Ravindra Vijay M, Bollo Robert J, Eli Ilyas M, Griauzde Julius, Lanpher Arianna, Klein Jennifer, Zhu Huirong, Brockmeyer Douglas L, Kestle John R W, Couldwell William T, Scott R Michael, Smith Edward
1Division of Pediatric Neurosurgery, Primary Children's Hospital, University of Utah, Salt Lake City, Utah.
2Department of Radiology, University of Michigan, Ann Arbor, Michigan.
J Neurosurg Pediatr. 2019 Jul 1;24(1):1-8. doi: 10.3171/2019.2.PEDS18731. Epub 2019 Apr 5.
Large experiences with the treatment of pediatric arteriovenous malformations (AVMs) remain relatively rare, with limited data on presentation, treatment, and long-term functional outcomes. Because of the expected long lifespan of children, caregivers are especially interested in outcome measures that assess quality of life. The authors' intention was to describe the long-term functional outcomes of pediatric patients who undergo AVM surgery and to identify predictors of sustained neurological deficits.
The authors analyzed a 21-year retrospective cohort of pediatric patients with intracranial AVMs treated with microsurgery at two institutions. The primary outcome was a persistent neurological deficit at last follow-up. Secondary outcome measures included modified Rankin Scale (mRS) score and independent living.
Overall, 97 patients (mean age 11.1 ± 4.5 years; 56% female) were treated surgically for intracranial AVMs (mean follow-up 77.5 months). Sixty-four patients (66%) presented with hemorrhage, and 45 patients (46%) had neurological deficits at presentation. Radiologically, 39% of lesions were Spetzler-Martin grade II. Thirty-seven patients (38%) with persistent neurological deficits at last follow-up were compared with those without deficits; there were no differences in patient age, presenting Glasgow Coma Scale score, AVM size, surgical blood loss, or duration of follow-up. Multivariate analysis demonstrated that a focal neurological deficit on presentation, AVM size > 3 cm, and lesions in eloquent cortex were independent predictors of persistent neurological deficits at long-term follow-up. Overall, 92% of the children had an mRS score ≤ 2 on long-term follow-up.
Pediatric patients with AVMs treated with microsurgical resection have good functional and radiological outcomes. There is a high rate (38%) of persistent neurological deficits, which were independently predicted by preoperative deficits, AVMs > 3 cm, and lesions located in eloquent cortex. This information can be useful in counseling families on the likelihood of long-term neurological deficits after cerebral AVM surgery.
小儿动静脉畸形(AVM)治疗方面的大规模经验仍然相对较少,关于其临床表现、治疗及长期功能转归的数据有限。鉴于儿童预期寿命较长,照护者尤其关注评估生活质量的转归指标。作者旨在描述接受AVM手术的小儿患者的长期功能转归,并确定持续性神经功能缺损的预测因素。
作者分析了在两家机构接受显微手术治疗的颅内AVM小儿患者的21年回顾性队列。主要转归是最后一次随访时的持续性神经功能缺损。次要转归指标包括改良Rankin量表(mRS)评分和独立生活能力。
总体而言,97例患者(平均年龄11.1±4.5岁;56%为女性)接受了颅内AVM的手术治疗(平均随访77.5个月)。64例患者(66%)表现为出血,45例患者(46%)在就诊时有神经功能缺损。影像学检查显示,39%的病变为Spetzler-MartinⅡ级。将最后一次随访时有持续性神经功能缺损的37例患者(38%)与无缺损的患者进行比较;患者年龄、就诊时的格拉斯哥昏迷量表评分、AVM大小、手术失血量或随访时间无差异。多因素分析表明,就诊时的局灶性神经功能缺损、AVM大小>3 cm以及功能区皮层的病变是长期随访时持续性神经功能缺损的独立预测因素。总体而言,92%的儿童在长期随访时mRS评分≤2。
接受显微手术切除治疗的小儿AVM患者具有良好的功能和影像学转归。持续性神经功能缺损的发生率较高(38%),术前缺损、AVM>3 cm以及位于功能区皮层的病变可独立预测其发生。这些信息有助于向家属咨询脑AVM手术后长期神经功能缺损的可能性。