Baylor University Medical Center, Texas A&M University, Dallas, Texas, USA.
J Gastroenterol Hepatol. 2014 Jan;29(1):6-25. doi: 10.1111/jgh.12392.
Diarrhea is best defined as passage of loose stools often with more frequent bowel movements. For clinical purposes, the Bristol Stool Form Scale works well to distinguish stool form and to identify loose stools. Laboratory testing of stool consistency has lagged behind. Acute diarrhea is likely to be due to infection and to be self-limited. As diarrhea becomes chronic, it is less likely to be due to infection; duration of 1 month seems to work well as a cut-off for chronic diarrhea, but detailed scientific knowledge is missing about the utility of this definition. In addition to duration of diarrhea, classifications by presenting scenario, by pathophysiology, and by stool characteristics (e.g. watery, fatty, or inflammatory) may help the canny clinician refine the differential diagnosis of chronic diarrhea. In this regard, a careful history remains the essential part of the evaluation of a patient with diarrhea. Imaging the intestine with endoscopy and radiographic techniques is useful, and biopsy of the small intestine and colon for histological assessment provides key diagnostic information. Endomicroscopy and molecular pathology are only now being explored for the diagnosis of chronic diarrhea. Interest in the microbiome of the gut is increasing; aside from a handful of well-described infections because of pathogens, little is known about alterations in the microbiome in chronic diarrhea. Serological tests have well-defined roles in the diagnosis of celiac disease but have less clearly defined application in autoimmune enteropathies and inflammatory bowel disease. Measurement of peptide hormones is of value in the diagnosis and management of endocrine tumors causing diarrhea, but these are so rare that these tests are of little value in screening because there will be many more false-positives than true-positive results. Chemical analysis of stools is of use in classifying chronic diarrhea and may limit the differential diagnosis that must be considered, but interpretation of the results is still evolving. Breath tests for assessment of carbohydrate malabsorption, small bowel bacterial overgrowth, and intestinal transit are fraught with technical limitations that decrease sensitivity and specificity. Likewise, tests of bile acid malabsorption have had limited utility beyond empirical trials of bile acid sequestrants.
腹泻最好的定义是通过松散的粪便经常更频繁的排便。为了临床目的,布里斯托尔粪便形态量表很好地区分了粪便的形态并识别出松散的粪便。粪便一致性的实验室检测落后了。急性腹泻可能是由感染引起的,并具有自限性。随着腹泻变为慢性,其不太可能由感染引起;1 个月的持续时间似乎很好地作为慢性腹泻的截止值,但关于该定义的实用性缺乏详细的科学知识。除了腹泻的持续时间外,根据出现的情况、病理生理学和粪便特征(例如水样、脂肪样或炎症性)进行分类可以帮助有经验的临床医生细化慢性腹泻的鉴别诊断。在这方面,仔细的病史仍然是评估腹泻患者的重要部分。使用内镜和放射技术对肠道进行成像很有用,对小肠和结肠进行活检以进行组织学评估提供了关键的诊断信息。内镜下黏膜活检和分子病理学目前仅用于慢性腹泻的诊断。人们对肠道微生物组的兴趣正在增加;除了少数因病原体引起的描述明确的感染外,对慢性腹泻中微生物组的改变知之甚少。血清学检测在诊断乳糜泻方面具有明确的作用,但在自身免疫性肠病和炎症性肠病中的应用定义不太明确。肽激素的测量对诊断和管理引起腹泻的内分泌肿瘤具有价值,但这些肿瘤非常罕见,以至于这些检测在筛查中几乎没有价值,因为假阳性结果会比真阳性结果多得多。粪便的化学分析在分类慢性腹泻方面具有一定的价值,并且可能会限制需要考虑的鉴别诊断,但结果的解释仍在不断发展。用于评估碳水化合物吸收不良、小肠细菌过度生长和肠道转运的呼吸试验存在技术限制,降低了敏感性和特异性。同样,胆汁酸吸收不良的检测除了经验性试验胆汁酸螯合剂之外,其应用也有限。