Evidence map›Paper›PMID 36803895›Full record

ArticleVaccine2023

Risk of COVID-19 breakthrough infection and hospitalization in individuals with comorbidities.

Peter D Smits, Samuel Gratzl, Michael Simonov, Senthil K Nachimuthu, Brianna M Goodwin Cartwright, Michael D Wang, Charlotte Baker, Patricia Rodriguez, Mackenzie Bogiages, Benjamin M Althouse and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 44 citations in OpenAlex.

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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.

Peter D SmitsTruveta, Inc, Bellevue, WA, United States.
Samuel GratzlTruveta, Inc, Bellevue, WA, United States.
Michael SimonovTruveta, Inc, Bellevue, WA, United States; Yale School of Medicine, New Haven, CT, United States.
Senthil K NachimuthuTruveta, Inc, Bellevue, WA, United States.
Brianna M Goodwin CartwrightTruveta, Inc, Bellevue, WA, United States.
Michael D WangTruveta, Inc, Bellevue, WA, United States.
Charlotte BakerTruveta, Inc, Bellevue, WA, United States.
Patricia RodriguezTruveta, Inc, Bellevue, WA, United States.
Mackenzie BogiagesTruveta, Inc, Bellevue, WA, United States.
Benjamin M AlthouseTruveta, Inc, Bellevue, WA, United States; University of Washington, Seattle, Washington, United States; New Mexico State University, Las Cruces, New Mexico, United States.
Nicholas L StuckyTruveta, Inc, Bellevue, WA, United States. Electronic address: nicholass@truveta.com.
Bellevue Hospital Center · USNew Mexico State University · USTruven Health Analytics (United States) · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
6 · The paper itself

Abstract

backgroundThe successful development of multiple COVID-19 vaccines has led to a global vaccination effort to reduce severe COVID-19 infection and mortality. However, the effectiveness of the COVID-19 vaccines wane over time leading to breakthrough infections where vaccinated individuals experience a COVID-19 infection. Here we estimate the risks of breakthrough infection and subsequent hospitalization in individuals with common comorbidities who had completed an initial vaccination series.

methodsOur study population included vaccinated patients between January 1, 2021 to March 31, 2022 who are present in the Truveta patient population. Models were developed to describe 1) time from completing primary vaccination series till breakthrough infection; and 2) if a patient was hospitalized within 14 days of breakthrough infection. We adjusted for age, race, ethnicity, sex, and year-month of vaccination.

resultsOf 1,218,630 patients in the Truveta Platform who had completed an initial vaccination sequence between January 1, 2021 and March 31, 2022, 2.85, 3.42, 2.75, and 2.88 percent of patients with CKD, chronic lung disease, diabetes, or are in an immunocompromised state experienced breakthrough infection, respectively, compared to 1.46 percent of the population without any of these four comorbidities. We found an increased risk of breakthrough infection and subsequent hospitalization in individuals with any of the four comorbidities when compared to individuals without these four comorbidities.

conclusionsVaccinated individuals with any of the studied comorbidities experienced an increased risk of breakthrough COVID-19 infection and subsequent hospitalizations compared to the people without any of the studied comorbidities. Individuals with immunocompromising conditions and chronic lung disease were most at risk of breakthrough infection, while people with CKD were most at risk of hospitalization following breakthrough infection. Patients with multiple comorbidities have an even greater risk of breakthrough infection or hospitalization compared to patients with none of the studied comorbidities. Individuals with common comorbidities should remain vigilant against infection even if vaccinated.

Indexed as

COVID-19Renal Insufficiency, ChronicBreakthrough InfectionsCOVID-19 VaccinesHospitalizationHumansCOVID-19 Vaccines

Identifiers

PMID36803895
PMCPMC9933320
OpenAlexW4321112673

What OpenQuestion holds

Textmetadata
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.