Cohort studyindependent cross-checkabstract checked★ key study I-LEG-109 standard review

Antibiotics and haemolysis in G6PD deficiency

Quinolones and risk of haemolysis in patients with glucose-6-phosphate dehydrogenase deficiency: a nationwide retrospective active-comparator cohort study.

Overview

Lavon O et al.. J Antimicrob Chemother 2026 · PMID 42522747 · DOI 10.1093/jac/dkag265

In 465,083 antibiotic courses, coded haemolysis occurred after fewer than 1 in 1,000 courses, with no clear excess for quinolones.

Does the study support the specific claim? No · Methodological quality: moderate

Original publication

Plain-language summary

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

Test whether quinolones cause haemolysis in G6PD deficiency.

How was the study done?

National database cohort vs penicillins.

How many people, animals or samples were studied?

64,861 patients.

What was actually found?

No clear increase.

How large was the observed effect?

aOR 1.29 (0.92-1.77).

What do the results mean in everyday life?

Ordinary antibiotics rarely cause haemolysis in G6PD deficiency.

What are the study's limitations?

Coded data; abstract only.

What does it say about Elawady's specific claim?

Contradicts the class-wide antibiotic claim.

Do the results apply to Germany and Europe?

Applicable.

What can explicitly not be concluded from this study?

It cannot exclude rare reactions in severe variants.

Scientific in-depth review

1. Full reference

Authors
Lavon O et al.
Journal
J Antimicrob Chemother
Year
2026
Identifier
PMID 42522747 DOI 10.1093/jac/dkag265 · PMC13416391
Verification
verified – PubMed efetch 2026-10-26 + Crossref works API
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

Not stated in abstract.

2. Research question

Are oral quinolone dispensations associated with haemolysis compared with penicillins in G6PD-deficient patients?

3. Study design and population

Study design
Cohort study – Nationwide retrospective active-comparator cohort (Clalit Health Services database)
Population

Patients with an ICD-coded diagnosis of G6PD deficiency receiving outpatient oral quinolone or penicillin

Country

Israel

Period

2010-2023

Sample size

465,083 dispensations among 64,861 patients

Inclusion and exclusion criteria

>=1 ICD code for G6PD deficiency; outpatient oral dispensation.

4. Methods and endpoints

Exposure / intervention

Oral quinolone

Comparator

Oral penicillin

Endpoints

Haemolysis-related diagnosis code within 30 days; jaundice; laboratory markers

Statistical methods

Logistic models adjusted for age, sex, Charlson index; within-patient subcohort

5. Actual results

Results

Coded haemolysis after 52/65,906 quinolone (0.079%) vs 198/399,177 penicillin episodes (0.050%); aOR 1.29 (95% CI 0.92-1.77). Age <=18 y: 5/8,865 vs 91/160,423, aOR 1.02 (0.36-2.26). Within-patient: 0.065% vs 0.061%, aOR 0.95 (0.65-1.37).

Absolute risks

Below 0.1% of courses in both groups (recalculated crude risk difference 0.029 percentage points).

Authors' conclusion

No detectable major increase in coded haemolysis with quinolones; small risks or risks in severe deficiency/young children not excluded.

6. Strengths

  • Very large sample
  • Active comparator
  • Within-patient analysis

7. Weaknesses

  • Coded outcomes
  • Variant severity unknown
  • Abstract only

8. Risk of bias

Orienting tool
ROBINS-I
Type of assessment
simplified assessment (abstract only)
Full formal assessment
no
Overall risk of bias
some concerns
Rationale

Outcome misclassification; confounding by indication partly addressed.

9. Assessment of the statistical interpretation

CI approximately log-symmetric; crude NNH would exceed 3,000 courses if causal (stats/C-LEG-05_lavon2026_quinolones.py).

10. Relevance to the specific claim

Shows that common antibiotics (penicillins, quinolones) are rarely followed by haemolysis in G6PD deficiency; contradicts the class-wide antibiotic claim of C-LEG-05.

11. Independent contrary findings

Some hospital leaflets list quinolones as drugs to avoid (I-LEG-110).

12. Transferability to Germany and Europe

Applicable to Mediterranean G6PD variants.

13. Overall methodological judgement

Reassuring real-world data on antibiotics; supports not withholding needed antibiotics.

Multidimensional assessment
Multidimensional assessment
Authenticity of the sourceverified
Methodological qualitymoderate
Risk of biassome concerns
Precision of resultsmoderate
Directnessdirect
Reproducibilitynot replicated
Consistency with the overall evidenceconsistent
Regional transferabilitymoderate
Adequacy of the interpretation (by the archive)not applicable

14. Open questions

Risk in severe variants and infants.

15. Linked fact checks