Evidence map›Paper›PMID 39101606›Full record

ArticleThe Journal of infectious diseases2024

Association of Pneumococcal Conjugate Vaccination With Severe Acute Respiratory Syndrome Coronavirus 2 Infection Among Older Adult Recipients of Coronavirus Disease 2019 Vaccines: A Longitudinal Cohort Study.

Joseph A Lewnard, Vennis Hong, Lindsay R Grant, Bradley K Ackerson, Katia J Bruxvoort, Magdalena Pomichowski, Adriano Arguedas, Alejandro Cané, Luis Jodar, Bradford D Gessner and 1 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Joseph A LewnardCenter for Computational Biology, School of Public Health.
Vennis HongDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.
Lindsay R GrantPfizer Vaccines, Collegeville, Pennsylvania.
Bradley K AckersonDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.
Katia J BruxvoortDepartment of Epidemiology, School of Public Health, University of Alabama at Birmingham.ORCID 0000-0001-8277-2431
Magdalena PomichowskiDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.
Adriano ArguedasPfizer Vaccines, Collegeville, Pennsylvania.
Alejandro CanéPfizer Vaccines, Collegeville, Pennsylvania.
Luis JodarPfizer Vaccines, Collegeville, Pennsylvania.ORCID 0000-0003-1246-530X
Bradford D GessnerPfizer Vaccines, Collegeville, Pennsylvania.
Sara Y TartofDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.

Funding

Pfizer
6 · The paper itself

Abstract

backgroundPneumococcal carriage is associated with increased acquisition and duration of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection among adults. While pneumococcal conjugate vaccines (PCVs) prevent carriage of vaccine-serotype pneumococci, their potential impact on coronavirus disease 2019 (COVID-19)-related outcomes remains poorly understood in populations with prevalent immunity against SARS-CoV-2.

methodsWe undertook a retrospective cohort study of adults aged ≥65 years in the Kaiser Permanente Southern California healthcare system who had received ≥2 COVID-19 vaccine doses, comparing risk of SARS-CoV-2 infection between 1 January 2021 and 31 December 2022 among recipients and nonrecipients of 13-valent PCV (PCV13) employing multiple strategies to mitigate bias from differential test-seeking behavior.

resultsThe ajusted hazard ratio of confirmed SARS-CoV-2 infection comparing PCV13 recipients to nonrecipients was 0.92 (95% confidence interval [CI], .90-.95), corresponding to prevention of 3.9 (95% CI, 2.6-5.3) infections per 100 person-years. Following receipt of 2, 3, and ≥4 COVID-19 vaccine doses, aHRs (95% CI) were 0.85 (.81-.89), 0.94 (.90-.97), and 0.99 (.93-1.04), respectively. The aHR (95% CI) for persons who had not received COVID-19 vaccination in the preceding 6 months was 0.90 (.86-.93), versus 0.94 (.91-.98) within 6 months after COVID-19 vaccination. Similarly, aHRs (95% CI) were 0.92 (.89-.94) for persons without history of documented SARS-CoV-2 infection, versus 1.00 (.90-1.12) for persons with documented prior infection.

conclusionsAmong older adults who had received ≥2 COVID-19 vaccine doses, PCV13 was associated with modest protection against SARS-CoV-2 infection. Protective effects of PCV13 were greater among individuals expected to have weaker immune protection against SARS-CoV-2 infection.

Indexed as

COVID-19COVID-19 VaccinesPneumococcal VaccinesSARS-CoV-2Vaccines, ConjugateAgedAged, 80 and overCaliforniaFemaleHumansLongitudinal StudiesMaleRetrospective StudiesVaccination13-valent pneumococcal vaccineCOVID-19 VaccinesPneumococcal VaccinesVaccines, Conjugateadult vaccinationpneumococcal conjugate vaccinepolymicrobial infectionsSARS-CoV-2Streptococcus pneumoniae

Identifiers

PMID39101606
PMCPMC11566223

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.