Literature DB >> 26001793

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

Giovanni Di Minno1, Rainer B Zotz2, Roseline d'Oiron3, Niels Bindslev4, Matteo Nicola Dario Di Minno5, Man-Chiu Poon6.   

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.

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Year:  2015        PMID: 26001793      PMCID: PMC5004418          DOI: 10.3324/haematol.2014.121475

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  21 in total

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Authors:  A T Nurden
Journal:  Thromb Haemost       Date:  1999-08       Impact factor: 5.249

2.  Use of recombinant factor VIIa in 3 patients with inherited type I Glanzmann's thrombasthenia undergoing invasive procedures.

Authors:  R d'Oiron; C Ménart; M C Trzeciak; P Nurden; E Fressinaud; M Dreyfus; Y Laurian; C Négrier
Journal:  Thromb Haemost       Date:  2000-05       Impact factor: 5.249

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Journal:  Thromb Diath Haemorrh       Date:  1975-12-15

Review 4.  A mini-review on platelet refractoriness.

Authors:  Paolo Rebulla
Journal:  Haematologica       Date:  2005-02       Impact factor: 9.941

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Authors:  L Tengborn; B Petruson
Journal:  Thromb Haemost       Date:  1996-06       Impact factor: 5.249

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Authors:  J N George; J P Caen; A T Nurden
Journal:  Blood       Date:  1990-04-01       Impact factor: 22.113

7.  An abnormal platelet glycoprotein pattern in three cases of Glanzmann's thrombasthenia.

Authors:  A T Nurden; J P Caen
Journal:  Br J Haematol       Date:  1974-10       Impact factor: 6.998

8.  The use of recombinant factor VIIa in children with inherited platelet function disorders.

Authors:  Antonio M Almeida; Kate Khair; Ian Hann; Ri Liesner
Journal:  Br J Haematol       Date:  2003-05       Impact factor: 6.998

9.  Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in Iran.

Authors:  G Toogeh; R Sharifian; M Lak; R Safaee; A Artoni; F Peyvandi
Journal:  Am J Hematol       Date:  2004-10       Impact factor: 10.047

Review 10.  Platelet transfusion refractoriness.

Authors:  Eldad Hod; Joseph Schwartz
Journal:  Br J Haematol       Date:  2008-05-28       Impact factor: 6.998

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  5 in total

Review 1.  Treatment of inherited thrombocytopenias.

Authors:  Carlo L Balduini
Journal:  Haematologica       Date:  2022-06-01       Impact factor: 11.047

2.  Severe Intestinal Bleeding in a Woman with Glanzmann Thrombasthenia.

Authors:  Raquel Mesquita; Inês Santos; Helena Monteiro
Journal:  Eur J Case Rep Intern Med       Date:  2018-02-22

Review 3.  Glanzmann Thrombasthenia: Perspectives from Clinical Practice on Accurate Diagnosis and Optimal Treatment Strategies.

Authors:  Natalie Mathews; Georges-Etienne Rivard; Arnaud Bonnefoy
Journal:  J Blood Med       Date:  2021-06-11

Review 4.  Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?

Authors:  Alan Nurden
Journal:  J Blood Med       Date:  2021-07-08

5.  Recognition and management of platelet-refractory bleeding in patients with Glanzmann's thrombasthenia and other severe platelet function disorders.

Authors:  Meera Chitlur; Madhvi Rajpurkar; Michael Recht; Michael D Tarantino; Donald L Yee; David L Cooper; Sriya Gunawardena
Journal:  Int J Gen Med       Date:  2017-04-03
  5 in total

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