纤维脂肪丝终末系带儿童接受手术治疗的预测因素。

Revue internationale de la Croix-rouge Pub Date : 2019-11-01 Print Date: 2020-02-01 DOI:10.3171/2019.8.PEDS19292
Osama N Kashlan, D Andrew Wilkinson, Hal Morgenstern, Siri S Khalsa, Cormac O Maher
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引用次数: 0

摘要

目的:增厚或脂肪性终丝是一种隐匿性病变,可导致拴系脊髓综合征,需要手术松解。本研究的目的是估算大量投保儿科人群中纤维脂肪脐带拴系综合征(TFFT)的发病率,确定TFFT患者的手术预测因素,并评估诊断算法:TFFT是根据ICD-9-CM中的脐带拴系代码(742.59)定义的,并排除了脊髓脊膜膨出、髓母细胞瘤、终末髓母细胞瘤、脑膜瘤和髓母细胞瘤的代码。作者利用 Optum Insight 数据库(2001-2014 年),确定了美国确诊为脐带拴系的儿科患者(小于 21 岁),并估算了该来源人群的脐带拴系发病率以及 14 年间脐带拴系患者的手术解拴概率。他们使用逻辑回归估算了诊断时的年龄、性别、Charlson 综合征指数 (CCI) 评分、Chiari 畸形 I 型诊断、鞘膜积液诊断以及手术概率对美国人口普查地区的影响(调整后 OR 和 95% CI)。最后,为了评估他们从 ICD-9 编码中识别 TFFT 的算法,作者在其所在机构诊断出的符合 ICD-9-CM 标准的 50 名儿童中估算了该算法的阳性预测值 (PPV):结果:共有 3218 例 TFFT 诊断,其中 482 例儿童患者在研究期间接受了系带松解术。估计发病率为12.0/100,000/年(95% CI为11.6-12.4/100,000/年)。女性的发病率略高于男性(12.7 vs 11.4 per 100,000/year )。0)、确诊时年龄为 7-11 岁的儿童比年龄小于 1 岁的儿童(OR 1.5,95% CI 1.1-2.0)、CCI 评分≥ 3 分的儿童比 0 分的儿童(OR 2.3,95% CI 1.4-3.8)、美国西部居民比美国东北部居民(OR 2.3,95% CI 1.6-3.5)。在作者所在机构的数据库中,TFFT 的 PPV 为 35/50(70.0%,95% CI 57.3%-82.7%),可在儿童阳性患者中识别出纤维脂肪性终丝引起的脐带系带:结论:有合并症或伴有鞘膜积液的患者接受TFFT解拴手术的风险较高。此外,美国西部的手术频率明显更高。这些发现表明,有必要对接受和未接受手术治疗的 TFFT 患者的长期疗效进行合作性前瞻性队列研究,以确定哪些患者应该接受手术治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictors of surgical treatment in children with tethered fibrofatty filum terminale.

Objective: Thickened or fatty filum terminale is an occult lesion that can cause tethered cord syndrome requiring surgical untethering. This study's objectives were to estimate the incidence of tethered fibrofatty filum terminale (TFFT) in a large insured pediatric population, identify predictors of surgery among those TFFT patients, and assess a diagnostic algorithm.

Methods: TFFT was defined according to the ICD-9-CM code for cord tethering (742.59), after excluding codes for diastematomyelia, lipomyelomeningocele, terminal myelocystocele, meningocele, and myelomeningocele. Utilizing the Optum Insight database for 2001-2014, the authors identified pediatric patients (< 21 years) in the US who were diagnosed with a tethered cord and estimated the TFFT incidence rates in that source population and the surgical untethering probability among TFFT patients over the 14-year period. Logistic regression was used to estimate the effects (adjusted OR and 95% CI) of age at diagnosis, sex, Charlson Comorbidity Index (CCI) score, diagnosis of Chiari malformation type I, diagnosis of syrinx, and the probability of surgery by US census region. Lastly, to evaluate their algorithm for identifying TFFT from ICD-9 codes, the authors estimated its positive predictive value (PPV) among 50 children who were diagnosed at their institution and met the ICD-9-CM criteria.

Results: There were 3218 diagnoses of TFFT, with 482 of these pediatric patients undergoing tethered cord release during the study period. The estimated incidence rate was 12.0 per 100,000/year (95% CI 11.6-12.4 per 100,000/year). The incidence rate was slightly higher in females than in males (12.7 vs 11.4 per 100,000/year). The probability of surgery in the total pediatric TFFT population was 15.0% (95% CI 13.8%-16.2%) and was greater in children with a syrinx (OR 2.2, 95% CI 1.6-3.0), children 7-11 years of age at diagnosis versus < 1 year (OR 1.5, 95% CI 1.1-2.0), CCI score ≥ 3 versus 0 (OR 2.3, 95% CI 1.4-3.8), and residents of the Western vs Northeastern US (OR 2.3, 95% CI 1.6-3.5). In the authors' own institution's database, the PPV of TFFT was 35/50 (70.0%, 95% CI 57.3%-82.7%) for identifying tethered cord due to fibrofatty filum terminale among childhood positives.

Conclusions: Patients with comorbidities or an associated syrinx showed a higher risk of untethering procedures for TFFT. Also, surgery was appreciably more frequent in the Western US. These findings signify the need for a collaborative prospective cohort study of long-term outcomes for TFFT patients with and without surgery to determine which patients should have surgery.

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