Meta-analysiscited by the Tayebat archiveabstract only checked A-PPI-06 standard review

PPIs and C. difficile in hospital

Clostridium difficile-associated diarrhea and proton pump inhibitor therapy: a meta-analysis.

Overview

Janarthanan S et al.. Am J Gastroenterol 2012 · PMID 22710578 · DOI 10.1038/ajg.2012.179

Pooled risk about 1.7-fold higher with PPIs.

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?

CDAD with PPIs.

How was the study done?

Meta-analysis.

How many people, animals or samples were studied?

23 studies.

What was actually found?

Higher incidence.

How large was the observed effect?

RR ≈1.69.

What do the results mean in everyday life?

Infection risk.

What are the study's limitations?

Observational; overlap.

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?

Causation.

Scientific in-depth review

1. Full reference

Authors
Janarthanan S, Ditah I, Adler DG, Ehrinpreis MN
Journal
Am J Gastroenterol
Year
2012
Identifier
PMID 22710578 DOI 10.1038/ajg.2012.179
Verification
verified – PubMed E-utilities efetch, 2026-10-25
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

not stated in abstract

2. Research question

Association between PPIs and C. difficile-associated diarrhoea in hospitalised patients

3. Study design and population

Study design
Meta-analysis – Meta-analysis of observational studies
Population

Hospitalised patients

Country

Multinational

Period

1990–2010

Sample size

23 studies, ~300,000 patients

Inclusion and exclusion criteria

see abstract

4. Methods and endpoints

Exposure / intervention

PPI use

Comparator

Non-use

Endpoints

CDAD

Statistical methods

Random-effects; Begg/Egger; trim-and-fill

5. Actual results

Results

Summary risk estimate 1.69 (1.395–1.974); cohort 2.31 (1.72–3.10); case-control 1.48 (1.25–1.75).

Absolute risks

not reported in abstract

Authors' conclusion

Sufficient evidence to suggest PPIs increase CDAD incidence; more prudent use recommended.

6. Strengths

  • Hospital focus

7. Weaknesses

  • Observational inputs
  • Only Medline/PubMed searched
  • Overlaps with A-PPI-05

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

Overlapping primary studies with A-PPI-05; not independent confirmation.

9. Assessment of the statistical interpretation

See results.

10. Relevance to the specific claim

C-PPI-02.

11. Independent contrary findings

Overlap with A-PPI-05.

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 with A-PPI-05; not independent.

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?

Association between PPIs and C. difficile-associated diarrhoea in hospitalised patients

B. What did the authors find?

Summary risk estimate 1.69 (1.395–1.974); cohort 2.31 (1.72–3.10); case-control 1.48 (1.25–1.75).

C. What conclusions do the authors themselves draw?

Sufficient evidence to suggest PPIs increase CDAD incidence; more prudent use recommended.

D. What does the archive derive from it?

Supports C. difficile claim.

E. Is this derivation scientifically justified?

Yes as association.

Adequacy of the interpretation (by the archive)
correctly reported