2019 - A Pediatric Epidemic Deformational Plagiocephalybrachycephaly and Congenital Muscular Torticollis
2019 - A Pediatric Epidemic Deformational Plagiocephalybrachycephaly and Congenital Muscular Torticollis
Pediatric healthcare providers are on the front lines to provide early identification and
treatment of plagiocephaly/brachycephaly and torticollis for those infants spending more
time supine/reclined and less time prone. Here’s why early intervention is so important.
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misshapen area is bilateral, the back of the head will widen Torticollis: Other associated
and may look tall or turricephalic. Incidence of DPB ranges problems
from 18% to 19.7%.3
Congenital muscular torticollis has an association with MA that can lead to long-term facial
asymmetry.1,12 Unilateral ramal height growth restriction, causing jaw asymmetry, results
from CMT due to abnormal muscle forces. Mandibular asymmetry can be identi ed by
approximating the mandible to the maxilla. The mandible will cant upward on the side of the
head tilt. Physical therapy for the torticollis will address the MA, which is important because
MA can affect feeding, especially the ability to achieve latch and adequate suction for
breastfeeding.13 Addressing MA early means a greater potential for improvement and
resolution. Craniofacial asymmetries, including MA, can become more severe with age when
delay or if CMT remains untreated.14
treatment of CMT is delayed
Most parents notice the attening or misshaping of their infant’s head shape between age 1
and 2 months. Parents and primary care physicians (PCPs) do not always recognize CMT
because presentation may be subtle. Parents tell us they mention their concern about
abnormal head shape and/or positional preference to their PCP but are told it will
spontaneously improve once the infant is rolling over and sitting upright. They are
discouraged when this does not happen. Although many PCPs believe what they are telling
concerned parents about spontaneous improvement, this is typically not the case unless
interventions are initiated much earlier in infancy.
In the United States in 2017, 3.8 million babies were born. As noted earlier, incidence of DPB
ranges from 18% to 19.7%-about 720,000 infants per year born with DPB.3 About 100 US
pediatric plastic surgery/cleft-craniofacial centers each see nearly 100 patients with these
diagnoses per month. This does not account for other providers including neurosurgeons or
pediatricians. Only about 100,000 of 720,000 infants per year are currently being identi ed
and treated, leaving 86% (620,000) unidenti ed and untreated. Given long-term, often
irreversible, sequelae, this is a serious problem.
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At our institution, the University of Pittsburgh Medical Center (UPMC) Children’s Hospital of
Pittsburgh, Pennsylvania, the cleft-craniofacial center is embedded in the pediatric plastic
surgery department. With more than 100 new patients referred to us monthly, most of whom
having both DPB and CMT, we developed a multidisciplinary clinic in 2010. Our
comprehensive team evaluation and treatment approach includes a nurse practitioner and a
physical therapist. With this approach, we are able to institute PT and aggressive
repositioning (AR) management at the initial appointment, beginning these conservative
measures as soon as possible. Combining these services saves time and money for parents
and/or guardians by eliminating the need to schedule a separate PT appointment.
Patients receive a wealth of information during a medical appointment, of which about 80%
is not retained once they leave the o ce.15 To reinforce our recommendations and
instruction, we have developed printed patient-education materials to increase
understanding and compliance. Handouts include information sheets on DPB and AR
techniques as well as brochures about tummy time and torticollis that describe home
exercises for CMT.
We also provide community outreach to our regional PCPs and pediatric therapists. Our
purpose is to increase awareness of these diagnoses and emphasize the small but critical
time frame available to institute conservative measures to treat DPB.
Diagnosis of DPB is determined by physical exam. The cranial exam is performed by having
the parent/guardian hold the infant in his/her lap while the nurse practitioner examines the
baby from the vertex view (Figure 1). This exam ascertains whether the DPB is unilateral or
bilateral. Unilateral DPB most frequently manifests in a parallelogram shape of the head
(Figure 2). The attened side of the head displaces the ear forward anteriorly, causing
forehead bossing and fullness of the cheek on the affected side. The orbital opening may be
larger on the affected side. Bilateral DPB results in signi cant brachycephaly (Figure 3).
Facial features are not as affected in brachycephalic patients unless both brachycephaly
and asymmetry are demonstrated.
When assessing the cranial vault, a hand caliper is used to measure the cranial index (CI),
also referred to as the cephalic ratio, de ned as the width divided by the length. The oblique
diagonal difference (ODD) is a measurement of the asymmetry of the cranial vault. The CI
and ODD provide objective guidelines with which to determine DPB severity (Figure 4).
Criteria for cranial vault measurements have not been standardized, but an ODD equal to or
greater than 12 mm (and/or con dence index [CI] ≥1.0) has been used to denote DPB as
severe. These measurements guide treatment decision-making; eg, mild DPB is treated
conservatively with AR and PT.
If the baby is aged 4.5 to 5 months or older and has moderate or severe cranial vault
measurements, the parent/guardian is offered HT as a choice. The infant must show
adequate head and neck control. We verify this developmental achievement by performing a
pull-to-sit test to ensure a strong chin tuck is present and there is no head lag (Figure 5). If
head lag exists, we recommend increasing tummy time to achieve improved head and neck
control and a return visit once adequate head and neck control is achieved. Helmets weigh
about 8 ounces, which is a signi cant weight to place on an infant’s head. Infant safety must
be ensured with HT as poor head and neck control combined with the weight of a helmet
could potentially compromise respiratory status.
Differential diagnosis
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Skull x-rays are rarely indicated or helpful. If the 3D CT scan shows craniosynostosis, the
patient is referred to a craniofacial surgeon. If the scan does not indicate craniosynostosis,
HT can be considered. Some asymmetric facial features observed in children with mild
hemifacial microsomia may also be seen in children with DPB and CMT. Children with
hemifacial microsomia, however, typically do not present with DPB and/or CMT.
The physical therapist evaluates the patient’s neck, spine, hips, feet, and provides gross
motor skill screening. If the infant has CMT, parents and/or guardians are educated about it,
taught exercises to begin immediately, and counseled on initiating PT services via
outpatient or early intervention (Birth-to-3). In our state, parents/guardians often opt for
early intervention because the state-funded programs do not require insurance and provide
the convenience of a physical therapist coming to the home, daycare, or sitter’s home. Such
services can take up to a month to initiate, so exercises must start right away. Frequency of
PT is weekly or every other week, becoming less frequent as the infant improves. Standard
of care for CMT is to continue with PT until the child is walking independently to ensure
gross motor milestones are achieved and performed symmetrically.11
Up to 99% of CMT resolves with PT and less than 0% to 1% requires surgical intervention.11
Often CMT manifests with soft tissue restriction of the neck and shoulders, including
bromatosis colli within the SCM in 10% to 50% of cases.1 Families are taught massage for
the soft tissue restrictions, which can take months to resolve. Also, a 10% to 14.9%
correlation of CMT with developmental hip dysplasia has been documented.1,16,17 The
physical therapist undertakes a clinical hip evaluation, and if there are any concerns, the
patient is referred to a pediatric healthcare provider or to orthopedics.
Initiating awake prone time immediately is crucial in the newborn period. Although parents
are well educated about the Back to Sleep campaign to prevent sudden infant death
syndrome, they rarely receive su cient information on the bene ts and techniques of
tummy time. Our brochure on tummy time reviews techniques for families to use to achieve
the goal of 81 minutes by age 4 months.2
Tummy time strengthens the infant’s neck and core and relieves pressure from the head. It
is inexpensive, easy to do, and does not require additional products or have associated
costs. It would be most bene cial if tummy time were reviewed by the pediatrician or
healthcare personnel within the practice during the rst newborn appointments. The slogan
“Back to sleep, tummy to play” establishes a simple but important message.
If patients are referred early, between age 0 and 4 months, we initiate the conservative
measures of AR and PT. Such techniques are effective then because the skull is soft and
malleable until age 5 to 6 months. We strongly support the AAP recommendations of
sleeping on a at, rm surface. Many families have their babies sleeping in reclined chairs,
which we believe exacerbates DPB and CMT. In an effort to minimize pressure on the
misshaped side of the head, we teach families to use AR. We use a receiving blanket rolled
up like a log and tucked behind the affected side of the head, shoulder, waist, and hip when
the baby is resting, especially in reclined chairs (eg, bouncy, Fisher Price Rock ‘n Play, or
swing chairs). The goal is to minimize reclined positioning and increase upright seating
when developmentally appropriate.
Upright chairs for emerging sitters (eg, Bumbo, Fisher Price Sit-Me-Up, Summer Infant,
BebePod) are recommended at age 3 to 4 months. These chairs provide necessary back
support but allow pressure to be removed from the head. They should be introduced in short
intervals, increased as the baby adjusts, and placed on the oor, never on a table or counter
due to concern over fall risk. Parents are encouraged to use front carriers in their daily
activities to remove pressure from the baby’s head.
Feeding techniques for both bottle-feeding and breastfeeding are provided to support the
head and neck, reducing pressure on the affected side of the skull. It is important to reduce
laying the baby’s affected side of the head on an arm or items like a pillow. Visual
stimulation encourages the baby to look to the opposite side from the DPB.
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We use AAP guidelines and state trooper guidelines for car-seat positioning.18 These
guidelines require the infant be safely buckled into the car seat and the blanket roll tucked
behind the affected side of the head, shoulder, and hip outside of straps and buckles. The
family is taught to take the infant out of the reclined car seat upon reaching their destination
to prevent further pressure on the affected side of the head. This can be done by holding the
baby, using a front carrier, or, when developmentally appropriate, the stroller. We offer a
prescription for AR if the baby is enrolled in daycare.
Patients return for further evaluation between age 4.5 and 5 months. If conservative
techniques have been effective in improving or halting progression of DPB and its severity
does not meet criteria for HT, we recommend continuing AR and PT. If between 4.5 and 5
months infants still show signi cant DPB and meet criteria, we offer HT and many parents
agree to it. Again, HT has proved most effective when the skull is still malleable, brain
growth is robust, and when initiated prior to the ossi cation process.19 We inform families
that DPB is a functional cosmetic issue because patients need to t into safety helmets
properly when they begin to ride bikes or play helmeted sports. Risk of concussion should
not be increased by an ill- tting helmet due to an abnormal head shape.
Although highly effective, HT can be time consuming and stigmatizing. Often, mothers tell
us they feel they have done something to cause this problem. Many cultures are not open to
HT. The potential adverse effects of HT include skin issues; ie, rashes, pressure areas,
wounds, contact dermatitis, and exacerbation of eczema, seborrhea, or cradle cap. Infants
also can become overheated when wearing helmets. Loss of work due to follow-up
appointments for adjustments can impact the family. Finally, HT can be very expensive and
insurance coverage may be lacking.
Of note, the AAP clinical report from 2011 found no evidence that molding helmets work any
better than repositioning for mild or moderate skull deformity.20 Based on studies available
then, the best use of helmets for severe deformity is at age 4 to 12 months because of the
greater malleability and rapid brain growth. Since 2011, however, newer, larger studies have
been completed on the e cacy of HT.
We propose, however, that AR and PT initiated early enough have the potential to be as
effective as HT in addressing DPB. Patients are rarely referred to us in this early critical
timeframe, but when they are, the conservative measures of AR and PT halt or reverse DPB,
resulting in substantial improvement and even negating the need for HT. Although it has not
been our experience, concerns exist about the overprescribing of HT, but that issue is
beyond the scope of this article’s focus.
The epidemic of DPB and CMT has caused a signi cant nancial burden on the healthcare
system, especially when HT is used. As the majority of infants are referred too late to
institute conservative measures, HT becomes the only option, one that we estimate costs
$3.6 million at our center for approximately 900 patients per year.
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The United States has over 100 craniofacial centers, and certainly speci c costs attributed
to this problem vary among them. Nevertheless, referencing our costs for HT as well as
plastic surgery consults and PT evaluations and sessions, and multiplying it by 100 centers
across the country, the rough gross estimate for costs nationwide quickly reaches more
than $1 billion. As well, this estimate does not include costs for patients treated by
neurosurgery centers or other providers, missed work, or transportation.
Prevention
Few medical issues occur with this prevalence in otherwise healthy infants, and little
attention has been paid to prevention or early treatment in light of the increased numbers of
infants with this diagnosis since 1992. Research supporting effective prevention strategies
is scant. We recently completed a pilot study approved by the Institutional Review Board
that demonstrated support of early referral resulting in less-frequent HT. A Finnish study
also has shown that initiating preventive education in the maternity ward from the time
infants are born provides signi cant reduction in the number of infants who develop
deformational plagiocephaly or require HT.4
Conclusion
Pediatric healthcare providers are in the best position to identify and manage DPB and CMT.
Evaluation of the infant’s head shape and range of motion of the neck should be
incorporated into the 1- and 2-month well-child appointments. If any concerns are noted, AR
and referral to PT should be initiated immediately.
Lack of intervention or suggesting it will resolve once the baby is rolling and sitting is
usually a fallacy. Conservative measures are most effective when the skull is still malleable
prior to onset of ossi cation. If no improvement is observed by the 4-month well-child
appointment, referral to a specialist is recommended. Early identi cation and treatment are
critical. They can dramatically improve the patient’s course and provide the momentum to
begin to minimize, and hopefully reverse, this epidemic.
References:
1. Karmel-Ross K. Congenital muscular torticollis. In: Campbell SK, Palisano RJ, Orlin MN,
eds. Physical Therapy for Children. 4th ed. St. Louis, MO: Elsevier Saunders; 2012:292-312.
2. Dudek-Shriber L, Zelazny S. The effects of prone positioning on the quality and acquisition
of developmental milestones in four-month-old infants. Pediatr Phys Ther. 2007;19(1):48-
55.
5. Cheng JC, Au AW. Infantile torticollis: a review of 624 cases. J Pediatr Orthop.
1994;14(6):802-808.
6. Cheng JC, Tang SP, Chen TM. Sternocleidomastoid pseudotumor and congenital
muscular torticollis in infants: a prospective study of 510 cases. J Pediatr. 1999;134(6):712-
716.
7. Cheng JC, Wong MW, Tang SP, Chen TM, Shum SL, Wong EM. Clinical determinants of the
outcome of manual stretching in the treatment of congenital muscular torticollis in infants.
A prospective study of eight hundred and twenty-one cases. J Bone Joint Surg Am. 2001;83-
A(5):679-687.
8. Do TT. Congenital muscular torticollis: current concepts and review of treatment. Curr
Opin Pediatr. 2006;18(1):26-29.
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10. Stellwagen L, Hubbard E, Chambers C, Jones KL. Torticollis, facial asymmetry and
plagiocephaly in normal newborns. Arch Dis Child. 2008;93(10):827-831.
12. Kawamoto HK, Kim SS, Jarrahy R, Bradley JP. Differential diagnosis of the idiopathic
laterally deviated mandible. Plast Reconstr Surg. 2009;124(5):1599-1609.
13. Wall V, Glass R. Mandibular asymmetry and breastfeeding problems: experience from 11
cases. J Hum Lact. 2006;22(3):328-334.
14. Jeong KY, Min KJ, Woo J, Yim SY. Craniofacial asymmetry in adults with neglected
congenital muscular torticollis. Ann Rehabil Med. 2015;39(3):440-450.
15. Bass PF. 3 steps to boost health literacy. Contemp Pediatr. 2018;35(1):13-14.
16. Jackson JC, Runge MM, Nye NS. Common questions about developmental dysplasia of
the hip. Am Fam Physician. 2014;90(12):843-850.
17. Kim SN, Shin YB, Kim W, et al. Screening for the coexistence of congenital muscular
torticollis and developmental dysplasia of hip. Ann Rehabil Med. 2011;35(4):485-490.
19. Kluba S, Kraut W, Reinert S, Krimmel M. What is the optimal time to start helmet therapy
in positional plagiocephaly? Plast Reconstr Surg. 2011;128(2):492-498.
20. Laughlin J, Luerssen TG, Dias MS; Committee on Practice and Ambulatory Medicine,
Section on Neurological Surgery. Prevention and management of positional skull
deformities in infants. Pediatrics. 2011;128(6):1236-1241. Erratum in: Pediatrics.
2012;129(3):595.
22. Steinberg JP, Rawlani R, Humphries LS, Rawlani V, Vicari FA. Effectiveness of
conservative therapy and helmet therapy for positional cranial deformation. Plast Reconstr
Surg. 2015;135(3):833-842.
23. Naidoo SD, Skolnick GB, Patel KB, Woo AS, Cheng AL. Long-term outcomes in treatment
of deformational plagiocephaly and brachycephaly using helmet therapy and repositioning:
a longitudinal cohort study. Childs Nerv Syst. 2015;31(9):1547-1552.
25. Flannery AM, Tamber MS, Mazzola C, et al. Congress of Neurological Surgeons
systematic review and evidence-based guidelines for the management of patients with
positional plagiocephaly: executive summary. Neurosurgery. 2016;79(5):623-624.
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A new study urges pediatricians to screen for cognitive challenges as children with PPB
age.
Flattening of the skull on the back or side of an infant’s head-also known as positional
plagiocephaly and/or brachycephaly (PPB)-is a common problem seen in pediatric practice.
Although attened skulls in infancy, often considered a benign issue, can be corrected, a
new study investigates the long-term cognitive outcomes of more severe malformations.
In a new study published in Pediatrics, researchers evaluated the long-term cognitive and
academic impact of PPB.1 In a separate study, published in the European Journal of
Pediatrics,2 37.8% of infants had some degree of plagiocephaly by age 8 to 12 weeks, and
another 15% presented with brachycephaly. Plagiocephaly is de ned as a attened head on
one side resulting in asymmetry, possibly accompanied by misaligned ears. In
brachycephaly, the back of the head becomes attened, resulting in a widened head and
occasional bulging of the forehead. These conditions can be caused by positioning in the
womb or after birth, with a spike in cases noted after the American Academy of Pediatrics
issued its recommendation that infants sleep at on their backs to prevent sudden infant
death syndrome (SIDS).
Not so benign?
Whereas these common conditions have long been thought to be a benign cosmetic issue,
the research team that developed the new Pediatrics study notes that associations have
been made between PPB and neurodevelopmental de cits.1
To test these associations further, a research team evaluated 336 children with a mean age
of 9 years who had had PPB in infancy. Researchers found that children with moderate to
severe PPB were more likely to have required some form of developmental intervention than
their peers, with 66% of the children who had PPB in infancy requiring intervention
compared with 21% of their peers. Twenty-eight percent of the children in the PPB cohort
had had mild PPB as infants and 72% had moderate to severe PPB. As for treatment during
infancy, 34% had worn orthotic helmets to treat their PPB, and 45% had torticollis-a twisting
of the neck muscles caused by positioning of the head.
Although mean cognitive and academic scores for the PPB cohort were generally within
average range, the research team notes that children with PPB scored lower on most
cognitive and achievement tests performed over the course of the study, with children who
had moderate to severe PPB scoring lower than those with mild cases.
“Children who had moderate to severe PPB in infancy had persistently lower scores on tests
of cognition and, to a lesser extent, academic achievement than children without PPB
(controls),” says lead author Brent Collett, PHD, an associate professor in the Department of
Psychiatry and Behavioral Sciences at the University of Washington School of Medicine,
Seattle. “Children who had mild PPB as infants did not differ from controls.”
The researchers stop short of stating that PPB has a causal relationship to developmental
problems but note that PPB might rather be used as a marker for developmental
vulnerability, and add that treating skull deformations may be less important than tracking
developmental progress and offering early intervention when needed.
Collett says it’s important for pediatricians to monitor patients with PPB, even after the
malformation is treated.
“For infants with more noticeable (moderate to severe) deformation, pediatricians should
provide developmental assessment and monitoring or refer infants to a developmental
specialist,” Collett says. “For infants with mild deformation, pediatricians could use the
results of our study to reassure parents who often worry about developmental effects.”
Collett says he hopes that the study will help guide pediatricians in the management of the
long-term effects of PPB.
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“We hope that our results will guide efforts to identify babies with
plagiocephaly/brachycephaly who would bene t from developmental
assessment/monitoring and early intervention, potentially offsetting case-control
differences like those observed in our study,” he says. “We also anticipate that our ndings
will prompt further research into strategies and tools that pediatricians could use to
evaluate the severity of deformation in their practice, which would guide referrals to
craniofacial centers, early interventionists, and other providers.”
References:
1. Collett BR. Wallace ER, Kartin D, Cunningham ML, Speltz ML. Cognitive outcomes and
positional plagiocephaly. Pediatrics. January 11, 2019. Epub ahead of print. Available at:
http://pediatrics.aappublications.org/content/early/2019/01/09/peds.2018-2373. Accessed
January 25, 2019.
The second part of this article on integrating oral health into primary pediatric care
discusses the important role of fluoride and fluoride varnish application for preventing dental
caries in children.
Table 1
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Topical uoride in the form of toothpaste (at-home use) and
varnish (in-o ce use) should be recommended for all
children starting at tooth eruption.2,5 The American
Academy of Pediatrics (AAP) and United States Preventive
Services Task Force (USPSTF) also recommends dietary
uoride supplements for all children who do not have an
adequate supply of uoride in their primary drinking water.
The AAP additionally recommends uoride mouth rinse use
Table 2
for children aged 6 years and older who are at high risk for
dental caries.2,6
TOPICAL FLUORIDE
Children should be encouraged to spit after brushing. Post-brushing rinsing with water
should be limited to provide optimal uoride exposure to the teeth from the toothpaste.2,9
Fluoride toothpaste, like all other medications, should be kept out of reach of small children.
Mouth rinses: Over-the-counter uoride rinses may be bene cial for use for children,
particularly those who have high caries risk or live in uoride-de cient areas. Mouth rinses
should be reserved for high-risk children aged older than 6 years who can rinse and spit.2,10
Alcohol-containing mouth rinses should be avoided in pediatric populations.9 Fluoride
mouth rinses, supplements, or gels can be used after brushing with uoride toothpaste.
Varnish: Fluoride varnish is a highly concentrated form of topical uoride that is applied to
teeth in a professionally supervised setting. Research shows uoride varnish is highly
effective in caries reduction with a decrease in caries incidence between 18% to 24% in 1
study and as high as 59% in another.11,12 The USPSTF “recommends that primary care
clinicians apply uoride varnish to the primary teeth of all infants and children starting at the
age of primary tooth eruption” through age 5 years.6 The recommended uoride varnish
dose is 0.25 mL unidose 5% NaF (2.26% F), and frequency is every 3 to 6 months, based on
the child’s caries risk considerations.2,13 Fluoride varnish application is easy and fast. A thin
layer should be placed on relatively dry teeth achieved by wiping the teeth with gauze.
2. Use gauze to blot the teeth dry. Varnish does not adhere well to teeth if they are wet.
3. Prepare for application by stirring the varnish and apply varnish to dried teeth, starting on
the back teeth. Apply a thin layer to all tooth surfaces with the supplied brush.
4. Apply varnish to the front teeth last. Saliva contamination after application is expected
and varnish sets on contact with saliva (Figure 3).
5. Provide caregiver instructions about varnish application after care (Table 1).13
Instructional videos of proper uoride varnish application technique can be viewed online in
the National Smiles for Life Curriculum Module 613: www.smilesforlifeoralhealth.com.
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Advocate in most states who can educate individuals and o ces on uoride varnish
application or provide support as questions arise about oral health integration into
practice.17
Developing a clinical work ow to include uoride varnish application can improve the oral
health of children within a practice. A recent Qualis Health White Paper offers speci c
strategies for integration of oral health into practice work ow.18
Dental providers may recommend other forms of topical uoride, including highly
concentrated uoride gels. However, these are generally not recommended for young
children aged younger than 6 years. In addition, silver diamine uoride is a modality now
being used in dentistry to help arrest caries in primary teeth.19,20
Lastly, uoridated community water aids in prevention of dental caries by up to 27%21 and
reduces dental expenditures per capita22 by providing both topical and systemic routes of
uoride. Fluoridated tap water use should be encouraged instead of bottled water use,
which may not contain uoride and may be more acidic than previously anticipated, thus
promoting demineralization of tooth structure.23 Parents who live in areas with uoridated
water should be asked if their child drinks uoridated water. Parents often use bottled water
and therefore their children may not be receiving the bene ts of uoridated water. Pediatric
medical and dental providers should continue to strongly advocate for community water
uoridation as it bene ts not only children, but the entire population.24
SYSTEMIC FLUORIDE
Challenges
The fear of uorosis has fueled some concerns about uoride use. Fluorosis occurs when
developing teeth are exposed to high quantities of uoride. Fluorosis presents as white
streaks or mottling on the tooth surface (Figure 4), with the milder presentations typically
not noticeable except by a trained dental professional.26 The risk of uorosis increases
when uoride is not used appropriately, such as eating large amounts of uoride toothpaste
during unsupervised brushing, or prescribing uoride to a child who already is drinking
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uoridated water. Recommend that caregivers always supervise young children during tooth
brushing and keep toothpaste in a safe location out of reach of young children, just like
other medications in the home.
Many other fears, such as uoride causing cancer or a low IQ, do not have a basis in
scienti c evidence. A good AAP website to refer to patients to help address these myths is
ilikemyteeth.org. It is important to understand concerns regarding uoride and seize the
opportunity to use motivational interviewing beginning with open-ended questions that
promote dialogue, such as: “What have you heard about uoride?” or “Help me understand
your concerns about uoride use.”
There may be times when you have given the family all the facts and they may continue to
refuse uoride. In these situations, it is best to make certain the patient has early and
consistent dental care to continue the discussion. Consistent messaging from the primary
care provider and dental specialists may help allay fears and encourage families to use
uoride.
References:
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1999-2004. Vital Health Stat 11. 2007;(248):1-92.
2. Clark MB, Slayton RL; Section on Oral Health. Fluoride use in caries prevention in the
primary care setting. Pediatrics. 2014;134(3):626-633.
3. US Department of Health and Human Services. Oral Health in America: A Report of the
Surgeon General. Executive summary. Rockville, MD: US Department of Health and Human
Services, National Institute of Dental and Craniofacial Research, National Institutes of
Health; 2000. Available at: https://www.nidcr.nih.gov/research/data-statistics/surgeon-
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5. Weyant RJ, Tracy SL, Anselmo T, et al; American Dental Association Council on Scienti c
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Care. Seattle, WA: Qualis Health; June 2015. Available at:
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caries management in children and adolescents, including those with special health care
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