P = 0.019). CONCLUSION In patients undergoing gastric ESD, TCS appears to be important for detecting synchronous double neoplasms. Advanced adenoma and cancer were more common in patients with at least two of the following conditions: hypertension, dyslipidemia, and diabetes mellitus. Caution is therefore especially warranted in patients with these risk factors.
Gastroenterology | 1998
Takako Sasai; Hideyuki Hiraishi; Takeshi Oinuma; T. Shimada; Akira Terano
that endoscopically negative patients with GER-related symptoms may have enhanced protective mechanisms. Aims: 1. To assess bicarbonate, non-bicarbonate, protein, transforming growth factor ct (TGFtx) and prostaglandin E 2 (PGE2) in salivary secretion in patients with endoscopically negative [E(-)] GERD. 2. To compare the obtained results with corresponding values in asymptomatic controls (C) and patients with RE~ Subjects & Methods: The study was conducted in 30 patients with RE (12F & 18M, mean age of 49), in 39 asymptomatic volunteers (16F & 23M, mean age of 40), and in 10 patients with E(-) GERD (SF & 5M, mean age of 40). Salivary secretions were collected under basal conditions, daring mastication, and during intraesophageal mechanical and chemical stimulation, mimicking the GER scenario, using an esophageal perfusion catheter. Salivary bicarbonate and non-bicarbonate were measured using Titra-Lab (Radiometer America, IL). Salivary protein was quantitated using Lowry method, whereas TGFot, and PGE z by RIA (Amersham, IL and Biomed. Technol. Inc. MA). Statistical analysis was implemented by E-Stat (Jandel Sci. CA) software. Results: Salivary bicarbonate in patients with E(-) GERD was significantly higher than in C and in RE during intraesophageal chemical stimulation (P < 0.05). Salivary protein was significantly higher in GERD E(-) than in and RE during intraesophageai mechanical and chemical stimulation (P < 0.05). Salivary TGFot output in GERD E(-) was significantly higher than in RE (P < 0.05) but not controls during intraesophageal mechanical stimulation. Salivary PGE z output, on the other hand, in GERD E(-) was significantly higher than in C (P < 0.05) but not RE during intraesophageal chemical stimulation. Conclusion: . A strong salivary secretory response to intraesophageal mechanical and chemical stimuli in patients with GERD E(-) in terms of bicarbonate, protein, TGFa, and PGE z seem to mediate resistance to the development of endoscopic mucosal changes by GER. ° This could explain t he lack of endoscopic esophagitis in the majority of GERD patients and could be a therapeutic target in future treatment strategies.