Evidence map›Paper›PMID 35305268›Full record

ArticleTransfusion2022

Acute drug-induced immune thrombocytopenia - A work of articaine.

Ingvild Jenssen Laegreid, Mats Irgen Olsen, Jon Inge Harr, Renathe Henriksen Grønli, Trude Victoria Mørtberg, Siw Leiknes Ernstsen, Maria Therese Ahlen

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Transfusion, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Ingvild Jenssen LaegreidThe Norwegian National Unit for Platelet Immunology, Department of Laboratory medicine, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0002-6379-4018
Mats Irgen OlsenDepartment of Hematology, Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway.
Jon Inge HarrDepartment of Anesthesiology Narvik, Division of Surgical Medicine and Intensive Care, University Hospital of North Norway, Narvik, Norway.
Renathe Henriksen GrønliThe Norwegian National Unit for Platelet Immunology, Department of Laboratory medicine, University Hospital of North Norway, Tromsø, Norway.
Trude Victoria MørtbergThe Norwegian National Unit for Platelet Immunology, Department of Laboratory medicine, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0003-0808-0183
Siw Leiknes ErnstsenThe Norwegian National Unit for Platelet Immunology, Department of Laboratory medicine, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0001-9515-0922
Maria Therese AhlenThe Norwegian National Unit for Platelet Immunology, Department of Laboratory medicine, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0002-3104-3818
University Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDrug-induced immune thrombocytopenia (DITP) is a rare, but serious complication to a wide range of medications. Upon suspicion, one should do a thorough clinical evaluation following proposed diagnostic criteria and seek laboratory confirmation. If confirmed, it is important to ensure avoidance of the drug in the future. STUDY DESIGN AND

methodsHerein, we describe a young adult male who experienced two bouts of severe thrombocytopenia following dental treatment. The thrombocytopenia was acknowledged due to unexpected hemorrhaging during the procedures. On both occasions, he was exposed to four different drugs, none commonly associated with DITP. After the second episode of severe procedural-related thrombocytopenia, an investigation into the cause was initiated. We describe the clinical approach to elucidate which of the four implicated drugs was responsible for thrombocytopenia and the laboratory work-up done to confirm that the reaction was antibody-mediated and identify the antibody's drug: glycoprotein specificity. An alternative drug was tested both in vivo and in vitro, to identify an option for future procedures.

resultsSequential exposure revealed the local anesthetic substance articaine to induce thrombocytopenia. Laboratory work-up confirmed drug-dependent antibodies (DDAbs) with specificity for the glycoprotein Ib/IX complex, swiftly identified by a bead-based Luminex assay. Further investigations by monoclonal antibody immobilization of platelet antigens assay (MAIPA) revealed a probable GPIb binding site. An alternative local anesthetic, lidocaine, was deemed safe for future procedures.

conclusionArticaine can induce rapid-onset, severe immune-mediated thrombocytopenia causing bleeding complications. A modified bead-based Luminex platelet antigen assay proved a useful addition in the DITP-investigation.

Indexed as

Purpura, Thrombocytopenic, IdiopathicThrombocytopeniaAnesthetics, LocalAntibodies, MonoclonalAutoantibodiesBlood PlateletsCarticaineHumansMaleAnesthetics, LocalAntibodies, MonoclonalAutoantibodiesCarticaineadverse effectarticainedrug-induced immune thrombocytopeniaGPIb/IXMAIPAthrombocytopenia

Identifiers

PMID35305268
PMCPMC9314149
OpenAlexW4220652650

What OpenQuestion holds

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LicenceCC BY-NC
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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.