Suppr超能文献

成人特发性巨直肠的临床特征与结局

Clinical features and outcomes of adult idiopathic megarectum.

作者信息

Wu Kyle, Little Robert D, Long Andrew, Khera Angela, Kamm Michael A, Basnayake Chamara

机构信息

St Vincent's Hospital Melbourne, Melbourne, Australia.

出版信息

Eur J Gastroenterol Hepatol. 2023 May 1;35(5):550-552. doi: 10.1097/MEG.0000000000002545. Epub 2023 Mar 18.

Abstract

OBJECTIVE

Idiopathic megarectum is characterized by abnormal, pronounced rectal dilatation in the absence of identifiable organic pathology. Idiopathic megarectum is uncommon and under-recognized. This study aims to describe the clinical features and management of idiopathic megarectum.

METHODS

A retrospective review was undertaken on patients diagnosed with idiopathic megarectum with or without idiopathic megacolon over a 14-year period until 2021. Patients were identified from the hospital's International Classification of Diseases codes, and pre-existing clinic patient databases. Patient demographics, disease characteristics, healthcare utilization and treatment history data were collected.

RESULTS

Eight patients with idiopathic megarectum were identified; half of the patients were female, with the median age of symptom onset being 14 years (interquartile range [IQR] 9-24). The median rectal diameter measured was 11.5 cm (IQR 9.4-12.1). The most common presenting symptom was constipation, bloating and faecal incontinence. All patients required prior sustained periods of regular phosphate enemas and 88% were using ongoing oral aperients. Concomitant anxiety and or depression were found in 63% of patients and 25% were diagnosed with an intellectual disability. Healthcare utilization was high with a median of three emergency department presentations or ward admissions related to idiopathic megarectum per patient over the follow-up period; 38% of patients required surgical intervention during the period of follow-up.

CONCLUSION

Idiopathic megarectum is uncommon and associated with significant physical and psychiatric morbidity and high healthcare utilization.

摘要

目的

特发性巨直肠的特征是在没有可识别的器质性病变的情况下出现异常、明显的直肠扩张。特发性巨直肠并不常见,且未得到充分认识。本研究旨在描述特发性巨直肠的临床特征和治疗方法。

方法

对截至2021年的14年间诊断为特发性巨直肠(无论是否伴有特发性巨结肠)的患者进行回顾性研究。通过医院的国际疾病分类编码和现有的临床患者数据库识别患者。收集患者的人口统计学资料、疾病特征、医疗利用情况和治疗史数据。

结果

共识别出8例特发性巨直肠患者;半数患者为女性,症状出现的中位年龄为14岁(四分位间距[IQR]9 - 24岁)。测量的直肠中位直径为11.5厘米(IQR 9.4 - 12.1)。最常见的症状是便秘、腹胀和大便失禁。所有患者之前都需要长期定期使用磷酸盐灌肠剂,88%的患者正在使用口服缓泻剂。63%的患者伴有焦虑和/或抑郁,25%的患者被诊断为智力残疾。医疗利用率很高,在随访期间,每位患者因特发性巨直肠平均有三次急诊科就诊或病房住院;38%的患者在随访期间需要手术干预。

结论

特发性巨直肠并不常见,与严重的身体和精神疾病以及高医疗利用率相关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验