Evidence map›Paper›PMID 24876561›Full record

ArticleBlood2014

Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults.

Sonata Jodele, Stella M Davies, Adam Lane, Jane Khoury, Christopher Dandoy, Jens Goebel, Kasiani Myers, Michael Grimley, Jack Bleesing, Javier El-Bietar and 4 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 222 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
222citing papers in PubMed, 5 pooled it
12.0field-weighted citation impact, top 1% 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.

NCT03384693 phase2completednot on this mapstarted 2018, after this paper: background citation

A Pilot Trial of Using Pre-Transplant Risk Stratification and Prophylactic Defibrotide to Prevent Serious Thrombotic Microangiopathy in High-Risk Hematopoietic Stem Cell Transplant Patients

TypeinterventionalSponsorUniversity of California, San FranciscoRan2018 to 2020Enrolled25ConditionsThrombotic MicroangiopathiesArmsDefibrotide
NCT07347990 narecruitingnot on this mapstarted 2026, after this paper: background citation

A Prospective, Multicenter, Single-Arm Study: Safety and Efficacy of Iptacopan in the Treatment of High-Risk Hematopoietic Stem Cell Transplantation-Associated Thrombotic Microangiopathy (TA-TMA)

TypeinterventionalSponsorFirst Affiliated Hospital of Zhejiang UniversityRan2026 to 2029Enrolled30ConditionsThrombotic Microangiopathy, Hematopoietic Stem Cell Transplantation (HSCT)Armsiptacopan
3 · Its place in the literature

Who cites it

222 citing papers in PubMed, 5 syntheses or guidelines pooled it, 400 citations in OpenAlex.

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  17. Causes and outcomes of pediatric thrombotic microangiopathy.Research and practice in thrombosis and haemostasis · 2026
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162 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 1 country.

Sonata JodeleDivision of Bone Marrow Transplantation and Immune Deficiency.
Stella M DaviesDivision of Bone Marrow Transplantation and Immune Deficiency.
Adam LaneDivision of Bone Marrow Transplantation and Immune Deficiency.
Jane KhouryDivision of Biostatistics and Epidemiology.
Christopher DandoyDivision of Bone Marrow Transplantation and Immune Deficiency.
Jens GoebelDivision of Nephrology and Hypertension, and.
Kasiani MyersDivision of Bone Marrow Transplantation and Immune Deficiency.
Michael GrimleyDivision of Bone Marrow Transplantation and Immune Deficiency.
Jack BleesingDivision of Bone Marrow Transplantation and Immune Deficiency.
Javier El-BietarDivision of Bone Marrow Transplantation and Immune Deficiency.
Gregory WallaceDivision of Bone Marrow Transplantation and Immune Deficiency.
Ranjit S ChimaDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; and.
Zachary PaffDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; and.
Benjamin L LaskinDivision of Nephrology, The Children's Hospital of Philadelphia, Philadelphia, PA.
Immune Deficiency Foundation · USCincinnati Children's Hospital Medical Center · USCancer Research And Biostatistics · USChildren's Hospital of Philadelphia · USHypertension Institute · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., TSEVAT, JOEL · 2012 to 2014
$9.9M
Pediatric Center--Gene Expression /Developmental ScienceK12HD028827 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Tina Lee Cheng · 2002 to 2026
$9.6M
NCRR NIH HHS UL1 RR026314NCRR NIH HHS UL1-RR026314-01
6 · The paper itself

Abstract

Transplant-associated thrombotic microangiopathy (TMA) leads to generalized endothelial dysfunction that can progress to multiorgan injury, and severe cases are associated with poor outcomes after hematopoietic stem cell transplantation (HSCT). Identifying patients at highest risk for severe disease is challenging. We prospectively evaluated 100 consecutive HSCT recipients to determine the incidence of moderate and severe TMA and factors associated with poor overall outcomes. Thirty-nine subjects (39%) met previously published criteria for TMA. Subjects with TMA had a significantly higher nonrelapse mortality (43.6% vs 7.8%, P < .0001) at 1 year post-HSCT compared with those without TMA. Elevated lactate dehydrogenase, proteinuria on routine urinalysis, and hypertension were the earliest markers of TMA. Proteinuria (>30 mg/dL) and evidence of terminal complement activation (elevated sC5b-9) in the blood at the time of TMA diagnosis were associated with very poor survival (<20% at 1 year), whereas all TMA subjects without proteinuria and a normal sC5b-9 serum concentration survived (P < .01). Based on these prospective observations, we conclude that severe TMA occurred in 18% of HSCT recipients in our cohort and propose an algorithm to identify the highest-risk patients who might benefit from prompt clinical interventions.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleFollow-Up StudiesGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunosuppressive AgentsMalePrognosisProspective StudiesRisk FactorsSurvival RateThrombotic MicroangiopathiesImmunosuppressive Agents

Identifiers

PMID24876561
PMCPMC4110664
OpenAlexW1993215990

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.