The effect of a therapeutic trial of high-dose rabeprazole on symptom response of patients with non-cardiac chest pain:: a randomized, double-blind, placebo-controlled, crossover trial

被引:60
作者
Dickman, R
Emmons, S
Cui, H
Sewell, J
Hernández, D
Esquivel, RF
Fass, R
机构
[1] So Arizona VA Hlth Care Syst, GI Sect, Neuroenter Clin Res Grp, Dept Med, Tucson, AZ 85723 USA
[2] Univ Arizona, Sch Med, Tucson, AZ USA
[3] Univ Arizona, Ctr Hlth Sci, Arizona Canc Ctr, Dept Biometry, Tucson, AZ USA
关键词
D O I
10.1111/j.1365-2036.2005.02620.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Therapeutic trials with high-dose lansoprazole and omeprazole have been shown to be sensitive clinical tools for diagnosing patients with gastro-oesophageal reflux disease-related non-cardiac chest pain. Aim: To determine the clinical value of a therapeutic trial of high-dose rabeprazole over 7 days in detecting patients with gastro-oesophageal reflux disease-related non-cardiac chest pain. Methods: Double-blind, randomized, placebo-controlled, crossover study. Patients referred by a cardiologist after a comprehensive cardiac work-up were enrolled into the study. Oesophageal mucosal disease was determined by upper endoscopy and 24-h oesophageal pH monitoring assessed acid exposure. Patients were then randomized to either placebo or rabeprazole 20 mg AM and 20 mg pm for 7 days. After a washout period of 1 week, patients crossed over to the other arm of the study for an additional 7 days. Patients completed a daily diary assessing severity and frequency of chest pain throughout the baseline, treatment and wash-out periods. The rabeprazole therapeutic trial was considered as a diagnostic tool, if chest pain scores improved >= 50% from baseline. Results: Of the 35 patients enrolled, 16 (46%) were diagnosed as gastro-oesophageal reflux disease-positive and 19 (54%) as gastro-oesophageal reflux disease-negative. Of the gastro-oesophageal reflux disease-positive patients, 12 of 16 (75%) had a significant symptom improvement on rabeprazole when compared with 3 of 16 (19%) on placebo (P=0.029). Of the gastro-oesophageal reflux disease-negative group, only two of 19 (11%) improved significantly on the medication and four of 19 (21%) on placebo (P=0.6599). The calculated sensitivity and specificity of the rabeprazole therapeutic trial was 75% and 90%, respectively. Conclusions: A rabeprazole therapeutic trial is highly sensitive and specific for diagnosing gastro-oesophageal reflux disease-related non-cardiac chest pain patients.
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页码:547 / 555
页数:9
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