Evidence map›Paper›PMID 42433599›Full record

Observational studyResearch and practice in thrombosis and haemostasis2026

Efficacy and safety of recombinant activated factor VII for secondary prophylaxis in patients with Glanzmann thrombasthenia.

Pablo García-Jaén, Nuria Fernández-Mosteirin, María Luisa Serrano, Susana Riesco, Carlos Aguilar, David Gabaldon, Sara Kanaan-Leis, Almudena González-Prieto, Raquel Portugal, María Carmen Mendoza and 10 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Pablo García-JaénServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
Nuria Fernández-MosteirinServicio de Hematología, Hospital Universitario Miguel Servet, Zaragoza, Spain.
María Luisa SerranoServicio de Pediatría, Complejo Asistencial de Soria, Soria, Spain.
Susana RiescoServicio de Pediatría, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain.
Carlos AguilarServicio de Hematología, Complejo Asistencial de Soria, Soria, Spain.
David GabaldonServicio de Pediatría, Complejo Asistencial Universitario de Burgos, Burgos, Spain.
Sara Kanaan-LeisServicio de Pediatría, Complejo Asistencial de Soria, Soria, Spain.
Almudena González-PrietoServicio de Pediatría, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain.
Raquel PortugalServicio de Pediatría, Complejo Asistencial Universitario de Burgos, Burgos, Spain.
María Carmen MendozaServicio de Pediatría, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain.
Carmen GilabertServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
Ana HortalServicio de Pediatría, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain.
Lorena Díaz-AjenjoCentro de Investigación del Cáncer-CSIC-Universidad de Salamanca (USAL), Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain.
Ana Lama-VillanuevaCentro de Investigación del Cáncer-CSIC-Universidad de Salamanca (USAL), Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain.
Alba Mei González-GalánCentro de Investigación del Cáncer-CSIC-Universidad de Salamanca (USAL), Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain.
Ana Sánchez-FuentesServicio de Hematología, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-U765, Murcia, Spain.
Rocío BenitoCentro de Investigación del Cáncer-CSIC-Universidad de Salamanca (USAL), Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain.
José RiveraServicio de Hematología, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-U765, Murcia, Spain.
José Ramón González-PorrasServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
José María BastidaServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glanzmann thrombasthenia (GT) is a rare inherited platelet disorder associated with recurrent and sometimes life-threatening bleeding. Recombinant activated factor VII (rFVIIa) is approved for treatment of bleeding episodes or surgical prophylaxis in patients with GT who are refractory or alloimmunized to platelet transfusions. However, evidence for its use as secondary prophylaxis remains scarce. Objectives: This study described the efficacy and safety of rFVIIa secondary prophylaxis in patients with GT and recurrent and uncontrolled bleeding despite standard therapy. Methods: A multicenter, retrospective study of patients with GT included in the Spanish Registry of Patients with Inherited Platelet Disorders (RETPLAC) was performed. We evaluated bleeding severity using the International Society on Thrombosis and Haemostasis (ISTH) bleeding assessment tool (BAT) and calculated the annualized bleeding rate (ABR) before and during rFVIIa prophylaxis. Results: Of the 37 patients with GT included in RETPLAC, 4 patients received regular rFVIIa prophylaxis due to recurrent severe bleeding. Median baseline ISTH-BAT score was 13.5 (IQR, 9.5-18), and median preprophylaxis ABR was 3 (IQR, 3-5.25). All patients received rFVIIa of 90 μg/kg, 3 twice weekly and 1 monthly. The median prophylaxis duration was 7.5 months (IQR, 6.75-12). Prophylaxis led to a 57.1% overall reduction in ABR, with resolution of severe bleeding in 2 patients and reduction in frequency in the remaining 2. Three patients achieved transfusion independence. All patients showed improvement in hemoglobin and iron profile. No thrombotic or adverse events occurred. Conclusion: Secondary prophylaxis with rFVIIa may be an effective option in patients with GT and recurrent severe bleeding unresponsive to standard therapy. Prospective studies are necessary to optimize dosing schedules and define its role in secondary prophylaxis.

Indexed as

Factor VIIaHemorrhageThrombastheniaAdolescentAdultFemaleHumansMaleRecombinant ProteinsRecurrenceRegistriesRetrospective StudiesSecondary PreventionSpainTreatment OutcomeFactor VIIarecombinant FVIIaRecombinant ProteinsbleedingGlanzmann thrombastheniaprophylaxisrecombinant activated factor VII

Identifiers

PMID42433599
PMCPMC13352059

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.