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Assessing Prenatal Alcohol Exposure History for Pediatric Patients: Practices Among U.S. Clinicians
Janae Dunkley1,2, Nicholas P Deputy3,4, Clark H Denny3
1Division of Birth Defects and Infant Disorders, National Center On Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, 4770 Buford Hwy NE, Atlanta, Chamblee, GA, 30341, USA. janae.dunkley@emory.edu.
Insights
Clinicians rarely screen for prenatal alcohol exposure (PAE) in all pediatric patients, missing opportunities to identify children with fetal alcohol spectrum disorders (FASDs). Improved training and support are needed for routine PAE history collection.
Area of Science:
- Pediatric healthcare
- Public health
- Clinical practice guidelines
Background:
- The American Academy of Pediatrics recommends screening for prenatal alcohol exposure (PAE) in pediatric patients.
- Screening facilitates identification of fetal alcohol spectrum disorders (FASDs) and access to interventions.
Purpose of the Study:
- To evaluate the frequency of PAE history assessment by clinicians in pediatric patient interactions.
- To determine the methods used by clinicians to ascertain PAE information.
Main Methods:
- Analysis of data from the Fall 2020 DocStyles web-based survey of 1754 primary healthcare professionals.
- Calculation of PAE assessment frequency by clinician specialty (pediatricians, family practitioners, NP/PAs) and patient population.
- Statistical comparison of assessment frequency across specialties using chi-square and Bonferroni tests.
Main Results:
- Approximately 70.5% of clinicians often/always obtained PAE history for children with developmental issues, 63.0% for adopted/foster children, and 60.7% for newborns.
- Less than half collected PAE history from parents of infants (47.6%) and new patients (38.2%).
- Pediatricians were more likely than family practitioners to collect PAE history for adopted/foster children (71.5% vs. 57.7%).
Conclusions:
- Prenatal alcohol exposure (PAE) history is not routinely obtained for all pediatric patients.
- Findings indicate a need for enhanced clinician training and practice support.
- Improved screening can aid in identifying and treating children at risk for FASDs.
Objectives:
The American Academy of Pediatrics recommends clinicians who treat pediatric patients screen for prenatal alcohol exposure (PAE) to facilitate the identification of children with fetal alcohol spectrum disorders and promote timely access to behavioral and cognitive interventions. We evaluated how frequently clinicians inquire about PAE in their pediatric patient interactions and the methods used to ascertain this information.
Methods:
We analyzed data from the Fall 2020 DocStyles survey, a web-based survey of primary healthcare professionals (n = 1754). Distributions for frequency of assessing PAE history for five pediatric populations and the methods used were calculated by clinician specialty (family practitioners [FP], pediatricians, and nurse practitioners/physician assistants [NP/PAs]) and overall. Chi-square and Bonferroni post-hoc tests determined whether frequency of assessing PAE history varied by specialty.
Results:
Among 779 clinicians serving pediatric patients, approximately 70.5%, 63.0%, and 60.7% reported often/always obtaining PAE history from parents of children with developmental/behavioral issues, adopted/foster children, and newborns, respectively. By contrast, less than half of respondents reported often/always collecting this information from parents of infants (47.6%) and new patients (38.2%). Most respondents reported collecting PAE history through interviews conducted by physicians or physician assistants (69.7%). Obtaining PAE history varied by specialty; pediatricians (71.5%) were more likely to collect PAE history for adopted/foster children when compared to FPs (57.7%, p = 0.003).
Conclusions For Practice:
PAE history is not routinely obtained for pediatric patients. These findings highlight the need for trainings and practice supports to aid clinicians in identifying and treating children at-risk of FASDs.
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