Evidence map›Paper›PMID 34698847›Full record

Observational studyJAMA network open2021

Association of Self-reported High-Risk Allergy History With Allergy Symptoms After COVID-19 Vaccination.

Lily Li, Lacey B Robinson, Rajesh Patel, Adam B Landman, Xiaoqing Fu, Erica S Shenoy, Dean M Hashimoto, Aleena Banerji, Paige G Wickner, Upeka Samarakoon and 3 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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  20. From Immunogen to COVID-19 vaccines: Prospects for the post-pandemic era.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    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

13 authors at 4 institutions in 1 country.

Lily LiDivision of Allergy and Clinical Immunology, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Lacey B RobinsonHarvard Medical School, Boston, Massachusetts.
Rajesh PatelHarvard Medical School, Boston, Massachusetts.
Adam B LandmanHarvard Medical School, Boston, Massachusetts.
Xiaoqing FuDivision of Rheumatology, Allergy and Immunology, Department of Medicine, Massachusetts General Hospital, Boston.
Erica S ShenoyHarvard Medical School, Boston, Massachusetts.
Dean M HashimotoHarvard Medical School, Boston, Massachusetts.
Aleena BanerjiHarvard Medical School, Boston, Massachusetts.
Paige G WicknerDivision of Allergy and Clinical Immunology, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Upeka SamarakoonDivision of Rheumatology, Allergy and Immunology, Department of Medicine, Massachusetts General Hospital, Boston.
Christian M ManciniDivision of Rheumatology, Allergy and Immunology, Department of Medicine, Massachusetts General Hospital, Boston.
Yuqing ZhangHarvard Medical School, Boston, Massachusetts.
Kimberly G BlumenthalHarvard Medical School, Boston, Massachusetts.
Massachusetts General Hospital · USHarvard University · USBrigham and Women's Hospital · USMass General Brigham · US

Funding

IMMUNOLOGIC BASIS OF RESISTANCE AND HYPERSENSITIVITYT32AI007306 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Nora Amanda Barrett, Joshua A Boyce · 1985 to 2026
$12.2M
The Clinical and Economic Impact of Penicillin AllergyK01AI125631 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI BLUMENTHAL, KIMBERLY GOLD · 2016 to 2021
$779k
NIAID NIH HHS K01 AI125631NIAID NIH HHS T32 AI007306
6 · The paper itself

Abstract

Importance: Allergic history in individuals with confirmed anaphylaxis to a messenger RNA (mRNA) COVID-19 vaccine is common. However, the risk factors for allergy symptoms after receiving the vaccine are unknown. Objective: To assess the association between self-reported history of high-risk allergy and self-reported allergic reactions after mRNA COVID-19 vaccination of health care employees. Design, Setting, and Participants: This cohort study obtained demographic, medical, and vaccine administration data of employees of Mass General Brigham from the institutional electronic health record. Employees who received at least 1 dose of an mRNA COVID-19 vaccine between December 14, 2020, and February 1, 2021, and who completed at least 1 postvaccination symptom survey in the 3 days after vaccination were included. Exposures: Self-reported history of high-risk allergy, defined as a previous severe allergic reaction to a vaccine, an injectable medication, or other allergen. Main Outcomes and Measures: The primary outcome was 1 or more self-reported allergic reactions in the first 3 days after dose 1 or dose 2 of an mRNA COVID-19 vaccine. Multivariable log binomial regression was used to assess the association between allergic reactions and high-risk allergy status. Results: A total of 52 998 health care employees (mean [SD] age, 42 [14] years; 38 167 women [72.0%]) were included in the cohort, of whom 51 706 (97.6%) received 2 doses of an mRNA COVID-19 vaccine and 474 (0.9%) reported a history of high-risk allergy. Individuals with vs without a history of high-risk allergy reported more allergic reactions after receiving dose 1 or 2 of the vaccine (11.6% [n = 55] vs 4.7% [n = 2461]). In the adjusted model, a history of high-risk allergy was associated with an increased risk of allergic reactions (adjusted relative risk [aRR], 2.46; 95% CI, 1.92-3.16), with risk being highest for hives (aRR, 3.81; 95% CI, 2.33-6.22) and angioedema (aRR, 4.36; 95% CI, 2.52-7.54). Conclusions and Relevance: This cohort study found that self-reported history of high-risk allergy was associated with an increased risk of self-reported allergic reactions within 3 days of mRNA COVID-19 vaccination. However, reported allergy symptoms did not impede the completion of the 2-dose vaccine protocol among a cohort of eligible health care employees, supporting the overall safety of mRNA COVID-19 vaccine.

Indexed as

2019-nCoV Vaccine mRNA-1273AdultBNT162 VaccineCase-Control StudiesCOVID-19COVID-19 VaccinesFemaleHumansHypersensitivityMaleMiddle AgedPandemicsProspective StudiesRisk FactorsSARS-CoV-2Self Report2019-nCoV Vaccine mRNA-1273BNT162 VaccineCOVID-19 Vaccines

Identifiers

PMID34698847
PMCPMC8548941
OpenAlexW3210747309

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.