Literature DB >> 31657709

Emergency management in patients with haemophilia A and inhibitors on prophylaxis with emicizumab: AICE practical guidance in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET.

Giancarlo Castaman1, Cristina Santoro2, Antonio Coppola3, Maria E Mancuso4, Rita C Santoro5, Sergio Bernardini6, Francesco R Pugliese7, Riccardo Lubrano8, Maria Golato9, Armando Tripodi10,4, Angiola Rocino11, Elena Santagostino4, Chiara Biasoli12, Alessandra Borchiellini13, Alberto Catalano14, Laura Contino15, Antonella Coluccia16, Dorina Cultrera17, Raimondo De Cristofaro18, Giovanni Di Minno19, Andrea Fabbri20, Massimo Franchini21, Gabriella Gamba22, Anna Chiara Giuffrida23, Paolo Gresele24, Adele Giampaolo25, Hamisa J Hassan26, Matteo Luciani27, Emanuela Marchesini28, Renato Marino29, Maria Gabriella Mazzucconi30, Angelo C Molinari31, Massimo Morfini32, Lucia D Notarangelo33, Lucia Peccarisi34, Flora Peyvandi35, Berardino Pollio36, Gianna Franca Rivolta3, Maria Pia Ruggieri37, Vittorio Sargentini38, Mario Schiavoni39, Laura Sciacovelli40, Maria Luisa Serino41, Sergio Siragusa42, Annarita Tagliaferri3, Sophie Testa43, Alberto Tosetto44, Stefania Zampogna45, Ezio Zanon46.   

Abstract

Emicizumab has been approved in several countries for regular prophylaxis in patients with congenital haemophilia A and FVIII inhibitors because it substantially reduces their bleeding risk and improves quality of life. However, although significantly less frequent, some breakthrough bleeds may still occur while on emicizumab, requiring treatment with bypassing or other haemostatic agents. Thrombotic complications have been reported with the associated use of activated prothrombin complex concentrates. In addition, when surgery/invasive procedures are needed while on emicizumab, their management requires multidisciplinary competences and direct supervision by experts in the use of this agent. Given this, and in order to expand the current knowledge on the use of emicizumab and concomitant haemostatic agents, and reduce the risk of complications in this setting, the Italian Association of Haemophilia Centres (AICE) here provides guidance on the management of breakthrough bleeds and surgery in emergency situations in patients with haemophilia A and inhibitors on emicizumab prophylaxis. This paper has been shared with other National Scientific Societies involved in the field.

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Year:  2019        PMID: 31657709      PMCID: PMC7141940          DOI: 10.2450/2019.0186-19

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  10 in total

1.  Emicizumab use in major orthopedic surgery.

Authors:  Craig D Seaman; Margaret V Ragni
Journal:  Blood Adv       Date:  2019-06-11

2.  Rescue factor VIII replacement to secure hemostasis in a patient with hemophilia A and inhibitors on emicizumab prophylaxis undergoing hip replacement.

Authors:  Elena Santagostino; Maria Elisa Mancuso; Cristina Novembrino; Luigi Piero Solimeno; Armando Tripodi; Flora Peyvandi
Journal:  Haematologica       Date:  2019-03-28       Impact factor: 9.941

Review 3.  Position paper on laboratory testing for patients with haemophilia. A consensus document from SISET, AICE, SIBioC and SIPMeL.

Authors:  Armando Tripodi; Rita C Santoro; Sophie Testa; Angelo C Molinari; Sergio Bernardini; Maria Golato; Giuseppe Lippi; Walter Ageno; Elena Santagostino
Journal:  Blood Transfus       Date:  2019-02-04       Impact factor: 3.443

Review 4.  Management of bleeding and invasive procedures in haemophilia A patients with inhibitor treated with emicizumab (Hemlibra® ): Proposals from the French network on inherited bleeding disorders (MHEMO), the French Reference Centre on Haemophilia, in collaboration with the French Working Group on Perioperative Haemostasis (GIHP).

Authors:  Sophie Susen; Yves Gruel; Anne Godier; Annie Harroche; Herve Chambost; Dominique Lasne; Antoine Rauch; Stephanie Roullet; Pierre Fontana; Jenny Goudemand; Emmanuel de Maistre; Valerie Chamouard; Bénédicte Wibaut; Pierre Albaladejo; Claude Négrier
Journal:  Haemophilia       Date:  2019-07-11       Impact factor: 4.287

5.  Safety analysis of rFVIIa with emicizumab dosing in congenital hemophilia A with inhibitors: Experience from the HAVEN clinical program.

Authors:  Gallia G Levy; Elina Asikanius; Peter Kuebler; Soraya Benchikh El Fegoun; Sille Esbjerg; Stephanie Seremetis
Journal:  J Thromb Haemost       Date:  2019-06-17       Impact factor: 5.824

6.  Emicizumab Prophylaxis in Hemophilia A with Inhibitors.

Authors:  Johannes Oldenburg; Johnny N Mahlangu; Benjamin Kim; Christophe Schmitt; Michael U Callaghan; Guy Young; Elena Santagostino; Rebecca Kruse-Jarres; Claude Negrier; Craig Kessler; Nancy Valente; Elina Asikanius; Gallia G Levy; Jerzy Windyga; Midori Shima
Journal:  N Engl J Med       Date:  2017-07-10       Impact factor: 91.245

7.  Emicizumab prophylaxis among infants and toddlers with severe hemophilia A and inhibitors-a single-center cohort.

Authors:  Assaf A Barg; Einat Avishai; Ivan Budnik; Sarina Levy-Mendelovich; Tami B Barazani; Gili Kenet; Tami Livnat
Journal:  Pediatr Blood Cancer       Date:  2019-07-26       Impact factor: 3.167

8.  Effects and Interferences of Emicizumab, a Humanised Bispecific Antibody Mimicking Activated Factor VIII Cofactor Function, on Coagulation Assays.

Authors:  Joanne I Adamkewicz; David C Chen; Ido Paz-Priel
Journal:  Thromb Haemost       Date:  2019-05-07       Impact factor: 5.249

9.  Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee.

Authors:  P W Collins; R Liesner; M Makris; K Talks; P Chowdary; E Chalmers; G Hall; A Riddell; C L Percy; C R Hay; D P Hart
Journal:  Haemophilia       Date:  2018-05       Impact factor: 4.287

10.  Factor VIII-Mimetic Function of Humanized Bispecific Antibody in Hemophilia A.

Authors:  Midori Shima; Hideji Hanabusa; Masashi Taki; Tadashi Matsushita; Tetsuji Sato; Katsuyuki Fukutake; Naoki Fukazawa; Koichiro Yoneyama; Hiroki Yoshida; Keiji Nogami
Journal:  N Engl J Med       Date:  2016-05-26       Impact factor: 91.245

  10 in total
  11 in total

1.  Psychometric Validation of the Haemo-QOL-A in Participants with Hemophilia A Treated with Gene Therapy.

Authors:  Jennifer Quinn; Kathleen A Delaney; Wing Yen Wong; Wolfgang Miesbach; Monika Bullinger
Journal:  Patient Relat Outcome Meas       Date:  2022-07-18

2.  Quantification of emicizumab by mass spectrometry in plasma of people with hemophilia A: A method validation study.

Authors:  Anouk A M T Donners; László Gerencsér; Kim C M van der Elst; Toine C G Egberts; Moniek P M de Maat; Albert Huisman; Rolf T Urbanus; Mohsin El Amrani
Journal:  Res Pract Thromb Haemost       Date:  2022-06-08

3.  B cell-activating factor modulates the factor VIII immune response in hemophilia A.

Authors:  Bhavya S Doshi; Jyoti Rana; Giancarlo Castaman; Mostafa A Shaheen; Radoslaw Kaczmarek; John Ss Butterfield; Shannon L Meeks; Cindy Leissinger; Moanaro Biswas; Valder R Arruda
Journal:  J Clin Invest       Date:  2021-04-15       Impact factor: 14.808

4.  Impact of novel hemophilia therapies around the world.

Authors:  Margareth C Ozelo; Gabriela G Yamaguti-Hayakawa
Journal:  Res Pract Thromb Haemost       Date:  2022-04-12

Review 5.  Bridging the Missing Link with Emicizumab: A Bispecific Antibody for Treatment of Hemophilia A.

Authors:  Georg Gelbenegger; Christian Schoergenhofer; Paul Knoebl; Bernd Jilma
Journal:  Thromb Haemost       Date:  2020-07-27       Impact factor: 5.249

Review 6.  Current and Emerging Approaches for Pain Management in Hemophilic Arthropathy.

Authors:  Roberta Gualtierotti; Francesco Tafuri; Sara Arcudi; Pier Luigi Solimeno; Jacopo Acquati; Laura Landi; Flora Peyvandi
Journal:  Pain Ther       Date:  2022-01-12

Review 7.  Advances in laboratory assessment of thrombosis and hemostasis.

Authors:  Jaewoo Song
Journal:  Blood Res       Date:  2022-04-30

Review 8.  Concomitant Use of rFVIIa and Emicizumab in People with Hemophilia A with Inhibitors: Current Perspectives and Emerging Clinical Evidence.

Authors:  Silvia Linari; Giancarlo Castaman
Journal:  Ther Clin Risk Manag       Date:  2020-05-22       Impact factor: 2.423

Review 9.  Confronting COVID-19: Issues in Hemophilia and Congenital Bleeding Disorders.

Authors:  Antonio Coppola; Annarita Tagliaferri; Gianna Franca Rivolta; Gabriele Quintavalle; Massimo Franchini
Journal:  Semin Thromb Hemost       Date:  2020-06-08       Impact factor: 4.180

10.  European principles of inhibitor management in patients with haemophilia: implications of new treatment options.

Authors:  C Hermans; P L F Giangrande; B O'Mahony; P de Kleijn; M Bedford; A Batorova; J Blatný; K Jansone
Journal:  Orphanet J Rare Dis       Date:  2020-08-24       Impact factor: 4.123

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