Meta-analysiscited by the Tayebat archiveabstract only checked A-PPI-05 standard review

PPIs and C. difficile – meta-analysis

Proton pump inhibitors therapy and risk of Clostridium difficile infection: Systematic review and meta-analysis.

Overview

Trifan A et al.. World J Gastroenterol 2017 · PMID 29085200 · DOI 10.3748/wjg.v23.i35.6500

PPI users had about twice the odds of C. difficile infection.

Does the study support the specific claim? Yes · Methodological quality: moderate

Original publication

Plain-language summary

Study explained simply
What did the researchers want to find out?

CDI risk with PPIs.

How was the study done?

Meta-analysis.

How many people, animals or samples were studied?

56 studies.

What was actually found?

Higher odds.

How large was the observed effect?

OR 1.99.

What do the results mean in everyday life?

Gut infection risk is a real concern.

What are the study's limitations?

Heterogeneity, publication bias.

What does it say about Elawady's specific claim?

Supports.

Do the results apply to Germany and Europe?

Applicable.

What can explicitly not be concluded from this study?

Exact size; causality.

Scientific in-depth review

1. Full reference

Authors
Trifan A, Stanciu C, Girleanu I, Stoica OC, Singeap AM, Maxim R, Chiriac SA, Ciobica A, Boiculese L
Journal
World J Gastroenterol
Year
2017
Identifier
PMID 29085200 DOI 10.3748/wjg.v23.i35.6500 · PMC5643276
Verification
verified – PubMed E-utilities efetch, 2026-10-25
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

Conflict-of-interest statement: The authors deny any conflict of interest.

2. Research question

Is PPI therapy associated with Clostridium difficile infection?

3. Study design and population

Study design
Meta-analysis – Systematic review and meta-analysis of case-control and cohort studies
Population

Adults in 56 observational studies

Country

Multinational

Period

1990–March 2017

Sample size

56 studies, 356,683 patients

Inclusion and exclusion criteria

see abstract

4. Methods and endpoints

Exposure / intervention

PPI use

Comparator

Non-use

Endpoints

CDI

Statistical methods

Random-effects pooled ORs; NOS quality; funnel plot

5. Actual results

Results

Pooled OR 1.99 (1.73–2.30); case-control 2.00; cohort 1.98; I² 85.4%; publication bias (P=0.002).

Absolute risks

not reported in abstract

Authors' conclusion

PPI use is associated with increased CDI risk; high-quality prospective studies needed to assess causality.

6. Strengths

  • Large number of studies
  • Consistent across subgroups

7. Weaknesses

  • Observational primary studies
  • High heterogeneity
  • Publication bias

8. Risk of bias

Orienting tool
AMSTAR 2
Type of assessment
simplified assessment (abstract only)
Full formal assessment
no
Overall risk of bias
some concerns
Rationale

AMSTAR-2-oriented: comprehensive search, but observational inputs, heterogeneity and publication bias.

9. Assessment of the statistical interpretation

See results.

10. Relevance to the specific claim

C-PPI-02.

11. Independent contrary findings

COMPASS: CDI doubled but n.s. with 13 events.

12. Transferability to Germany and Europe

High: European (Swedish, UK, Dutch, German) data show similar associations; PPIs are widely used in Germany.

13. Overall methodological judgement

Consistent association, causality probable but magnitude uncertain.

Multidimensional assessment
Multidimensional assessment
Authenticity of the sourceverified
Methodological qualitymoderate
Risk of biassome concerns
Precision of resultsmoderate
Directnessdirect
Reproducibilityreplicated
Consistency with the overall evidenceconsistent
Regional transferabilityhigh
Adequacy of the interpretation (by the archive)correctly reported

14. Open questions

15. Linked fact checks

Use by the Tayebat archive

Note: according to the archive, the studies were compiled by the archive operators. Whether Dr. Elawady himself cited this study is not established.

What the archive says about the study

Listed in the archive bibliography of the acid-blockers rule without its own interpretation; used implicitly to support the rule summary ('long-term suppression turns against the body: CKD, bacterial overgrowth, C. difficile, pneumonia, B12 and magnesium deficiency, hip fractures, microbiome change, excess mortality').

A. What was actually studied?

Is PPI therapy associated with Clostridium difficile infection?

B. What did the authors find?

Pooled OR 1.99 (1.73–2.30); case-control 2.00; cohort 1.98; I² 85.4%; publication bias (P=0.002).

C. What conclusions do the authors themselves draw?

PPI use is associated with increased CDI risk; high-quality prospective studies needed to assess causality.

D. What does the archive derive from it?

Supports the C. difficile part of the summary.

E. Is this derivation scientifically justified?

Yes as association; size uncertain.

Adequacy of the interpretation (by the archive)
correctly reported