Literature DB >> 16834735

Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitors.

J Astermark1, M Morado, A Rocino, H M van den Berg, M von Depka, A Gringeri, L Mantovani, R P Garrido, M Schiavoni, A Villar, J Windyga.   

Abstract

The management of patients with inhibitors is an important challenge in haemophilia care. The lack of randomized controlled trials means that clinical decisions are generally based on subjective opinions, and purchasers' attention is likely to focus on the costs of treatment. In order to assess the current management of inhibitor patients and use of immune tolerance induction therapy (ITI) in Europe, we performed a survey within a European network of 21 comprehensive care centres from 14 countries (the European Haemophilia Therapy Standardisation Board). The survey identified a total of 381 patients with inhibitors attending the centres, 211 (55.4%) of whom had never been exposed to ITI. Between 1998 and 2003, the centres performed 233 procedures and 114 (48.9%) were successful. The survey demonstrated that dosing, which is the time to start and stop the ITI, the type of concentrate to use and the definition of success varied among the centres. Well-designed trials are warranted to guide decision-making, but in the absence of these studies we have developed consensus guidance for the management of inhibitor patients based on current clinical practice, as identified by the survey, and review of the literature.

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Year:  2006        PMID: 16834735     DOI: 10.1111/j.1365-2516.2006.01296.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  17 in total

Review 1.  Key issues in inhibitor management in patients with haemophilia.

Authors:  Keith Gomez; Robert Klamroth; Johnny Mahlangu; Maria E Mancuso; María E Mingot; Margareth Castro Ozelo
Journal:  Blood Transfus       Date:  2013-12-03       Impact factor: 3.443

Review 2.  Immune tolerance induction for patients with severe hemophilia A: a critical literature review.

Authors:  Massimo Franchini; Giuseppe Lippi
Journal:  J Thromb Thrombolysis       Date:  2011-11       Impact factor: 2.300

3.  6 Factor VIII Concentrates, Factor VIII/von Willebrand Factor Concentrates, Factor IX Concentrates, Activated Prothrombin Complex Concentrates.

Authors: 
Journal:  Transfus Med Hemother       Date:  2009       Impact factor: 3.747

4.  Principles of treatment and update of recommendations for the management of haemophilia and congenital bleeding disorders in Italy.

Authors:  Angiola Rocino; Antonio Coppola; Massimo Franchini; Giancarlo Castaman; Cristina Santoro; Ezio Zanon; Elena Santagostino; Massimo Morfini
Journal:  Blood Transfus       Date:  2014-10       Impact factor: 3.443

5.  The International Immune Tolerance Induction Study and its follow-up study on Japanese hemophilia A patients with inhibitors.

Authors:  Akira Yoshioka; Eizaburo Ishii; Tamaki Ueno; Ikuya Usami; Masao Kobayashi; Ryoji Kobayashi; Manabu Sotomatsu; Akira Shirahata; Takashi Suzuki; Masashi Taki; Yasushi Ishida; Tadashi Matsushita; Midori Shima; Keiji Nogami; Michio Sakai; Hisato Kigasawa; Katsuyuki Fukutake
Journal:  Int J Hematol       Date:  2015-02-18       Impact factor: 2.490

Review 6.  Current and evolving features in the clinical management of haemophilia.

Authors:  Antonio Coppola; Massimo Morfini; Ernesto Cimino; Antonella Tufano; Anna M Cerbone; Giovanni Di Minno
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

7.  Survey of the anti-factor IX immunoglobulin profiles in patients with hemophilia B using a fluorescence-based immunoassay.

Authors:  B Boylan; A S Rice; A T Neff; M J Manco-Johnson; C L Kempton; C H Miller
Journal:  J Thromb Haemost       Date:  2016-09-17       Impact factor: 5.824

8.  Hematopoietic stem-cell gene therapy of hemophilia A incorporating a porcine factor VIII transgene and nonmyeloablative conditioning regimens.

Authors:  Lucienne M Ide; Bagirath Gangadharan; Kuang-Yueh Chiang; Christopher B Doering; H Trent Spencer
Journal:  Blood       Date:  2007-06-14       Impact factor: 22.113

9.  Syngeneic transplantation of hematopoietic stem cells that are genetically modified to express factor VIII in platelets restores hemostasis to hemophilia A mice with preexisting FVIII immunity.

Authors:  Qizhen Shi; Scot A Fahs; David A Wilcox; Erin L Kuether; Patricia A Morateck; Nicole Mareno; Hartmut Weiler; Robert R Montgomery
Journal:  Blood       Date:  2008-05-21       Impact factor: 22.113

10.  New treatments in hemophilia: insights for the clinician.

Authors:  Karin Knobe; Erik Berntorp
Journal:  Ther Adv Hematol       Date:  2012-06
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