کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5629908 | 1580282 | 2016 | 6 صفحه PDF | دانلود رایگان |
- ACD implantation is associated with a significantly lower reherniation rate in MRI.
- The total number of reoperations is similar between study groups.
- In the ACD group there is a significantly higher incidence of endplate erosions.
Sequestrectomy alone represents a procedure for the treatment of lumbar disc herniation. For selected cases, an anulus closure device (ACD) can be implanted which may result in lower reoperation rates. However, comparative magnetic resonance imaging (MRI) changes and their clinical relevance of both procedures are unclear and have not been reported so far.Clinical and MRI data of patients after limited discectomy with ACD implantation (group ACD; NÂ =Â 45) and patients after sequestrectomy alone (group S; NÂ =Â 40) with primary lumbar disc herniation were compared retrospectively. Pain intensity on the visual analogue pain scale (VAS), oswestry disability index (ODI) or the patient satisfaction index (PSI) were collected. Disc signal intensity, Modic type changes, endplate reactions, anular tears and reherniations were investigated using MRI before and <18Â months postoperative. Morphologic changes were correlated with clinical outcome.There was no difference in VAS back, VAS leg or ODI/PSI after the operation although group S showed significantly more reherniations in MRI. The overall rate of repeated surgery at the same level was similar with a trend in favour of the ACD group (PÂ =Â 0.729). Significantly more patients of the ACD group experienced endplate erosions after surgery (PÂ <Â 0.001). Both groups experienced progression of disc signal intensity, Modic type changes, and anular tears with most MRI signs being without clinical relevance.ACD implantation is associated with a significantly lower reherniation rate in MRI but showed a significantly higher rate of endplate erosions. The structural changes do not appear to be clinically relevant.
Journal: Journal of Clinical Neuroscience - Volume 34, December 2016, Pages 288-293