Identifying patients with undiagnosed primary biliary cholangitis using a clinical management process.

IF 3.7 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Agustin Castiella, Maria José Sánchez-Iturri, Jon Stampa, Beatriz Fernandez, Iñigo Garaizabal, Alvaro Prada, Silvia Torrente, Leire Aburruza, Eva Zapata
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Abstract

Introduction and objectives: Early diagnosis of primary biliary cholangitis (PBC) is fundamental, as treatment with ursodeoxycholic acid (UDCA) prevents its progression. The aim of our study is to investigate undiagnosed patients in our region and to treat retrieved patients.

Patients and methods: Analysis of databases (immunology, biochemistry and other data from their medical records) was performed between January 2019 and December 2021. PBC was diagnosed if anti-mitochondrial antibodies were positive (>1:80) and alkaline phosphatase (AP) was chronically elevated in the absence of other liver disease. Identified patients were contacted.

Results: A total of 306 patients were identified and 221 had previously been diagnosed with PBC and were undergoing treatment. Fifty-one patients did not meet the current criteria for diagnosis and treatment at their last blood test. Six patients had died by the time the study started. Finally, we found 28 patients with a probable diagnosis of PBC who could benefit from treatment (9.6%). We contacted all 28 patients and 16 (57.14%) of them agreed to come to our hospital for diagnosis confirmation, ultrasound and fibroscan. All of them were women, aged between 46 and 74 years (mean 61.18, SD 9.19). Laboratory analysis showed a mean AP of 144.25 (SD 71.03) and mean GGPT of 115.62 (SD 98.42). Mean bilirubin was 0.55 (SD 0.22). Fibroscan showed a mean value of 6.05 kPa. UDCA was initiated in 14 patients; two patients refused treatment.

Conclusions: The use of hospital databases enabled us to diagnose and treat 16 (57.14%) of the 28 detected patients.

使用临床管理程序识别未确诊的原发性胆管炎患者。
简介和目的:早期诊断原发性胆管炎(PBC)是基础,因为熊去氧胆酸(UDCA)治疗可防止其进展。本研究的目的是调查本地区未确诊的患者并治疗复发患者。患者和方法:在2019年1月至2021年12月期间,对数据库(免疫学、生物化学和其他医疗记录数据)进行了分析。如果抗线粒体抗体阳性(>1:80)和碱性磷酸酶(AP)在没有其他肝脏疾病的情况下长期升高,则诊断为PBC。联系了已确认的患者。结果:共有306例患者被确定,其中221例先前被诊断为PBC并正在接受治疗。51例患者最后一次血检不符合现行诊断和治疗标准。到研究开始时,已有6名患者死亡。最后,我们发现28例可能诊断为PBC的患者可以从治疗中获益(9.6%)。我们联系了所有28例患者,其中16例(57.14%)同意来我院进行诊断确认、超声和纤维扫描。所有患者均为女性,年龄在46 ~ 74岁之间(平均61.18岁,SD 9.19)。实验室分析显示平均AP为144.25 (SD 71.03),平均GGPT为115.62 (SD 98.42)。平均胆红素为0.55 (SD 0.22)。纤维扫描显示平均值为6.05 kPa。14例患者开始UDCA;两名患者拒绝治疗。结论:利用医院数据库对28例检出患者中的16例(57.14%)进行了诊断和治疗。
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
Annals of hepatology
Annals of hepatology 医学-胃肠肝病学
CiteScore
7.90
自引率
2.60%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.
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