口服胆酸盐激发试验的初步临床经验:来自2023-2024早期准入计划的结果

Stuart C. Gordon, James Burton, Bhaktasharan Patel, EAP Participants
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引用次数: 0

摘要

用于代偿性晚期慢性肝病的口服胆酸盐刺激试验于2023-2024年通过早期准入计划(EAP)推出。测试提供给了美国5个肝脏中心的16名临床医生。测试的患者(n = 129)代表了一系列的病因和疾病分期。最主要的临床用途是:(1)告知内镜检查静脉曲张的决定(n = 56, 43%);(2)确定大食管静脉曲张(LEV)的风险(n = 92, 71%);(3)监测疾病进展或治疗效果的基线(n = 33, 26%)。该测试的疾病严重程度指数(DSI)根据门脉高压和LEV的风险对患者进行分层:低危49例(38%),中危31例(24%),高危49例(38%)。在临床实践中,DSI≤18.3对避免EGD的潜在影响(38%)与先前验证研究中观察到的结果(41%)相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Initial Clinical Experience With the Oral Cholate Challenge Test: Results From the 2023–2024 Early Access Program

Initial Clinical Experience With the Oral Cholate Challenge Test: Results From the 2023–2024 Early Access Program

The oral cholate challenge test of liver health, intended for use in compensated advanced chronic liver disease, was launched through an Early Access Program (EAP) in 2023–2024. Tests were provided to 16 clinicians at five liver centres across the US. The tested patients (n = 129) represented a range of etiologies and stages of disease. Top clinical uses were: (1) informing the decision for endoscopy to test for varices (n = 56, 43%), (2) defining risk for large oesophageal varices (LEV) (n = 92, 71%), and (3) baseline for monitoring disease progression or treatment effects (n = 33, 26%). The test's disease severity index (DSI) stratified patients according to risk for portal hypertension and LEV: 49 (38%) low risk, 31 (24%) moderate risk and 49 (38%) high risk. The potential impact of DSI ≤ 18.3 on EGD avoidance (38%) in clinical practice replicated that which was observed in prior validation studies (41%).

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