Key result
Prohemostatic therapy in critical bleeding carries ~31% 30-day mortality across observational cohorts.
Why the study?
The outcome of patients receiving goal-directed prohemostatic therapy as part of hemostatic resuscitation remains unanswered.
What are the clinical outcomes and predictors of mortality in critically ill patients receiving goal-directed prohemostatic therapy?
Observational (n=287)
What are the clinical outcomes and predictors of mortality in critically ill patients receiving goal-directed prohemostatic therapy?
In critically ill patients receiving goal-directed prohemostatic therapy, 30-day mortality is high (31%), with varying rates of thromboembolic events depending on the specific agent used.
High mortality and varying thromboembolic risks warrant caution with prohemostatic agents; hypothesis-generating for agent-specific safety in goal-directed therapy.
The Danish Capital Region Blood Bank operates a 24/7 on-call service staffed with physicians specialized in hemostatic management to guide clinicians in hemostatic resuscitation, including administration of prohemostatic therapy (PHT). The outcome of patients who receive PHT as part of hemostatic resuscitation remains unanswered. The objective of this study was therefore to investigate clinical outcome of patients receiving PHT managed by the on-call service. We identified 287 patients who received PHT during 2015-16, of which 161 (59%) received fibrinogen concentrate (FC), 111 (39%) received prothrombin complex concentrate (PCC), and 15 (5%) received recombinant factor VIIa (rFVIIa) as the first product. Patients were critically ill with a 30-day mortality of 31%. Among FC recipients, cardiothoracic admission, non-trauma, and antithrombotics predicted survival. FC recipients had lower platelet count and thrombelastography clot strengths than the other PHT groups and within the group, these factors predicted mortality. The symptomatic thromboembolic event (TE) rate at 30 days was 5%. For PCC recipients, vitamin K antagonists predicted survival, while rivaroxaban predicted mortality. TE rate was 2%. We did not identify factors associated with survival in the small group of rFVIIa recipients. TE rate was 13%. In summary, trauma and coagulopathy predicted mortality in patients who received FC and our data suggest that optimization of PHT algorithms may be possible. Outcome of patients who received PCC was comparable to results reported elsewhere and its use may be safe in a setting as reported here. Recombinant FVIIa was rarely used but had the highest incidence of arterial thromboembolism.
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Vigstedt et al. (2022) conducted an observational in Critically ill requiring hemostatic resuscitation (n=287). Prohemostatic therapy was evaluated on 30-day mortality. Among 287 critically ill patients receiving prohemostatic therapy, 30-day mortality was 31%, with thromboembolic event rates of 5% for fibrinogen concentrate, 2% for PCC, and 13% for rFVIIa.
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