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Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series.
Iorio, A; Barbara, A M; Makris, M; Fischer, K; Castaman, G; Catarino, C; Gilman, E; Kavakli, K; Lambert, T; Lassila, R; Lissitchkov, T; Mauser-Bunschoten, E; Mingot-Castellano, M E; Ozdemir, N; Pabinger, I; Parra, R; Pasi, J; Peerlinck, K; Rauch, A; Roussel-Robert, V; Serban, M; Tagliaferri, A; Windyga, J; Zanon, E.
Afiliação
  • Iorio A; Department of Clinical Epidemiology and Biostastics, McMaster University, Hamilton, ON, Canada.
  • Barbara AM; Department of Clinical Epidemiology and Biostastics, McMaster University, Hamilton, ON, Canada.
  • Makris M; Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.
  • Fischer K; Van Creveldkliniek University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Castaman G; San Bortolo Hospital, Vicenza, Italy.
  • Catarino C; Congenital Coagulopathies Centre, Santa Maria Hospital, Lisbon, Portugal.
  • Gilman E; Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.
  • Kavakli K; Department of Pediatric Hematology, Ege University Children's Hospital, Izmir, Turkey.
  • Lambert T; Centre de traitement des Hemophiles de Bicetre, Paris, France.
  • Lassila R; Department of Hematology, Cancer Center, Helsinki University Hospital, Helsinki, Finland.
  • Lissitchkov T; Haematology Hospital "Joan Pavel", Sofia, Bulgaria.
  • Mauser-Bunschoten E; Van Creveldkliniek University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Mingot-Castellano ME; Regional University Hospital of Málaga, Málaga, Spain.
  • Ozdemir N; Istanbul University Haemophilia Centre, Istanbul, Turkey.
  • Pabinger I; Department of Medicine I, Haemophilia Centre, Medical University of Vienna, Vienna, Austria.
  • Parra R; Hospital Vall d'Hebron, Barcelona, Spain.
  • Pasi J; Barts and the London School of Medicine, London, UK.
  • Peerlinck K; Haemophilia Center, Universitaire Ziekenhuis Gasthuisberg, Leuven, Belgium.
  • Rauch A; Département d'Hématologie Transfusion, Centre Hospitalier Régional Universitaire de Lille, Lille, France.
  • Roussel-Robert V; Regional Reference Centre for Inherited Bleeding Disorders, University Hospital of Parma, Parma, Italy.
  • Serban M; Hôpital Cochin, Paris, France.
  • Tagliaferri A; European Haemophilia Center, Paediatric Clinical Emergency Hospital Louis Turcanu, Timisoara, Romania.
  • Windyga J; Department of Disorders of Haemostasis and Internal Medicine, Institute of Haematology & Transfusion Medicine, Warsaw, Poland.
  • Zanon E; Haemophilia Centre, Azienda Universitaria Ospedaliera di Padova, Padova, Italy.
Haemophilia ; 23(2): 255-263, 2017 Mar.
Article em En | MEDLINE | ID: mdl-28205285
ABSTRACT

BACKGROUND:

Development of inhibitors is the most serious complication in haemophilia A treatment. The assessment of risk for inhibitor formation in new or modified factor concentrates is traditionally performed in previously treated patients (PTPs). However, evidence on risk factors for and natural history of inhibitors has been generated mostly in previously untreated patients (PUPs). The purpose of this study was to examine cases of de novo inhibitors in PTPs reported in the scientific literature and to the EUropean HAemophilia Safety Surveillance (EUHASS) programme, and explore determinants and course of inhibitor development.

METHODS:

We used a case series study design and developed a case report form to collect patient level data; including detection, inhibitor course, treatment, factor VIII products used and events that may trigger inhibitor development (surgery, vaccination, immune disorders, malignancy, product switch).

RESULTS:

We identified 19 publications that reported 38 inhibitor cases and 45 cases from 31 EUHASS centres. Individual patient data were collected for 55/83 (66%) inhibitor cases out of 12 330 patients. The median (range) peak inhibitor titre was 4.4 (0.5-135.0), the proportion of transient inhibitors was 33% and only two cases of 12 undergoing immune tolerance induction failed this treatment. In the two months before inhibitor development, surgery was reported in nine (22%) cases, and high intensity treatment periods reported in seven (17%) cases.

CONCLUSIONS:

By studying the largest cohort of inhibitor development in PTPs assembled to date, we showed that inhibitor development in PTPs, is on average, a milder event than in PUPs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: História Natural Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Revista: Haemophilia Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: História Natural Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Revista: Haemophilia Ano de publicação: 2017 Tipo de documento: Article