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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.
Collins, P W; Liesner, R; Makris, M; Talks, K; Chowdary, P; Chalmers, E; Hall, G; Riddell, A; Percy, C L; Hay, C R; Hart, D P.
Affiliation
  • Collins PW; School of Medicine, Cardiff University, UK.
  • Liesner R; Great Ormond Street Hospital, London, UK.
  • Makris M; University of Sheffield, Sheffield, UK.
  • Talks K; Royal Victoria Infirmary, Newcastle, UK.
  • Chowdary P; Royal Free Hospital, London, UK.
  • Chalmers E; Royal Hospital for Children, Glasgow, UK.
  • Hall G; John Radcliffe Hospital, Oxford, UK.
  • Riddell A; Royal Free Hospital, London, UK.
  • Percy CL; Queen Elizabeth Hospital, Birmingham, UK.
  • Hay CR; Central Manchester University Hospitals, Manchester, UK.
  • Hart DP; Barts and The London School of Medicine and Dentistry, Queen Mary University London, Royal London Hospital, London, UK.
Haemophilia ; 24(3): 344-347, 2018 May.
Article de En | MEDLINE | ID: mdl-30070072
ABSTRACT
Emicizumab is a bispecific antibody that activates FX to FXa in the absence of FVIII. It has been shown to reduce bleeding episodes in people with haemophilia A complicated by a FVIII inhibitor. Despite the protection against bleeds, some breakthrough bleeds are inevitable and these may require additional haemostatic treatment. Emicizumab has been associated with severe adverse events when co-administered with activated prothrombin complex concentrate. To minimize the risk of adverse events, the UK Haemophilia Centre Doctors' Organisation issues the following updated interim guidance to its Inhibitor Guidelines for managing patients receiving Emicizumab based on the limit published information available in February 2018.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteur VIII / Recommandations comme sujet / Anticorps bispécifiques / Anticorps monoclonaux humanisés / Hémophilie A / Hémorragie Type d'étude: Guideline Limites: Humans Langue: En Journal: Haemophilia Sujet du journal: HEMATOLOGIA Année: 2018 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteur VIII / Recommandations comme sujet / Anticorps bispécifiques / Anticorps monoclonaux humanisés / Hémophilie A / Hémorragie Type d'étude: Guideline Limites: Humans Langue: En Journal: Haemophilia Sujet du journal: HEMATOLOGIA Année: 2018 Type de document: Article Pays d'affiliation: Royaume-Uni