Effect of population screening and treatment for Helicobacter pylori on dyspepsia and quality of life in the community: a randomised controlled trial
Infection with Helicobacter pylori is the main cause of peptic-ulcer disease. Treatment of this infection might lower the prevalence of dyspepsia in the community and improve quality of life. We investigated this possibility in a double-blind randomised controlled trial. Individuals aged 40–49 years...
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Veröffentlicht in: | The Lancet (British edition) 2000-05, Vol.355 (9216), p.1665-1669 |
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Sprache: | eng |
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Zusammenfassung: | Infection with
Helicobacter pylori is the main cause of peptic-ulcer disease. Treatment of this infection might lower the prevalence of dyspepsia in the community and improve quality of life. We investigated this possibility in a double-blind randomised controlled trial.
Individuals aged 40–49 years were randomly selected from the lists of 36 primary-care centres. A researcher interviewed participants with a validated dyspepsia questionnaire and the psychological general wellbeing index (PGWB).
H pylori status was assessed by the carbon-13-labelled urea breath test. Infected participants were randomly assigned active treatment (omeprazole 20 mg, clarithromycin 250 mg, and tinidazole 500 mg, each twice daily for 7 days) or identical placebo. Participants were followed up at 6 months and 2 years.
Of 32 929 individuals invited, 8455 attended and were eligible; 2324 were positive for
H pylori and were assigned active treatment (1161) or placebo (1163). 1773 (76%) returned at 2 years. Dyspepsia or symptoms of gastro-oesophageal reflux were reported in 247 (28%) of 880 in the treatment group and 291 (33%) of 871 in the placebo group (absolute-risk reduction 5% [95% CI 1–10]).
H pylori treatment had no significant effect on quality of life (mean difference in PGWB score between groups 0·86 [−0·33 to 2·05]).
Community screening and treatment for
H pylori produced only a 5% reduction in dyspepsia. This small benefit had no impact on quality of life. |
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ISSN: | 0140-6736 1474-547X |
DOI: | 10.1016/S0140-6736(00)02236-4 |