{"title":"P4。腰椎后路椎间融合术后椎笼后移的预防","authors":"Hiroyuki Aono MD","doi":"10.1016/j.xnsj.2025.100628","DOIUrl":null,"url":null,"abstract":"<div><h3>BACKGROUND CONTEXT</h3><div>Cage retropulsion following posterior lumbar interbody fusion (PLIF) is a rare but serious complication requiring revision surgery in many cases.</div></div><div><h3>PURPOSE</h3><div>To investigate this complication and potential preventive measures, we retrospectively analyzed a series of PLIF procedures performed at our institution using a consistent surgical technique.</div></div><div><h3>STUDY DESIGN/SETTING</h3><div>This is a retrospective study.</div></div><div><h3>PATIENT SAMPLE</h3><div>We reviewed the surgical database of our institution for PLIF procedures performed between June 2006 and May 2024 for degenerative lumbar disease. Patients who underwent PLIF and were followed up for at least six months postoperatively were included in this study.</div></div><div><h3>OUTCOME MEASURES</h3><div>Cage retropulsion was defined as posterior migration of the cage into the spinal canal, by lateral radiographs at latest follow up.</div></div><div><h3>METHODS</h3><div>All PLIF procedures were performed using a standardized technique involving bilateral facetectomy, subtotal discectomy, thorough local bone grafting (at least two strut bone blocks with two box-type cages), and pedicle screw instrumentation. Patient demographics (age, sex) and the number of fused levels were also analyzed.</div></div><div><h3>RESULTS</h3><div>A total of 918 patients were included in this study (97% follow-up rate). The cohort consisted of 316 males and 602 females with a mean age of 71 years. A total of 1,133 levels were fused (one-level: 887, two-level: 119, three-level: 6). Ninety-two PLIF procedures were performed to treat adjacent segment disease. No cases of cage retropulsion were observed.</div></div><div><h3>CONCLUSIONS</h3><div>The reported incidence of cage retropulsion after PLIF/TLIF ranges from 0.8% to 4.7%. Risk factors include older age, high body mass index, multi-level fusion, cage size and shape, endplate injury, and disc space morphology. We believe that our consistent surgical technique, particularly emphasizing thorough discectomy and bone grafting, may have contributed to the absence of cage retropulsion in our series.</div></div><div><h3>FDA Device/Drug Status</h3><div>Intervertebral disc cage (Approved for this indication).</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"22 ","pages":"Article 100628"},"PeriodicalIF":2.5000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"P4. Prevention for cage retropulsion following posterior lumbar interbody fusion\",\"authors\":\"Hiroyuki Aono MD\",\"doi\":\"10.1016/j.xnsj.2025.100628\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>BACKGROUND CONTEXT</h3><div>Cage retropulsion following posterior lumbar interbody fusion (PLIF) is a rare but serious complication requiring revision surgery in many cases.</div></div><div><h3>PURPOSE</h3><div>To investigate this complication and potential preventive measures, we retrospectively analyzed a series of PLIF procedures performed at our institution using a consistent surgical technique.</div></div><div><h3>STUDY DESIGN/SETTING</h3><div>This is a retrospective study.</div></div><div><h3>PATIENT SAMPLE</h3><div>We reviewed the surgical database of our institution for PLIF procedures performed between June 2006 and May 2024 for degenerative lumbar disease. Patients who underwent PLIF and were followed up for at least six months postoperatively were included in this study.</div></div><div><h3>OUTCOME MEASURES</h3><div>Cage retropulsion was defined as posterior migration of the cage into the spinal canal, by lateral radiographs at latest follow up.</div></div><div><h3>METHODS</h3><div>All PLIF procedures were performed using a standardized technique involving bilateral facetectomy, subtotal discectomy, thorough local bone grafting (at least two strut bone blocks with two box-type cages), and pedicle screw instrumentation. Patient demographics (age, sex) and the number of fused levels were also analyzed.</div></div><div><h3>RESULTS</h3><div>A total of 918 patients were included in this study (97% follow-up rate). The cohort consisted of 316 males and 602 females with a mean age of 71 years. A total of 1,133 levels were fused (one-level: 887, two-level: 119, three-level: 6). Ninety-two PLIF procedures were performed to treat adjacent segment disease. No cases of cage retropulsion were observed.</div></div><div><h3>CONCLUSIONS</h3><div>The reported incidence of cage retropulsion after PLIF/TLIF ranges from 0.8% to 4.7%. Risk factors include older age, high body mass index, multi-level fusion, cage size and shape, endplate injury, and disc space morphology. We believe that our consistent surgical technique, particularly emphasizing thorough discectomy and bone grafting, may have contributed to the absence of cage retropulsion in our series.</div></div><div><h3>FDA Device/Drug Status</h3><div>Intervertebral disc cage (Approved for this indication).</div></div>\",\"PeriodicalId\":34622,\"journal\":{\"name\":\"North American Spine Society Journal\",\"volume\":\"22 \",\"pages\":\"Article 100628\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"North American Spine Society Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666548425000484\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"North American Spine Society Journal","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666548425000484","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
P4. Prevention for cage retropulsion following posterior lumbar interbody fusion
BACKGROUND CONTEXT
Cage retropulsion following posterior lumbar interbody fusion (PLIF) is a rare but serious complication requiring revision surgery in many cases.
PURPOSE
To investigate this complication and potential preventive measures, we retrospectively analyzed a series of PLIF procedures performed at our institution using a consistent surgical technique.
STUDY DESIGN/SETTING
This is a retrospective study.
PATIENT SAMPLE
We reviewed the surgical database of our institution for PLIF procedures performed between June 2006 and May 2024 for degenerative lumbar disease. Patients who underwent PLIF and were followed up for at least six months postoperatively were included in this study.
OUTCOME MEASURES
Cage retropulsion was defined as posterior migration of the cage into the spinal canal, by lateral radiographs at latest follow up.
METHODS
All PLIF procedures were performed using a standardized technique involving bilateral facetectomy, subtotal discectomy, thorough local bone grafting (at least two strut bone blocks with two box-type cages), and pedicle screw instrumentation. Patient demographics (age, sex) and the number of fused levels were also analyzed.
RESULTS
A total of 918 patients were included in this study (97% follow-up rate). The cohort consisted of 316 males and 602 females with a mean age of 71 years. A total of 1,133 levels were fused (one-level: 887, two-level: 119, three-level: 6). Ninety-two PLIF procedures were performed to treat adjacent segment disease. No cases of cage retropulsion were observed.
CONCLUSIONS
The reported incidence of cage retropulsion after PLIF/TLIF ranges from 0.8% to 4.7%. Risk factors include older age, high body mass index, multi-level fusion, cage size and shape, endplate injury, and disc space morphology. We believe that our consistent surgical technique, particularly emphasizing thorough discectomy and bone grafting, may have contributed to the absence of cage retropulsion in our series.
FDA Device/Drug Status
Intervertebral disc cage (Approved for this indication).