Treatment of non-ulcer dyspepsia: a meta-analysis of placebo-controlled prospective studies

Citation
Hd. Allescher et al., Treatment of non-ulcer dyspepsia: a meta-analysis of placebo-controlled prospective studies, SC J GASTR, 36(9), 2001, pp. 934-941
Citations number
46
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
ISSN journal
00365521 → ACNP
Volume
36
Issue
9
Year of publication
2001
Pages
934 - 941
Database
ISI
SICI code
0036-5521(200109)36:9<934:TONDAM>2.0.ZU;2-X
Abstract
Background: Dyspeptic symptoms are commonly reported complaints in clinical practice and are mostly the result of functional disorders. Empirical trea tment with histamine H-2-receptor blockers or gastroprokinetics for 2-4 wee ks has frequently been proposed as first line management of these patients. The clinical trials which support the use of these agents, show a high var iation in clinical success rate and benefit of these treatments. Methods: T he available clinical trials were evaluated, pooled where appropriate and s ubjected to a meta-analysis with the principal goal to provide valid treatm ent recommendations for patients with non-ulcer dyspepsia. In the present m eta-analysis 19 studies on gastroprokinetics (cisapride, domperidone) and 1 0 studies on histamine H-2-receptor antagonists (cimetidine, ranitidine) we re included. Results: Based on these studies, a total of 1540 patients were evaluated for histamine H-2-receptor antagonists (verum n = 786, placebo n = 754) and 1235 patients for gastroprokinetics (verum n = 616, placebo n = 619). The probability for treatment success compared to placebo was 0.2026 (0.1261; 0.2791) for histamine H-2-receptor antagonists and 0.4029 (0.3042 ; 0.5069) for gastroprokinetics. Conclusions: Based on these data both trea tments are significantly more effective than placebo in the symptomatic tre atment of non-ulcer dyspepsia, with gastroprokinetics (cisapride, domperido ne) being more effective than histamine H-2-receptor antagonists (cimetidin e, ranitidine).