The NexGen LPS-flex to the knee prosthesis at a minimum of three years
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, T.-H. | - |
dc.contributor.author | Lee, D.-H. | - |
dc.contributor.author | Bin, S.-I. | - |
dc.date.accessioned | 2021-09-09T15:47:54Z | - |
dc.date.available | 2021-09-09T15:47:54Z | - |
dc.date.created | 2021-06-17 | - |
dc.date.issued | 2008 | - |
dc.identifier.issn | 0301-620X | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/125307 | - |
dc.description.abstract | We carried out a prospective study to assess the clinical outcome, complications and survival of the NexGen Legacy posterior-stabilised-Flex total knee replacement (TKR) in a consecutive series of 278 knees between May 2003 and February 2005. Mean follow-up for 259 TKRs (98.2%) was 3.8 years (3.0 to 4.8). Annual follow-up showed improvement in the Knee Society scores (paired t-test, p < 0.05). At the last follow-up, the mean maximum flexion was 135° (110° to 150°). Two knees showed radiolucent lines, but revision was not required because the patients were asymptomatic. Revision was required in one case because of infection, but there were no prosthesis-related revisions. There were no other complications. The estimated survival rate at four years with revision for any reason and prosthesis-related problems was 99.6% and 100%, respectively. This relatively large study indicates that the legacy posterior stabilised-Flex design provides excellent short-term outcome but warrants ongoing evaluation to confirm the long-term durability and functioning of the implant. ©2008 British Editorial Society of Bone and Joint Surgery. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.subject | adult | - |
dc.subject | aged | - |
dc.subject | article | - |
dc.subject | controlled study | - |
dc.subject | female | - |
dc.subject | follow up | - |
dc.subject | human | - |
dc.subject | infection | - |
dc.subject | knee prosthesis | - |
dc.subject | major clinical study | - |
dc.subject | male | - |
dc.subject | outcome assessment | - |
dc.subject | postoperative complication | - |
dc.subject | priority journal | - |
dc.subject | prospective study | - |
dc.subject | prosthesis failure | - |
dc.subject | survival | - |
dc.subject | survival rate | - |
dc.subject | total knee replacement | - |
dc.subject | Aged | - |
dc.subject | Aged, 80 and over | - |
dc.subject | Arthroplasty, Replacement, Knee | - |
dc.subject | Female | - |
dc.subject | Follow-Up Studies | - |
dc.subject | Humans | - |
dc.subject | Knee Joint | - |
dc.subject | Knee Prosthesis | - |
dc.subject | Male | - |
dc.subject | Middle Aged | - |
dc.subject | Osteoarthritis, Knee | - |
dc.subject | Postoperative Complications | - |
dc.subject | Prospective Studies | - |
dc.subject | Prosthesis Design | - |
dc.subject | Range of Motion, Articular | - |
dc.subject | Treatment Outcome | - |
dc.title | The NexGen LPS-flex to the knee prosthesis at a minimum of three years | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, D.-H. | - |
dc.identifier.doi | 10.1302/0301-620X.90B10.21050 | - |
dc.identifier.scopusid | 2-s2.0-53849148920 | - |
dc.identifier.bibliographicCitation | Journal of Bone and Joint Surgery - Series B, v.90, no.10, pp.1304 - 1310 | - |
dc.relation.isPartOf | Journal of Bone and Joint Surgery - Series B | - |
dc.citation.title | Journal of Bone and Joint Surgery - Series B | - |
dc.citation.volume | 90 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 1304 | - |
dc.citation.endPage | 1310 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | adult | - |
dc.subject.keywordPlus | aged | - |
dc.subject.keywordPlus | article | - |
dc.subject.keywordPlus | controlled study | - |
dc.subject.keywordPlus | female | - |
dc.subject.keywordPlus | follow up | - |
dc.subject.keywordPlus | human | - |
dc.subject.keywordPlus | infection | - |
dc.subject.keywordPlus | knee prosthesis | - |
dc.subject.keywordPlus | major clinical study | - |
dc.subject.keywordPlus | male | - |
dc.subject.keywordPlus | outcome assessment | - |
dc.subject.keywordPlus | postoperative complication | - |
dc.subject.keywordPlus | priority journal | - |
dc.subject.keywordPlus | prospective study | - |
dc.subject.keywordPlus | prosthesis failure | - |
dc.subject.keywordPlus | survival | - |
dc.subject.keywordPlus | survival rate | - |
dc.subject.keywordPlus | total knee replacement | - |
dc.subject.keywordPlus | Aged | - |
dc.subject.keywordPlus | Aged, 80 and over | - |
dc.subject.keywordPlus | Arthroplasty, Replacement, Knee | - |
dc.subject.keywordPlus | Female | - |
dc.subject.keywordPlus | Follow-Up Studies | - |
dc.subject.keywordPlus | Humans | - |
dc.subject.keywordPlus | Knee Joint | - |
dc.subject.keywordPlus | Knee Prosthesis | - |
dc.subject.keywordPlus | Male | - |
dc.subject.keywordPlus | Middle Aged | - |
dc.subject.keywordPlus | Osteoarthritis, Knee | - |
dc.subject.keywordPlus | Postoperative Complications | - |
dc.subject.keywordPlus | Prospective Studies | - |
dc.subject.keywordPlus | Prosthesis Design | - |
dc.subject.keywordPlus | Range of Motion, Articular | - |
dc.subject.keywordPlus | Treatment Outcome | - |
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