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披露还是隐瞒?成年患者对癫痫性猝死披露的看法。

To reveal or conceal? Adult patient perspectives on SUDEP disclosure.

作者信息

Long Lucretia, Cotterman-Hart Sheri, Shelby Jennae

机构信息

The Ohio State University Department of Neurology, 395 W 12th St, 7th floor, Columbus, OH 43201, United States of America.

The Ohio State University Department of Neurology, 395 W 12th St, 7th floor, Columbus, OH 43201, United States of America.

出版信息

Epilepsy Behav. 2018 Sep;86:79-84. doi: 10.1016/j.yebeh.2018.06.026. Epub 2018 Jul 9.

Abstract

OBJECTIVE

The study aimed to evaluate adult patient or caregiver feelings and viewpoints about sudden unexpected death in epilepsy (SUDEP) awareness.

BACKGROUND

The decision to discuss SUDEP with patients and families has created much debate. Many healthcare providers (HCPs) are hesitant to discuss SUDEP because of the perception of evoking unnecessary fear in patients while others argue that informing patients about SUDEP may enhance patient compliance, improve seizure control, and aid in saving lives. This study quantifies patient viewpoints regarding their right to information, requirements of disclosure, and initial responses of fear and patient motivation toward behavioral change.

DESIGN/METHODS: This was a prospective random sample survey of adult patients with epilepsy or their caregivers. Every third eligible adult patient with epilepsy or caregiver was given a one-page SUDEP information sheet promoted by the Epilepsy Foundation of America. Participants were then asked if they were interested in completing an eight-item questionnaire assessing their perception of the information.

RESULTS

Ninety-four of ninety-six subjects completed the survey (98%). One hundred percent (n = 94) of responders felt they had a right to be informed about SUDEP, and 95% felt that their HCP should be required to inform them. Respondents also indicated that SUDEP awareness motivated them for better medication adherence (89%) and management of lifestyle factors that lower seizure threshold (88%). Thirty percent endorsed increased fear. However, 100% of those patients or caregivers who endorsed fear still felt it was their right to be informed. Patients who endorsed fear were also more likely to be interested in nonpharmacologic treatment options as a result of SUDEP disclosure.

CONCLUSIONS

Patients and caregivers feel it is their right to be informed about SUDEP, irrespective of evoked fear. The vast majority of participants endorsed a requirement for HCPs to disclose related information. While some participants endorsed fear, most agreed that SUDEP awareness motivated them to better manage factors that trigger seizures. Patient education regarding SUDEP may play a key role in encouraging modifying lifestyle factors that lower seizure threshold and facilitate more aggressive interventions in patients with pharmacoresistant epilepsy.

摘要

目的

本研究旨在评估成年患者或照料者对癫痫性猝死(SUDEP)认知的感受和观点。

背景

与患者及其家属讨论SUDEP的决定引发了诸多争议。许多医疗服务提供者(HCPs)因担心在患者中引发不必要的恐惧而不愿讨论SUDEP,而其他人则认为告知患者SUDEP可能会提高患者的依从性、改善癫痫发作控制并有助于挽救生命。本研究量化了患者对信息权、披露要求以及恐惧的初始反应和患者行为改变动机的观点。

设计/方法:这是一项对成年癫痫患者或其照料者的前瞻性随机抽样调查。每第三位符合条件的成年癫痫患者或照料者会收到一份由美国癫痫基金会推广的关于SUDEP的单页信息表。然后询问参与者是否有兴趣完成一份评估他们对该信息认知的八项问卷。

结果

96名受试者中有94名完成了调查(98%)。100%(n = 94)的受访者认为他们有权了解SUDEP,95%的人认为应该要求他们的HCP告知他们。受访者还表示,对SUDEP的认知促使他们更好地坚持服药(89%)以及管理降低癫痫发作阈值的生活方式因素(88%)。30%的人认可恐惧增加。然而,100%认可恐惧的患者或照料者仍认为他们有权了解相关信息。认可恐惧的患者由于SUDEP的披露也更有可能对非药物治疗选择感兴趣而。

结论

患者和照料者认为他们有权了解SUDEP,无论是否引发恐惧。绝大多数参与者认可要求HCPs披露相关信息。虽然一些参与者认可恐惧,但大多数人同意对SUDEP的认知促使他们更好地管理引发癫痫发作的因素。关于SUDEP的患者教育可能在鼓励改变降低癫痫发作阈值的生活方式因素以及促进对药物难治性癫痫患者进行更积极的干预方面发挥关键作用。

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