Evidence map›Paper›PMID 42703612›Full record

ArticleOpen forum infectious diseases2026

Residual Disparities in US Adults Hospitalized due to All-Cause Pneumonia Following Implementation of Childhood 13-Valent Pneumococcal Conjugate Vaccine in National Immunization Program.

Mark H Rozenbaum, Ahuva Averin, Derek Weycker, Rotem Lapidot, Amanda Miles, Maria J Tort, Paula Peyrani, Jeffrey Vietri, Alexander Lonshteyn, Stephen I Pelton

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mark H RozenbaumHTA Value & Evidence, Pfizer Inc, Capelle A/d Ijssel, The Netherlands.
Ahuva AverinEvidence & Strategy, Avalere Health, Washington, District of Columbia, USA.ORCID https://orcid.org/0000-0002-4490-7021
Derek WeyckerEvidence & Strategy, Avalere Health, Washington, District of Columbia, USA.
Rotem LapidotDivision of Infectious Diseases, Rambam Health Care Campus, Haifa, Israel.ORCID https://orcid.org/0000-0002-4398-1588
Amanda MilesReal World Evidence and Epidemiology, Pfizer Inc, New York, New York, United States.ORCID https://orcid.org/0009-0001-6486-6896
Maria J TortUS Vaccines Medical Affairs, Pfizer Inc, Collegeville, Pennsylvania, United States.ORCID https://orcid.org/0000-0002-6088-451X
Paula PeyraniUS Vaccines Medical Affairs, Pfizer Inc, Collegeville, Pennsylvania, United States.ORCID https://orcid.org/0000-0001-8958-1734
Jeffrey VietriHTA Value & Evidence, Pfizer Inc, Collegeville, Pennsylvania, United States.ORCID https://orcid.org/0000-0002-5610-3098
Alexander LonshteynEvidence & Strategy, Avalere Health, Washington, District of Columbia, USA.
Stephen I PeltonDepartment of Pediatrics, Boston Medical Centre, Boston, Massachusetts, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Use of 13-valent pneumococcal conjugate vaccine (PCV13) has reduced the burden of pneumococcal disease among both children and adults. Research has indicated that some population subgroups have benefited more than others. This study estimated rates of inpatient all-cause pneumonia among US adults by age, race, comorbidity profile, and household income (HHI), before and after universal recommendation for PCV13 in children and targeted recommendation for use in adults. Methods: A retrospective observational study was conducted using Optum's de-identified Clinformatics Data Mart Database (2007-2019). Adults aged ≥18 years were stratified by age, race, comorbidity profile (low-risk, at-risk/high-risk), and annual household income. Inpatient all-cause pneumonia episodes were identified via relevant Results: Among 38.7 million US adults, inpatient all-cause pneumonia rates decreased from the pre-PCV13 to post-PCV13#2 period among all age groups (eg, 72.9 to 38.2 among 18- to 49-year-olds and 1621.8 to 1326.0 among ≥75-year-olds). Irrespective of age, rates generally decreased from the pre-PCV13 to post-PCV13#2 period within subgroups defined by race, comorbidity profile, and HHI; the greatest relative reductions were observed among persons aged 18-49 years. During the post-PCV13#2 period, the highest rates of inpatient all-cause pneumonia persisted in Black adults, at-risk/high-risk adults, and adults with HHI <$100 000. Conclusions: Despite reductions in inpatient all-cause pneumonia following pediatric PCV13 introduction, residual disparities persist for Black, at-risk/high-risk, and low- and middle-income adults. Strategies to reduce persistent disparities in disease burden among affected adults should be considered and implemented.

Indexed as

adultscomorbidityherd immunitypneumococcal vaccinessocioeconomic factors

Identifiers

PMID42703612
PMCPMC13546781

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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.