Recombinant Activated Factor VII in Aortic Surgery for Patients Under Hypothermic Circulatory Arrest.

Purpose: We aimed to identify the risk factors of critical bleeding and investigate the safety of recombinant activated factor VII (rFVIIa) in aortic surgery under hypothermic circulatory arrest (HCA). Patients and
Methods: The present single-center retrospective study compared the baseline characteristics of 144 patients who underwent aortic surgery under HCA at our institute. Among the total cohort of 144 patients, 42 received rFVIIa (rFVIIa group), while the remaining 102 patients did not (non-rFVIIa group). Perioperative bleeding and transfusions, postoperative 30-day mortality, and adverse events (AEs) were analyzed in 29 propensity score-matched pairs.
Results: Before surgery, the rFVIIa group demonstrated a greater number of shocks (p=0.019), higher JapanSCORE II mortality rate (p=0.033), low platelet count (p=0.015) and fibrinogen (p<0.001) level, prolonged activated partial thromboplastin time (aPTT) (p=0.005) and prothrombin time international normalized ratio (PT-INR) (p=0.006), and longer aortic cross clamp time (p=0.049). Postoperative bleeding, transfusion, 30-day mortality, and AEs were comparable between the groups both in the entire-unmatched cohort and propensity score matching cohort.
Conclusion: Preoperative shock, higher JapanSCORE II mortality rates, low platelet and fibrinogen levels, prolonged aPTT and PT-INR, and longer aortic clamping time might be risk factors for excessive bleeding and indicate the need for rFVIIa treatment. The present study suggests that rFVIIa can be safely used to address critical and continuous bleeding in spite of adequate transfusion and supplementation of other coagulation factors in aortic surgery under HCA, without an increase in 30-day mortality and AEs.

Introduction

Management of bleeding is an important and often urgent concern for anesthesiologists and cardiac surgeons, especially during aortic surgery. Currently, hypothermic circulatory arrest (HCA) with cerebral perfusion is a safe standard strategy in thoracic aortic surgery to lower the incidence of perioperative stroke.1–4 However, HCA causes coagulopathy because of both cardiopulmonary bypass (CPB) and hypothermia, which may result in life-threatening bleeding.5,6 In such cases of bleeding, massive transfusion of packed red blood cells (PRBC), fresh frozen plasma (FFP), and platelet concentrate (PC) is performed. Occasionally, the condition necessitates further administration of other hemostatic agents, such as fibrinogen concentrates, prothrombin complex, and recombinant activated factor VII (rFVIIa). However, researchers have not yet assessed the risk factors for such critical bleeding events even following adequate transfusion protocol and administration of other coagulation factors, ie fibrinogen concentrates and prothrombin complex, which necessitates rFVIIa treatment in aortic surgery under HCA.

rFVIIa was developed as a treatment agent for bleeding episodes in hemophilia. Nonetheless, its off-label use in cardiac surgery has increased since the first report in 2000.7 In 2008, rFVIIa was most frequently used in cardiac surgery (29%) and trauma (29%) in the USA, compared to its use for hemophilia A and B (2.7%).8 Numerous studies have investigated the efficacy and safety of rFVIIa in cardiac surgery.9,10 However, only few studies have focused on its off-label use in aortic surgery.11,12 Moreover, these studies only included patients with acute aortic dissection (AAD) or those who underwent aortic surgery without HCA. Therefore, the safety of rFVIIa for life-threatening bleeding in aortic surgery under HCA remains unclear.

Furthermore, the occurrence rate of thromboembolic complications following administration of rFVIIa in patients who underwent aortic surgery under HCA should be investigated. In a meta-analysis study, Levi et al reported that treatment with high dose rFVIIa on an off-label basis increased the risk of arterial thromboembolic events in patients due to several conditions, such as spontaneous central nervous system bleeding, trauma, spinal surgery, and cardiac surgery.13 In a particular cohort that underwent non-aortic cardiac surgery, ie coronary artery bypass grafting and/or valve surgery without HCA, Gill et al reported a trend towards an increased occurrence of adverse events, including stroke.9 However, massive coagulopathy would be exist in patients suffering from critical bleeding in aortic surgery under HCA, and association between thromboembolic complications and the use of rFVIIa in this particular cohort has not been well investigated.

Thus, we intended to identify the risk factors of uncontrollable bleeding in aortic surgery under HCA and to elucidate the safety of off-label rFVIIa use for life-threatening bleeding events.

Materials and Methods

Study Design and Patient Population

We retrospectively analyzed 162 patients who underwent aortic surgery under HCA between April 2014 and March 2019 at a single institution. Cases of redo and salvage surgeries (requiring cardiopulmonary resuscitation before surgery) were excluded. Of the remaining 144 patients, 42 patients received rFVIIa (rFVIIa group), while 102 patients did not (non-rFVIIa group). We analyzed the preoperative patient characteristics, perioperative bleeding and transfusions, postoperative adverse events (AEs), and 30-day mortality. Postoperative 30-day mortality and thrombosis-related AEs were the primary endpoints. In contrast, postoperative bleeding and transfusions were the secondary endpoints. AEs were defined as follows: disabling stroke (postoperative persistent neurological deficits caused by thromboembolic events, confirmed by computed tomography (CT) scan or magnetic resonance imaging); minor stroke (postoperative temporary neurological deficits with recovery at discharge or at transfer to another hospital), and renal failure (serum creatinine >2.0 mg/dl and doubling of the preoperative value, or the new onset of hemodialysis). Myocardial infarction (MI), pulmonary embolism (PE), deep venous thrombosis, and other AEs were comprehensively diagnosed by physical examinations, laboratory tests, CT, electrocardiography, echocardiography, or color Doppler sonography (where appropriate).

The Asahikawa Medical University Hospital approved the off-label use of rFVIIa. The Institutional Review Board of Asahikawa Medical University approved this study (No. 19078). While the need for written informed consent for enrollment in this study was waived due to the retrospective study design. The research content has been open for public consumption and the patients were granted the right to refuse participation in the present study. On the other hand, written informed consent to use rFVIIa had been obtained from the participants. In cases of elective or urgent surgery, written informed consent was obtained directly from the patients preoperatively. In cases of emergency surgery, written informed consent was obtained from a family member of the patient.

Anesthetic Methods

Once in the operating room, standard monitoring was performed using five-channel electrocardiography, pulse oximetry, and direct arterial or indirect blood pressure monitoring. General anesthesia was performed using the target-controlled intravenous infusion of propofol, continuous infusion of remifentanil, and single-dose administration of fentanyl. Propofol was infused to maintain a bispectral index within the range of 40–60. Sevoflurane or Desflurane were also administered if the attending anesthesiologist judged it to be necessary. Rocuronium was administered to facilitate endotracheal intubation and to provide adequate muscle relaxation during surgery when necessary. After intubation, a central venous catheter and transesophageal echocardiography probe were inserted. After completing the surgical procedures, the patients were sedated using a continuous infusion of propofol and dexmedetomidine while intubated and were transported to the intensive Care unit (ICU).

Surgical Procedures

Median sternotomy was performed in all cases. Before CPB, we administered heparin (300 U/kg) to maintain an activated clotting time of >480 s during CPB. CPB was established using bicaval venous cannulation. Arterial cannulation is generally performed at the level of the ascending aorta or femoral artery in some AAD cases. Following CPB establishment, mild (>28°C) to moderate (20.1–28°C) hypothermia was applied. Myocardial protection was achieved by antegrade or retrograde cardioplegia in cases of thoracic aortic aneurysm (TAA) or AAD, respectively. The ascending aorta was clamped and transected during systemic cooling, and proximal anastomosis of the aorta was performed. The rectal temperature upon reaching the target temperature induced HCA. Simultaneously, retrograde cerebral perfusion was initiated and eventually switched to antegrade selective cerebral perfusion by cannulation of the supra-aortic arch vessels. Moreover, the patients underwent distal anastomosis of the ascending aorta or aortic arch during the HCA. Following the end of the distal anastomosis, perfusion of the lower body was restarted from the side branch of the prosthesis, and rewarming was initiated. Moreover, anastomoses of the supra-aortic arch vessels were performed following distal anastomosis of the aorta in case of total arch replacement. Concomitant procedures were performed when required.

Intraoperative and Postoperative Management of Bleeding and Transfusion

Following weaning from CPB, heparin was antagonized by protamine administration (1:1 ratio to the applied heparin dosage). Subsequently, a transfusion was initiated. Hemoglobin <8 g/dL resulted in PRBC transfusion. Cell saver blood was also administered. In our institute, the cell saver blood was considered in the bleeding amount, although nearly all the cell saver blood was returned to the patients. Moreover, FFP was transfused upon detecting prolonged activated partial thromboplastin time (aPTT) or prothrombin time international normalized ratio (PT-INR). PC transfusion occurred when platelets (Plt) were <8 × 109. In addition, the patients were administered cryoprecipitate when fibrinogen was <1.5 g/L. Fibrinogen <1.5 g/L following cryoprecipitate transfusion resulted in fibrinogen concentrate administration. rFVIIa was administered on observing continuous excessive bleeding despite the correction of surgical bleeding, pH, temperature, and adequate transfusion. Cryoprecipitate, fibrinogen concentrate, and rVIIa were only used in the operating room. After achieving adequate hemostasis in the operative field, as assessed by the surgeon, the patients were transferred to the ICU. Re-exploration was considered in the ICU if the total bleeding amount from the chest tubes exceeded 400 mL/h regardless of adequate transfusion.

Indication and Administration Dose of rFVIIa

As aforementioned, rFVIIa was administered upon observing continuous excessive bleeding despite the adjustments for surgical bleeding, pH, temperature, and adequate transfusion. In the early period of the present series, 5 mg of rFVIIa was administrated in most cases (n=20). However, with the accumulation of clinical experience, 2 mg or 1 mg of rFVIIa was mainly administered in the late period (n=22). Repetitive administration was warranted only in one patient (5 mg + 2 mg).

Statistical Analyses

While the categorical variables are presented as numbers and percentages, the continuous variables are presented as medians. We performed propensity score matching (PSM) to balance the risk factors for outcomes between the groups. The propensity score (PS) was obtained from a logistic regression model with forced entry method, including variables presented in Table 1, except for concomitant surgery and JapanSCORE II. JapanSCORE II was not considered for PS because it represents the risk-adjusted mortality and preoperatively expected morbidity, based on the Japan Cardiovascular Surgery Database (JCVSD).12 Thus, age, sex, BMI, AAD/TAA, emergency surgery, malperfusion, preoperative shock, cardiac tamponade, GCS<8, smoking, hypertension, diabetes mellitus, liver dysfunction, anticoagulant treatment, and laboratory data before surgery (Hb, Plt, APTT, PT-INR, fibrinogen, serum creatinine, total arch replacement, CPB time, aortic clamp time, lowest rectal temperature, and HCA time) were included in the logistic regression model with forced entry method to generate propensity score. Patients were matched 1:1 using the nearest neighbor matching method without replacement, and a caliper width of 0.2 of the standard deviation of the logit of the estimated PS. This resulted in 29 out of the possible 42 pairs. We calculated standardized mean differences before and after PSM to assess the balance of variables between the groups. Unmatched sub-cohorts were compared using the Fisher's exact test and Mann–Whitney U-test for categorical and continuous variables, respectively. Following PSM, we performed the McNemar test and Wilcoxon signed rank test for the categorical and continuous variables, respectively. PSM was performed using EZR (Saitama Medical Center, Jichi Medical University, Saitama, Japan), a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria).14 All other statistical analyses were performed using Statistical Package for the Social Sciences for Windows (version 26.0; IBM Corp., Armonk, NY, USA). We analyzed the baseline characteristics in an unmatched population. Perioperative bleeding, transfusion, and postoperative outcomes were analyzed in the matched population. The statistical significance was defined as p<0.05.

Table 1

Baseline and Operative Characteristics

Characteristic	Before Matching				After Matching
	rFVIIa (n=42)	Non-rFVIIa (n=102)	p-value	SMD	rFVIIa (n=29)	Non-rFVIIa (n=29)	p-value	SMD
Age (y)	76.5 (69.5, 82.3)	73.5 (66.0, 79.0)	0.065	0.150	75.0 (65.0, 81.0)	78.0 (68.5, 80.5)	0.820	0.192
Sex (Male)	24 (57.1%)	57 (55.9%)	1.000	0.025	17 (58.6%)	18 (62.1%)	1.000	0.071
Body mass index (kg/m2)	23.1 (19.8, 26.8)	22.8 (20.8, 26.3)	0.610	0.180	23.1 (20.4, 27.3)	21.5 (20.0, 24.7)	0.370	0.237
AAD/TAA	27 (64.3%)/15 (35.7%)	53 (52.0%)/49 (48.0%)	0.200	0.252	16 (55.2%)/13 (44.8%)	16 (55.2%)/13 (44.8%)	1.000	<0.001
Emergency surgery	27 (64.3%)	51 (50.0%)	0.142	0.292	16 (55.2%)	17 (58.6%)	1.000	0.07
Malperfusion	5 (11.9%)	9 (8.8%)	0.550	0.101	3 (10.3%)	2 (6.9%)	1.000	0.123
Shock (requiring hemodynamic support)	6 (14.3%)	3 (2.9%)	0.019	0.413	3 (10.3%)	2 (6.9%)	1.000	0.123
Cardiac tamponade	8 (19.0%)	8 (7.8%)	0.077	0.333	5 (17.2%)	6 (20.7%)	1.000	0.088
GCS <8	1 (2.4%)	3 (2.9%)	1.000	0.035	1 (3.4%)	2 (6.9%)	1.000	0.156
Smoking	7 (16.7%)	27 (26.5%)	0.281	0.240	5 (17.2%)	5 (17.2%)	1.000	<0.001
Hypertension	33 (78.6%)	78 (76.5%)	0.831	0.050	24 (82.8%)	24 (82.8%)	1.000	<0.001
Diabetes mellitus	7 (16.7%)	12 (11.8%)	0.428	0.141	5 (17.2%)	6 (20.7%)	1.000	0.088
Liver dysfunction	6 (14.3%)	8 (7.8%)	0.234	0.206	3 (10.3%)	4 (13.8%)	1.000	0.106
Anticoagulant treatment	5 (11.9%)	10 (9.8%)	0.766	0.068	2 (6.9%)	3 (10.3%)	1.000	0.123
Antiplatelet treatment	7 (16.7%)	17 (16.7%)	1.000	<0.001	6 (20.7%)	7 (24.1%)	1.000	0.083
JapanSCORE II 30-day mortality (%)	8.4 (5.6, 14.0)	6.1 (3.9, 10.2)	0.033	0.355	6.9 (4.3, 11.1)	7.1 (4.4, 13.5)	0.665	0.088
Hemoglobin (g/dl)	11.5 (10.0, 13.6)	12.5 (10.8, 14.0)	0.092	0.285	11.9 (10.0, 13.7)	11.7 (10.2, 13.6)	0.811	0.101
Platelet count (109/L)	157 (124, 188)	177 (142, 213)	0.015	0.401	158 (126, 179)	168 (130, 188)	0.787	0.074
APTT (s)	31.2 (27.4, 37.7)	28.4 (26.2, 31.9)	0.005	0.284	31.1 (27.5, 35.2)	30.3 (27.2, 34.8)	0.795	0.190
PT-INR	1.07 (1.00, 1.24)	1.02 (0.96, 1.10)	0.006	0.314	1.05 (0.98, 1.18)	1.06 (1.00, 1.14)	0.964	0.056
Fibrinogen (g/L)	2.43 (1.62, 2.96)	2.90 (2.46, 3.91)	<0.001	0.668	2.64 (1.77, 3.29)	2.45 (2.21, 2.97)	0.922	0.053
Serum creatinine (mg/dl)	0.94 (0.72, 1.11)	0.87 (0.70, 1.10)	0.427	0.149	0.94 (0.75, 1.12)	1.00 (0.78, 1.25)	0.160	0.195
Surgery
Primary procedure			0.146	0.274			1.000	<0.001
Total arch replacement	19 (45.%2)	60 (58.8%)			14 (48.3%)	14 (48.3%)
Hemiarch replacement	23 (54.8%)	42 (41.2%)			15 (51.7%)	15 (51.7%)
Concomitant procedure	14 (33.3%)	26 (25.5%)	0.413	0.173	9 (31.0%)	8 (27.6%)	1.000	0.076
None	28 (66.7%)	76 (74.5%)			20 (69.0%)	21 (72.4%)
AVR or AVP	3 (7.1%)	4 (3.9%)			2 (6.9%)	2 (6.9%)
Bentall	2 (4.8%)	1 (1.0%)			1 (3.4%)	0 (0%)
David	3 (7.1%)	7 (6.9%)			2 (6.9%)	3 (10.3%)
CABG	7 (16.7%)	11 (10.8%)			4 (13.8%)	3 (10.3%)
Others	0 (0%)	3 (2.9%)			0 (0%)	0 (0%)
CPB time (min)	169 (145, 230)	169 (142, 192)	0.136	0.437	161 (136, 227)	177 (136, 216)	0.754	0.084
ACC time (min)	110 (88, 146)	97 (79, 121)	0.049	0.376	102 (80, 141)	110 (75, 123)	0.462	0.119
Lowest rectal temperature (°C)	27.5 (25.7, 27.9)	26.1 (25.3, 27.6)	0.043	0.421	27.4 (25.6, 27.9)	26.6 (25.4, 27.8)	0.546	0.183
HCA time (min)	40 (28, 49)	39.5 (29.0, 53.0)	0.986	0.094	40 (28, 50)	36 (25, 56)	0.829	0.039

Notes: The number of “concomitant procedures” means the number of patients who added some sort of adjunct procedure including AVR, AVP, Bentall, David, CABG, and others. Abbreviations: AAD, acute aortic dissection; ACC, aortic cross clamp; APTT, activated partial thromboplastin time; AVP, aortic valvuloplasty; AVR, aortic valve replacement; CABG, coronary artery bypass grafting; CPB, cardiopulmonary bypass; GCS, Glasgow coma scale; HCA, hypothermic circulatory arrest; PT-INR, prothrombin time international normalized ratio; rFVIIa, recombinant activated factor VII; SMD, standardized mean difference; and TAA, thoracic aortic aneurysm.

Results

Baseline and Operative Characteristics

Table 1 summarizes the baseline and operative characteristics. Before PSM, the number of shock patients (p=0.019) and JapanSCORE II 30-day mortality rates (p=0.033) were significantly higher in the rFVIIa group. While Plt (p=0.015) and fibrinogen (p<0.001) were significantly lower, aPTT (p=0.005) and PT-INR (p=0.006) were prolonged in the rFVIIa group. The rFVIIa group demonstrated longer aortic clamp time (p=0.049) and higher lowest body temperature (p=0.043). Following PSM, none of the characteristics were significantly different between the groups.

Perioperative Bleeding and Transfusion

Table 2 summarizes the perioperative amounts of bleeding and transfusion.

Table 2

Perioperative Bleeding and Blood Products in the Entire Unmatched and Propensity-Score Matched Populations

Characteristic	Before Matching			After Matching
	rFVIIa (n = 42)	Non-rFVIIa (n = 102)	p-value	rFVIIa (n = 29)	Non-rFVIIa (n = 29)	p-value
Bleeding volume intra-OP (mL)	6492 (3643, 11,502)	3652 (2425, 5207)	<0.001	6773 (4019, 10,185)	3639 (2399, 6627)	0.012
PRBC intra-OP (unit)	30 (20, 37)	20 (12, 24)	<0.001	26 (19, 34)	20 (12, 24)	0.048
FFP intra-OP (unit)	36 (24, 47)	22 (16, 30)	<0.001	34 (20, 46)	24 (18, 32)	0.021
PC intra-OP (unit)	50 (40, 60)	40 (40, 60)	0.099	55 (40, 60)	40 (40, 60)	0.472
Cryoprecipitate intra-OP (unit)	12 (12, 24)	12 (12, 12)	0.002	12 (12, 24)	12 (12, 12)	0.405
rFVIIa (µg/kg)	56 (35, 85)	-		56 (32, 83)	-
Fibrinogen concentrate (g)	3 (0, 3)	0 (0, 0)	<0.001	3 (0, 3)	0 (0, 0)	<0.001
Bleeding volume until 12 h (mL)	1099 (598, 1425)	655 (469, 1098)	0.005	790 (490, 1470)	740 (540, 1233)	0.071
PRBC until 12 h (unit)	3 (0, 6)	2 (0, 5)	0.082	2 (0, 6)	2 (0, 5)	0.370
FFP until 12 h (unit)	7 (4, 10)	4 (4, 8)	0.040	6 (4, 9)	6 (4, 8)	0.576
PC until 12 h (unit)	0 (0, 20)	0 (0, 0)	0.005	0 (0, 20)	0 (0, 10)	0.967

Abbreviations: FFP, fresh frozen plasma; OP, operation; PC, platelet concentrates; PRBC, packed red blood cells; rFVIIa, recombinant activated factor VII.

In the entire unmatched cohort, intraoperative bleeding and amount of transfusion were significantly higher in the rFVIIa group than the non-rFVIIa group, as a matter of course because rFVIIa was administrated in patients with critical bleeding in the present series.

These significant differences were seen also in the PSM cohort. Intraoperative bleeding (p=0.012), PRBC transfusion (p=0.048), and FFP (p=0.021) were significantly higher in the rFVIIa group. Patients in the rFVIIa group received a significantly greater amount of fibrinogen concentrate (p<0.001). The median intraoperative dose of rFVIIa was 56 μg/kg.

Postoperative bleeding and amount of transfusion were significantly higher in the rFVIIa group than non-rFVIIa group in the entire unmatched cohort, however, those differences were not seen after PSM.

Mortality and Postoperative Adverse Events

The results of postoperative outcomes are shown in Table 3. Regarding laboratory data after surgery, Plt was significantly lower (p < 0.001) and PT-INR (p < 0.001) was shorter in rFVIIa group. There were no significant differences between the groups with regard to primary and secondary endpoints.

Table 3

Postoperative Data and Complications in the Entire Unmatched and Propensity-Score Matched Populations

	Before Matching			After Matching
	rFVIIa (n = 42)	Non-rFVIIa (n = 102)	p-value	rFVIIa (n = 29)	Non-rFVIIa (n = 29)	p-value
Laboratory data after surgery
Hb (g/dl)	10.6 (9.3, 11.6)	10.3 (9.6, 12.0)	0.476	10.6 (9.0, 11.5)	10.5 (9.5, 11.8)	0.381
Plt (109 /L)	97 (74, 133)	138 (106, 167)	<0.001	97 (73, 137)	142 (106, 169)	<0.001
APTT (s)	46.6 (33.4, 56.3)	38.5 (35.0, 47.3)	0.017	45.2 (33.6, 55.1)	37.1 (33.4, 44.0)	0.206
PT-INR	0.84 (0.80, 1.01)	1.15 (1.10, 1.24)	<0.001	0.86 (0.81, 1.03)	1.13 (1.08, 1.18)	<0.001
Fibrinogen (g/L)	2.15 (1.85, 2.85)	2.26 (1.97, 2.67)	0.021	2.10 (1.79, 2.59)	2.39 (2.06, 2.69)	0.846
Serum creatinine* (mg/dl)	1.21 (0.89, 1.73)	1.31 (1.07, 1.74)	0.604	1.21 (0.94, 1.72)	1.10 (0.83, 1.63)	0.226
Intubation time (h)	17 (10, 53)	16 (11, 51)	0.046	25 (12, 96)	16 (10, 42)	0.991
Deep sternal wound infection	1 (2.4%)	1 (1.0%)	0.500	1 (3.4%)	0 (0%)	1.000
Septicemia	2 (4.8%)	3 (2.9%)	0.629	0 (0%)	1 (3.4%)	1.000
Renal failure**	5 (11.9%)	11 (10.8%)	1.000	1 (3.4%)	3 (10.3%)	0.500
Paraparesis	2 (4.8%)	3 (2.9%)	0.629	1 (3.4%)	1 (3.4%)	1.000
Deep venous thrombosis	0 (0%)	2 (2.0%)	1.000	0 (0%)	1 (3.4%)	1.000
Pulmonary embolism	0 (0%)	0 (0%)		0 (0%)	0 (0%)
Myocardial infarction	0 (0%)	0 (0%)		0 (0%)	0 (0%)
Stroke	3 (7.1%)	5 (4.9%)	0.692	1 (3.4%)	1 (3.4%)	1.000
Minor stroke	2 (4.8%)	1 (1.0%)	0.204	1 (3.4%)	0 (0%)	1.000
Disabling stroke	1 (2.4%)	4 (3.9%)	1.000	0 (0%)	1 (3.4%)	1.000
Cardiac tamponade	1 (2.4%)	3 (2.9%)	1.000	0 (0%)	1 (3.4%)	1.000
Re-exploration	4 (9.5%)	4 (3.9%)	0.231	4 (13.8%)	3 (10.3%)	1.000
30-day mortality	3 (7.1%)	2 (2.0%)	0.148	1 (3.4%)	1 (3.4%)	1.000

Notes: *Peak postoperative, **Serum creatinine > 2.0 mg/dl and more than twice before surgery, or requiring newly hemodialysis.

Abbreviations: APTT, activated partial thromboplastin time; Plt, platelet; PT-INR, prothrombin time international normalized ratio; rFVIIa, recombinant activated factor VII.

In the entire un-matched cohort, 30-day mortality was 7.1% in rFVIIa group and 2.0% in non-rFVIIa group (p=0.148). Stroke occurred in 3 patients (2 minor and 1 disabling stroke) in rFVIIa group and in 5 patients (1 minor and 4 disabling stroke) in non-rFVIIa group (p=0.692). There were no case of postoperative MI or PE in both groups. DVT occurred in 2 patients only in non-rFVIIa group (p=1.000) and cardiac tamponade occurred in one patient in rFVIIa group and in 3 patients in non-rFVIIa group (p=1.000). Re-exploration was performed 9.5% in rFVIIa group and 3.9% in non-rFVIIa group (p=0.231). All other postoperative adverse events were also comparable between the groups.

In PSM cohort, 30-day mortality was 3.4% in both groups (p = 1). One patient (3.4%) in rFVIIa had postoperative minor stroke and one patient (3.4%) in non-rFVIIa had disabling stroke, respectively (p = 1.000). There were no case of postoperative MI or PE in both groups. DVT and cardiac tamponade were detected 1 case (3.4%) in non-rFVIIa group, respectively. Re-exploration was performed 13.8% in rFVIIa group and 10.3% in non-rFVIIa group (p = 1.000). All other postoperative adverse events were also comparable between the groups.

Association Between the Administered Dose of rFVIIa and Mortality/Stroke

Twenty patients who received 5 mg (n=19) or 7 mg (n=1) of rFVIIa were classified as group H and 22 patients who received 2 mg (n=19) or 1 mg (n=1) were classified as group L, and the mortality and thromboembolic complications were compared. Mortality was 10% (n=2/20) in group H and 4.5% (n=1/22) in group L (p=0.493). Stroke rates of 5% in group H (n=1/20, 2 minor strokes) and 9.1% in group L (n=2/22, 1 disabling and 1 minor stroke) were observed.

Comparison Between AAD and TAA Regarding the Detected Risk Factors for the Use of rFVIIa

As already described, 80 patients with AAD and 64 patients with TAA were included in the present study. rFVIIa was administrated in 27 (12.5%) patients with AAD and 15 (23.4%) patients with TAA, including three rupture cases. The results of this sub-analysis are shown in Table 4. Briefly, the preoperative condition, including indicators for coagulopathy, was worse in the AAD group than in the TAA group; however, the outcome was comparative.

Table 4

Comparison Between Acute Aortic Dissection and Thoracic Aortic Aneurysm Regarding the Detected Risk Factors for rFVIIa Use and Outcomes

Characteristic	AAD (n=80)	TAA (n=64)	p-value
Use of rFVIIa	27 (12.5%)	15 (23.4%)	0.176
Age (y)	75.0 (66.5, 82.0)	71.5 (66.0, 78.0)	0.070
Sex (Male)	35 (43.7%)	46 (71.9%)	0.001
Shock (requiring hemodynamic support)	9 (11.3%)	0 (0%)	0.005
JapanSCORE II 30-day mortality rate	8.30(5.85, 13.2)	4.60 (2.70, 8.45)	<0.001
Platelet count (109/L)	157 (129, 190)	184 (158, 246)	<0.001
APTT (s)	31 (27, 37)	28 (26, 31)	0.022
PT-INR	1.08 (1.01, 1.21)	0.99 (0.93, 1.04)	<0.001
Fibrinogen (g/L)	253(177, 374)	291 (256, 393)	0.022
Aortic clamp time (min)	100 (77, 122)	103 (81, 122)	0.532
Lowest rectal temperature (°C)	26.5 (25.5, 27.7)	26.3 (25.4, 27.9)	0.915
Re-exploration	5 (6.3%)	3 (4.7%)	0.684
Stroke	5 (6.3%)	3 (4.7%)	0.684
30-day Mortality	4 (5.0%)	1 (1.6%)	0.382

Abbreviations: rFVIIa, recombinant activated factor VII; APTT, activated partial thromboplastin time; PT-INR, prothrombin time international normalized ratio.

Discussion

Few studies have reported on the off-label use of rFVIIa in aortic surgery, with no previous study focusing on the safety of rFVIIa in aortic surgery under HCA.10,11 However, the high possibility of massive bleeding necessitates an evaluation of the safety of off-label rFVIIa use in aortic surgery under HCA. The crucial findings of the present study were as follows: (i) preoperative shock, coagulopathic state in laboratory tests, higher JapanSCORE II 30-day mortality rate, and longer aortic clamp time might be associated with excessive bleeding in aortic surgery under HCA and (ii) rFVIIa application did not result in a significant increase in the postoperative 30-day mortality and AEs in aortic surgery under HCA.

Preoperative shock and coagulopathy increased the risk of intraoperative bleeding, which might require rFVIIa administration. Preoperative shock in our patients was caused by AAD. Guan et al reported that intense prothrombin generation and excessive systemic fibrinolysis occur in AAD before surgery, thereby leading to prolonged consumption coagulopathy, excessive bleeding, and complications.15 On the other hand, researchers have also described coagulopathy in aortic aneurysms with increased intensity upon rupture.16 In the present study, there were three ruptured TAA cases and all the patients received rFVIIa therapy. Regardless of the underlying pathology, the rFVIIa group demonstrated significantly lower Plt and fibrinogen levels, prolonged aPTT, and PT-INR before PSM. This resulted in a significantly greater amount of intraoperative bleeding and transfusion.

In the present study, JapanSCORE II was used to estimate operative mortality because it is routinely calculated in all patients in our institute. JapanSCORE II is a calculated operative risk similar to EuroSCORE. However, it is based on JCVSD. JapanSCORE II more precisely reflects operative risk in Japan than EuroSCORE.17 In the present study, the higher frequency of AAD, emergent surgery, and shock might result in higher operative risk in the rFVIIa group. Despite a lower actual mortality rate than the calculated value, JapanSCORE II appeared to be a reliable risk predictor.

The clinical impact of HCA-induced coagulopathy is well known. However, the underlying mechanism is still unclear. Hypothermia and CPB are factors that cause coagulopathy. However, several studies have reported that the lowest body temperature is not associated with bleeding.2,4 In the present study, the lowest temperature was significantly higher in the rFVIIa group. Nevertheless, intraoperative bleeding was significantly higher in the rFVIIa group than that in the control group. In other words, the lowest temperature was not strongly associated with coagulopathy. Meanwhile, the aortic clamp time in the present study was significantly longer and supposedly associated with excessive bleeding. There are few reports on the relationship between coagulopathy and aortic clamp time. Moreover, longer aortic clamp time reportedly causes both fibrinogen consumption and accumulation of tissue plasminogen activator. Nonetheless, the underlying mechanism is unclear.18

The efficacy of off-label rFVIIa use has been repeatedly reported. However, most of the latter studies involved patients who underwent cardiac surgery,7–10 where the efficacy was demonstrated with respect to the amount of perioperative bleeding, transfusion, and re-exploration.7–10 However, a previous study on AAD surgery reported on significantly greater perioperative bleeding, transfusion, and re-exploration, following rFVIIa administration.19 In the present study, the rFVIIa group demonstrated significantly higher intraoperative bleeding and transfusion, in addition to significantly lower postoperative Plt. The severity of coagulopathy in aortic surgery under HCA is expectedly much higher than that in general cardiac surgery. Therefore, consumption coagulopathy may have persisted even after rFVIIa treatment. According to Paparella et al, intense thrombin generation in patients with AAD stimulates platelet activation and dysfunction, and promotes coagulation factor consumption and excessive fibrinolysis, which collectively result in excessive bleeding.20 Consumption coagulopathy and platelet dysfunction have been not only reported in AAD but also in TAA.21 Patients in the rFVIIa group in aortic surgery under HCA might continue to suffer from life-threatening bleeding and require a greater amount of transfusion if not treated with rFVIIa. Therefore, rFVIIa in aortic surgery under HCA plays an important role in rescue therapy.

The safety of rFVIIa, especially regarding thromboembolic complications, is still unclear and depends on several factors, such as patient characteristics, transfusion, and the dose of rFVIIa utilized. A randomized trial reported no significant increase in mortality, rather a numeric increase in AEs including stroke.9 Alfirevic et al reported higher mortality and renal morbidity in the rFVIIa group.22 The aforementioned studies focused on complex cardiac surgery. Other studies on AAD or aortic surgery demonstrated no significant increase in postoperative mortality or AEs.11,19 From these previous studies, one may assume that the prophylactic use of rFVIIa in patients with preserved coagulation condition could increase thromboembolic complications, but therapeutic use in patients having coagulation disorder would be safe. The results of the present study support this hypothesis. Intense thrombin generation in aortic surgery under HCA causes platelet dysfunction, consumptive coagulopathy, and excessive fibrinolysis. Based on the above-mentioned factors, a low frequency of thromboembolic AEs might result from rFVIIa therapy in aortic surgery.

The safety dose or optimal protocol for rFVIIa in cardiac surgery is still unknown. Researchers have reported on the safety and efficacy of a dose ranging between 35 μg/kg to 70 μg/kg in general cardiac surgery.23 Several studies have described the efficacy of low-dose rFVIIa <20 μg/kg.10 However, considering the severity of coagulopathy in aortic surgery under HCA, a higher dose may also be acceptable A dose <90 μg/kg is considered safe in patients without hemophilia.24 In the present study, the median dose of rFVIIa was 56 μg/kg, and patients did not demonstrate an increase in mortality or thromboembolic AEs. Moreover, the sub-analysis conducted in the present study demonstrated that the administration of a high dose of rFVIIa (more than 5 mg) was not associated with an increased mortality and stroke rate. This finding suggests that the administration dose is not associated with the postoperative complications, and that rFVIIa could be used repeatedly until adequate hemostasis is obtained. However, the present study does not determine the sufficient dose for adequate hemostasis in patients who experience critical bleeding during aortic surgery under HCA, which warrants further investigation. We administered rFVIIa following the correction of other hemostatic parameters, which was in compliance with current recommendations.22

Since rFVIIa is considered expensive, its cost effectiveness should also be discussed. In Japan, the cost of 1 mg rFVIIa is 85,276 yen. On the other hand, the cost of 2 units of PRBC (400 mL), 2 units of FFP (240 mL), and 20 units of PC (250 mL) are 17,194; 18,322; and 163,471 yen, respectively. It indicates that the cost of 2 mg rFVIIa is comparable to additional 20 units of PC in a situation of critical intraoperative bleeding. From the perspective of cost effectiveness and patients’ safety, administration of rFVIIa as a rescue therapy for critical bleeding in aortic surgery under HCA could be justified.

Limitations

Our study had several limitations. First, this was a single-center, retrospective, observational study with a small sample size. Second, the decision to use rFVIIa and its timing as a rescue therapy was made by the individual anesthesiologists and operating surgeons; thus, a definite criterion for the use of rFVIIa could not be clarified in the present study. Third, we performed PSM based on different characteristics before rFVIIa treatment. Nevertheless, there were several unmeasured confounders. Fourth, we observed a difference in intraoperative transfusions, which might have affected the amount of intraoperative bleeding and rFVIIa administration. However, it was impossible to equalize the number of intraoperative transfusions because of the retrospective observational study design. Despite the aforementioned limitations, this is the first study to focus on the use of rFVIIa in aortic surgery under HCA and could serve as a basis for further, large-volume studies focusing on coagulopathy during aortic surgery under HCA.

Conclusion

Preoperative shock, higher JapanSCORE II mortality rates, low Plt and fibrinogen, prolonged aPTT and PT-INR, and longer aortic clamp time might be risk factors for excessive bleeding, thus necessitating rFVIIa treatment. The present study suggests that rFVIIa can be used for critical and continuous bleeding in spite of adequate transfusion and supplementation of other coagulation factors during aortic surgery under HCA, without an increase in 30-day mortality and AEs. Nevertheless, further prospective randomized studies are warranted owing to the critical limitations of the present study.