(18) Peds Flashcards

1
Q

Four Principles of Child Development

A
  1. Child development proceeds along a predictable pathway.
    - Child development proceeds along a predictable pathway governed
    by the maturing brain. You can measure age-specific milestones and use
    them to characterize development as normal or abnormal. Because your
    health care visit and physical examination take place at one point in time,
    you need to determine where the child fits along a developmental trajectory.
    Milestones are achieved in an order than can be anticipated. Loss of milestones
    is always concerning
  2. The range of normal development is wide.
    - The range of normal development is wide. Children mature at different
    rates. Each child’s physical, cognitive, and social development should
    fall within a broad developmental range
  3. Various physical, social, and environmental factors, as well as diseases, can
    affect child development and health.
    - Various physical, social, and environmental factors, as well as diseases,
    can affect child development and health. For example, chronic illnesses, child abuse,
    and poverty can all cause detectable physical abnormalities and alter the rate and
    course of development. Additionally, children with physical or cognitive disabilities
    may not follow the expected age-specific developmental trajectory
  4. The child’s developmental level affects how you conduct the history and
    physical examination
    - The child’s developmental level affects how you conduct the clinical
    history and physical examination. For example, interviewing a 5-year-old is fundamentally different than interviewing an adolescent. Both order and
    style differ from the adult examination. Before performing a physical examination,
    attempt to ascertain the child’s approximate developmental level and
    adapt your physical examination to that level. An understanding of normal
    child development helps you achieve these tasks
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2
Q

Key Components of Pediatric

Health Promotion

A
  1. Age-appropriate developmental achievement of the child
    ● Physical (maturation, growth, puberty)
    ● Motor (gross and fine motor skills)
    ● Cognitive (developmental milestones, language, school performance)
    ● Emotional (self-regulation, mood, temperament, self-efficacy, self-esteem,
    independence)
    ● Social (social competence, self-responsibility, integration with family and
    community, peer interactions)
  2. Health supervision visits
    ● Periodic assessment of clinical and oral health
    ● More frequent health supervision visits for children with special health
    care needs
  3. Integration of physical examination findings with health promotion
  4. Immunizations
  5. Screening procedures
  6. Anticipatory guidance4,8
    ● Healthy habits
    ● Nutrition and healthy eating
    ● Safety and prevention of injury
    ● Physical activity
    ● Sexual development and sexuality
    ● Self-responsibility, efficacy, and healthy self-esteem
    ● Family relationships (interactions, strengths, supports)
    ● Positive parenting strategies
    ● Emotional and mental health
    ● Oral health
    ● Recognition of illness
    ● Sleep
    ● Screen time
    ● Prevention of risky behaviors (e.g., tobacco, alcohol and drug use, unprotected
    sex)
    ● School and vocation
    ● Peer relationships
    ● Community interactions
  7. Partnership among health care provider, child/adolescent, and family
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3
Q

Tips for Examining Newborns

A

● Examine the newborn in the presence of the parents.
● Swaddle and then undress the newborn as the examination proceeds.
● Dim the lights and rock the newborn to encourage the eyes to open.
● Observe feeding, if possible, particularly breast-feeding.
● Demonstrate calming maneuvers to parents (e.g., swaddling).
● Observe and teach parents about transitions as the newborn arouses.
● A typical sequence for the examination of the newborn:
● Careful observation before (and during) the examination
● Heart
● Lungs
● Head, neck, and clavicles
● Ears and mouth
● Hips
● Abdomen and genitourinary system
● Lower extremities, back
● Eyes, whenever they are spontaneously open or at end of examination
● Skin, as you go along
● Neurologic system

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4
Q

Apgar Score.

A

an assessment of the newborn
immediately after birth. Its five components classify the newborn’s neurologic
recovery from the stress of birth and immediate adaptation to extrauterine life.
Score each newborn at 1 and 5 minutes after birth according to the following
table. Scoring is based on a 3-point scale (0, 1, or 2) for each component. Total
scores range from 0 to 10. Scoring may continue at 5-minute intervals until
the score is >7. If the 5-minute Apgar score is 8 or more, proceed to a more
complete examination.

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5
Q

Apgar Scoring System

A

HR: absent, <100, >100
Resp. effort: absent, slow/irregular, good/strong
Muscle tone: flaccid, some flexion, active
Reflex irritability: none, grimace, vigorous cry
Color: blue/pale, pink body/blue extremities, pink all over

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6
Q

Apgar 1-min score

A

8-10 normal
5-7 some nervous system depression
0-4 severe depression, require immediate resuscitation

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7
Q

Apgar 5-min score

A

8-10: normal

0-7: high risk for subsequent central nervous system and other organ system dysfunction

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8
Q

Ballard Scoring System

A

estimates
gestational age to within 2 weeks, even in extremely premature infants.

chart on pg 806

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9
Q

Gestational Age classification at birth

A

preterm: <34 weeks
late preterm: 34-36 weeks
term: 37-42 weeks
postterm: >42 weeks

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10
Q

Birth weight classification

A

extremely low: <1000g
very low: <1500g
low: <2500g
normal:>2500g

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11
Q

newborn classifications

A

small for gestation age: <10%
appropriate for gestation age: 10-90th %
large for gestation age: >90%

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12
Q

Most normal, full-term newborns

A

lie in a symmetric
position, with the limbs semiflexed and the legs partially abducted at the hip.
Note the baby’s spontaneous motor activity with flexion and extension alternating
between the arms and legs. The fingers are usually flexed in a tight fist, but
may extend in slow athetoid posturing movements. You will observe brief tremors
of the body and extremities during vigorous crying, and even at rest.

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13
Q

What a Newborn Can Do

A

Core Elements
● Newborns use all five senses. For example, they will look at human faces and
turn to a parent’s voice.
● Newborns are unique individuals. Marked differences exist in temperaments,
personality, behavior, and learning.
● Newborns interact dynamically with caregivers—a two-way street!
Examples of Complex Newborn Behavior
Habituation Ability to selectively and progressively shut out negative
stimuli (e.g., a repetitive sound)
Attachment A reciprocal, dynamic process of interacting and bonding
with the caregiver
State regulation Ability to modulate the level of arousal in response to different
degrees of stimulation (e.g., self-consoling)
Perception Ability to regard faces, turn to voices, quiet in presence of
singing, track colorful objects, respond to touch, and
recognize familiar scents

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14
Q

newborn to 1 year height/weight

A

weight - triple

height - increase by 50%

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15
Q

newborn physical development

A

Physical growth during infancy is faster than at
any other age.12 By 1 year, the infant’s birth weight should have tripled and
height increased by 50% from weight and height at birth.
Newborns have surprising abilities, such as fixing upon and following human
faces. Neurologic development progresses centrally to peripherally. Thus, newborns
learn head control before trunk control and use of arms and legs before
use of hands and fingers (Fig. 18-9).
Activity, exploration, and environmental manipulation contribute to learning. By
3 months, normal infants lift the head and clasp the hands. By 6 months, they roll
over, reach for objects, turn to voices, and possibly sit with support. With increasing
peripheral coordination, infants reach for objects, transfer them from hand to
hand, crawl, stand by holding on, and play with objects by banging and grabbing.
At 1 year a child may be standing and putting objects in the mouth

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16
Q

Newborn: cognitive and language development

A

Exploration fosters increased
understanding of self and environment. Infants learn cause and effect (e.g., shaking
a rattle produces sound), object permanence, and use of tools. By 9 months, they
may recognize the examiner as a stranger deserving wary cooperation, seek comfort
from parents during examinations, and actively manipulate reachable objects (e.g.,
your stethoscope). Language development proceeds from cooing at 2 months, to
babbling at 6 months, to saying one to three words by 1 year

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17
Q

newborn: social and emotional development

A

Understanding of self and
family also matures. Social tasks include bonding, attachment to caregivers, and
trust that caregivers will meet their needs (Fig. 18-11). Temperaments vary.
Some infants are predictable, adaptable, and respond positively to new stimuli;
others are less so and respond intensely or negatively. Because environment
affects social development, observe the infant’s interactions with caregivers

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18
Q

Developmental Milestones during infancy

A

p. 810, figure 18-11

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19
Q

Tips for Examining Infants

A

DISTRACTION!
● Approach the infant gradually, using a toy or object for distraction.
● Perform as much of the examination as possible with the infant in the parent’s lap.
● Speak softly to the infant or mimic the infant’s sounds to attract attention.
● If the infant is cranky, make sure he or she is well fed before proceeding.
● Ask a parent about the infant’s strengths to elicit useful developmental and
parenting information.
● Don’t expect to do a head-to-toe examination in a specific order. Work with
what the infant gives you and save the mouth and ear examination for last.

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20
Q

The AAP recommends that health care providers use a standardized developmental
screening instrument for infants as young as several months of age.
Several developmental screening instruments have been tested widely and validated
in many nations. In general, these instruments assess five critical domains
of infant/child development:

A

gross motor, fine motor, cognitive (or problem-solving),

communication, and personal/social domains of development

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21
Q

For babies born

prematurely, adjust expected developmental milestones for the gestational age up to

A

24 months

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22
Q

The AAP and the group Bright Futures4 recommend health supervision visits for
infants at the following ages:

A

at birth, at 3 to 5 days, by 1 month, and at 2, 4, 6,

9, and 12 months

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23
Q

? is one of the most important

indicators of infant health

A

Measurement of growth

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24
Q

The most important tools for assessing somatic growth are

A

the growth charts
which are published by the National Center for Health Statistics (www.cdc.
gov/nchsv)16 and also the World Health Organization (www.who.int).

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25
Q
Although obtaining
accurate blood pressure readings in
infants is challenging (Fig. 18-17), this
measurement is nevertheless important
for
A

some high-risk infants and should

be routinely performed after age 3 years.

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26
Q

HRs:
birth-1 month
1-6 months
6-12 months

A

140 (90-190)

130 (80-180)

115 (75-155)

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27
Q

RR newborn

A

30-60
The respiratory rate may vary considerably from moment to moment in the
newborn, with alternating periods of rapid and slow breathing (called “periodic
breathing”)

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28
Q

tachypnea from birth-1 year

A

Commonly accepted cutoffs for defining tachypnea are >60/min from birth to
2 months, and >50/min from 2 to 12 months

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29
Q

infants and temperature

A

Because
fever is so common in infants
and children, obtain an accurate
body temperature when
you suspect infection. Axillary
and thermal-tape skin
temperature recordings in
infants and children are inaccurate.
Auditory canal temperatures
are accurate.
Rectal temperatures are the
most accurate for infants
Body temperature in infants and children is less constant than in adults. The
average rectal temperature is higher in infancy and early childhood, usually
above 99°F (37.2°C) until after age 3 years. Body temperature may fluctuate as
much as 3°F during a single day, approaching 101°F (38.3°C) in normal children,
particularly in late afternoon and after vigorous activity

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30
Q

Newborns and Infants: Skin Inspection

A

Examine the skin of the newborn or infant carefully to identify
both normal markings and potentially abnormal ones. The photos on pp. 818–820
demonstrate normal markings. The newborn’s skin has a unique characteristic
texture and appearance. The texture is soft and smooth because it is thinner than
the skin of older children. Within the first 10 minutes after birth a normal newborn
progresses from generalized cyanosis to pinkness. In lighter-skinned
infants, an erythematous flush, giving the skin the appearance of a “boiled lobster,”
is common during the first 8 to 24 hours after which the normal pale pink
coloring predominates.
Vasomotor changes in the dermis and subcutaneous tissue—a response to cooling
or chronic exposure to radiant heat—can produce a lattice-like, bluish mottled
appearance (cutis marmorata), particularly on the trunk, arms, and legs. This
response to cold may last for months in normal infants. Acrocyanosis, a blue cast
to the hands and feet when exposed to cold (see p. 818), is very common in
newborns for the first few days and may recur throughout early infancy. Occasionally
in newborns, a remarkable color change (harlequin dyschromia) appears
with transient cyanosis of one half of the body or one extremity, presumably from
temporary vascular instability.
The amount of melanin in the skin of newborns varies, affecting pigmentation.
Black newborns may have a lighter skin color initially, except in the nail beds,
genitalia, and ear folds which are dark at birth. A dark or bluish pigmentation
over the buttocks and lower lumbar regions is common in newborns of African,
Asian, and Mediterranean descent. These areas, called slate blue patches, result
from pigmented cells in the deep layers of the skin; they become less noticeable
with age and usually disappear during childhood. Document these pigmented areas
to avoid later concern about bruising.
At birth, there is a fine, downy growth of hair called lanugo over the entire body,
especially the shoulders and back. This hair is shed within the first few weeks.
Lanugo is prominent in premature infants. Hair thickness on the head varies
considerably among newborns and is not predictive of later hair growth. All of the original hair is shed within months and is replaced with a new crop, sometimes
of a different color.
Inspect the newborn closely for a series of common skin conditions. At birth, a
cheesy white material called vernix caseosa, composed of sebum and desquamated
epithelial cells, covers the body. Some newborns have edema over their hands,
feet, lower legs, pubis, and sacrum; this disappears within a few days. Superficial
desquamation of the skin is often noticeable 24 to 36 hours after birth, particularly
in postterm babies (>40 weeks gestation), and it can last for 7 to 10 days.
You should be able to identify four common dermatologic conditions in newborns—
miliaria rubra, erythema toxicum, pustular melanosis, and milia—which
are shown on p. 819. None of these is clinically significant.
Note any signs of trauma from the birth process and the use of forceps or suction;
these signs disappear but should prompt a careful neurologic examination.

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31
Q

Newborns/Infants: Jaundice inspection

A

Carefully examine and touch the newborn’s skin to assess
the level of jaundice. Normal “physiologic” jaundice, which occurs in half
of all newborns, appears on the second or third day, peaks at about the fifth
day, and usually disappears within a week (although it may persist longer
in breast-fed infants). Jaundice is best seen in natural daylight rather than
artificial light. Newborn jaundice appears to progress from head to toe, with
more intense jaundice on the upper body and less intense yellow color in
the lower extremities.
To detect jaundice, apply pressure to the skin (Fig. 18-19) to press out the normal
pink or brown color. A yellowish “blanching” indicates jaundice

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32
Q

newborns/infants: vascular markings

A

A common vascular marking is the “salmon patch”
(also known as nevus simplex, “flame nevi,” telangiectatic nevus, or capillary
hemangioma). These flat, irregular, light pink patches (see p. 819) are most often
seen on the nape of the neck (“stork bite”), upper eyelids, forehead, or upper
lip (“angel kisses”). They are not true nevi, but result from distended capillaries.
They often disappear by 1 year of age and are covered by the hairline

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33
Q

newborns/infants: palpation

A

Palpate the newborn or infant’s skin to assess the degree of hydration,
or turgor. Roll a fold of loosely adherent skin on the abdominal wall
between your thumb and forefinger to determine its consistency. The skin in
well-hydrated infants returns to its normal position immediately upon release.
Delay in return is a phenomenon called “tenting” and usually occurs in children
with significant dehydration

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34
Q

Acrocyanosis

A

This bluish discoloration usually appears in the palms and
soles. Cyanotic congenital heart disease can present with severe
acrocyanosis

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35
Q

Jaundice

A

Physiologic jaundice occurs during days 2 to 5 of life and progresses
from head to toe as it peaks. Extreme jaundice may
signify a hemolytic process or biliary or liver disease.

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36
Q

Miliaria Rubra

A

Scattered vesicles on an erythematous base, usually on the face
and trunk, result from obstruction of the sweat gland ducts; this
condition disappears spontaneously within weeks

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37
Q

Erythema Toxicum

A

Usually appearing on days 2 to 3 of life, this rash consists of
erythematous macules with central pinpoint vesicles scattered
diffusely over the entire body. They appear similar to
flea bites. These lesions are of unknown etiology but disappear
within 1 week of birth

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38
Q

Pustular Melanosis

A

Seen more commonly in black infants, the rash presents at
birth as small vesiculopustules over a brown macular base;
these can last for several months

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39
Q

Milia

A

Pinhead-sized smooth white raised areas without surrounding
erythema on the nose (seen here), chin, and forehead result from
retention of sebum in the openings of the sebaceous glands.
Although occasionally present at birth, milia usually appear
within the first few weeks and disappears over several weeks

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40
Q

Eyelid Patch

A

This birthmark fades, usually within the first year of life

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41
Q

Salmon Patch

A

Also called the “stork bite,” or “angel kiss,” this splotchy pink
mark fades with age

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42
Q

Café-au-lait Spots

A

These light-brown pigmented lesions usually have borders and
are uniform. They are noted in more than 10% of black infants. If
more than five café-au-lait spots exist, consider the diagnosis of neurofibromatosis

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43
Q

Slate Blue Patches

A

These are more common among dark-skinned babies. It is
important to note them so that they are not mistaken for
bruises

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44
Q

newborns/infants: sutures and fontanelles

A

Membranous tissue spaces called sutures separate
the bones of the skull from one another. The areas where the major sutures intersect
in the anterior and posterior portions of the skull are known as fontanelles.
Examine the sutures and fontanelles carefully
On palpation, the sutures feel like ridges and the fontanelles like soft concavities.
The anterior fontanelle at birth measures 4 to 6 cm in diameter and usually
closes between 2 and 26 months of age (90% between 7 and 19 months). The
posterior fontanelle measures 1 to 2 cm at birth and usually closes by 2 months
Carefully examine the fontanelle, because its fullness reflects intracranial pressure.
Palpate the fontanelle while the baby is sitting quietly or being held upright.
Clinicians often palpate the fontanelles at the beginning of the examination. In
normal infants, the anterior fontanelle is soft and flat. A full anterior fontanelle
with increased intracranial pressure is seen when a baby cries or vomits. Pulsations
of the fontanelle reflect the peripheral pulse and are normal (and parents
often inquire about them). Learn to palpate the fontanelle because a bulging
fontanelle is concerning for increased intracranial pressure and a depressed
fontanelle may suggest dehydration.
Inspect the scalp veins carefully to assess for dilatation

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45
Q

infants/newborns: skull symmetry and head circumference

A

Carefully assess skull
symmetry (Fig. 18-21). Various conditions
can cause asymmetry; some are benign,
while others reflect underlying pathology.
Look for asymmetric head swelling. A
newborn’s scalp may be swollen over the
occipitoparietal region. This is called
caput succedaneum and results from capillary
distention and extravasation of
blood and fluid resulting from the vacuum
effect of rupture of the amniotic
sac. This swelling typically crosses suture
lines and resolves in 1 to 2 days.
The premature infant’s head at birth is relatively long in the occipitofrontal diameter
and narrow in the bitemporal diameter (dolichocephaly). Usually, the skull
shape normalizes within 1 to 2 years
Pick up the infant and examine the skull shape from behind. Asymmetry of the
cranial vault (positional plagiocephaly) occurs when an infant lies mostly on one
side, resulting in a flattening of the parieto-occipital region on the dependent
side and a prominence of the frontal region on the ipsilateral side. It disappears
as the baby becomes more active and spends less time in one position, and symmetry
is almost always restored. Interestingly, the current trend to have newborns
sleep on their backs to reduce the risk for sudden infant death syndrome (SIDS)
has resulted in more cases of positional plagiocephaly (Fig. 18-22). This condition
can be prevented by frequent repositioning (providing “tummy time” when the
infant is awake).
Measure the head circumference (p. 814) to detect abnormally large head size
(macrocephaly) or small head size (microcephaly), both of which may signify an
underlying disorder affecting the brain.
Palpate along the suture lines. A raised, bony ridge at a suture line suggests craniosynostosis.
Palpate the infant’s skull with care. The cranial bones generally appear “soft” or
pliable; they will normally become firmer with increasing gestational age

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46
Q

newborns/infants: facial symmetry

A

Check the face of infants for symmetry. In utero positioning
may result in transient facial asymmetries. If the head is flexed on the sternum,
a shortened chin (micrognathia) may result. Pressure of the shoulder on the
jaw may create a temporary lateral displacement of the mandible.
Examine the face for an overall impression of the facies; it is helpful to compare
with the face of the parents. A systematic assessment of a child with abnormalappearing
facies can identify specific syndromes.18 The box on the next page
describes steps for evaluating fa

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47
Q

Evaluating a Newborn or Child with

Possible Abnormal Facies

A

Carefully review the history, especially:
● Family history
● Pregnancy
● Perinatal history
Note abnormalities on other parts of the physical examination, especially:
● Growth
● Development
● Other dysmorphic somatic features
Perform measurements (and plot percentiles), especially:
● Head circumference
● Height
● Weight
Consider the three mechanisms of facial dysmorphogenesis:
● Deformations from intrauterine constraint
● Disruptions from amniotic bands or fetal tissue
● Malformations from intrinsic abnormality in face/head or brain
Examine the parents and siblings:
● Similarity to a parent may be reassuring (e.g., large head) but may also be an
indication of a familial disorder
Try to determine whether the facial features fit a recognizable syndrome,
comparing with:
● References (including measurements) and pictures of syndromes
● Tables/databases of combinations of features

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48
Q

Chvostek Sign

A

Percuss the cheek to check for Chvostek sign, which is present
in some metabolic disturbances and occasionally in normal infants. Percuss at
the top of the cheek just below the zygomatic bone in front of the ear, using the
tip of your index or middle finger

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49
Q

newborn/infants: eyes

A

Newborns keep their eyes closed except during brief awake periods.
If you attempt to separate their eyelids, they will tighten them even more.
Bright light causes infants to blink, so use subdued lighting. Awaken the baby
gently and support the baby in a sitting position; often the eyes open.
To examine the eyes of infants and young children, use some tricks to encourage
cooperation. Small colorful toys are useful as fixation devices in examining the
eyes.
Newborns may look at your
face and follow a bright light if
you catch them during an alert
period. Some newborns can
follow your face and turn their
heads 90° to each side. Examine
infants for eye movements.
Hold the baby upright, supporting
the head. Rotate yourself
with the baby slowly in one
direction. This usually causes
the baby’s eyes to open, allowing
you to examine the sclerae,
pupils, irises, and extraocular
movements (Fig. 18-23). The
baby’s eyes gaze in the direction
you are turning. When the rotation stops, the eyes look in the opposite direction,
after a few nystagmoid movements.
During the first 10 days of life, the eyes may stare in one direction if just the head
is turned without moving the body (doll’s eye reflex).
During the first few months of life, some infants have intermittent crossed eyes
(intermittent alternating convergent strabismus, or esotropia) or laterally deviated
eyes (intermittent alternating divergent strabismus, or exotropia).
Look for abnormalities or congenital problems in the sclera and pupils. Subconjunctival
hemorrhages are common in newborns and resolve within a
couple of weeks. The eyes of many newborns are edematous from the birth
process.
Observe pupillary reactions by response to light or by covering each eye with
your hand and then uncovering it. Although there may be initial asymmetry in
the size of the pupils, over time they should be equal in size and reaction to
light.
Inspect the irises carefully for abnormalities Examine the conjunctiva for swelling or redness. Most newborn nurseries use an
antibiotic eye ointment to help prevent gonococcal eye infection.
You will not be able to measure the visual acuity of newborns or infants. You can
use visual reflexes to indirectly assess vision: direct and consensual pupillaryconstriction in response to light, blinking in response to bright light (optic
blink reflex), and blinking in response to quick movement of an object toward
the eyes.

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50
Q

Visual Milestones of Infancy

A
Birth - Blinks, may regard face
1 month - Fixes on objects
1½–2 months - Coordinated eye movements
3 months - Eyes converge, baby reaches
toward a visual stimulus
12 months - Acuity around 20/60–20/80
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51
Q

newborns/infants: Ophthalmoscopic Examination.

A

For the ophthalmoscopic examination,
with the newborn awake and eyes open, examine the red retinal (fundus) reflex
by setting the ophthalmoscope at 0 diopters and viewing the pupil from about
10 inches. Normally, a red or orange color is reflected from the fundus through
the pupil.
A thorough ophthalmoscopic examination is difficult in young infants but may
be needed if ocular or neurologic abnormalities are noted. The cornea can ordinarily
be seen at +20 diopters, the lens at +15 diopters, and the fundus at 0
diopters.
Examine the optic disc area as you would for an adult. In infants, the optic disc
is difficult to visualize but is lighter in color, with less macular pigmentation. The
foveal light reflection may not be visible. Papilledema is rare in infants because
the fontanelles and open sutures accommodate any increased intracranial pressure,
sparing the optic discs.

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52
Q

newborns/infants: ears

A

The physical examination of the ears of infants is important because many
abnormalities can be detected, including structural problems, otitis media, and
hearing loss.
The goals are to determine the position, shape, and features of the ear and to detect
abnormalities. Note ear position in relation to the eyes. An imaginary line drawn
across the inner and outer canthi of the eyes should cross the pinna or auricle;
if the pinna is below this line the infant has low-set ears. Draw this imaginary
line across the face of the baby on p. 821; note that it crosses the pinna.
Otoscopic examination of the newborn’s ear can detect only patency of the ear
canal because accumulated vernix caseosa obscures the tympanic membrane for
the first few days of life A small skin tab, cleft, or pit found just forward of the tragus represents a remnant
of the first branchial cleft and usually has no significance. However, occasionally
it may also be associated with renal disease and acquired hearing loss if
there is a family history of hearing loss.
The infant’s ear canal is directed downward from the outside; therefore, pull
the auricle gently downward, not upward, for the best view of the eardrum.
Once the tympanic membrane is visible, note that the light reflex is diffuse; it
does not become cone-shaped for several months.
The acoustic blink reflex is a blinking of the infant’s eyes in response to a sudden
sharp sound. You can produce it by snapping your fingers or using a bell, beeper,
or other noisemaking device approximately 1 foot from the infant’s ear. Be sure you
are not producing an airstream that may cause the infant to blink. This reflex may
be difficult to elicit during the first 2 to 3 days of life. After it is elicited several times
within a brief period, the reflex disappears, a phenomenon known as habituation.
This crude test of hearing certainly is not diagnostic. Most newborns in the United
States undergo hearing screenings, which are mandatory in the majority of states

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53
Q

Signs That an Infant Can Hear

A

0–2 mo: Startle response and blink to a sudden noise
Calming down with soothing voice or music
2–3 mo: Change in body movements in response to sound
Change in facial expression to familiar sounds
Turning eyes and head to sound
3–4 mo: Turning to listen to voices and conversation
6–7 mo: Appropriate language development

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54
Q

infants/newborns: nose and sinuses

A

The most important component of the examination of the infant nose is to test
for patency of the nasal passages. You can do this by gently occluding each nostril
alternately while holding the infant’s mouth closed. This usually will not cause
stress because most infants are nasal breathers. Some infants are obligate nasal
breathers and have difficulty breathing through their mouths. Do not occlude
both nares simultaneously, as this will cause considerable distress.
Inspect the nose to ensure that the nasal septum is midline.
At birth, the maxillary and the ethmoid sinuses are present. Palpation of the
sinuses of newborns is not helpful.

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55
Q

newborns/infants: mouth and pharynx

A

Use both inspection with a tongue depressor and flashlight and palpation to inspect
the mouth and pharynx (Fig. 18-24). One method employs the parent to hold theinfant’s head and arms. The newborn’s
mouth is edentulous and the alveolar
mucosa is smooth with finely serrated
borders. Occasionally, pearl-like retention
cysts are seen along the alveolar
ridges and are easily mistaken for teeth;
these disappear within 1 or 2 months.
Petechiae are commonly found on the
soft palate after birth.
Palpate the upper hard palate to make sure it is intact. Epstein pearls, tiny white
or yellow, rounded mucous retention cysts, are located along the posterior midline
of the hard palate. They disappear within months.
Cysts may be noted on the tongue or mouth. Thyroglossal duct cysts may open
under the tongue.
Infants produce little saliva during the first 3 months. Older infants produce a
lot of saliva and drool frequently.
Inspect the tongue. The frenulum varies in tightness; sometimes it extends
almost to the tip and other times it is short, limiting protrusion of the tongue
(ankyloglossia or tongue tie).
You will often see a whitish covering on the tongue. If this coating is from milk,
it can be easily removed by scraping or wiping it away. Use a tongue depressor
or your gloved finger to wipe away the coating.
While there is a predictable pattern of tooth eruption, there is wide variation in the
age at which teeth appear. A rule of thumb is that a child will have 1 tooth for
each month of age between 6 and 26 months, up to a maximum of 20 primary
teeth.
The pharynx of the infant is best seen while the baby is crying. You will likely have
difficulty using a tongue depressor because it produces a strong gag reflex. Infants
do not have prominent lymphoid tissue so you will probably not visualize the
tonsils which increase in size as children grow.
Listen to the quality of the infant’s cry. Normal infants have a lusty, strong cry. The
following box lists some unusual types of infant cries

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56
Q

Abnormal Infant Cries (If Persistent)

A

Shrill or high pitched:
Increased intracranial pressure. Also in newborns born to
narcotic-addicted mothers.

Hoarse: Hypocalcemic tetany or congenital hypothyroidism

Continuous
inspiratory
and expiratory
stridor:
Upper airway obstruction from various lesions (e.g., a polyp
or hemangioma), a relatively small larynx (infantile laryngeal
stridor), or a delay in the development of the cartilage
in the tracheal rings (tracheomalacia)

Absence of cry: Severe illness, vocal cord paralysis, or profound brain damage

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57
Q

newborns/infants: neck

A

Palpate the lymph nodes of the neck and assess for any additional masses such as
congenital cysts (Fig. 18-25). Because the necks of infants are short, it is best to
palpate the neck while infants are lying supine, whereas older children are best
examined while sitting. Check the position of the thyroid cartilage and trachea.
In newborns, palpate the clavicles and look for evidence of a fracture. If present,
you may feel a break in the contour of the bone, tenderness, crepitus at the fracture
site, and may notice limited movement of the arm on the affected side.

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58
Q

newborns/infants: thorax and lungs

A

The infant’s thorax is more rounded than that of adults. The thin chest wall has
little musculature; thus, lung and heart sounds are transmitted quite clearly. The
bony and cartilaginous rib cage is soft and pliant. The tip of the xiphoid process
often protrudes anteriorly, immediately beneath the skin

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59
Q

newborns/infants: thorax and lungs inspection

A

Carefully assess respirations and breathing patterns. Newborns,
especially those born prematurely, show periods of normal rate (30 to 40 per
minute) alternating respirations that may even cease for 5 to 10 seconds. This
alternating pattern of rapid and slow breathing is called “periodic respiration” or
“periodic breathing.”
Do not rush to the stethoscope. Instead, observe the infant carefully as demonstrated
in Figure 18-26, which demonstrates locations for retractions among
infants. Inspection is easiest when infants are not crying; thus, work with the
parents to settle the child. Observe for 30 to 60 seconds, note general appearance,
respiratory rate, color, nasal component of breathing, audible breath
sounds, and work of breathing, as described below.
Because infants are obligate nasal breathers, observe their nose as they breathe.
Look for nasal flaring. Observe breathing with the infant’s mouth closed or during
nursing or sucking on a bottle to assess for nasal patency. Listen to the sounds of
breathing; note any grunting, audible wheezing, or lack of breath sounds (obstruction).
Nasal flaring, grunting, retractions, and wheezing are all signs of respiratory distress.
Observe two aspects of the infant’s breathing: audible breath sounds and work of
breathing. These are particularly relevant in assessing both upper and lower respiratory
illness. Studies in countries with poor access to chest radiographs have found these signs at least as useful as auscultation. Any of the abnormalities listed
below should raise concern about underlying respiratory pathology.
In healthy infants, the ribs do not move much during quiet breathing. Any outward
movement is produced by descent of the diaphragm which compresses the
abdominal contents and in turn shifts the lower ribs outward.
Pulmonary disease causes increased abdominal breathing and can result in
retractions (chest indrawing), an indicator of pulmonary disease before 2 years
of age.
Chest indrawing is inward movement of the skin between the ribs during inspiration.
Movement of the diaphragm primarily affects breathing with little assistance
from the thoracic muscles. As mentioned in the preceding table, four types
of retractions can be noted in infants: suprasternal, intercostal, substernal, and
subcostal.
Thoracoabdominal paradox, inward movement of the chest and outward movement
of the abdomen during inspiration (abdominal breathing), is a normal finding in
newborns (but not older infants). It persists during active, or rapid eye movement
(REM), sleep even when it is no longer seen during wakefulness or quiet sleep
because of the decreased muscle tone of active sleep. As muscle strength increases
and chest wall compliance decreases with age, abdominal breathing should no
longer be noted. If observed, it may signify respiratory disease

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60
Q

observing respiration before you touch the child: general appearance

A

Inability to feed or smile

Lack of consolability

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61
Q

observing respiration before you touch the child: respiratory rate

A

Tachypnea (see p. 815), apnea

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62
Q

observing respiration before you touch the child: color

A

Pallor or cyanosis

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63
Q

observing respiration before you touch the child: nasal component of breathing

A
Nasal flaring (enlargement of both nasal
openings during inspiration)
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64
Q

observing respiration before you touch the child: audible breath sounds

A

Grunting (repetitive, short expiratory sound)
Wheezing (musical expiratory sound)
Stridor (high-pitched, inspiratory noise)
Obstruction (lack of breath sounds)

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65
Q

observing respiration before you touch the child: work of breathing

A

Nasal flaring (excessive movement of nares)
Grunting (expiratory noises)
Retractions (chest indrawing):
Supraclavicular (soft tissue above clavicles)
Intercostal (indrawing of the skin between ribs)
Substernal (at xiphoid process)
Subcostal (just below the costal margin)

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66
Q

newborns/infants: thorax and lungs - palpation

A

Assess tactile fremitus by palpation. Place your hand on the
chest when the infant cries or makes noise. Place your hand or fingertips over
each side of the chest and feel for symmetry in the transmitted vibrations.
Percussion is not helpful in infants except in extreme instances. The infant’s
chest is hyperresonant throughout, and it is difficult to detect abnormalities
on percussion.

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67
Q

newborns/infants: thorax and lungs - auscultation

A

After performing these maneuvers, you are ready for auscultation.
Infant breath sounds are louder and harsher than those of adults because
the stethoscope is closer to the origin of the sounds. It is often difficult to distinguish
transmitted upper airway sounds from sounds originating in the chest.
Upper airway sounds tend to be loud, transmitted symmetrically throughout the
chest, and loudest as you move your stethoscope toward the neck. They are usually
coarse inspiratory sounds. Lower airway sounds are loudest over the site of
pathology, are often asymmetric, and often occur during expiration
Expiratory sounds usually arise from an intrathoracic source, whereas inspiratory
sounds can arise from an extrathoracic airway such as the trachea or from
an intrathoracic source. During expiration, the diameter of the intrathoracic airways
decreases because radial forces from the surrounding lung do not “tether”
the airways open as occurs during inspiration. Higher flow rates during inspiration
produce turbulent flow, resulting in appreciable sounds.
Expiratory sounds usually arise from an intrathoracic source, whereas inspiratory
sounds can arise from an extrathoracic airway such as the trachea or from
an intrathoracic source. During expiration, the diameter of the intrathoracic airways
decreases because radial forces from the surrounding lung do not “tether”
the airways open as occurs during inspiration. Higher flow rates during inspiration
produce turbulent flow, resulting in appreciable sounds.

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68
Q

infants/newborns: heart inspection

A

Before examining the heart itself, observe the infant carefully for any
cyanosis. Acrocyanosis in the newborn is discussed on pages 816 and 918. It is
important to detect central cyanosis because it is always abnormal and because
many congenital cardiac abnormalities, as well as respiratory diseases, present with
cyanosis.20
Recognizing minimal degrees of cyanosis requires care. Look inside the body
(i.e., the inside of the mouth, the tongue, or the conjunctivae) in addition to
assessing skin color. A true strawberry pink is normal, whereas any hint of
raspberry red suggests desaturation and requires urgent evaluation.
The distribution of the cyanosis should be evaluated. An oximetry reading will
confirm desaturation.
Observe the infant for general signs of health. The infant’s nutritional status,
responsiveness, irritability, and fatigue are all clues that may be useful in evaluating
cardiac disease. Note that noncardiac findings (see box on the next page) are
often present in infants with cardiac disease.
Observe the respiratory rate and pattern to help distinguish the degree of illness
and cardiac versus pulmonary diseases. An increase in respiratory effort is
expected from pulmonary diseases, whereas in cardiac disease there may be
tachypnea without increased work of breathing (called “peaceful tachypnea”)
until heart failure becomes significant.

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69
Q

Cardiac Causes of Central Cyanosis in

Infants and Children

A

Immediately at birth Transposition of the great arteries
Pulmonary valve atresia
Severe pulmonary valve stenosis
Possibly Ebstein malformation

Within a few days after birth All of the above plus:
Total anomalous pulmonary venous return
Hypoplastic left heart syndrome
Truncus arteriosus (sometimes)
Single ventricle variants

Weeks, months, or years of life All of the above plus:
Pulmonary vascular disease with atrial,
ventricular, or great vessel shunting
(right-to-left shunting)

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70
Q

Noncardiac Findings Commonly Present in

Infants with Cardiac Disease

A
Poor feeding 
Tachypnea 
Poor overall appearance
Failure to thrive Hepatomegaly 
Weakness
Irritability 
Clubbing 
Fatigue
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71
Q

newborn/infant: heart palpation

A

Palpation of the chest wall will allow you to assess volume changes
within the heart. For example, a hyperdynamic precordium reflects a big volume
change.
The point of maximal cardiac impulse, or PMI, is not always palpable in infants and
is affected by respiratory patterns, a full stomach, and the infant’s positioning. It
is usually an interspace higher than in adults during the first few years of life
because the heart lies more horizontally within the chest.
Thrills are palpable when turbulence within the heart or great vessels is transmitted
to the surface. Knowledge of the structures of the precordium helps pinpoint
the origin of the thrill. Thrills are easiest to feel with your palm or the base of
your fingers rather than your fingertips. Thrills have a somewhat rough, vibrating
quality. Figure 18-27 shows locations of thrills that occur in infants and
children from various cardiac abnormalities

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72
Q

newborn/infant: pulses

A

The major branches of the aorta can be assessed by evaluation of
the peripheral pulses. All neonates should have an evaluation of all pulses at the
time of their newborn examination. In neonates and infants, the brachial artery
pulse in the antecubital fossa is easier to feel than the radial artery pulse at the wrist.
Both temporal arteries should be felt just in front of the ear.
Palpate the femoral pulses. They lie in the midline just below the inguinal crease,
between the iliac crest and the symphysis pubis. Take your time to search for
femoral pulses; they are difficult to detect in chubby, squirming infants. If you
first flex the infant’s thighs on the abdomen, this may overcome the reflex flexion
that occurs when you then extend the legs.
Palpate the pulses in the lower extremities
using your index or middle finger.
The dorsalis pedis and posterior tibial
pulses (Fig. 18-28) may be difficult to
feel unless there is an abnormality
involving aortic run-off. Normal pulses
should have a sharp rise and should be
firm and well localized.
As discussed on p. 814, carefully measure the blood pressure of infants and children
(using an appropriate-sized infant blood pressure cuff) as part of the cardiac
examination.

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73
Q

newborn/infant: heart auscultation

A

You can evaluate the heart rhythm more easily in infants by
listening to the heart than by feeling the peripheral pulses; in older children
assess the rhythm either way.
Infants and children commonly have a normal sinus dysrhythmia, with the
heart rate increasing on inspiration and decreasing on expiration, sometimes
quite abruptly. This normal finding can be identified by its repetitive nature and
its correlation with respiration.
Many neonates and some older children have premature atrial or ventricular
beats that are often described as “skipped” beats. You can usually eradicate them
by increasing their intrinsic sinus rate through exercise such as crying in an
infant or jumping in an older child, although they may also be more frequent
in the postexercise period. In a completely healthy child, they are usually benign
and rarely persist.
In addition to trying to detect splitting of the S2, listen for the intensity of A2 and
P2. The aortic, or first component of the second sound at the base, is normally
louder than the pulmonic, or second component (Fig. 18-29).
You may detect third heart sounds which are low-pitched, early diastolic sounds
best heard at the lower left sternal border, or apex; they reflect rapid ventricular
filling. These are frequently heard in children and are normal.
Fourth heart sounds represent decreased ventricular compliance, suggesting heart
failure.
You may also detect an apparent gallop (widely split S2 that varies), in the presence
of a normal heart rate and rhythm. This is frequently found in normal
children and does not represent pathology

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74
Q

characteristics of normal variants of heart rhythms in children

A

p. 835

75
Q

newborns/infants: heart murmurs

A

One of the most challenging aspects of the cardiac examination
in children is the evaluation of heart murmurs. In addition to listening
to a squirming, perhaps uncooperative child, a major challenge is distinguishing
common benign murmurs from unusual or pathologic ones. Characterize heart
murmurs in infants and children by noting their specific location (e.g., left upper
sternal border, not just left sternal border), timing, intensity, and quality. If
each murmur is delineated completely, the diagnosis is usually made clinically,
and laboratory tools such as ECG, chest x-ray, and echocardiography are needed
for confirmation and better characterization.
An important rule of thumb is that, by definition, benign murmurs in children have
no associated abnormal findings. Many (but not all) children with serious cardiac
malformations have signs and symptoms other than a heart murmur obtainable
on careful history or examination. Many have noncardiac signs and symptoms,
including evidence of genetic defects that may offer helpful diagnostic
clues.
Most children, if not all, will have one or more functional, or benign, heart murmurs
before reaching adulthood.21–23 It is important to identify functional murmurs
by their specific qualities rather than by their intensity. You will learn to
recognize the common functional murmurs of infancy and childhood, which
under most circumstances do not require evaluation.
The box on the next page characterizes two benign heart murmurs in infants
according to their locations and key characteristics
In some infants, you will detect a soft, somewhat ejectile murmur, not over the
precordium but over the lung fields, particularly in the axillae. This represents
peripheral pulmonary artery flow and is partly the result of inadequate pulmonary
artery growth in utero (when there is little pulmonary blood flow) and the
sharp angle at which the pulmonary artery curves backward. In the absence of
any physical findings to suggest additional underlying diseases, this peripheral
pulmonary flow murmur (which is common) can be considered benign and usually
disappears by 1 year.
When you detect a murmur in a child, note all of the qualities as described in
Chapter 9, The Cardiovascular System, to help you distinguish pathologic murmurs
from benign murmurs. Heart murmurs that reflect underlying structural heart
disease are easier to evaluate if you have a good knowledge of intrathoracic anatomy
and the functional cardiac changes following birth and if you understand the
physiologic basis for heart murmurs. Understanding these physiologic changes can
help you distinguish pathologic murmurs from benign heart murmurs in children.

76
Q

2 common benign murmurs in infants:

A
  1. Closing ductus (newborns) - Transient, soft, ejection, systolic
    Upper left sternal border
  2. Peripheral pulmonary flow murmur (newborn - 1 year) - Soft, slightly ejectile, systolic
    Upper left sternal border, radiating to lung fields
    and axillae
77
Q

Physiologic Basis for Some Pathologic

Heart Murmurs

A

Change in Pulmonary Vascular Resistance
Heart murmurs that are dependent on a postnatal drop in pulmonary vascular resistance,
allowing turbulent flow from the high-pressure systemic circuit to the lowerpressure
pulmonary circuit, are not audible until such a drop has occurred. Except in
premature infants, murmurs of a ventricular septal defect or PDA are not heard in the
first few days of life and usually become audible after a week to 10 days.
Obstructive Lesions
Obstructive lesions, such as pulmonic and aortic stenosis, are caused by normal
blood flow through two small valves. They are not dependent on a drop in pulmonary
vascular resistance. They are audible at birth.
Pressure Gradient Differences
Murmurs of atrioventricular valve regurgitation are audible at birth because of the
high-pressure gradient between the ventricle and its atrium.
Changes Associated with Growth of Children
Some murmurs do not follow the patterns above, but become audible because
of alterations in normal blood flow that occur with growth. For example, even
though it is an obstructive defect, aortic stenosis may not be audible until considerable
growth has occurred and is frequently not heard until adulthood, although
a congenitally abnormal valve is responsible. Similarly, the pulmonary flow murmur
of an atrial septal defect may not be heard for a year or more because right
ventricular compliance gradually increases and the shunt becomes larger, eventually
producing a murmur caused by too much blood flow across a normal pulmonic
valve.

78
Q

newborns/infants: breasts

A

The breasts of the newborn in both males and females are often enlarged from
maternal estrogen effect; this may last several months. The breasts may also be
engorged with a white liquid, sometimes colloquially called “witch’s milk,” which
may last 1 or 2 weeks

79
Q

newborn/infants: abdomen inspection

A

Inspect the abdomen with the infant lying supine (and, optimally,
asleep). The infant’s abdomen is protuberant as a result of poorly developed
abdominal musculature. You will easily notice abdominal wall blood vessels and
intestinal peristalsis.
Inspect the newborn’s umbilical cord to detect abnormalities. Normally, there are
two thick-walled umbilical arteries and one larger but thin-walled umbilical vein
which is usually located at the 12 o’clock position.
The umbilicus in the newborn may have a long cutaneous portion (umbilicus
cutis) which is covered with skin, and an amniotic portion (umbilicus amnioticus)
which is covered by a firm gelatinous substance. The amniotic portion dries up
and falls off within 2 weeks, whereas the cutaneous portion retracts to be flush
with the abdominal wall.
Inspect the area around the umbilicus for redness or swelling.
Umbilical hernias are detectable by a few weeks of age. Most disappear by 1 year,
nearly all by 5 years.
In some normal infants, you will notice a diastasis recti. This involves separation
of the two rectus abdominis muscles, causing a midline ridge most apparent
when the infant contracts the abdominal muscles. A benign condition in most
cases, it resolves during early childhood

80
Q

infant/newborn: abdominal auscultation

A

Auscultation of a quiet infant’s abdomen is easy. You may hear
an orchestra of musical tinkling bowel sounds upon placement of your stethoscope
on the infant’s abdomen

81
Q

infant/newborn: abdominal percussion and palpation

A

You can percuss an infant’s abdomen as you
would an adult’s, but may note greater tympanitic sounds because of the infant’s
propensity to swallow air. Percussion is useful for determining the size of organs
and abdominal masses.
It is easy to palpate an infant’s abdomen because infants like being touched. A
useful technique to relax the infant is to hold the legs flexed at the knees and
hips with one hand and palpate the abdomen with the other. A pacifier may
quiet the infant in this position.
When palpating the liver, start gently low in the abdomen, moving upward with
your fingers. This technique helps to identify an extremely enlarged liver that
extends down into the pelvis. With a careful examination, you can feel the liver
edge in most infants, 1 to 3 cm below the right costal margin.
One technique for assessing liver size in infants is simultaneous percussion and
auscultation.24 Percuss and simultaneously auscultate, noting a change in sound
as you percuss over the liver or beyond it. Of note, a scratch test (described on
page 880 for older children) can be attempted in infants.
The spleen, like the liver, is felt easily in most infants. It is soft with a sharp edge
and it projects downward like a tongue from under the left costal margin. The
spleen is moveable and rarely extends more than 1 to 2 cm below the left costal
margin.
Palpate the other abdominal structures. You will commonly note pulsations in the
epigastrium caused by the aorta. This is felt on deep palpation to the left of the
midline.
You may be able to palpate the kidneys of infants by carefully placing the fingers
of one hand in front of and those of the other behind each kidney. The descending
colon is a sausage-like mass in the left lower quadrant.
Once you have identified the normal structures in the infant’s abdomen, use
palpation to identify abnormal masses.

82
Q

newborn/infant: male genitalia

A

Inspect the male genitalia with the infant supine noting the appearance of the
penis, testes, and scrotum. The foreskin completely covers the glans penis. It is
nonretractable at birth though you may be able to retract it enough to visualize
the external urethral meatus. The foreskin gradually loosens over months to
years and becomes retractable. The rate of circumcision had declined over several
decades in North America and varies worldwide, depending on cultural practices,
but is now recommended by the AAP and by experts in many parts of the world
due to reduced rates of HIV and other infections among circumcised males.
Inspect the shaft of the penis, noting any abnormalities on the ventral surface.
Make sure the penis appears straight.
Inspect the scrotum noting rugae which should be present by 40 weeks gestation.
Scrotal edema may be present for several days following birth because of the
effect of maternal estrogen.
Palpate the testes in the scrotal sacs, proceeding downward from the external
inguinal ring to the scrotum. If you feel a testis up in the inguinal canal, gently
milk it downward into the scrotum. The newborn’s testes should be about
10 mm in width and 15 mm in length and should lie in the scrotal sacs most
of the time.
In about 3% of neonates, one or both testes cannot be felt in the scrotum or
inguinal canal. This raises concern of cryptorchidism. In two thirds of these cases,
both testes are descended by 1 year of age.
Examine the testes for swelling within
the scrotal sac and over the inguinal
ring. If you detect swelling in the scrotal
sac try to differentiate it from the
testis. Note whether the size changes
when the infant increases abdominal
pressure by crying. See if your fingers
can get above the mass, trapping it in
the scrotal sac. Apply gentle pressure
to try to reduce the size of the mass
and note any tenderness. Note whether
it transilluminates (Fig. 18-30).

83
Q

newborn/infant: female genitalia

A

In the newborn female, the genitalia will be prominent due to the effects of
maternal estrogen. The labia majora and minora have a dull pink color in lightskinned
infants and may be hyperpigmented in dark-skinned infants. During the
first few weeks of life there is often a milky white vaginal discharge that may be
blood tinged and is not a cause for concern. This estrogenized appearance of
the genitalia decreases during the first year of life.
Examine the different structures systematically, including the size of the clitoris,
the color and size of the labia majora, and any rashes, bruises, or external lesions
(Fig. 18-31). Next, separate the labia majora at their midpoint with the thumb
of each hand, or as shown in Figs. 18-83 and 18-84 below.
Inspect the urethral orifice and the labia minora. Assess the hymen, which in
newborns and infants is a thickened, avascular structure with a central orifice,
covering the vaginal opening. You should note a vaginal opening, although the
hymen will be thickened and redundant. Note any discharge.

84
Q

newborn/infant: rectal exam

A

The rectal examination generally is not performed for infants or children
unless there is question of patency of the anus or an abdominal mass. In such
cases, flex the infant’s hips and fold the legs to the head. Use your lubricated and
gloved pinky to perform the examination.

85
Q

newborn/infant: musculoskeletal

A

Enormous changes in the musculoskeletal system occur during infancy. Much of
the examination of the infant focuses on detection of congenital abnormalities,
particularly in the hands, spine, hips, legs, and feet. Combine the musculoskeletal
examination with the neurologic and developmental examination.
The newborn’s hands are clenched. Because of the palmar grasp reflex (see the
discussion on the nervous system, p. 849) you will need to help the infant extend
the fingers. Inspect the fingers carefully, noting any defects.
Palpate along the clavicle noting any lumps, tenderness, or crepitus; these may
indicate a fracture.
Inspect the spine carefully. Although major defects of the spine such as meningomyelocele
are obvious and often detected by ultrasound before birth, subtle
abnormalities may include pigmented spots, hairy patches, or deep pits. These
abnormalities, if present within 1 cm or so of the midline, may overlie external
openings of sinus tracts that extend to the spinal canal. Do not probe sinus tracts
because of the potential risk for introducing infection. Palpate the spine in the
lumbosacral region, noting any deformities of the vertebraeExamine the newborn and infant’s hips carefully at each examination for signs
of dislocation.26,27 Figures 18-32 to 18-36 and discussion cover the two major
techniques, one to test for the presence of a posteriorly dislocated hip (Ortolani
test) (Fig. 18-32), and another to test for the ability to sublux or dislocate an
intact but unstable hip (Barlow test)
Make sure the baby is relaxed for these techniques. For the Ortolani test, place
the baby supine with the legs pointing toward you. Flex the legs to form right
angles at the hips and knees, placing your index fingers over the greater trochanter
of each femur and your thumbs over the lesser trochanters (Fig. 18-34).
Abduct both hips simultaneously until the lateral aspect of each knee touches
the examining table
For the Barlow test, place
your hands in the same
position as for the Ortolani
test. Pull the leg forward
and adduct with
posterior force; that is,
press in the opposite
direction with your
thumbs moving down
toward the table and outward
(Fig. 18-36). Feel
for any movement of the
head of the femur laterally.
Normally, there is no
movement and the hip
feels “stable.”
Test for femoral shortening using the Galeazzi or Allis sign. Place the feet (with
knee flexed and sacrum flat on the table) together and note any difference in
knee heights.
Examine a newborn or infant’s legs and feet to detect developmental abnormalities.
Assess symmetry, bowing, and torsion of the legs. There should be no discrepancy
in leg length. It is common for normal infants to have asymmetric thigh
skin folds, but if you do detect asymmetry, make sure you perform the instability
tests because dislocated hips are commonly associated with this finding.
Most newborns are bowlegged, reflecting their curled-up intrauterine position
Some normal infants exhibit twisting or torsion of the tibia inwardly or outwardly
on its longitudinal axis. Parents may be concerned about a toeing in
or toeing out of the foot and an awkward gait, all of which are usually normal.
Tibial torsion usually corrects itself during the second year of life after months of
weight bearing
Examine the feet of newborns
and infants. At birth,
the feet may appear deformed
from retaining their intrauterine
positioning, often
turned inward (Fig. 18-37).
You should be able to correct
the feet to the neutral
and even to an overcorrected
position (Fig. 18-38).
Scratch or stroke along the
outer edge to see if the foot
assumes a normal position.
The normal newborn’s foot
has several benign features
that may initially cause concern.
The newborn’s foot
appears flat because of a
plantar fat pad. There is
often inversion of the foot,
elevating the outer margin
(see p. 922). Other babies will
have adduction of the forefoot
without inversion, called
metatarsus adductus which
requires close follow-up.
Still others will have adduction
of the entire foot. Finally, most toddlers have some pronation during early
stages of weight-bearing with eversion of the foot. In all of these normal variants
the abnormal position can be easily overcorrected past midline. They all tend to
resolve within 1 or 2 years

86
Q

infant/newborn: nervous system

A

The examination of the nervous system in infants includes techniques that are
highly specific to this particular age. Unlike many neurologic abnormalities in
adults that produce asymmetric localized findings, neurologic abnormalities in
infants often present as developmental abnormalities such as failure to do ageappropriate
tasks. Therefore, the neurologic and developmental examinations
need to proceed together. A developmental abnormality should prompt you to pay
particular attention to the neurologic examination.
The neurologic screening examination of all newborns should include assessment
of mental status, gross and fine motor function, tone, cry, deep tendon
reflexes, and primitive reflexes. More detailed examination of cranial nerve function
and sensory function are indicated if you suspect any abnormalities from the
history or screening The neurologic examination can reveal extensive disease but will not pinpoint
specific functional deficits or minute lesions

87
Q

infant/newborn: motor function and tone

A

Assess
the motor tone of newborns and infants,
first by carefully observing their position
at rest and testing their resistance
to passive movement.
Further, assess tone as you move each
major joint through its range of motion,
noting any spasticity or flaccidity. Hold the
baby in your hands to determine whether
the tone is normal, increased, or decreased
(Fig. 18-39). Either increased or decreased
tone may indicate intracranial disease
although such disease is usually accompanied
by a number of other signs.

88
Q

infants/newborns: sensory function

A

You can test for sensory function of the newborn in only a
limited way. Test for pain sensation by flicking the infant’s palm or sole with your
finger. Observe for withdrawal, arousal, and change in facial expression. Do not
use a pin to test for pain.

89
Q

newborns/infants: cranial nerves

A
I Olfactory Very difficult to test
II Visual acuity Have infant regard your face and look
for facial response and tracking.
II, III Response to
light
Darken room, raise infant to sitting
position to open eyes.
Use light and test for optic blink reflex
(blink in response to light).
Use the otoscope’s light (without speculum)
to assess pupillary responses
III, IV, VI Extraocular
movements
Observe how well the infant tracks
your smiling face (or a bright light)
and whether the eyes move
together.
V Motor Test rooting reflex.
Test sucking reflex (watch infant suck
breast, bottle, or pacifier) and
strength of suck.
VII Facial Observe infant crying and smiling; note
symmetry of face.
VIII Acoustic Test acoustic blink reflex (blinking of
both eyes in response to a loud
noise).
Observe tracking in response to sound.
IX, X Swallow Observe coordination during
swallowing.
Gag Test for gag reflex.
XI Spinal accessory Observe symmetry of shoulders.
XII Hypoglossal Observe coordination of sucking,
swallowing, and tongue thrusting.
Pinch nostrils; observe reflex opening
of mouth with tip of tongue to
midline.
90
Q

newborns/infants: deep tendon reflexes

A

The deep tendon reflexes are present in newborns
but may be difficult to elicit and may vary in their intensity because the
corticospinal pathways are immature. Their exaggerated presence or their
absence has little diagnostic significance, unless this response is different from
results of previous testing or extreme responses are observed or they are very
asymmetric.
Use the same techniques to elicit deep tendon reflexes as you would for an adult.
You can substitute your index or middle finger for the reflex hammer as shown
in Figure 18-40.
The triceps, brachioradialis, and abdominal reflexes are difficult to elicit before
6 months of age. The anal reflex is present at birth and important to elicit if a
spinal cord lesion is suspected.
In newborns, a positive Babinski response to plantar stimulation (dorsiflexion of
big toe and fanning of other toes) can be elicited and may persist for several
months.
In order to best elicit the ankle reflex of an infant, grasp the infant’s malleolus
with one hand and abruptly dorsiflex the ankle (Fig. 18-41). You may note rapid,
rhythmic plantar flexion of the newborn’s foot (ankle clonus) in response to this
maneuver. Up to 10 beats are normal in newborns and young infants; this is
unsustained ankle clonus.

91
Q

newborn/infants: primitive reflexes

A

Evaluate the newborn’s and infant’s developing central
nervous system by assessing infantile automatisms, called primitive reflexes.
These develop during gestation, are generally demonstrable at birth, and disappear
at defined ages. Abnormalities in these primitive reflexes suggest neurologic
disease and merit more intensive investigation.

92
Q

newborn/infants: development

A

Refer to the developmental milestones on p. 810 and to the
items on a standardized developmental screening instrument to learn which agespecific
developmental tasks to evaluate. By observation and play with the
infant, you can do both a developmental screening examination and an assessment
for gross and fine motor achievement. Specifically, look for weakness by
observing sitting, standing, and transitions. Note station, or the posture of sitting
or standing. Assess fine motor development in a similar way, combining the
neurologic and developmental examination. Key milestones include the development
of the pincer grasp, ability to manipulate objects with the hands, and
more precise tasks, such as building a tower of cubes or scribbling. Fine and
gross motor development progresses in a proximal to distal direction.
Assess the infant’s cognitive and social–emotional development as you proceed
with the comprehensive neurologic and developmental examination. Some neurologic
abnormalities produce deficits or slowing in cognitive and social development.
Infants who have developmental delay may have abnormalities on the
neurologic examination because much of the examination is based on age-specific
norms.
A normative measure of development is the developmental quotient,30 shown
here:
Development quotient = × 1 00
Development age
Chronologic age
Assess the development of an infant or child using standard scales for each type
of development. Assign to each child a gross motor developmental quotient, a
fine motor developmental quotient, a cognitive developmental quotient, and so
forth. Importantly, these estimates are never a perfect assessment of a child’s
development or potential because both can change over time

Developmental Quotients:
>85% normal
70-85% possibly delayed
<70% delayed

93
Q

Palmar Grasp Reflex

A
Place your fingers
into the infant’s
hands and press
against the palmar
surfaces.
The infant will flex all
fingers to grasp
your fingers.
Birth to
3–4 mo
94
Q

Plantar Grasp Reflex

A
Touch the sole at the
base of the toes.
The toes will curl.
Birth to
6–8 mo
95
Q

Rooting Reflex

A
Stroke the perioral
skin at the corners
of the mouth.
The mouth will open
and the infant will
turn the head
toward the stimulated
side and
suck.
Birth to
3–4 mo
96
Q

Moro Reflex (Startle)

A
Hold the infant
supine, supporting
the head, back,
and legs. Abruptly
lower the entire
body about 2 feet.
The arms will abduct
and extend, hands
will open, and legs
will flex. The
infant may cry.
Birth to 4 mo
97
Q

Asymmetric Tonic Neck Reflex

A
With the infant
supine, turn head
to one side, holding
jaw over shoulder.
The arms/legs on
side to which head
is turned will
extend while the
opposite arm/leg
will flex. Repeat
on other side.
Birth to 2 mo
98
Q

Trunk Incurvation (Galant) Reflex

A
Support the infant
prone with one
hand and stroke
one side of the
back 1 cm from
midline, from
shoulder to buttocks.
The spine will curve
toward the stimulated
side.
Birth to 2 mo
99
Q

Landau Reflex

A
Suspend the infant
prone with one
hand.
The head will lift up,
and the spine will
straighten.
Birth to 6 mo
100
Q

Parachute Reflex

A
Suspend the infant
prone and slowly
lower the head
toward a surface.
The arms and legs
will extend in a
protective fashion.
8 mo and
does not
disappear
101
Q

Positive Support Reflex

A
Hold the infant
around the trunk
and lower until the
feet touch a flat
surface.
The hips, knees, and
ankles will extend,
the infant will
stand up, partially
bearing weight,
sagging after
20–30 seconds.
Birth or 2 mo
until 6 mo
102
Q

Placing and Stepping Reflexes

A
Hold the infant
upright as in
positive support
reflex. Have one
sole touch the
tabletop.
The hip and knee of
that foot will flex
and the other foot
will step forward.
Alternate stepping
will occur.
Birth (best
after 4
days; variable
age
to disappear)
103
Q

Early Childhood: physical development

A

After infancy, the rate of physical growth slows
by approximately half. After 2 years, toddlers gain about 2 to 3 kg and grow 5 cm per
year. Physical changes are impressive. Chubby, clumsy toddlers transform into
leaner, more muscular preschoolers.
Gross motor skills also develop quickly. Almost all children walk by 15 months,
run well by 2 years, and pedal a tricycle and jump by 4 years. Fine motor skills
develop through neurologic maturation and environmental manipulation
(Fig. 18-42). The 18-month-old who scribbles becomes a 2-year-old who draws
lines and then a 4-year-old who makes circles

104
Q

Early Childhood: cognitive and language development

A

Toddlers move from sensorimotor
learning (through touching and looking) to symbolic thinking, solving
simple problems, remembering songs, and engaging in imitative play. Language
develops with extraordinary speed. An 18-month-old with 10 to 20 words
becomes a 2-year-old with three-word sentences, and a 3-year-old who converses
well. By 4 years, preschoolers form complex sentences. They remain preoperational,
however, without sustained logical thought processes.

105
Q

Early Childhood: social and emotional development

A

New intellectual pursuits are surpassed
only by an emerging drive for independence (Fig. 18-43). Because toddlers
are impulsive and have poor self-regulation, temper tantrums are common.
Self-regulation is an important developmental task with a wide range of normal

106
Q

Early Childhood: milestones table

A

pg.853

107
Q

Middle Childhood: physical development

A

Children grow steadily but more slowly. Strength
and coordination improve dramatically with more participation in activities
(Fig. 18-45). This is also when children with physical disabilities or chronic illnesses
become more aware of their limitations

108
Q

Middle Childhood: cognitive and language development

A

Children become “concrete
operational”—capable of limited logic and more complex learning. They remain
rooted in the present with little ability to understand consequences or abstractions.
School, family, and environment greatly influence learning (Fig. 18-46). A
major developmental task is self-efficacy, or the ability to thrive in different situations.
Language becomes increasingly complex.

109
Q

Middle Childhood: social and emotional development

A

Children become progressively
more independent, initiating activities and enjoying accomplishments. Achievements
are critical for self-esteem and developing a “fit” within major social structures—
family, school, and peer activity groups. Guilt and poor self-esteem also
may emerge. Family and environment contribute enormously to the child’s selfimage.
Moral development remains simple and concrete with a clear sense of
“right and wrong.”

110
Q

Middle Childhood

A

Middle childhood is an active
period of growth and development. Goal-directed exploration, increased physical
and cognitive abilities, and achievements by trial and error mark this stage. The
physical examination is more straightforward during this age period, but always
consider the developmental stages and tasks that school-aged children are facing.

111
Q

middle childhood physical developmental tasks

A

characteristic:
Enhanced strength and coordination
Competence in various tasks
and activities

health care needs:
Screening for strengths,
assessing problems
Involving parents
Support for disabilities
Anticipatory guidance: safety,
exercise, nutrition, sleep
112
Q

middle childhood cognitive developmental tasks

A
characteristic:
“Concrete operational:” focus on
the present
Emphasis on short-term consequences
Achievement of knowledge and
skills, self-efficacy

healthcare needs:
Support; screening for skills
and school performance

113
Q

middle childhood social developmental tasks

A

characteristic:
Achieving good “fit” with family,
friends, school

healthcare needs:
Assessment, support, advice
about interactions including
peer relationships
Sustained self-esteem Support, emphasis on
strengths
Evolving self-identity Understanding, advice, support

114
Q

children: obtaining health history

A

An important aspect of examining children is that parents are usually watching
and taking part in the interaction, providing you the opportunity to observe the
parent–child interaction. Note whether the child displays age-appropriate behaviors.
Assess the “goodness of fit” between parents and child. Although some
abnormal interactions may result from the unnatural setting of the examination
room, others may be a consequence of interactional problems. Careful observation
of the child’s interactions with parents and the child’s unstructured play in
the examination room can reveal abnormalities in physical, cognitive, and social
development or issues with parent–child relationship.
Normal toddlers are occasionally terrified or angry at the examiner. Often, they
are completely uncooperative. Most eventually warm up to you. If this behavior
continues or is not developmentally appropriate, there may be an underlying
behavioral or developmental abnormality. Older, school-aged children have more
self-control and prior experience with clinicians and are generally cooperative
with the examination.

115
Q

Abnormalities Detected While Observing Play

A
Behaviorala
Poor parent–child interactions
Sibling rivalry
Inappropriate parental discipline
“Difficult temperament”
Developmental
Gross motor delay
Fine motor delay
Language delay (expressive or
receptive)
Delay in social or emotional tasks
Social or Environmental
Parental stress, depression
Risk for abuse or neglect
Neurologic
Weakness
Abnormal posture
Spasticity
Clumsiness
Attentional problems, hyperactivity
Autistic features
Musculoskeletal abnormalities
116
Q

assessing younger children

A

One challenge in examining children in this age group is avoiding a physical
struggle, a crying child, or a distraught parent. Accomplishing this successfully
is one aspect of the “art of medicine” in the practice of pediatrics.
Gain the child’s confidence and allay the child’s fears from the start of the encounter.
Your approach will vary with the circumstances of the visit. A health supervision
visit allows greater rapport than a visit when the child is ill.
The child should remain dressed during the interview to minimize the child’s
apprehension. It also allows you to interact more naturally and observe the child
playing, interacting with the parents, and undressing and dressing.
Toddlers who are of 9 to 15 months may have stranger anxiety, a fear of strangers
that is developmentally normal. It signals the toddler’s growing awareness that
the stranger is new. You should not approach these toddlers quickly. Play can
help the child warm up to you. Make sure they remain solidly in their parent’s
lap throughout much of the examination and that the parent remains close when
the child is on the examination table
Engage children in age-appropriate conversation. Ask simple questions about
their illness or toys. Compliment their appearance or behavior, tell a story, or
play a simple game (Fig. 18-47). If a child is shy, turn your attention to the parent
to allow the child to warm up gradually. Also, sometimes the parent is anxious.
Helping the parent relax or asking them to help by reading to the child or
playing with the child can help relax everyone in the examination room.
With certain exceptions, physical examination does not require use of the examining
table; it can be done on the floor or with the child in a parent’s lap. The key
is to engage the child’s cooperation. For young children who resist undressing,
expose only the body part being examined. When examining siblings, begin with
the oldest child who is more likely to cooperate and set a good example. Approach
the child pleasantly. Explain each step as you perform it. Continue conversing
with the family to provide distraction
Plan the examination to start with the
least distressing procedures and end
with the most distressing ones, usually
involving the throat and ears. Begin
with parts that can be done with the
child sitting such as examining the
eyes or palpating the neck. Lying down
may make a child feel vulnerable, so
change positions with care. Once a
child is supine, begin with the abdomen,
saving throat and ears or genitalia
for last. You may need a parent’s help to
restrain the child for examination of
the ears or throat; however, use of formal restraints is inappropriate. Patience,
distraction, play, flexibility in the order of the examination, and a caring but firm and
gentle approach, are all key to successfully examining the young child (Fig. 18-48).
Children are usually accompanied by a parent or caregiver. Even when alone,
they are often seeking health care at the request of their parent; indeed, the parent
is usually sitting in the waiting room. When interviewing a child, you need
to consider the needs and perspectives of both the child and the caregivers

117
Q

useful strategies for examining kids 1-4

A
Examine a child sitting on parent’s lap.
Try to be at the child’s eye level.
First examine the child’s toy or teddy
bear, then the child.
Let the child do some of the examination
(e.g., move the stethoscope). Then go
back and “get the places we missed.”
Ask the toddler who keeps pushing you
away to “hold your hand.” Then have
the toddler “help you” with the
examination.
Some toddlers believe that if they can’t
see you, then you aren’t there. Perform
the examination while the child stands
on the parent’s lap, facing the parent.
If 2-yr-olds are holding something in
each hand (such as tongue depressors),
it is more difficult for them to
fight or resist.
Hand the child an age-appropriate book
and engage the child in reading.
118
Q

useful toys/aids for examining kids 1-4

A
“Blow out” the otoscope light.
“Beep” the stethoscope on your nose.
Make tongue-depressor puppets.
Use the child’s own toys for play.
Jingle your keys to test for hearing.
Shine the otoscope through the tip of
your finger (or the child’s finger) to
show it doesn’t hurt, “lighting it
up,” and then examine the child’s
ears with it.
Use age-appropriate toys and books.
119
Q

Kids: establishing rapport

A

Begin the
interview by greeting and establishing
rapport with each person present
(Fig. 18-50). Refer to the child by
name rather than by “him” or “her.”
Clarify the role or relationship of all of
the adults and children. “Now, are you
Jimmy’s grandmother?” “Please help
me by telling me Jimmy’s relationship
to everyone here.” Address the parents
as “Mr. Smith” and “Ms. Smith” rather
than by their first names or “Mom” or
“Dad.” When the family structure is
not immediately clear, you may avoid
embarrassment by asking directly about other members. “Who else lives in the
home?” “Who is Jimmy’s father?” “Do you live together?” Do not assume that just
because parents are separated, only one parent is actively involved in the child’s
life. Families come in many varieties—these include traditional families, single
parents, separated/divorced parents, blended, same-sex parents, kinship families,
foster families, and adoptive families.
Use your personal experiences with children to guide how you interact in a
health care setting. To establish rapport, meet children on their own level. Eye
contact on their level, participating in playful engagement, and talking about
what interests them are always good strategies. Ask children about their clothes,
one of their toys, what book or TV show they like, or their adult companion in
an enthusiastic but gentle style. Spending time at the beginning of the interview to
calm and connect with an anxious child can put both the child and the caregiver at ease.

120
Q

kids: working with families

A

One challenge when several people are present is deciding
to whom to direct your questions. While eventually you need to get information
from both the child and the parent, it is useful to start with the child.
Asking simple open-ended questions like “Are you sick? . . . Tell me about it,” followed
by more specific questions, often provides much of the clinical data. The
parents can then verify the information, add details that give you the larger context,
and identify other issues you need to address. Sometimes children are embarrassed
to begin, but once the parent has started the conversation, direct questions back to
the child. Characterize symptom attributes the same way you do with adults.
Your mom tells me that you get stomachaches. Tell me about them.
Show me where you get the pain. What does it feel like?
Is it sharp like a pinprick, or does it ache?
Does it stay in the same spot, or does it move around?
What helps make it go away? What makes it worse?
What do you think causes it?
The presence of family members allows you to observe how they interact with
the child. A child may be able to sit still or may get restless and start fidgeting.
Watch how the parents set, or fail to set, limits when needed.

121
Q

kids: multiple agendas

A

Each individual in the room, including the clinician, may
have a different idea about the nature of the problem and what needs to be done
about it. Discover as many of these perspectives and agendas as possible. Family
members who are not present (e.g., the absent parent or grandparent) may also
have concerns. Ask about those concerns, too. “If Suzie’s father were here today,
what questions or concerns would he have?” “Have you, Mrs. Jones, discussed
this with your mother or anyone else?” “What does she think?”
For example, Mrs. Jones brings Suzie in for abdominal pain because she is worried
that Suzie may have an ulcer and is also worried about Suzie’s eating habits.
Suzie is not worried about the belly pain, but is uneasy about the changes in her
body and about getting fat. Mr. Jones thinks that Suzie’s schoolwork is not getting
enough attention. You, as the clinician, need to balance these concerns with
what you see as a healthy 12-year-old girl in early puberty with some mild functional
abdominal pain and appropriate concern for possible emerging obesity.
Your goals need to include uncovering the concerns of each person and helping
the family to be realistic about the range of “normal.”

122
Q

kids: family as resource

A

In general, family members provide most of the
care and are your natural allies in promoting the child’s health. Being open to a
wide range of parenting behaviors helps to make this alliance. Raising a child
reflects cultural, socioeconomic, and family practices. It is important to respect the
tremendous variation in these practices. A good strategy is to view the parents as
experts in the care of their child and yourself as their consultant. This demonstrates
respect for the parents’ care and minimizes their likelihood of discounting or ignoring
your advice. Parents face many challenges raising children, so practitioners
need to be supportive, not judgmental. Comments like, “Why didn’t you bring him
in sooner?” or “What did you do that for?” do not improve your rapport with the
parent. Statements acknowledging the hard work of parenting and praising
successes are always appreciated. “Mr. Smith, you are doing such a wonderful job
with Bobby. Being a parent takes so much work and Bobby’s behavior here today
clearly shows your efforts. We might have some suggestions for you at the end of
the visit.” Or to the child, “Bobby you are so lucky to have such a wonderful dad.”

123
Q

kids: hidden agendas

A

As with adults, the chief complaint
may not relate to the real reason the parent has brought
the child to see you (Fig. 18-51). The complaint may be
a bridge to concerns that may not seem like a legitimate
reason to go to the clinician. Create a trusting atmosphere
that allows parents to be open about all their concerns
by asking facilitating questions such as:
Do you have any other concerns about Randy?
Was there anything else that you wanted to tell/ask
me today?

124
Q

The AAP and Bright Futures periodicity schedules for children include health
supervision visits at

A

12, 15, 18, and 24 months followed by annual visits when
the child is 3 and 4 years old.
An additional visit at 30 months is also
recommended to assess the child’s development.

125
Q

This is a critical age for preventing childhood obesity as many children begin their
trajectory toward obesity between ages

A

3 and 4 years

126
Q

health promotion: 5-10 years

A

The AAP and Bright Futures periodicity
schedules for children recommend
annual health supervision visits during
this period.8 As for earlier ages, these
visits present opportunities to assess
the child’s physical, mental, and
developmental health and the parent–
child relationship and the child’s
relationships with peers and school
performance (Fig. 18-52). Once again,
health promotion should be incorporated
into all interactions with
children and families.
Older children enjoy talking directly with the examiner. In addition to discussing
health, safety, development, and anticipatory guidance with parents, include the
child in these conversations using age-appropriate language and concepts. Discuss
the child’s experience and perceptions of school, interactions with peers,
and other cognitive and social activities. Focus on healthy habits such as good
nutrition, exercise, reading, stimulating activities, health sleep hygiene, screen
time, and safety.
About 12% to 20% of children have some
type of chronic physical, developmental,
or mental condition.33 These children
should be seen more frequently for
monitoring, disease management, and
preventive care (Fig. 18-53). Some
behaviors that become established at
this age can lead to or exacerbate
chronic conditions such as obesity or
eating disorders. Health promotion is
critical to optimize healthy habits and
minimize unhealthy ones. Helping
families and children with chronic diseases
deal most effectively with these
disorders is a key part of health promotion.
For all children, health promotion involves assessing and promoting the family’s
overall health.
The specific components of the health supervision visit for older children are the
same as the components for younger children. Emphasize school performance
and experiences as well as appropriate and safe sports and activities and healthy
peer relationships.

127
Q

After age 2 years children should grow at least

During puberty, growth.

A

5 cm per year.

velocity increases

128
Q

head circumference is measured until

A

24 months

129
Q

BMI in kids

A

underweight: <5%
healthy 5-85%
overweight 85-95%
obese >95%

130
Q

BP in kids

A

p.864

131
Q

HR in kids

A

1-2y/o: 110 (70-150)
2-6y/o: 103 (68-138)
6-10y/o: 95 (65-125)

132
Q

RR in kids

A

20-40 early childhood
15-25 late childhood
reach adult levels by 15 y/o

133
Q

The best single physical finding for ruling out pneumonia is:

A

absence of tachypnea

tachypnea in kids >1y/o is RR>40

134
Q

childhood temperature methods

A

auditory canal b/c easy and no discomfort

135
Q

The two most important components of the eye examination for young children
are

A

to determine whether the gaze is conjugate or symmetric

to test visual
acuity in each eye

136
Q

Conjugate Gaze in kids

A

The corneal light reflex test and the cover–uncover test

are particularly useful in young children

137
Q

childhood visual acuity tests

A

<3 y/o: the simplest examination is to assess for fixation preference by alternately
covering one eye; the child with normal vision will not object, but a child
with poor vision in one eye will object to having the good eye covered

> 4y/o: eye charts (shapes, E)

138
Q

Acuity by childhood age

A

3 months - eyes converge, baby reaches

12 months - 20/200

<4 y/o - 20/40

> 4 y/o - 20/30

139
Q

how to pull auricle fo kid ear exam

A

the auricle must be pulled upward,

outward, and backward to afford the best view.

140
Q

Tips for Conducting the Otoscopic Examination

A

● Use the best angle of the otoscope.
● Use the largest possible speculum.
● A larger speculum allows you to better visualize the tympanic membrane
and is less painful since it is not inserted as far as a smaller speculum.
● A small speculum may not provide a seal for pneumatic otoscopy.
● Don’t apply too much pressure which will cause the child to cry and may cause
false-positive results on pneumatic otoscopy.
● Insert the speculum ¼ to ½ inch into the canal.
● First find the landmarks.
● Careful—sometimes the ear canal resembles the tympanic membrane.
● Note whether the tympanic membrane is abnormal.
● Remove cerumen if it is blocking your view, using one of the following:
● Special plastic curettes
● A moistened microtipped cotton swab
● Flushing of ears for older children
● Special instruments that can also be purchased.

141
Q

2 was to hold otoscope for kid exam

A

■ The first is the method generally used in adults, with the otoscope handle
pointing upward or laterally while you pull up on the auricle. Hold the
lateral aspect of your hand that has the otoscope against the child’s head to
provide a buffer against sudden movements by the patient (Figs. 18-61 and
18-62).
■ The second position, with the handle of the otoscope pointing down
toward the child’s feet, is preferred by many pediatricians because of the
angle of the auditory canal in children. While holding the otoscope with the
handle pointing down, pull up on the auricle. Steady your hand against
the child’s head and pull up on the auricle with that hand, while you hold
the otoscope with the other hand

142
Q

childhood: nose

A

Maxillary sinuses are noted on x-rays
by age 4 years, sphenoid sinuses by
age 6 years, and frontal sinuses by age
6 to 7 years. The sinuses of older children
can be palpated as in adults,
looking for tenderness.45 Transillumination
of the paranasal sinuses of younger children has poor sensitivity and
specificity for diagnosing sinusitis or fluid in the sinuses

143
Q

Tooth Types and Age of Eruption

A

Central incisor

  • 5-8 m
  • 6-8 y

Lateral incisor

  • 5-11 m
  • 7-9 y

Cuspids

  • 24-30 m
  • 11-12 y

First bicuspids
- 10-12 y

Second bicuspids
- 10-12 y

First molars

  • 16-20 m
  • 6-7 y

Second molars

  • 24-30 m
  • 11-13 y

Third molars
- 17-22 y

144
Q

Tonsils in kids

A

Note the size, position, symmetry, and appearance of the tonsils. The peak growth
of tonsillar tissue is between 8 and 16 years (Fig. 18-54). The size of the tonsils
varies considerably in children and is often categorized on a scale of 1+ to 4+,
with 1+ being easy visibility of the gap between the tonsils, and 4+ being tonsils
that touch in the midline with the mouth wide open. The tonsils in children
often appear more obstructive than they really are.
Tonsils in children usually have deep crypts on their surfaces, which often have
white concretions or food particles protruding from their depths. This does not
indicate disease

145
Q

hypernasal speech suggests

A

submucosal cleft palate

146
Q

nasal voice plus snoring suggests

A

adenoidal hypertrophy

147
Q

hoarse voice plus cough suggests

A

viral infection (croup)

148
Q

rocks in mouth suggests

A

tonsilitis

149
Q

The vast majority of enlarged lymph nodes in children are due to

A

infections
(mostly viral, but sometimes bacterial) and not due to malignant disease,
even though the latter is a concern for many parents

150
Q

Kids and Nuchal Rigidity

A

In children, the presence of nuchal rigidity
is a more reliable indicator of meningeal
irritation than Brudzinski sign or
Kernig sign. To detect nuchal rigidity in
older children, ask the child to sit with
legs extended on the examining table.
Normally, children should be able to sit
upright and touch their chins to their
chests. Younger children can be persuaded
to flex their necks by having
them follow a small toy or light beam.
You also can test for nuchal rigidity with
the child lying on the examining table,
as shown in Figure 18-72. Nearly all
children with nuchal rigidity will be
extremely sick, irritable, and difficult
to examine. In many countries the
incidence of bacterial meningitis has
plummeted because of vaccinations.

151
Q

Kids- inspiration:expiration

A

The
normal ratio is about 1:1.

Prolonged inspirations or expirations are a clue to disease
location. Degree of prolongation and effort or “work of breathing” are related
to disease severity.

152
Q

Kids and murmurs

A

Preschool and school-aged children often have benign
murmurs (see figure on p. 879). The most common (Still’s murmur) is a grade
I–II/VI, musical, vibratory, early and midsystolic murmur with multiple overtones
located over the mid or lower left sternal border; it may also be heard over
the carotid arteries. Carotid artery compression will usually cause the precordial
murmur to disappear. This murmur may be extremely variable and may be
accentuated when cardiac output is increased, as occurs with fever or exercise.
The murmur will diminish as the child goes from supine to sitting to standing.
In preschool or school-aged children,
you may detect a venous hum. This is a
soft, hollow, continuous sound, louder
in diastole, heard just below the right
clavicle (Fig. 18-76). It can be completely
eliminated by maneuvers that
affect venous return, such as lying
supine, changing head position, or
jugular venous compression. It has the
same quality as breath sounds and is
therefore frequently overlooked.
The murmur heard in the carotid area
or just above the clavicles is known as
a carotid bruit. It is early and midsystolic
with a slightly harsh quality. It is
usually louder on the left and may be
heard alone or in combination with the
Still’s murmur. It may be completely
eradicated by carotid artery compression

153
Q

Still’s murmur

A

benign

preschool or early school age

Grade I–II/VI, musical, vibratory
Multiple overtones
Early and midsystolic
Mid/lower left sternal border
Frequently also a carotid bruit
154
Q

Venous hum

A

benign

preschool or early school age

Soft, hollow, continuous
Louder in diastole
Under clavicle
Can be eliminated by maneuvers

155
Q

carotid bruit

A

benign

preschool or later

Early and midsystolic
Usually louder on left
Eliminated by carotid compression

156
Q

pulmonary flow murmur

A

benign

preschool or school age

Grade 2–3 systolic ejection
Loudest at pulmonary auscultation area
Harsh, nonvibratory
Intensity increases when in the supine

157
Q

liver span chart

A

pg. 880

158
Q

spleen in kids

A

The spleen, like the liver, is felt easily in most children. It too is soft with a sharp
edge, and it projects downward like a tongue from under the left costal margin.
The spleen is moveable and rarely extends more than 1 to 2 cm below the costal
margin

159
Q

kids leg development

A

During early infancy, there is a common and normal progression from bowleggedness
(Fig. 18-87) that begins to disappear at about 18 months of age, often
followed by transition toward knock-knees. The knock-knee pattern (Fig. 18-88)
is usually maximal by age 3 to 4 years and gradually corrects by age 9 or 10 years.

Children may toe in when they begin to
walk. This may increase up to 4 years
of age and then gradually disappear by
about 10 years of age

160
Q

Strategies to Assess Cranial Nerves in

Young Children: I Olfactory

A

Testable in older children

161
Q

Strategies to Assess Cranial Nerves in

Young Children: II Visual Acuity

A

Use Snellen chart after age 3 yrs.
Test visual fields as for an adult.
A parent may need to hold the
child’s head

162
Q

Strategies to Assess Cranial Nerves in

Young Children: III,IV,VI Extraocular Movements

A

Have the child track a light or an
object (a toy is preferable). A
parent may need to hold the
child’s head

163
Q

Strategies to Assess Cranial Nerves in

Young Children: V Motor

A
Play a game with a soft cotton
ball to test sensation.
Have the child clench the teeth
and chew or swallow some
food
164
Q

Strategies to Assess Cranial Nerves in

Young Children: VII Facial

A
Have the child “make faces” or
imitate you as you make faces
(including moving your eyebrows)
and observe symmetry
and facial movements.
165
Q

Strategies to Assess Cranial Nerves in Young Children: VII Acoustic

A
Perform auditory testing after
age 4 yrs.
Whisper a word or command
behind the child’s back and
have the child repeat it
166
Q

Strategies to Assess Cranial Nerves in Young Children: IX, X Swallow and Gag

A
Have the child stick the “whole
tongue out” or “say ‘ah’.”
Observe movement of the
uvula and soft palate.
Test the gag reflex
167
Q

Strategies to Assess Cranial Nerves in Young Children: Spinal Accessory

A
Have the child push your hand
away with his head. Have the
child shrug his shoulders while
you push down with your
hands to “see how strong you
are.”
168
Q

Strategies to Assess Cranial Nerves in

Young Children: Hypoglossal

A

Ask the child to “stick out your

tongue all the way.”

169
Q

adolescents: physical development

A

Adolescence is the period of transition from
childhood to adulthood. The physical transformation generally occurs over a
period of years, beginning at an average age of 10 years in girls and 11 years in
boys. On average, girls end pubertal development with a growth spurt by age
14 years and boys by age 16 years. The age of onset and duration of puberty
vary widely, although the stages follow the same sequence in all adolescents.
Early adolescents are preoccupied with these physical changes

170
Q

adolescents: cognitive development

A

Although less obvious, cognitive changes
during adolescence are as dramatic as changes in physique. Most adolescents
progress from concrete to formal operational thinking, acquiring an ability to
reason logically and abstractly and to consider future implications of current
actions (Fig. 18-95). Although the interview and examination resemble those of
adults, keep in mind the wide variability in cognitive development of adolescents
and their often erratic and still limited ability to see beyond simple solutions.
Moral thinking becomes sophisticated with lots of time spent debating issues.
Recent evidence shows that brain development (especially in the right prefrontal
cortex) probably continues well into the twenties

171
Q

adolescents: social and emotional development

A

Adolescence is a tumultuous
time, marked by the transition from family-dominated influences to increasing
autonomy and peer influence (Fig. 18-96). The struggle for identity, independence,
and eventually intimacy leads to stress, health-related problems, and
often, high-risk behaviors. This struggle also provides an important opportunity
for health promotion.

172
Q

developmental tasks of adolescence chart

A

p. 890-1

173
Q

The key to successfully examining adolescents

is

A

a comfortable, confidential

environment

174
Q

adolescents: HR

A

10-14 y/o: 85 (55-115)

>15 y/o: 60-100

175
Q

adolescents: heart

A

The benign pulmonary flow murmur is a grade I–II/VI soft, nonharsh murmur with
the timing characteristics of an ejection murmur, beginning after the first sound and
ending before the second sound, but without the marked crescendo–decrescendo
quality of an organic ejection murmur. If you hear this murmur, evaluate whether the pulmonary closure sound is of normal intensity and whether splitting of the second
heart sound is eliminated during expiration. An adolescent with a benign pulmonary
ejection murmur will have normal intensity and normally split second heart sounds.
The pulmonary flow murmur may also be heard in the presence of volume overload
from any cause such as chronic anemia, and following exercise. It may
persist into adulthood

176
Q

Pulmonary Flow Murmur

A

older child, adolescence and later

benign

Grade I–II/VI soft, nonharsh
Ejection in timing
Upper left sternal border
Normal P2

177
Q

signs of female puberty

A

The first easily detectable sign of puberty
is usually the appearance of breast buds although pubic hair sometimes appears
earlier. The average age of the appearance of pubic hair has decreased in recent
years, and current consensus is that the appearance of pubic hair as early as 7
years can be normal, particularly in dark-skinned girls who develop secondary
sexual characteristics at an earlier age

178
Q

Sexual Maturity Rating in Girls: Breasts

A

Stage 1: Preadolescent
- elevation of nipple only

Stage 2: Breast Bud Stage

  • elevation of breast and nipple as a small mound
  • enlargement of areolar diameter

Stage 3:

  • Further enlargement of elevation of breast and areola
  • no separation of their contours

Stage 4:
- Projection of areola and nipple to form a secondary mound above the level of
breast

Stage 5: Mature Stage
- projection of nipple only
- areola has receded to general contour of the breast (although in some normal
individuals the areola continues to form a secondary mound)

179
Q

first sign of male puberty

A

The first reliable sign of puberty starting between
ages 9 and 13.5 years is an increase in the size of the testes.

(Next, pubic hair appears,
along with progressive enlargement of the penis. The complete change from preadolescent to adult anatomy requires about 3 years, with a range of 1.8 to 5 years)

180
Q

Sexual maturity Rating in Boys

A
Stage 1: Preadolescent
Pubic hair - no pubic hair except for the fine body hair (vellus hair) similar to that on the abdomen
Penis - same size and proportions as in
childhood
Testes & Scrotum - same size
and proportions as in
childhood

Stage 2:
Pubic hair - Sparse growth of long, slightly pigmented, downy hair, straight or only
slightly curled, chiefly at
the base of the penis
Penis - Slight or no enlargement
Testes & Scrotum - Testes larger; scrotum larger, somewhat reddened,
and altered in texture

Stage 3:
Pubic hair - Darker, coarser, curlier hair spreading sparsely over the pubic symphysis
Penis - Larger, especially in length
Testes & Scrotum - Further enlarged

Stage 4:
Pubic hair - Coarse and curly hair, as in the adult; area covered greater than in stage 3, but not as great as in the
adult and not yet including
the thighs
Penis - Further enlarged in length and breadth, with development of the glans
Testes & Scrotum - Further enlarged; scrotal skin darkened

Stage 5: Adult
Pubic hair - Hair adult in quantity and quality, spreads to the medial surfaces of the
thighs but not up over the abdomen
Penis - Adult in size and shape
Testes & Scrotum - Adult in size and shape

181
Q

Sexual Maturity Ratings in Girls: Pubic Hair

A

Stage 1: Preadolescent
- no pubic hair except for the fine body hair (vellus hair) similar to that on the abdomen

Stage 2: Sparse growth of long, slightly pigmented, downy hair, straight or
only slightly curled, chiefly along the labia

Stage 3: Darker, coarser, curlier hair, spreading sparsely over the pubic symphysis

Stage 4: Coarse and curly hair as in adults; area covered greater than in stage 3
but not as great as in the adult and not yet including the thighs

Stage 5: Hair adult in quantity and quality, spreads on the medial surfaces of the thighs but not up over the abdomen

182
Q

Scoliosis Screening

A
First,
examine the patient standing assessing
symmetry of shoulders, scapula, and
hips. Then have the child bend forward
with the knees straight and
head hanging straight down between
extended arms (Adams forward bend
test).

If you detect scoliosis use a scoliometer
to test for the degree of scoliosis.
Have the teen bend forward again as
described above. Place the scoliometer over the spine at a point of maximum
prominence making sure that the spine is parallel to the floor at that point, as
shown in Figure 18-102. If needed, move the scoliometer up and down the spine
to find the point of maximal prominence. An angle greater than 7° on the scoliometer
is a reason for concern and often used as a threshold for referral to a
specialist. Of note, the sensitivity and specificity of both the Adams forward bend
test and scoliometer vary greatly according to the skill and experience of the
examiner.
You can also use a plumb line, a string
with a weight attached, to assess symmetry
of the back (Fig. 18-103). Place
the top of the plumb line at C7 and
have the child stand straight. The
plumb line should extend to the gluteal
crease (not shown here).

183
Q

Scoliosis is more common in kids w/

A

neuro or musculoskeletal abnormalities

184
Q

Screening for Musculoskeletal Exam for Sports

A

(1) Stand straight, facing forward
(2) move neck in all directions
(3) shrug shoulders
(4) hold arms out to the side against resistance
(5) hold arms out to side w/ elbows bent 90 degrees, raise and lower arms
(6) hold arms out, completely bend, straighten elbows
(7) hold arms down, bend elbows 90 degrees, pronate and supinate forearms
(8) make a fist, clench, and then spread fingers
(9) squat and suck walk for 4 steps forward
(10) stand straight w/ arms at sides facing back
(11) bend forward w knees straight and touch toes
(12) stand on heels and rise to the toes