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误诊是麦克尔病诊断延迟的一个重要因素。

Misdiagnosis is an important factor for diagnostic delay in McArdle disease.

作者信息

Scalco Renata Siciliani, Morrow Jasper M, Booth Suzanne, Chatfield Sherryl, Godfrey Richard, Quinlivan Ros

机构信息

MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK; CAPES Foundation, Ministry of Education of Brazil, Brasilia, DF, Brazil.

MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience, University College London Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

出版信息

Neuromuscul Disord. 2017 Sep;27(9):852-855. doi: 10.1016/j.nmd.2017.04.013. Epub 2017 May 3.

Abstract

Diagnosis of McArdle disease is frequently delayed by many years following the first presentation of symptoms to a health professional. The aim of this study was to investigate the importance of misdiagnosis in delaying diagnosis of McArdle disease. The frequency of misdiagnosis, duration of diagnostic delay, categories of misdiagnoses and inappropriate medical interventions were assessed in 50 genetically confirmed patients. The results demonstrated a high frequency of misdiagnosis (90%, n = 45/50) most commonly during childhood years (67%; n = 30/45) compared with teenage years and adulthood (teenage: n = 7/45; adult n = 5/45; not known n = 3/45). The correct diagnosis of McArdle disease was rarely made before adulthood (median age of diagnosis 33 years). Thirty-one patients (62%) reported having received more than one misdiagnosis; the most common were "growing pains" (40%, n = 20) and "laziness/being unfit" (46%, n = 23). A psychiatric/psychological misdiagnosis was significantly more common in females than males (females 6/20; males 1/30; p < 0.01). Of the 45 patients who were misdiagnosed, 21 (47%) received incorrect management. This study shows that most patients with McArdle disease received an incorrect explanation of their symptoms providing evidence that misdiagnosis plays an important part in delaying implementation of appropriate medical advice and management to this group of patients.

摘要

从首次向医疗专业人员报告症状起,麦克尔迪氏病的诊断常常会延迟许多年。本研究的目的是调查误诊在麦克尔迪氏病诊断延迟中的重要性。在50例经基因确诊的患者中评估了误诊频率、诊断延迟时长、误诊类别及不恰当的医疗干预措施。结果显示误诊频率很高(90%,n = 45/50),最常见于儿童期(67%;n = 30/45),相比青少年期和成年期(青少年期:n = 7/45;成年期:n = 5/45;情况不明:n = 3/45)。麦克尔迪氏病很少在成年前得到正确诊断(诊断的中位年龄为33岁)。31例患者(62%)报告曾不止一次被误诊;最常见的误诊是“生长痛”(40%,n = 20)和“懒惰/身体不适”(46%,n = 23)。女性的精神科/心理科误诊显著多于男性(女性6/20;男性1/30;p < 0.01)。在45例被误诊的患者中,21例(47%)接受了错误的治疗。本研究表明,大多数麦克尔迪氏病患者对其症状得到了错误的解释,这证明误诊在延迟向这组患者提供适当医疗建议和治疗方面起到了重要作用。

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