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Ann Thorac Surg 2007;84:1373-1374
© 2007 The Society of Thoracic Surgeons
a The Trauma Program and the Department of Surgery, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada
b Canadian Forces Health Services, Ottawa, Ontario, Canada
c St. Georges Hospital, University of London, London, United Kingdom
d Royal Army Medical Corps, British Army, London, United Kingdom
e Carbonear General Hospital, Newfoundland, Ottawa, Ontario, Canada
f Department of Critical Care Medicine, University of Ottawa, Ottawa, Ontario, Canada
Accepted for publication May 11, 2007.
* Address correspondence to Dr Tien, Sunnybrook Health Sciences Centre, 2075 Bayview Ave, Suite H186, Toronto, Ontario, M4N 3M5, Canada (Email: homer.tien{at}sunnybrook.ca).
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| Introduction |
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Recently, recombinant activated coagulation factor VII (rFVIIa [NovoSeven, Novo Nordisk Pharmaceuticals Inc, Princeton, NJ]) has been proposed as an adjuvant therapy for exsanguinating trauma patients with coagulopathy [3]. To date, the use of rFVIIa in trauma-related hemoptysis has been limited to one case of diffuse alveolar hemorrhage from coagulopathy after blunt thoracic injury [4]. We report the successful use of rFVIIa in treating massive hemoptysis from penetrating thoracic trauma in a noncoagulopathic patient treated in a military field hospital in Afghanistan.
A 23-year-old Afghanistan man sustained a gunshot wound to his left chest and was evacuated to a Canadian Forces field hospital in Kandahar. On admission he was alert and his systolic blood pressure was 85 mm Hg; his pulse rate was 125 beats per minute, and his respiratory rate was 35 per minute. His oxygen saturation was 85%. He had a small wound in his left axilla and a large wound over his anterior chest (Fig 1). There were no retained bullets.
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A thoracotomy revealed a severely contused left upper lobe. Otherwise there was no retained hemothorax, cardiac injury, or great vessel injury. The Canadian field hospital holds approximately 6 dosages of rFVIIa. As thoracotomy was initiated, 4,800 mcg of rFVIIa (approximately 90 mcg/kg) was administered on the belief that the patient had an exsanguinating thoracic hemorrhage. Within 1 minute the hemoptysis was controlled and the patients ventilation improved, such that he was placed on the mechanical ventilator. We then terminated the operation without performing a left upper lobectomy as the patient did not have a significant air leak and had no further hemorrhage. The patient remained ventilated for 7 days, and he was discharged home within 2 weeks.
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We report a case in which rFVIIa successfully controlled massive hemoptysis related to a pulmonary contusion from a gunshot wound to the left chest. The rFVIIa becomes active after forming a complex with tissue factor, which is only exposed to circulating blood at the site of injury. Formation of the tissue factor-rFVIIa complex then initiates activation of factors IX and X, inducing a thrombin burst and faster formation of the fibrin clot [3]. In our patient, administration of rFVIIa may have accelerated thrombosis within ruptured arterioles in the macerated left upper lobe of lung, stopping the intra-alveolar hemorrhage and the resulting hemoptysis.
The rFVIIa may have a role in treating massive hemoptysis in the military setting. Military surgeons may see relatively high volumes of penetrating thoracic trauma while deployed, and yet may not have the expertise of experienced thoracic surgeons for performing anatomical pulmonary resections [6]. In addition, military field hospitals usually do not have interventional radiologic capabilities to perform embolization.
Recombinant activated coagulation factor VII (rFVIIa) is approved to treat hemorrhage in hemophiliacs, but it is increasingly being used in massively exsanguinating, coagulopathic trauma patients. However, rFVIIa has not been shown to improve survival in these patients [7]. One explanation is that any reduction in bleeding achieved by administering rFVIIa may have been overshadowed by the severity of their physiologic derangements.
The rFVIIa may be beneficial in cases where adverse outcomes are less related to the absolute volume of bleeding, but to its location. For example, the "off-label" use of rFVIIa has improved survival in noncoagulopathic patients suffering from spontaneous, nontraumatic intracerebral hemorrhage [8]. Certainly, the volume reduction achieved by using rFVIIa for this indication was extremely modest, but was shown to be associated with a profound survival benefit. Likewise, rFVIIa use should be considered in traumatic hemoptysis cases where physiologic consequences of intra-alveolar hemorrhage predominate. In these cases the danger from hemorrhage is primarily to ventilation and impaired gas exchange, which may be improved by relatively modest reductions in intra-alveolar bleeding. Future studies on rFVIIa use in trauma patients should also focus on ventilatory and oxygenation measurements as intermediate outcomes, especially in patients with documented pulmonary injury.
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