Xu Kevin Young, Nascimento Fábio A, Lin Binx Yezhe, Park Tae Woo, Maust Donovan T, Samples Hillary, Bushnell Greta A
Department of Psychiatry, Washington University School of Medicine in Saint Louis, St Louis, Missouri, USA.
Department of Neurology, Washington University School of Medicine in Saint Louis, St Louis, Missouri, USA.
BMJ Neurol Open. 2024 Sep 18;6(2):e000767. doi: 10.1136/bmjno-2024-000767. eCollection 2024.
Characterising benzodiazepine (BZD) prescribing to individuals with psychogenic non-epileptic seizures (PNES) is important for optimising PNES outcomes, but existing data is lacking.
Using a nationwide administrative claims database (2016-2022), incident PNES was defined as an International classification of diseases, tenth revision, clinical modification (ICD-10-CM) diagnosis in an inpatient or outpatient healthcare encounter after a 1-year period with no documented diagnosis. We described clinical characteristics of adults with incident PNES and estimated the prevalence of outpatient BZD treatment in the baseline year and 30-day follow-up period, with secondary analyses stratifying by baseline ES, anxiety and/or insomnia diagnoses, representing common indications for BZD receipt. We used logistic regression to evaluate predictors of post-PNES BZD receipt.
Among 20 848 adults with incident PNES diagnosis, 33.1% and 15.1% received BZDs in the year and month prior to PNES diagnosis, respectively, and 18.1% received BZDs in the month following a PNES diagnosis; 5.4% of those without prior BZD prescriptions received BZDs after diagnosis. The median days' supply was 30 days, with clonazepam, alprazolam and lorazepam representing the most common BZDs prescribed after PNES. Most people who received BZDs in the month prior to PNES diagnosis remained on BZDs in the month after PNES diagnosis (62.9%), with similar findings in the subcohorts without ES, anxiety and/or insomnia. Baseline BZD receipt and anxiety disorders, but not baseline ES diagnoses, were strong independent predictors of post-PNES BZD receipt.
While new BZD initiation is rare after PNES, most individuals with BZD scripts 1 month before PNES continue scripts after diagnosis.
了解苯二氮䓬类药物(BZD)在精神性非癫痫性发作(PNES)患者中的处方情况对于优化PNES的治疗效果很重要,但目前缺乏相关数据。
利用全国性行政索赔数据库(2016 - 2022年),将新发PNES定义为在1年无相关诊断记录后,在住院或门诊医疗就诊时的国际疾病分类第十次修订版临床修订本(ICD - 10 - CM)诊断。我们描述了新发PNES成人患者的临床特征,并估计了基线年份和30天随访期内门诊BZD治疗的患病率,进行了二级分析,按基线精神性症状(ES)、焦虑和/或失眠诊断分层,这些是BZD用药的常见指征。我们使用逻辑回归评估PNES后BZD用药的预测因素。
在20848例新发PNES诊断的成人患者中,分别有33.1%和15.1%在PNES诊断前一年和一个月接受了BZD治疗,18.1%在PNES诊断后一个月接受了BZD治疗;在诊断前未使用过BZD处方的患者中,5.4%在诊断后接受了BZD治疗。BZD供应天数中位数为30天,氯硝西泮、阿普唑仑和劳拉西泮是PNES后最常用的BZD。大多数在PNES诊断前一个月接受BZD治疗的患者在PNES诊断后一个月仍继续使用BZD(62.9%),在无ES、焦虑和/或失眠的亚组中也有类似发现。基线BZD用药和焦虑症,而非基线ES诊断,是PNES后BZD用药的强有力独立预测因素。
虽然PNES后开始新的BZD治疗很少见,但大多数在PNES前1个月有BZD处方的患者在诊断后继续用药。