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Clinical Science  |   February 2005
Recombinant Coagulation Factor VIIa in Major Liver Resection: A Randomized, Placebo-controlled, Double-blind Clinical Trial
Author Affiliations & Notes
  • J Peter A. Lodge, M.D., F.R.C.S.
    *
  • Sven Jonas, M.D.
  • Elie Oussoultzoglou, M.D.
  • Massimo Malagó, M.D.
    §
  • Christian Jayr, M.D.
  • Daniel Cherqui, M.D.
    #
  • Matthias Anthuber, M.D.
    **
  • Darius F. Mirza, M.S., F.R.C.S.
    ††
  • Luce Kuhlman, M.D.
    ‡‡
  • Wolf-Otto Bechstein, M.D.
    §§
  • Juan Carlos Meneu Díaz, M.D.
    ∥∥
  • Jack Tartiere, M.D.
    ##
  • Daniel Eyraud, M.D.
    ***
  • Marianne Fridberg, M.Sc.
    †††
  • Elisabeth Erhardtsen, D.V.M.
    ‡‡‡
  • Oliver Mimoz, M.D.
    §§§
  • * Professor of Surgery, St. James’s University Hospital. † Professor, Campus Virchow-Klinikum. ‡ Hospital Practitioner, Hospital Haute-Pierre, Strasbourg, France. § Professor of Surgery and Transplantation, Essen University Clinic. ∥ Research Director, Institut Gustave Rousy. # Professor, Hospital Henri-Mondor. ** Professor, Regensburg University Clinic. †† Consultant Hepatobiliary and Transplant Surgeon, The Queen Elizabeth Hospital. ‡‡ Hospital Consultant in Anesthesiology, Paul Brousse University Hospital Center. §§ Professor of Surgery and Chairman of the Department of General and Vascular Surgery, University Hospital Frankfurt am Main. ∥∥Staff Surgeon, Hospital “12 de Octubre.” ## Hospital Practitioner in Anesthesiology and Intensive Care, Anesthesia and Intensive Care Department, Pr JL Gerard Unit, Centre Hospitalier Universitaire de la Côte de Nacre. *** Associate Professor, Hospital Pitié Salpétriére. ††† Clinical Research Associate, ‡‡‡ Medical Director, Novo Nordisk A/S, Bagsvaerd, Denmark. §§§ Professor, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
Article Information
Clinical Science / Coagulation and Transfusion / Gastrointestinal and Hepatic Systems / Hematologic System
Clinical Science   |   February 2005
Recombinant Coagulation Factor VIIa in Major Liver Resection: A Randomized, Placebo-controlled, Double-blind Clinical Trial
Anesthesiology 2 2005, Vol.102, 269-275. doi:
Anesthesiology 2 2005, Vol.102, 269-275. doi:
DESPITE improvements in surgical techniques during the past two decades, hepatic resection is often associated with significant intraoperative blood loss, primarily occurring from branches of the hepatic veins damaged during parenchymal transection or as a result of mobilization of tumors.1 Recent estimates show that perioperative blood transfusion is required in approximately 25–40% of unselected patients undergoing partial hepatectomy.2–6 In addition to the inherent difficulties in adequately replacing blood components especially in cases of severe bleeding, allogeneic blood transfusion constitutes a risk factor for intraoperative and postoperative morbidity, including viral disease transmission, transfusion reactions, and an increased risk of postoperative infectious complications.7–9 The existence of an adverse effect of blood transfusion on tumor recurrence is still controversial10,11 but may be a further argument for reducing the need for blood transfusions. The latter point is especially pertinent for major liver resection, which is mostly performed for malignant disease. Many surgical techniques for vascular control in hepatic resection have been advocated. Techniques such as partial and total vascular exclusion are routinely used but may induce ischemic liver injury and, in the latter case, hemodynamic complications.12–14 Therefore, there is a need for treatment modalities that may induce a primary hemostatic effect.
Recombinant activated coagulation factor VII (rFVIIa, NovoSeven®; NovoNordisk A/S, Copenhagen, Denmark) is currently registered for perioperative prophylaxis and treatment of bleeding episodes in hemophilia patients with inhibitors against coagulation factors VIII and IX and in the European Union for patients with acquired hemophilia, FVII deficiency, and Glanzmann thrombasthenia who are refractory to platelets. Pharmacologic doses of rFVIIa have been shown to enhance thrombin generation on locally activated platelets, thereby contributing to the formation of a stabilized and lysis-resistant fibrin plug at the site of vessel injury.15,16 Patients experiencing bleeding in any situation of potentially suboptimal thrombin generation, including intraoperative depression of the coagulation system, may thus potentially benefit from dosing with rFVIIa. A hemostatic effect of rFVIIa has recently been demonstrated in patients with normal coagulation systems in a double-blind, placebo-controlled trial in retropubic prostatectomy, where a single bolus of 40 μg/kg rFVIIa in the early operative phase significantly reduced blood loss, transfusion requirements, and operating time when compared with placebo.17 
The current randomized, controlled, double-blind, multi-national trial was designed to evaluate the efficacy and safety of rFVIIa in noncirrhotic patients undergoing major liver resection.
Materials and Methods
Patients
Noncirrhotic adults (≥ 18 yr of age) scheduled to undergo partial hepatectomy for liver cancer/metastasis, benign tumors, or both were recruited into the trial at 13 hospitals throughout France, Spain, Germany, and the United Kingdom (see 1). A further requirement for inclusion was planned anatomical resection of three or more segments of the liver or planned nonanatomical resection of a volume equivalent to two or more segments of the liver parenchyma. Exclusion criteria included known hereditary bleeding disorders; the planned use of autologous blood transfusion, low-molecular-weight heparin before hepatectomy, tissue glue or hemodilution therapy during surgery, or hemostatic drugs for prophylactic purposes; renal insufficiency requiring dialysis; clinically documented portal vein or deep vein thrombosis or a history of the latter within the preceding 6 months; severe cardiovascular disease or previous myocardial/pulmonary infarction or stroke within the preceding 6 months; anticoagulation therapy not discontinued within 48 h before surgery; active bleeding; and the use of nonsteroidal antiinflammatory drugs within 7 days before surgery. The study protocol was approved by local ethics committees in the participating countries, and the trial was conducted according to standards of good clinical practice. All patients gave written informed consent.
Study Drug Administration
Patients were equally randomized in center blocks to receive an injection of either 20 or 80 μg/kg rFVIIa or placebo. Randomization was computer-generated and was performed after patient eligibility assessments on the day of surgery by means of a central interactive voice response system set up by Novo Nordisk A/S. The trial drug was administered as a slow intravenous injection within 5 min before the first skin cut to ensure sufficient amounts of rFVIIa in the liver circulation during surgical procedures and before any clamping procedures were performed. A second identical dose was given 5 h after the first skin cut if the surgery time was anticipated to exceed 6 h. This was done to achieve adequate plasma concentrations of rFVIIa during extended surgical procedures, given the expected half-life of rFVIIa of approximately 2.5 h.18 
Blinding
To maintain blinding, an equal volume of trial drug per body weight was administered to all patients, irrespective of treatment group allocation. Furthermore, central laboratory analysis results for prothrombin time, which might reveal treatment allocation, were not transferred from the laboratory to the investigators or the sponsor before the trial was completed. Local laboratory results on prothrombin time or international normalized ratio were reviewed by an unblinded third party.
Hepatectomy and Transfusion Procedures
Partial hepatectomy was performed according to local standard practice at the participating centers in France, Spain, Germany, and the United Kingdom. Unless deviations were clinically indicated, the following transfusion guidelines were adhered to: erythrocytes were administered when the hematocrit was less than 25%; fresh frozen plasma was administered when clinically indicated as evaluated by the attending surgeon; platelet concentrate was administered when the platelet count was less than 30,000/mm2; and cryoprecipitates or fibrinogen concentrate was administered when the fibrinogen concentration was less than 1.0 g/l. Prophylactic systemic administration of hemostatic drugs and low-molecular-weight heparin was not allowed before surgery, but treatment could be initiated if critical bleeding occurred during surgery. Topical administration of hemostatic drugs/agents was allowed in those cases where overt bleeding occurred even though transfusion guidelines were followed. During the postsurgical period, the hematocrit was to be kept above 28%. Blood samples were drawn at 15 and 60 min after the first skin cut and then at 1-hour intervals until completion of surgery for the determination of blood biochemistry, coagulation-related parameters, and plasma concentrations of rFVIIa. Treatment with low-molecular-weight heparin at maximum doses of 10,000 U every 24 h for at least 1 day was initiated at completion of surgery. Patients were monitored for 7 days after surgery or until discharge from the hospital, whichever came first.
Endpoints
The primary endpoint was whether patients required erythrocyte transfusion during surgery or the 48-h period after surgery (perioperative period). Efficacy was furthermore assessed by the amount of erythrocytes transfused, change in hematocrit, the proportion of patients who required perioperative transfusions of fresh frozen plasma, and total surgery time (from first skin cut to wound closure). Blood loss during surgery was assessed as the volume collected in suction containers and sponges/dressings/swabs minus the irrigation volume, and blood loss after surgery was evaluated using surgical drain volume 0–24 h after surgery, as well as hematocrit measured herein, as endpoints. Safety was assessed by the occurrence of adverse events, focusing on thromboembolic adverse events and bleeding complications, the former evaluated by Doppler examination of the hepatic vessels (before surgery, within 48 h after surgery, and otherwise if indicated) and lower extremities (before surgery and every 24 h until 3 days after surgery). Also, changes in coagulation-related parameters (prothrombin time, platelet count, and the concentrations of fibrinogen, D-dimer, prothrombin fragments 1 and 2, thrombin-antithrombin complex, and antithrombin III) and blood biochemistry (serum creatinine, calcium, potassium, sodium, bilirubin, serum albumin, alanine aminotransferase, aspartate aminotransferase, and alkaline phosphatase) were monitored.
Statistics
The trial size was planned to detect a 50% relative reduction in the proportion of patients requiring perioperative erythrocyte transfusions from 40% in the placebo group to 20% in the rFVIIa groups with 80% statistical power at a significance level of 5%. This translated to a sample size of 180 patients, 60 per treatment group. The perioperative period was defined as spanning the intraoperative period and the 48-h postsurgical period.
The comparison of the three treatment groups with respect to the primary endpoint, i.e.  , the proportion of the patients requiring perioperative erythrocyte transfusions, was conducted with use of a logistic regression model. Treatment group, country, baseline hematocrit, whether clamping was performed (defined as portal triad, inferior vena cava clamping, or both), type of resection (according to the Brisbane 2000 terminology19), and surgery type (hepatectomy vs.  rehepatectomy) were included as covariates in the model. Residual diagnostics were used to check the statistical assumptions of the model.
Analysis of the treatment effect on the proportion of patients requiring fresh frozen plasma during the perioperative period was conducted as for the primary endpoint. Amounts of erythrocytes transfused during the perioperative period were compared between treatment groups using a two-sided Jonckheere-Terpstra test. This test was also applied for comparisons of treatment effects on requirements for systemic hemostatic drug as well as for other secondary endpoints, with the one exception of changes in hematocrit, which were analyzed using F tests. In all the above-mentioned analyses, the type I error was set to 5%. All randomized patients who were dosed were included in the safety analyses, whereas efficacy data presented herein pertain to all randomized patients who were dosed and underwent liver resection.
Results
Between January 2001 and January 2002, 204 eligible patients were included in the trial. Four patients were withdrawn before dosing, the reasons being the investigator’s decision not to perform a partial hepatectomy, noncompliance with the protocol, failure to obtain a drug dispensing form before surgery, and patient withdrawal of consent. A flow diagram of patient allocation is outlined in figure 1. Baseline characteristics and prognostic factors were similar across treatment groups (table 1). Six patients in the placebo group, five in the 20-μg/kg group, and two in the 80-μg/kg group received a second dose 5 h after the initial injection as a result of an extended surgery period.
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
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Table 1. Baseline Characteristics and Prognostic Factors (Efficacy Population) 
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Table 1. Baseline Characteristics and Prognostic Factors (Efficacy Population) 
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Efficacy
Results are summarized in table 2. The proportion of patients who required perioperative transfusion of erythrocytes (the primary endpoint) was 37% (23 of 63) in the placebo group, 41% (26 of 63) in the 20-μg/kg group, and 25% (15 of 59) in the 80-μg/kg group. The overall effect of rFVIIa treatment was not statistically significant (logistic regression model; P  = 0.09). Mean erythrocyte requirements for patients receiving erythrocytes were 1,024 ml in the placebo group, 1,354 ml in the 20-μg/kg rFVIIa group, and 1,036 ml in the 80-μg/kg rFVIIa group (P  = 0.78).
Table 2. Trial Results 
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Table 2. Trial Results 
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The mean volume of blood loss during surgery was 1,422 ml in the placebo group, 1,372 ml in the 20-μg/kg group, and 1,073 ml in the 80-μg/kg group (P  = 0.07). The reduction in hematocrit from before surgery to last observation during surgery was smallest in the 80-μg/kg group, with a statistically significant overall effect of treatment (P  = 0.04), even though the amount of erythrocytes transfused during surgery was not greater in the 80-μg/kg group. However, the reduction in hematocrit during surgery was larger in the 20-μg/kg group than in the placebo group. No significant difference between treatment groups was found with respect to requirement for fresh frozen plasma or systemic hemostatic drug, operating time, total volume collected in surgical drains in the 24-h postsurgical period, or for the percentage of hematocrit measured herein (table 2).
Data on plasma FVII clotting activity are depicted in figure 2. As expected, measured maximum plasma concentration and area under the concentration curve seem to increase approximately proportionally with dose. Prothrombin time was significantly shortened with rFVIIa dosing, the effect being prolonged at the 80-μg/kg dose level when compared with the effect of 20 μg/kg (fig. 3).
Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
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Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
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Safety
Of the 200 dosed patients, 158 patients had 487 adverse events (table 3). The most frequently reported adverse events included nausea, constipation, fever, hypotension, and insomnia, and there were no apparent differences between dose groups in the types or frequencies of adverse events reported. All nonthromboembolic serious adverse events were considered by the investigators as unlikely to be related to trial drug treatment. Three thromboembolic events were observed in each of the three treatment groups. The total of nine events was comprised of the following.
Table 3. Adverse Events 
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Table 3. Adverse Events 
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Four events of deep venous thrombosis.
All four events (two in the placebo group diagnosed at day 1 after dosing and two in the 80-μg/kg group diagnosed at days 2 and 3 after dosing, respectively) were without clinical symptoms and were thus only recognized through the protocol-specified routine Doppler examinations.
Two events of pulmonary embolism.
A 62-yr-old patient of the 20-μg/kg group was diagnosed with a right basal segment arterial pulmonary embolism at day 2 after dosing. Doppler examination before the events showed no signs of deep vein thrombosis. A 58-yr-old patient of the 80-μg/kg group was diagnosed with a left apical pulmonary embolism at day 7 after dosing. Two days after the event, a Doppler ultrasound examination indicated a partial thrombosis of the left internal jugular vein corresponding to the site of central venous catheter placement. Doppler ultrasonography before the event and 4 days after the event did not indicate deep venous thrombosis in the lower extremities. Both patients recovered completely from the events.
An event of partial portal vein thrombosis experienced by a patient in the placebo group.
Five days after extended hepatic resection and administration of trial drug, a 67-yr-old woman of the placebo group experienced fever, abdominal pain, and clouding of consciousness with signs of hepatic failure. A computed tomography scan indicated a partial portal venous thrombus at the stump of the ligated right portal vein. The thrombus was protruding into the main portal vein without impairment of the flow. Doppler ultrasonography confirmed good portal venous flow. The patient died of hepatic failure, most probably as a consequence of the extended hepatic resection performed 2 weeks previously.
Two events of myocardial infarction experienced by patients in the 20-μg/kg group.
A 79-yr-old man experienced posterior myocardial infarction 1 day after administration of the trial drug. Subsequent angiography showed moderate left ventricle–apical hypokinesia and severe left main stem and triple vessel disease. The patient underwent coronary surgery and recovered completely. A 74-yr-old man experienced worsening of liver, renal, and respiratory function 4 days after receiving the trial drug and undergoing hepatic resection and extensive abdominal surgery. The patient subsequently had a hypotensive episode but recovered quickly after colloid therapy. An electrocardiogram showed a possible myocardial infarction, but this was unconfirmed because creatinine kinase concentrations were already increased. Renal, hepatic, and respiratory functions deteriorated over the course of the day, and chest radiographs suggested pulmonary edema. The condition of the patient continued to worsen, and he died from multiorgan failure 7 days later.
Seven adverse events recorded during the trial period had a fatal outcome, with death occurring on average 28 days after trial drug dosing (range, 9–92 days). Three deaths occurred in the placebo group, and four deaths occurred in the 20-μg/kg treatment group (causes of death were hepatic failure, pneumonia, pulmonary edema, and multiorgan failure). All seven deaths were evaluated by the investigators as unlikely to be related to the trial drug.
Bleeding complications, as defined by the investigators, occurred with similar frequencies across treatment groups (P  = 0.73). Furthermore, no clinically significant adverse changes in the investigated coagulation-related parameters were observed, and there were no indications of systemic activation of the coagulation cascade. A statistically significantly greater increase from baseline to 1 h after dosing (P  < 0.01) and to 24 h after dosing (P  = 0.04) was observed for D-dimer when comparing rFVIIa groups to placebo, which is consistent with the expected mode of action of rFVIIa. No significant differences between dose groups were observed for platelets, fibrinogen, prothrombin fragments 1 and 2, thrombin–antithrombin complex, or antithrombin III, although it should be noted that data for prothrombin fragments 1 and 2 and thrombin–antithrombin complex were inconclusive because of methodologic problems related to drawing of blood at some of the trial centers.
Discussion
This was a placebo-controlled, double-blind study of the effect of a single presurgical bolus injection of either 20 or 80 μg/kg rFVIIa administered to noncirrhotic patients undergoing major liver resection. No statistically significant overall effect of rFVIIa treatment across treatment groups was observed with respect to the proportion of patients requiring perioperative erythrocyte transfusions (primary endpoint) or other endpoints on transfusion and blood loss. The trial was dimensioned to detect a 50% relative reduction with respect to the primary endpoint, and the number of patients included would thus be expected to be insufficient to statistically verify any smaller relative reduction on the primary endpoint. A larger trial, powered for a smaller but still clinically relevant effect on transfusion requirements, would be needed to better evaluate any hemostatic effect of rFVIIa in this patient population. Prothrombin time was significantly shortened with rFVIIa dosing. However, the clinical relevance of this in vitro  effect of rFVIIa remains to be determined.
The administration of a procoagulant such as rFVIIa to patients with otherwise normal coagulation systems might raise concerns that patients would be exposed to a higher risk of thromboembolic events. In this trial, the prevalence of thromboembolic events in these immobilized, anesthetized, noncoagulopathic patients undergoing major liver surgery did not differ between placebo-treated and rFVIIa-treated patients. Although there was a tendency for the thromboembolic events to be more severe in the rFVIIa-treated patients, the number of events is too small to draw any conclusions. The 1% overall incidence of pulmonary embolism observed in the current study corresponds to the incidence previously observed in cancer surgery.20 Moreover, no indications of systemic activation of the coagulation cascade were observed. The absence of systemic activation of the coagulation system with rFVIIa may be explained by its mode of action, confining propagation of coagulation to the site of injury of the vessel wall.15,16 Given the localized effect of rFVIIa, an increased incidence of thromboembolic complications or intravascular coagulation after dosing with rFVIIa would not be expected and has indeed not been observed previously.17,21 The low trial-related mortality rate of 3.5% (0.0% in the 80-μg/kg dose group) is in line with previous observations, where operative mortality of less than 10% has been reported in many series6,22 and is to be expected in this noncirrhotic patient population. No statistically significant effect of rFVIIa on mortality was observed. However, the trial was not powered to investigate mortality.
It should be noted that routine monitoring of laboratory coagulation parameters during surgery could potentially reveal dose group allocation. The effect of such bias on trial results, however, is judged to be small because of the requirement of adherence to protocol-defined transfusion guidelines.
In conclusion, dosing with 20 or 80 μg/kg rFVIIa did not raise safety concerns in this patient population without preexisting coagulopathy undergoing major liver resection. No statistically significant effect of rFVIIa across treatment groups was observed for transfusion requirements or blood loss. Further trials are needed to establish the hemostatic potential of rFVIIa in this clinical setting.
The authors thank the patients and the hospital staff participating in the trial, as well as Allan Blemings, M.Sc. (Statistician), and Karsten Soendergaard, M.Sc. (Clinical Researcher), both at Novo Nordisk A/S, Copenhagen, Denmark.
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Appendix: Participating Principal Investigators and Hospitals
United Kingdom  : J. Peter A. Lodge, M.D., F.R.C.S., Professor of Surgery, St. James’s University Hospital, Leeds; Darius F. Mirza, M.S., F.R.C.S., Consultant Hepatobiliary and Transplant Surgeon, The Queen Elizabeth Hospital, The Liver and Hepatobiliary Unit, Birmingham. Germany  : Sven Jonas, M.D., Professor, Campus Virchow-Klinikum, Berlin; Massimo Malagó, M.D., Professor of Surgery and Transplantation, Essen University Clinic, Department of General Surgery and Transplantation, Essen; Matthias Anthuber, M.D., Professor, Regensburg University Clinic, Regensburg; Wolf-Otto Bechstein, M.D., Professor of Surgery, Chairman of the Department of General and Vascular Surgery, University Hospital Frankfurt am Main. France  : Daniel Cherqui, M.D., Professor, Hospital Henri-Mondor, Department of General and Digestive Surgery, Paris; Christian Jayr, M.D., Research Director, Institut Gustave Rousy, Anesthesiology Department, Villejuif; Luce Kuhlman, M.D., Hospital Consultant in Anesthesiology, Paul Brousse University Hospital Center, Department of Hepatobiliary Surgery, Villejuif; Jack Tartiere, M.D., Hospital Practitioner in Anesthesiology and Intensive Care, CHU de la Côte de Nacre, Anesthesia and Intensive Care Department, Pr JL Gerard Unit, Caen; Daniel Eyraud, M.D., Associate Professor, Anesthesiology and Intensive Care Unit, Hospital Pitié Salpétriére, Paris; Elie Oussoultzoglou, M.D., Hospital Practitioner, Hospital Haute-Pierre, Strasbourg. Spain  : Juan Carlos Meneu Díaz, M.D., Staff Surgeon, Hospital “12 de Octubre,” General and Digestive Surgery and Liver Transplantation Unit, Madrid.
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
Fig. 1. Flow diagram of patient allocation. rFVIIa = recombinant factor VIIa. 
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Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
Fig. 2. Plasma factor VII clotting activity (FVII:C; mean and SD) by treatment group. Normal range: 0.54–1.23 U/ml. Plasma FVII clotting activity was significantly higher (pairwise comparisons based on  t  tests using Dunnett adjustment;  P  < 0.01) in the rFVIIa dose groups relative to placebo for all time points except for 5 h after dosing in the 20-μg/kg group. 
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Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
Fig. 3. Prothrombin time (mean and SD) by treatment group. Normal range: 10.7–13.0 s. Prothrombin time was significantly shorter (Student  t  test for unequal variances;  P  < 0.05) in the rFVIIa dose groups relative to placebo for all time points except for 4 and 5 h after dosing in the 20-μg/kg group. 
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Table 1. Baseline Characteristics and Prognostic Factors (Efficacy Population) 
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Table 1. Baseline Characteristics and Prognostic Factors (Efficacy Population) 
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Table 2. Trial Results 
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Table 2. Trial Results 
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Table 3. Adverse Events 
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Table 3. Adverse Events 
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