Evidence map›Paper›PMID 35238382›Full record

ArticleRheumatology (Oxford, England)2022

Safety of the BNT162b2 mRNA COVID-19 vaccine in patients with familial Mediterranean fever.

Liran Shechtman, Karney Lahad, Avi Livneh, Chagai Grossman, Amit Druyan, Eitan Giat, Merav Lidar, Sarit Freund, Uri Manor, Alon Pomerantz and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. 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

12 authors at 5 institutions in 1 country.

Liran ShechtmanDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Karney LahadDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Avi LivnehDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Chagai GrossmanDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Amit DruyanDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.
Eitan GiatRheumatology Unit, Sheba Medical Center, Tel-Hashomer.
Merav LidarSackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.
Sarit FreundFaculty of Industrial Engineering and Management, Ruppin Academic Center.
Uri ManorSackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv.
Alon PomerantzFaculty of Medicine, Hebrew University of Jerusalem, Jerusalem.
Daniel VeroslavskiRappaport Faculty of Medicine, Technion University, Haifa.
Ilan Ben-ZviDepartment of Internal Medicine F, Sheba Medical Center, Tel-Hashomer.ORCID 0000-0002-9160-3098
Tel Aviv University · ILSheba Medical Center · ILHebrew University of Jerusalem · ILRuppin Academic Center · ILTechnion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesEvidence suggests a possible association between the COVID-19 vaccine and autoimmune disease flares or new onset of various autoinflammatory manifestations, such as pericarditis and myocarditis. The objective of this study was to assess the safety of an mRNA-based BNT162b2 anti-COVID-19 vaccine in individuals with FMF, a prototypic autoinflammatory disease.

methodsPatients participating in this study fulfilled the criteria for diagnosis of FMF, were older than 18 years and received at least one dose of the vaccine. Data on baseline characteristics, features of FMF, post-vaccination side effects, and disease flares were acquired using electronic medical files and telephone interviews.

resultsA total of 273 FMF patients were recruited for the study. >95% were vaccinated with two doses of the vaccine. The rates of local reactions following the first and second vaccine doses were 65.5% and 60%, respectively, and 26% and 50.4%, respectively, for systemic adverse events. These rates are lower than those reported for the general population from real-world and clinical trial settings. Postvaccination FMF activity remained stable in most patients. None of the patients reported an attack of pericarditis or myocarditis, considered the most serious vaccine-associated adverse events. Patients with a more active FMF disease and patients harboring the M694V mutation had a significantly higher rate of post-vaccination systemic side effects and attacks.

conclusionThe BNT162b2 mRNA COVID-19 vaccine is safe in patients with FMF. Our results support the administration of this vaccine to FMF patients according to guidelines applicable to the general population.

Indexed as

BNT162 VaccineCOVID-19Familial Mediterranean FeverMyocarditisPericarditisHumansRNA, MessengerBNT162 VaccineRNA, MessengerCOVID-19FMFmRNAvaccine

Identifiers

PMID35238382
PMCPMC8903441
OpenAlexW4214887441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.