首页> 外文期刊>Journal of child and adolescent psychopharmacology >Establishing a Pediatric Acute-Onset Neuropsychiatric Syndrome Clinic: Baseline Clinical Features of the Pediatric Acute-Onset Neuropsychiatric Syndrome Cohort at Karolinska Institutet
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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:建立儿科急性发作神经精神综合征诊断:Karolinska Institutet小儿急性发作神经精神综合征综合征综合征综合征

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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 psychiatric/neuropsychiatric 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:小儿急性发作神经精神综合征(平底锅)是一种描述性临床实体,由精神疾病和体细胞症状突然发作,导致功能显着丧失功能。良好特征的PANS患者的数据有限,尚未确定生物标志物,缺乏指导治疗的固体证据基础。在这项研究中,我们展示了我们对瑞典队列中包括的前45名患者的系统评估的经验。方法:2014 - 2018年期间,我们的诊所接受了有关疑似平台的100个推荐。所有患者均经过儿童/青少年精神病学家和临床心理学家或护士的标准化精神病/医学评估。患有严重症状的人也被儿科神经科医生和儿科病毒学家评估。在不同时间点获得实验室测试,试图捕获活性疾病状态。结果:在100张推荐中,45人达到严格的粉丝标准,并同意参加长期的后续研究。摄入量的中位年龄为7.2年(范围3.0-13.1),56%是男性。九十三个百分之均为急性/非典型症状发作的标准,并在发病方面进行感染。 16%的百分比对截止粉丝的发病症状的自身免疫或炎症性疾病发病。最常见的发病症状是强迫性疾病(89%),焦虑(78%)和情绪萎靡(71%)。 24%的百分比具有预先存在的自身免疫疾病(AD)和18%的预先存在的精神病/神经精神诊断。六十四个生物亲属至少有一个精神疾病和76%的至少一种广告或炎症疾病。补体激活(37%),白细胞减少症(20%),阳性抗核抗体(17%)和升高的甲状腺抗体(11%)是最常见的实验室发现。结论:在我们的PANS队列中,与广告联系有强烈迹象表明。需要进一步的工作来确定所确定的任何潜在的生物标志物是否在临床上有用。使用瑞典国家寄存器的这些患者的长期随访将能够更深入地了解本患者组的过程。

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