枕骨髁和寰椎异常对 I 型奇异畸形合并鞘膜积液患者枕颈椎融合术效果的影响:Park-Reeves 鞘膜积液研究联合会的一项研究。

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY Journal of neurosurgery. Pediatrics Pub Date : 2024-04-01 DOI:10.3171/2024.1.PEDS23229
Alexander T. Yahanda, J. Koueik, Laurie L. Ackerman, P. D. Adelson, Gregory W Albert, Philipp R. Aldana, Tord D Alden, Richard C E Anderson, David F Bauer, Tammy Bethel-Anderson, K. Bierbrauer, D. Brockmeyer, Joshua Chern, Daniel E Couture, David J Daniels, B. Dlouhy, Susan R Durham, R. Ellenbogen, R. Eskandari, Herbert E Fuchs, Gerald A. Grant, P. Graupman, Stephanie Greene, Jeffrey P Greenfield, Naina L. Gross, Daniel J Guillaume, Todd C. Hankinson, Gregory G. Heuer, M. Iantosca, B. Iskandar, Eric M. Jackson, G. Jallo, James M Johnston, Bruce A Kaufman, Robert F. Keating, Nickalus R. Khan, Mark D. Krieger, Jeffrey R. Leonard, C. Maher, F. Mangano, Jonathan E Martin, J. G. McComb, Sean McEvoy, Thanda Meehan, Arnold H. Menezes, Michael S. Muhlbauer, Brent R O'Neill, G. Olavarria, J. Ragheb, Nathan Selden, Manish N Shah, C. Shannon, J. Shimony, Matthew D Smyth, S. Stone, J. Strahle, M. Tamber, James Torner, G. Tuite, Elizabeth Tyler-Kabara, S. Wait, J. Wellons, William E Whitehead, Tae Sung Park, D. D. Lim
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Tamber, James Torner, G. Tuite, Elizabeth Tyler-Kabara, S. Wait, J. Wellons, William E Whitehead, Tae Sung Park, D. D. Lim","doi":"10.3171/2024.1.PEDS23229","DOIUrl":null,"url":null,"abstract":"OBJECTIVE\nCongenital anomalies of the atlanto-occipital articulation may be present in patients with Chiari malformation type I (CM-I). However, it is unclear how these anomalies affect the biomechanical stability of the craniovertebral junction (CVJ) and whether they are associated with an increased incidence of occipitocervical fusion (OCF) following posterior fossa decompression (PFD). The objective of this study was to determine the prevalence of condylar hypoplasia and atlas anomalies in children with CM-I and syringomyelia. The authors also investigated the predictive contribution of these anomalies to the occurrence of OCF following PFD (PFD+OCF).\n\n\nMETHODS\nThe authors analyzed the prevalence of condylar hypoplasia and atlas arch anomalies for patients in the Park-Reeves Syringomyelia Research Consortium database who underwent PFD+OCF. Condylar hypoplasia was defined by an atlanto-occipital joint axis angle (AOJAA) ≥ 130°. Atlas assimilation and arch anomalies were identified on presurgical radiographic imaging. This PFD+OCF cohort was compared with a control cohort of patients who underwent PFD alone. The control group was matched to the PFD+OCF cohort according to age, sex, and duration of symptoms at a 2:1 ratio.\n\n\nRESULTS\nClinical features and radiographic atlanto-occipital joint parameters were compared between 19 patients in the PFD+OCF cohort and 38 patients in the PFD-only cohort. Demographic data were not significantly different between cohorts (p > 0.05). The mean AOJAA was significantly higher in the PFD+OCF group than in the PFD group (144° ± 12° vs 127° ± 6°, p < 0.0001). In the PFD+OCF group, atlas assimilation and atlas arch anomalies were identified in 10 (53%) and 5 (26%) patients, respectively. These anomalies were absent (n = 0) in the PFD group (p < 0.001). Multivariate regression analysis identified the following 3 CVJ radiographic variables that were predictive of OCF occurrence after PFD: AOJAA ≥ 130° (p = 0.01), clivoaxial angle < 125° (p = 0.02), and occipital condyle-C2 sagittal vertical alignment (C-C2SVA) ≥ 5 mm (p = 0.01). A predictive model based on these 3 factors accurately predicted OCF following PFD (C-statistic 0.95).\n\n\nCONCLUSIONS\nThe authors' results indicate that the occipital condyle-atlas joint complex might affect the biomechanical integrity of the CVJ in children with CM-I and syringomyelia. 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引用次数: 0

摘要

目的I型奇异畸形(CM-I)患者可能存在寰枕关节的先天性异常。然而,目前尚不清楚这些异常如何影响颅椎间隙(CVJ)的生物力学稳定性,也不清楚这些异常是否与后窝减压术(PFD)后枕颈融合(OCF)发生率的增加有关。本研究的目的是确定髁突发育不良和寰椎异常在患有 CM-I 和鞘膜积液的儿童中的发病率。作者还研究了这些异常对 PFD(PFD+OCF)后发生 OCF 的预测作用。方法作者分析了 Park-Reeves 浆膜肌瘤研究联合会数据库中接受 PFD+OCF 的患者中髁突发育不良和寰弓异常的患病率。髁突发育不良的定义是寰枕关节轴角(AOJAA)≥130°。寰枕关节轴角(AOJAA)≥130°定义为髁突发育不良。PFD+OCF组患者与单独接受PFD的对照组患者进行了比较。结果比较了 PFD+OCF 组中 19 名患者和单纯 PFD 组中 38 名患者的临床特征和寰枕关节影像学参数。两组患者的人口统计学数据无明显差异(P > 0.05)。PFD+OCF 组的平均 AOJAA 明显高于 PFD 组(144° ± 12° vs 127° ± 6°,p < 0.0001)。在 PFD+OCF 组中,分别有 10 名(53%)和 5 名(26%)患者发现寰椎同化和寰椎弓异常。而在 PFD 组中则没有这些异常(n = 0)(p < 0.001)。多变量回归分析确定了以下 3 个 CVJ 影像学变量可预测 PFD 后 OCF 的发生:AOJAA ≥ 130° (p = 0.01)、Clivoaxial 角度 < 125° (p = 0.02)、枕髁-C2 矢状垂直对齐 (C-C2SVA) ≥ 5 mm (p = 0.01)。作者的研究结果表明,枕髁-atlas 关节复合体可能会影响 CM-I 和鞘膜积液患儿 CVJ 的生物力学完整性。他们描述了 AOJAA 指标作为 PFD 后发生 OCF 的独立预测因素的作用。术前对这些骨骼异常的识别可用于指导手术规划和治疗患有复杂CM-I并同时伴有骨质病变的患者。
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The role of occipital condyle and atlas anomalies on occipital cervical fusion outcomes in Chiari malformation type I with syringomyelia: a study from the Park-Reeves Syringomyelia Research Consortium.
OBJECTIVE Congenital anomalies of the atlanto-occipital articulation may be present in patients with Chiari malformation type I (CM-I). However, it is unclear how these anomalies affect the biomechanical stability of the craniovertebral junction (CVJ) and whether they are associated with an increased incidence of occipitocervical fusion (OCF) following posterior fossa decompression (PFD). The objective of this study was to determine the prevalence of condylar hypoplasia and atlas anomalies in children with CM-I and syringomyelia. The authors also investigated the predictive contribution of these anomalies to the occurrence of OCF following PFD (PFD+OCF). METHODS The authors analyzed the prevalence of condylar hypoplasia and atlas arch anomalies for patients in the Park-Reeves Syringomyelia Research Consortium database who underwent PFD+OCF. Condylar hypoplasia was defined by an atlanto-occipital joint axis angle (AOJAA) ≥ 130°. Atlas assimilation and arch anomalies were identified on presurgical radiographic imaging. This PFD+OCF cohort was compared with a control cohort of patients who underwent PFD alone. The control group was matched to the PFD+OCF cohort according to age, sex, and duration of symptoms at a 2:1 ratio. RESULTS Clinical features and radiographic atlanto-occipital joint parameters were compared between 19 patients in the PFD+OCF cohort and 38 patients in the PFD-only cohort. Demographic data were not significantly different between cohorts (p > 0.05). The mean AOJAA was significantly higher in the PFD+OCF group than in the PFD group (144° ± 12° vs 127° ± 6°, p < 0.0001). In the PFD+OCF group, atlas assimilation and atlas arch anomalies were identified in 10 (53%) and 5 (26%) patients, respectively. These anomalies were absent (n = 0) in the PFD group (p < 0.001). Multivariate regression analysis identified the following 3 CVJ radiographic variables that were predictive of OCF occurrence after PFD: AOJAA ≥ 130° (p = 0.01), clivoaxial angle < 125° (p = 0.02), and occipital condyle-C2 sagittal vertical alignment (C-C2SVA) ≥ 5 mm (p = 0.01). A predictive model based on these 3 factors accurately predicted OCF following PFD (C-statistic 0.95). CONCLUSIONS The authors' results indicate that the occipital condyle-atlas joint complex might affect the biomechanical integrity of the CVJ in children with CM-I and syringomyelia. They describe the role of the AOJAA metric as an independent predictive factor for occurrence of OCF following PFD. Preoperative identification of these skeletal abnormalities may be used to guide surgical planning and treatment of patients with complex CM-I and coexistent osseous pathology.
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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