Pediatric Idiopathic Intracranial Hypertension: Clinical Presentations, Risk Factors, and Prognostic Indicator

IF 0.4 4区 医学 Q4 PEDIATRICS Iranian Journal of Pediatrics Pub Date : 2024-04-20 DOI:10.5812/ijp-143360
Narjes Jafari, Golazin Shahbodagh, Amir Hossein Hassani, Mohammad Nikoohemmat
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Abstract

Background: Idiopathic intracranial hypertension (IIH) is characterized by elevated cerebrospinal fluid pressure without space-occupying lesions, infections, or alterations in brain parenchyma. Diagnosing IIH in children poses a significant challenge for pediatricians, given the often nonspecific nature of clinical signs and symptoms. Objectives: Our study aims to evaluate the clinical presentations and potential risk factors among pediatric individuals diagnosed with IIH, considering the limited research in this particular domain. Methods: Clinical data from pediatric patients diagnosed with IIH who sought care at Tehran's primary referral children's hospitals were collected from 2013 to 2021, spanning eight years. These patients were subsequently contacted to follow up on the presence of persistent headaches and visual problems. Detailed records of their initial signs and symptoms were documented. To identify prognostic factors associated with persistent headaches and visual problems in pediatric IIH patients, binary logistic regression analysis was conducted. Results: A total of 81 pediatric patients were included in the study, with a mean age of 13.56 ± 4.404 years at the time of their IIH diagnosis. The most frequently reported clinical symptom among these patients was headache, observed in 85.2% of cases, followed by diplopia (50.6%), visual impairment (46.9%), and nausea with/without vomiting (44.4%). Furthermore, a substantial proportion of the patients were underweight (weight percentiles < 3). Our analysis showed that male patients and those without strabismus experienced significantly more recurrent episodes of IIH (P = 0.013 and P = 0.013, respectively). Notably, recurrent episodes and higher weight percentiles emerged as predictive factors for future persistent visual problems within our study population (P = 0.032 and P = 0.045, respectively). Conclusions: Recurrence of IIH was significantly less in female patients and those with strabismus. Additionally, we found that both lower and higher weight percentiles, as well as the occurrence of recurrent episodes, served as predictive factors for the development of persistent visual problems. However, our model could not predict persistent headaches.
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小儿特发性颅内高压:临床表现、风险因素和预后指标
背景:特发性颅内高压(IIH)的特点是脑脊液压力升高,但无空间占位性病变、感染或脑实质改变。由于临床症状和体征通常不具有特异性,因此诊断儿童 IIH 对儿科医生来说是一项重大挑战。研究目的考虑到这一特定领域的研究有限,我们的研究旨在评估被诊断为 IIH 的儿科患者的临床表现和潜在风险因素。研究方法从 2013 年到 2021 年,我们收集了在德黑兰主要转诊儿童医院就诊的被诊断为 IIH 的儿科患者的临床数据,时间跨度长达八年。随后与这些患者取得联系,对其是否存在持续性头痛和视力问题进行随访。他们最初的体征和症状都有详细记录。为了确定与小儿IIH患者持续性头痛和视力问题相关的预后因素,我们进行了二元逻辑回归分析。结果:研究共纳入了 81 名儿童患者,他们被诊断为 IIH 时的平均年龄为(13.56 ± 4.404)岁。这些患者中最常见的临床症状是头痛,占 85.2%,其次是复视(50.6%)、视力障碍(46.9%)和恶心伴/不伴呕吐(44.4%)。此外,相当一部分患者体重不足(体重百分位数小于 3)。我们的分析表明,男性患者和无斜视患者的 IIH 复发率明显更高(分别为 P = 0.013 和 P = 0.013)。值得注意的是,在我们的研究人群中,反复发作和较高的体重百分位数成为未来持续性视觉问题的预测因素(分别为 P = 0.032 和 P = 0.045)。结论女性患者和斜视患者的 IIH 复发率明显较低。此外,我们还发现,较低和较高的体重百分位数以及反复发作的情况都是导致持续性视力问题的预测因素。但是,我们的模型无法预测持续性头痛。
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来源期刊
CiteScore
0.90
自引率
20.00%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Iranian Journal of Pediatrics (Iran J Pediatr) is a peer-reviewed medical publication. The purpose of Iran J Pediatr is to increase knowledge, stimulate research in all fields of Pediatrics, and promote better management of pediatric patients. To achieve the goals, the journal publishes basic, biomedical, and clinical investigations on prevalent diseases relevant to pediatrics. The acceptance criteria for all papers are the quality and originality of the research and their significance to our readership. Except where otherwise stated, manuscripts are peer-reviewed by minimum three anonymous reviewers. The Editorial Board reserves the right to refuse any material for publication and advises that authors should retain copies of submitted manuscripts and correspondence as the material cannot be returned. Final acceptance or rejection rests with the Editors.
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