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使用骨整合植入物的脊柱骨盆固定术:上市后监测分析以确定失败率。

Spinopelvic Fixation Using an Osseointegrative Implant: Analysis of Postmarket Surveillance to Determine the Failure Rate.

作者信息

Eastlack Robert K, Menger Richard P, Turner Jay D, Ashcraft Kara R, Carlton Recking W, Kleck Christopher J

机构信息

Department of Orthopedic Surgery, Scripps Institute, La Jolla, CA, USA.

Department of Neurosurgery, University of Southern Alabama, Mobile, AL, USA.

出版信息

Int J Spine Surg. 2025 Jun 12;19(3):273-278. doi: 10.14444/8720.

Abstract

BACKGROUND

Adult spinal deformities, affecting up to 60% of individuals older than 60 years, often require long segment fusions. Constructs spanning the lumbosacral junction commonly include pelvic fixation. Despite robust pelvic fixation, distal junctional failure, such as pseudoarthrosis, bone fracture, and instrumentation failure, occurs in 24%-34% of these cases. A novel implant designed for both durable pelvic fixation and sacroiliac joint fusion was recently cleared by the US Food and Drug Administration. This implant is engineered to address some of the pelvic fixation failure mechanisms by reducing motion at the lumbosacral junction and sacroiliac joint while decreasing stress on S1 pedicle screws and S2AI implants.

OBJECTIVE

To determine the failure rate of a novel osseointegrative implant for spinopelvic fixation/fusion.

STUDY DESIGN

Analysis of manufacturer postmarket surveillance database.

METHODS

A postmarket surveillance database was analyzed to determine the type and rate of complaints and revisions of a novel osseointegrative implant. These were then compared with the published literature.

RESULTS

A total of 15,628 implants were identified in 6907 patients. The postmarket surveillance of the novel screw fusion device revealed a low complaint rate of 0.75% and no postoperative implant breakage. Revision procedures were mostly due to set screw dissociation (0.4%) and implant loosening (0.15%), which was primarily linked to pre-existing conditions or infection. The mean (SD) time from index procedure to the complaint was 7.1 (5.4) months.

CONCLUSIONS

Compared with published literature, this novel osseointegrative implant demonstrates a significantly lower incidence of set screw dissociation than traditional pelvic screws with no incidence of breakage or back out, underscoring its durable integration with bone, with low rates of revisions and mechanical failures.

CLINICAL RELEVANCE

A novel osseointegrative implant offers reduced rates of mechanical failures and revisions, helping to reduce complications in pelvic fixation procedures.

摘要

背景

成人脊柱畸形影响高达60%的60岁以上个体,通常需要长节段融合。跨越腰骶关节的结构通常包括骨盆固定。尽管骨盆固定稳固,但这些病例中仍有24%-34%会发生远端交界性失败,如假关节形成、骨折和内固定失败。一种专为持久骨盆固定和骶髂关节融合设计的新型植入物最近获得了美国食品药品监督管理局的批准。该植入物旨在通过减少腰骶关节和骶髂关节的活动,同时减轻S1椎弓根螺钉和S2AI植入物上的应力,来解决一些骨盆固定失败机制。

目的

确定一种新型骨整合植入物用于脊柱骨盆固定/融合的失败率。

研究设计

对制造商售后监测数据库进行分析。

方法

对一个售后监测数据库进行分析,以确定一种新型骨整合植入物的投诉类型和发生率以及翻修情况。然后将这些结果与已发表的文献进行比较。

结果

在6907例患者中总共识别出15628枚植入物。对这种新型螺钉融合装置的售后监测显示投诉率较低,为0.75%,且术后无植入物断裂。翻修手术主要是由于定位螺钉分离(0.4%)和植入物松动(0.15%),这主要与既往存在的情况或感染有关。从初次手术到投诉的平均(标准差)时间为7.1(5.4)个月。

结论

与已发表的文献相比,这种新型骨整合植入物的定位螺钉分离发生率明显低于传统骨盆螺钉,且无断裂或退出情况,突出了其与骨的持久整合,翻修率和机械故障发生率较低。

临床意义

一种新型骨整合植入物可降低机械故障和翻修率,有助于减少骨盆固定手术中的并发症。

相似文献

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[Clinical and therapeutic analysis of 22 patients with traumatic spinopelvic dissociation].22例创伤性脊柱骨盆分离患者的临床与治疗分析
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2025 Jun 15;39(6):692-700. doi: 10.7507/1002-1892.202504029.

本文引用的文献

9
Adult spinal deformity.成人脊柱畸形。
Lancet. 2019 Jul 13;394(10193):160-172. doi: 10.1016/S0140-6736(19)31125-0. Epub 2019 Jul 11.

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