Randomised controlled trialindependent cross-checkfull text checked★ key study I-PPI-106 in-depth review
Most people could stop unnecessary acid blockers
An App-Based Proton Pump Inhibitor Discontinuation Tool: A Multicentre, Open-Label, Randomised Superiority Trial.
Overview
Koggel LM et al.. United European Gastroenterol J 2026 · PMID 42894466 · DOI 10.1002/ueg2.70297
Among outpatients without a reason for long-term PPIs, 86% using an app and 64% using a leaflet had stopped after 2 months.
Does the study support the specific claim? No · Methodological quality: moderate
Plain-language summary
Study explained simply
- What did the researchers want to find out?
Help people stop unneeded PPIs.
- How was the study done?
Randomised trial, app vs brochure.
- How many people, animals or samples were studied?
163 Dutch outpatients.
- What was actually found?
86% vs 64% stopped; few side effects.
- How large was the observed effect?
RR 1.34 (1.11-1.61).
- What do the results mean in everyday life?
Stopping is usually possible with good information.
- What are the study's limitations?
Short follow-up; self-report.
- What does it say about Elawady's specific claim?
Contradicts 'cannot stop'.
- Do the results apply to Germany and Europe?
Directly applicable.
- What can explicitly not be concluded from this study?
Cannot tell how many restart later.
Scientific in-depth review
1. Full reference
- Authors
- Koggel LM et al.
- Journal
- United European Gastroenterol J
- Year
- 2026
- Identifier
- PMID 42894466 DOI 10.1002/ueg2.70297
- Verification
- verified – PubMed efetch 2026-10-26 + Crossref 2026-10-26
- Retracted
- no
- Corrections
- none
- Extent checked
- full text
- Conflicts of interest and funding
No sponsor or funder; one author co-founded the app company; others report industry funding unrelated (full text)
2. Research question
Does an app-based discontinuation tool improve stopping of PPIs used without a chronic indication?
3. Study design and population
- Study design
- Randomised controlled trial – Multicentre, open-label, adaptive randomised superiority trial
- Population
Adults using daily PPI >=4 weeks without chronic indication (Dutch GP guideline), outpatients of 3 Dutch hospitals
- Country
Netherlands
- Period
May 2022 - March 2023
- Sample size
174 randomised; 163 analysed
- Inclusion and exclusion criteria
Excluded if physician deemed PPI necessary, prior upper GI surgery, no smartphone, limited life expectancy
4. Methods and endpoints
- Exposure / intervention
App with information and tapering guidance
- Comparator
Information brochure
- Endpoints
Discontinuation at 2 months (<=1 tablet in prior 14 days); adverse events
- Statistical methods
Risk ratio; adaptive sample size with Pocock-type correction
5. Actual results
- Results
Discontinued: 66/77 (86%) app vs 55/86 (64%) brochure; RR 1.34 (1.11-1.61). Adverse events 18/121 (15%) of those who stopped vs 6/42 (14%) who did not; 4/121 (3%) possibly attributable to discontinuation.
- Absolute risks
64-86% stopped within 2 months; 3% had adverse events possibly due to stopping
- Authors' conclusion
An app-based intervention significantly improves discontinuation of inappropriate PPI use compared with a brochure.
6. Strengths
- Randomised
- Patients without indication (target group)
- Full text read
7. Weaknesses
- Open label, self-reported outcome
- Only 2-month follow-up
- Mid-trial sample-size adaptation
- App developer among authors
8. Risk of bias
- Orienting tool
- RoB 2
- Type of assessment
- simplified assessment (abstract only)
- Full formal assessment
- no
- Overall risk of bias
- some concerns
- Rationale
Self-reported outcome, unblinded, sample size adaptation.
9. Assessment of the statistical interpretation
Recomputed RR 1.34 (1.12-1.61) matches; Wilson CI for brochure arm 53%-73% (stats/C-PPI-06_07_rebound_discontinuation.py).
10. Relevance to the specific claim
Direct evidence that most people taking PPIs without an indication can stop within 2 months, even with only a brochure.
11. Independent contrary findings
Long-term relapse unknown.
12. Transferability to Germany and Europe
Directly applicable to Europe.
13. Overall methodological judgement
Strong contradiction of 'one cannot stop'.
| Multidimensional assessment | |
|---|---|
| Authenticity of the source | verified |
| Methodological quality | moderate |
| Risk of bias | some concerns |
| Precision of results | moderate |
| Directness | direct |
| Reproducibility | not replicated |
| Consistency with the overall evidence | consistent |
| Regional transferability | high |
| Adequacy of the interpretation (by the archive) | not applicable |
14. Open questions
Sustained discontinuation beyond 2 months.
15. Linked fact checks
- PPIs create dependency: the drug 'manufactures the disease it claims to treat', so that a short course for a passing complaint turns into chronic dependence and one 'cannot stop'. – Studies contradicting or limiting the claim
- PPIs are widely prescribed without a real indication (for example by doctors of other specialties to 'protect the stomach') and are now sold freely. – Studies supporting the claim