Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK.
Department of Pediatrics, Christian Medical College, Ludhiana, India.
Cochrane Database Syst Rev. 2021 Nov 1;11(11):CD009027. doi: 10.1002/14651858.CD009027.pub4.
Neurocysticercosis is the most common parasitic infection of the brain. Epilepsy is the most common clinical presentation, though people may also present with headache, symptoms of raised intracranial pressure, hydrocephalus, and ocular symptoms depending upon the localisation of the parasitic cysts. Anthelmintic drugs, antiepileptic drugs (AEDs), and anti-oedema drugs, such as steroids, form the mainstay of treatment. This is an updated version of the Cochrane Review previously published in 2019.
To assess the effects (benefits and harms) of AEDs for the primary and secondary prevention of seizures in people with neurocysticercosis. For the question of primary prevention, we examined whether AEDs reduce the likelihood of seizures in people who had neurocysticercosis but had not had a seizure. For the question of secondary prevention, we examined whether AEDs reduce the likelihood of further seizures in people who had had at least one seizure due to neurocysticercosis. As part of primary prevention studies, we also aimed to examine which AED was beneficial in people with neurocysticercosis in terms of duration, dose, and side-effect profile.
For the 2021 update of this review, we searched the Cochrane Register of Studies (CRS Web), MEDLINE, and LILACS to January 2021. CRS Web includes randomised or quasi-randomised, controlled trials from CENTRAL, the Specialised Registers of Cochrane Review Groups, including Epilepsy, PubMed, Embase, ClinicalTrials.gov, and the World Health Organisation International Clinical Trials Registry Platform. We also checked the reference lists of identified studies, and contacted experts and colleagues in the field to search for additional and ongoing studies.
Randomised and quasi-randomised controlled trials. Single-blind, double-blind, or unblinded studies were eligible for inclusion.
We followed standard methodological procedures expected by Cochrane. Two review authors independently selected trials for inclusion and extracted the relevant data. The primary outcomes of interest were: proportion of individuals experiencing seizures, and time to first seizure post randomisation. Secondary outcomes included: seizure freedom, number of withdrawals, side effects, number of people seizure free with short or long durations of treatment, quality of life, therapy costs, hospitalisations, and mortality. We used an intention-to-treat analysis for the primary analysis. We calculated odds ratio (OR) for dichotomous data (proportion of individuals who experienced seizures, were seizure free for a specific time period (12 or 24 months), withdrew from treatment, developed drug-related side effects or complications, were seizure-free with each treatment policy, mortality), and planned to use mean difference (MD) for continuous data, if any continuous data were identified (quality of life, cost of treatment). We intended to evaluate time to first seizure after randomisation by calculating hazard ratios (HRs). We assessed precision using 95% confidence intervals (CIs). We stratified the analysis by treatment comparison. We also considered the duration of drug usage, co-medications, and the length of follow-up.
We did not find any trials that investigated the role of AEDs in preventing seizures among people with neurocysticercosis, presenting with symptoms other than seizures. We did not find any trials that directly compared individual AEDs for primary prevention in people with neurocysticercosis. We included four trials that evaluated the efficacy of short-term versus longer-term AED treatment for people with solitary neurocysticercosis (identified on computed tomography (CT) scan) who presented with seizures. In total, 466 people were enrolled. These studies compared AED treatment durations of 6, 12, and 24 months. The risk of seizure recurrence with six months of treatment compared with 12 to 24 months of treatment was inconclusive (odds ratio (OR) 1.34, 95% confidence interval (CI) 0.73 to 2.47; three studies, 360 participants; low-certainty evidence). The risk of seizure recurrence with six to 12 months of treatment compared with 24 months of treatment was inconclusive (OR 1.36, 95% CI 0.72 to 2.57; three studies, 385 participants; very low-certainty evidence). Two studies compared seizure recurrence with CT findings, and suggested that persistent and calcified lesions had a higher recurrence risk, and suggest longer duration of treatment with AEDs. One study reported no side effects, while the rest did not comment on side effects of the drugs. None of the studies addressed the quality of life of the participants. These studies had methodological deficiencies, such as small sample sizes, and a possibility of bias due to lack of blinding, which affect the results of the review.
AUTHORS' CONCLUSIONS: Despite neurocysticercosis being the most common cause of epilepsy worldwide, there is currently no evidence available regarding the use of AEDs as seizure prophylaxis among people presenting with symptoms other than seizures. For those presenting with seizures, there is no reliable evidence regarding the duration of treatment required. Therefore, there is a need for large scale randomised controlled trials to address these questions.
脑囊虫病是最常见的脑部寄生虫感染。癫痫是最常见的临床表现,但根据寄生虫囊肿的位置,人们也可能出现头痛、颅内压升高、脑积水和眼部症状。抗蠕虫药物、抗癫痫药物(AEDs)和类固醇等消肿药物是治疗的主要方法。这是之前于 2019 年发表的 Cochrane 综述的更新版本。
评估 AEDs 用于预防神经囊尾蚴病患者的原发性和继发性癫痫发作的效果(益处和危害)。对于原发性预防问题,我们检查了 AED 是否降低了神经囊尾蚴病但未发生癫痫发作的人的癫痫发作可能性。对于继发性预防问题,我们检查了 AED 是否降低了已经因神经囊尾蚴病而至少发生一次癫痫发作的人的进一步癫痫发作的可能性。作为原发性预防研究的一部分,我们还旨在检查在神经囊尾蚴病患者中,哪种 AED 在持续时间、剂量和副作用方面具有益处。
为了对本综述进行 2021 年的更新,我们检索了 Cochrane 对照试验注册库(CRS Web)、MEDLINE 和 LILACS,检索日期截至 2021 年 1 月。CRS Web 包括来自 CENTRAL、专门的 Cochrane 综述组的随机或半随机对照试验,包括癫痫组、PubMed、Embase、ClinicalTrials.gov 和世界卫生组织国际临床试验注册平台。我们还检查了已确定研究的参考文献,并联系了该领域的专家和同事,以搜索其他正在进行的研究。
随机和半随机对照试验。单盲、双盲或非盲研究都有资格纳入。
我们遵循了 Cochrane 预期的标准方法学程序。两位综述作者独立选择试验进行纳入并提取相关数据。主要结局包括:个体发生癫痫发作的比例,以及随机分组后首次癫痫发作的时间。次要结局包括:癫痫发作无发作、停药、副作用、接受每种治疗方案无癫痫发作的人数、生活质量、治疗费用、住院和死亡率。我们对主要分析进行了意向性治疗分析。我们为二分类数据(发生癫痫发作的个体比例、在特定时间段(12 或 24 个月)无癫痫发作、停药、出现药物相关副作用或并发症、接受每种治疗方案无癫痫发作、死亡率)计算了优势比(OR),如果确定了任何连续数据(生活质量、治疗费用),则计划使用均数差(MD)。我们打算通过计算风险比(HR)来评估随机分组后首次癫痫发作的时间。我们使用 95%置信区间(CI)来评估精度。我们按治疗比较进行了分层。我们还考虑了药物使用的持续时间、合并用药和随访时间。
我们没有发现任何研究调查 AED 在预防除癫痫发作以外的神经囊尾蚴病症状患者的癫痫发作中的作用。我们没有发现任何直接比较神经囊尾蚴病患者(在计算机断层扫描 (CT) 扫描上确定)短期与长期 AED 治疗效果的研究。我们纳入了四项评估单一神经囊尾蚴病患者短期与长期 AED 治疗效果的研究,这些患者有癫痫发作。总共有 466 人参与。这些研究比较了 6、12 和 24 个月的 AED 治疗时间。与 12 至 24 个月的治疗相比,6 个月的治疗后癫痫复发的风险尚无定论(优势比 (OR) 1.34,95%置信区间 (CI) 0.73 至 2.47;三项研究,360 名参与者;低确定性证据)。与 6 至 12 个月的治疗相比,24 个月的治疗后癫痫复发的风险尚无定论(OR 1.36,95% CI 0.72 至 2.57;三项研究,385 名参与者;非常低确定性证据)。两项研究比较了癫痫发作与 CT 发现之间的关系,并表明持续和钙化病变的复发风险更高,并表明需要更长时间的 AED 治疗。一项研究报告无副作用,其余研究未对药物的副作用发表意见。这些研究均未涉及参与者的生活质量。这些研究存在方法学缺陷,例如样本量小,以及由于缺乏盲法而存在偏倚的可能性,这些都影响了综述的结果。
尽管脑囊虫病是全世界最常见的癫痫发作原因,但目前尚无证据表明 AED 可用于预防除癫痫发作以外的症状患者的癫痫发作。对于有癫痫发作的患者,尚不清楚需要多长时间的治疗。因此,需要进行大规模的随机对照试验来解决这些问题。