IntroductionThe appropriate strategy for trauma-induced coagulopathy management is under debate. We report the treatment of major trauma using mainly coagulation factor concentrates.MethodsThis retrospective analysis included trauma patients who received ≥ 5 units of red blood cell concentrate within 24 hours. Coagulation management was guided by thromboelastometry (ROTEM®). Fibrinogen concentrate was given as first-line haemostatic therapy when maximum clot firmness (MCF) measured by FibTEM (fibrin-based test) was <10 mm. Prothrombin complex concentrate (PCC) was given in case of recent coumarin intake or clotting time measured by extrinsic activation test (EXTEM) >1.5 times normal. Lack of improvement in EXTEM MCF after fibrinogen concentrate administration was an indication for platelet concentrate. The observed mortality was compared with the mortality predicted by the trauma injury severity score (TRISS) and by the revised injury severity classification (RISC) score.ResultsOf 131 patients included, 128 received fibrinogen concentrate as first-line therapy, 98 additionally received PCC, while 3 patients with recent coumarin intake received only PCC. Twelve patients received FFP and 29 received platelet concentrate. The observed mortality was 24.4%, lower than the TRISS mortality of 33.7% (P = 0.032) and the RISC mortality of 28.7% (P > 0.05). After excluding 17 patients with traumatic brain injury, the difference in mortality was 14% observed versus 27.8% predicted by TRISS (P = 0.0018) and 24.3% predicted by RISC (P = 0.014).ConclusionsROTEM®-guided haemostatic therapy, with fibrinogen concentrate as first-line haemostatic therapy and additional PCC, was goal-directed and fast. A favourable survival rate was observed. Prospective, randomized trials to investigate this therapeutic alternative further appear warranted.
ROTEM-based diagnosis of HF predicted outcome. Further independent predictors of death were combination of HF with hemorrhagic shock, low PC, and prolonged CFT in ROTEM. ROTEM-based point of care testing in the emergency room is thus able to identify prognostic factors such as prolonged CFT and low platelet contribution to clot firmness (MCF(EX) - MCF(FIB)) earlier than standard laboratory-based monitoring.
About one third of all blood components
transfused intraoperatively is used in cardiac surgery,
whereas mortality of cardiosurgical patients correlates
nearly linear with the number of transfused units of
packed red blood cells. Acquired platelet function disorders
play a major role in perioperative bleeding in cardiac
surgery. Therefore, the use of point-of-care-suitable
platelet function analyzers seems to be reasonable in this
field. Methods: Platelet function analyzer PFA-100®, rotational
thrombelastometry (ROTEM®), and multiple
platelet function analyzer (Multiplate®) are in principle
applicable for point-of-care testing. Since these three analyzers
monitor different aspects of platelet function and
have different limitations, the selection of the right test
system depends on the right question. Results: Perioperative
use of platelet function analyzers is helpful in prediction
of blood loss in cardiac surgery. Perioperative
usage of blood components and their respective costs
can be reduced by an appropriate coagulation management.
Conclusion: Algorithms for perioperative coagulation
management based on point-of-care testing permit a
fast diagnostic and goal-directed therapy of coagulation
and functional platelet disorders. The possibility to reduce
the mortality of patients and the overall cost for
hospital stay is subject of further studies.
MEA reliably detected the effects of aspirin. Notably, 500 mg aspirin caused complete inhibition of arachidonic acid-induced platelet aggregation for 2 days in all volunteers. Aggregation returned to baseline values with a wide interindividual variation in time course by day 5. No resting time for the blood sample was required for ASPItest or TRAPtest. These assays can be implemented as real POC tests. The reproducibility of the assays studied here is within the range of modern POC analyzers.
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