Evidence map›Paper›PMID 35479064›Full record

ReviewFrontiers in immunology2022

Molecular Diagnosis Is Vital to the Accurate Classification and Management of Thrombotic Thrombocytopenic Purpura in Children.

Cecile L Karsenty, Susan E Kirk, Hannah L Helber, Jose M Esquilin, Jenny M Despotovic, Amanda B Grimes

Open access · goldAbstract readReview
In one paragraph

Review 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. A compound heterozygousFrontiers in medicine · 2024
    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

6 authors at 2 institutions in 1 country.

Cecile L KarsentyDepartment of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX, United States.
Susan E KirkDepartment of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX, United States.
Hannah L HelberDepartment of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX, United States.
Jose M EsquilinMethodist Children's Hospital, San Antonio, TX, United States.
Jenny M DespotovicDepartment of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX, United States.
Amanda B GrimesDepartment of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX, United States.
Baylor College of Medicine · USMethodist Children’s Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thrombotic thrombocytopenic purpura (TTP) is a rare but potentially life-threatening hematologic disease, presenting a myriad of diagnostic and management challenges in children. Here, we provide a review of this disorder and discuss 2 exemplary cases of TTP occurring in adolescents, emphasizing the need for consideration of late-onset congenital TTP (cTTP). We demonstrate the importance of early confirmation of ADAMTS13 enzyme deficiency and the presence or absence of ADAMTS13 inhibitor in order to rapidly initiate the appropriate life-saving therapies. Ultimately, molecular testing is paramount to distinguishing between congenital and acquired immune-mediated TTP.

Indexed as

Purpura, Thrombotic ThrombocytopenicAdolescentChildHumansADAMTS13congenital TTPimmune-mediated TTPinhibitorpediatric

Identifiers

PMID35479064
PMCPMC9038040
OpenAlexW4223413374

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.