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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="research-article"><?properties manuscript?><front><journal-meta><journal-id journal-id-type="nlm-journal-id">101631607</journal-id><journal-id journal-id-type="pubmed-jr-id">42487</journal-id><journal-id journal-id-type="nlm-ta">Curr Dev Disord Rep</journal-id><journal-id journal-id-type="iso-abbrev">Curr Dev Disord Rep</journal-id><journal-title-group><journal-title>Current developmental disorders reports</journal-title></journal-title-group><issn pub-type="epub">2196-2987</issn></journal-meta><article-meta><article-id pub-id-type="pmid">26317063</article-id><article-id pub-id-type="pmc">4547360</article-id><article-id pub-id-type="doi">10.1007/s40474-015-0057-3</article-id><article-id pub-id-type="manuscript">NIHMS703600</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Improving Recognition of Children Affected by Prenatal Alcohol
Exposure: Detection of Exposure in Pediatric Care</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Bax</surname><given-names>Ami C.</given-names></name><degrees>MS, MD</degrees><xref ref-type="aff" rid="A1">a</xref></contrib><contrib contrib-type="author"><name><surname>Geurts</surname><given-names>Carrie D.</given-names></name><degrees>MS, APRN, CNP</degrees><xref ref-type="aff" rid="A1">a</xref></contrib><contrib contrib-type="author"><name><surname>Balachova</surname><given-names>Tatiana N.</given-names></name><degrees>PhD</degrees><xref ref-type="aff" rid="A1">a</xref></contrib></contrib-group><aff id="A1"><label>a</label>University of Oklahoma Health Sciences Center, Department
of Pediatrics, Section on Developmental and Behavioral Pediatrics; 1100 N.E.
13<sup>th</sup> Street, Oklahoma City, OK 73117</aff><author-notes><fn id="FN1"><p id="P1"><email>carrie-geurts@ouhsc.edu</email>;
<email>tatiana-balachova@ouhsc.edu</email></p></fn><corresp id="CR1"><bold>Address correspondence to:</bold> Ami C. Bax, 1100 N.E.
13<sup>th</sup> Street, Oklahoma City, OK 73117
[<email>ami-bax@ouhsc.edu</email>], 405-271-8858 (phone), 405-271-2931
(fax).</corresp></author-notes><pub-date pub-type="nihms-submitted"><day>17</day><month>7</month><year>2015</year></pub-date><pub-date pub-type="ppub"><day>1</day><month>9</month><year>2015</year></pub-date><pub-date pub-type="pmc-release"><day>01</day><month>9</month><year>2016</year></pub-date><volume>2</volume><issue>3</issue><fpage>165</fpage><lpage>174</lpage><!--elocation-id from pubmed: 10.1007/s40474-015-0057-3--><abstract><p id="P2">Early identification of fetal alcohol spectrum disorders (FASDs) is
important for providing services and preventing secondary disabilities. Recent
studies indicate that many FASDs are undiagnosed, partly because there is a need
to improve detection of prenatal alcohol exposure (PAE). The aims of this review
are to characterize existing practices for assessing PAE in pediatric care,
identify the most efficient, promising methods of detecting PAE, and recognize
the knowledge and practice gaps. This review indicates that maternal
self-reports remain the most common method utilized in routine clinical practice
and highlights promising methods of PAE identification, including a single binge
drinking question. The review yields few studies describing existing strategies
to assess PAE in pediatric practice and identifies knowledge gaps that need to
be addressed for improving recognition of FASDs in pediatric practice.</p></abstract><kwd-group><kwd>Prenatal alcohol exposure</kwd><kwd>Fetal alcohol spectrum disorders</kwd><kwd>Fetal alcohol syndrome</kwd><kwd>Neurobehavioral Disorder Associated with Prenatal Alcohol Exposure
(ND-PAE)</kwd><kwd>Women</kwd><kwd>Alcohol use</kwd><kwd>Pregnancy</kwd></kwd-group></article-meta></front><body><sec sec-type="intro" id="S1"><title>Introduction</title><p id="P3">Accurate identification of FASDs is important for providing services and
preventing disorders secondary to FASDs. Research indicates that early diagnosis of
a child affected by prenatal alcohol exposure (PAE) is associated with better health
and life outcomes [<xref rid="R1" ref-type="bibr">1</xref>]. However, FASDs remain
largely underdiagnosed. The Centers for Disease Control and Prevention (CDC)
acknowledged that FASD surveillance is inadequate and that the number of children
adversely affected by in-utero exposure to alcohol is underestimated [<xref rid="R2" ref-type="bibr">2&#x02022;&#x02022;</xref>]. The CDC Fetal Alcohol
Syndrome (FAS) Surveillance Network (FASSNet) II [<xref rid="R2" ref-type="bibr">2&#x02022;&#x02022;</xref>] utilized medical records in several states and
identified 0.3 children with FAS per 1,000 children aged 7-9 years. This figure is
significantly lower than the prevalence reported by active case ascertainment
studies, in which an expert evaluates children in person; these studies estimated
2-to-7 children affected by FAS and 20-to-50 affected by FASDs per 1,000 children in
the U.S. and Western Europe, approximately 2% to 5% of the population [<xref rid="R3" ref-type="bibr">3&#x02022;&#x02022;</xref>]. Another study reported the
prevalence of FASDs among first grade students in a representative Midwestern US
community as 6-9 per 1,000 children, Partial Fetal Alcohol Syndrome (PFAS) as 11-17
per 1,000 children, and the overall rate of FASDs as 24-48 per 1,000 children, or
2.4% to 4.8% [<xref rid="R4" ref-type="bibr">4</xref>]. A recent study reported that
86.5% of foster and adopted youth with FASDs were undiagnosed (80.1%) or were
diagnosed incorrectly within the FASD spectrum (6.4%) prior to a comprehensive
evaluation in a specialized clinic [<xref rid="R5" ref-type="bibr">5&#x02022;&#x02022;</xref>].</p><p id="P4">Data about women's alcohol consumption indicate that more children may be
affected by PAE and be at high risk for FASDs. Per the CDC Behavioral Risk Factor
Surveillance System (BRFSS), 7.6% of pregnant women report consuming alcohol in the
past 30 days; 1.4% report binge drinking, defined as consuming four or more
alcoholic drinks (standard-sized drink equivalents are included in <xref ref-type="fig" rid="F1">Figure 1</xref>) per occasion during the past 30 days
[<xref rid="R6" ref-type="bibr">6&#x02022;</xref>]. According to BRFSS data,
among non-pregnant women of childbearing age, the prevalence of any alcohol use in
the last 30 days is 51.5% and the prevalence of binge drinking is 15%, which is
higher among young women who are more likely to have children, including women aged
18&#x02013;24 years (24.2%) and 25&#x02013;34 years (19.9%) [<xref rid="R6" ref-type="bibr">6</xref>]. Moreover, about half of pregnancies in U.S. are unintended,
and a woman may not know she is pregnant until 4-6 weeks of gestation [<xref rid="R7" ref-type="bibr">7</xref>]. Given that women often continue to consume
alcohol at pre-pregnancy levels until they become aware of their pregnancy [<xref rid="R8" ref-type="bibr">8</xref>], there is a high likelihood of PAE before
pregnancy recognition, with binge drinking of particular concern because it causes
high blood alcohol concentration. Therefore, many pregnancies may be affected by PAE
early on, placing children at risk for FASDs.</p><p id="P5">Some cases might not be diagnosed because of the syndromic nature of FASDs,
the lack of pathognomonic features, and the negative perceptions associated with
alcohol use during pregnancy. The physical features of FAS are often subtle, and the
hallmark facial features (smooth philtrum, thin vermillion, small palpebral
fissures) are not always fully apparent at birth [<xref rid="R9" ref-type="bibr">9</xref>], are difficult to accurately assess without precise measurement
[<xref rid="R10" ref-type="bibr">10</xref>], and sometimes become less apparent
with age. Fox et al. [<xref rid="R2" ref-type="bibr">2&#x02022;&#x02022;</xref>] noted
that healthcare providers inadequately recognize facial features of FAS and often
fail to document the features in the patient's records with over half of health
providers in this study reporting that they received no training in recognizing
FASDs. Several genetic syndromes may present with similar features and require
differential diagnosis. Furthermore, physical features may not be present in Partial
FAS (PFAS) and in non-dysmorphic FASDs, including Neurobehavioral Disorder
Associated with Prenatal Alcohol Exposure (ND-PAE), a new diagnostic category
introduced in the Diagnostic and Statistical Manual of Mental Disorders
5<sup>th</sup> Edition (DSM 5) [<xref rid="R11" ref-type="bibr">11</xref>]. The
ND-PAE was established to recognize individuals who do not meet full criteria for
FAS, but have impairments in neurocognitive, self-regulatory, and adaptive
functioning, and known PAE [<xref rid="R11" ref-type="bibr">11</xref>]. The
introduction of ND-PAE in the DSM 5 emphasizes the importance of identifying PAE.
Unlike FAS, which can be diagnosed without information about PAE history, diagnosing
ND-PAE and other non-dysmorphic FASDs requires a confirmed history of more than
minimal prenatal exposure. The &#x0201c;minimal&#x0201d; exposure is defined as
1-to-13 drinks/month and no more than 2 drinks per one occasion [<xref rid="R11" ref-type="bibr">11</xref>]. Therefore, accurate detection of PAE is
necessary to improve identification of children with FASDs and provide services to
prevent adverse outcomes.</p><p id="P6">This paper focuses on detection of PAE to improve the identification of FASDs
in pediatric practice. The primary aims of this article are to 1) characterize
existing practice and strategies to assess PAE in pediatric care, 2) identify the
most efficient, promising methods of detecting PAE, and 3) recognize the knowledge
and practice gaps that must be addressed in order to improve recognition of FASDs in
pediatric practice.</p></sec><sec id="S2"><title>Review of PAE screening practices and strategies among pediatric and other
clinicians</title><p id="P7">A systematic literature search was conducted for studies reporting on PAE
screening practices among pediatric clinicians, related guidelines, and barriers to
alcohol screening and FASD identification. Because an initial search identified few
studies focusing on screening among pediatric clinicians, the search was expanded to
include obstetricians, family physicians, and other healthcare providers who
provided salient information about PAE screening processes, knowledge base, or
competence. Since this review focused on PAE screening among pediatric clinicians,
data about other physicians&#x02019; practices were only included for comparison
purposes. No comprehensive review of alcohol screening by other health care
providers was conducted. Studies were excluded if they focused on an overview of
FASDs/FAS or its diagnostic process, or if they did not address eliciting a maternal
self-report of PAE.</p><p id="P8">We searched the Ovid Medline and PubMed search engines using a date range of
&#x0003c;1946 to February Week 2 2015&#x0003e; for &#x0201c;alcohol and pregnancy and
screen&#x0201d; AND &#x0201c;physician's practice patterns/or pediatrics/ or
pediatrician.&#x0201d; Adding &#x0201c;self-report&#x0201d; to this search or
substituting it for &#x0201c;screen&#x0201d; yielded the same or fewer results. We
also performed a search to find articles on the topic of &#x0201c;Physician awareness
and screening for fetal alcohol syndrome,&#x0201d; and conducted a general
GoogleScholar search on these terms. Our overall search yielded 27 articles. After
excluding articles based on the above criteria and those unavailable in full text,
two articles were identified as relevant to our primary question of current
pediatric screening practices and strategies to identify alcohol consumption during
pregnancy. Six additional articles addressed our question in other provider
populations and/or assessed pediatric attitudes regarding screening for PAE. An
additional search was conducted to examine reports about promising methods of
identification of alcohol consumption during pregnancy and barriers and challenges
to PAE identification.</p><sec id="S3"><title>Professional guidelines on detecting PAE</title><p id="P9">The U.S. Surgeon General (2005) issued a statement that health
professionals should inquire routinely about alcohol consumption by women of
childbearing age, inform them of the risks of alcohol consumption during
pregnancy, and advise them not to drink alcoholic beverages during pregnancy
[<xref rid="R12" ref-type="bibr">12</xref>]. Per these guidelines, pregnant
women and women who consider becoming pregnant or may become pregnant should
abstain from alcohol. Because approximately half of pregnancies are unplanned
and women often do not recognize pregnancy until 4-6 weeks gestation, sexually
active women of childbearing age who do not consistently use effective
contraception and combine the possibility of pregnancy with risky drinking are
at high risk for an alcohol-exposed pregnancy. Although the specific amount of
alcohol that can cause an FASD is unknown, the at-risk drinking threshold has
been established as &#x0003e; 7 standard drinks per week or &#x0003e; 3 standard
drinks on a day [<xref rid="R13" ref-type="bibr">13</xref>] or &#x02265; 4
standard drinks on a single occasion (i.e., binge drinking that results in a
0.08% gram or higher blood alcohol concentration) [<xref rid="R14" ref-type="bibr">14</xref>].</p><p id="P10">The Substance Abuse and Mental Health Services Administration recommends
Screening, Brief Intervention, and Referral to Treatment (SBIRT) as part of
routine health care in numerous settings, including primary care, emergency
departments, trauma centers, and other community care centers [<xref rid="R15" ref-type="bibr">15</xref>]. The American Academy of Obstetricians
and Gynecologists (ACOG) guidelines recommend screening for problematic drinking
for all women seeking obstetric&#x02013;gynecologic care annually and within the
first trimester of pregnancy, with early intervention strategies encouraging
healthy behaviors and appropriate referrals to a substance abuse professional
when indicated [<xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R17" ref-type="bibr">17</xref>]. ACOG recommends the T-ACE (Tolerance, Annoyance, Cut
Down, Eye-Opener) and CAGE (Cut Back, Annoyed, Guilty, Eye-Opener) screening
tools [<xref rid="R17" ref-type="bibr">17</xref>]. The American Academy of
Family Physicians recommends universal alcohol use screening for all women of
childbearing age and for mothers of patients with clinical features worrisome
for FASDs (facial dysmorphia, growth deficiencies, central nervous system
impairment) [<xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R19" ref-type="bibr">19</xref>]. The FASD Advisory Workgroup in Canada recognizes that
there is no general consensus for screening for alcohol use in women of
childbearing age, and issues recommendations to improve screening and recording
processes of alcohol use among women of child-bearing age [<xref rid="R20" ref-type="bibr">20</xref>]. The recommendations include a three-level PAE
identification model: 1) practice-based approaches, such as motivational
interviewing and supportive dialogue, implemented by health care providers when
talking to women about alcohol use, 2) structured questionnaires, such as CAGE
or T-ACE, and 3) biological tests to confirm the presence of alcohol or a drug,
the level of exposure, and the presence of multiple drugs.</p><p id="P11">As part of routine adolescent care, the American Academy of Pediatrics
Bright Futures [<xref rid="R21" ref-type="bibr">21</xref>-<xref rid="R23" ref-type="bibr">23</xref>] recommends a universal substance use screening, brief
intervention, and referral to treatment protocol, using CRAFFT, a
developmentally appropriate screening tool for alcohol and drug use [<xref rid="R21" ref-type="bibr">21</xref>, <xref rid="R22" ref-type="bibr">22</xref>]. However, the framework for screening for parental substance
use, including maternal alcohol use during pregnancy in pediatric practice is
limited. The parent is not the pediatrician's patient, so there is no financial
reimbursement for parental screening or a brief intervention. Furthermore, if a
clinician encounters concerns for problematic substance use, referring the
parent to appropriate treatment resources becomes a challenge. Even in the
setting of adolescent pregnancy, where both the mother and the child are
pediatric patients, there are no clear recommendations for PAE screening,
prevention, and treatment with appropriate resources.</p><p id="P12">A review of the professional guidelines indicates some similarities;
however, there is a lack of consistency in methods and recording results in
medical records and no consensus regarding whether all pediatric patients should
be screened for PAE [<xref rid="R18" ref-type="bibr">18</xref>, <xref rid="R19" ref-type="bibr">19</xref>]. In order to identify FASDs in children
and provide effective treatment, pediatric clinicians ultimately bear the
responsibility for detecting PAE and, therefore, are tasked with the challenge
of screening the mothers of their patients. Although primary care and obstetric
clinicians have been tasked with screening and brief interventions to reduce
at-risk drinking and prevent FASDs, the identification of maternal alcohol
consumption is a relatively new task for pediatric clinicians. There is
uncertainty about the actions that a pediatrician is expected to implement if a
mother reports alcohol or drug use and about whether the pediatrician is
expected to conduct a brief intervention or refer the parent for treatment if
indicated. Understanding the current practices of pediatric clinicians is
crucial to facing these challenges and improving identification of PAE.</p></sec><sec id="S4"><title>Prenatal alcohol screening practices among pediatric and other
clinicians</title><p id="P13">Studies indicated that many pediatricians do not routinely screen their
patients for PAE. Vagnerelli et al. [<xref rid="R24" ref-type="bibr">24</xref>]
reported that 59% of Italian neonatologists, 78.4% of Italian pediatricians, and
60% of Spanish pediatricians endorsed always asking new mothers about ethanol
consumption during pregnancy. Over 90% of all clinicians who reported PAE
screening among new mothers used general questions, with less than 10% reporting
use of standardized screening tools [<xref rid="R24" ref-type="bibr">24</xref>].
Nanson et al. [<xref rid="R25" ref-type="bibr">25</xref>] obtained information
about screening practices among Canadian pediatricians and family and general
physicians (FP/GP); pediatricians were less likely to screen mothers about their
alcohol use during pregnancy than were FP/GP (58.3% vs 77.4%). An earlier survey
asked a small sample of Texas practitioners what percentage of colleagues they
believed screened for FAS, and the mean response was 30%; however, this study
did not specifically examine the practitioners&#x02019; screening practices
[<xref rid="R26" ref-type="bibr">26</xref>].</p><p id="P14">Other medical providers, including obstetricians and FP/GP, often
routinely conduct PAE screening with pregnant and non-pregnant women of
childbearing age, but utilization of standard screening tools is limited [<xref rid="R26" ref-type="bibr">26</xref>]. A survey of Canadian family physicians
revealed that while 75% reported asking pregnant patients about alcohol use,
they were unaware of current screening methods to accurately gauge alcohol use
among women [<xref rid="R27" ref-type="bibr">27</xref>]. Another Canadian study
found that 94% of family physicians, midwives, and obstetricians reported asking
their pregnant patients about alcohol use; however, only 74% of family
physicians, 45% of obstetricians, and 20% of midwives utilized a standard
screening tool [<xref rid="R28" ref-type="bibr">28</xref>]. According to Tough
[<xref rid="R28" ref-type="bibr">28</xref>], less than 50% of Canadian
healthcare providers caring for women in the preconception period reported
frequently discussing smoking, alcohol use, or addiction history. Arnold et al.
[<xref rid="R29" ref-type="bibr">29</xref>] found that only 38% of medical
students and residents at an U.S. university reported always screening their
pregnant patients for alcohol use, suggesting that there is a need to educate
practicing clinicians and trainees about the importance of PAE screening. In
general, few articles reported the specific methods used to screen for PAE.</p></sec><sec id="S5"><title>Barriers to screening for PAE</title><p id="P15">Pediatric clinicians face many barriers to accurate detection of PAE,
given the social stigma, legal implications, and other factors. Women
under-report alcohol consumption because of embarrassment, fear, or beliefs that
small amounts of alcohol are inconsequential [<xref rid="R30" ref-type="bibr">30</xref>, <xref rid="R31" ref-type="bibr">31</xref>]. Coles [<xref rid="R30" ref-type="bibr">30</xref>] noted that alcohol use is reported less
frequently than other drug use in medical records. Many adopted and foster care
children are at high risk of having had PAE, yet they are often no longer in the
care of their biological mother. Clinicians must thus rely upon secondary
reports of maternal alcohol use during pregnancy. Because many children have
come into the care of other biological relatives or the foster care system,
exposure information must often be obtained from medical/social service records
or by hearsay. Studies have shown that information yielded in this manner is
often less accurate than direct maternal self-report, contributing to the
under-diagnosis of FASDs [<xref rid="R30" ref-type="bibr">30</xref>]. When
pediatric clinicians have contact with their patients&#x02019; biological
mothers, many find it difficult and feel uncomfortable asking parents about
their alcohol use, and if the history is not obtained in a sensitive manner,
parents may feel blamed for wrong-doing. Mothers may not reveal their alcohol
use during pregnancy because of guilt or fear of legal actions that could result
in losing their job, children, or relationships [<xref rid="R31" ref-type="bibr">31</xref>].</p><p id="P16">Clinicians may be reluctant to document PAE due to concerns with
mandatory reporting of child maltreatment. ACOG states, &#x0201c;Seeking
obstetric-gynecologic care should not expose a woman to criminal or civil
penalties or the loss of custody of her children&#x0201d; [<xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R17" ref-type="bibr">17</xref>]. Discussing
the role of obstetrician-gynecologists in substance abuse reporting and
pregnancy, ACOG has expressed concerns that the threat of prosecution is an
ineffective strategy in reducing the incidence of alcohol or drug abuse; it may
deter women from seeking prenatal care which would be contrary to the child and
maternal welfare [<xref rid="R16" ref-type="bibr">16</xref>].</p><p id="P17">The new Child Abuse Prevention and Treatment Act (CAPTA) [<xref rid="R32" ref-type="bibr">32</xref>] does not require clinicians to report
maternal alcohol use or PAE to Child Protective Services (CPS). However, if a
child is diagnosed with FAS/FASDs, clinicians are required to make a referral to
CPS so that safe care plans and services are initiated. Additional laws
regarding FASDs may differ based on the state in which the clinician practices.
These new laws and procedures can improve services for children diagnosed with
FASDs but could also increase challenges in obtaining accurate self-reports
about alcohol use during pregnancy. When children are older at their first
referral, diagnosis relies on the maternal recall of alcohol use after a period
of years by a woman who may not remember well or may have some motivation,
conscious or unconscious, to downplay the extent of use [<xref rid="R30" ref-type="bibr">30</xref>]. Pediatric clinicians should be aware of the reporting
guidelines for reporting FASDs to child welfare and reporting guidelines related
to maternal alcohol use within their states and include during their regular
discussion of consent to evaluation/treatment and disclosure with the family.
Health care professionals may be encouraged to work with state legislators to
ensure that legislation support education and services to women instead of
punishing pregnant women for substance use.</p><p id="P18">In addition, if a mother reveals alcohol misuse, a pediatrician may feel
uncomfortable because of limited skills, time, or resources necessary to
adequately respond to the reported problem. Many pediatric clinicians lack
screening and brief intervention (SBI) skills and knowledge of community
resources on alcohol misuse. Since pediatricians are already tasked with
providing SBI for substance abuse in adolescent patients with high risk for
pregnancy [<xref rid="R21" ref-type="bibr">21</xref>, <xref rid="R22" ref-type="bibr">22</xref>, <xref rid="R23" ref-type="bibr">23</xref>, <xref rid="R33" ref-type="bibr">33</xref>], they may be well-poised to assist in
providing SBI to mothers of their patients who report at-risk drinking. However,
there are barriers to reimbursement for a brief intervention for a parent, a
lack of skills to conduct SBI, and no formal pediatric guidelines for such
services. Pediatricians need guidelines, training, and resources for improving
detection of PAE in their patients and should be provided with specific
instructions if they are to help prevent future PAE and FASDs.</p><p id="P19">Several studies have surveyed clinicians to inquire about their
perception of barriers to eliciting a self-report of PAE. A survey of U.S.
obstetricians identified several barriers, including physician bias due to own
alcohol misuse, lack of training, poor awareness of the problem and its effects,
denial that FAS occurs in private practice, time limitations, lack of interest,
fear of offending the patient, and fear that patients will lie [<xref rid="R34" ref-type="bibr">34</xref>]. Another study reported that family
physicians and obstetricians were 60% more likely to identify time constraints
as a barrier to discussing alcohol use during pregnancy with women than were
midwives, and almost half of all providers felt that existing information
available for discussing PAE not in a useful form for clients [<xref rid="R28" ref-type="bibr">28</xref>]. An in-depth focus group of prenatal
care providers in San Francisco indicated that practice setting strongly
influenced providers&#x02019; screening and counseling of pregnant women about
tobacco, alcohol, and illicit drug use. Providers with larger settings, like
county hospitals and the Health Maintenance Organization (HMO), reported more
resources, compared with private practitioners. HMO providers were also more
likely to report using standardized questionnaires and toxicology screening in
pregnancy. In contrast, private practices appeared to offer greater continuity
of care and patient-provider relationships [<xref rid="R35" ref-type="bibr">35</xref>]. Clinicians have also reported the lack of training and
confidence about FAS/FASDs as barriers to identification and diagnosis. In a
study of Toronto family physicians, 49% reported little confidence in their
ability to diagnose FAS; 81% felt their training was inadequate [<xref rid="R27" ref-type="bibr">27</xref>]. Italian and Spanish neonatologists and
pediatricians also had low confidence in their ability to diagnose FAS and
FASDs, with over 50% feeling that they needed more information regarding
FAS/FASD identification in newborns and children [<xref rid="R24" ref-type="bibr">24</xref>].</p></sec><sec id="S6"><title>Biomarkers in detecting PAE</title><p id="P20">Biological tests utilize maternal or child specimens, such as urine,
blood, hair, meconium, and umbilical cord samples [<xref rid="R36" ref-type="bibr">36</xref>]. Biomarkers of PAE include direct ethanol
metabolites/conjugation products, such as fatty acid ethyl esters (FAEEs),
phosphatidylethanol (PEth), ethyl glucuronide (EtG), and ethyl sulfate (EtS),
and indirect ethanol-induced protein alterations, such as gamma
glutamyltranspeptidase (GGT) [<xref rid="R37" ref-type="bibr">37</xref>, <xref rid="R38" ref-type="bibr">38&#x02022;</xref>, <xref rid="R39" ref-type="bibr">39</xref>-<xref rid="R41" ref-type="bibr">41</xref>]. Several studies
indicate that biomarkers reveal higher prevalence of alcohol use during
pregnancy than do maternal self-reports. A study indicated a fivefold increase
in detection of PAE from a meconium FAEE test compared with traditional
self-reports in a population-based sample in Canada [<xref rid="R42" ref-type="bibr">42</xref>]. A recent review reported PAE prevalence 4.3 times
higher when testing meconium than relying on maternal self-reports [<xref rid="R43" ref-type="bibr">43</xref>]. These approaches are promising for
detecting PAE. However, there are several drawbacks: (1) the methods are costly
and may be invasive, (2) nearly two-thirds of problem drinkers do not have
elevated test values, (3) scores may be elevated due to other factors, such as
maternal diabetes or diet, and (4) the methods do not indicate either the amount
or the time period of drinking [<xref rid="R41" ref-type="bibr">41</xref>].
Traditionally utilized biomarkers, such as urine and blood testing, only provide
information about drinking within the last several hours. Other biomarkers, such
as meconium or hair testing, provide information about PAE during the last two
trimesters of pregnancy. However, these methods are expensive, detect heavier
alcohol use, and may be less reliable in detecting moderate or social drinking.
In addition, no currently known biomarker can detect exposure during the first
trimester.</p><p id="P21">When a pediatric clinician orders biomarkers on an infant, results may
reveal information about the mother, who is not their patient, which raises an
ethical concern. Universal biomarker screening raises additional ethical
questions. Implementing informed consent to patients about testing and providing
biomarker screening only to those who consented reduces the benefits of testing,
since patients who consumed alcohol are more likely to refuse testing [<xref rid="R44" ref-type="bibr">44</xref>]. However, testing without patient
consent would violate the patient's right for autonomy. An additional
consideration is that if biomarker screenings were to be routinely used,
intervention resources would need to be available [<xref rid="R36" ref-type="bibr">36</xref>]. Identification of PAE in older children is even more
challenging, as no current laboratory test can detect and quantify PAE in older
children.</p><p id="P22">Some hospitals have implemented targeted biomarker screening and may
have established algorithms to determine risk for PAE (e.g., specific concerns
due to lack of prenatal care, premature birth, low birth weight, or mother's
intoxication at admission; personal communication with Raja Nandyal, M.D., and
Vadim Ivanov, M.D., neonatologists at University of Oklahoma Children's
Hospital, February 2015). However, there is no commonly accepted algorithm or
procedure to record biomarker results in maternal medical charts, and
transferring the information to the child's health records had been inconsistent
in the U.S. and Canada [<xref rid="R20" ref-type="bibr">20</xref>].</p><p id="P23">Although biomarker screening could offer advantages over maternal
self-reports, research is needed to further validate biomarkers and improve PAE
detection [<xref rid="R45" ref-type="bibr">45</xref>]. Given these limitations,
maternal self-report remains the most common method to assess for PAE in
clinical practice.</p></sec><sec id="S7"><title>Strategies for improving identification of PAE through maternal
self-report</title><p id="P24">Self-reports about alcohol consumption have been demonstrated to
reliably reflect women's alcohol consumption. Babor et al. [<xref rid="R46" ref-type="bibr">46</xref>] indicated that, in clinical trials of
research volunteers, self-report measurements are accurate. Biomarker tests and
collateral informant reports do not add sufficient data to warrant their routine
use. However, most published data regarding the reliability of self-reports were
obtained from volunteers who provided anonymous or confidential information in
research studies. A physician asking about alcohol use as part of a clinic
appointment in which information is not anonymous and is likely to be included
in the patient's medical record makes self-reports more likely to be affected by
a social desirability bias. A recent study reported that in-depth research
interviews revealed more alcohol use among pregnant women than was recorded
during routine clinical care appointments with these women [<xref rid="R47" ref-type="bibr">47</xref>].</p><p id="P25">Several approaches to improve the accuracy of self-reports of alcohol
consumption and PAE identification have been identified. Physicians can improve
self-report accuracy by asking questions in a sensitive and nonjudgmental manner
[<xref rid="R33" ref-type="bibr">33</xref>-<xref rid="R36" ref-type="bibr">36</xref>] and when embedding questions about alcohol use in the routine
prenatal history that includes nutrition, exercise, and avoidance of
environmental toxins, such as nicotine/second-hand smoke. In order to increase
accurate and truthful reporting, the woman must be alcohol- and drug- free when
interviewed, and the interviewer must use simple language and provide word
questions clearly [<xref rid="R48" ref-type="bibr">48</xref>]. Asking a woman
about her drinking patterns before she became pregnant is another strategy that
could elicit more accurate estimates of first-trimester drinking and alcohol use
later during pregnancy [<xref rid="R49" ref-type="bibr">49</xref>]. Robles et
al. [<xref rid="R50" ref-type="bibr">50</xref>] found that self-reported alcohol
consumption is moderately reliable over 3-month and 5-month time periods, and
longer timeframes have been documented to improve sensitivity of self-reports in
women of childbearing age [<xref rid="R51" ref-type="bibr">51</xref>]. A summary
of PAE screening recommendations for pediatric practice is included in <xref ref-type="table" rid="T1">Table 1</xref>. <xref ref-type="fig" rid="F2">Figure 2</xref> provides a suggested algorithm for implementing PAE
screening and appropriate action plans based upon risks identified within a
pediatric practice.</p></sec><sec id="S8"><title>Screening instruments to identify alcohol use during pregnancy</title><p id="P26">A number of screening measures have been implemented for screening for
at-risk drinking in different settings. Two of the instruments have been
designed and validated specifically to detect the risk for alcohol use during
pregnancies in women, TWEAK (Tolerance, Worried, Eye-opener, Amnesia, Kut down)
and T-ACE [<xref rid="R52" ref-type="bibr">52</xref>-<xref rid="R54" ref-type="bibr">54</xref>]. These measures have been tested in diverse obstetric
samples and demonstrated good performance in PAE identification [<xref rid="R52" ref-type="bibr">52</xref>, <xref rid="R55" ref-type="bibr">55</xref>-<xref rid="R57" ref-type="bibr">57</xref>]. In addition, the
AUDIT-C (Alcohol Use Disorders Identification Test alcohol consumption
questions) has demonstrated sensitivity in identification of prenatal alcohol
use among women [<xref rid="R58" ref-type="bibr">58</xref>]. Most women who
consume alcohol during pregnancy do not meet criteria for alcohol use disorders
and may not be identified with commonly used instruments, such as the standard
AUDIT (Alcohol Use Disorders Identification Test) [<xref rid="R59" ref-type="bibr">59</xref>]. For example, the CAGE questionnaire and SMAST (Short
Michigan Alcoholism Screening Test) were designed to identify hazardous and
harmful drinking and alcohol dependency and were tested in specific populations
(e.g., heavy-drinkers, males) [<xref rid="R60" ref-type="bibr">60</xref>]. These
instruments do not accurately identify drinking among women [<xref rid="R15" ref-type="bibr">15</xref>, <xref rid="R16" ref-type="bibr">16</xref>, <xref rid="R58" ref-type="bibr">58</xref>]. T-ACE and TWEAK,
simple screening instruments designed for identifying women who consume alcohol
during pregnancy, are particularly valuable and detecting the risk for PAE.</p></sec><sec id="S9"><title>Single question to identify alcohol use during pregnancy</title><p id="P27">Even brief instruments consisting of a few questions may be difficult to
implement in a busy pediatric practice. Recent studies indicate that a
single-question can be used for screening. The National Institute on Alcohol
Abuse and Alcoholism recommended the Single &#x0201c;Binge&#x0201d; Drinking
Question (SBDQ) (&#x0201c;How often did you have &#x02265; 4 drinks on one
occasion?&#x0201d;) to screen people whose drinking puts them at risk of an
alcohol use disorder [<xref rid="R13" ref-type="bibr">13</xref>]. Recent studies
found that the SBDQ accurately identified patients with at-risk drinking in
primary care [<xref rid="R61" ref-type="bibr">61</xref>] and also identified
women whose drinking placed them at risk of PAE [<xref rid="R62" ref-type="bibr">62</xref>-<xref rid="R64" ref-type="bibr">64</xref>]. These findings
support the use of SBDQ to identify prenatal alcohol use. However, the studies
were conducted in research settings, and additional research is needed to
evaluate the performance of the measure in pediatric care settings. It is
reasonable, though, to conclude that the SBDQ and screening instruments,
including T-ACE and TWEAK, are feasible and effective for PAE identification and
can be recommended for implementation in pediatric care settings.</p></sec></sec><sec sec-type="conclusions" id="S10"><title>Conclusions</title><p id="P28">Screening women for at-risk drinking and high risk for alcohol-exposed
pregnancies has been recommended for primary care, and is widely accepted as a part
of routine care by many practitioners. Recent findings regarding the clinical
features and prevalence of FASDs and new DSM 5 guidelines for diagnosing ND-PAE
highlight the importance of improving PAE identification in pediatric settings.
Thus, pediatric clinicians are tasked with eliciting accurate maternal self-reports
of alcohol use during pregnancy. Since women are more likely to provide accurate
reports of prenatal alcohol use retrospectively, pediatric clinicians should be
reassured that they are in the best position to engage in this discussion and can
prompt accurate information about PAE.</p><p id="P29">Although challenges in PAE identification have been reported, a significant
body of research and clinical guidelines support pediatric clinicians in
identification of PAE. Currently, maternal self-reports about alcohol use are a more
practical method of PAE detection than biological methods. Several self-report
methods, including the SBDQ, have shown validity [<xref rid="R52" ref-type="bibr">52</xref>, <xref rid="R55" ref-type="bibr">55</xref>, <xref rid="R63" ref-type="bibr">63</xref>-<xref rid="R66" ref-type="bibr">66</xref>]. These approaches
need further evaluation in clinical settings to determine their accuracy when
implemented by pediatric professionals. Studies have indicated that many clinicians
feel they lack the confidence, skills, and time to effectively screen for PAE, and
that they need training in effective screening methods that require minimal time
[<xref rid="R24" ref-type="bibr">24</xref>, <xref rid="R27" ref-type="bibr">27</xref>, <xref rid="R34" ref-type="bibr">34</xref>]. However, few studies
have examined the general frequency and methods of PAE screening practices used by
pediatricians. Additional measures, such as screening by nurses and other health
care professionals, incorporating screening tools in electronic medical records, and
utilization of tablets/electronic system screening, can be utilized in pediatric
offices. By improving recognition of PAE via accurate maternal self-reports,
pediatric clinicians can improve early identification of FASDs, ensure services and
early interventions for children with FASDs to prevent secondary disabilities, and
potentially contribute to prevention of PAE in future pregnancies. </p></sec></body><back><ack id="S11"><title>Acknowledgments</title><p>The authors wish to thank Kathy Kyler of the University of Oklahoma Health Sciences
Center for her help with editing the manuscript. The publication was partially
supported by Research Grant Number R01AA016234 from the National Institutes of
Health/National Institute on Alcohol Abuse and Alcoholism and Fogarty International
Center (Brain Disorders in the Developing World: Research Across the Lifespan) and a
Cooperative Agreement with the University of Missouri (Sub-award Number C00399-76;
DHHS/CDC Grant Award U84DD000884). The contents of this article are solely the
responsibility of the authors and do not necessarily represent the official views of
the NIH and CDC.</p></ack><fn-group><fn id="FN2"><p id="P30">Compliance with Ethics Guidelines</p><p id="P31">Conflict of Interest</p><p id="P32">Ami C. Bax, Carrie D. Geurts, and Tatiana N. Balachova declare that they
have no conflict of interest.</p></fn><fn id="FN3"><p id="P33">Human and Animal Rights and Informed Consent</p><p id="P34">This article does not contain any studies with human or animal subjects
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Alcohol Abuse and Alcoholism. A Pocket Guide for Alcohol Screening and Brief
Intervention. 2005. Rockville, MD: National Institutes of Health, 2005.)
Available at <ext-link ext-link-type="uri" xlink:href="http://pubs.niaaa.nih.gov/publications/Practitioner/PocketGuide/pocket_guide.htm">http://pubs.niaaa.nih.gov/publications/Practitioner/PocketGuide/pocket_guide.htm</ext-link>.
Produced by the American College of Gynecologists and Obstetricians [ACOG]
.</p></caption><graphic xlink:href="nihms-703600-f0001"/></fig><fig id="F2" orientation="portrait" position="float"><label>Figure 2</label><caption><p>Suggested algorithms for assessing prenatal alcohol exposure: action plan. aPAE:
prenatal alcohol exposure; bND-PAE: neurobehavioral disorder associated with
prenatal alcohol exposure; cSBI: screening and brief intervention/referral to
treatment. (Data adapted with permission from: Balachova T. Screening for
prenatal alcohol exposure. Alcohol Related Neurodevelopmental Disabilities and
Prenatal Alcohol Exposure Workgroup Meeting, American Academy of Pediatrics, Elk
Grove Village, February 24, 2014) [<xref rid="R68" ref-type="bibr">68</xref>].</p></caption><graphic xlink:href="nihms-703600-f0002"/></fig><table-wrap id="T1" position="float" orientation="portrait"><label>Table 1</label><caption><p>Prenatal alcohol exposure screening recommendations for pediatric settings
(SUPER)</p></caption><table frame="void" rules="all"><thead><tr><td rowspan="1" colspan="1"/></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold><underline>S</underline></bold>upport</td><td align="left" valign="top" rowspan="1" colspan="1">&#x02022; Provide empathy and support in a
non-judgemental manner.</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold><underline>U</underline></bold>niversally Screen with
Evidence-based screening tool</td><td align="left" valign="top" rowspan="1" colspan="1">&#x02022; Universally screen for PAE<sup><xref ref-type="table-fn" rid="TFN1">a</xref></sup> prenatally and in
the newborn period; selectively screen throughout
childhood.<break/>&#x02022; Embed alcohol screening in routine prenatal
questioning regarding other health behaviors prior and during pregnancy:
nutrition, vitamin use, physical exercise, and the avoidance of
environmental toxins, such as nicotine and second-hand
smoke.<break/>&#x02022; To &#x0201c;normalize&#x0201d; the questioning
about alcohol use, start with a general statement, like &#x0201c;I ask
all my patients' parents standard health questions to understand factors
that may affect the health of their child.&#x0201d;<break/>&#x02022;
Perform frequent developmental screening if PAE is identified.</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold><underline>P</underline></bold>re-pregnancy and
<bold><underline>P</underline></bold>regnancy alcohol use</td><td align="left" valign="top" rowspan="1" colspan="1">&#x02022; To approach the topic of alcohol and
quickly determine whether prenatal exposure occurred, the following set
of questions is recommended:<break/>&#x000a0;&#x000a0;&#x000a0;&#x000a0;1.
&#x0201c;In the 3 months before you knew you were pregnant, how many
times did you have 4 or more alcohol drinks in a
day?&#x0201d;<break/>&#x000a0;&#x000a0;&#x000a0;&#x000a0;2. &#x0201c;During
your pregnancy, how many times did you have any
alcohol?&#x0201d;<break/>&#x02022; If a positive response is given to
either question above, it is recommended that the clinician follow up to
determine the level of PAE by
asking:<break/>&#x000a0;&#x000a0;&#x000a0;&#x000a0;3. &#x0201c;During your
pregnancy, on average, how many days per week did you have any
alcohol?&#x0201d;<break/>&#x000a0;&#x000a0;&#x000a0;&#x000a0;4. &#x0201c;During your
pregnancy, on a typical day when you had an alcoholic beverage, how many
drinks did you have?&#x0201d;<break/>&#x000a0;&#x000a0;&#x000a0;&#x000a0;5.
&#x0201c;During your pregnancy, what was the maximum number of drinks that you
had in a day?&#x0201d;</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold><underline>E</underline></bold>ducate</td><td align="left" valign="top" rowspan="1" colspan="1">&#x02022; Educate women about the risks of
alcohol use during pregnancy and advise them to avoid alcohol
consumption while pregnant or when conception is possible.</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1"><bold><underline>R</underline></bold>ecord,
<bold><underline>R</underline></bold>eport,
<bold><underline>R</underline></bold>efer</td><td align="left" valign="top" rowspan="1" colspan="1">&#x02022; Any affirmative answer to above
questions indicates maternal at-risk drinking and minimal or higher
PAE.<break/>&#x02022; The presence of PAE (pre-pregnancy binge drinking,
during pregnancy any alcohol use) and, if possible, the PAE level
(during pregnancy the number of drinking days/week, average number of
drinks/day, and the maximum number of drinks/day) must be documented in
the child's medical record. Documentation of PAE in child's medical
records is important for diagnosing ND-PAE<sup><xref ref-type="table-fn" rid="TFN2">b</xref></sup> or other FASD condtions at the time of
the evaluation or later if disorders become evident later in
life.<break/>&#x02022; Guidelines should be followed for the child with
PAE, including a referral to a developmental specialist.<break/>&#x02022;
Consider legal reporting guidelines for reporting FASDs to Child
Welfare; include during regular discussion of treatment consent and
disclosure with the family.<break/>&#x02022; If maternal at-risk drinking
and PAE is identified, a brief intervention/referral for the mother is
indicated to prevent PAE in a future pregnancy and reduce her own health
risk.</td></tr></tbody></table><table-wrap-foot><fn id="TFN1"><label>a</label><p id="P35">PAE: prenatal alcohol exposure</p></fn><fn id="TFN2"><label>b</label><p id="P36">ND-PAE: neurobehavioral disorder associated with prenatal alcohol
exposure (Data adapted with permission from: Balachova T. Screening for
prenatal alcohol exposure. Alcohol Related Neurodevelopmental Disabilities
and Prenatal Alcohol Exposure Workgroup Meeting, American Academy of
Pediatrics, Elk Grove Village, February 24, 2014) [<xref rid="R68" ref-type="bibr">68</xref>].</p></fn></table-wrap-foot></table-wrap></floats-group></article>