Astley Susan J, Bledsoe Julia M, Davies Julian K, Thorne John C
University of Washington, Seattle, WA, USA.
Adv Pediatr Res. 2017;4(3). doi: 10.12715/apr.2017.4.13. Epub 2017 Oct 30.
As clinicians strive to achieve consensus worldwide on how best to diagnose fetal alcohol spectrum disorders (FASD), the most recent FASD diagnosstic systems exhibit convergence and divergence. Applying these systems to a single clinical population illustrates contrasts between them, but validation studies are ultimately required to identify the best system. Currently, only the 4-Digit Code has published comprehensive validation studies.
The 4-Digit Code and Hoyme 2016 FASD systems were applied to the records of 1,392 patients evaluated for FASD at the University of Washington to: 1) Compare the diagnostic criteria and tools used by each system, 2) Compare the prevalence and concordance of diagnostic outcomes and assess measures of validity.
Only 38% of patients received concordant diagnoses. The Hoyme criteria rendered half as many diagnoses under the umbrella of FASD (n=558) as the 4-Digit Code (n=1,092) and diagnosed a much higher proportion (53%) as fetal alcohol syndrome/partial fetal alcohol syndrome (FAS/PFAS) than the 4-Digit Code (7%). Key Hoyme factors contributing to discordance included relaxation of facial criteria (40% had the Hoyme FAS face, including patients with confirmed absence of alcohol exposure); setting alcohol exposure thresholds prevented 1/3 with confirmed exposure from receiving FAS/FASD diagnoses; and setting minimum age limits for Alcohol-Related Neurodevelopmental Disorder prevented 79% of alcohol-exposed infants with neurodevelopmental impairment a FASD diagnosis. The Hoyme Lip/Philtrum Guides differ substantively from the 4-Digit Lip-Philtrum Guides and thus are not valid for use with the 4-Digit Code.
All FASD diagnostic systems need to publish comprehensive validation studies to identify which is the most accurate, reproducible, and medically valid.
随着临床医生努力在全球范围内就如何最好地诊断胎儿酒精谱系障碍(FASD)达成共识,最新的FASD诊断系统呈现出趋同与分歧。将这些系统应用于单一临床群体可说明它们之间的差异,但最终需要进行验证研究以确定最佳系统。目前,只有四位数编码系统发表了全面的验证研究。
将四位数编码系统和霍伊姆2016年FASD系统应用于华盛顿大学接受FASD评估的1392例患者的记录,以:1)比较每个系统使用的诊断标准和工具;2)比较诊断结果的患病率和一致性,并评估有效性指标。
只有38%的患者得到了一致的诊断。在FASD范畴内,霍伊姆标准做出的诊断数量(n = 558)仅为四位数编码系统(n = 1092)的一半,且诊断为胎儿酒精综合征/部分胎儿酒精综合征(FAS/PFAS)的比例(53%)远高于四位数编码系统(7%)。导致不一致的关键霍伊姆因素包括面部标准的放宽(40%有霍伊姆FAS面容,包括确认无酒精暴露的患者);设定酒精暴露阈值使三分之一确认有暴露的患者无法获得FAS/FASD诊断;以及设定酒精相关神经发育障碍的最低年龄限制使79%有神经发育障碍的酒精暴露婴儿无法获得FASD诊断。霍伊姆唇/人中指南与四位数唇-人中指南有实质性差异,因此不适用于四位数编码系统。
所有FASD诊断系统都需要发表全面的验证研究,以确定哪一个最准确、可重复且在医学上有效。