Jerrell Jeanette M, McIntyre Roger S
Department of Neuropsychiatry and Behavioral Science, University of South Carolina School of Medicine, Columbia.
Departments of Psychiatry and Pharmacology, University of Toronto, Toronto, Canada.
Prim Care Companion CNS Disord. 2016 Mar 3;18(2). doi: 10.4088/PCC.15m01901. eCollection 2016.
The greater severity and burden of illness in individuals with early onset schizophrenia (ie, before age 18 years) deserves further investigation, specifically regarding its prevalence in community-based treatment and its association with other psychiatric or medical conditions.
A retrospective cohort design was employed using the South Carolina Medicaid claims database covering outpatient and inpatient medical services from January 1, 1999, through December 31, 2013, to identify patients aged ≤ 17 years with a diagnosis of schizophrenia spectrum disorders (ICD-9-CM). Logistic regression was used to examine the factors differentiating childhood- versus adolescent-onset schizophrenia in a community-based system of care.
Early onset schizophrenia was diagnosed in 613 child and adolescent cases during the study epoch or 0.2% of this population-based cohort. The early onset cohort was primarily male (64%) and black (48%). The mean length of time followed in the Medicaid dataset was 12.6 years. Within the early onset cohort, 22.5% were diagnosed at age ≤ 12 years and 77.5% were diagnosed as adolescents. The childhood-onset subgroup was twice as likely to have speech, language, or educational disabilities and an attention-deficit/hyperactivity disorder diagnosis but significantly less likely to have schizophrenia or schizoaffective disorder, an organic brain disorder or mental retardation/intellectual disability, or a substance use disorder (adjusted OR = 2.01, 2.26, 0.38, 0.31, 0.47, and 0.32, respectively) compared to the adolescent-onset subgroup.
Primary care providers should identify and maintain surveillance of cases of pediatric neurodevelopmental disorders, which appear to be highly comorbid and genetically related, and refer them early and promptly for specialized treatment.
早发性精神分裂症患者(即18岁之前发病)病情更为严重,疾病负担更大,这值得进一步研究,特别是关于其在社区治疗中的患病率以及与其他精神或躯体疾病的关联。
采用回顾性队列设计,利用南卡罗来纳州医疗补助索赔数据库,该数据库涵盖了1999年1月1日至2013年12月31日的门诊和住院医疗服务,以识别诊断为精神分裂症谱系障碍(国际疾病分类第九版临床修订本)的17岁及以下患者。在基于社区的医疗系统中,采用逻辑回归分析来研究区分儿童期与青少年期发病精神分裂症的因素。
在研究期间,613例儿童和青少年被诊断为早发性精神分裂症,占该人群队列的0.2%。早发性队列主要为男性(64%)和黑人(48%)。医疗补助数据集中的平均随访时间为12.6年。在早发性队列中,22.5%在12岁及以下被诊断,77.5%在青少年期被诊断。与青少年期发病亚组相比,儿童期发病亚组出现言语、语言或教育障碍以及注意力缺陷多动障碍诊断的可能性高出两倍,但患精神分裂症或分裂情感性障碍、器质性脑障碍或精神发育迟滞/智力残疾、或物质使用障碍的可能性显著降低(校正比值比分别为2.01、2.26、0.38、0.31、0.47和0.32)。
初级保健提供者应识别并持续监测小儿神经发育障碍病例,这些病例似乎高度共病且与遗传相关,并应尽早及时将他们转诊至专科治疗。