Evidence map›Paper›PMID 37482552›Full record

Trial reportScientific reports2023

Adjunctive intravenous then oral vitamin C for moderate and severe community-acquired pneumonia in hospitalized adults: feasibility of randomized controlled trial.

Stephen T Chambers, Malina Storer, Amy Scott-Thomas, Sandy Slow, Jonathan Williman, Michael Epton, David R Murdoch, Sarah Metcalf, Anitra Carr, Heather Isenman and 1 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% of its field
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
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

11 authors at 4 institutions in 1 country.

Stephen T ChambersDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand. steve.chambers@otago.ac.nz.
Malina StorerCanterbury Respiratory Research Group, Canterbury District Health Board, Christchurch, New Zealand.
Amy Scott-ThomasDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.
Sandy SlowDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.
Jonathan WillimanBiostatistics and Computation Biology Unit, University of Otago, Christchurch, New Zealand.
Michael EptonCanterbury Respiratory Research Group, Canterbury District Health Board, Christchurch, New Zealand.
David R MurdochDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.
Sarah MetcalfDepartment of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand.
Anitra CarrDepartment of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.
Heather IsenmanDepartment of Infectious Diseases, Christchurch Hospital, Canterbury District Health Board, Christchurch, New Zealand.
Michael MazeCanterbury Respiratory Research Group, Canterbury District Health Board, Christchurch, New Zealand.
University of Otago · NZCanterbury District Health Board · NZChristchurch Hospital · NZLincoln University · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients hospitalised with community acquired pneumonia (CAP) have low peripheral blood vitamin C concentrations and limited antioxidant capacity. The feasibility of a trial of vitamin C supplementation to improve patient outcomes was assessed. Participants with moderate and severe CAP (CURB-65 ≥ 2) on intravenous antimicrobial treatment were randomised to either intravenous vitamin C (2.5 g 8 hourly) or placebo before switching to oral intervention (1 g tds) for 7 days when they were prescribed oral antimicrobial therapy. Of 344 patients screened 75 (22%) were randomised and analysed. The median age was 76 years, and 43 (57%) were male. In each group, one serious adverse event that was potentially intervention related occurred, and one subject discontinued treatment. Vitamin C concentrations were 226 µmol/L in the vitamin C group and 19 µmol/L in the placebo group (p < 0.001) after 3 intravneous doses. There were no signficant differences between the vitamin C and placebo groups for death within 28 days (0 vs. 2; p = 0.49), median length of stay (69 vs. 121 h; p = 0.07), time to clinical stability (22 vs. 49 h; p = 0.08), or readmission within 30 days (1 vs. 4; p = 0.22). The vitamin C doses given were safe, well tolerated and saturating. A randomised controlled trial to assess the efficacy of vitamin C in patients with CAP would require 932 participants (CURB-65 ≥ 2) to observe a difference in mortality and 200 participants to observe a difference with a composite endpoint such as mortality plus discharge after 7 days in hospital. These studies are feasible in a multicentre setting.

Indexed as

Ascorbic AcidPneumoniaAdultAgedFeasibility StudiesFemaleHumansInfusions, IntravenousMaleVitaminsAscorbic AcidVitamins

Identifiers

PMID37482552
PMCPMC10363531
OpenAlexW4385117352

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.