Use of prothrombin complex concentrate for excessive bleeding after cardiac surgery
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Published on: July 31, 2016
Vrigina Arnékian1, Julien Camous, Soly Fattal
1Cardiothoracic Intensive Care Unit, Centre Chirurgical Marie Lannelongue, Le Plessis Robinson, France.
Insights
Low-dose prothrombin complex concentrates (PCCs) effectively reduced bleeding after cardiopulmonary bypass (CPB). This study evaluated PCC
Area of Science:
- Cardiovascular Surgery
- Hematology
- Anesthesiology
Background:
- Excessive bleeding is a significant complication following cardiopulmonary bypass (CPB).
- Prothrombin complex concentrates (PCCs) are sometimes used off-label to manage post-CPB bleeding.
- Clinical and biological efficacy of PCC in this setting requires further evaluation.
Purpose of the Study:
- To retrospectively assess the clinical and biological efficacy of prothrombin complex concentrates (PCCs).
- To evaluate PCC's effectiveness in managing excessive bleeding after cardiopulmonary bypass (CPB).
- To compare PCC with other hemostatic therapies in the post-CPB setting.
Main Methods:
- Retrospective chart review of patients undergoing cardiac surgery with CPB over two years.
- Identification of patients treated for active bleeding with hemostatic therapy.
- Quantification of chest tube blood loss, coagulation parameters, and thromboembolic complications.
Main Results:
- Seventy-seven patients were included: 24 received PCC alone (Group I), 26 received fresh frozen plasma (Group II), and 27 received both (Group III).
- Group I showed a significant difference in initial blood loss compared to Group III (P=0.02).
- Re-exploration for bleeding occurred in 4% of Group I, 8% of Group II, and 37% of Group III (P=0.002).
Conclusions:
- Low-dose prothrombin complex concentrate administration significantly decreased postoperative bleeding after CPB.
- PCC demonstrated efficacy in reducing the need for re-exploration due to bleeding.
- Further research may support the use of PCC for managing post-cardiopulmonary bypass bleeding.
Objectives:
Prothrombin complex concentrates (PCCs) are sometimes used as 'off label' for excessive bleeding after cardiopulmonary bypass (CPB). The main objective of this study was to retrospectively evaluate the clinical and biological efficacy of PCC in this setting.
Methods:
We reviewed the charts of all patients who had undergone cardiac surgery under CPB in our institution for 2 years. Patients treated for active bleeding with haemostatic therapy were identified. Chest tube blood loss was quantified postoperatively in the first 24 h. Coagulation parameters were recorded at intensive care unit admission and in the patient's first 24 h. Thromboembolic complications were also ascertained.
Results:
Seventy-seven patients out of the 677 studied (11.4%) were included: PCC was solely administered in 24 patients (group I), fresh frozen plasma in 26 (group II) and both in 27 (group III). The mean dose of PCC was 10.0 UI/kg ± 3.5 for group I vs 14.1 UI/kg ± 11.2 for group III (P = 0.09). Initial blood loss in the first hour was different between the three groups (P = 0.05): 224 ± 131 ml for group I, 369 ± 296 ml for group II and 434 ± 398 ml for group III. Only group I vs group III presented a significant difference (P = 0.02). Variations of blood loss over time were no different according to the treatment groups (P = 0.12). Reductions in blood loss expressed in percentage showed no difference between the three groups after 2 h: 54.5% (68.6-30.8) for group I; 45.0% (81.6-22.2) for group II; 57.6 (76.0-2.1) for group III; (P = 0.89). Re-exploration for bleeding involved 1 patient in group I (4%), 2 in group II (8%) and 10 in group III (37%) (P = 0.002). Except for fibrinogen, variations of prothrombin time, activated partial thromboplastin time and platelets with time were not different according to the treatment groups. Cerebral infarction occurred in one patient in group II.
Conclusions:
Administration of low-dose of PCC significantly decreased postoperative bleeding after CPB.
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