Evidence map›Paper›PMID 42820515›Full record

Trial reportCritical care science2026

A secondary analysis of the SODa-BIC randomized clinical trial using multiple hierarchical composite outcomes.

Humphrey G M Walker, Alastair Brown, Kyle C White, Mairead McNamara, D Jamie Cooper, Tomoko Fujii, Alisa M Higgins, Carol L Hodgson, Leanlove Navarra, Alistair Nichol and 19 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Critical care science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors.

Humphrey G M WalkerDepartment of Critical Care, St Vincent's Hospital - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-3502-2288
Alastair BrownDepartment of Critical Care, St Vincent's Hospital - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-3137-4895
Kyle C WhiteSchool of Clinical Sciences, Faculty of Health, Queensland University of Technology - Brisbane, QLD, Australia.ORCID http://orcid.org/0000-0002-0129-8297
Mairead McNamaraAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.
D Jamie CooperAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-5872-9051
Tomoko FujiiAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-3854-4081
Alisa M HigginsAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-8295-7559
Carol L HodgsonDepartment of Critical Care, University of Melbourne - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-9002-2075
Leanlove NavarraIntensive Care Unit, Wellington Hospital - Wellington, New Zealand.ORCID http://orcid.org/0009-0000-6621-7016
Alistair NicholAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-4689-1238
Sandra PeakeAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-6682-7973
Alvaro Rea-NetoDepartment of Clinical Medicine, Universidade Federal do Paraná - Curitiba (PR), Brazil.ORCID http://orcid.org/0000-0001-5524-0907
Paul SecombeAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-1137-0512
Fiona OsborneAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0009-0009-0235-579X
Hugh BurrillAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0009-0004-4212-4527
Emily SeeDepartment of Critical Care, University of Melbourne - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-4436-4319
Meredith YoungDepartment of Intensive Care and Hyperbaric Medicine, The Alfred Hospital - Melbourne, VIC, Australia.
Fernando Godinho ZampieriDepartment of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta - Edmonton, AB, Canada.ORCID http://orcid.org/0000-0001-9315-6386
Mark PlummerDepartment of Critical Care, University of Melbourne - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-9640-1911
Connor ChristieDepartment of Intensive Care Medicine, Royal Adelaide Hospital - Adelaide, SA, Australia.ORCID http://orcid.org/0009-0002-6847-3499
Leo NunninkIntensive Care Unit, Princess Alexandra Hospital - Woolloongabba, QLD, Australia.ORCID http://orcid.org/0000-0002-9242-8690
Josephine MackayIntensive Care Unit, Princess Alexandra Hospital - Woolloongabba, QLD, Australia.ORCID http://orcid.org/0009-0006-0472-8885
Shay McGuinnessCardiothoracic and Vascular Intensive Care Unit, Auckland City Hospital - Auckland, New Zealand.ORCID http://orcid.org/0000-0003-0620-4787
Joradee MarmolIntensive Care Unit, Wellington Hospital - Wellington, New Zealand.
Ravindranath TiruvoipatiDepartment of Intensive Care Medicine, Frankston Hospital - Frankston, VIC, Australia.ORCID http://orcid.org/0000-0003-3800-902X
Michael BaileyAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-5551-1401
Paul J YoungDepartment of Critical Care, University of Melbourne - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-3428-3083
Andrew UdyAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-6284-2022
Ary Serpa NetoDepartment of Critical Care, University of Melbourne - Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-1520-9387

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Sodium Bicarbonate for Metabolic Acidosis in the ICU (SODa-BIC) trial assessed the effect of sodium bicarbonate on Major Adverse Kidney Events at 30 days (MAKE30) in critically ill patients with metabolic acidosis. Although the trial demonstrated no significant difference in the primary outcome, the individual components showed differing magnitudes and directions of effect; we undertook an exploratory analysis of the SODa-BIC trial using different hierarchical outcomes to better understand potential treatment effects of sodium bicarbonate.

methodsPost-hoc analysis of the SODa-BIC trial. All patients included in the SODa-BIC trial were eligible. The primary outcome was a win ratio analysis with a hierarchy consisting of death, requirement for renal replacement therapy, persistent renal dysfunction, and hospital length of stay. Several sensitivity and subgroup analyses were conducted.

resultsThe primary analysis resulted in 59,250 pairs from 488 patients. Consistent with the SODa-BIC analysis, there was no overall evidence of a treatment effect of sodium bicarbonate, with a win ratio of 0.97 (95%CI 0.79 - 1.19) and a Desirability of Outcome Ranking probability of 0.49 (95%CI 0.45 - 0.54). A majority of pairwise comparisons were resolved by mortality and hospital length of stay. Evidence of significant treatment effect modification was observed across subgroups defined by acute kidney injury and severity of acidemia.

conclusionIn this post-hoc analysis of the SODa-BIC trial, the use of hierarchical composite outcomes did not alter the neutral overall interpretation of the original trial. However, this analysis provides additional insight into the relative contribution of individual components of the primary outcome.

Indexed as

AcidosisSodium BicarbonateAcute Kidney InjuryCritical IllnessFemaleHumansIntensive Care UnitsLength of StayMaleMiddle AgedSecondary Data AnalysisTreatment OutcomeSodium Bicarbonate

Identifiers

PMID42820515
PMCPMC13690031

What OpenQuestion holds

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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.