ABSTRACTS
OCTUBRE
2007
PEDIATRICS Vol. 120
No. 4 October 2007, pp.
e788-e794 (doi:10.1542/peds.2006-3765)
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Amir Kugelman, MDa,
Brian Reichman, MBChBb,c, Irena Chistyakov, MDa, Valentina
Boyko, MScb, Orna Levitski, BAb, Liat Lerner-Geva, MD,
PhDb,c, Arieh Riskin, MDa, David Bader, MD, MHAa
in collaboration with the Israel Neonatal Network
OBJECTIVE. The objective of this study was to identify
factors that were associated with death after discharge from the
NICU of very low birth weight infants in a population-based study.
METHODS. From a national cohort of 13430 very low
birth weight infants who were born in Israel from 1995 to 2003,
10602 infants were discharged from the hospital and composed the
study population. Demographic and clinical data regarding the
pregnancy, delivery, and neonatal course were obtained from the
Israel national very low birth weight infant database. Data on each
case of death during the postdischarge period until 1 year of age
were provided by the Ministry of Health from national linked birth
and death certificates. Univariate analyses and a multivariable
logistic regression analyses were performed to examine the perinatal
and neonatal risk factors for postdischarge death.
RESULTS. The postdischarge mortality rate was 7.5 per
1000 (80 of 10602 infants discharged from the hospital). The death
rate was significantly higher in non-Jewish infants, infants who
were born to young mothers, and infants who were born to low-educated
mothers. After adjustment for demographic characteristics and perinatal
and neonatal variables, postdischarge mortality was independently
associated with congenital malformations, neonatal seizures,
necrotizing enterocolitis, and bronchopulmonary dysplasia.
CONCLUSION. Although the postdischarge death rate was
relatively low in our cohort of very low birth weight infants,
attention should be focused on the subgroups of infants who are at
higher risk to decrease their mortality further.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e815-e825 (doi:10.1542/peds.2006-3122)
Patrick Van
Reempts, MD, PhDa, Ludwig Gortner, MD, PhDb, David
Milligan, MDc, Marina Cuttini, MD, PhDd, Stavros Petrou,
PhDe, Rocco Agostino, MDf, David Field, MDg,
Lya den Ouden, MD, PhDh, Klaus Børch, MDi, Jan Mazela, MDj,
Manuel Carrapato, MDk, Jennifer Zeitlin, DScl for the
MOSAIC Research Group
OBJECTIVES. We sought to compare guidelines for level
III units in 10 European regions and analyze the characteristics of
neonatal units that care for very preterm infants.
METHODS. The MOSAIC (Models of Organising Access to
Intensive Care for Very Preterm Births) project combined a
prospective cohort study on all births between 22 and 31 completed
weeks of gestation in 10 European regions and a survey of neonatal
unit characteristics. Units that admitted
5
infants at <32 weeks of gestation were included in the analysis (N
= 111). Place of hospitalization of infants who were admitted to
neonatal care was analyzed by using the cohort data (N =
4947). National or regional guidelines for level III units were
reviewed.
RESULTS. Six of 9 guidelines for level III units
included minimum size criteria, based on number of intensive care
beds (6 guidelines), neonatal admissions (2), ventilated patients
(1), obstetric intensive care beds (1), and deliveries (2). The
characteristics of level III units varied, and many were small or
unspecialized by recommended criteria: 36% had fewer than 50 very
preterm annual admissions, 22% ventilated fewer than 50 infants
annually, and 28% had fewer than 6 intensive care beds. Level II
units were less specialized, but some provided mechanical
ventilation (57%) or high-frequency ventilation (20%) or had
neonatal surgery facilities (17%). Sixty-nine percent of level III
and 36% of level I or II units had continuous medical coverage by a
qualified pediatrician. Twenty-two percent of infants who were
<28 weeks of gestation were treated in units that admitted fewer
than 50 very preterm infants annually (range: 2%–54% across the
study regions).
CONCLUSIONS. No consensus exists in Europe about size
or other criteria for NICUs. A better understanding of the
characteristics associated with high-quality neonatal care is
needed, given the high proportion of very preterm infants who are
cared for in units that are considered small or less specialized by
many recommendations.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e992-e1001 (doi:10.1542/peds.2006-2775)
Donald B. Bailey,
Jr, PhDa, Lauren Nelson, PhDb, Kathy Hebbeler, PhDc
and Donna Spiker, PhDc
OBJECTIVE. The purpose of this work was to examine
factors related to perceived impact of early intervention on
children with disabilities and their families.
METHODS. A nationally representative sample of
2100
parents completed a 40-minute telephone interview near their child's
third birthday. Structural equation modeling examined the relationships
between 3 support variables (quality of child services, quality of
family services, and family/community support) and 2 outcomes at 36
months (impact on child and impact on family) and determined whether
these relationships were mediated by 2 perceptual variables (optimism
and confidence in parenting) or moderated by 5 demographic variables
(poverty, maternal education, ethnicity, age of initial Individual
Family Service Plan, and health at 36 months).
RESULTS. Perceived impact of early intervention on
both child and family were significantly related to each other. The
quality of child services was related to impact on the child but not
on the family. The quality of family services was related to both
child and family impact. Informal support was not related to
perceived impact on children or families but was strongly related to
confidence in parenting and optimism. Neither optimism nor
confidence in parenting mediated the relationships between services
or supports and perceived impact. Minority families and families of
children with poor health reported lower quality of services, but
these characteristics did not moderate the relationships between
services and perceived impact on the child. However, both poverty
status and minority status were associated with perceptions of
impact on the family.
CONCLUSIONS. Findings reinforce the role of
high-quality services in maximizing perceived impact. They also
highlight the important role of informal support in promoting
optimism and confidence in parenting. Poverty status, minority
status, and poor health of the child are salient factors in
predicting lower perceived quality of and benefit from services.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e1017-e1027 (doi:10.1542/peds.2006-3482)
Gale A. Richardson,
PhDa, Lidush Goldschmidt, PhDb and Cynthia Larkby, PhDa
OBJECTIVE. There has been a limited amount of research
on the long-term effects of prenatal cocaine exposure on growth of
the infant, and there has been no use of longitudinal growth models.
We investigated the effects of prenatal cocaine exposure on
offspring growth from 1 through 10 years of age by using a
repeated-measures growth-curve model.
METHODS. Women were enrolled from a prenatal clinic
and interviewed at the end of each trimester of pregnancy about
their cocaine, crack, alcohol, marijuana, tobacco, and other drug
use. Fifty percent of the women were white, and 50% were black.
Follow-up assessments occurred at 1, 3, 7, and 10 years of age.
RESULTS. Cross-sectional analyses showed that children
exposed to cocaine during the first trimester (n = 99) were smaller
on all growth parameters at 7 and 10 years, but not at 1 or 3
years, than the children who were not exposed to cocaine during the
first trimester (n = 125). The longitudinal analyses indicated that
the growth curves for the 2 groups diverged over time: children who
were prenatally exposed to cocaine grew at a slower rate than
children who were not exposed. These analyses controlled for other
factors associated with child growth.
CONCLUSIONS. To our knowledge, this is the first study
of the long-term effects of prenatal cocaine exposure to conduct
longitudinal growth-curve analyses using 4 time points in childhood.
Children who were exposed to cocaine during the first trimester grew
at a slower rate than those who were not exposed. These findings indicate
that prenatal cocaine exposure has a lasting effect on child development.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e1028-e1034 (doi:10.1542/peds.2006-3433)
Ohad Ronen, MDa,
Atul Malhotra, MDb and Giora Pillar, MD, PhDc
OBJECTIVE. Obstructive sleep apnea has a strong male
predominance in adults but not in children. The collapsible portion
of the upper airway is longer in adult men than in women (a property
that may increase vulnerability to collapse during sleep). We sought
to test the hypothesis that in prepubertal children, pharyngeal
airway length is equal between genders, but after puberty boys have
a longer upper airway than girls, thus potentially contributing to this
change in apnea propensity.
METHODS. Sixty-nine healthy boys and girls who had
undergone computed tomography scans of their neck for other reasons
were selected from the computed tomography archives of Rambam and
Carmel hospitals. The airway length was measured in the midsagittal plane
and defined as the length between the lower part of the posterior
hard palate and the upper limit of the hyoid bone. Airway length and
normalized airway length/body height were compared between the
genders in prepubertal (4- to 10-year-old) and postpubertal (14- to
19-year-old) children.
RESULTS. In prepubertal children, airway length was
similar between boys and girls (43.2 ± 5.9 vs 46.8 ±
CONCLUSIONS. Although boys have equal or shorter
airway length compared with girls among prepubertal children, after
puberty, airway length and airway length normalized for body height
are significantly greater in boys than in girls. These data suggest
that important anatomic changes at puberty occur in a gender-specific
manner, which may be important in explaining the male predisposition
to pharyngeal collapse in adults.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e1035-e1042 (doi:10.1542/peds.2006-3567)
Katsumi Mizuno, MD,
PhD, Yoshiko Nishida, MD, Motohiro Taki, MD, Satoshi Hibino, MD, Masahiko
Murase, MD, Motoichirou Sakurai, MD, PhD and Kazuo Itabashi, MD, PhD
OBJECTIVE. Preterm infants with bronchopulmonary
dysplasia often demonstrate sucking difficulties. The aim of this
study was to determine whether the severity of bronchopulmonary
dysplasia affects not only coordination among
suck–swallow–respiration but also sucking endurance and performance
itself.
PATIENTS AND METHODS. Twenty very low birth weight
infants were studied. Infants with anomalies or intraventricular
hemorrhage were excluded from the evaluation. Subjects were divided
into 3 groups: no bronchopulmonary dysplasia (7 infants),
bronchopulmonary dysplasia without home oxygen therapy (7 infants),
and bronchopulmonary dysplasia with home oxygen therapy (6 infants).
In addition to sucking efficiency, pressure, frequency, duration,
and duration of sucking burst, length of deglutition apnea, number
of swallows per burst, and respiratory rate were also measured
during bottle-feeding at 40 weeks' postmenstrual age. In addition, PCO2
and oxygen saturation were measured at rest and during
bottle-feeding.
RESULTS. Infants with severe bronchopulmonary
dysplasia demonstrated not only the lowest sucking pressure and
sucking frequency, shortest sucking burst duration, and lowest
feeding efficiency but also the lowest frequency of swallows during
the run and the longest deglutition apnea. The respiratory rate was
highest, and the decrease in oxygen saturation was largest, in
infants with severe bronchopulmonary dysplasia.
CONCLUSIONS. Feeding problems depend on the severity
of bronchopulmonary dysplasia. Infants with bronchopulmonary
dysplasia demonstrated not only poor feeding coordination but also
poor feeding endurance and performance.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 723-733 (doi:10.1542/peds.2006-1939)
Robin J. Edison,
MD, MPHa, Kate Berg, PhDa, Alan Remaley, MDb,
Richard Kelley, MD, PhDc, Charles Rotimi, PhDd, Roger E.
Stevenson, MDe and Maximilian Muenke, MDa
OBJECTIVE. The objective of this study was to assess
whether low maternal serum cholesterol during pregnancy is
associated with preterm delivery, impaired fetal growth, or
congenital anomalies in women without identified major risk factors
for adverse pregnancy outcome.
METHODS. Mother-infant pairs were retrospectively
ascertained from among a cohort of 9938 women who were referred to
South Carolina prenatal clinics for routine second-trimester serum
screening. Banked sera were assayed for total cholesterol; <10th percentile
of assayed values (159 mg/dL at mean gestational age of 17.6 weeks)
defined a "low total cholesterol" prenatal risk category.
Eligible women were aged 21 to 34 years and nonsmoking and did not
have diabetes; neonates were liveborn after singleton gestations.
Total cholesterol values of eligible mothers were adjusted for
gestational age at screening before risk group assignment. The study
population included 118 women with low total cholesterol and 940
women with higher total cholesterol. Primary analyses used
multivariate regression models to compare rates of preterm delivery,
fetal growth parameters, and congenital anomalies between women with
low total cholesterol and control subjects with mid–total
cholesterol values >10th percentile but <90th percentile.
RESULTS. Prevalence of preterm delivery among mothers
with low total cholesterol was 12.7%, compared with 5.0% among
control subjects with mid–total cholesterol. The association of
low maternal serum cholesterol with preterm birth was observed only
among white mothers. Term infants of mothers with low total cholesterol
weighed on average
CONCLUSIONS. Total serum cholesterol <10th
population percentile was strongly associated with preterm delivery
among otherwise low-risk white mothers in this pilot study
population. Term infants of mothers with low total cholesterol
weighed less than control infants among both racial groups.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 770-777 (doi:10.1542/peds.2007-0514)
Renée A. Shellhaas,
MDa,b, Adina I. Soaita, MD, DPHc and Robert R. Clancy, MDa,b
BACKGROUND. Conventional electroencephalography
remains the gold standard for the diagnosis and quantification of
neonatal seizures. However, amplitude-integrated
electroencephalography (aEEG) is being introduced to neonatal
intensive care as an adjunct for neonatal seizure detection.
OBJECTIVES. This study's purpose was to determine the
sensitivity of neonatal seizure detection in a single
electroencephalogram channel (C3
C4),
used to simulate the raw signal from which aEEG is derived. We also
aimed to determine the sensitivity of seizure detection by
neonatologists by using aEEG and to establish those neonatal seizure
characteristics that are associated with their correct detection by
aEEG.
METHODS. Conventional electroencephalograms with
neonatal seizures were reviewed for electroencephalogram background
and neonatal seizure characteristics (site of onset, duration, and
peak-to-peak amplitude). The presence, duration, and peak-to-peak
amplitude of each seizure were simultaneously noted in a single
electroencephalogram channel (C3
C4).
aEEGs generated from this channel were reviewed for background and
seizures by 6 neonatologists with varying aEEG interpretation
expertise.
RESULTS. A total of 851 neonatal seizures from 125
conventional electroencephalograms were analyzed. The patients' conceptional
ages were 34 to 50 weeks. Because 94% of the conventional
electroencephalograms had
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neonatal seizure visible in C3
C4,
and 78% of all neonatal seizures appeared in the C3
C4
channel, the theoretical sensitivity of seizure detection in a
single electroencephalogram channel was high. However, seizures were
briefer and lower in amplitude in C3
C4
compared with conventional electroencephalography. Neonatologists identified
seizures in 22% to 57% of the 125 records of neonatal seizure. They
detected 12% to 38% of the 851 individual seizures. Multivariate
analysis revealed that the appearance of seizures in C3
C4,
neonatal seizure duration, seizure amplitude, seizure count per
hour, and neonatologists' experience with aEEG interpretation all
correlated with neonatal seizure detection.
CONCLUSIONS. Even among physicians who have extensive
experience, many neonatal seizures are difficult to detect on an
aEEG, especially when they are infrequent, brief, or of low
amplitude.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 778-784 (doi:10.1542/peds.2007-0540)
E. Juulia Paavonen,
MD, PhD, BSocSca, Sonja Strang-Karlsson, MDb,c, Katri
Räikkönen, PhDa, Kati Heinonen, PhDa, Anu-Katriina
Pesonen, PhDa, Petteri Hovi, MDb,c, Sture Andersson, MD,
PhDc, Anna-Liisa Järvenpää, MD, PhDc, Johan G. Eriksson,
MD, PhDb,d and Eero Kajantie, MD, PhDb,c
OBJECTIVE. We investigated whether very low birth
weight (<
METHODS. The study was a retrospective longitudinal
study of 158 young adults born with very low birth weight and 169
term-born control subjects (aged 18.5–27.1 years). The principal
outcome variable was sleep-disordered breathing defined as chronic snoring.
RESULTS. The crude prevalence of chronic snoring was
similar in both groups: 15.8% for the very low birth weight group
versus 13.6% for the control group. However, after controlling for
the confounding variables in multivariate logistic regression models
(age, gender, current smoking, parental education, height, BMI, and
depression), chronic snoring was 2.2 times more likely in the very
low birth weight group compared with the control group. In addition,
maternal smoking during pregnancy was significantly and
independently of very low birth weight related to risk of sleep-disordered
breathing. Maternal preeclampsia, standardized birth weight, and,
for very low birth weight infants, small-for-gestational-age status
were not related to sleep-disordered breathing.
CONCLUSIONS. Premature infants with very low birth
weight have a twofold risk of sleep-disordered breathing as young
adults. In addition, maternal smoking during pregnancy increases the
risk of sleep-disordered breathing by more than twofold.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 785-792 (doi:10.1542/peds.2007-0211)
OBJECTIVES. Periventricular hemorrhagic infarction is
a serious complication of germinal matrix-intraventricular
hemorrhage in premature infants. Our objective was to determine the
neurodevelopmental and adaptive outcomes of periventricular
hemorrhagic infarction survivors and identify early cranial
ultrasound predictors of adverse outcome.
METHODS. We retrospectively evaluated all cranial
ultrasounds of 30 premature infants with periventricular hemorrhagic
infarction and assigned a cranial ultrasound–based periventricular
hemorrhagic infarction severity score (range: 0–3) on the
basis of whether periventricular hemorrhagic infarction (1) involved
2
territories, (2) was bilateral, or (3) caused midline shift. We then
performed neuromotor, visual function, and developmental evaluations
(Mullen Scales of Early Learning, Vineland Adaptive Behavior Scale).
Developmental scores below 2 SD from the mean were defined as abnormal.
RESULTS. Median adjusted age at evaluation was 30
months (range: 12–66 months). Eighteen subjects (60%) had abnormal
muscle tone, and 7 (26%) had visual field defects. Developmental
delays involved gross motor (22 [73%]), fine motor (17 [59%]), visual
receptive (13 [46%]), expressive language (11 [38%]), and cognitive (14
[50%]) domains. Impairment in daily living and socialization was
documented in 10 (33%) and 6 (20%) infants, respectively. Higher
cranial ultrasound–based periventricular hemorrhagic infarction
severity scores predicted microcephaly and abnormalities in gross
motor, visual receptive, and cognitive function.
CONCLUSIONS. In the current era, two thirds of
periventricular hemorrhagic infarction survivors develop significant
cognitive and/or motor abnormalities, whereas adaptive skills are
relatively spared. Higher cranial ultrasound–based periventricular
hemorrhagic infarction severity scores predict worse outcome in
several modalities and may prove to be a valuable tool for prognostication.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 793-804 (doi:10.1542/peds.2007-0440)
BACKGROUND. Studies of very preterm infants have
demonstrated impairments in multiple neurocognitive domains. We
hypothesized that neuromotor and executive-function deficits may
independently contribute to school failure.
METHODS. We studied children who were born at
25
completed weeks' gestation in the United Kingdom and Ireland in 1995
at early school age. Children underwent standardized cognitive and
neuromotor assessments, including the Kaufman Assessment Battery for
Children and NEPSY, and a teacher-based assessment of academic
achievement.
RESULTS. Of 308 surviving children, 241 (78%) were
assessed at a median age of 6 years 4 months. Compared with 160 term
classmates, 180 extremely preterm children without cerebral palsy
and attending mainstream school performed less well on 3 simple
motor tasks: posting coins, heel walking, and 1-leg standing. They
more frequently had non–right-hand preferences (28% vs 10%) and more
associated/overflow movements during motor tasks. Standardized
scores for visuospatial and sensorimotor function performance
differed from classmates by 1.6 and 1.1 SDs of the classmates'
scores, respectively. These differences attenuated but remained
significant after controlling for overall cognitive scores. Cognitive,
visuospatial scores, and motor scores explained 54% of the variance
in teachers' ratings of performance in the whole set; in the
extremely preterm group, additional variance was explained by
attention-executive tasks and gender.
CONCLUSIONS. Impairment of motor, visuospatial, and
sensorimotor function, including planning, self-regulation, inhibition,
and motor persistence, contributes excess morbidity over cognitive
impairment in extremely preterm children and contributes independently
to poor classroom performance at 6 years of age.
PEDIATRICS Vol. 120 No. 4 October 2007, pp. e1097-e1106 (doi:10.1542/peds.2006-2083)
Swaddling was an almost universal child-care practice
before the 18th century. It is still tradition in certain parts of
the Middle East and is gaining popularity in the United Kingdom, the
United States, and the Netherlands to curb excessive crying. We have
systematically reviewed all articles on swaddling to evaluate its
possible benefits and disadvantages. In general, swaddled infants
arouse less and sleep longer. Preterm infants have shown improved
neuromuscular development, less physiologic distress, better motor
organization, and more self-regulatory ability when they are
swaddled. When compared with massage, excessively crying infants cried
less when swaddled, and swaddling can soothe pain in infants. It is
supportive in cases of neonatal abstinence syndrome and infants with
neonatal cerebral lesions. It can be helpful in regulating
temperature but can also cause hyperthermia when misapplied. Another
possible adverse effect is an increased risk of the development of
hip dysplasia, which is related to swaddling with the legs in
extension and adduction. Although swaddling promotes the favorable
supine position, the combination of swaddling with prone position
increases the risk of sudden infant death syndrome, which makes it
necessary to warn parents to stop swaddling if infants attempt to
turn. There is some evidence that there is a higher risk of
respiratory infections related to the tightness of swaddling. Furthermore,
swaddling does not influence rickets onset or bone properties. Swaddling
immediately after birth can cause delayed postnatal weight gain
under certain conditions, but does not seem to influence breastfeeding
parameters.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 855-864 (doi:10.1542/peds.2007-0078)
Although asthma is the most common cause of cough,
wheeze, and dyspnea in children and adults, asthma is often
attributed inappropriately to symptoms from other causes. Cough that
is misdiagnosed as asthma can occur with pertussis, cystic fibrosis,
primary ciliary dyskinesia, airway abnormalities such as
tracheomalacia and bronchomalacia, chronic purulent or suppurative
bronchitis in young children, and habit-cough syndrome. The
respiratory sounds that occur with the upper airway obstruction
caused by the various manifestations of the vocal cord dysfunction
syndrome or the less common exercise-induced laryngomalacia are
often mischaracterized as wheezing and attributed to asthma. The
perception of dyspnea is a prominent symptom of hyperventilation
attacks. This can occur in those with or without asthma, and
patients with asthma may not readily distinguish the perceived
dyspnea of a hyperventilation attack from the acute airway
obstruction of asthma. Dyspnea on exertion, in the absence of other
symptoms of asthma or an unequivocal response to albuterol, is most
likely a result of other causes. Most common is the dyspnea
associated with normal exercise limitation, but causes of dyspnea on
exertion can include other physiologic abnormalities including
exercise-induced vocal cord dysfunction, exercise-induced
laryngomalacia, exercise-induced hyperventilation, and
exercise-induced supraventricular tachycardia. A careful history,
attention to the nature of the respiratory sounds that are present,
spirometry, exercise testing, and blood-gas measurement provide
useful data to sort out the various causes and avoid inappropriate
treatment of these pseudo-asthma clinical manifestations.
PEDIATRICS
Vol. 120 No. 4 October 2007, pp. 898-921 (doi:10.1542/peds.2007-2333)
Key Words: hearing screening
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THE POSITION STATEMENT |
The Joint Committee on Infant Hearing (JCIH) endorses early detection
of and intervention for infants with hearing loss. The goal of early
hearing detection and intervention (EHDI) is to maximize linguistic
competence and literacy development for children who are deaf or
hard of hearing. Without appropriate opportunities to learn
language, these children will fall behind their hearing peers in
communication, cognition, reading, and social-emotional development.
Such delays may result in lower educational and employment levels in
adulthood.1 To maximize the outcome for infants who are
deaf or hard of hearing, the hearing of all infants should be
screened at no later than 1 month of age. Those who do not pass
screening should have a comprehensive audiological evaluation at no
later than 3 months of age. Infants with confirmed hearing loss
should receive appropriate intervention at no later than 6 months of
age from health care and education professionals with expertise in
hearing loss and deafness in infants and young children. Regardless
of previous hearing-screening outcomes, all infants with or without
risk factors should receive ongoing surveillance of communicative
development beginning at 2 months of age during well-child visits in
the medical home.2 EHDI systems should guarantee seamless transitions
for infants and their families through this process.
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2007 JCIH POSITION STATEMENT UPDATES |