From the Department of Radiology (R.T., C.S., R.K., T.A., D.J.A.), Phoenix Children's Hospital, Phoenix, Arizona.
University of Arizona College of Medicine, Phoenix (R.T., C.S., R.K., D.J.A.), Phoenix, Arizona.
AJNR Am J Neuroradiol. 2019 Aug;40(8):1422-1426. doi: 10.3174/ajnr.A6131. Epub 2019 Jul 11.
Spinal muscular atrophy, a genetic disease resulting in loss of motor function, presents from in utero to adulthood. Depending on progression and secondary scoliosis, spinal stabilization may be necessary. When planning intrathecal access in these patients, spinal anatomy is the most important factor. Therefore, when planning intrathecal nusinersen injections, we subdivided patients with spinal muscular atrophy into simple-versus-complex spine subgroups. Our purpose was to present our experience with our first 42 transforaminal intrathecal nusinersen injections.
We reviewed 31 consecutive patients with spinal muscular atrophy types 1-3 who presented for intrathecal nusinersen injections from March 2017 to September 2018. Nine children had complex spines (ie, spinal instrumentation and/or fusion) and required preprocedural imaging for route planning for subarachnoid space access via transforaminal or cervical approaches.
A total of 164 intrathecal nusinersen injections were performed in 31 children 4-226 months of age, with 100% technical success in accessing the subarachnoid space. Nine patients with complex spinal anatomy underwent 45 intrathecal nusinersen injections; 42 of 45 procedures were performed via a transforaminal approach with the remaining 3 via cervical techniques. There were no complications.
Our initial experience has resulted in a protocol-driven approach based on simple or complex spinal anatomy. Patients with simple spines do not need preprocedural imaging or imaging-guided intrathecal nusinersen injections. In contrast, the complex spine subgroup requires preprocedural imaging for route planning and imaging guidance for therapy, with the primary approach being the transforaminal approach for intrathecal nusinersen injections.
脊髓性肌萎缩症是一种导致运动功能丧失的遗传性疾病,可发生于胎儿至成年期。根据进展情况和继发性脊柱侧凸,可能需要脊柱稳定。在为这些患者规划鞘内入路时,脊柱解剖结构是最重要的因素。因此,在规划鞘内注射诺西那生钠时,我们将脊髓性肌萎缩症患者分为简单脊柱与复杂脊柱亚组。我们的目的是报告我们对前 42 例经椎间孔鞘内注射诺西那生钠的经验。
我们回顾了 2017 年 3 月至 2018 年 9 月期间因鞘内注射诺西那生钠而就诊的 31 例脊髓性肌萎缩症 1-3 型连续患者。9 例儿童有复杂脊柱(即脊柱内固定和/或融合),需要术前影像学检查以规划经椎间孔或颈椎入路进入蛛网膜下腔的路线。
31 例 4-226 月龄儿童共进行了 164 次鞘内注射诺西那生钠,100%技术上成功进入蛛网膜下腔。9 例复杂脊柱解剖患者进行了 45 次鞘内注射诺西那生钠;45 次中有 42 次经椎间孔入路进行,3 次经颈椎技术进行。无并发症发生。
我们的初步经验产生了一种基于简单或复杂脊柱解剖结构的方案驱动方法。简单脊柱患者不需要术前影像学检查或影像学引导的鞘内注射诺西那生钠。相比之下,复杂脊柱亚组需要术前影像学检查以规划入路,并在治疗时进行影像学引导,主要入路为经椎间孔鞘内注射诺西那生钠。