HALP(血红蛋白、白蛋白、淋巴细胞和血小板)评分能否区分肝外胆管梗阻患者肝外胆汁淤积的良恶性原因?

Northern clinics of Istanbul Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI:10.14744/nci.2024.23169
Ibrahimhalil Dusunceli, Zeynep Gok Sargin, Umut Celik, Fatih Sargin
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引用次数: 0

摘要

目的:胆汁淤积性疾病是一种常见的疾病,根据其病因分为良性和恶性。HALP是一种独特的营养免疫标志物,它结合了包括血红蛋白和白蛋白在内的营养状况指标,以及淋巴细胞和血小板计数等免疫功能标志物。我们研究了HALP评分在肝外胆汁淤积症患者中区分良恶性原因的能力。方法:采用横断面、回顾性研究方法。在2020年1月1日至2022年1月1日期间,被诊断为肝外胆汁淤积的患者被纳入研究。通过无创成像方法、内窥镜逆行胰胆管造影(ERCP)和组织活检结果确诊。根据肝外胆道梗阻的类型分为良性和恶性两组。HALP评分的计算方法是将患者的白蛋白(g/L)、血红蛋白(g/L)和淋巴细胞计数(/L)相乘,除以血小板计数(/L)。结果:216例肝外胆汁淤积121例为良性因素,以胆总管结石为主;95例为恶性因素,以胰头癌为主。结论:HALP评分不能区分肝外胆汁淤积的良恶性原因。
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Can HALP (Hemoglobin, albumin, lymphocyte, and platelet) score distinguish malignant and benign causes of extrahepatic cholestasis in patients with extrahepatic bile duct obstruction?

Objective: Cholestatic diseases are common and classified as benign or malignant based on their etiology. HALP is a unique nutritional immune marker that combines indicators of nutritional status, including hemoglobin and albumin, with immune function markers like lymphocyte and platelet counts. We investigated the HALP score's ability to differentiate between benign and malignant causes in extrahepatic cholestasis patients.

Methods: This research was designed as cross-sectional and retrospective. Between 1 January 2020-1 January 2022, patients diagnosed with extrahepatic cholestasis were included. The diagnoses were confirmed using non-invasive imaging methods, ERCP (endoscopic retrograde cholangiopancreatography), and tissue biopsy results. Based on the type of extrahepatic biliary obstruction, either benign or malignant, the patients were divided into two groups. The HALP score was calculated by multiplying the patient's albumin (g/L), hemoglobin (g/L), and lymphocyte count (/L) and dividing by the platelet count (/L).

Results: In 121 of 216 patients, extrahepatic cholestasis was caused by benign factors, mostly choledocholithiasis, while malignant causes, predominantly pancreatic head cancer, were responsible for extrahepatic cholestasis in 95 patients. The malignant cholestasis group had significantly higher bilirubin levels (p<0.001), lower hemoglobin levels (p=0.005), lower albumin levels (p<0.001), higher lymphocyte counts (p<0.001), and higher platelet levels (p=0.001) compared to the benign cholestasis group. There was no considerable difference in the HALP score between the two groups, as indicated by a p-value of 0.741.

Conclusion: The HALP score could not distinguish between benign and malignant causes of extrahepatic cholestasis.

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