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《Lennox-Gastaut 综合征的疾病负担:系统文献回顾》。

The burden of illness in Lennox-Gastaut syndrome: a systematic literature review.

机构信息

Epilepsy Center Frankfurt Rhine-Main, Center of Neurology and Neurosurgery, University Hospital and Goethe-University Frankfurt, Schleusenweg 2-16 (Haus 95), 60528, Frankfurt am Main, Germany.

LOEWE Center for Personalized and Translational Epilepsy Research (CePTER), Goethe-University Frankfurt, Frankfurt am Main, Germany.

出版信息

Orphanet J Rare Dis. 2023 Mar 1;18(1):42. doi: 10.1186/s13023-023-02626-4.

Abstract

BACKGROUND

Lennox-Gastaut syndrome (LGS) is a severe developmental and epileptic encephalopathy characterized by drug-resistant epilepsy with multiple seizure types starting in childhood, a typical slow spike-wave pattern on electroencephalogram, and cognitive dysfunction.

METHODS

We performed a systematic literature review according to the PRISMA guidelines to identify, synthesize and appraise the burden of illness in LGS (including "probable" LGS). Studies were identified by searching MEDLINE, Embase and APA PsychInfo, Cochrane's database of systematic reviews, and Epistemonikos. The outcomes were epidemiology (incidence, prevalence or mortality), direct and indirect costs, healthcare resource utilization, and patient and caregiver health-related quality of life (HRQoL).

RESULTS

The search identified 22 publications evaluating the epidemiology (n = 10), direct costs and resource (n = 10) and/or HRQoL (n = 5). No studies reporting on indirect costs were identified. With no specific ICD code for LGS in many regions, several studies had to rely upon indirect methods to identify their patient populations (e.g., algorithms to search insurance claims databases to identify "probable" LGS). There was heterogeneity between studies in how LGS was defined, the size of the populations, ages of the patients and length of the follow-up period. The prevalence varied from 4.2 to 60.8 per 100,000 people across studies for probable LGS and 2.9-28 per 100,000 for a confirmed/narrow definition of LGS. LGS was associated with high mortality rates compared to the general population and epilepsy population. Healthcare resource utilization and direct costs were substantial across all studies. Mean annual direct costs per person varied from $24,048 to $80,545 across studies, and home-based care and inpatient care were significant cost drivers. Studies showed that the HRQoL of patients and caregivers was adversely affected, although only a few studies were identified. In addition, studies suggested that seizure events were associated with higher costs and worse HRQoL. The risk of bias was low or moderate in most studies.

CONCLUSIONS

LGS is associated with a significant burden of illness featuring resistant seizures associated with higher costs and worse HRQoL. More research is needed, especially in evaluating indirect costs and caregiver burden, where there is a notable lack of studies.

摘要

背景

Lennox-Gastaut 综合征(LGS)是一种严重的发育性和癫痫性脑病,其特征为儿童期开始出现多种类型的耐药性癫痫发作、脑电图上典型的慢棘慢波模式、以及认知功能障碍。

方法

我们根据 PRISMA 指南进行了系统文献回顾,以确定、综合和评估 LGS(包括“可能”的 LGS)的疾病负担。通过搜索 MEDLINE、Embase 和 APA PsychInfo、Cochrane 系统评价数据库和 Epistemonikos 来识别研究。结果为流行病学(发病率、患病率或死亡率)、直接和间接成本、医疗资源利用以及患者和照护者的健康相关生活质量(HRQoL)。

结果

搜索确定了 22 项评估流行病学(n=10)、直接成本和资源(n=10)和/或 HRQoL(n=5)的研究。没有发现报告间接成本的研究。由于在许多地区没有 LGS 的特定 ICD 编码,因此一些研究不得不采用间接方法来确定其患者人群(例如,使用算法搜索保险索赔数据库以确定“可能”的 LGS)。研究之间在 LGS 的定义、人群规模、患者年龄和随访时间长度方面存在异质性。在“可能”的 LGS 中,患病率在各研究之间从每 100,000 人 4.2 至 60.8 不等,而在确诊/狭义定义的 LGS 中,患病率为每 100,000 人 2.9 至 28 不等。与一般人群和癫痫人群相比,LGS 的死亡率较高。所有研究均显示医疗资源利用和直接成本较高。各研究中人均年直接成本从 24,048 美元到 80,545 美元不等,家庭护理和住院护理是主要的成本驱动因素。研究表明,患者和照护者的 HRQoL 受到不利影响,尽管仅确定了少数研究。此外,研究表明癫痫发作与更高的成本和更差的 HRQoL 相关。大多数研究的偏倚风险较低或中等。

结论

LGS 与疾病负担显著相关,其特征为耐药性癫痫发作,与更高的成本和更差的 HRQoL 相关。需要进一步研究,特别是在评估间接成本和照护者负担方面,因为这方面的研究明显不足。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88b9/9979426/5fa3692c5ba3/13023_2023_2626_Fig1_HTML.jpg

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