Patient: AX-919

MEDICAL REPORT
Protected Document: █ █ █ B-10070 █ █ █

Intake Date: - - -
Intake Time: 11:30
Patient Name: DOCTOR : AX-919 - Julian Qar




MEDICAL NARRATIVE
[Intake doctor: J-QAR]
[Assist: HAZE]

JQ [AX-919] presents to the ED med bay after Csilla arrival complaining of lower extremity tenderness, bleeding, fatigue, swelling, and severe pain at the titanium femoral junction.

Upon first inspection, clear signs of tearing present at the base of the titanium ring holding the limb in place. Irritation present where the pin and neurological synth patch attachments placed.

Further visual observation show signs of severe muscular atrophy. The vascular line connecting the titanium unit to the synthetic femoral artery shows fraying and collapse.

Discussing patient history for causality: the patient believes their injury is a result of overuse and improper distribution of weight and calibrations during introductory cybernetic augmentation procedure.

Epidural was given on L2 vert - note JQ [AX-919] has shielding of the spinal cord and brain stem present and within working condition. No abnormalities present.
[Note: Patient may consider material upgrade on cord shield.]

Treatment plan and diagnosis: Full amputation of the organic right lower limb, replace limb with titanium cybernetic augments.


TESTING & DRUG ADMINISTRATION:

Reflex Test: Minimal response.

Movement Test: Major limp and disturbance in normal gait present. See notes above regarding calibration and weight distribution.

Xray Diagnostic Results: All bones within LRL had shown no titanium covering, organic tissues left intact. Titanium rod present in place of organic marrow.


Blood panel results: High white blood cell count, bacteria present on rapid culture. Results conclude early stages of Cellulitis. CVAD installed due to patients' limited vascular access. Intravenous Doxysylon administered for preventive measures.

Patient weight with augmentations: 354kg

Limb Weight after removal: 15kg [Weight at the first installment: 21kg]



DISCHARGE INSTRUCTIONS
The patient should limit movement for the next four weeks following the procedure. Phantom limb symptoms may be present. Physical therapy is recommended to ensure the cybernetic limb is in working order. Routine calibration may be needed to ensure the distribution of weight is adequate. CVAD should remain in place for four weeks following the procedure to ensure organic tissues were not compromised due to the early stages of patient infection. Patients should be able to perform light activity at work, no heavy lifting for four weeks.

Medical Director


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