Evidence map›Paper›PMID 26728503›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2016

Achievements, challenges and unmet needs for haemophilia patients with inhibitors: Report from a symposium in Paris, France on 20 November 2014.

Y Dargaud, A Pavlova, S Lacroix-Desmazes, K Fischer, M Soucie, S Claeyssens, D W Scott, R d'Oiron, G Lavigne-Lissalde, G Kenet and 5 more

Open access · greenAbstract readConference Proceedings
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Advances and innovations in haemophilia treatment.Nature reviews. Drug discovery · 2018
    Review
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

15 authors at 11 institutions in 5 countries.

Y DargaudUnite d'Hemostase Clinique, Hopital Cardiologique Louis Pradel, Universite Lyon 1, Lyon, France.
A PavlovaInstitute of Experimental Haematology and Transfusion Medicine, University Clinic, Bonn, Germany.
S Lacroix-DesmazesINSERM UMRS 1138, Immunopathologie et immuno-intervention thérapeutique, Centre de Recherche des Cordeliers, Paris, France.
K FischerVan Creveldkliniek (HP C01.425), University Medical Center Utrecht, Utrecht, The Netherlands.
M SoucieDivision of Blood Disorders, National Center for Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
S ClaeyssensChu Purpan Pav. Centre Hospitalier Lefebvre, Centre Rgal de l'Hemophilie, Toulouse, France.
D W ScottDepartment of Medicine, Uniformed Services, University for the Health Sciences, Bethesda, MD, USA.
R d'OironCentre de Traitement de l'Hémophilie et des Maladies Hémorragiques Constitutionnelles, Hôpitaux Universitaires Paris Sud - Site Bicêtre, Le Kremlin-Bicêtre, France.
G Lavigne-LissaldeLaboratoire d'Hématologie et Consultations d'Hématologie Biologique Centre Hospitalier Universitaire de Nîmes, Place du Pr R. Debré Nîmes, France.
G KenetNational Hemophilia Institute, Sheba Medical Center, Tel-Hashomer, Tel Aviv University, Tel Aviv, Israel.
C Escuriola EttingshausenHemophilia Centre Rhein-Main HZRM, Frankfurt-Mörfelden, Germany.
A Borel-DerlonHaemophilia and von Willebrand Disease Centre, University Hospital of Caen, Caen.
T LambertHemophilia Care Center, Bicêtre AP-HP Hospital and Faculté de Médecine Paris XI, Paris, France.
G PastaUOSD di Ortopedia e Traumatologia, Centro Emofilia 'Angelo Bianchi Bonomi', Fondazione IRCCS Ca'Granda Ospedale Maggiore Policlinico, Milano, Italy.
C NégrierHaematology Department, Director Hemophilia Comprehensive Care Center, Hopital Louis Pradel, Université Lyon 1, Bron Cedex, France.
Hôpital Louis Pradel · FRCentre de Recherche des Cordeliers · FRCentre Hospitalier Universitaire de Nîmes · FRCentre Hospitalier Universitaire de Toulouse · FRFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITNational Center on Birth Defects and Developmental Disabilities · USSheba Medical Center · ILUniformed Services University of the Health Sciences · USUniversité de Caen Normandie · FRUniversité Paris-Saclay · FRUniversity Medical Center Utrecht · NL

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Over the past 20 years, there have been many advances in haemophilia treatment that have allowed patients to take greater control of their disease. However, the development of factor VIII (FVIII) inhibitors is the greatest complication of the disease and a challenge in the treatment of haemophilia making management of bleeding episodes difficult and surgical procedures very challenging. A meeting to discuss the unmet needs of haemophilia patients with inhibitors was held in Paris on 20 November 2014. Topics discussed were genetic and non-genetic risk factors for the development of inhibitors, immunological aspects of inhibitor development, FVIII products and inhibitor development, generation and functional properties of engineered antigen-specific T regulatory cells, suppression of immune responses to FVIII, prophylaxis in haemophilia patients with inhibitors, epitope mapping of FVIII inhibitors, current controversies in immune tolerance induction therapy, surgery in haemophilia patients with inhibitors and future perspectives for the treatment of haemophilia patients with inhibitors. A summary of the key points discussed is presented in this paper.

Indexed as

AntibodiesEpitope MappingFactor VIIIHemophilia AHumansImmune ToleranceImmunity, CellularParisAntibodiesFactor VIIIFVIII productsgeneticshaemophiliainhibitorsprophylaxissurgery

Identifiers

PMID26728503
PMCPMC4989271
OpenAlexW2300804841

What OpenQuestion holds

Textmetadata
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.