The effect of cisapride in maintaining symptomatic remission in patients with gastro-oesophageal reflux disease

被引:24
作者
Hatlebakk, JG
Johnsson, F
Vilien, M
Carling, L
Wetterhus, S
Thogersen, T
机构
[1] CTY HOSP KONGSVINGER,DEPT MED,KONGSVINGER,NORWAY
[2] UNIV LUND HOSP,DEPT SURG,S-22185 LUND,SWEDEN
[3] CTY HOSP BOLLNAS,DEPT MED,BOLLNAS,SWEDEN
[4] CENT HOSP,DEPT MED,HOLBAEK,DENMARK
[5] CTY HOSP VARDE,DEPT MED,VARDE,DENMARK
关键词
cisapride; gastro-oesophageal reflux disease; maintenance therapy; reflux symptoms;
D O I
10.3109/00365529709002988
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Successful treatment of gastro-oesophageal reflux disease (GORD) has traditionally been assessed as healing of reflux oesophagitis, which may not be relevant in patients with moderate disease. In these patients symptom relief and patient satisfaction with therapy are of fundamental importance. Cisapride has well-documented prokinetic effects and may be well suited for long-term therapy of GORD, but its effectiveness in purely symptomatic treatment is unknown. We therefore compared two dosage regimens of cisapride with placebo over a period of 6 months in patients with evidence of gastrooesophageal reflux, initially treated with antisecretory medication, with regard to maintaining symptom relief and satisfaction with treatment. Methods: Five hundred and thirty-five patients with reflux oesophagitis grade 1 (n = 293) or 2 (n = 124) or with no reflux oesophagitis but pathologic 24-h pH-metry (n = 118) achieved satisfactory symptom relief with an H-2-receptor antagonist or proton pump inhibitor within 4-8 weeks. In a double-blind randomized, parallel-group study, they were then treated with cisapride, 20 mg at night or 20 mg twice daily, or placebo and followed up for a maximum period of 6 months. Relapse was defined as dissatisfaction with therapy or an average consumption of more than two antacid tablets a day. Results: Median time to relapse was 63 days for cisapride, 20 mg twice daily; 59 days for cisapride, 20 mg at night; and 49 days for placebo. Time to relapse was not significantly different (P = 0.09). Presence and grade of oesophagitis at base line, type of therapy before randomization, and pattern of non-reflux symptoms at base line did not influence these findings significantly. Conclusion: The study indicates that cisapride is of limited value in maintenance therapy of GORD in patients in whom symptom relief has been accomplished with potent antisecretory medication. This 'step-down' approach to therapy seems disadvantageous in the long-term therapy of GORD.
引用
收藏
页码:1100 / 1106
页数:7
相关论文
共 24 条
[11]   SYMPTOMATIC GASTROESOPHAGEAL REFLUX, ABNORMAL ESOPHAGEAL ACID EXPOSURE, AND MUCOSAL ACID SENSITIVITY ARE 3 SEPARATE, THOUGH RELATED, ASPECTS OF GASTROESOPHAGEAL REFLUX DISEASE [J].
HOWARD, PJ ;
MAHER, L ;
PRYDE, A ;
HEADING, RC .
GUT, 1991, 32 (02) :128-132
[12]   EPIDEMIOLOGY OF GASTROESOPHAGEAL REFLUX DISEASE [J].
HOWARD, PJ ;
HEADING, RC .
WORLD JOURNAL OF SURGERY, 1992, 16 (02) :288-293
[13]  
KIMMIG JM, 1995, ALIMENT PHARM THERAP, V9, P281
[14]  
LEPOUTRE L, 1987, GASTROENTEROLOGY, V92, P1501
[15]   SYMPTOMATIC GASTROESOPHAGEAL REFLUX - INCIDENCE AND PRECIPITATING FACTORS [J].
NEBEL, OT ;
FORNES, MF ;
CASTELL, DO .
AMERICAN JOURNAL OF DIGESTIVE DISEASES, 1976, 21 (11) :953-956
[16]   NOCTURNAL INTRAGASTRIC ACIDITY DURING AND AFTER A PERIOD OF DOSING WITH EITHER RANITIDINE OR OMEPRAZOLE [J].
PREWETT, EJ ;
HUDSON, M ;
NWOKOLO, CU ;
SAWYERR, AM ;
POUNDER, RE .
GASTROENTEROLOGY, 1991, 100 (04) :873-877
[17]  
SAVARY M, 1977, MANUEL ATLAS ENDOSCO
[18]   HEALING AND PREVENTION OF RELAPSE OF REFLUX ESOPHAGITIS BY CISAPRIDE [J].
TOUSSAINT, J ;
GOSSUIN, A ;
DERUYTTERE, M ;
HUBLE, F ;
DEVIS, G .
GUT, 1991, 32 (11) :1280-1285
[19]   EFFECT OF CISAPRIDE ON RELAPSE OF REFLUX ESOPHAGITIS, HEALED WITH AN ANTISECRETORY DRUG [J].
TYTGAT, GNJ ;
HANSEN, OJA ;
CARLING, L ;
DEGROOT, GH ;
GELDOF, H ;
GLISE, H ;
EFSKIND, P ;
ELSBORG, L ;
KARVONEN, AL ;
OHLIN, B ;
SOLHAUG, OH ;
VERMEERSCH, B .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1992, 27 (03) :175-183
[20]  
TYTGAT GNJ, 1995, ALIMENT PHARM THERAP, V9, P271