The international, prospective Glanzmann Thrombasthenia Registry: treatment modalities and outcomes of non-surgical bleeding episodes in patients with Glanzmann thrombasthenia

Giovanni Di Minno, Rainer B Zotz, Roseline d'Oiron, Niels Bindslev, Matteo Nicola Dario Di Minno, Man-Chiu Poon, Glanzmann Thrombasthenia Registry Investigators, Grifi Fathia, Sidi Mansour Nourredine, Mesli Naïma, Hamdi Selma, Belhani Meriem, Touhami Hadj, Max Heistinger, Paul Alexander Kyrle, Christel Van Geet, Veerle Labarque, Angelina Stoyanova, Katya Sapunarova, Caroline Oudot, Roseline d'Oiron, Gruel Yves, Albert Faradji, Achille Aouba, Nathalie Trillot, Alain Marquès-Verdier, Claire Pouplard, Rainer B Zotz, Roswith Eisert, Ingvild Birschmann, Mario von Depka Prondzinski, Maximillian Kirchmaier, Markus Rieke, Daniele Pillitteri, Agota Schlammadinger, Csongor Kiss, Laszlo Nemes, Gavino Piseddu, Giovanni Di Minno, Antonio Coppola, Paola Giordano, Elisabetta Sacchi, Michele Schiavulli, Paula Frouke Ypma, Meijer Karina, Maria Kruip, Pieter Kamphuisen, Britta Laros Van Gorkom, Karly Hamulyak, Rienk Yde Johan Tamminga, Tahir Shamsi, Munira Borhany, Rosario Perez Garrido, Victor Jiménez-Yuste, Erik Berntorp, Karin Knobe, Dimitrios Tsakiris, Brigitte Brand, John D Grainger, Kate Khair, Jayashree Motwani, Paula Bolton-Maggs, Marcella Torres, Giovanni Di Minno, Rainer B Zotz, Roseline d'Oiron, Niels Bindslev, Matteo Nicola Dario Di Minno, Man-Chiu Poon, Glanzmann Thrombasthenia Registry Investigators, Grifi Fathia, Sidi Mansour Nourredine, Mesli Naïma, Hamdi Selma, Belhani Meriem, Touhami Hadj, Max Heistinger, Paul Alexander Kyrle, Christel Van Geet, Veerle Labarque, Angelina Stoyanova, Katya Sapunarova, Caroline Oudot, Roseline d'Oiron, Gruel Yves, Albert Faradji, Achille Aouba, Nathalie Trillot, Alain Marquès-Verdier, Claire Pouplard, Rainer B Zotz, Roswith Eisert, Ingvild Birschmann, Mario von Depka Prondzinski, Maximillian Kirchmaier, Markus Rieke, Daniele Pillitteri, Agota Schlammadinger, Csongor Kiss, Laszlo Nemes, Gavino Piseddu, Giovanni Di Minno, Antonio Coppola, Paola Giordano, Elisabetta Sacchi, Michele Schiavulli, Paula Frouke Ypma, Meijer Karina, Maria Kruip, Pieter Kamphuisen, Britta Laros Van Gorkom, Karly Hamulyak, Rienk Yde Johan Tamminga, Tahir Shamsi, Munira Borhany, Rosario Perez Garrido, Victor Jiménez-Yuste, Erik Berntorp, Karin Knobe, Dimitrios Tsakiris, Brigitte Brand, John D Grainger, Kate Khair, Jayashree Motwani, Paula Bolton-Maggs, Marcella Torres

Abstract

Standard treatment for Glanzmann thrombasthenia is platelet transfusion. Recombinant activated factor VII has been shown to be successful in patients with Glanzmann thrombasthenia with platelet antibodies or who are refractory to platelet transfusions. The Glanzmann Thrombasthenia Registry prospectively collected worldwide information on the effectiveness and safety of platelet transfusion, recombinant activated factor VII and/or antifibrinolytics for the treatment of bleeds in patients with Glanzmann thrombasthenia. Data relating to 829 non-surgical bleeding episodes were entered into the Glanzmann Thrombasthenia Registry (severe/moderate: 216/613; spontaneous/post-traumatic: 630/199). Recombinant activated factor VII alone was used in 124/829 bleeds, recombinant activated factor VII+antifibrinolytics in 107/829, platelets±antifibrinolytics in 312/829, antifibrinolytics alone in 219/829, and recombinant activated factor VII+platelets±antifibrinolytics in 67/829. The proportion of successful treatments to stop bleeding was 91.0% in cases treated with recombinant activated factor VII only, 82.7% for recombinant activated factor VII+antifibrinolytics, 72.7% for treatment with recombinant activated factor VII+platelets±antifibrinolytics, 78.8% for platelets±antifibrinolytics and 84.7% for antifibrinolytics alone. Treatment failure was documented in 18 bleeding events (2% of the total treatments), the majority of which were in patients receiving treatment with antifibrinolytics; bleeding re-started in 6% of bleeds after initial effective treatment. Thirty-five adverse events were reported, none of which was a thromboembolic event. Among treatments that included recombinant activated factor VII, only one patient reported three possibly drug-related non-serious adverse events (nausea, dyspnea and headache). To conclude, non-surgical bleeds were common and often severe in Glanzmann thrombasthenia; both platelets and recombinant activated factor VII appeared to be effective, and with good safety profiles, for the treatment of non-surgical bleeds. This trial was registered at clinicaltrials.gov identifier: NCT01476423.

Copyright© Ferrata Storti Foundation.

Figures

Figure 1.
Figure 1.
Chart depicting the flow of admissions into the GTR and the data used for primary and secondary analyses. *One admission was considered both a surgical procedure and a bleeding episode. †Data used for the primary effectiveness analysis (performed in 2012). ‡Data used for the secondary data analysis (performed in 2014). All data were included in the safety analysis.

Source: PubMed

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