Why are rare diseases underdiagnosed? A clinical management study on detection of primary biliary cholangitis in primary care.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES
Francesco Donato, Marie Graciella Pigozzi, Giulia Colarieti, Marco Festa, Erminio Tabaglio
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Abstract

Background: There are about 7,000 rare diseases that affect 10% of the world population. Primary biliary cholangitis, an autoimmune chronic liver disease of the interlobular bile ducts, is one of the most common causes of chronic cholestasis. However, it is a rare, often underdiagnosed and undertreated, disease which can lead to cirrhosis and liver failure. We aimed to assess the proportion of undetected primary biliary cholangitis patients in primary care through a clinical management process.

Methods: We made two extractions of the clinical data concerning liver diseases, risk factors and laboratory tests from the databases of a sample of general practitioners, with a check and correction of mistakes. The clinical data of the patients without liver disease and major risk factors, and with serum Alkaline Phosphatase above the laboratory reference values, were re-evaluated by each general practitioner with an expert gastroenterologist. The patients with elevated Alkaline Phosphatase values and without evidence of intrahepatic or extrahepatic causes of cholestasis were considered suspected for primary biliary cholangitis and assessed for antimitochondrial antibodies test and specialist' s evaluation, according to present guidelines.

Results: A total of 20,480 adults attending 14 general practitioners in the province of Brescia, Northern Italy, were included in the study. Nine patients had a prior primary biliary cholangitis diagnosis, with a prevalence of 43.9/100000. After excluding 2094 (10.2%) patient with liver diseases or other causes of cholestasis, 121 subjects with Alkaline Phosphatase above the reference values were re-evaluated by the general practitioners and gastroenterologist, and 27 patients without symptoms or signs of cholestasis were considered suspected for primary biliary cholangitis: 9 of them were tested for antimitochondrial antibodies, and three new primary biliary cholangitis cases were detected (+33%).

Discussion and conclusions: This study shows that there is a not negligible burden of undetected cases of adult rare diseases that can be diagnosed in primary care, through a disease management procedure, without modifying the routine clinical practice.

罕见疾病为何诊断不足?关于在初级保健中发现原发性胆汁性胆管炎的临床管理研究。
背景:全球约有 7000 种罕见病,影响着 10% 的人口。原发性胆汁性胆管炎是小叶间胆管的一种自身免疫性慢性肝病,是慢性胆汁淤积症最常见的病因之一。然而,它是一种罕见的疾病,往往诊断不足、治疗不及时,可导致肝硬化和肝功能衰竭。我们的目的是通过临床管理流程评估基层医疗机构中未发现的原发性胆汁性胆管炎患者的比例:我们从全科医生样本数据库中提取了两次有关肝病、风险因素和实验室检查的临床数据,并进行了检查和纠错。没有肝病和主要危险因素,但血清碱性磷酸酶高于实验室参考值的患者的临床数据,由每位全科医生和一位消化内科专家重新评估。碱性磷酸酶值升高且无肝内或肝外原因导致胆汁淤积的患者被认为疑似原发性胆汁性胆管炎,并根据现行指南进行抗线粒体抗体检测和专家评估:意大利北部布雷西亚省的 14 名全科医生共接诊了 20480 名成年人。9名患者曾被诊断为原发性胆汁性胆管炎,发病率为43.9/10万。在排除了2094名(10.2%)患有肝病或其他原因导致胆汁淤积的患者后,121名碱性磷酸酶高于参考值的受试者接受了全科医生和消化科医生的重新评估,27名没有胆汁淤积症状或体征的患者被认为疑似原发性胆汁性胆管炎:其中9人接受了抗线粒体抗体检测,发现了3个新的原发性胆汁性胆管炎病例(+33%):这项研究表明,成人罕见病中未被发现的病例数量不容忽视,这些病例可以通过疾病管理程序在初级保健中得到诊断,而无需改变常规临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annali di igiene : medicina preventiva e di comunita
Annali di igiene : medicina preventiva e di comunita HEALTH CARE SCIENCES & SERVICES-
CiteScore
3.40
自引率
0.00%
发文量
69
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