Syringo-Subarachnoid Shunt for the Treatment of Persistent Syringomyelia Following Decompression for Chiari Type I Malformation: Surgical Results

被引:33
作者
Soleman, Jehuda [1 ,2 ,3 ]
Roth, Jonathan [1 ,2 ,3 ]
Bartoli, Andrea [4 ]
Rosenthal, Daniel [1 ,2 ,3 ]
Korn, Akiva [1 ,2 ,3 ]
Constantini, Shlomi [1 ,2 ,3 ]
机构
[1] Tel Aviv Univ, Sourasky Med Ctr, Dept Neurosurg, Tel Aviv, Israel
[2] Tel Aviv Univ, Sourasky Med Ctr, Dept Pediat Neurosurg, Tel Aviv, Israel
[3] Tel Aviv Univ, Dana Childrens Hosp Tel Aviv, Tel Aviv, Israel
[4] Geneva Univ Hosp, Dept Neurosurg, Geneva, Switzerland
关键词
Chiari I malformation; Electrophysiologic monitoring; Foramen magnum decompression; Posterior columns; Spinal cord; Syringomyelia; Syringo-subarachnoid shunt; POSTERIOR-FOSSA DECOMPRESSION; CRITICAL-APPRAISAL; CHILDREN; SURGERY;
D O I
10.1016/j.wneu.2017.08.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Approximately 30% of patients treated with foramen magnum decompression (FMD) for Chiari I-associated syringomyelia will show persistence, recurrence, or progression of the syrinx. OBJECTIVE: This study evaluates the clinical and radiologic outcomes of syringo-subarachnoid shunt (SSS) as the treatment for persistent syringomyelia after FMD. METHODS: Data were collected retrospectively. The primary outcome measurement was neurologic function (assessed with the Modified Japanese Orthopedic Association [mJOA] scale). Secondary outcome measurements were surgical complications, reoperation rate, and syrinx status on magnetic resonance imaging (MRI). RESULTS: Twenty-one patients (14 females [66.7%]) underwent SSS, either concurrent to the FMD or at a later stage. Two minor surgical complications were seen: a wound dehiscence and postoperative kyphosis, both requiring revision surgery. No major complication or mortality occurred. The median change in the mJOA score was an improvement of 3 out of a possible 17 points on the scale (mean follow-up, 24.9 months). Expressed as a percentage, overall improvement was 11.8% (95% confidence interval [CI], 5.9-17.6; P < 0.001). On postoperative MRI, shrinkage of the syrinx was seen in all but 1 patient in whom the syrinx remained unchanged. Expressed as percentage, the improvement of the syrinx surface was 76.3% (95% CI, 65.0-87.7; P < 0.001), and the improvement of syrinx span was 36.4% (95% CI, 21.8-50.9; P < 0.05). CONCLUSION: SSS for persistent, recurrent, or increasing syrinx following FMD for Chiari I malformation is a safe and effective surgical treatment when performed selectively by an experienced neurosurgeon.
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页码:836 / 843
页数:8
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