Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-12-01 Epub Date: 2024-06-26 DOI:10.1007/s00381-024-06517-2
Jinggang J Ng, Linda M Saikali, Zachary D Zapatero, Benjamin B Massenburg, Meagan Wu, Dominic J Romeo, Gregory G Heuer, Scott P Bartlett, Jesse A Taylor, Jordan W Swanson, Shih-Shan Lang
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Abstract

Purpose: Treatment of subjects with refractory idiopathic intracranial hypertension (IIH) or shunted hydrocephalus with chronic shunt complications is challenging. What is the role for cranial vault expansion, particularly utilizing posterior vault distraction osteogenesis (PVDO), in these cases? This study assesses medium-term efficacy of cranial vault expansion in this unique patient population.

Methods: A retrospective review was conducted of patients who underwent cranial vault expansion from 2008 to 2023 at the Children's Hospital of Philadelphia. Subjects who did not have a diagnosis of primary craniosynostosis were included in the study. Demographic information, medical history, and perioperative details were collected from medical records. Primary outcomes were the rate of CSF diversion procedures and resolution of presenting signs and symptoms. Secondary outcomes were perioperative and 90-day complications and reoperation requirement.

Results: Among 13 included subjects, nine (69.2%) patients had a primary diagnosis of shunted hydrocephalus and 4 (30.8%) patients had IIH. Twelve (92.3%) subjects underwent posterior vault distraction osteogenesis (PVDO) and one (7.7%) underwent posterior vault remodeling (PVR). All 4 patients with IIH demonstrated symptomatic improvement following PVDO, including resolution of headaches, vomiting, and/or papilledema. Among 9 patients with shunted hydrocephalus, CSF diversion requirement decreased from 2.7 ± 1.6 procedures per year preoperatively to 1.2 ± 1.8 per year following cranial vault expansion (p = 0.030). The mean postoperative follow-up was 4.1 ± 2.1 years and four (30.8%) patients experienced complications within 90 days of surgery, including infection (n = 2), CSF leak (n = 1), and elevated ICP requiring lumbar puncture (n = 1). Four (30.8%) patients underwent repeat cranial vault expansion for recurrence of ICP-related symptoms. At most recent follow-up, 7 of 9 patients with shunted hydrocephalus demonstrated symptomatic improvement.

Conclusion: Cranial vault expansion reduced intracranial hypertension-related symptomology as well as the rate of CSF diversion-related procedures in patients with refractory IIH and shunted hydrocephalus without craniosynostosis, and should be considered in those who have significant shunt morbidity.

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进一步穹隆:颅骨穹隆扩张术治疗无原发性颅骨发育不良的颅脑比例失调。
目的:治疗难治性特发性颅内高压(IIH)或分流脑积水慢性分流并发症具有挑战性。颅穹隆扩张,尤其是利用后穹隆牵张成骨术(PVDO)在这些病例中的作用是什么?本研究评估了颅穹隆扩张术在这一特殊患者群体中的中期疗效:我们对 2008 年至 2023 年期间在费城儿童医院接受颅骨穹隆扩张术的患者进行了回顾性研究。研究对象包括未确诊为原发性颅骨发育不良的患者。研究人员从病历中收集了受试者的人口统计学信息、病史和围手术期的详细信息。主要结果是脑脊液转移手术率和症状与体征的缓解率。次要结果是围手术期和 90 天内的并发症以及再次手术的要求:在纳入的 13 名受试者中,9 名(69.2%)患者的主要诊断为分流性脑积水,4 名(30.8%)患者为 IIH。12名患者(92.3%)接受了后穹隆牵张成骨术(PVDO),1名患者(7.7%)接受了后穹隆重塑术(PVR)。所有 4 位 IIH 患者在接受 PVDO 后症状均有所改善,包括头痛、呕吐和/或乳头水肿的缓解。在 9 名分流脑积水患者中,CSF 分流需求从术前的每年 2.7 ± 1.6 次减少到颅顶扩张后的每年 1.2 ± 1.8 次(p = 0.030)。术后平均随访时间为 4.1 ± 2.1 年,4 名(30.8%)患者在术后 90 天内出现并发症,包括感染(2 例)、脑脊液漏(1 例)和需要腰椎穿刺的 ICP 升高(1 例)。4名患者(30.8%)因ICP相关症状复发而再次接受了颅穹隆扩张手术。在最近的随访中,9 名分流脑积水患者中有 7 人的症状有所改善:结论:颅骨穹隆扩张术可减少难治性 IIH 和分流性脑积水(无颅骨发育不良)患者的颅内高压相关症状以及 CSF 分流相关手术的发生率。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
期刊最新文献
Correction: Imaging features of pediatric meningiomas: emphasis on unusual locations. Correction: Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Radiographic severity is associated with worse executive function in metopic craniosynostosis. Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome. Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis.
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