Evidence map›Paper›PMID 35146746›Full record

ReviewBritish journal of haematology2022

TTP: From empiricism for an enigmatic disease to targeted molecular therapies.

Nuno A G Graça, Bérangère S Joly, Jan Voorberg, Karen Vanhoorelbeke, Nicolas Béranger, Agnès Veyradier, Paul Coppo

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of haematology, 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
1.4field-weighted citation impact, top 19% 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, 19 citations in OpenAlex.

  1. Revisiting the PLASMIC score and the future of ADAMTS13 prediction.Blood vessels, thrombosis & hemostasis · 2026
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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

7 authors at 4 institutions in 3 countries.

Nuno A G GraçaDepartment of Molecular Hematology, Sanquin-Academic Medical Center, Landsteiner Laboratory, Amsterdam, The Netherlands.ORCID 0000-0001-5694-1836
Bérangère S JolyService d'hématologie biologique and EA3518- Institut universitaire d'hématologie, Groupe Hospitalier Saint Louis-Lariboisière, AP-HP, Université Paris Diderot, Paris, France.ORCID 0000-0003-0151-337X
Jan VoorbergDepartment of Molecular Hematology, Sanquin-Academic Medical Center, Landsteiner Laboratory, Amsterdam, The Netherlands.ORCID 0000-0003-4585-2621
Karen VanhoorelbekeLaboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.ORCID 0000-0003-2288-8277
Nicolas BérangerService d'hématologie biologique and EA3518- Institut universitaire d'hématologie, Groupe Hospitalier Saint Louis-Lariboisière, AP-HP, Université Paris Diderot, Paris, France.
Agnès VeyradierService d'hématologie biologique and EA3518- Institut universitaire d'hématologie, Groupe Hospitalier Saint Louis-Lariboisière, AP-HP, Université Paris Diderot, Paris, France.ORCID 0000-0001-7773-5003
Paul CoppoCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, Paris, France.ORCID 0000-0002-4618-2095
Université Paris Cité · FRAmsterdam UMC Location University of Amsterdam · NLResearch Institute for Chromatography · BESorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 100th anniversary of the first description of Thrombotic Thrombocytopenic Purpura (TTP) as a disease by Dr. Eli Moschcowitz approaches. For many decades, TTP remained mostly a mysterious fatal condition, where diagnosis was often post-mortem. Initially a pentad of symptoms was identified, a pattern that later revealed to be fallible. Sporadic observations led to empiric interventions that allowed for the first impactful breakthrough in TTP treatment, almost 70 years after its first description: the introduction of plasma exchange and infusions as treatments. The main body of knowledge within the field was gathered in the latest three decades: patient registries were set and proved crucial for advancements; the general mechanisms of disease have been described; the diagnosis was refined; new treatments and biomarkers with improvements on prognosis and management were introduced. Further changes and improvements are expected in the upcoming decades. In this review, we provide a brief historic overview of TTP, as an illustrative example of the success of translational medicine enabling to rapidly shift from a management largely based on empiricism to targeted therapies and personalized medicine, for the benefit of patients. Current management options and present and future perspectives in this still evolving field are summarized.

Indexed as

Purpura, Thrombotic ThrombocytopenicADAMTS13 ProteinEmpiricismHumansMolecular Targeted TherapyPlasma ExchangeADAMTS13 Protein

Identifiers

PMID35146746
PMCPMC9304236
OpenAlexW4211166432

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.