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2019年冠状病毒病大流行期间成年癫痫患者的医疗保健可及性、心理社会结局与心理健康

Health care access, psychosocial outcomes and mental health in adults living with epilepsy during the COVID-19 pandemic.

作者信息

Mc Carthy L, Mathew B, Blank L J, Van Hyfte G, Gotlieb E, Goldstein J, Agarwal P, Kwon C S, Singh A, Fields M, Marcuse L, Yoo J Y, Sivarak E, Gururangan K, Navis A, Jetté N

机构信息

Department of Neurology, Icahn school of Medicine at Mount Sinai, New York, NY, USA.

Department of Neurology, Icahn school of Medicine at Mount Sinai, New York, NY, USA; Institute for Healthcare Delivery Science, Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Epilepsy Behav. 2024 Feb;151:109617. doi: 10.1016/j.yebeh.2023.109617. Epub 2024 Jan 13.

Abstract

PURPOSE

People living with epilepsy (PLWE) have a higher prevalence of mental health comorbidities and poorer psychosocial outcomes compared to the general population. The aim of this study was to examine psychosocial outcomes, mental health, healthcare accessibility, and seizure burden in PLWE during the COVID-19 pandemic.

METHODS

We conducted a cross-sectional study of adults with epilepsy treated in an urban multicenter health system from 2021 to 2022. A standardized questionnaire assessed for COVID-19 history, comorbidities, access to antiseizure medications (ASMs) and neurological care, seizure burden, and psychosocial outcomes (e.g., employment, social and financial support). The Patient Health Questionnaire-9 (PHQ-9) and Generalized Anxiety Disorder-7 (GAD-7) were administered to evaluate for depression and anxiety. Frequency and proportions for categorical variables and median and interquartile ranges for continuous variables were calculated.

RESULTS

Fifty-five PLWE participated (95 % response rate). Median age was 40 years (IQR 31.5-66.5), 61.8 % were women, 47.3 % had a bachelor's degree or higher and 29.1 % each had Medicaid and Medicare insurance. Race (from highest to lowest %) was: 32.7 % White, 20 % Black, 20 % Latinx, 14.5 % Asian, and 12.7 % selected "other" or "prefer not to say." COVID-19 had been diagnosed in 21.8 % of participants. Symptoms of anxiety and depression were self-reported by 43.6 % and 34.5 % of patients, respectively, with many describing this symptom as new post-pandemic (37.5 % and 31.6 %, respectively). Using validated scales, 52.7 % had depression (PHQ-9 score ≥ 5) with 30.9 % having moderate/severe depression (PHQ-9 score ≥ 10), while 29.1 % had probable generalized anxiety disorder (GAD-7 score ≥ 8). Seizure burden increased in 21.8 % of participants, while 20 % reported fewer seizures and 29.1 % were seizure free since the COVID-19 pandemic. Economic impacts of the pandemic included job loss (25 % amongst those employed at onset of pandemic), new or worsened financial difficulties (40 %), and new or worsened social support issues (30.9 %). Of all participants, 18.2 % reported difficulties accessing ASMs and 25.5 % cancelled visits, but of those with cancelled visits, 78.6 % had their appointments rescheduled as a telehealth visit.

CONCLUSION

Our cohort of PLWE experienced some challenges during the COVID-19 pandemic including poorer mental health and financial and employment-related stressors. Encouragingly, healthcare access was relatively spared during the COVID-19 crisis, with some patients even reporting a reduction in seizure burden. However, PLWE require ongoing psychosocial support with particular attention to decompensation of mental health and social stressors that may be exacerbated by the COVID-19 pandemic.

摘要

目的

与普通人群相比,癫痫患者(PLWE)心理健康合并症的患病率更高,心理社会结局更差。本研究的目的是调查2019冠状病毒病(COVID-19)大流行期间PLWE的心理社会结局、心理健康、医疗可及性和癫痫发作负担。

方法

我们对2021年至2022年在城市多中心卫生系统接受治疗的成年癫痫患者进行了一项横断面研究。一份标准化问卷评估了COVID-19病史、合并症、抗癫痫药物(ASM)的可及性和神经科护理、癫痫发作负担以及心理社会结局(如就业、社会和经济支持)。使用患者健康问卷-9(PHQ-9)和广泛性焦虑障碍-7(GAD-7)评估抑郁和焦虑情况。计算分类变量的频率和比例以及连续变量的中位数和四分位间距。

结果

55名PLWE参与研究(应答率95%)。中位年龄为40岁(四分位间距31.5 - 66.5),61.8%为女性,47.3%拥有学士学位或更高学历,29.1%的人分别拥有医疗补助和医疗保险。种族(从高到低%)为:32.7%白人、20%黑人、20%拉丁裔、14.5%亚洲人,12.

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