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Vol. 19. Issue S1.
Abstracts of the 2020 Annual meeting of the Mexican Association of Hepatology (AMH) – XV Congreso Nacional de Hepatología (23-25 de julio)
Pages 16 (September 2020)
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Vol. 19. Issue S1.
Abstracts of the 2020 Annual meeting of the Mexican Association of Hepatology (AMH) – XV Congreso Nacional de Hepatología (23-25 de julio)
Pages 16 (September 2020)
34
Open Access
Characterization of patients with primary sclerosing cholangitis in a third level hospital
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V. López Ladrón de Guevara, C. Alonzo García, A. Vélez Carrión, F. Thomas Lora, B. Astudillo Romero, E. Márquez Guillén, C. Moctezuma Velázquez, N.C. Flores García, G. Castro Narro, A. Torre Delgadillo
Departamento de Gastroenterología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México
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Background and aim: Primary sclerosing cholangitis (CEP) is a syndrome of unknown cause, but it may be the result of an environmental insult that occurs in patients genetically susceptible to the disease, which would indicate an autoimmune component. Aim: To describe the clinical characteristics, treatment and complications of patients with Primary Sclerosing Cholangitis

Material and methods: Design: retrospective, cross-sectional study. It was held at INNSZ during 2009-2019. 40 patients were included with the diagnosis of Primary Sclerosing Cholangitis, Both genders, ages 18-69 years. Statistic analysis: Percentages, means, medians with standard deviation were used. The X2 test was used. A value of p0.05 was considered statistically significant with a 95% confidence interval. The analysis was carried out using the statistical package SPSS® v. 25

Results: The number of patients was 40, male predominance in 52.5%, with a median age of 53 years and body mass index of 22.9. 22.7% of the patients had arterial hypertension and Type 2 Diabetes Mellitus as comorbidity. Cholecystectomy was the surgical antecedent in 29.5%. The predominant symptom at the time of diagnosis was jaundice in 57.5%. Primary large duct sclerosing cholangitis was observed in 92.5%, cirrhosis in 83%. and association with ulcerative colitis in 67.6%. 77% of the patients received ursodeoxycholic acid. Recurrent cholangitis presented in 37.5%. Liver transplant 30%, mortality was 12.5%, identifying as cause of death: n=2 due to complications from liver cirrhosis, n=1 due to infection, n=1 due to liver transplant complications and n=1 due to cholangiocarcinoma.

Conclusions: 1. Primary Sclerosing Cholangitis was presented predominantly in men, with a median of aged 53 years and associated with UC, 77% of the patients received medical treatment with AUDC. 2. Complications: recurrent cholangitis and dominant stenosis. 3. Liver transplant in 30%. 4. Main cause of death was due to complications associated with liver cirrhosis.

Conflicts of interest: The authors have no conflicts of interest to declare.

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