Abstract

The publication of Australian fetal alcohol spectrum disorder (FASD) diagnostic guidelines marks an important step forward in Australia’s efforts to prevent FASD. But do we need yet another set of FASD guidelines? At the 5th International FASD Conference, the ever growing number of FASD diagnostic guidelines was identified as a core area of concern by leaders in FASD worldwide. All agreed we need to strive to adopt a single set of guidelines. It is essential that FASD diagnosis advance to incorporate new knowledge and technology. But to date, the field of FASD has seen multiple sets of guidelines published that do not address the important question-How is the performance of these new guidelines superior to the performance of existing guidelines to warrant/justify their introduction into the medical literature?The Australian guidelines include FAS, PFAS and Neurodevelopmental Disorder-Alcohol Exposed (ND-AE). This latter group includes individuals with severe CNS abnormalities without the physical features of FAS. This is the group the 4-Digit-Code calls Static-Encephalopathy-Alcohol-Exposed (SE-AE). The criteria for FAS, PFAS, and ND-AE (or what the 4-Digit-Code calls SE-AE) are identical between the Australian and 4-Digit-Code guidelines with the exception of one very small, but very consequential difference in facial criteria for PFAS. The 4-Digit-Code requires a Rank 3 FAS facial phenotype for PFAS (J Popul Ther Clin Pharmacol20(3):e416–e467, 2013); the Australian guidelines relax the criteria to include the Rank 2 FAS facial phenotype. This relaxation of the criteria renders the facial phenotype NOT specific to prenatal alcohol exposure as confirmed in published empirical studies. If the facial phenotype is not specific to (caused only by) prenatal alcohol exposure one can no longer validly call the outcome PFAS. When one makes a diagnosis of FAS (full or partial), one is stating explicitly that the individual has a syndrome caused by prenatal alcohol exposure. One is also stating explicitly that the biological mother drank alcohol during pregnancy and, as a result, harmed her child. These are bold conclusions to draw and are not without medical, ethical, and even legal consequences. So the question remains-Why go against the published empirical evidence and relax the PFAS facial criteria into the normal range?

Highlights

  • The field of fetal alcohol spectrum disorder (FASD) has seen multiple sets of guidelines published that do not address the important question-How is the performance of these new guidelines superior to the performance of existing guidelines to warrant/justify their introduction into the medical literature [2]? At the 5th International FASD Conference in 2013, the ever growing number of FASD diagnostic guidelines was identified as a core area of concern by leaders in FASD worldwide

  • This study clearly demonstrated that the partial fetal alcohol syndrome (PFAS) facial phenotype proposed in the Australian guidelines is not observed exclusively among children damaged by prenatal alcohol exposure

  • When one makes a diagnosis of FAS, one is stating explicitly that the individual has a syndrome caused by prenatal alcohol exposure

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Summary

Background

We recently published Australian recommendations for FASD screening and diagnosis [1] with the aim of supporting clinical decisionmaking to improve the identification, management and prevention of these disorders based on a standard national approach. In her commentary on our recommendations, Astley has raised some important questions about the need for these guidelines, the publication of this work and the recommended criteria for the diagnosis of partial fetal alcohol syndrome (PFAS). Competing interests The author declares that she has no competing interests

21. Astley S
Findings
23. Institute of Medicine
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