Evidence map›Paper›PMID 42472834›Full record

SynthesisCritical care (London, England)2026

Sodium bicarbonate therapy in severe metabolic acidemia: an individual patient data meta-analysis of the BICAR-ICU and BICAR-ICU2 trials.

Maxime Fosset, Joris Pensier, Matthieu Jabaudon, Laurent Bitker, Audrey De Jong, Gerald Chanques, Helena Huguet, Nicolas Molinari, Samir Jaber, Boris Jung

Abstract readMeta-Analysis
In one paragraph

Synthesis in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Maxime Fosset *Medical Intensive Care Unit, CHU Montpellier, 191, Avenue du Doyen Gaston Giraud, Montpellier, Cedex 5, 34295, France.
Joris Pensier *Department of Anesthesia and Intensive Care unit, St-Eloi Hospital, Regional University Hospital of Montpellier, University of Montpellier, CEDEX 5, Montpellier, France.
Matthieu JabaudonDepartment of Perioperative Medicine, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Laurent BitkerMedical Intensive Care Unit, La Croix Rousse Hospital, Lyon, France.
Audrey De JongDepartment of Anesthesia and Intensive Care unit, St-Eloi Hospital, Regional University Hospital of Montpellier, University of Montpellier, CEDEX 5, Montpellier, France.
Gerald ChanquesDepartment of Anesthesia and Intensive Care unit, St-Eloi Hospital, Regional University Hospital of Montpellier, University of Montpellier, CEDEX 5, Montpellier, France.
Helena HuguetEpidemiology and Clinical Research Department, Montpellier University Hospital, Université de Montpellier, Montpellier, France.
Nicolas MolinariIDESP, Univ Montpellier, INSERM, PreMEdical, INRIA, CHU Montpellier, Montpellier, France, University of Montpellier, Montpellier, 34295, France.
Samir JaberDepartment of Anesthesia and Intensive Care unit, St-Eloi Hospital, Regional University Hospital of Montpellier, University of Montpellier, CEDEX 5, Montpellier, France.
Boris JungMedical Intensive Care Unit, CHU Montpellier, 191, Avenue du Doyen Gaston Giraud, Montpellier, Cedex 5, 34295, France. b-jung@chu-montpellier.fr.ORCID 0000-0003-2522-1531

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTwo randomized trials (BICAR-ICU and BICAR-ICU2) evaluated intravenous sodium bicarbonate therapy in patients with severe metabolic acidemia but yielded inconclusive results. We performed an individual patient data meta-analysis to assess its effects on 90-day mortality and renal replacement therapy (RRT) use, and search for heterogeneity of treatment effects across prespecified subgroups.

methodsWe performed an individual patient data meta-analysis of the BICAR-ICU and BICAR-ICU2 trials, including adults with severe metabolic acidemia (pH ≤ 7.20). Patients were randomized to receive intravenous sodium bicarbonate titrated to a pH ≥ 7.30 or no sodium bicarbonate. The primary outcome was 90-day mortality. Secondary outcomes included RRT initiation and dialysis-free days. Prespecified subgroup analyses explored treatment-effect heterogeneity by acidemia depth (pH ≤ 7.10 vs. > 7.10), severe acute kidney injury (AKI) status, and serum lactate (< 2mmol/L vs. ≥2mmol/L).

resultsA total of 1,016 patients was included (509 sodium bicarbonate, 507 control). Sodium bicarbonate therapy did not significantly reduce 90-day mortality compared to control (58.3% vs. 60.6%; risk ratio [RR], 0.96; 95%CI, 0.86-1.07; p = 0.51). However, it significantly reduced RRT initiation (34.8% vs. 50.7%; RR, 0.69; 95%CI, 0.60-0.79; p < 0.001, number needed to treat: 6.3) and increased dialysis-free days (incidence rate ratio, 1.10; 95%CI, 1.06-1.14; p < 0.001). A significant interaction was observed with acidemia depth (p-for-interaction = 0.006): in patients with pH ≤ 7.10, sodium bicarbonate reduced 90-day mortality (RR, 0.80; 95%CI, 0.68-0.93; p = 0.004); no benefit was seen with pH > 7.10 (RR, 1.05; 95%CI, 0.92-1.21; p = 0.47). No significant interactions were observed for severe AKI status (p-for-interaction = 0.11) nor serum lactate (p-for-interaction = 0.22).

conclusionsSodium bicarbonate therapy did not reduce overall 90-day mortality but decreased RRT use and suggested a mortality benefit in patients with the most profound acidemia (pH ≤ 7.10). These findings invite a reconsideration of current paradigms, suggesting timely correction of severe metabolic acidemia to avoid RRT in some patients.

Indexed as

AcidosisSodium BicarbonateAgedFemaleHumansIntensive Care UnitsMaleMiddle AgedRandomized Controlled Trials as TopicRenal Replacement TherapySodium BicarbonateAcidemiaHeterogeneity of treatment effectICUMeta-analysisSodium bicarbonate

Identifiers

PMID42472834
PMCPMC13393698

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.