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Multicenter Study
. 2025 Jul 8;9(13):3238-3248.
doi: 10.1182/bloodadvances.2024015494.

Critical bleeding in adults and children with immune thrombocytopenia: a multicenter cohort study

Affiliations
Multicenter Study

Critical bleeding in adults and children with immune thrombocytopenia: a multicenter cohort study

Emily Sirotich et al. Blood Adv. .

Abstract

Critical bleeding in patients with immune thrombocytopenia (ITP) is a life-threatening hematologic emergency. This study aimed to describe the frequency, management, and outcomes of critical bleeds among adults and children with ITP. We conducted a retrospective cohort study of patients with ITP who presented to the emergency room with a platelet count <20 × 109/L across 7 centers in the United States and Canada between 2010 and 2019. Of 1226 patients (n = 296 adults; n = 930 children), 28 (2.3%) had critical bleeds (adults, n = 15 [median age, 68 years]; children, n = 13 [median age, 11 years]). Of patients with critical bleeds, 12 adults (80.0%) and 6 children (46.2%) had intracranial hemorrhage (ICH). For adults, the common interventions used to treat critical bleeds were platelet transfusions (n = 11 [73.3%]), corticosteroids (n = 10 [66.7%]), and IV immunoglobulin (n = 8 [53.3%]), and for children, common interventions were IV immunoglobulin (n = 10 [76.9%]), corticosteroids (n = 8 [61.5%]), platelet transfusions (n = 8 [61.5%]), thrombopoietin receptor agonists (n = 4 [30.8%]), and antifibrinolytic agents (n = 4 [30.8%]). For both adults and children, the most common treatment combination was corticosteroids, IV immunoglobulin, and platelet transfusion (n = 6 [40.0%] vs n = 6 [46.2%]). The median time from presentation to first treatment was 6.9 hours for adults and 3.5 hours for children. Overall, 9 patients (32.1%) with critical ITP bleeds died, including 7 adults (46.7%) and 2 children (15.4%). Critical bleeding in patients with ITP was rare but frequently fatal, especially among older adults with ICH and when treatments were delayed.

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Conflict of interest statement

Conflict-of-interest disclosure: A.C. reports personal fees from Synergy, Sanofi, Pfizer, MingSight, and UpToDate, outside the submitted work. R.F.G. reports research funding from Agios, Novartis, and Sobi; and had a consultancy role with Agios, Sanofi, and Sobi, outside the submitted work. M.P.L. reports personal fees from Novartis Dova, Principia, argenx, Rigel, Sobi, Sanofi, Janssen, and UpToDate; and research funding from Novartis Dova, Principia, argenx, Rigel, Sobi, Sanofi, and Janssen. A.P. served on an advisory board for Biomarin and received authorship royalties from UpToDate. D.M.A. reports research grants from Rigel; and personal fees from Rigel, Amgen, Medison, Daiichi Sankyo, Sobi, Principia, Chugai, Alpine, argenx, Sanofi, and UpToDate, outside the submitted work. The remaining authors declare no competing financial interests.

Figures

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Graphical abstract
Figure 1.
Figure 1.
Recruitment of patients with ITP.

References

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