创伤外科杂志
創傷外科雜誌
창상외과잡지
JOURNAL OF AUMATIC SURGERY
2014年
1期
29-31
,共3页
羟基磷灰石%聚酰胺%骨缺损%人工骨
羥基燐灰石%聚酰胺%骨缺損%人工骨
간기린회석%취선알%골결손%인공골
hydroxyapatite%polyamide%bone defect%artificial bone
目的:观察纳米羟基磷灰石/聚酰胺66( n-HA/PA66)复合生物活性人工骨在四肢骨缺损术中填充植骨的安全性和临床疗效。方法对87例四肢骨手术后骨缺损,包括四肢松质骨暴力压缩骨折导致骨缺损和干骺端良性骨肿瘤术后骨缺损的患者,采用n-HA/PA66复合生物活性人工骨填充植骨。术前、术后1周及3、6、12个月分别摄X线片及CT,观察骨缺损的修复生长和植骨融合情况。结果随访6~28个月(平均8个月),伤口均甲级愈合,无切口感染、非特异炎症反应和排斥反应; X线片和CT检查示:术后骨缺损区域填充良好,密度较松质骨稍低,材料与周围骨边界清楚;术后1个月,骨缺损区密度逐渐升高,可见植骨周围模糊,有少量新生骨痂形成;术后3个月,骨缺损区密度明显升高,植骨周围间隙开始向中心融合成片,更多新生骨痂影融合;术后6个月,骨缺损区密度明显升高,大量新生骨痂形成。临床骨愈合时间为术后3~7个月,平均3.8个月,愈合率为91.5%。结论纳米羟基磷灰石/聚酰胺66复合生物活性人工骨用于治疗四肢骨缺损,能与植骨区骨生长融合,无不良反应,疗效满意,是一种安全有效的骨缺损植骨填充材料。
目的:觀察納米羥基燐灰石/聚酰胺66( n-HA/PA66)複閤生物活性人工骨在四肢骨缺損術中填充植骨的安全性和臨床療效。方法對87例四肢骨手術後骨缺損,包括四肢鬆質骨暴力壓縮骨摺導緻骨缺損和榦骺耑良性骨腫瘤術後骨缺損的患者,採用n-HA/PA66複閤生物活性人工骨填充植骨。術前、術後1週及3、6、12箇月分彆攝X線片及CT,觀察骨缺損的脩複生長和植骨融閤情況。結果隨訪6~28箇月(平均8箇月),傷口均甲級愈閤,無切口感染、非特異炎癥反應和排斥反應; X線片和CT檢查示:術後骨缺損區域填充良好,密度較鬆質骨稍低,材料與週圍骨邊界清楚;術後1箇月,骨缺損區密度逐漸升高,可見植骨週圍模糊,有少量新生骨痂形成;術後3箇月,骨缺損區密度明顯升高,植骨週圍間隙開始嚮中心融閤成片,更多新生骨痂影融閤;術後6箇月,骨缺損區密度明顯升高,大量新生骨痂形成。臨床骨愈閤時間為術後3~7箇月,平均3.8箇月,愈閤率為91.5%。結論納米羥基燐灰石/聚酰胺66複閤生物活性人工骨用于治療四肢骨缺損,能與植骨區骨生長融閤,無不良反應,療效滿意,是一種安全有效的骨缺損植骨填充材料。
목적:관찰납미간기린회석/취선알66( n-HA/PA66)복합생물활성인공골재사지골결손술중전충식골적안전성화림상료효。방법대87례사지골수술후골결손,포괄사지송질골폭력압축골절도치골결손화간후단량성골종류술후골결손적환자,채용n-HA/PA66복합생물활성인공골전충식골。술전、술후1주급3、6、12개월분별섭X선편급CT,관찰골결손적수복생장화식골융합정황。결과수방6~28개월(평균8개월),상구균갑급유합,무절구감염、비특이염증반응화배척반응; X선편화CT검사시:술후골결손구역전충량호,밀도교송질골초저,재료여주위골변계청초;술후1개월,골결손구밀도축점승고,가견식골주위모호,유소량신생골가형성;술후3개월,골결손구밀도명현승고,식골주위간극개시향중심융합성편,경다신생골가영융합;술후6개월,골결손구밀도명현승고,대량신생골가형성。림상골유합시간위술후3~7개월,평균3.8개월,유합솔위91.5%。결론납미간기린회석/취선알66복합생물활성인공골용우치료사지골결손,능여식골구골생장융합,무불량반응,료효만의,시일충안전유효적골결손식골전충재료。
Objective To observe the therapeutic efficacy and safety of the bioactive artificial bone by nano-hydroxyapatite/polyamide 66(n-HA/PA66) in treating the limb bone defect.Methods Eighty-seven cases of limb bone defect ,which resulted from limb cancellated bone compression fracture or metaphysis innocuousness tu -morectomy,were treated by padding bioactive artificial bone by nano-hydroxyapatite/polyamide 66(n-HA/PA66). X ray examination and CT were taken preoperatively and at 1 week,3,6,and 12 months postoperatively to observe the bone repair and bone graft fusion.Results All patients were followed up for 8 months (ranging 6-28 months). All patients got good wound healing ,without infection ,non-specify inflammatory reaction ,and serious complications . X-ray and CT examination revealed:bone defect area was well filled after operation ,its bone density was lower than the cancellous bone and the materials had clear boundary with the surrounding bone ;at 1 month after operation ,the bone defect density gradually increased ,showing blurring around the bone ,and a small amount of callus formation;at 3 months after operation ,the bone defect density was significantly increased with more callus fusion ;at 6 months after operation,the bone defect density was significantly increased with a large number of callus formation .The clinical bone healing time was at 3 to 7 months postoperatively (averaging 3.8 months),and the healing rate was 91.5%. Conclusion Bioactive artificial bone by nano-hydroxyapatite/polyamide 66 is a satisfactory and effective material for treating limb bone defect ,which can get expecting fusion without any adverse effect .