Collins Jack C, Wheeler Amanda J, McMillan Sara S, Hu Jie, El-Den Sarira, Roennfeldt Helena, O'Reilly Claire L
The University of Sydney School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Menzies Health Institute Queensland, Griffith University, Nathan, Australia.
Health Expect. 2024 Dec;27(6):e70122. doi: 10.1111/hex.70122.
Psychotropic medications are a common treatment modality for people living with severe and persistent mental illness (SPMI). While effective in reducing relapse and hospitalisation, psychotropic medications cause numerous side effects, varying in nature and severity. Identification and management of side effects is crucial in the ongoing management of SPMI.
To characterise the side effects of psychotropic medications, experienced by a sample of consumers living with SPMI, using a validated tool.
Consumers with SPMI living in the community were recruited from all 25 community pharmacies across four Australian regions, which were allocated to the intervention arm of the Bridging the Gap between Physical and Mental Illness (PharMIbridge) randomised controlled trial (RCT).
Responses to the My Medicines & Me Questionnaire (M3Q).
Consumers (n = 156) most frequently reported side effects in the categories of sleep-related side effects (80.8%, n = 126), mood-related side effects (75.6%, n = 118) and weight and appetite changes (60.3%, n = 107). Daytime somnolence was the most reported individual side effect (68.6%, n = 107). Mood-related side effects were ranked as the most bothersome, followed by sleep-related side effects and weight and appetite changes. More than one-quarter (29.5%, n = 46) of consumers reported choosing not to take their medications due to side effects. Consumers more frequently told family and friends about the side effects rather than healthcare professionals.
An overwhelming majority of consumers experienced at least one side effect attributed to their psychotropic medication, with many experiencing multiple. These findings highlight the critical need to regularly engage with consumers to discuss, identify and manage side effects to treatment burden, reduce risk of non-adherence and improve their treatment experience.
The PharMIbridge RCT included a training programme and intervention service that was co-designed and co-delivered with people with lived experience of mental illness. The research team, expert advisory panel and mentors who supported the delivery and implementation of the training and intervention included participants who have lived experience of mental illness or caring for someone with mental illness.
ANZCTR12620000577910.
精神药物是重度持续性精神疾病(SPMI)患者常用的治疗方式。虽然精神药物在减少复发和住院方面有效,但会引发许多副作用,其性质和严重程度各不相同。识别和管理副作用对于SPMI的持续治疗至关重要。
使用经过验证的工具,描述SPMI患者样本所经历的精神药物副作用。
从澳大利亚四个地区的所有25家社区药房招募社区中的SPMI消费者,这些药房被分配到“弥合身心疾病差距(PharMIbridge)”随机对照试验(RCT)的干预组。
对“我的药物与我问卷(M3Q)”的回答。
消费者(n = 156)最常报告的副作用类别为睡眠相关副作用(80.8%,n = 126)、情绪相关副作用(75.6%,n = 118)以及体重和食欲变化(60.3%,n = 107)。日间嗜睡是报告最多的个体副作用(68.6%,n = 107)。情绪相关副作用被列为最困扰的,其次是睡眠相关副作用以及体重和食欲变化。超过四分之一(29.5%,n = 46)的消费者报告因副作用而选择不服用药物。消费者更常将副作用告知家人和朋友,而非医疗保健专业人员。
绝大多数消费者经历了至少一种归因于其精神药物的副作用,许多人经历了多种副作用。这些发现凸显了定期与消费者沟通以讨论、识别和管理副作用的迫切需求,以减轻治疗负担、降低不依从风险并改善他们的治疗体验。
PharMIbridge RCT包括一个与有精神疾病生活经历的人共同设计和共同提供的培训计划和干预服务。支持培训和干预实施的研究团队、专家咨询小组和导师包括有精神疾病生活经历或照顾精神疾病患者的参与者。
ANZCTR12620000577910。