腰椎间盘退行性疾病患者核替代候选筛查。

SAS journal Pub Date : 2008-06-01 eCollection Date: 2008-01-01 DOI:10.1016/SASJ-2007-0116-RR
Ioannis Pappou, Frank Cammisa, Elias Papadopoulos, Peter Frelinghuysen, Federico Girardi
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引用次数: 1

摘要

背景:核置换是一种新兴的手术治疗退行性椎间盘疾病(DDD)和腰痛(LBP)。虽然临床经验最广泛的是假体椎间盘核PDN (Raymedica, Minneapolis, Minnesota),但该装置的植入有严格的适应症。本研究的目的是确定退行性椎间盘病变手术治疗合并其他外科手术的患者中有多少比例可以选择核替代植入。方法:回顾性分析85例保守治疗失败的腰痛手术融合、椎间盘置换术或环成形术患者的病历和影像资料。1级病变53例,2级病变32例,共117个治疗级别。有以下影像学禁忌症的患者依次被排除:(1)Schmorl淋巴结和> 50%的椎间盘间隙塌陷;(2)MRI上的不规则/凸终板;(3)完全撕裂和大环缺损(即不完全撕裂和完全撕裂均被排除,但局部环缺损的患者被认为有资格进行核置换);(4)BMI > 30。结果:59个级别(50.4%)对核替代装置治疗无影像学禁忌症。10例BMI > 30的患者中有12个级别被排除在外。总体而言,117个水平中有47个(40.2%)对假核装置没有禁忌症。L5-S1水平是最常治疗的水平(117,47%中的55个),但只有25.5%没有放射禁忌症,总体上只有21.8%的水平适合核替代装置。较高比例的病例(分别为68.8%和72.7%)上腰椎节段(L3-4和L4-5)无放射禁忌证。纳入BMI标准后,这一比例分别降至50%和59.1%。结论:外科医生在为DDD患者提供核置换治疗时,必须评估终板完整性、椎间盘高度、终板形状、环完整性和BMI。
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Screening for nuclear replacement candidates in patients with lumbar degenerative disc disease.

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.

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