Minimal change oesophagitis: a disease with characteristic differences to erosive oesophagitis

被引:49
作者
Nakamura, T
Shirakawa, K
Masuyama, H
Sugaya, H
Hiraishi, H
Terano, A
机构
[1] Dokkyo Univ, Sch Med, Dept Endoscopy, Mibu, Tochigi 3210293, Japan
[2] Dokkyo Univ, Sch Med, Dept Gastroenterol, Mibu, Tochigi, Japan
关键词
D O I
10.1111/j.1365-2036.2005.02469.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The majority of gastro-ocsophageal reflux disease (GERD) seems to be non-erosive reflux disease. Nonerosive reflux disease includes minimal change oesophagitis (whitish or reddish, oedematous change and erosion that is not regarded as mucosal break) and no endoscopic abnormalities. Aim: To investigate the accurate proportion of those with minimal change oesophagitis and to clarify its characteristics. In addition, we evaluated the effect of famotidine (40 mg/ day) in those with minimal change. Methods: Prospective endoscopic assessment was performed for consecutive 606 out-patients. Of the 582 patients suitable for analysis, 347 were non-treated. The latter were divided into those with erosive GERD or minimal change, and their endoscopic findings and characteristics were compared. Results: Among 3 4 7 non-treated patients, 8 8 (25%) had erosive GERD and 249 (72%) had minimal change. Compared with patients who have erosive GERD and those with minimal change, the latter were less likely to have hiatal hernia or bile reflux, but more likely to have gastric atrophy. Symptomatic patients (n = 55) with minimal change oesophagitis were more likely to have hiatal hernia than those who were asymptomatic (n= 194). Most patients preferred taking famotidine on-demand, during a 4-week follow-up period. Conclusions: Most non-erosive reflux disease can be classified as minimal change oesophagitis, and that have different characteristics from erosive GERD. On-demand famotidine may be a suitable alternative treatment for patients with minimal change disease.
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页码:19 / 26
页数:8
相关论文
共 21 条
[1]   The endoscopic assessment of esophagitis: A progress report on observer agreement [J].
Armstrong, D ;
Bennett, JR ;
Blum, AL ;
Dent, J ;
deDombal, FT ;
Galmiche, JP ;
Lundell, L ;
Margulies, M ;
Richter, JE ;
Spechler, SJ ;
Tytgat, GNJ ;
Wallin, L .
GASTROENTEROLOGY, 1996, 111 (01) :85-92
[2]  
Avidan B, 2001, AM J GASTROENTEROL, V96, P41
[3]  
Carlsson R, 1998, SCAND J GASTROENTERO, V33, P1023
[4]   Updated guidelines for the diagnosis and treatment of Gastroesophageal reflux disease [J].
DeVault, KR ;
Castell, DO .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (01) :190-200
[5]   There is no difference in the disease severity of gastro-oesophageal reflux disease between patients infected and not infected with Helicobacter pylori [J].
Fallone, CA ;
Barkun, AN ;
Mayrand, S ;
Wakil, G ;
Friedman, G ;
Szilagyi, A ;
Wheeler, C ;
Ross, D .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 20 (07) :761-768
[6]   Report of the Asia-Pacific consensus on the management of gastroesophageal reflux disease [J].
Fock, KM ;
Talley, N ;
Hunt, R ;
Fass, R ;
Nandurkar, S ;
Lam, SK ;
Goh, KL ;
Sollano, J .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2004, 19 (04) :357-367
[7]  
Fujimoto K, 2003, J GASTROENTEROL, V38, P3
[8]   Proportion of reflux esophagitis in 6010 Japanese adults: prospective evaluation by endoscopy [J].
Furukawa, N ;
Iwakiri, R ;
Koyama, T ;
Okamoto, K ;
Yoshida, T ;
Kashiwagi, Y ;
Ohyama, T ;
Sakata, H ;
Fujimoto, K .
JOURNAL OF GASTROENTEROLOGY, 1999, 34 (04) :441-444
[9]   Impact of hiatal hernia on histological pattern of non-erosive reflux disease [J].
Gatopoulou, A ;
Mimidis, K ;
Giatromanolaki, A ;
Papadopoulos, V ;
Polychronidis, A ;
Lyratzopoulos, N ;
Sivridis, E ;
Minopoulos, G .
BMC GASTROENTEROLOGY, 2005, 5 (1)
[10]   Review article: The role of the hiatus hernia in gastro-oesophageal reflux disease [J].
Gordon, C ;
Kang, JY ;
Neild, PJ ;
Maxwell, JD .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 20 (07) :719-732