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磁控生长棒的禁忌症:早发性脊柱侧弯治疗专家共识

Contraindications to magnetically controlled growing rods: consensus among experts in treating early onset scoliosis.

作者信息

Matsumoto Hiroko, Sinha Rishi, Roye Benjamin D, Ball Jacob R, Skaggs Kira F, Brooks Jaysson T, Welborn Michelle C, Emans John B, Anari Jason B, Johnston Charles E, Akbarnia Behrooz A, Vitale Michael G, Murphy Robert F

机构信息

Department of Orthopedic Surgery, Columbia University Irving Medical Center, New York, NY, 10032, USA.

Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, 10032, USA.

出版信息

Spine Deform. 2022 Nov;10(6):1289-1297. doi: 10.1007/s43390-022-00543-3. Epub 2022 Jul 3.

DOI:10.1007/s43390-022-00543-3
PMID:35780448
Abstract

PURPOSE

The purpose of this study was to describe contraindications to the magnetically controlled growing rod (MCGR) in patients with early onset scoliosis (EOS) by establishing consensus amongst expert surgeons who treat these patients frequently.

METHODS

Nine pediatric spine surgeons from an international EOS study group participated in semi-structured interviews via email to identify factors that influence decision making in the use of MCGR. A 39-question survey was then developed to specify these factors as contraindications for MCGR-these included patient age and size, etiology, medical comorbidities, coronal and sagittal curve profiles, and skin and soft tissue characteristics. Pediatric spine surgeons from the EOS international study group were invited to complete the survey. A second 29-item survey was created to determine details and clarify results from the first survey. Responses were analyzed for consensus (> 70%), near consensus (60-69%), and no consensus/variability (< 60%) for MCGR contraindication.

RESULTS

56 surgeons of 173 invited (32%) completed the first survey, and 64 (37%) completed the second survey. Responders had a mean of over 15 years in practice (range 1-45) with over 6 years of experience with using MCGR (range 2-12). 71.4% of respondents agreed that patient size characteristics should be considered as contraindications, including BMI (81.3%) and spinal height (84.4%), although a specific BMI range or a specific minimum spinal height were not agreed upon. Among surgeons who agreed that skin and soft tissue problems were contraindications (78.6%), insufficient soft tissue (98%) and skin (89%) to cover MCGR were specified. Among surgeons who reported curve stiffness as a contraindication (85.9%), there was agreement that this curve stiffness should be defined by clinical evaluation (78.2%) and by traction films (72.3%). Among surgeons who reported sagittal curve characteristics as contraindications, hyperkyphosis (95.3%) and sagittal curve apex above T3 (70%) were specified. Surgeons who indicated the need for repetitive MRI as a contraindication (79.7%) agreed that image quality (72.9%) and not patient safety (13.6%) was the concern. In the entire cohort, consensus was not achieved on the following factors: patient age (57.4%), medical comorbidities (46.4%), etiology (53.6%), and coronal curve characteristics (58.9%).

CONCLUSION

Surgeon consensus suggests that MCGR should be avoided in patients who have insufficient spinal height to accommodate the MCGR, have potential skin and soft tissue inadequacy, have too stiff a spinal curve, have too much kyphosis, and require repetitive MRI, particularly of the spine. Future data-driven studies using this framework are warranted to generate more specific criteria (e.g. specific degrees of kyphosis) to facilitate clinical decision making for EOS patients.

LEVEL OF EVIDENCE

Level V-expert opinion.

摘要

目的

本研究旨在通过在经常治疗早发性脊柱侧弯(EOS)患者的专家外科医生之间达成共识,描述EOS患者使用磁控生长棒(MCGR)的禁忌证。

方法

来自国际EOS研究组的9名儿科脊柱外科医生通过电子邮件参与了半结构化访谈,以确定影响MCGR使用决策的因素。随后制定了一项包含39个问题的调查问卷,将这些因素具体列为MCGR的禁忌证,包括患者年龄和体型、病因、内科合并症、冠状面和矢状面曲线形态以及皮肤和软组织特征。邀请EOS国际研究组的儿科脊柱外科医生完成该调查问卷。还创建了第二项包含29个条目的调查问卷,以确定细节并阐明第一项调查问卷的结果。对MCGR禁忌证的回答进行了分析,分为达成共识(>70%)、接近共识(60 - 69%)以及未达成共识/存在差异(<60%)。

结果

173名受邀外科医生中有56名(32%)完成了第一项调查问卷,64名(37%)完成了第二项调查问卷。受访者的平均从业年限超过15年(范围1 - 45年),使用MCGR的经验超过6年(范围2 - 12年)。71.4%的受访者同意患者体型特征应被视为禁忌证,包括体重指数(BMI)(81.3%)和脊柱高度(84.4%),尽管未就具体的BMI范围或特定的最小脊柱高度达成一致。在同意皮肤和软组织问题为禁忌证的外科医生中(78.6%),明确指出软组织(98%)和皮肤(89%)不足以覆盖MCGR。在报告曲线僵硬为禁忌证的外科医生中(85.9%),一致认为这种曲线僵硬应由临床评估(78.2%)和牵引片(72.3%)来定义。在报告矢状面曲线特征为禁忌证的外科医生中,明确指出了后凸畸形(95.3%)和矢状面曲线顶点高于T3(70%)。表示需要重复进行磁共振成像(MRI)作为禁忌证的外科医生(79.7%)一致认为关注的是图像质量(72.9%)而非患者安全(13.6%)。在整个队列中,以下因素未达成共识:患者年龄(57.4%)、内科合并症(46.4%)、病因(53.6%)以及冠状面曲线特征(58.9%)。

结论

外科医生的共识表明,对于脊柱高度不足以容纳MCGR、存在潜在皮肤和软组织不足、脊柱曲线过僵、后凸畸形过大以及需要重复进行MRI(尤其是脊柱MRI)的患者,应避免使用MCGR。有必要利用该框架进行未来的数据驱动研究以生成更具体的标准(如特定程度的后凸畸形),以便为EOS患者的临床决策提供便利。

证据水平

V级——专家意见。

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