Evidence map›Paper›PMID 31950979›Full record

Trial reportJAMA2020

Effect of Vitamin C, Hydrocortisone, and Thiamine vs Hydrocortisone Alone on Time Alive and Free of Vasopressor Support Among Patients With Septic Shock: The VITAMINS Randomized Clinical Trial.

Tomoko Fujii, Nora Luethi, Paul J Young, Daniel R Frei, Glenn M Eastwood, Craig J French, Adam M Deane, Yahya Shehabi, Ludhmila A Hajjar, Gisele Oliveira and 20 more

3 registry-linked trialsAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 216 papers, 19 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
216citing papers in PubMed, 19 pooled it
–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.

NCT03333278 phase2completednot on this map

The VitamIn C, HydrocorTisone and ThiAMINe in Patients With Septic Shock Trial (VITAMINS Trial) - A Prospective, Feasibility, Pilot, Multi-centre, Randomised, Open-label Controlled Trial

TypeinterventionalSponsorAustralian and New Zealand Intensive Care Research CentreRan2018 to 2019Enrolled216ConditionsShock, Septic, Critically Ill, Vasoplegic Syndrome, SepsisArmsVitamin C, Thiamine, Hydrocortisone,
NCT05192213 phase3terminatednot on this mapstarted 2021, after this paper: background citation

Vitamin C, Hydrocortisone and Thiamine in Patients With Septic Shock: a Randomized Clinical Study (VITAMIN TRIAL)

TypeinterventionalSponsorHospital Sirio-LibanesRan2021 to 2022Enrolled71ConditionsSepsis, Septic ShockArmsVitamin C, Placebo
NCT05840718 completednot on this mapstarted 2023, after this paper: background citation

Impact of Thiamine Supplementation on Clinical Outcomes of Patients With Septic Shock: a Retrospective Before-after Study

TypeobservationalSponsorHospital Sao DomingosRan2023 to 2023Enrolled73ConditionsSeptic ShockArmsThiamin
3 · Its place in the literature

Who cites it

216 citing papers in PubMed, 19 syntheses or guidelines pooled it.

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  2. Corticosteroids for treating sepsis in children and adults.The Cochrane database of systematic reviews · 2025
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  9. IV Vitamin C in Sepsis: A Latest Systematic Review and Meta-Analysis.International journal of clinical practice · 2023
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  11. Intravenous vitamin C use and risk of severity and mortality in COVID-19: A systematic review and meta-analysis.Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition · 2022
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156 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Tomoko FujiiAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Nora LuethiAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Paul J YoungIntensive Care Unit, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand.
Daniel R FreiDepartment of Anaesthesia and Pain Medicine, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand.
Glenn M EastwoodAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Craig J FrenchAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Adam M DeaneDepartment of Medicine, University of Melbourne, Royal Melbourne Hospital, Parkville, Australia.
Yahya ShehabiCritical Care and Perioperative Services, School of Clinical Sciences, Monash University and Monash Health, Melbourne, Victoria, Australia.
Ludhmila A HajjarCancer Institute of the State of Sao Paulo, Sao Paulo, Brazil.
Gisele OliveiraCancer Institute of the State of Sao Paulo, Sao Paulo, Brazil.
Andrew A UdyAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Neil OrfordAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Samantha J EdneyIntensive Care Unit, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand.
Anna L HuntIntensive Care Unit, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand.
Harriet L JuddIntensive Care Unit, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand.
Laurent BitkerIntensive Care Unit, Austin Hospital, Heidelberg, Victoria, Australia.
Luca CioccariAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Thummaporn NaorungrojIntensive Care Unit, Austin Hospital, Heidelberg, Victoria, Australia.
Fumitaka YanaseAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Samantha BatesDepartment of Intensive Care, Anaesthesia, Pain, and Perioperative Medicine, Footscray Hospital, Western Health, Footscray, Melbourne, Victoria, Australia.
Forbes McGainDepartment of Intensive Care, Anaesthesia, Pain, and Perioperative Medicine, Footscray Hospital, Western Health, Footscray, Melbourne, Victoria, Australia.
Elizabeth P HudsonMelbourne Medical School, University of Melbourne, Parkville, Victoria, Australia.
Wisam Al-BassamCritical Care and Perioperative Services, School of Clinical Sciences, Monash University and Monash Health, Melbourne, Victoria, Australia.
Dhiraj Bhatia DwivediCritical Care and Perioperative Services, School of Clinical Sciences, Monash University and Monash Health, Melbourne, Victoria, Australia.
Chloe PeppinCritical Care and Perioperative Services, School of Clinical Sciences, Monash University and Monash Health, Melbourne, Victoria, Australia.
Phoebe McCrackenDepartment of Intensive Care and Hyperbaric Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
Judit OroszDepartment of Intensive Care and Hyperbaric Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
Michael BaileyAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Rinaldo BellomoAustralian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
VITAMINS Trial Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: It is unclear whether vitamin C, hydrocortisone, and thiamine are more effective than hydrocortisone alone in expediting resolution of septic shock. Objective: To determine whether the combination of vitamin C, hydrocortisone, and thiamine, compared with hydrocortisone alone, improves the duration of time alive and free of vasopressor administration in patients with septic shock. Design, Setting, and Participants: Multicenter, open-label, randomized clinical trial conducted in 10 intensive care units in Australia, New Zealand, and Brazil that recruited 216 patients fulfilling the Sepsis-3 definition of septic shock. The first patient was enrolled on May 8, 2018, and the last on July 9, 2019. The final date of follow-up was October 6, 2019. Interventions: Patients were randomized to the intervention group (n = 109), consisting of intravenous vitamin C (1.5 g every 6 hours), hydrocortisone (50 mg every 6 hours), and thiamine (200 mg every 12 hours), or to the control group (n = 107), consisting of intravenous hydrocortisone (50 mg every 6 hours) alone until shock resolution or up to 10 days. Main Outcomes and Measures: The primary trial outcome was duration of time alive and free of vasopressor administration up to day 7. Ten secondary outcomes were prespecified, including 90-day mortality. Results: Among 216 patients who were randomized, 211 provided consent and completed the primary outcome measurement (mean age, 61.7 years [SD, 15.0]; 133 men [63%]). Time alive and vasopressor free up to day 7 was 122.1 hours (interquartile range [IQR], 76.3-145.4 hours) in the intervention group and 124.6 hours (IQR, 82.1-147.0 hours) in the control group; the median of all paired differences was -0.6 hours (95% CI, -8.3 to 7.2 hours; P = .83). Of 10 prespecified secondary outcomes, 9 showed no statistically significant difference. Ninety-day mortality was 30/105 (28.6%) in the intervention group and 25/102 (24.5%) in the control group (hazard ratio, 1.18; 95% CI, 0.69-2.00). No serious adverse events were reported. Conclusions and Relevance: In patients with septic shock, treatment with intravenous vitamin C, hydrocortisone, and thiamine, compared with intravenous hydrocortisone alone, did not significantly improve the duration of time alive and free of vasopressor administration over 7 days. The finding suggests that treatment with intravenous vitamin C, hydrocortisone, and thiamine does not lead to a more rapid resolution of septic shock compared with intravenous hydrocortisone alone. Trial Registration: ClinicalTrials.gov Identifier: NCT03333278.

Indexed as

Administration, IntravenousAgedAnti-Inflammatory AgentsAscorbic AcidDrug Therapy, CombinationFemaleHospital MortalityHumansHydrocortisoneMaleMiddle AgedShock, SepticThiamineVasoconstrictor AgentsVitaminsAnti-Inflammatory AgentsAscorbic AcidHydrocortisoneThiamineVasoconstrictor AgentsVitamins

Identifiers

PMID31950979
PMCPMC7029761

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.