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Selective mutism: a consensus based care pathway of good practice.

机译:选择性默:基于共识的良好实践护理途径。

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BACKGROUND: Selective mutism (SM) now acknowledged as an anxiety condition, tends to be a poorly understood, highly complex and vastly under-recognised clinical entity. Children with SM are a vulnerable group as the condition is not the remit of any one professional group. This inevitably leads to delay in formal diagnosis and management. There is a lack of systematic research on which to base guidelines for management. AIM: To develop, agree and validate key principles underlying the management of SM through a consensus process involving international experts, in order to create a local care pathway. METHODS: A local multi-agency consultation process developed 11 statements, which were felt to be the key principles underpinning a potential care pathway for managing SM. Thirteen recognised experts from North America, Europe and Australia participated in a modified Delphi process involving two rounds using a Likert-scale and free commentary. Both quantitative and qualitative analyses were used in the validation or revision of the statements at each stage. RESULTS: Response rates were 100% for Round 1 and 84.6% for Round 2. Despite the differing professional backgrounds and service contexts, by successive revision and/or revalidation of statements, it was possible to arrive at a consensus about key principles relating to early recognition, assessment and intervention. The agreed key principles are presented together with the resulting local care pathway. CONCLUSION: Through a Delphi process, agreement was reached by a multidisciplinary group of professionals, on key principles that underpin the timely identification, assessment and management of children with SM. These include the potential for staff in school/preschool settings to identify SM and that intervention programmes should generally be based in these settings. Children with SM should receive assessment for possible coexisting disorders, whether developmental, emotional or behavioural and additional specific intervention given for these. Agreementwas reached as to what constitutes clinical progress, intervals for monitoring progress, criteria for referral onwards for multidisciplinary specialist assessment and the role of selective serotonin reuptake inhibitor (SSRI) medication. A consensus methodology has been successfully used to compensate for the lack of evidence base and harness the expertise of a relatively small number of experienced professionals in order to provide a basis for the future development of services.
机译:背景:选择性默症(SM)现在被认为是一种焦虑症,它往往是一个知之甚少,高度复杂且未被广泛认可的临床实体。患有SM的儿童是弱势群体,因为条件不是任何一个专业群体的责任。这不可避免地导致正式诊断和管理的延迟。缺乏系统的研究作为管理指南的基础。目的:通过涉及国际专家的共识程序,开发,同意和验证SM管理基础的关键原则,以创造本地护理途径。方法:当地的多机构咨询程序制定了11项声明,这些声明被认为是管理SM的潜在护理途径的关键原则。来自北美,欧洲和澳大利亚的13名知名专家参加了经过改进的Delphi程序,该过程包括使用Likert量表和免费评论的两轮比赛。在每个阶段的陈述的确认或修订中均使用了定量和定性分析。结果:第一轮的回应率为100%,第二轮的回应率为84.6%。尽管专业背景和服务背景不同,但通过对陈述的连续修改和/或重新验证,就与早期有关的关键原则达成了共识。认可,评估和干预。介绍了商定的关键原则以及由此产生的本地护理途径。结论:通过德尔福过程,一个多学科的专业人员小组就关键原则达成了协议,这些原则为及时识别,评估和管理SM儿童提供了基础。这些包括学校/学前班环境中的员工识别SM的潜力,干预计划通常应基于这些环境。患有SM的儿童应接受对可能并存的疾病的评估,无论是发育,情感还是行为,都应针对这些疾病进行额外的特殊干预。就什么构成临床进展,监测进展的间隔,多学科专科医生评估的转诊标准以及选择性5-羟色胺再摄取抑制剂(SSRI)药物的作用达成了共识。已经成功地使用一种共识方法来弥补缺乏证据的基础,并利用相对较少的经验丰富的专业人员的专业知识,以便为服务的未来发展提供基础。

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