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Anterior Cervical Discectomy and Fusion Performed Using a CaO-SiO2-P2O5-B2O3 Bioactive Glass Ceramic or Polyetheretherketone Cage Filled with Hydroxyapatite/& beta;-Tricalcium Phosphate: A Prospective Randomized Controlled Trial

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dc.contributor.authorPark, Jiwon-
dc.contributor.authorPark, Sang-Min-
dc.contributor.authorHam, Dae-Woong-
dc.contributor.authorHong, Jae-Young-
dc.contributor.authorKim, Ho-Joong-
dc.contributor.authorYeom, Jin S.-
dc.date.accessioned2024-01-09T17:34:19Z-
dc.date.available2024-01-09T17:34:19Z-
dc.date.issued2023-06-
dc.identifier.issn2077-0383-
dc.identifier.issn2077-0383-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/70891-
dc.description.abstractA CaO-SiO2-P2O5-B2O3 bioactive glass-ceramic (BGS-7) spacer provides high mechanical stability, produces a chemical bond to the adjacent endplate, and facilitates fusion after spine surgery. This prospective, randomized, single-blind, non-inferiority trial aimed to evaluate the radiographic outcomes and clinical efficacy of anterior cervical discectomy and fusion (ACDF) using a BGS-7 spacer for treating cervical degenerative disorders. Thirty-six patients underwent ACDF using a BGS-7 spacer (Group N), and 40 patients underwent ACDF using polyetheretherketone (PEEK) cages filled with a mixture of hydroxyapatite (HA) and & beta;-tricalcium phosphate (& beta;-TCP) for the treatment of cervical degenerative disorders. The spinal fusion rate was assessed 12 months postoperatively using three-dimensional computed tomography (CT) and dynamic radiographs. Clinical outcomes included patient-reported outcome measures, visual analog scale scores for neck and arm pain, and scores from the neck disability index (NDI), European Quality of Life-5 Dimensions (EQ-5D), and 12-item Short Form Survey (SF-12v2). All participants were randomly assigned to undergo ACDF using either a BGS-7 spacer or PEEK cage filled with HA and & beta;-TCP. The primary outcome was the fusion rate on CT scan image at 12 months after ACDF surgery based on a per-protocol strategy. Clinical outcomes and adverse events were also assessed. The 12-month fusion rates for the BGS-7 and PEEK groups based on CT scans were 81.8% and 74.4%, respectively, while those based on dynamic radiographs were 78.1% and 73.7%, respectively, with no significant difference between the groups. There were no significant differences in the clinical outcomes between the two groups. Neck pain, arm pain, NDI, EQ-5D, and SF-12v2 scores significantly improved postoperatively, with no significant differences between the groups. No adverse events were observed in either group. In ACDF surgery, the BGS-7 spacer showed similar fusion rates and clinical outcomes as PEEK cages filled with HA and & beta;-TCP.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleAnterior Cervical Discectomy and Fusion Performed Using a CaO-SiO2-P2O5-B2O3 Bioactive Glass Ceramic or Polyetheretherketone Cage Filled with Hydroxyapatite/& beta;-Tricalcium Phosphate: A Prospective Randomized Controlled Trial-
dc.typeArticle-
dc.identifier.doi10.3390/jcm12124069-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL MEDICINE, v.12, no.12-
dc.description.isOpenAccessY-
dc.identifier.wosid001014494200001-
dc.identifier.scopusid2-s2.0-85164034265-
dc.citation.number12-
dc.citation.titleJOURNAL OF CLINICAL MEDICINE-
dc.citation.volume12-
dc.type.docTypeArticle-
dc.publisher.location스위스-
dc.subject.keywordAuthorACDF-
dc.subject.keywordAuthorcervical-
dc.subject.keywordAuthorfusion rate-
dc.subject.keywordAuthorglass ceramics-
dc.subject.keywordAuthorPEEK cage-
dc.subject.keywordPlusINTERBODY FUSION-
dc.subject.keywordPlusBGS-7-
dc.subject.keywordPlusALLOGRAFT-
dc.subject.keywordPlusSPACER-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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