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非典型神经性厌食症的诊断应排除那些终生患有神经性厌食症的患者:对沃尔什、哈根和洛克伍德(2022年)的评论。

Atypical anorexia nervosa diagnosis should exclude those with lifetime anorexia nervosa: Commentary on Walsh, Hagan, and Lockwood (2022).

作者信息

Eddy Kamryn T, Breithaupt Lauren

机构信息

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, Massachusetts, USA.

Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Int J Eat Disord. 2023 Apr;56(4):838-840. doi: 10.1002/eat.23924. Epub 2023 Feb 28.

Abstract

Atypical anorexia nervosa (AN) is not well-defined. Walsh, Hagan, and Lockwood (2022) review the data on atypical AN published in the last decade demonstrating overwhelming clinical similarities between atypical AN and AN. As written, atypical AN includes at least three clinical presentations that may not have the same underlying illness, and in turn, may have different prognoses and treatment needs: (1) higher-weight AN; (2) prodromal AN; and (3) partial remission from AN. While useful for the first two presentations, we suggest that the atypical AN diagnosis is not appropriate for those in partial remission from AN. Extant data document symptom fluctuation is part of illness course in AN rather than crossover to a distinct disorder. Further, lifetime AN carries the greatest risk for relapse to low-weight, premature death, and medical morbidities. Finally, emerging data support unique biobehavioral mechanisms in AN suggesting its combination with atypical AN is premature. Therefore, at this time, we recommend that the atypical AN diagnosis be reserved for those without lifetime AN. We encourage research to test and validate operational definitions of atypical AN and partial remission from AN, and further suggest documentation of lifetime AN across the eating disorders given its prognostic value.

摘要

非典型神经性厌食症(AN)的定义并不明确。沃尔什、哈根和洛克伍德(2022年)回顾了过去十年发表的关于非典型AN的数据,表明非典型AN与AN之间存在压倒性的临床相似性。如前所述,非典型AN包括至少三种临床表现,它们可能没有相同的潜在疾病,进而可能有不同的预后和治疗需求:(1)体重较高的AN;(2)前驱性AN;以及(3)AN部分缓解。虽然这对于前两种表现形式有用,但我们认为非典型AN诊断不适用于AN部分缓解的患者。现有数据表明,症状波动是AN病程的一部分,而非转变为一种截然不同的疾病。此外,终生AN复发至低体重、过早死亡和医学并发症的风险最大。最后,新出现的数据支持AN中独特的生物行为机制,这表明将其与非典型AN合并还为时过早。因此,目前我们建议非典型AN诊断仅适用于无终生AN的患者。我们鼓励开展研究以测试和验证非典型AN及AN部分缓解的操作定义,并鉴于其预后价值,进一步建议记录进食障碍患者的终生AN情况。

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