Published · Updated · 2 min read
Metamizole versus ibuprofen after cesarean delivery: no pain difference detected, renal safety uncertain
What it means for practice
In women with preeclampsia with severe features, the trial did not establish an advantage of metamizole over ibuprofen for pain or blood pressure. These findings should not be interpreted as evidence of equivalence or equal renal safety.
Summary
A quadruple-blind randomized trial compared metamizole with ibuprofen for analgesia after cesarean delivery in women with preeclampsia with severe features. The trial was conducted at a tertiary maternity hospital in northeastern Brazil. It assessed analgesic effectiveness and short-term safety, particularly blood-pressure trajectory and renal function.
Of 74 participants, 38 received oral metamizole 1 g and 36 received ibuprofen 400 mg every 6 hours for up to 5 days. Intravenous tramadol was available for rescue analgesia. The co-primary outcomes were postoperative pain category on the visual analogue scale and acute kidney injury.
Key findings
- The distribution of pain categories did not differ between groups on day 1 (exact P=.45) or day 2 (exact P=.55).
- On day 1, rescue analgesia was required by 18.4% of participants receiving metamizole versus 38.9% receiving ibuprofen; the risk difference was −20.5 percentage points (95% confidence interval −39.1 to 0.1).
- Acute kidney injury occurred in 3 of 38 women (7.9%) versus 1 of 36 (2.8%); the risk ratio was 2.84 (95% confidence interval 0.31–26.08; Fisher P=.62).
- No group-by-time interaction was detected for systolic or diastolic blood pressure. Severe hypertensive episodes were rare in both groups.
Limitations: the trial was not designed to establish equivalence or non-inferiority. The acute kidney injury estimate was highly imprecise; comparative renal safety remains uncertain and requires adequately powered studies.
Source
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Pordeus ACB, Katz L, Maia MT, et al. Metamizole (dipyrone) versus ibuprofen for post-cesarean analgesia in women with preeclampsia with severe features: a quadruple-blind, randomized, active-comparator trial. Am J Obstet Gynecol MFM. 2026:102162. doi:10.1016/j.ajogmf.2026.102162
PubMed 42966477 DOI 10.1016/j.ajogmf.2026.102162 Original: pubmed.ncbi.nlm.nih.gov
Reviewed by: DrugCard editorial team ·
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