Ketogenic Diet: Parental Experiences and Expectations.

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Journal of Child Neurology Pub Date : 2024-01-01 Epub Date: 2024-02-05 DOI:10.1177/08830738241227066
Elizabeth Orr, Robyn Whitney, Nandini Nandeesha, Eric H Kossoff, Rajesh RamachandranNair
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引用次数: 0

Abstract

Background: The ketogenic diet may be difficult for some patients and their families to implement and can impact physical, emotional, and social well-being.

Methods: Through principles of fundamental qualitative description, we completed an exploratory study on parents' experiences and expectations on the use and efficacy of the ketogenic diet for children with medically refractory epilepsy.

Results: Seventeen parents (10 mothers and 7 fathers) of 12 children with epilepsy participated. At the time of the interview, parents had experienced an average of 25 months of ketogenic diet treatment for their child (range 2 months to 98 months). Half of the caregivers learned about the ketogenic diet from their neurologist, whereas the remainder had heard about it from another source (ie, the internet). Most caregivers' (n = 13) diet expectations were related to seizure control. However, child development (n = 5) and quality of life (n = 5) were also crucial to some. Physical impacts of the diet were most commonly gastrointestinal for children (n = 9). Social and emotional effects were noted in some older children with typical development. Most caregivers described negative impacts on finances (n = 15), relationships (n = 14), and emotional well-being (ie, stress) (n = 12). Caregivers benefited from the ketogenic diet team's regular communication, close follow-up, and family-centered care.

Conclusions: Despite the impacts that the ketogenic diet may have on caregivers' emotional and social well-being, the positive impacts of the diet were felt to outweigh any perceived risks. Effects (both positive and negative) on quality of life and child development (eg, social, emotional, cognitive) are essential for caregivers and require additional investigation.

生酮饮食:父母的经历和期望。
背景:生酮饮食对一些患者及其家庭来说可能难以实施,并可能影响身体、情感和社会福祉:通过基本的定性描述原则,我们完成了一项探索性研究,了解了家长对药物难治性癫痫患儿使用生酮饮食的经验和期望以及生酮饮食的疗效:12 名癫痫患儿的 17 名家长(10 名母亲和 7 名父亲)参加了研究。在接受访谈时,父母平均已为其子女经历了 25 个月的生酮饮食治疗(2 个月至 98 个月不等)。半数照顾者是从神经科医生那里了解到生酮饮食的,其余的则是从其他渠道(即互联网)了解到的。大多数照顾者(13 人)对饮食的期望与控制癫痫发作有关。然而,儿童发育(5 人)和生活质量(5 人)对一些人来说也至关重要。饮食对儿童身体的影响最常见的是胃肠道影响(9 人)。一些发育正常的大龄儿童则受到了社会和情感方面的影响。大多数照顾者描述了对经济(15 人)、人际关系(14 人)和情绪健康(即压力)(12 人)的负面影响。生酮饮食团队的定期沟通、密切跟踪和以家庭为中心的护理让护理者受益匪浅:尽管生酮饮食可能会对照顾者的情绪和社会福祉产生影响,但人们认为生酮饮食的积极影响大于任何预期风险。对生活质量和儿童发展(如社交、情感和认知)的影响(包括正面和负面影响)对照顾者至关重要,需要进行更多调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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