Evidence map›Paper›PMID 35657850›Full record

Trial reportPloS one2022

The safety of co-administration of Bacille Calmette-Guérin (BCG) and influenza vaccines.

Paola Villanueva, Ushma Wadia, Nigel W Crawford, Nicole L Messina, Tobias R Kollmann, Michaela Lucas, Laurens Manning, Peter Richmond, Laure F Pittet, Nigel Curtis

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

10 authors at 4 institutions in 1 country.

Paola VillanuevaDepartment of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.ORCID 0000-0002-6504-2979
Ushma WadiaWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.
Nigel W CrawfordDepartment of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Nicole L MessinaDepartment of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Tobias R KollmannWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.ORCID 0000-0003-2403-9762
Michaela LucasSchool of Medicine, University of Western Australia, Perth, WA, Australia.
Laurens ManningWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.ORCID 0000-0003-4334-5351
Peter RichmondWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.
Laure F PittetDepartment of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Nigel CurtisDepartment of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
Royal Children's Hospital · AUThe Kids Research Institute Australia · AUThe University of Melbourne · AUThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the emergence of novel vaccines and new applications for older vaccines, co-administration is increasingly likely. The immunomodulatory effects of BCG could theoretically alter the reactogenicity of co-administered vaccines. Using active surveillance in a randomised controlled trial, we aimed to determine whether co-administration of BCG vaccination changes the safety profile of influenza vaccination.

methodsParticipants who received influenza vaccine alone (Influenza group) were compared with those who also received BCG-Denmark vaccine in the contralateral arm (Influenza+BCG group). Data on the influenza vaccination site were collected using serial questionnaires and active follow-up for 3 months post vaccination.

resultsOf 1351 participants in the Influenza+BCG group and 1418 participants in the Influenza group, 2615 (94%) provided influenza vaccine safety data. There was no significant difference in the proportion of participants with any local adverse reaction between the Influenza+BCG group and the Influenza group (918/1293 [71.0%] versus (906/1322 [68.5%], p = 0.17). The proportion of participants reporting any pain, erythema and tenderness at the influenza vaccination site were similar in both groups. Swelling was less frequent (81/1293 [6.3%] versus 119/1322 (9.0%), p = 0.01) and the maximal diameter of erythema was smaller (mean 1.8 cm [SD 2.0] versus 3.0 cm [SD 2.5], p<0.001) in the Influenza+BCG group. Sixteen participants reported serious adverse events: 9 participants in the Influenza+BCG group and 7 in the Influenza group.

conclusionsAdverse events following influenza vaccination are not increased when BCG is co-administered.

Indexed as

BCG VaccineInfluenza, HumanInfluenza VaccinesHumansVaccinationBCG VaccineInfluenza Vaccines

Identifiers

PMID35657850
PMCPMC9165819
OpenAlexW4282036495

What OpenQuestion holds

Textmetadata
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.