Component

Sepsis mortality at day 28

Independent measured endpoint or substance; model, assay and exposure are retained in each linked finding.

2 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Day-28 mortality was 25/84 (29.8%) with C versus 38/82 (46.3%) with placebo (P=0.03), in an exploratory analysis without adjustment for multiple comparisons.

    L-Ascorbic acid → Sepsis mortality at day 28 source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    CITRIS-ALI: double-blind multicenter randomized trial; 170 initially randomized, three subsequently excluded without receiving C, 167 in the reported analysis (84 C, 83 placebo).
    exposure
    IV vitamin C 50 mg/kg in 5% dextrose every six hours for 96 hours versus dextrose placebo.
    limitations
    One of 46 secondary outcomes; 43 were nonsignificant. Different eligibility and endpoint hierarchy from LOVIT. The signal is hypothesis-generating, and no cellular mediator was proven.
    nutrient_topic
    Vitamin C research collection; topical membership is not evidence of a direct dietary effect. · Vitamin C
    organism
    Homo sapiens
    plain_language
    This smaller trial reported a possible survival benefit, although its main endpoints were negative.
    primary_references
    [c-fowler2019] Effect of Vitamin C Infusion on Organ Failure and Biomarkers of Inflammation and Vascular Injury in Patients With Sepsis and Severe Acute Respiratory Failure: The CITRIS-ALI Randomized Clinical Trial (2019). https://pubmed.ncbi.nlm.nih.gov/31573637/ DOI: 10.1001/jama.2019.11825
    tissue_or_cell_type
    Human blood or whole-person endpoints

    Vitamin C: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1755–1765

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · CITRIS-ALI: double-blind multicenter randomized trial; 170 initially randomized, three subsequently excluded without receiving C, 167 in the reported analysis (84 C, 83 placebo). · source_derived_draft · unverified_draft

    ### c-citris-exploratory-mortality-signal Day-28 mortality was 25/84 (29.8%) with C versus 38/82 (46.3%) with placebo (P=0.03), in an exploratory analysis without adjustment for multiple comparisons. Condition category: normal nutrient_topic: Vitamin C research collection; topical membership is not evidence of a direct dietary effect. plain_language: This smaller trial reported a possible survival benefit, although its main endpoints were negative. organism: Homo sapiens tissue_or_cell_type: Human blood or whole-person endpoints experimental_model: CITRIS-ALI: double-blind multicenter randomized trial; 170 initially randomized, three subsequently excluded without receiving C, 167 in the reported analysis (84 C, 83 placebo). limitations: One of 46 secondary outcomes; 43 were nonsignificant. Different eligibility and endpoint hierarchy from LOVIT. The signal is hypothesis-generating, and no cellular mediator was proven. exposure: IV vitamin C 50 mg/kg in 5% dextrose every six hours for 96 hours versus dextrose placebo. [c-fowler2019] Effect of Vitamin C Infusion on Organ Failure and Biomarkers of Inflammation and Vascular Injury in Patients With Sepsis and Severe Acute Respiratory Failure: The CITRIS-ALI Randomized Clinical Trial (2019). https://pubmed.ncbi.nlm.nih.gov/31573637/ DOI: 10.1001/jama.2019.11825
    Complete structured claim and evidence
  2. Day-28 mortality was 35.4% versus 31.6% (RR 1.17, 95% CI 0.98–1.40), while the combined primary endpoint was significant.

    L-Ascorbic acid → Sepsis mortality at day 28 source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    LOVIT: multicenter placebo-controlled randomized ICU trial; 872 randomized, 863 in primary analysis, with sepsis and vasopressor use.
    exposure
    IV vitamin C 50 mg/kg every six hours for up to 96 hours versus matched placebo.
    limitations
    Confidence interval includes no difference; neither a proven mortality increase alone nor evidence of identical mortality.
    nutrient_topic
    Vitamin C research collection; topical membership is not evidence of a direct dietary effect. · Vitamin C
    organism
    Homo sapiens
    plain_language
    The combined endpoint and mortality alone had different statistical results.
    primary_references
    [c-lamontagne2022] Intravenous Vitamin C in Adults with Sepsis in the Intensive Care Unit (2022). https://pubmed.ncbi.nlm.nih.gov/35704292/ DOI: 10.1056/nejmoa2200644
    tissue_or_cell_type
    Human blood or whole-person endpoints

    Vitamin C: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1707–1717

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · LOVIT: multicenter placebo-controlled randomized ICU trial; 872 randomized, 863 in primary analysis, with sepsis and vasopressor use. · source_derived_draft · unverified_draft

    ### c-lovit-mortality-component Day-28 mortality was 35.4% versus 31.6% (RR 1.17, 95% CI 0.98–1.40), while the combined primary endpoint was significant. Condition category: normal nutrient_topic: Vitamin C research collection; topical membership is not evidence of a direct dietary effect. plain_language: The combined endpoint and mortality alone had different statistical results. organism: Homo sapiens tissue_or_cell_type: Human blood or whole-person endpoints experimental_model: LOVIT: multicenter placebo-controlled randomized ICU trial; 872 randomized, 863 in primary analysis, with sepsis and vasopressor use. limitations: Confidence interval includes no difference; neither a proven mortality increase alone nor evidence of identical mortality. exposure: IV vitamin C 50 mg/kg every six hours for up to 96 hours versus matched placebo. [c-lamontagne2022] Intravenous Vitamin C in Adults with Sepsis in the Intensive Care Unit (2022). https://pubmed.ncbi.nlm.nih.gov/35704292/ DOI: 10.1056/nejmoa2200644
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards