Suicide, Stimulants, and Selective Serotonin Reuptake Inhibitors: A Retrospective Chart Review.

IF 1.5 4区 医学 Q2 PEDIATRICS
Reena Thomas, Austin Sellers, Jamie L Fierstein, Mark Cavitt, Jeffrey Alvaro, Neil Goldenberg
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引用次数: 0

Abstract

Background: Previous studies suggest that selective serotonin reuptake inhibitors (SSRIs) may increase the risk of suicide among children and youth, although the association between suicide risk and the combination of SSRIs with other medication such as stimulants in this population remains unclear. This study explored whether the combination of SSRIs with stimulants influenced suicide risk. Methods: A retrospective cohort study was conducted at a single children's hospital campus-based ambulatory psychiatric clinic between September 1, 2017, and September 30, 2020. Subjects were 6-21 years of age and prescribed either stimulants or stimulants and SSRIs only. The primary outcome was suicidal thoughts and behaviors (STB), defined by documented suicidal thoughts, plans, or behaviors. Firth logistic regression evaluated associations between medication class and STB. Results: Among 349 patients, the prevalence of STB was 5.7% (n = 20). In unadjusted model, patients prescribed SSRIs and stimulants had a 2.9-fold increase of STB compared to patients prescribed stimulants only, along with increasing age, male sex, and the diagnoses of anxiety and/or depression. In the final model adjusted for each of these factors, the observed association of medication regiment with STB was attenuated (odds ratio [OR]: 1.3, confidence interval [CI]: 0.3-4.9, p = 0.7). The magnitude of the adjusted association between depressive diagnosis and STB was notable (OR: 3.6, CI: 1.0-12.6, p = 0.049). Conclusions: Among patients followed in a children's hospital-based ambulatory psychiatric clinic, a combination medication regimen of SSRIs and stimulants after adjusting for genetic sex, age, anxiety diagnosis, and depression diagnosis, the observed association between STB and combination stimulant and SSRI treatment was attenuated. This finding suggests that other factors, including depression, may have contributed to the association between SSRI treatment and STB. Larger, prospective studies of the relationship between combination pharmacotherapy and suicide risk are warranted to guide clinical/pharmacological decision making and to better clarify these relationships.

自杀、兴奋剂和选择性羟色胺再摄取抑制剂:回顾病历
背景:以往的研究表明,选择性血清素再摄取抑制剂(SSRIs)可能会增加儿童和青少年的自杀风险,但这一人群的自杀风险与 SSRIs 与兴奋剂等其他药物联用之间的关系仍不清楚。本研究探讨了 SSRIs 与兴奋剂联用是否会影响自杀风险。研究方法一项回顾性队列研究于 2017 年 9 月 1 日至 2020 年 9 月 30 日在一家儿童医院的门诊精神科诊所进行。受试者年龄为 6-21 岁,处方为兴奋剂或仅处方为兴奋剂和 SSRIs。主要结果是自杀想法和行为(STB),即有记录的自杀想法、计划或行为。费斯逻辑回归评估了药物类别与 STB 之间的关联。结果显示在 349 名患者中,STB 患病率为 5.7%(n = 20)。在未经调整的模型中,与仅服用刺激剂的患者相比,服用 SSRIs 和刺激剂的患者 STB 患病率增加了 2.9 倍,同时患者的年龄、性别和焦虑和/或抑郁诊断也在增加。在对这些因素进行调整后的最终模型中,观察到的药物治疗与 STB 的关系有所减弱(几率比 [OR]:1.3,置信区间 [CI]:0.3-4.9,P = 0.7)。抑郁症诊断与 STB 之间的调整后关联程度显著(OR:3.6,CI:1.0-12.6,P = 0.049)。结论在一家儿童医院门诊精神病诊所接受随访的患者中,在对遗传性别、年龄、焦虑诊断和抑郁诊断进行调整后,发现 STB 与刺激剂和 SSRI 联合治疗之间的关联有所减弱。这一发现表明,包括抑郁症在内的其他因素可能导致了 SSRI 治疗与 STB 之间的关联。有必要对联合药物治疗与自杀风险之间的关系进行更大规模的前瞻性研究,以指导临床/药物治疗决策,并更好地阐明这些关系。
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来源期刊
CiteScore
3.60
自引率
5.30%
发文量
61
审稿时长
>12 weeks
期刊介绍: Journal of Child and Adolescent Psychopharmacology (JCAP) is the premier peer-reviewed journal covering the clinical aspects of treating this patient population with psychotropic medications including side effects and interactions, standard doses, and research on new and existing medications. The Journal includes information on related areas of medical sciences such as advances in developmental pharmacokinetics, developmental neuroscience, metabolism, nutrition, molecular genetics, and more. Journal of Child and Adolescent Psychopharmacology coverage includes: New drugs and treatment strategies including the use of psycho-stimulants, selective serotonin reuptake inhibitors, mood stabilizers, and atypical antipsychotics New developments in the diagnosis and treatment of ADHD, anxiety disorders, schizophrenia, autism spectrum disorders, bipolar disorder, eating disorders, along with other disorders Reports of common and rare Treatment Emergent Adverse Events (TEAEs) including: hyperprolactinemia, galactorrhea, weight gain/loss, metabolic syndrome, dyslipidemia, switching phenomena, sudden death, and the potential increase of suicide. Outcomes research.
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