Evidence map›Paper›PMID 31329369›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2019

Origins and organization of the NHLBI State of the Science Workshop: Generating a national blueprint for future research on factor VIII inhibitors.

Denise E Sabatino, Steven W Pipe, Diane J Nugent, J Michael Soucie, W Craig Hooper, W Keith Hoots, Donna M DiMichele

Open access · bronzeAbstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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 5 institutions in 1 country.

Denise E SabatinoPerelman School of Medicine, The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID https://orcid.org/0000-0002-6116-5453
Steven W PipeUniversity of Michigan, Ann Arbor, Michigan.ORCID https://orcid.org/0000-0003-2558-2089
Diane J NugentChildren's Hospital of Orange County, University of California at Irvine, Irvine, California.
J Michael SoucieDivision of Blood Disorders, Centers for Disease Control and Prevention, Atlanta, Georgia.
W Craig HooperDivision of Blood Disorders, Centers for Disease Control and Prevention, Atlanta, Georgia.
W Keith HootsDivision of Blood Diseases and Resources, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Donna M DiMicheleDivision of Blood Diseases and Resources, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Centers for Disease Control and Prevention · USNational Institutes of Health · USChildren's Hospital of Orange County · USChildren's Hospital of Philadelphia · USUniversity of Michigan · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

introductionThe major complication of protein replacement therapy for haemophilia A is the development of anti-FVIII antibodies or inhibitors that occur in 25%-30% of persons with severe haemophilia A. Alternative therapeutics such as bypassing agents or immune tolerance induction protocols have additional challenges and are not always effective.

aimAssemble a National Heart, Lung and Blood Institute (NHLBI) State of the Science (SOS) Workshop to generate a national blueprint for research on inhibitors to solve the problem of FVIII immunogenicity.

methodsAn Executive Steering Committee was formed in October 2017 to establish the scientific focus and Scientific Working Groups for the SOS Workshop in May 2018. Four working groups were assembled to address scientific priorities in basic, translational and clinical research on inhibitors.

resultsWorking Group 1 was charged with determining the scientific priorities for clinical trials to include the integration of non-intravenous, non-factor therapeutics including gene therapy into the standard of care for people with haemophilia A with inhibitors. Working Group 2 established the scientific priorities for 21st-century data science and biospecimen collection for observational inhibitor cohort studies. The scientific priorities for acquiring an actionable understanding of FVIII immunogenicity and the immunology of the host response and FVIII tolerance were developed by Working Group 3. Working Group 4 designed prospective pregnancy/birth cohorts to study FVIII immunogenicity, inhibitor development and eradication.

conclusionThe NHLBI SOS Workshop generated a focused summary of scientific priorities and implementation strategies to overcome the challenges of eradicating and preventing inhibitors in haemophilia A.

Indexed as

National Institutes of Health (U.S.)Clinical Trials as TopicEducationFactor VIIIHemophilia AHumansResearchUnited StatesFactor VIIIfactor VIIIhaemophiliaimmune responseinhibitor formation

Identifiers

PMID31329369
PMCPMC7235928
OpenAlexW2963560358

What OpenQuestion holds

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LicenceTDM
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.