• Journal of Korean Neurosurgical Society
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• 제67권3호
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• pp.354-363
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• 2024

Objective : This study aims to determine the optimal dose of recombinant-human bone morphogenic protein-2 (rhBMP-2) for successful bone fusion in minimally invasive lateral lumbar interbody fusion (MIS LLIF). Previous studies show that rhBMP is an effective alternative to autologous iliac crest bone graft, but the optimal dose remains uncertain. The study analyzes the fusion rates associated with different rhBMP doses to provide a recommendation for the optimal dose in MIS LLIF. Methods : Ninety-three patients underwent MIS LLIF using demineralized bone matrix (DBM) or a mixture of rhBMP-2 and DBM as fusion material. The group was divided into the following three groups according to the rhBMP-2 usage : group A, only DBM was used (n=27); group B, 1 mg of rhBMP-2 per 5 mL of DBM paste (n=41); and group C, 2 mg of rhBMP-2 per 5 mL of DBM paste (n=25). Demographic data, clinical outcomes, postoperative complication and fusion were assessed. Results : At 12 months post-surgery, the overall fusion rate was 92.3% according to Bridwell fusion grading system. Groups B and C, who received rhBMP-2, had significantly higher fusion rates than group A, who received only DBM. However, there was no significant increase in fusion rate when the rhBMP-2 dosage was increased from group B to group C. The groups B and C showed significant improvement in back pain and Oswestry disability index compared to the group A. The incidence of screw loosening was decreased in groups B and C, but there was no significant difference in the occurrence of other complications. Conclusion : Usage of rhBMP-2 in LLIF surgery leads to early and increased final fusion rates, which can result in faster pain relief and return to daily activities for patients. The benefits of using rhBMP-2 were not significantly different between the groups that received 1 mg/5 mL and 2 mg/5 mL of rhBMP-2. Therefore, it is recommended to use 1 mg of rhBMP-2 with 5 mL of DBM, taking both economic and clinical aspects into consideration.

• Journal of Korean Neurosurgical Society
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• 제64권6호
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• pp.933-943
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• 2021

Objective : Percutaneous pedicle screw (PPS) fixation is a needle based procedure that requires fluoroscopic image guidance. Consequently, radiation exposure is inevitable for patients, surgeons, and operation room staff. We hypothesize that reducing the production of radiation emission will result in reduced radiation exposure for everyone in the operation room. Research was performed to evaluate reduction of radiation exposure by modifying imaging manner and mode of radiation source. Methods : A total of 170 patients (680 screws) who underwent fusion surgery with PPS fixation from September 2019 to March 2020 were analyzed in this study. Personal dosimeters (Polimaster Ltd.) were worn at the collar outside a lead apron to measure radiation exposure. Patients were assigned to four groups based on imaging manner of fluoroscopy and radiation modification (pulse mode with reduced dose) : continuous use without radiation modification (group 1, n=34), intermittent use without radiation modification (group 2, n=54), continuous use with radiation modification (group 3, n=26), and intermittent use with radiation modification (group 4, n=56). Post hoc Tukey Honest significant difference test was used for individual comparisons of radiation exposure/screw and fluoroscopic time/screw. Results : The average radiation exposure/screw was 71.45±45.75 µSv/screw for group 1, 18.77±11.51 µSv/screw for group 2, 19.58±7.00 µSv/screw for group 3, and 4.26±2.89 µSv/screw for group 4. By changing imaging manner from continuous multiple shot to intermittent single shot, 73.7% radiation reduction was achieved in the no radiation modification groups (groups 1, 2), and 78.2% radiation reduction was achieved in the radiation modification groups (groups 3, 4). Radiation source modification from continuous mode with standard dose to pulse mode with reduced dose resulted in 72.6% radiation reduction in continuous imaging groups (groups 1, 3) and 77.3% radiation reduction in intermittent imaging groups (groups 2, 4). The average radiation exposure/screw was reduced 94.1% by changing imaging manner and modifying radiation source from continuous imaging with standard fluoroscopy setting (group 1) to intermittent imaging with modified fluoroscopy setting (group 4). A total of 680 screws were reviewed postoperatively, and 99.3% (675) were evaluated as pedicle breach grade 0 (<2 mm). Conclusion : The average radiation exposure/screw for a spinal surgeon can be reduced 94.1% by changing imaging manner and modifying radiation source from real-time imaging with standard dose to intermittent imaging with modified dose. These modifications can be instantly applied to any procedure using fluoroscopic guidance and may reduce the overall radiation exposure of spine surgeons.

• 대한골관절종양학회지
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• 제10권2호
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• pp.88-95
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• 2004

목적: 통증을 동반한 유골 골종의 치료는 일반적으로 수술적 절제로 이루어졌으나, 그 침습성으로 인하여 술후 통증 및 일정 동안의 회복 시간이 필요하였다. 최소 침습적인 방법인 경피적 고주파 열치료를 이용한 유골 골종의 치료는 술 후 통증이 적고, 회복이 빠르며, 재발은 수술적 방법과 비슷한 것으로 보고되어 있다. 이에 저자들은 본원에서 시행한 경피적 고주파 열치료의 임상 결과를 보고하고자 한다. 대상 및 방법: 1999년 4월에서 2004년 5월 사이에 삼성서울병원에 내원하여 유골 골종으로 진단된 환자 22명, 22례를 전산화 단층 촬영 도움 하에 경피적 고주파 열치료를 시행하였다. 평균 연령은 26.5(7~55)세였고, 남자가 15명, 여자가 7명이었다. 이 중 2례는 외부에서 치료 받은 후 재발한 경우였다. 병변의 위치는 대퇴골 13, 경골 4, 비골 1, 상완골 1, 장골 1, 좌골 1, 천골 1례였다. 시술 전 3례에서 경피적 생검을 시행하여 확진 하였고, 나머지는 임상양상 및 방사선 소견으로 진단하였다. 전신 또는 척추 마취 하에 전산화 단층 촬영으로 병소의 위치를 확인한 후 고주파 전극을 병소의 중심부에 위치한 후, 섭씨 80에서 90도로 평균 6(3~8)분간 가열하였다. 외래 추시 및 전화 통화로 증상 호전 여부 및 일상 생활 정도를 추적 관찰하였으며, 평균 추시 기간은 30(4~62)개월 이었다. 결과: 추시 중 19례(86%)에서 통증이 소실되었고, 2례에서는 시술 후 각각 5개월, 12개월에 병변이 재발하였으며, 1례에서는 재발의 증거 없이 지속되는 통증이 있었다. 시술 후 4시간 정도 침상 안정 후 바로 보조기 없이 보행이 가능하였으며, 화상으로 인한 근육 손상이 발생한 1례를 제외한 21례 환자들은 합병증 없이 시술 후 평균 1.9일에 퇴원하였다. 재발이 확인된 2례는 다시 고주파 열치료를 시행하여 증상이 모두 소실되었다. 결론: 유골 골종의 치료에 있어서 전산화 단층 촬영 도움 하 경피적 고주파 열치료는 최소 침습적인 방법으로 술후 통증이 적으며, 회복이 빠르고, 안전하면서, 이제까지 보고된 수술적 절제의 결과와 비교할 만한 우수한 성적을 나타내었다.