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Establishing a Pediatric Acute-Onset Neuropsychiatric Syndrome Clinic: Baseline Clinical Features of the Pediatric Acute-Onset Neuropsychiatric Syndrome Cohort at Karolinska Institutet

机译:建立小儿急性发作神经精神病综合症诊所:Karolinska研究所的小儿急性发作神经精神病综合症基线临床特征

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摘要

>Objectives: Pediatric acute-onset neuropsychiatric syndrome (PANS) is a descriptive clinical entity defined by the abrupt onset of psychiatric and somatic symptoms leading to significant loss of function. Data on well-characterized PANS patients are limited, biomarkers have yet to be identified, and a solid evidence base to guide treatment is lacking. In this study, we present our experience of a systematic evaluation of the first 45 patients included in a Swedish cohort.>Methods: During the period 2014–2018, our clinic received 100 referrals regarding suspected PANS. All patients underwent a standardized psychiatric/medical evaluation by a child/adolescent psychiatrist and a clinical psychologist or a nurse. Those with severe symptoms were also assessed by a pediatric neurologist and a pediatric rheumatologist. Laboratory tests were obtained at different time points in an attempt to capture an active disease state.>Results: Of the 100 referrals, 45 met strict PANS criteria and consented to participate in a long-term follow-up study. The median age at intake was 7.2 years (range 3.0–13.1) and 56% were male. Ninety-three percent fulfilled both criteria for acute/atypical onset of PANS symptoms and having had an infection in relation to onset. Sixteen percent had an onset of an autoimmune or inflammatory disorder in temporal relation to the onset of PANS-related symptoms. The most common onset symptoms were obsessive-compulsive disorder (89%), anxiety (78%), and emotional lability (71%). Twenty-four percent had a preexisting autoimmune disease (AD) and 18% a preexisting psychiatriceuropsychiatric diagnosis. Sixty-four percent of biological relatives had at least one psychiatric disorder and 76% at least one AD or inflammatory disorder. Complement activation (37%), leukopenia (20%), positive antinuclear antibodies (17%), and elevated thyroid antibodies (11%) were the most common laboratory findings.>Conclusions: In our PANS cohort, there was a strong indication of an association with AD. Further work is needed to establish whether any of the potential biomarkers identified will be clinically useful. Long-term follow-up of these patients using the Swedish national registers will enable a deeper understanding of the course of this patient group.
机译:>目的:小儿急性发作性神经精神病综合症(PANS)是一种描述性临床实体,由突然出现的精神病和躯体症状导致严重功能丧失所定义。表征良好的PANS患者的数据有限,尚未确定生物标志物,并且缺乏指导治疗的可靠证据基础。在这项研究中,我们介绍了系统评估瑞典队列中前45例患者的经验。>方法:在2014-2018年期间,我们的诊所收到了100例有关可疑PANS的转诊报告。所有患者均由儿童/青少年精神科医生和临床心理学家或护士进行了标准化的精神病/医学评估。儿科神经科医生和儿科风湿病医师也对症状严重的患者进行了评估。 >结果:在100个转诊患者中,有45个符合严格的PANS标准并同意参加长期随访研究。摄入时的中位年龄为7.2岁(范围3.0-13.1),其中56%为男性。百分之九十三的人既符合PANS症状急性/非典型发作的标准,又符合与感染相关的标准。有16%的人与PANS相关症状的发作在时间上有自身免疫性或炎性疾病的发作。最常见的发作症状是强迫症(89%),焦虑症(78%)和情绪不稳(71%)。 24%的患者患有先前的自身免疫性疾病(AD),18%的患者患有先前的精神病/神经精神病学诊断。有64%的生物学亲属患有至少一种精神病,至少有76%患有AD或炎症。补体激活(37%),白细胞减少症(20%),抗核抗体阳性(17%)和甲状腺抗体升高(11%)是最常见的实验室检查结果。>结论:在我们的PANS队列中,有强烈的迹象表明与AD相关。需要进一步的工作来确定鉴定出的任何潜在生物标记物是否在临床上有用。使用瑞典国家注册簿对这些患者进行长期随访将使人们对该患者病程有更深入的了解。

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