Safety and Efficacy of Syringoperitoneal Shunting with a Programmable Shunt Valve for Syringomyelia Associated with Extensive Spinal Adhesive Arachnoiditis: Technical Note
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作者:
Naito, Kentaro
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Osaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, JapanOsaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, Japan
Naito, Kentaro
[1
]
Yamagata, Toru
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Osaka City Gen Hosp, Dept Neurosurg, Osaka, JapanOsaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, Japan
Yamagata, Toru
[2
]
Ohata, Kenji
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Osaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, JapanOsaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, Japan
Ohata, Kenji
[1
]
Takami, Toshihiro
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Osaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, JapanOsaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, Japan
Takami, Toshihiro
[1
]
机构:
[1] Osaka City Univ, Dept Neurosurg, Grad Sch Med, Osaka, Japan
[2] Osaka City Gen Hosp, Dept Neurosurg, Osaka, Japan
OBJECTIVE: Although syringomyelia associated with extensive spinal adhesive arachnoiditis (SAA) can be a progressive disease that has potentially devastating clinical consequences, its surgical resolution has remained poorly defined. The aim of the present study was to verify the safety and efficacy of syringoperitoneal shunting for syringomyelia associated with extensive SAA. METHODS: The present retrospective study included 15 patients who had undergone syringoperitoneal shunting with a programmable shunt valve for the diagnosis of syringomyelia associated with extensive SAA from October 2012 to June 2018. The shunt pressure was appropriately adjusted according to the postoperative sequential clinical condition and change in syringomyelia evaluated using magnetic resonance imaging. The average postoperative follow-up duration was 32.7 months. RESULTS: No surgery-related complications such as shunt dysfunction or infection occurred during the follow-up period, except for 2 patients with minor issues with the shunt tube. The average shunt pressure at the last follow-up examination was 4.5 cm H2O. The findings from the clinical assessment suggested that the average grade on the sensory pain scale was 2.9 before surgery and had improved significantly to 2.5 at the most recent follow-up examination. Radiological analysis suggested that improvement of syringomyelia was noted in 14 of the 15 patients (93.3%), with no cases of radiological aggravation. No recurrence of syringomyelia developed during the follow-up period in the present study. CONCLUSION: Syringoperitoneal shunting with a programmable shunt valve was safe and effective for clinical control of syringomyelia associated with extensive SAA. Long-term follow-up is mandatory to monitor for shunt dysfunction and mechanical trouble.