A Case Report of a Patient who Achieved Recovery of Walking Independence with the Adjustment of the Prosthesis after Bilateral Leg Amputation and Spinal Cord Injury.
- VernacularTitle:両下腿切断と脊髄損傷を同時に受傷したが，義足の調整により歩行自立した1例の報告
- Author:
Masamune EBARA
1
;
Rina ABE
1
;
Dai FUJIWARA
2
;
Kentaro KANARI
1
;
Tsuyoshi MIZUSHIRI
1
;
Shinichi IZUMI
3
Author Information
- Keywords: spinal cord injury; paraplegia; below-the-knee amputation; prosthesis; multiple disability
- From:The Japanese Journal of Rehabilitation Medicine 2023;60(9):799-804
- CountryJapan
- Language:Japanese
- Abstract: This report describes a case of an amputee with a lumber spinal cord injury who successfully recovered ambulation with the use of prosthesis.A 30-year-old man with schizophrenia underwent amputation of the lower legs and concurrently developed lumbar spinal cord injury from of a suicide attempt. After the treatment of stump plasty and posterior fusion, the patient was transferred to our facility. Lower-extremity prostheses for both legs were fitted, and orthostatic training was commenced following admission. During the initial evaluation, the patient could not maintain a stable standing position because of weakness in the hip extensor muscle. An inflexion angle of the prosthesis was set to 0° to extend the knee joint and achieve standing stability. Appropriate adjustments of the prosthesis were made as required, specifically addressing the paraplegia caused by his lumbar spinal cord injury. Thus, the patient successfully regained ambulation with the treatment.Recovering walking independence after bilateral lower leg amputations or paraplegia caused by lumber spinal cord injury is not uncommon. However, this case is unique in that the muscle weakness caused by lumbar spinal cord injury presented unforeseen difficulties for the patient to achieve ambulation, which is not ordinarily observed in amputation rehabilitation cases. No similar cases have been reported in which patients concurrently suffered from both these conditions in Japan；therefore, this case is extremely rare.
