Solutions to common issues in the use of LAIs.

IF 4.6 3区 医学 Q2 CLINICAL NEUROLOGY
Stephen R Saklad
{"title":"Solutions to common issues in the use of LAIs.","authors":"Stephen R Saklad","doi":"10.1017/S1092852925100552","DOIUrl":null,"url":null,"abstract":"<p><p>Long-acting injectable (LAI) antipsychotics are highly effective tools for managing serious mental illness, yet their clinical utility is often compromised by logistical and pharmacological complexities. This review serves as a practical guide to optimizing LAI therapy by addressing common clinical hurdles. Maintaining a consistent injection schedule is essential to successful treatment. To improve adherence, clinicians should implement proactive reminder systems-such as phone calls or text messages-and involve family or caregivers in the care plan. When injections are delayed, management strategies must be tailored to the specific medication and the length of the \"dosing window\". For example, aripiprazole monohydrate (Abilify Maintena) allows a ±7 day window, whereas paliperidone palmitate (Invega Sustenna) provides a +14 day window. If these windows are exceeded, catch-up protocols may involve administering the next dose as soon as possible, utilizing supplemental oral antipsychotics for a bridge period (e.g., 14 days for aripiprazole or 21 days for risperidone), or restarting initiation loading regimens entirely. Clinically significant drug interactions, such as the reduction of aripiprazole or risperidone levels by carbamazepine, can lead to symptom breakthrough. Conversely, CYP450 inhibitors like fluvoxamine or fluoxetine may increase antipsychotic concentrations, necessitating dose reductions. Adverse effects, including drug-induced Parkinsonism and akathisia, should be managed by reducing the LAI dose or switching to agents with lower risk profiles, such as aripiprazole-based products. For akathisia, short-term adjunctive treatments like vitamin B6 or mirtazapine may be utilized until dose adjustments reach steady state. Patient-centered care requires a collaborative approach to substance use, which can exacerbate symptoms or interfere with LAI effectiveness. Clinicians must also engage in nonjudgmental discussions when patients request a return to oral therapy, carefully considering the pharmacokinetic properties of the LAI to time the transition safely. Ultimately, a proactive management plan that addresses these clinical variables is essential for reducing relapse risk and improving long-term quality of life.</p>","PeriodicalId":10505,"journal":{"name":"CNS Spectrums","volume":" ","pages":"S45-S50"},"PeriodicalIF":4.6000,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13064721/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CNS Spectrums","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/S1092852925100552","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Long-acting injectable (LAI) antipsychotics are highly effective tools for managing serious mental illness, yet their clinical utility is often compromised by logistical and pharmacological complexities. This review serves as a practical guide to optimizing LAI therapy by addressing common clinical hurdles. Maintaining a consistent injection schedule is essential to successful treatment. To improve adherence, clinicians should implement proactive reminder systems-such as phone calls or text messages-and involve family or caregivers in the care plan. When injections are delayed, management strategies must be tailored to the specific medication and the length of the "dosing window". For example, aripiprazole monohydrate (Abilify Maintena) allows a ±7 day window, whereas paliperidone palmitate (Invega Sustenna) provides a +14 day window. If these windows are exceeded, catch-up protocols may involve administering the next dose as soon as possible, utilizing supplemental oral antipsychotics for a bridge period (e.g., 14 days for aripiprazole or 21 days for risperidone), or restarting initiation loading regimens entirely. Clinically significant drug interactions, such as the reduction of aripiprazole or risperidone levels by carbamazepine, can lead to symptom breakthrough. Conversely, CYP450 inhibitors like fluvoxamine or fluoxetine may increase antipsychotic concentrations, necessitating dose reductions. Adverse effects, including drug-induced Parkinsonism and akathisia, should be managed by reducing the LAI dose or switching to agents with lower risk profiles, such as aripiprazole-based products. For akathisia, short-term adjunctive treatments like vitamin B6 or mirtazapine may be utilized until dose adjustments reach steady state. Patient-centered care requires a collaborative approach to substance use, which can exacerbate symptoms or interfere with LAI effectiveness. Clinicians must also engage in nonjudgmental discussions when patients request a return to oral therapy, carefully considering the pharmacokinetic properties of the LAI to time the transition safely. Ultimately, a proactive management plan that addresses these clinical variables is essential for reducing relapse risk and improving long-term quality of life.

长效注射抗精神病药物使用中常见问题的解决方法。
长效注射(LAI)抗精神病药物是治疗严重精神疾病的高效工具,但其临床应用往往受到后勤和药理学复杂性的影响。本综述通过解决常见的临床障碍,作为优化LAI治疗的实用指南。保持一致的注射时间表是成功治疗的关键。为了提高依从性,临床医生应该实施主动提醒系统,如电话或短信,并让家人或护理人员参与护理计划。当注射延迟时,管理策略必须根据具体药物和“给药窗口”的长度进行调整。例如,一水阿立哌唑(Abilify Maintena)允许±7天的窗口,而棕榈酸帕利哌酮(Invega Sustenna)提供+14天的窗口。如果超过了这些窗口期,补药方案可能包括尽快给药下一剂,在一段过渡期内(例如,阿立哌唑14天,利培酮21天)使用补充口服抗精神病药物,或者完全重新开始起始负荷方案。临床显著的药物相互作用,如卡马西平降低阿立哌唑或利培酮水平,可导致症状突破。相反,CYP450抑制剂如氟伏沙明或氟西汀可能增加抗精神病药浓度,需要减少剂量。不良反应,包括药物性帕金森氏症和静坐症,应通过减少LAI剂量或改用风险较低的药物,如阿立哌唑类产品来控制。对于静坐症,可以使用短期辅助治疗,如维生素B6或米氮平,直到剂量调整达到稳定状态。以患者为中心的护理需要对药物使用采取协作方法,这可能会加剧症状或干扰LAI的有效性。当患者要求恢复口服治疗时,临床医生也必须进行非判断性的讨论,仔细考虑LAI的药代动力学特性,以安全地选择过渡时间。最终,解决这些临床变量的前瞻性管理计划对于降低复发风险和改善长期生活质量至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CNS Spectrums
CNS Spectrums 医学-精神病学
CiteScore
6.20
自引率
6.10%
发文量
239
审稿时长
>12 weeks
期刊介绍: CNS Spectrums covers all aspects of the clinical neurosciences, neurotherapeutics, and neuropsychopharmacology, particularly those pertinent to the clinician and clinical investigator. The journal features focused, in-depth reviews, perspectives, and original research articles. New therapeutics of all types in psychiatry, mental health, and neurology are emphasized, especially first in man studies, proof of concept studies, and translational basic neuroscience studies. Subject coverage spans the full spectrum of neuropsychiatry, focusing on those crossing traditional boundaries between neurology and psychiatry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书