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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Incidence of delayed intracranial hypertension in children with isolated sagittal synostosis following open calvarial vault reconstruction
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Incidence of delayed intracranial hypertension in children with isolated sagittal synostosis following open calvarial vault reconstruction

机译:开放颅骨拱顶重建后患儿患儿颅内高血压延迟颅内高血压的发病率

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Purpose Delayed intracranial hypertension (DIH) occurs most frequently in children with syndromic or multi-suture synostosis after surgical correction. The rarity of DIH in children with isolated non-syndromic sagittal synostosis (ISS) warrants follow-up evaluation by large craniofacial centers until skeletal maturity. This study reports the incidence of DIH in children following open repair for ISS by our center's craniofacial team. Methods A single-center retrospective study of patients who underwent open calvarial vault remodeling (CVR) for ISS at our institution between November 2000 and November 2012 was performed. Syndromic and multi-suture synostosis patients were excluded. Demographic and follow-up data were extracted from the medical record for analysis until July 2017. Results One hundred five patients with ISS were identified who had undergone CVR in the aforementioned timeframe. Average age at initial surgery was 11.7 +/- 15.32 months. Mean follow-up in our craniofacial clinic was 4.94 +/- 3.53 years, with 69 patients (65.7%) having follow-up in craniofacial clinic >= 3 years and 74 (70.5%) having follow-up >= 3 years in any clinic at our institution. Four patients (3.8%) had intracranial pressure (ICP) monitors placed for symptoms concerning for DIH, one of which (0.95%) had confirmed DIH and underwent a second surgical procedure at 7.4 years of age. The patient presented late initially, having his first operation at 1.56 years of age. Conclusion One patient out of 105 (0.95%) developed DIH, confirmed by ICP monitoring, and required reoperation. The occurrence of DIH, albeit rare, remains an important topic to include in parental discussions and mandates long-term follow-up in this population.
机译:目的延迟颅内高血压(DIH)在手术校正后患有综合征或多缝合髁突发病的儿童中最常出现。具有孤立的非综合征矢状突触病(ISS)患儿DIH的稀有性(ISS)认证大型颅面中心的跟进评估,直至骨骼成熟。本研究报告了我们中心的颅面型开放式修理后DIH在儿童的发病率。方法执行对2000年11月至2012年11月在我们的机构中​​开放的颅骨拱形重塑(CVR)进行开放的Calvarial金库重塑(CVR)的单中心回顾性研究。综合征和多缝合线突发患者被排除在外。从医疗记录中提取人口和后续数据,直到2017年7月到7月。结果鉴定了在上述时间框架中经历了CVR的ISS的1万名患者。初始手术的平均年龄为11.7 +/- 15.32个月。我们的颅面诊所的平均随访4.94 +/- 3.53岁,患有69名患者(65.7%)在颅面诊所的后续行动> = 3岁,74(70.5%)在任何后续行动> = 3年诊所在我们的机构。四名患者(3.8%)具有颅内压(ICP)显示有关DIH的症状,其中一种(0.95%)已确认DIH,并在74岁时进行第二次外科手术。患者最初呈现,他的第一次运作在1.56岁。结论105(0.95%)开发DIH的一名患者,通过ICP监测证实,并进行了预先运行。 DIH的发生仍然是罕见的,仍然是包括在父母讨论中的重要课题,并在这群人口中任务长期后续行动。

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