University of Washington, Division of Gastroenterology and Hepatology, Seattle, Washington, USA.
Department of Medicine Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, Washington, USA.
Am J Gastroenterol. 2023 Jun 1;118(6):1096-1100. doi: 10.14309/ajg.0000000000002211. Epub 2023 Feb 3.
We compared critical flicker frequency (CFF) thresholds obtained using a novel portable device "Beacon" with thresholds from the commercially available Lafayette Flicker Fusion System (Lafayette-FFS) in patients with cirrhosis.
One hundred fifty-three participants with chronic liver disease underwent CFF testing using Beacon and Lafayette-FFS with a method-of-limits and/or forced-choice protocol.
Beacon demonstrated excellent test-retest reliability (intraclass correlation 0.91-0.97) and good correlation with the Lafayette-FFS values (intraclass correlation 0.77-0.84). Forced-choice CFF were on average 4.1 Hz higher than method-of-limits descending CFFs.
Beacon can be self-administered by patients with chronic liver disease and cirrhosis to measure CFF, a validated screening test for minimal hepatic encephalopathy.
我们比较了使用新型便携式设备“Beacon”获得的临界闪烁频率(CFF)阈值与 Lafayette 闪烁融合系统(Lafayette-FFS)的商业可用阈值,该系统用于肝硬化患者。
153 名慢性肝病患者使用 Beacon 和 Lafayette-FFS 进行 CFF 测试,采用极限法和/或迫选法方案。
Beacon 表现出极好的测试-重测可靠性(组内相关系数 0.91-0.97),与 Lafayette-FFS 值具有良好的相关性(组内相关系数 0.77-0.84)。迫选 CFF 平均比极限法下降 CFF 高 4.1Hz。
Beacon 可由慢性肝病和肝硬化患者自行使用,以测量临界闪烁频率(CFF),这是一种用于最小型肝性脑病的验证性筛选测试。