Evidence map›Paper›PMID 36275662›Full record

ArticleFrontiers in immunology2022

Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report.

Romana Rysava, Martina Peiskerova, Vladimir Tesar, Jan Benes, Martin Kment, Ágnes Szilágyi, Dorottya Csuka, Zoltán Prohászka

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Aplastic Anemia Following COVID-19 Vaccination: A Systematic Review of Case Reports and Case Series.International journal of hematology-oncology and stem cell research · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. The Rationale of Complement Blockade of the MCPInternational journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

8 authors at 3 institutions in 2 countries.

Romana RysavaDepartment of Nephrology, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.
Martina PeiskerovaDepartment of Nephrology, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.
Vladimir TesarDepartment of Nephrology, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.
Jan BenesUniversity Hospital, Charles University - Faculty of Medicine, Hradec Králové, Czechia.
Martin KmentDepartment of Clinical and Transplant Pathology, Institute of Clinical and Experimental Medicine (IKEM), Prague, Czechia.
Ágnes SzilágyiDepartment of Internal Medicine and Hematology, Semmelweis University, Budapest, Hungary.
Dorottya CsukaDepartment of Internal Medicine and Hematology, Semmelweis University, Budapest, Hungary.
Zoltán ProhászkaDepartment of Internal Medicine and Hematology, Semmelweis University, Budapest, Hungary.
Charles University · CZSemmelweis University · HUInstitute of Clinical and Experimental Medicine · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atypical hemolytic uremic syndrome (aHUS), also called complement-mediated hemolytic uremic syndrome (CM-HUS), is a rare disease caused by dysregulation in the alternative complement activation pathway. It is a life-threatening condition causing ischemia of a number of organs, and it typically causes acute kidney injury. This disorder may be triggered by various factors including viral or bacterial infections, pregnancy, surgery, and injuries. In about 60% of cases, the genetic origin of the disease can be identified-commonly mutations affecting complementary factor H and MCP protein. Eculizumab, a monoclonal antibody to the C5 component of the complement, represents the current effective treatment.We describe a case of a young woman with a previous history of polyvalent allergies, who developed atypical hemolytic uremic syndrome after vaccination with mRNA vaccine against SARS-CoV-2. The disease manifested by scleral bleeding, acute renal insufficiency, anemia, and thrombocytopenia. The patient was treated with

Indexed as

Acute Kidney InjuryAtypical Hemolytic Uremic SyndromeCOVID-19Antibodies, MonoclonalComplement Factor HComplement System ProteinsCOVID-19 VaccinesFemaleHumansmRNA VaccinesRNA, MessengerSARS-CoV-2VaccinationAntibodies, MonoclonalComplement Factor HComplement System ProteinsCOVID-19 VaccinesmRNA VaccinesRNA, Messengeracute kidney injuryatypical hemolytic uremic syndromecomplementeculizumabgenetic riskmRNA vaccine against SARS-CoV-2ravulizumabthrombotic microangiopathies

Identifiers

PMID36275662
PMCPMC9580272
OpenAlexW4297491642

What OpenQuestion holds

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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.