Successful use of recombinant activated factor VII (eptacog alfa, Novoseven®) in a refractory bleeding during pediatric cardiac surgery: a case report
© The Author(s) 2015
Received: 27 May 2015
Accepted: 4 August 2015
Published: 30 November 2015
A 2-year-and-7-month-old boy underwent an emergent reconstruction surgery of the right ventricle-pulmonary artery (RV-PA) conduit. Although he was successfully weaned from cardiopulmonary bypass (CPB) after reconstruction of the RV-PA conduit, the bleeding continued despite the massive transfusion of red blood cell (RBC), fresh frozen plasma (FFP), and platelets. Because of persistent bleeding and abnormal coagulation laboratory results, we administered the recombinant activated factor VII (rFVIIa), which was not approved for use in the treatment of post-CPB coagulopathy. After administration of rFVIIa, his coagulation data dramatically improved, the bleeding decreased, and the operation was able to be finished.
KeywordsPediatric cardiac surgery Refractory bleeding rFVIIa Acquired hemophilia A
There have been increasing numbers of reports of “off-label” use of the recombinant activated factor VII (rFVIIa) to achieve hemostasis in various situations including traumatic intractable bleeding [1, 2], cardiac surgery [3, 4], and obstetrical massive bleeding . However, there are few data regarding the appropriate use of rFVIIa, especially in pediatric patients. Here, we report a case of successful administration of rFVIIa for refractory post-cardiopulmonary bypass (CPB) bleeding in a child undergoing repeated cardiac surgery.
A 2-year-and-7-month-old boy with 22q11.2 deletion syndrome (height, 86 cm; body weight, 10 kg) was scheduled for an emergent surgery to reconstruct the right ventricle-pulmonary artery (RV-PA) conduit to remove its compression on his right coronary artery, causing the right ventricular failure. He was associated with tetralogy of Fallot, pulmonary atresia, major aortopulmonary collateral arteries, and right aortic arch. He underwent a systemic-pulmonary shunt (left subclavian artery to central pulmonary artery) at 1 month of age and right unifocalization and right Blalock-Taussig shunt at 1 year and 3 months of age. When he was 2 years and 7 months old, he underwent RV-PA conduit and pulmonary artery plasty. After the procedure, because of the poor contraction of the right ventricle, weaning from CPB failed and extracorporeal membrane oxygenation (ECMO) was instituted, from which he was weaned on postoperative day 11.
Twenty-two days after surgery, cardiac catheterization revealed that his right coronary artery was compressed by the RV-PA conduit, and the emergent reconstitution of the RV-PA conduit was scheduled on the same day.
Coagulation profile before and after administration of rFVIIa
Prior to rFVIIa
1 h after rFVIIa
5 h after rFVIIa
130–400 × 103
CPB time was 340 min, and his body temperature during CPB was 32 °C. Operation time was 639 min, and anesthesia time was 688 min. Total blood loss was 1480 ml, and required blood products were RBC 690, FFP 725, and platelets 250 ml, respectively.
Five hours after the administration of rFVIIa, coagulation data were comparable to the preoperative values (Table 1) and the total bleeding dose was less than 1 ml/kg/h. No additional rFVIIa was necessary. No thromboembolic events were noted after its administration.
Fifty-two days after the second surgery, his sternum and skin were able to be closed, and he was discharged from PICU on day 157.
We reported the use of rFVIIa in a child complicated with persistent bleeding after cardiac surgery under CPB. Because massive transfusion of FFP and platelets failed to control post-CPB bleeding, we decided to use rFVIIa though we knew that post-CPB coagulopathy was not a licensed indication. In this case, rFVIIa was administrated without previous parental informed consent for its use. The administration of rFVIIa dramatically improved his coagulation data and reduced blood loss.
Recombinant FVIIa is a hemostatic agent developed for the treatment of hemophilia A or B with inhibitors (antibodies) to coagulation factor VIII or IX. Currently, it is also approved to patients with congenital factor VII deficiency or the patients who have acquired antibodies to factor VIII, which is called as acquired hemophilia A. Furthermore, there have been increasing numbers of reports describing the off-label use of rFVIIa, which was effective in controlling refractory bleeding in nonhemophilic patients [1–4].
Uncontrolled bleeding after CPB is a critical problem especially in young children undergoing complex cardiac repair. The proposed mechanisms of the post-CPB coagulopathy in these young patients include (1) large circuit priming volume compared to the circulating blood volume, leading to dilution of platelets and coagulation factors; (2) long, complex cardiac repairs with extensive suture lines; (3) effects of hypothermia on both plasma coagulation factors and platelet function; (4) consumption of coagulation factors due to tissue injury, contact activation, and transfusion of suctioned pericardial blood; and (5) residual heparin or other anticoagulants [3, 5]. Adding to the repeated procedures, our patient was on the ECMO until 11 days before and underwent cardiac catheterization a few hours before the surgery in the unstable hemodynamic and debilitating state. These conditions might have further influenced the coagulation derangement, as partly shown by the abnormal data of PT, PT-INR, and APTT before surgery (Table 1).
There is no consensus on how to manage post-CPB coagulopathy in pediatric patients. The transfusion of platelets is the initial treatment for ongoing bleeding after adequate heparin neutralization in many institutions [3, 6]. However, if bleeding continues despite platelet administration, institutions vary in their transfusion approach.
The congenital Cardiac Anesthesia Society (CCAS) Task Force recommends that rFVIIa can be considered for the management of post-CPB bleeding refractory to maximal standard hemostatic therapy in pediatric cardiac surgery . This criterion for use of rFVIIa could be applied to our case.
It is not clear how the administration of rFVIIa worked dramatically in reducing bleeding in this case. The high dose of FVIIa might have stimulated the coagulation cascade by the activation of factors IX and X in combination with factors VIII and V through TF-dependent mechanism. Or the high dose of FVIIa might have stimulated the coagulation cascade, leading to subsequent thrombin generation through TF-independent mechanism. The latter mechanism seems more plausible because this pathway is enabled only when the high dose of FVIIa is provided and does not require the presence of factors V, VIII, and IX.
To exclude the possibility of acquired hemophilia A, the measurement of antibodies to coagulation factor VIII is required, which we did not perform in this case.
Concerning the dosage of rFVIIa, Pychyńska-Pokorska et al. reported that the effective dose in cardiac surgery was 131.7 ± 69.8 μg/kg in neonates, 104.6 ± 36.0 μg/kg in infants, and 44.6 ± 15.3 μg/kg in children older than 1 year of age . A systematic literature review showed that the effective dose was 93.2 μg/kg, the frequency of administration was 2, and the most common administration interval was 2 h . Since neonates and infants have immature coagulation system than adults , and the plasma clearance of rFVIIa is significantly higher in children than in adults (67 ml/kg/h in children, 36.6 ml/kg/h in adults) , children might require larger dose of rFVIIa than adults to achieve appropriate hemostasis. Considering the age and body weight of our patient, our dose of 100 μg/kg is comparable with the recommended dose.
One of the complications of administering rFVIIa is a thromboembolic event , especially in the patients with ECMO . It is stated that we should properly assess the risk-benefit of administration rFVIIa under ECMO . A thromboembolic event was not noted in our patient.
We experienced a case of a successful “off-label” use of rFVIIa in a pediatric cardiac surgery. In the case of massive post-CPB bleeding refractory to standard hemostatic therapy, the administration of rFVIIa may be taken into consideration. To accumulate the successful cases is important to define the criteria of uses of rFVIIa in the future.
Written informed consent was obtained from the parent of the patient for publication of this case report. A copy of the written consent is available for review by the Editor of this journal.
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
- Yao D, Li Y, Wang J, Yu W, Li N, Li J. Effects of recombinant activated factor VIIa on abdominal trauma patients. Blood Coagul Fibrinolysis. 2014;25:33–8.View ArticlePubMedGoogle Scholar
- Brown CV, Sowery L, Curry E, Valadka AB, Glover CS, Grabarkewitz K, et al. Recombinant factor VIIa to correct coagulopathy in patients with traumatic brain injury presenting to outlying facilities before transfer to the regional trauma center. Am Surg. 2012;78:57–60.PubMedGoogle Scholar
- Guzzetta NA, Russell IA, Williams GD. Review of the off-label use of recombinant activated factor VII in pediatric cardiac surgery patients. Anesth Analg. 2012;115:364–78.View ArticlePubMedGoogle Scholar
- Zatta A, Mcquilten Z, Kandane-Rathnayake R, Isbister J, Dunkley S, Mcneil J, et al. The Australian and New Zealand Haemostasis Registry: ten years of data on off-licence use of recombinant activated factor VII. Blood Transfus. 2015;13:86–99.PubMed CentralPubMedGoogle Scholar
- Barua A, Rao VP, Ramesh B, Barua B, El-Shafei H. Salvage use of activated recombinant factor VII in the management of refractory bleeding following cardiac surgery. J Blood Med. 2011;2:131–4.PubMed CentralView ArticlePubMedGoogle Scholar
- Hornykewycz S, Odegard KC, Castro RA, Zurakowski D, Pigula F, DiNardo JA. Hemostatic consequences of a non-fresh or reconstituted whole blood small volume cardiopulmonary bypass prime in neonates and infants. Paediatr Anaesth. 2009;19:854–61.View ArticlePubMedGoogle Scholar
- Pychyńska-Pokorska M, Pągowska-Klimek I, Krajewski W, Moll JJ. Use of recombinant activated factor VII for controlling refractory postoperative bleeding in children undergoing cardiac surgery with cardiopulmonary bypass. J Cardiothorac Vasc Anesth. 2011;25:987–94.View ArticlePubMedGoogle Scholar
- Levi M, Levy JH, Andersen HF, Truloff D. Safety of recombinant activated factor VII in randomized clinical trials. N Engl J Med. 2010;363:1791–800.View ArticlePubMedGoogle Scholar
- Dominguez TE, Brown KL. Activated recombinant factor VII and extracorporeal membrane oxygenation: everything is all right, nothing is wrong? Pediatr Crit Care Med. 2010;11:155–6.View ArticlePubMedGoogle Scholar