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腰椎退行性椎间盘疾病患者核置换候选者的筛选

Screening for nuclear replacement candidates in patients with lumbar degenerative disc disease.

作者信息

Pappou Ioannis, Cammisa Frank, Papadopoulos Elias, Frelinghuysen Peter, Girardi Federico

机构信息

Hospital for Special Surgery, New York, New York.

出版信息

SAS J. 2008 Jun 1;2(2):114-9. doi: 10.1016/SASJ-2007-0116-RR. eCollection 2008.

Abstract

BACKGROUND

Nuclear replacement is an emerging surgical treatment for degenerative disc disease (DDD) and low back pain (LBP). While clinical experience is most extensive with the prosthetic disc nucleus PDN (Raymedica, Minneapolis, Minnesota), strict indications apply for the implantation of this device. The purpose of this study was to ascertain what percentage of patients treated surgically for degenerative disc disease with other surgical procedures would have been candidates for nuclear replacement implantation.

METHODS

The charts and films of 85 consecutive patients with failed conservative management for LBP treated surgically with fusion, disc replacement, or annuloplasty were retrospectively reviewed. There were 53 patients with 1-level disease and 32 with 2-level disease, accounting for 117 treated levels. Patients with the following radiographic contraindications to nuclear replacement were serially eliminated: (1) Schmorl's nodes and > 50% collapse of the disc space, (2) irregular/convex endplates on the MRI, (3) complete tears and large annular defects (ie, both incomplete tears and complete tears were eliminated, but patients with local annular deficiency were deemed eligible for nuclear replacement), and (4) a BMI > 30.

RESULTS

Fifty-nine levels (50.4%) had no radiographic contraindications to treatment with a nuclear replacement device. Twelve levels in 10 patients with a BMI > 30 were excluded. Overall, 47 out of 117 levels (40.2%) had no contraindications to a prosthetic nucleus device. The L5-S1 level was the most commonly treated level (55 out of 117, 47%), but only 25.5% had no radiographic contraindications, and overall only 21.8% of the levels were suitable for a nuclear replacement device. Upper lumbar levels (L3-4 and L4-5) had no radiographic contraindications in a higher percentage of cases (68.8% and 72.7%, respectively). The inclusion of the BMI criteria reduced these percentages to 50% and 59.1%, respectively.

CONCLUSIONS

The surgeon has to assess endplate integrity, disc height, endplate shape, annular integrity, and BMI when offering nuclear replacement as treatment for patients with DDD.

摘要

背景

核置换是一种用于治疗椎间盘退变疾病(DDD)和腰痛(LBP)的新兴外科治疗方法。虽然人工椎间盘髓核(PDN,Raymedica公司,明尼阿波利斯,明尼苏达州)的临床经验最为丰富,但该装置的植入有严格的适应症。本研究的目的是确定采用其他外科手术治疗椎间盘退变疾病的患者中,有多大比例适合进行核置换植入。

方法

回顾性分析85例经手术治疗(融合术、椎间盘置换术或纤维环成形术)的LBP保守治疗失败患者的病历和影像学资料。其中,单节段疾病患者53例,双节段疾病患者32例,共治疗117个节段。对核置换有以下影像学禁忌症的患者依次予以排除:(1)Schmorl结节和椎间盘间隙塌陷>50%;(2)MRI上终板不规则/凸起;(3)完全撕裂和大的纤维环缺损(即不完全撕裂和完全撕裂均排除,但局部纤维环缺损患者被认为适合核置换);(4)BMI>30。

结果

59个节段(50.4%)没有核置换治疗的影像学禁忌症。排除10例BMI>30患者的12个节段。总体而言,117个节段中有47个(40.2%)没有人工髓核装置的禁忌症。L5-S1节段是最常治疗的节段(117个中的55个,47%),但只有25.5%没有影像学禁忌症,总体上只有21.8%的节段适合核置换装置。上腰椎节段(L3-4和L4-5)无影像学禁忌症的比例更高(分别为68.8%和72.7%)。纳入BMI标准后,这些比例分别降至50%和59.1%。

结论

在为DDD患者提供核置换治疗时,外科医生必须评估终板完整性、椎间盘高度、终板形状、纤维环完整性和BMI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bc0/4365830/ea8ab242d6ff/SAS-2-2007-0116-RR-g001.jpg

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