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A 25-year-old man presented to the trauma center with a close-range shotgun wound to the left proximal thigh.
The patient was awake and alert with a heart rate of 120 beats per minute and a systolic blood pressure of 90 mm Hg. A pressure dressing on the left proximal thigh which was applied in the field was half-saturated with blood. No arterial pulses were palpable in the left foot.
The most appropriate first step in the management of this patient in addition to resuscitation is:
CT of the abdomen.
Duplex ultrasound distal to the wound.
X-ray of the left groin and thigh.
An X-ray of the left groin and thigh documented that all pellets were in the proximal thigh inferior to the left inguinal ligament. A blood specimen was sent for type and crossmatch (no massive transfusion protocol available at the time), a cephalosporin antibiotic was administered, and the patient was moved to the operating room.
The preferred operative approach would be:
Pass a retrograde endovascular balloon occlusion of the aorta (REBOA) device through the right groin.
Make a left extraperitoneal renal transplant incision for proximal control.
Apply an aortic compression device on top of the pressure dressing.
Make a longitudinal incision in the left groin proximal to the wound.
A longitudinal incision was made in the left groin to allow for proximal control of the left common femoral artery and distal control of the left femoral vein. After encircling both femoral vessels with vessel loops, a vascular clamp was applied to the left common femoral artery and the time was noted. Bleeding from the open wound decreased significantly. A separate longitudinal incision was then made distal to the open wound. After elevation of the left sartorius muscle, the mid-left superficial femoral artery and femoral vein were mobilized and clamped. The distal femoral vein in the groin was then clamped as well.
The proximal and distal incisions in the left groin and thigh were extended into the open wound as the pressure dressing was removed. Clipping and tying of multiple vessels in the lacerated muscles of the thigh reduced bleeding considerably. There were multiple pellet wounds over a 15 cm length in both the left superficial femoral artery and the left femoral vein. After vigorous resuscitation with blood and products, the patient’s heart rate was 95 beats per minute and the systolic blood pressure was 110 mm Hg.
The most appropriate management of both vascular injuries is:
Intravenous tubing shunts into the artery and vein.
Umbilical vein graft to the artery, ligate vein.
Polytetrafluoroethylene (PTFE) grafts to the artery and vein.
Saphenous vein graft to the artery, PTFE graft to the vein.
As the patient was now reasonably stable, the injured segment of the left superficial femoral artery was resected. Fogarty balloon catheters were then passed proximally and distally. After two negative (no thrombus/embolus) passes of the balloon catheter, “regional” heparin (50 units unfractionated heparin/mL saline) was administered 20 mL proximally and 20 mL distally (total 2000 units). A reversed autogenous saphenous vein graft from the right thigh was then inserted into the left superficial femoral artery with a medial extra-anatomic route to avoid the 7 cm blast cavity through the muscles of the thigh. After removal of the vascular clamps on the artery, palpable left pedal pulses were noted.
The injured segment of the left femoral vein was excised. Proximal and distal vascular clamps were removed sequentially to flush out any thrombus. An 8 mm externally supported polytetrafluoroethylene (PTFE) graft was then inserted into the left femoral vein just lateral to the saphenous vein graft in the artery (figure 1).
A “prophylactic” two-skin incision, four-compartment below-left knee fasciotomy was performed. Vigorous debridement of the lacerated and contused skin, subcutaneous tissue, and muscles in the left thigh was performed, and the cavity was packed with fine mesh gauze.
The patient did well postoperatively, and the blast cavity was clean on the eighth postoperative day (figure 2). A venogram on the 10th postoperative day demonstrated patency of the externally supported PTFE graft (figure 3).
Starting on the 12th postoperative day, pus was noted to be present on the gauze dressing in the blast cavity as it was removed. This continued for another 15 days. At this point, the chief surgical resident on the trauma service met with the attending surgeon for violating his own well-known rule—“wounds that don’t heal contain dead tissue, infected tissue, cancer, or a foreign body.” The patient had reoperations on postoperative days 27 and 35; portions of the shotgun shell were removed on both occasions from the depths of the blast cavity (figure 4), and the blast cavity healed subsequently by secondary intention. At the time of discharge on postoperative day 40, the patient was advised to stop smoking and start a daily walking program, and was placed on oral aspirin 81 mg orally every 12 hours for 3 months.
Shotgun injuries to the extremities result in a wide spectrum of injuries. This is best explained by the following statement by the late Roger T Sherman (President of the American Association for the Surgery of Trauma from 1978 to 1979): “classification of shotgun wounds entails consideration of barrel length, bore, choke, load, wadding, and range as well as high or low brass charges.”1 In addition Sherman and Parrish1 in 1963 classified shotgun wounds as “penetrating” (assailant >7 yards from the victim), “perforating” (3–7 yards), and “massive” (<3 yards).
A patient with a close-range shotgun wound will often have many or all of the components of a “mangled extremity,” that is, injuries to the soft tissue, artery, vein, bone, and nerve.2 In the patient described, there were no injuries to the bone nor nerve, and this contributed to his eventual excellent recovery.
In the modern era this patient would have had QuikClot Combat Gauze (Z-Medica, Wallingford, Connecticut) inserted into the bleeding wound and a tourniquet placed superior to it.3 4 Whether a tourniquet or pressure dressing is in place, proximal and distal arterial and venous control is attained outside the blast cavity. Once the femoral vein is clamped superior to the area of injury, venous hemorrhage from lacerated muscle increases significantly. Controlling this delays insertion of the arterial interposition graft. So it is worthwhile to have a member of the surgical team start to retrieve the greater saphenous vein from the contralateral thigh while hemostasis is completed in the injured thigh.
Many surgeons would have inserted temporary intraluminal shunts into the injured artery and vein in such a patient.5 The vascular injuries in the patient described were 15 cm in length, so insertion of an Argyle (Cardinal Health, Dublin, Ohio) or the Pruitt F3 carotid artery shunt (LeMaitre Vascular, Burlington, Massachusetts) would have been impossible. An alternate choice would be large-bore blood tubing, whereas an Argyle thoracostomy tube could have been used in the femoral vein.5 6
The choice of an externally supported PTFE graft for interposition into the femoral vein is still controversial. The time required to create a 15 cm panel or spiral vein graft would have been unacceptable in this critically ill patient. The advantages of PTFE graft interposition into large peripheral veins include the following: (1) appropriate sizes off the shelf; (2) ease of insertion; (3) decreased bleeding from the area of injury and distal fasciotomy sites; (4) low infection rate when covered by viable tissue; and (5) long period of patency when externally supported grafts are used in patients placed on aspirin postoperatively (author’s observation).7 8
The major lesson learned from the management of this patient, however, is that removal of all retained fragments of a close-range shotgun wound (wadding and others) once the patient’s life and limb have been saved is mandatory. Failure to do so will result in chronic infection, purulent drainage, and failure of the blast cavity to heal.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent Not required.
Provenance and peer review Commissioned; internally peer reviewed.
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