首页> 外文期刊>Orthopaedic surgery >Safety and Efficacy of Minimally Invasive Transforaminal Lumbar Interbody Fusion Combined with Gelatin Sponge Impregnated with Dexamethasone and No Drainage Tube after Surgery in the Treatment of Lumbar Degenerative Disease
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Safety and Efficacy of Minimally Invasive Transforaminal Lumbar Interbody Fusion Combined with Gelatin Sponge Impregnated with Dexamethasone and No Drainage Tube after Surgery in the Treatment of Lumbar Degenerative Disease

机译:微创型突变体腰椎腰椎椎体椎体椎体椎体椎体椎体椎体椎体椎体椎间椎体蛋白末端浸渍在腰椎退行性疾病治疗后浸渍浸渍浸渍的明胶海绵。

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Objective The aim of the present study was to use a gelatin sponge impregnated with dexamethasone, combined with minimally invasive transforaminal lumbar interbody fusion (MIS‐TLIF) and no drainage tube after the operation for early postoperative recurrence of root pain caused by edema. Methods A prospective case series study was designed. From September 2015 to January 2018, eligible patients diagnosed with lumbar degenerative disease underwent MIS‐TLIF combined with a gelatin sponge impregnated with dexamethasone and no drainage tube after surgery. The short‐term clinical data were collected, such as visual analog scale (VAS) scores for low back pain and leg pain preoperatively and on postoperative days (POD) 1–10, time bedridden postoperatively, and length of hospital stay postoperatively. Long‐term indicators include the Japanese Orthopaedic Association (JOA) score, the Oswestry Disability Index (ODI) score, and the 36‐Item Short‐Form Health Survey (SF‐36) score, evaluated preoperatively and 1?week, 3?months, and more than 1?year postoperatively. Results Complete clinical data was obtained for 139 patients. All patients were followed up for more than 12?months (13.7?±?3.3?months). The average bedridden period was 1.5?±?0.4?days and hospital stays were 2.7?±?0.9?days. The VAS score of leg and back pain on POD 1–10 were all decreased compared with preoperation (all P ?0.0001). At the last follow up, the VAS scores for back pain and leg pain (0.69?±?0.47; 1.02?±?0.55) and the ODI score (11.1?±?3.5) decreased (all P ?0.0001), and the JOA score (27.1?±?3.2) and the SF‐36 (physical component summary, 50.5?±?7.3; mental component summary, 49.4?±?8.9) increased (all P ?0.0001) compared with preoperative values. Patients' early and long‐term levels of satisfaction postoperatively were 92.8% and 97.8%, respectively. At POD 7 and the last follow‐up, the improvement rate of the JOA score, respectively, was 41.8%?±?10.6% and 87.7%?±?8.2%, and clinical effects assessed as significantly effective according to the improvement rate of the JOA score was 16.5% and 66.9%, respectively. There were 2 (1.4%) cases with complications, including 1 (0.7%) case of wound infection and 1 (0.7%) case of deep vein thrombosis. There were no device‐related complications or neurological injuries. Conclusion Use of a gelatin sponge impregnated with dexamethasone combined with MIS‐TLIF and no drainage tube after the operation, compared with previous studies, appears to be safe and feasible to reduce recurrent back pain and leg pain after decompression in the treatment of lumbar degenerative disease.
机译:目的目的是本研究的目的是使用浸渍用地塞米松的明胶海绵,与微创的牙体腰椎胸部融合(MIS-TLIF)联合,并且在手术中没有排水管,以便于水肿引起的根疼痛的术后复发。方法设计了一项潜在案例系列研究。从2015年9月到2018年1月,符合条件患者诊断患有腰椎退化疾病的患者,接受了MIS-TLIF与浸渍在手术后浸渍的明胶海绵,没有排水管。收集短期临床数据,例如术前和术后术后疼痛和腿部疼痛的视觉模拟规模(VAS)评分,术后卧位,术后卧床卧位,以及术后医院的长度。长期指标包括日本矫形协会(JOA)得分,OSWestry残疾指数(ODI)得分,以及36项短型健康调查(SF-36)得分,评估术前和1个?周,3个月,3个月术后超过1年的年份。结果为139名患者提供了完整的临床数据。所有患者均超过12个月(13.7?±3.3个月)。平均卧床期为1.5?±0.4?天和医院住宿是2.7?±0.9?天。与施用相比,POD 1-10上的腿部和背部疼痛的VAS分数均降低(所有P <0.0001)。在最后一次跟进时,血管疼痛和腿部疼痛的变化(0.69?±0.47; 1.02?±0.55)和ODI得分(11.1?±3.5)减少(所有P <0.0001),和JOA得分(27.1?±3.2)和SF-36(物理组件摘要,50.5?±7.3;精神组分摘要,49.4?±α.8.9)与术前值相比,增加(所有P <0.0001)。患者的早期和长期满意度术后分别为92.8%和97.8%。在Pod 7和最后的随访中,JOA得分的提高率分别为41.8%?±10.6%和87.7%?±8.2%,并根据提高率评估为明显有效的临床效果Joa得分分别为16.5%和66.9%。有2例(1.4%)的并发症病例,包括1(0.7%)伤口感染情况,1(0.7%)深静脉血栓形成的情况。没有设备相关的并发症或神经损伤。结论使用浸渍地塞米松的明胶海绵与MIS-TLIF浸渍,与先前的研究相比,在手术后没有排水管,似乎是安全可行的,以减少腰椎退行性疾病治疗后减少复发后疼痛和腿部疼痛。

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