Detection and Management of Tethered Cord in Anorectal Malformation: A Survey of Pediatric Neurosurgeons in the United States.

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY
Caitlin A Smith, Lauren N Nicassio, Samuel E Rice-Townsend, Jeffrey R Avansino, Jason S Hauptman
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引用次数: 1

Abstract

Introduction: The reported prevalence of tethered spinal cord in patients with anorectal malformations (ARMs) ranges from 9% to 64%. Practice patterns surrounding the diagnosis and management of tethered cord (TC) are suspected to vary, with consideration to the type of spine imaging, adjunct imaging modalities, what patients are offered surgical intervention, and how patients are followed after detethering. We sought to determine what consensus, if any, exists among pediatric neurosurgeons in the USA in terms of diagnosis and management of TC and, specifically, patients with TC and ARM.

Methods: A survey was sent to members of the American Society of Pediatric Neurosurgeons (ASPN). Members of the ASPN received an email with a link to an anonymous REDCap survey that asked about their experience with detethering procedures, indications for surgery, diagnostic tools used, and follow-up protocols.

Results: The survey was completed by 93 of the 192 ASPN members (48%). When respondents were asked about the total number of all simple filum detetherings they performed annually, 61% (N = 57) indicated they perform less than 10 for all TC patients. Ninety-three percent (N = 87) of neurosurgeons performed these procedures in patients with simple filum TC and ARM patients (TC + ARM) specifically. When asked about prophylactic detethering in those with a confirmed diagnosis of low-lying conus and with a filum fatty terminale, 59.1% (N = 55) indicated they would offer this to TC + ARM patients regardless of their age. Regarding preoperative workup for simple filum detethering, all respondents indicated they would order an MRI in both TC and TC + ARM patients, with a minority also requiring additional testing such as urodynamics, neurodevelopmental assessments, and anorectal manometry for both groups. When following patients postoperatively, almost all respondents indicated they would require clinical neurosurgical follow-up with a clinic visit (100% in all simple filum TC patients, 98.9% in fatty filum/low-lying conus TC + ARM patients), but there was wide variation in the use of other tools such as urological testing, neurodevelopmental assessment, and anorectal manometry.

Discussion/conclusions: A wide variety of diagnostic criteria and indication for procedural intervention exists for management of TC patients with and without ARM. Further studies are needed to determine outcomes. Prospective protocols need to be developed and evaluated to standardize care for this patient population and determine best practices.

肛肠畸形系索的检测和处理:美国儿科神经外科医生的调查。
导读:据报道,肛肠畸形(ARMs)患者脊髓栓系的患病率从9%到64%不等。考虑到脊柱成像的类型、辅助成像方式、对哪些患者进行手术干预以及如何随访患者,怀疑围绕脊髓栓系(TC)的诊断和治疗的实践模式各不相同。我们试图确定美国儿科神经外科医生在TC的诊断和管理方面,特别是TC和ARM患者,是否存在共识。方法:向美国儿科神经外科学会(ASPN)成员发送调查问卷。ASPN的成员收到一封电子邮件,其中附有REDCap匿名调查的链接,询问了他们在脱缆手术、手术指征、使用的诊断工具和后续协议方面的经验。结果:192名ASPN成员中有93人(48%)完成了调查。当受访者被问及他们每年进行的所有简单的丝栓术的总数时,61% (N = 57)表示他们对所有TC患者进行的检查少于10次。93% (N = 87)的神经外科医生专门对单纯丝状TC和ARM患者(TC + ARM)进行了这些手术。当被问及确诊为低位圆锥和终末脂肪丝的患者是否需要预防性松脱术时,59.1% (N = 55)的患者表示,无论年龄大小,他们都会为TC + ARM患者提供这种治疗。关于简单的丝栓术前检查,所有受访者都表示他们会在TC和TC + ARM患者中进行MRI检查,少数患者还需要额外的检查,如尿动力学、神经发育评估和两组的肛肠测压。在术后随访患者时,几乎所有受访者都表示他们需要临床神经外科随访并就诊(所有单纯丝状TC患者为100%,脂肪丝状/低位结节TC + ARM患者为98.9%),但在使用其他工具(如泌尿科检查、神经发育评估和肛肠测压)方面存在很大差异。讨论/结论:对于合并或不合并ARM的TC患者,存在各种各样的诊断标准和手术干预指征。需要进一步的研究来确定结果。需要制定和评估前瞻性方案,以规范对这一患者群体的护理并确定最佳做法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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