中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
35期
6643-6646
,共4页
韩成龙%刘杨%姜超%朱洪勋%杨卫良
韓成龍%劉楊%薑超%硃洪勛%楊衛良
한성룡%류양%강초%주홍훈%양위량
聚醚醚酮融合器%纳米人工骨%脊髓型颈椎病%椎间融合%医学植入物
聚醚醚酮融閤器%納米人工骨%脊髓型頸椎病%椎間融閤%醫學植入物
취미미동융합기%납미인공골%척수형경추병%추간융합%의학식입물
背景:聚醚醚酮聚合物在体内外实验表明,它与人体组织有良好的相容性,最接近骨的弹性模量,并具有良好的塑性和硬度,是最佳的椎间融合器材料.目的:评价锚定聚醚醚酮椎间融合器结合纳米人工骨在脊髓型颈椎病前路间盘切除后椎体间融合效果.方法:回顾性分析2007-05/2009-09哈尔滨医科大学附属第一医院骨科收治的脊髓型颈椎病患者17例,男12例,女5例;年龄55(42~67)岁.均采用前路间盘切除后锚定聚醚醚酮融合器结合纳米人工骨椎间融合治疗.JOA评分评价神经功能恢复情况;术前、术后3个月X射线检查测量椎间高度,侧位像过伸过曲位观察融合情况.结果与结论:术后17例患者症状均有所改善,在术后的几天内,患者的下肢肌力增加,术后肢体的灵活性较术前改善.术后3个月JOA评分较术前明显提高,手术节段稳定,椎间高度恢复满意.无并发症发生,所有病例经X射线证实均达到牢固融合.结果说明锚定聚醚醚酮融合器可以使颈椎手术节段获得即刻稳定,锚定聚醚醚酮融合器结合纳米人工骨手术创伤小,手术时间短,融合效果确定,并发症较低,是治疗脊髓型颈椎病一种良好的选择.
揹景:聚醚醚酮聚閤物在體內外實驗錶明,它與人體組織有良好的相容性,最接近骨的彈性模量,併具有良好的塑性和硬度,是最佳的椎間融閤器材料.目的:評價錨定聚醚醚酮椎間融閤器結閤納米人工骨在脊髓型頸椎病前路間盤切除後椎體間融閤效果.方法:迴顧性分析2007-05/2009-09哈爾濱醫科大學附屬第一醫院骨科收治的脊髓型頸椎病患者17例,男12例,女5例;年齡55(42~67)歲.均採用前路間盤切除後錨定聚醚醚酮融閤器結閤納米人工骨椎間融閤治療.JOA評分評價神經功能恢複情況;術前、術後3箇月X射線檢查測量椎間高度,側位像過伸過麯位觀察融閤情況.結果與結論:術後17例患者癥狀均有所改善,在術後的幾天內,患者的下肢肌力增加,術後肢體的靈活性較術前改善.術後3箇月JOA評分較術前明顯提高,手術節段穩定,椎間高度恢複滿意.無併髮癥髮生,所有病例經X射線證實均達到牢固融閤.結果說明錨定聚醚醚酮融閤器可以使頸椎手術節段穫得即刻穩定,錨定聚醚醚酮融閤器結閤納米人工骨手術創傷小,手術時間短,融閤效果確定,併髮癥較低,是治療脊髓型頸椎病一種良好的選擇.
배경:취미미동취합물재체내외실험표명,타여인체조직유량호적상용성,최접근골적탄성모량,병구유량호적소성화경도,시최가적추간융합기재료.목적:평개묘정취미미동추간융합기결합납미인공골재척수형경추병전로간반절제후추체간융합효과.방법:회고성분석2007-05/2009-09합이빈의과대학부속제일의원골과수치적척수형경추병환자17례,남12례,녀5례;년령55(42~67)세.균채용전로간반절제후묘정취미미동융합기결합납미인공골추간융합치료.JOA평분평개신경공능회복정황;술전、술후3개월X사선검사측량추간고도,측위상과신과곡위관찰융합정황.결과여결론:술후17례환자증상균유소개선,재술후적궤천내,환자적하지기력증가,술후지체적령활성교술전개선.술후3개월JOA평분교술전명현제고,수술절단은정,추간고도회복만의.무병발증발생,소유병례경X사선증실균체도뢰고융합.결과설명묘정취미미동융합기가이사경추수술절단획득즉각은정,묘정취미미동융합기결합납미인공골수술창상소,수술시간단,융합효과학정,병발증교저,시치료척수형경추병일충량호적선택.
BACKGROUND: In vivo and in vitro experiments have demonstrated that polyetheretherketone (PEEK) polymer is the best cervical fusion cage material due to its good biocompatibility, elastic modulus similar to human bone, and satisfactory plasticity and hardness.OBJECTIVE: To assess the outcomes of polyetheretherketone (PEEK) cage filled with nano-artificial bone following anterior cervical discectomy and fusion (ACDF) in patients with cervical spondylotic myelopathy.METHODS: In total 17 patients with cervical spondylotic myelopathy were collected from the Department of Orthopedics, First Affiliated Hospital of Harbin Medical University between May 2007 and September 2009. There were 12 males and 5 females,averaging 55 (range 42-67) years of age. All patients underwent ACDF using PEEK cage filled with nano-artificial bone. Patients'neurological functions were assessed on the basis of Japanese Orthopaedic Association (JOA) scoring system. The distance between the midpoint of the upper end plate and lower end plate was measured as interboby height. Radiographs with the neck in lateral flexion and extension were obtained to evaluate fusion results.RESULTS AND CONCLUSIONS: Seventeen patients with cervical spondylotic myelopathy participated in the final analysis.Almost all patients had symptomatic improvement. Within postoperative several days, muscle strength of lower limb was increased, and limb was more flexible after surgery than prior to surgery. At 3 months after surgery, JOA scores were significantly increased compared to prior to surgery, the operated segments were stable and disc space height was satisfactory. In addition, no complications were found, and all cases achieved solid fusion, as confirmed by radiographs. These findings suggest that the immediate stability of the operated segments can be obtained by anchoring PEEK cage, and the nano-artificial bone-filled PEEK cage is safe, simple, and with relatively few complications. It is therefore a good choice for patients with cervical spondylotic myelopathy.