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当产前酒精暴露情况不明时,诊断胎儿酒精综合征需要高度的面部特异性和阳性预测值。

High facial specificity and positive predictive value are required to diagnose fetal alcohol syndrome when prenatal alcohol exposure is unknown.

作者信息

Astley Hemingway Susan J

机构信息

University of Washington, Seattle WA 98195 USA.

出版信息

Adv Pediatr Res. 2020;7(4). Epub 2020 Nov 6.

PMID:37228766
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10208451/
Abstract

BACKGROUND

Facial criteria with high specificity and positive predictive value (PPV) to prenatal alcohol exposure (PAE) are required to diagnose fetal alcohol syndrome (FAS) when documentation of PAE is unavailable. Not all fetal alcohol spectrum disorder (FASD) diagnostic guidelines appear to meet these criteria.

METHODS

A dataset generated from a 10-year FAS screening of 1,602 children in fostercare conducted by the University of Washington FAS Diagnostic & Prevention Network was used to determine how well the FAS facial phenotype, microcephaly and growth deficiency (individually and in combination at varying levels of magnitude) predicted PAE.

RESULTS

The 4-Digit-Code Rank 4 FAS facial phenotype was the only outcome that provided sufficient PPV and specificity to PAE (100%) to allow the facial phenotype to serve as confirmation of PAE in a diagnostic setting when PAE is unknown. Even minimal relaxation of the phenotype (e.g., Face Rank 3) resulted in PPV (35%) and specificity (88.7%) values too low to use as confirmation of PAE. Further relaxation of the facial criteria, as defined by the Hoyme et al., 2016 FASD guidelines, resulted in even lower PPV (17.9%) and specificity (76.6%); both too low to serve as confirmation of PAE in a diagnostic setting. The presence of all three physical features of FAS (Hoyme et al FAS facial phenotype, growth and OFC ≤10 percentile) did not increase PPV beyond chance (52%).

CONCLUSIONS

FASD diagnostic guidelines that use relaxed criteria for the FAS facial phenotype risk misdiagnosing and over-diagnosing FAS and partial FAS when PAE is unknown.

摘要

背景

当无法获得产前酒精暴露(PAE)的记录时,需要具有高特异性和阳性预测值(PPV)的面部标准来诊断胎儿酒精综合征(FAS)。并非所有胎儿酒精谱系障碍(FASD)诊断指南似乎都符合这些标准。

方法

使用华盛顿大学FAS诊断与预防网络对1602名寄养儿童进行的为期10年的FAS筛查生成的数据集,以确定FAS面部表型、小头畸形和生长发育迟缓(单独以及不同程度组合)对PAE的预测效果。

结果

4位数字编码等级4的FAS面部表型是唯一对PAE具有足够PPV和特异性(100%)的结果,使得在PAE未知的诊断环境中,面部表型可作为PAE的确认依据。即使对面部表型进行最小程度的放宽(例如面部等级3),PPV(35%)和特异性(88.7%)值也会过低,无法用作PAE的确认依据。按照Hoyme等人2016年FASD指南所定义的对面部标准进一步放宽,会导致更低的PPV(17.9%)和特异性(76.6%);两者都过低,无法在诊断环境中用作PAE的确认依据。FAS的所有三个身体特征(Hoyme等人的FAS面部表型、生长发育和枕额径≤第10百分位数)的存在并没有使PPV超出偶然概率(52%)而增加。

结论

当PAE未知时,使用放宽的FAS面部表型标准的FASD诊断指南有对FAS和部分FAS进行误诊和过度诊断的风险。

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18q12.3-q21.1 microdeletion detected in the prenatally alcohol-exposed dizygotic twin with discordant fetal alcohol syndrome phenotype.
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