Prevention of nonsteroidal anti-inflammatory drug-induced small-intestinal injury by prostaglandin: a pilot randomized controlled trial evaluated by capsule endoscopy

被引:105
作者
Fujimori, Shunji [1 ]
Seo, Tsuguhiko [1 ]
Gudis, Katya [1 ]
Ehara, Akihito [1 ]
Kobayashi, Tsuyoshi [1 ]
Mitsui, Keigo [1 ]
Yonezawa, Masaoki [1 ]
Tanaka, Shu [1 ]
Tatsuguchi, Atsushi [1 ]
Sakamoto, Choitsu [1 ]
机构
[1] Nippon Med Sch, Div Gastroenterol, Dept Internal Med, Bunkyo Ku, Tokyo 1138603, Japan
关键词
PLACEBO-CONTROLLED TRIAL; INDUCED GASTRIC-ULCER; DOUBLE-BLIND; GASTROINTESTINAL COMPLICATIONS; RHEUMATOID-ARTHRITIS; HEALTHY-SUBJECTS; PLUS OMEPRAZOLE; MUCOSAL INJURY; MISOPROSTOL; NSAID;
D O I
10.1016/j.gie.2008.08.017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: There is no known preventive agent against nonsteroidal anti-inflammatory drug (NSAID) induced small-intestinal injury. Objective: To evaluate by capsule endoscopy whether coadministration of prostaglandin (PG) can prevent small-intestinal damage induced by short-term NSAID treatment. Design: Single-blind, randomized, controlled trial. Setting: All procedures were performed at Nippon Medical School. Subjects: Thirty-four healthy male Volunteers. Methods: All subjects were randomly assigned to 2 groups: an NSAID-control group, who underwent NSAID (diclofenac sodium, 25 mg 3 times daily) and omeprazole (20 mg once daily) treatment, and an NSAID-PG group, who received PG (misoprostol, 200 mu g 3 times daily) in addition to the same NSAID-omeprazole treatment. Eligible Subjects, 15 per group, underwent capsule endoscopy before and 14 days after treatment. Main Outcome Measurements: The number of mucosal breaks at capsule endoscopy. Results: NSAID treatment significantly increased the mean (SD) number of mucosal breaks per subject, from a basal level of 0.1 +/- 0.3 up to 2.9 +/- 6.3 lesions in the NSAID-control group (P = .012). In contrast, there was no significant change in the mean number of mucosal breaks before and after PG cotreatment (P = 0.42). Thus, the mean number of posttreatment mucosal breaks per subject was significantly higher in the NSAID-control group than in the NSAID-PG group (P = .028). There was a significant increase in the percentage of subjects in the NSAID-control group, with at least I mucosal break after treatment (from 6.7% to 53.3%), whereas there was no change in the incidence of mucosal breaks in the NSAID-PG group, which remained at 13.3%. (P = .002). Limitations: Single-center, open-label study. Conclusions: PG cotherapy reduced the incidence of small-intestinal lesions induced by a 2-week administration of diclofenac sodium. (Gastrointest Endosc 2009;69:1339-46.)
引用
收藏
页码:1339 / 1346
页数:8
相关论文
共 26 条
[1]   MISOPROSTOL COMPARED WITH SUCRALFATE IN THE PREVENTION OF NONSTEROIDAL ANTIINFLAMMATORY DRUG-INDUCED GASTRIC-ULCER - A RANDOMIZED, CONTROLLED TRIAL [J].
AGRAWAL, NM ;
ROTH, S ;
GRAHAM, DY ;
WHITE, RH ;
GERMAIN, B ;
BROWN, JA ;
STROMATT, SC .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (03) :195-200
[2]   GASTROINTESTINAL DAMAGE ASSOCIATED WITH THE USE OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS [J].
ALLISON, MC ;
HOWATSON, AG ;
TORRANCE, CJ ;
LEE, FD ;
RUSSELL, RI .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (11) :749-754
[3]   A randomized trial of rofecoxib for the chemoprevention of colorectal adenomas [J].
Baron, John A. ;
Sandler, Robert S. ;
Bresalier, Robert S. ;
Quan, Hui ;
Riddell, Robert ;
Lanas, Angel ;
Bolognese, James A. ;
Oxenius, Bettina ;
Horgan, Kevin ;
Loftus, Susan ;
Morton, Dion G. .
GASTROENTEROLOGY, 2006, 131 (06) :1674-1682
[4]   MISOPROSTOL REDUCES INDOMETHACIN-INDUCED CHANGES IN HUMAN SMALL INTESTINAL PERMEABILITY [J].
BJARNASON, I ;
SMETHURST, P ;
FENN, CG ;
LEE, CE ;
MENZIES, TS ;
LEVI, AJ .
DIGESTIVE DISEASES AND SCIENCES, 1989, 34 (03) :407-411
[5]   SIDE-EFFECTS OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS ON THE SMALL AND LARGE-INTESTINE IN HUMANS [J].
BJARNASON, I ;
HAYLLAR, J ;
MACPHERSON, AJ ;
RUSSELL, AS .
GASTROENTEROLOGY, 1993, 104 (06) :1832-1847
[6]   Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[7]   Review article: prevention of non-steroidal anti-inflammatory drug gastrointestinal complications - review and recommendations based on risk assessment [J].
Chan, FKL ;
Graham, DY .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 19 (10) :1051-1061
[8]   NONSTEROIDAL ANTIINFLAMMATORY DRUG-ASSOCIATED GASTROPATHY - INCIDENCE AND RISK FACTOR MODELS [J].
FRIES, JF ;
WILLIAMS, CA ;
BLOCH, DA ;
MICHEL, BA .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 (03) :213-222
[9]   Diagnosis and treatment of obscure gastrointestinal bleeding using combined capsule endoscopy and double balloon endoscopy: 1-year follow-up study [J].
Fujimori, S. ;
Seo, T. ;
Gudis, K. ;
Tanaka, S. ;
Mitsui, K. ;
Kobayashi, T. ;
Ehara, A. ;
Yonezawa, M. ;
Tatsuguchi, A. ;
Sakamoto, C. .
ENDOSCOPY, 2007, 39 (12) :1053-1058
[10]   Small bowel mucosal injury is reduced in healthy subjects treated with celecoxib compared with ibuprofen plus omeprazole, as assessed by video capsule endoscopy [J].
Goldstein, J. L. ;
Eisen, G. M. ;
Lewis, B. ;
Gralnek, I. M. ;
Aisenberg, J. ;
Bhadra, P. ;
Berger, M. F. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2007, 25 (10) :1211-1222