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Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study

BACKGROUND: Bleeding diathesis after aortic valve operation and ascending aorta replacement (AV–AA) is managed with fresh-frozen plasma (FFP) and platelet concentrates. The aim was to compare haemostatic effects of conventional transfusion management and FIBTEM (thromboelastometry test)-guided fibri...

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Autores principales: Rahe-Meyer, N., Pichlmaier, M., Haverich, A., Solomon, C., Winterhalter, M., Piepenbrock, S., Tanaka, K. A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683341/
https://www.ncbi.nlm.nih.gov/pubmed/19411671
http://dx.doi.org/10.1093/bja/aep089
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author Rahe-Meyer, N.
Pichlmaier, M.
Haverich, A.
Solomon, C.
Winterhalter, M.
Piepenbrock, S.
Tanaka, K. A.
author_facet Rahe-Meyer, N.
Pichlmaier, M.
Haverich, A.
Solomon, C.
Winterhalter, M.
Piepenbrock, S.
Tanaka, K. A.
author_sort Rahe-Meyer, N.
collection PubMed
description BACKGROUND: Bleeding diathesis after aortic valve operation and ascending aorta replacement (AV–AA) is managed with fresh-frozen plasma (FFP) and platelet concentrates. The aim was to compare haemostatic effects of conventional transfusion management and FIBTEM (thromboelastometry test)-guided fibrinogen concentrate administration. METHODS: A blood products transfusion algorithm was developed using retrospective data from 42 elective patients (Group A). Two units of platelet concentrate were transfused after cardiopulmonary bypass, followed by 4 u of FFP if bleeding persisted, if platelet count was ≤100×10(3) µl(−1) when removing the aortic clamp, and vice versa if platelet count was >100×10(3) µl(−1). The trigger for each therapy step was ≥60 g blood absorbed from the mediastinal wound area by dry swabs in 5 min. Assignment to two prospective groups was neither randomized nor blinded; Group B (n=5) was treated according to the algorithm, Group C (n=10) received fibrinogen concentrate (Haemocomplettan(®) P/Riastap, CSL Behring, Marburg, Germany) before the algorithm-based therapy. RESULTS: A mean of 5.7 (0.7) g fibrinogen concentrate decreased blood loss to below the transfusion trigger level in all Group C patients. Group C had reduced transfusion [mean 0.7 (range 0–4) u vs 8.5 (5.3) in Group A and 8.2 (2.3) in Group B] and reduced postoperative bleeding [366 (199) ml vs 793 (560) in Group A and 716 (219) in Group B]. CONCLUSIONS: In this pilot study, FIBTEM-guided fibrinogen concentrate administration was associated with reduced transfusion requirements and 24 h postoperative bleeding in patients undergoing AV–AA.
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spelling pubmed-26833412009-05-19 Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study Rahe-Meyer, N. Pichlmaier, M. Haverich, A. Solomon, C. Winterhalter, M. Piepenbrock, S. Tanaka, K. A. Br J Anaesth Critical Care BACKGROUND: Bleeding diathesis after aortic valve operation and ascending aorta replacement (AV–AA) is managed with fresh-frozen plasma (FFP) and platelet concentrates. The aim was to compare haemostatic effects of conventional transfusion management and FIBTEM (thromboelastometry test)-guided fibrinogen concentrate administration. METHODS: A blood products transfusion algorithm was developed using retrospective data from 42 elective patients (Group A). Two units of platelet concentrate were transfused after cardiopulmonary bypass, followed by 4 u of FFP if bleeding persisted, if platelet count was ≤100×10(3) µl(−1) when removing the aortic clamp, and vice versa if platelet count was >100×10(3) µl(−1). The trigger for each therapy step was ≥60 g blood absorbed from the mediastinal wound area by dry swabs in 5 min. Assignment to two prospective groups was neither randomized nor blinded; Group B (n=5) was treated according to the algorithm, Group C (n=10) received fibrinogen concentrate (Haemocomplettan(®) P/Riastap, CSL Behring, Marburg, Germany) before the algorithm-based therapy. RESULTS: A mean of 5.7 (0.7) g fibrinogen concentrate decreased blood loss to below the transfusion trigger level in all Group C patients. Group C had reduced transfusion [mean 0.7 (range 0–4) u vs 8.5 (5.3) in Group A and 8.2 (2.3) in Group B] and reduced postoperative bleeding [366 (199) ml vs 793 (560) in Group A and 716 (219) in Group B]. CONCLUSIONS: In this pilot study, FIBTEM-guided fibrinogen concentrate administration was associated with reduced transfusion requirements and 24 h postoperative bleeding in patients undergoing AV–AA. Oxford University Press 2009-06 2009-05-02 /pmc/articles/PMC2683341/ /pubmed/19411671 http://dx.doi.org/10.1093/bja/aep089 Text en © 2009 The Author(s)
spellingShingle Critical Care
Rahe-Meyer, N.
Pichlmaier, M.
Haverich, A.
Solomon, C.
Winterhalter, M.
Piepenbrock, S.
Tanaka, K. A.
Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title_full Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title_fullStr Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title_full_unstemmed Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title_short Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
title_sort bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study
topic Critical Care
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683341/
https://www.ncbi.nlm.nih.gov/pubmed/19411671
http://dx.doi.org/10.1093/bja/aep089
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