Registration/cleaning |
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Cannulation of femoral artery |
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Supine positioning, head, and palms facing up (use nylon plates if necessary)
Sharp incision into the femoral triangle (skin, fascia, ca. 100 mm), followed by blunt dissection
Place sutures under proximal and distal end of exposed femoral artery
Incise longitudinally the femoral artery with a 10‐mm incision
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No. 4 scalpel handle, No. 21 scalpel blades, Adson forceps, dressing forceps, blunt/blunt curved scissors, retractors, aneurysm hooks |
Body fixation |
20 L of injection solution (70 kg cadaver; needs to be decreased or increased depending on individual cadaver) |
Use standard cannula, first placing inferiorly into distal limb, then placing superiorly; make sure the unused side is sutured
Perfuse cadaver until tissues become firm (“goose‐pimpled appearance”), and foam starts forming from the airways (mouth, nose)
Recommended pressure settings: 1,500‐2,000 mm H2O or 0.2‐0.3 bars
If perfusion seems unsuccessful use other sites (contralateral femoral artery, carotid artery), trocar for peripheral perfusion should only be used as a last resort
Suture incisions
Fill out report form
Wrap corpse in body bag, store, and transport at ambient conditions
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Metal cannula, needle holders, curved needles, injection pump, suture material |
Brain fixation (can be done as part of the initial fixation or at a later stage) |
20 ml formalin mixed with 100 ml injection solution |
Bilateral: skin incision of 20 mm, 10‐15 mm lateral to median sagittal plane, drill 6‐mm hole and place a needle anteromedially through dura mater
Remove cerebrospinal fluid and inject 50 ml (37% formaldehyde)
Close burr hole with bee wax and suture
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No. 4 scalpel handle, No. 21 scalpel blades, 6‐mm drill, bee wax, syringe |
Conservation and long‐term storage |
Phenoxyethanol (1 Vol%), optional Arquad‐75 (0.1 Vol%) |
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Storage at room temperature (warehouse 10‐25°C), polyethylene foil |
Treatment of mold growth |
Phenoxyethanol (2.4 Vol%, 120 ml), Arquad‐75 (0.25 Vol%, 1.25 ml) in 5 L water |
Spray suspected surfaces with 2% Trigene, and all specimens with the 2.4% phenoxyethanol solution, repeat once after 2 hours
Clean thoroughly all containers and instruments
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