Evidence map›Paper›PMID 36055875›Full record

ArticleVaccine2022

No significant increase in Guillain-Barré syndrome after COVID-19 vaccination in adults: A vaccine adverse event reporting system study.

M Jaffry, F Mostafa, K Mandava, S Rosario, Y Jagarlamudi, K Jaffry, J Kornitzer, K Jedidi, H Khan, N Souayah

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Neurolymphomatosis mimicking a Guillain-Barré syndrome triggered by COVID-19 vaccination.Neuropathology : official journal of the Japanese Society of Neuropathology · 2025
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  4. Article
  5. Observational
  6. Article
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  8. Review
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  10. Article
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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

10 authors at 3 institutions in 1 country.

M JaffryDepartment of Neurology, Rutgers New Jersey Medical School, Newark, NJ, USA.
F MostafaDepartment of Mathematics and Statistics, Texas Tech University, Lubbock, TX, USA.
K MandavaDepartment of Neurology, Rutgers New Jersey Medical School, Newark, NJ, USA.
S RosarioDepartment of Marketing, Columbia Business School, New York City, NY, USA.
Y JagarlamudiKhoury College of Computer Science, Northeastern University, Boston, MA, USA.
K JaffryDepartment of Neurology, Rutgers New Jersey Medical School, Newark, NJ, USA.
J KornitzerDepartment of Neurology, Rutgers New Jersey Medical School, Newark, NJ, USA; New Jersey Pediatric Neuroscience Institute, Morristown, NJ, USA.
K JedidiDepartment of Marketing, Columbia Business School, New York City, NY, USA.
H KhanDepartment of Public Health, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
N SouayahDepartment of Neurology, Rutgers New Jersey Medical School, Newark, NJ, USA. Electronic address: souayani@njms.rutgers.edu.
Rutgers, The State University of New Jersey · USTexas Tech University · USNortheastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the association between Guillain-Barré syndrome (GBS) and COVID-19 vaccination.

backgroundOn July 13, 2021, the US Food and Drug Administration (FDA) released a new warning that Johnson & Johnson COVID-19 vaccine could increase the risk of developing GBS.

methodsThe reporting rate of adult GBS after COVID-19 vaccination, ascertained with Brighton criteria, was compared with the reporting rate after other vaccinations during the same time period, and also compared with the reporting rate during control periods. Statistical methods such as proportion tests, and Pearson's chi-squared test were utilized to identify significant relationships. Self-controlled and case centered analyses were conducted. A machine learning model was utilized to identify the factors associated with a worse outcome defined as emergency room (ER) or doctor visits, hospitalizations, and deaths.

resultsThe reporting rate of GBS after COVID-19 vaccination was significantly higher than after influenza and other vaccinations (49.7, 0.19, 0.16 per 10 million, p < 0.0001). However, the reporting rate was within the incidence range of GBS in the general population. Using self-controlled and case centered analyses, there was a significant difference in the reporting rate of GBS after COVID-19 vaccination between the risk period and control period (p < 0.0001). There was an estimated 0.7-1.7 per million excess reports of GBS within 6 weeks of COVID-19 vaccination. Machine learning model demonstrated that female gender and age between 18 and 44 are associated with worse outcome. No association was found between the onset interval of GBS and its prognosis.

conclusionsAlthough the reporting rate of GBS after COVID-19 vaccination was not statistically different than that of the general population, the increased reporting of GBS within the first 6 weeks after COVID-19 vaccination, more so than with other vaccinations, suggests that some cases of GBS are temporally associated with COVID-19 vaccination. However, there is a reduction in the reporting rate of GBS after other vaccines, compared to reporting rates pre-COVID-19, highlighting limitations inherent in any passive surveillance system. These findings warrant continuous analysis of GBS after COVID-19 vaccination. Further improvement of the machine learning model is needed for clinical use.

Indexed as

COVID-19COVID-19 VaccinesGuillain-Barre SyndromeAdolescentAdultFemaleHumansVaccinationYoung AdultCOVID-19 VaccinesCOVID-19 vaccinationGuillan Barre syndromeMachine learningSARS-CoV-2Vaccine adverse events

Identifiers

PMID36055875
PMCPMC9393181
OpenAlexW4292553234

What OpenQuestion holds

Textmetadata
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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.