Division of Psychotic Disorders, McLean Hospital, Belmont, MA (Moran, Shinn, Nielsen, Cohen, Erkol, Merchant, Mujica, Ongur); Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital, Boston (Moran, Skinner); Department of Psychiatry, Harvard Medical School, Boston (Moran, Shinn, Rao, Taylor, Perlis, Ongur); Department of Psychiatry, Massachusetts General Hospital, Boston (Rao, Taylor, Perlis).
Am J Psychiatry. 2024 Oct 1;181(10):901-909. doi: 10.1176/appi.ajp.20230329. Epub 2024 Sep 12.
Amphetamine prescribing has increased in the United States in recent years. Previous research identified an increased risk of incident psychosis with prescription amphetamines. The purpose of this study was to examine the impact of dose levels of prescription amphetamines on the risk of this rare but serious adverse outcome.
A case-control study using electronic health records was conducted to compare the odds of incident psychosis or mania with past-month exposure to prescription amphetamines. Case subjects were patients ages 16-35 hospitalized at McLean Hospital for incident psychosis or mania between 2005 and 2019. Control subjects were patients with an initial psychiatric hospitalization for other reasons, most commonly depression and/or anxiety. Amphetamine doses were converted to dextroamphetamine equivalents and divided into terciles. Secondary analyses evaluated the odds of psychosis or mania with methylphenidate use.
Among 1,374 case subjects and 2,748 control subjects, the odds of psychosis and mania were increased for individuals with past-month prescription amphetamine use compared with no use (adjusted odds ratio=2.68, 95% CI=1.90-3.77). A dose-response relationship was observed; high doses of amphetamines (>30 mg dextroamphetamine equivalents) were associated with 5.28-fold increased odds of psychosis or mania. Past-month methylphenidate use was not associated with increased odds of psychosis or mania compared with no use (adjusted odds ratio=0.91, 95% CI=0.54-1.55).
Although use of hospitalized control subjects excludes individuals with less severe disease, leading to selection bias, the study results suggest that caution should be exercised when prescribing high doses of amphetamines, with regular screening for symptoms of psychosis or mania.
近年来,美国的安非他命处方量有所增加。先前的研究表明,处方安非他命会增加出现精神病的风险。本研究旨在探讨处方安非他命的剂量水平对这种罕见但严重不良后果的风险的影响。
采用电子病历进行病例对照研究,比较过去一个月接触处方安非他命与精神病或躁狂发作的几率。病例组患者为 2005 年至 2019 年间在麦克莱恩医院因精神病或躁狂发作住院的 16-35 岁患者。对照组患者为因其他原因首次住院的患者,最常见的是抑郁症和/或焦虑症。将安非他命剂量转换为右旋安非他命当量,并分为三分位数。二次分析评估了使用哌甲酯的精神病或躁狂发作的几率。
在 1374 名病例组患者和 2748 名对照组患者中,与未使用相比,过去一个月使用处方安非他命的个体精神病和躁狂发作的几率增加(调整后的优势比=2.68,95%置信区间=1.90-3.77)。观察到剂量反应关系;高剂量的安非他命(>30 毫克右旋安非他命当量)与精神病或躁狂发作的几率增加 5.28 倍相关。与未使用相比,过去一个月使用哌甲酯与精神病或躁狂发作的几率增加无关(调整后的优势比=0.91,95%置信区间=0.54-1.55)。
尽管使用住院对照组患者排除了疾病程度较轻的个体,从而导致选择偏倚,但研究结果表明,在开处高剂量安非他命时应谨慎,并定期筛查精神病或躁狂的症状。