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Reference
Range Values
for Pediatric Care
2ND EDITION
Editor
Lamia Soghier, MD, MEd, FAAP
Contributing Editors
Karen Fratantoni, MD, MPH, FAAP
Christine Reyes, MD, FCAP
Assistant Editor
Kristin Mullins, PhD
American Academy of Pediatrics Publishing Staff
Mary Lou White, Chief Product and Services Officer/SVP, Membership, Marketing, Publishing
Mark Grimes, Vice President, Publishing
Carrie Peters, Editor, Professional/Clinical Publishing
Theresa Wiener, Production Manager, Clinical and Professional Publications
Amanda Helmholz, Medical Copy Editor
Peg Mulcahy, Manager, Art Direction and Production
Linda Smessaert, MSIMC, Senior Marketing Manager, Professional Resources
Mary Louise Carr, MBA, Marketing Manager, Clinical Publications
EDITOR
Lamia M. Soghier, MD, MEd, FAAP
Assistant Professor of Pediatrics
The George Washington University School of Medicine and
Health Sciences
Medical Director, Neonatal Intensive Care Unit
Children’s National Health System
Washington, DC
CONTRIBUTING EDITORS
Karen Fratantoni, MD, MPH, FAAP
Assistant Professor of Pediatrics
The George Washington University School of Medicine and
Health Sciences
Medical Director, Complex Care Program
Children’s National Health System
Washington, DC
ASSISTANT EDITOR
Kristin Mullins, PhD
Associate Director of Chemistry, Point of Care Testing, and Clinical
Laboratory Support Services
Children’s National Health System
Washington, DC
iv Reference Range Values for Pediatric Care
CONTRIBUTORS
Sarah Goff, RD, LD, CNSC
Pediatric Clinical Dietitian
Children’s National Health System
Washington, DC
CONTENTS
Introduction...............................................................................................xiii
1. Conversions....................................................................................1
Conversion Formulas.............................................................................. 1
Temperature Conversion........................................................................ 1
Fahrenheit to Celsius Conversion...................................................... 2
Weight Conversion.................................................................................. 3
Newborn Weight Conversion Chart................................................. 3
Infant and Toddler Weight Conversion Chart.................................. 4
3. Growth..........................................................................................19
Determining Body Surface Area.......................................................... 19
Growth Charts....................................................................................... 20
Average Growth Velocity by Age-group........................................ 20
Fenton Preterm Growth Chart—Boys............................................. 21
Fenton Preterm Growth Chart—Girls............................................. 22
WHO Birth to 24 Months: Boys—Head Circumference-
for-age and Weight-for-length Percentiles................................ 23
WHO Birth to 24 Months: Boys—Length-for-age and
Weight-for-age Percentiles.......................................................... 24
WHO Birth to 24 Months: Girls—Head Circumference-
for-age and Weight-for-length Percentiles................................ 25
WHO Birth to 24 Months: Girls—Length-for-age and
Weight-for-age Percentiles.......................................................... 26
vi Reference Range Values for Pediatric Care
4. Blood Pressure.............................................................................59
Blood Pressure Nomograms................................................................. 59
Healthy Term Newborns During the First 12 Hours
After Birth..................................................................................... 59
Preterm and Full-term Newborns During the First Day
After Birth (According to Birth Weight).................................... 60
Preterm and Full-term Newborns During the First Day
After Birth (According to Gestational Age).............................. 61
Preterm and Full-term Newborns According to Post
Conceptional Age......................................................................... 62
Children Younger Than 1 Year......................................................... 63
Blood Pressure Levels for Boys by Age and
Height Percentile.......................................................................... 64
Blood Pressure Levels for Girls by Age and
Height Percentile.......................................................................... 66
viii Reference Range Values for Pediatric Care
6. Hyperbilirubinemia Management............................................109
Risk Nomogram................................................................................... 109
Phototherapy Nomogram................................................................... 110
Exchange Transfusion Nomogram.................................................... 111
12. Appendixes..............................................................................157
Acetaminophen Toxicity Nomogram............................................. 158
Rabies Guidelines............................................................................. 159
Rabies Postexposure Prophylaxis Schedule—
United States, 2010................................................................. 159
Immunization Schedules.................................................................. 160
Recommended Immunization Schedule for
Children and Adolescents Aged 18 Years
or Younger—United States, 2018.......................................... 160
Contents xi
INTRODUCTION
Reference Range Values for Pediatric Care was created in response
to an overwhelming need from pediatricians, pediatric residents,
nurse practitioners, pediatric nurses, and other pediatric providers
who acknowledged the utility of the Reference Range Values section
in the first edition of Quick Reference Guide to Pediatric Care, part of
the American Academy of Pediatrics (AAP) point-of-care offerings,
which also include the American Academy of Pediatrics Textbook of
Pediatric Care and Pediatric Care Online.
This handbook was designed with the busy practitioner in mind.
Compact and clear-cut, it provides the most commonly used ref-
erence range values, charts, and formulas at your fingertips. The
values span the gamut of age-groups, from newborn to adolescence,
with a particular emphasis on the values needed for the treatment
of preterm newborns younger than 37 weeks’ gestation. This focus
is complemented by sections that address common newborn scores
(eg, APGAR Score, New Ballard Score) as well as the AAP new-
born hyperbilirubinemia management charts. In this new (second)
edition, sections on antibiotics and anticonvulsant medications have
been expanded and now also include other commonly used drugs
with recommended serum drug target levels; preterm and neonatal
populations continue to be highlighted to assist any pediatrician
responsible for the complex dosing for this age-group. Two experi-
enced pediatric pharmacists, Laura Leathers, PharmD, BCPPS, and
Sara Rooney, PharmD, BCPS, BCPPS, have reviewed and revised this
section. In addition, 2 pediatric/neonatal dietitians, Sarah Goff, RD,
LD, CNSC, and Victoria C. Snelgrove, RD, LD, CNSC, CLC, provide
current reference ranges for nutritional requirements for growing
infants, toddlers, children, and adolescents. The handbook continues
to feature pain scales, growth measures for extremities, and the AAP
immunization and periodicity schedules.
In writing the second edition of Reference Range Values for
Pediatric Care, we would like to thank Carrie Peters, Mark Grimes,
and the AAP editorial team. We would also like to give a spe-
cial thanks to Andrea Estrada, MD (pediatric endocrinology), at
Children’s National Health System for her contribution to the text.
xiv Reference Range Values for Pediatric Care
TEMPERATURE CONVERSION
Celsius: °C = (5/9) × (°F − 32)
Fahrenheit: °F = (9/5) × (°C + 32)
2 Reference Range Values for Pediatric Care
Conversions
15 425 879 1,332 1,786 2,240 2,693 3,147 3,600 4,054 4,508 4,961
3
4
Infant and Toddler Weight Conversion Chart
Infant/toddler weight conversion chart. Oregon Patient Safety Commission Web site. https://oregonpatientsafety.org/docs/newsletters/Inf_Tod_
Weight_Conversion_Poster.pdf. Accessed February 6, 2019. Content developed by the Oregon Patient Safety Commission (OPSC). Learn more
Conversions
about OPSC at https://oregonpatientsafety.org. Used with permission.
5
2. Scales and Scoring
APGAR Score
Points
0 Points 1 Point 2 Points Totaled
Activity
Limp Some flexion Active motion
(muscle tone)
Grimace
Cry or active
(reflex No response Grimace
withdrawal
irritability)
Appearance Acrocyanotic
Completely
(skin color/ Pale or blue (body pink,
pink
complexion) extremities blue)
Respiration,
Weak cry; hypo Good;
including Absent
ventilation crying
breathing
8
MATURATIONAL ASSESSMENT OF GESTATIONAL AGE (New Ballard Score)
NAME SEX
HOSPITAL NO. BIRTH WEIGHT
RACE LENGTH
DATE/TIME OF BIRTH HEAD CIRCUMFERENCE
DATE/TIME OF EXAM EXAMINER
New Ballard Score
NEUROMUSCULAR MATURITY
SCORE
NEUROMUSCULAR SCORE RECORD
SCORE Neuromuscular
MATURITY SIGN
1 0 1 2 3 4 5 HERE Physical
Reference Range Values for Pediatric Care
Total
POSTURE
MATURITY RATING
SQUARE WINDOW SCORE WEEKS
(Wrist)
90º 90º 60º 45º 30º 0º
10 20
ARM RECOIL 5 22
180º 140-180º 110-140º 90-110º 90º
0 24
POPLITEAL ANGLE 5 26
180º 160º 140º 120º 100º 90º 90º
10 28
SCARF SIGN 15 30
20 32
HEEL TO EAR 25 34
30 36
TOTAL NEUROMUSCULAR
35 38
MATURITY SCORE
PHYSICAL MATURITY 40 40
SCORE RECORD 45 42
PHYSICAL
SCORE
MATURITY SIGN
1 0 1 2 3 4 5 HERE 50 44
sticky gelatinous superficial cracking parchment leathery
smooth pink peeling
SKIN friable red pale areas deep cracking cracked
visible veins and/or rash,
transparent translucent few veins rare veins no vessels wrinkled
GESTATIONAL AGE
(weeks)
HOSPITAL NO. BIRTH WEIGHT
SCARF SIGN
RACE LENGTH 15 30
DATE/TIME OF BIRTH HEAD CIRCUMFERENCE 20 32
DATE/TIME
HEEL TO EAR OF EXAM EXAMINER
25 34
AGE WHEN EXAMINED
30 36
APGAR SCORE: 1 MINUTE 5 MINUTES 10 MINUTES
TOTAL NEUROMUSCULAR
35 38
MATURITY SCORE
NEUROMUSCULAR
PHYSICAL
PHYSICAL MATURITYMATURITY
MATURITY 40 40
SCORE
NEUROMUSCULAR SCORE
SCORE RECORD
RECORD 45 42
PHYSICAL SCORE Neuromuscular
SIGN SCORE
MATURITY
MATURITYSIGN
1 HERE Physical
1 00 11 22 33 44 55 HERE 50 44
Total
sticky gelatinous superficial cracking parchment leathery
POSTURE smooth pink peeling
SKIN friable red pale areas deep cracking cracked
visible veins and/or rash,
transparent translucent few veins rare veins no vessels wrinkled
GESTATIONAL AGE
MATURITY RATING
SQUARE WINDOW (weeks)
LANUGO none sparse abundant thinning bald areas mostly bald SCORE WEEKS
(Wrist) By dates
90º 90º 60º 45º 30º 0º
10
By ultrasound 20
heel-toe anterior
PLANTAR 50 mm faint creases creases over By exam
ARM RECOIL 40-50 mm: 1 transverse 5 22
SURFACE no crease red marks ant. 2/3 entire sole
40 mm: 2 180º 140-180º crease only
110-140º 90-110º 90º
0 24
stippled
barely flat areola raised areola full areola
POPLITEAL
BREAST areola 5 26
ANGLE imperceptible perceptible no bud 3-4 mm bud 5-10 mm bud
1-2 mm bud
180º 160º 140º 120º 100º 90º 90º
10 28
lids fused lids open sl. curved well-curved formed
and firm thick cartilage
EYE/EAR
SCARF SIGN loosely: 1 pinna flat pinna; soft; pinna; soft but 15 30
ear stiff
tightly: 2 stays folded slow recoil ready recoil instant recoil
20 32
GENITALS testes in testes testes
scrotum flat, scrotum empty testes down
HEEL TO EAR upper canal descending pendulous
(Male) smooth faint rugae good rugae 25 34
rare rugae few rugae deep rugae
prominent prominent 30 36
GENITALS clitoris majora and majora
clitoris and majora large
TOTAL NEUROMUSCULAR
prominent clitoris and small minora equally cover clitoris
(Female) enlarging minora small 35 38
and labia flat labia minora prominent and minora
MATURITY SCORE
minora
PHYSICAL MATURITY 40 40
Abbreviations: ant., anterior; exam, examination; sl., slightly.
TOTAL PHYSICAL RECORD
Reproduced
PHYSICAL al. New
with permission from Ballard JL, Khoury JC, Wedig K, et SCORE 45 42
Ballard score, expanded to include extremely premature infants. J Pediatr. MATURITY SCORE SCORE
MATURITY SIGN
1991;119(3):417–423. 1 0 1 2 3 4 5 HERE 50 44
sticky gelatinous superficial cracking parchment leathery
smooth pink peeling
SKIN friable
Figure 83-1 red Maturational and/or rash,
pale
of areas deep cracking
gestational age cracked
(new Ballard score).
visible veins assessment
transparent translucent few veins rare veins no vessels wrinkled
GESTATIONAL AGE
(weeks)
LANUGO none sparse abundant thinning bald areas mostly bald
By dates
By ultrasound
heel-toe anterior
PLANTAR 50 mm faint creases creases over By exam
Scales and Scoring
stippled
barely flat areola raised areola full areola
BREAST imperceptible areola
perceptible no bud 3-4 mm bud 5-10 mm bud
1-2 mm bud
PAIN SCALES
Category Scoring
0 1 2
Face No particular Occasional grimace or Frequent to constant
expression or frown, withdrawn, disin quivering chin,
smile terested clenched jaw
Legs Normal position Uneasy, restless, tense Kicking, or legs
or relaxed drawn up
Activity Lying quietly, Squirming, shifting back Arched, rigid, or
normal position, and forth, tense jerking
moves easily
Cry No cry (awake Moans or whimpers, Crying steadily,
or asleep) occasional complaint screams or sobs,
frequent complaints
Consolability Content, Reassured by occasional Difficult to console or
relaxed touching, hugging, or be comfort
ing talked to; distractible
Merkel SI, Voepel-Lewis T, Shayevitz JR, Malviya S. The FLACC: a behavioral scale for scoring post
operative pain in young children. Pediatr Nurs. 1997;23(3):293–297. © The Regents of the University
of Michigan.
Neonatal Pain, Agitation, and Sedation Scale (NPASS)
Sedation/
Sedation Pain Pain/Agitation
Assessment
Criteria −2 −1 0/0 1 2
Crying/ No cry with Moans or cries No sedation/ Irritable or crying at High-pitched or
irritability painful stimuli minimally with no pain intervals silent-continuous cry
painful stimuli signs Consolable Inconsolable
Behavior/ No arousal to Arouses minimally No sedation/ Restless, squirming Arching, kicking
state any stimuli to stimuli no pain Awakens frequently Constantly awake or arouses
No spontaneous Little spontaneous signs minimally/no movement
movement movement (not sedated)
Facial Mouth lax Minimal expres No sedation/ Any pain expression Any pain expression
expression No expression sion with stimuli no pain intermittent continual
signs
Extremities/ No grasp reflex Weak grasp reflex No sedation/ Intermittent clenched Continual clenched toes,
tone Flaccid tone ↓ muscle tone no pain toes, clenched fists, or clenched fists, or finger
signs finger splay splay
Body not tense Body tense
Vital signs No variability <10% variability No sedation/ ↑ 10%–20% from ↑ >20% from baseline
HR, RR, with stimuli from baseline no pain baseline Sao2 ≤75% with stimulation—
BP, Sao2 Hypoventilation with stimuli signs Sao2 76%–85% with slow ↑
or apnea stimulation—quick ↑ Out of sync/fighting ventilator
11
12 Reference Range Values for Pediatric Care
ASSESSMENT OF SEDATION
• Sedation is scored in addition to pain for each behavioral and
physiological criterion to assess the infant’s response to stimuli.
• Sedation does not need to be assessed/scored with every pain
assessment/score.
• Sedation is scored from 0 → −2 for each behavioral and
physiological criterion, then summed and noted as a negative
score (0 → −10).
—— A score of 0 is given if the infant has no signs of sedation, does
not underreact.
• Desired levels of sedation vary according to the situation.
—— “Deep sedation” → goal score of −10 to −5.
—— “Light sedation” → goal score of −5 to −2.
—— Deep sedation is not recommended unless an infant is receiving
ventilatory support, related to the high potential for hypoventi-
lation and apnea.
• A negative score without the administration of opioids/sedatives
may indicate
—— The premature infant’s response to prolonged or persistent
pain/stress
—— Neurological depression, sepsis, or another pathology
ASSESSMENT OF PAIN/AGITATION
• Pain assessment is the fifth vital sign—assessment for pain should
be included in every vital sign assessment.
• Pain is scored from 0 → +2 for each behavioral and physiological
criterion, then summed.
—— Points are added to the premature infant’s pain score and based
on the gestational age to compensate for the limited ability to
behaviorally communicate pain.
—— Total pain score is documented as a positive number (0 → +11).
• Treatment/interventions are suggested for scores >3.
—— Interventions for known pain/painful stimuli are indicated
before the score reaches 3.
• The goal of pain treatment/intervention is a score ≤3.
Scales and Scoring 13
PARALYSIS/NEUROMUSCULAR BLOCKADE
• It is impossible to behaviorally evaluate a paralyzed infant for pain.
• Increases in HR and BP at rest or with stimulation may be the only
indicator of a need for more analgesia.
• Analgesics should be administered continuously by drip or
around-the-clock dosing.
—— Higher, more frequent doses may be required if the infant is
postoperative, has a chest tube, or has another pathology (such
as necrotizing enterocolitis) that would normally cause pain.
—— Opioid doses should be increased by 10% every 3–5 d, as toler-
ance will occur without symptoms of inadequate analgesia.
SCORING CRITERIA
CRYING/IRRITABILITY
−2 → No response to painful stimuli
—— No cry with needle sticks
—— No reaction to endotracheal tube or nares suctioning
—— No response to caregiving
−1 → Moans, sighs, or cries (audible or silent) minimally to painful
stimuli (eg, needle sticks, endotracheal tube or nares suctioning,
caregiving)
0 → No sedation signs or no pain/agitation signs
+1 → Infant irritable/crying at intervals—but can be consoled
—— If intubated, intermittent silent cry
+2 → Any of the following signs:
—— Cry is high-pitched.
—— Infant cries inconsolably.
—— If intubated, silent-continuous cry.
14 Reference Range Values for Pediatric Care
BEHAVIOR/STATE
−2 → Does not arouse or react to any stimuli:
—— Eyes continually shut or open
—— No spontaneous movement
−1 → Little spontaneous movement, arouses briefly and/or minimally
to any stimuli
—— Opens eyes briefly
—— Reacts to suctioning
—— Withdraws to pain
0 → No sedation signs or no pain/agitation signs
+1 → Any of the following signs:
—— Restless, squirming
—— Awakens frequently/easily with minimal or no stimuli
+2 → Any of the following signs:
—— Kicking
—— Arching
—— Constantly awake
—— No movement or minimal arousal with stimulation
(not sedated, inappropriate for gestational age or
clinical situation)
FACIAL EXPRESSION
−2 → Any of the following signs:
—— Mouth lax
—— Drooling
—— No facial expression at
rest or with stimuli
−1 → Minimal facial expression
with stimuli
0→ N o sedation signs or no pain/
agitation signs
+1 → Any pain facial expression
observed intermittently
+2 → Any pain facial expression continual
Scales and Scoring 15
EXTREMITIES/TONE
−2 → Any of the following signs:
—— No palmar or planter grasp can be elicited.
—— Flaccid tone.
−1 → Any of the following signs:
—— Weak palmar or planter grasp can be elicited.
—— Decreased tone.
0 → No sedation signs or no pain/agitation signs
+1 → Intermittent (<30 seconds’ duration) observation of toes and/or
hands as clenched, or fingers splayed
—— Body is not tense.
+2 → Any of the following signs:
—— Frequent (≥30 seconds’ duration) observation of toes and/or
hands as clenched, or fingers splayed.
—— Body is tense/stiff.
VITAL SIGNS: HR, BP, RR, Sao2
−2 → Any of the following signs:
—— No variability in vital signs with stimuli
—— Hypoventilation
—— Apnea
—— Ventilated infant—no spontaneous respiratory effort
−1 → Vital signs that show little variability with stimuli—<10% from
baseline
0 → No sedation signs or no pain/agitation signs
+1 → Any of the following signs:
—— HR, RR, and/or BP are 10%–20% above baseline.
—— With care/stimuli, infant de-saturates minimally to
moderately (Sao2 76%–85%) and recovers quickly
(within 2 min).
+2 → Any of the following signs:
—— HR, RR, and/or BP are >20% above baseline.
—— With care/stimuli, infant de-saturates severely (Sao2 <75%)
and recovers slowly (>2 min).
—— Out of sync/fighting ventilator.
16 Reference Range Values for Pediatric Care
CROUP SCORE
Croup is a respiratory illness that usually occurs in infants and
young children and may manifest with barking cough, stridor with
inspiration, and hoarseness. Severity scores, such as the Westley
Croup Score, can help the clinician distinguish between mild symp-
toms and severe symptoms and can be used to monitor response to
treatment. An online calculator may be found at www.mdcalc.com/
westley-croup-score.
3. Growth
DETERMINING BODY SURFACE AREA
Based on the nomogram, a straight line joining the patient’s height
and weight will intersect the center column at the calculated body
surface area (BSA). For children of normal height for weight, use the
child’s weight in pounds, and then read across to the corresponding
BSA in meters squared. Alternatively, you can use Mosteller’s formula.
Nomogram
Height For children of SA Weight
cm in normal height m2 lb kg
and weight 180 80
90 160 70
1.30
2.0 140
80 1.20 1.9 130 60
240 70 1.10 1.8 120
1.7 110 50
220 85 1.00 1.6 100
60 1.5
80 90 40
200 .90 1.4
190 75 50 80
1.3
180 70 .80 1.2 70
30
Surface area in meters squared
170 40 1.1 60
65 .70
160 1.0 25
60 50
150 0.9
30 .60 45 20
140 55
.55 40
0.8
Weight in pounds
130 50 .50 35
0.7 15
120 30
20 .45
45
110 0.6 25
.40
100 40 10
15 .35 0.5 20 9.0
90 18 8.0
35
16 7.0
.30 0.4
80 14
6.0
30 10
12
28 9 .25 5.0
70
8 10
26 0.3 9 4.0
24 7 8
60
6 .20 7
22 3.0
6
20 5 2.5
50 0.2
19 5
18 4 .15 2.0
17 4
40 16
3 1.5
15
3
14
13
.10 1.0
30 12 2 0.1
GROWTH CHARTS
Average Growth Velocity by Age-group
Head Circumference
Age Weight Height (cm/wk)
Preterm infant 15–20 g/kg/d 0.8–1.1 cm/wk 0.8–1
<2 kg
Preterm infant 20–30 g/d 0.8–1.1 cm/wk 0.8–1
>2 kg
0–4 mo 23–34 g/d 0.8–0.93 cm/wk 0.38–0.48
4–8 mo 10–16 g/d 0.37–0.47 cm/wk 0.16–0.2
8–12 mo 6–11 g/d 0.28–0.37 cm/wk 0.08–0.11
12–16 mo 5–9 g/d 0.24–0.33 cm/wk 0.04–0.08
16–20 mo 4–9 g/d 0.21–0.29 cm/wk 0.03–0.06
20–24 mo 4–9 g/d 0.19–0.26 cm/wk 0.02–0.04
2–6 y 5–8 g/d 5–8 cm/y NA
6–10 y NA
Appendix A - 4 Growth 21
Fig. A-4.1
Fenton Preterm Growth Chart—Boys
APP
Appendix A 1313
Growth 23
From National Center for Health Statistics. WHO growth standards are recommended for use in the U.S. for
infants and children 0 to 2 years of age. Centers for Disease Control and Prevention Web site. https://www.cdc.
gov/growthcharts/who_charts.htm. Updated September 9, 2010. Accessed February 6, 2019.
24 Reference Range Values for Pediatric Care
From National Center for Health Statistics. WHO growth standards are recommended for use in the U.S. for
infants and children 0 to 2 years of age. Centers for Disease Control and Prevention Web site. https://www.cdc.
gov/growthcharts/who_charts.htm. Updated September 9, 2010. Accessed February 6, 2019.
Growth 25
From National Center for Health Statistics. WHO growth standards are recommended for use in the
U.S. for infants and children 0 to 2 years of age. Centers for Disease Control and Prevention Web
site. https://www.cdc.gov/growthcharts/who_charts.htm. Updated September 9, 2010. Accessed
February 6, 2019.
26 Reference Range Values for Pediatric Care
From National Center for Health Statistics. WHO growth standards are recommended for use in the U.S. for
infants and children 0 to 2 years of age. Centers for Disease Control and Prevention Web site. https://www.
cdc.gov/growthcharts/who_charts.htm. Updated September 9, 2010. Accessed February 6, 2019.
Growth 27
12 13 14 15 16 17 18 19 20
Mother’s Stature Father’s Stature cm in
Date Age Weight Stature BMI*
AGE (YEARS) 76
95
190
74
90
185 S
75
72
180 T
50 70 A
175 T
25 68 U
170 R
10 66
165 E
in cm 3 4 5 6 7 8 9 10 11 5
64
160 160
62 62
155 155
S 60 60
T 150 150
A 58
T 145
U 56
140 105 230
R
54
E 135 100 220
52
130 95 95 210
50
125 90 200
90
48 190
120 85
46 180
115 80
75
44 170
110 75
42 160
105 50 70
150 W
40
100 65 140 E
25
38 I
95 60 130 G
10
36 90 5 H
55 120
T
34 85 50 110
32 80 45 100
30
40 90
80 35 35 80
W 70 70
30 30
E 60 60
I 25 25
G 50 50
H 20 20
40 40
T
15 15
30 30
10 10
lb kg AGE (YEARS) kg lb
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
Abbreviations: BMI,
Published May 30, body
2000 mass index;
(modified CDC, Centers for Disease Control and Prevention.
11/21/00).
SOURCE: Developed by the National Center for Health Statistics in collaboration with
From National CenterCenter
the National for Health Statistics.
for Chronic Clinical
Disease growthand
Prevention charts.
HealthCenters for Disease
Promotion (2000). Control
and Prevention Web site. https://www.cdc.gov/growthcharts/clinical_charts.htm. Updated
http://www.cdc.gov/growthcharts
June 16, 2017. Accessed February 6, 2019.
28 Reference Range Values for Pediatric Care
35
34
33
32
31
30
95
29
BMI 28
90
27 27
26 85 26
25 25
75
24 24
23 23
50
22 22
21 21
25
20 20
10
19 19
5
18 18
17 17
16 16
15 15
14 14
13 13
12 12
2 2
kg/m AGE (YEARS) kg/m
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
Abbreviations: BMI,
Published May 30, body
2000 mass index;
(modified CDC, Centers for Disease Control and Prevention.
10/16/00).
SOURCE: Developed by the National Center for Health Statistics in collaboration with
From National Center Center
the National for Health Statistics.
for Chronic Clinical
Disease growthand
Prevention charts. Centers
Health for Disease
Promotion (2000). Control
and Prevention Web site. https://www.cdc.gov/growthcharts/clinical_charts.htm. Updated
http://www.cdc.gov/growthcharts
June 16, 2017. Accessed February 6, 2019.
Growth 29
12 13 14 15 16 17 18 19 20
Mother’s Stature Father’s Stature cm in
Date Age Weight Stature BMI*
AGE (YEARS) 76
190
74
185 S
72
180 T
70 A
95
175 T
90
68 U
170 R
75 66
165 E
in cm 3 4 5 6 7 8 9 10 11 50
64
160 25 160
62 62
155 10 155
60 5 60
150 150
58
145
56
140 105 230
54
S 135 100 220
T 52
A 130 95 210
50
T 125 90 200
U
48 190
R 120 85
E 95 180
46
115 80
44 170
110 90 75
42 160
105 70
150 W
40 75
100 65 140 E
38 I
95 60 130 G
50
36 90 H
55 120
25 T
34 85 50 110
10
32 80
5
45 100
30
40 90
80 35 35 80
W 70 70
30 30
E 60 60
I 25 25
G 50 50
H 20 20
40 40
T
15 15
30 30
10 10
lb kg AGE (YEARS) kg lb
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
Abbreviations: BMI,
Published May 30, body
2000 mass index;
(modified CDC, Centers for Disease Control and Prevention.
11/21/00).
SOURCE: Developed by the National Center for Health Statistics in collaboration with
From National CenterCenter
the National for Health Statistics.
for Chronic Clinical
Disease growthand
Prevention charts. Centers
Health for Disease
Promotion (2000). Control and
Preventionhttp://www.cdc.gov/growthcharts
Web site. https://www.cdc.gov/growthcharts/clinical_charts.htm. Updated June 16, 2017.
Accessed February 6, 2019.
30 Reference Range Values for Pediatric Care
Abbreviations: BMI, body mass index; CDC, Centers for Disease Control and Prevention.
From National Center for Health Statistics. Clinical growth charts. Centers for Disease Control and
Prevention Web site. https://www.cdc.gov/growthcharts/clinical_charts.htm. Updated June 16, 2017.
Accessed February 6, 2019.
Growth 31
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Boys
Weight-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Boys
Length-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Boys
Head Circumference-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Boys
Weight-for-length Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Girls
Weight-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Girls
Length-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Girls
Head Circumference-for-age Percentiles
Growth Charts for Children With Down Syndrome, Birth to 36 Months: Girls
Weight-for-length Percentiles
BIBLIOGRAPHY
Brooks J, Day S, Shavelle R, Strauss D. Low weight, morbidity, and mortality in
children with cerebral palsy: new clinical growth charts. Pediatrics. 2011;128(2):
e299–e307
Butler M, Lee P, Whitman B, eds. Management of Prader-Willi Syndrome. 3rd
ed. New York, NY: Springer-Verlag; 2006
Health Resources and Services Administration. The CDC Growth Charts for
Children with Special Health Care Needs Web site. http://depts.washington.
edu/growth/cshcn/text/page2b.htm. Accessed February 6, 2019
Horton WA, Rotter JI, Rimoin DL, Scott CI, Hall JG. Standard growth curves for
achondroplasia. J Pediatr. 1978;93(3):435–438
Kline AD, Barr M, Jackson LG. Growth manifestations in the Brachmann-de
Lange syndrome. Am J Med Genet. 1993;47(7):1042–1049
Lyon AJ, Preece MA, Grant DB. Growth curves for girls with Turner syndrome.
Arch Dis Child. 1985;60(10):932–935
Morris CA, Demsey SA, Leonard CO, Dilts C, Blackburn BL. Natural history of
Williams syndrome: physical characteristics. J Pediatr. 1988;113(2):318–326
Pyeritz RE. Growth and anthropometrics in the Marfan syndrome. In:
Papadatos CJ, Bartsocas CS, eds. Endocrine Genetics and Genetics of Growth.
New York, NY: Alan R. Liss Inc; 1985
Pyeritz RE. Marfan syndrome and related disorders. In: Rimoin DL, Pyeritz RE,
Korf B, eds. Emery and Rimoin’s Principles and Practice of Medical Genetics. 5th
ed. New York, NY: Churchill Livingstone; 2006
Ranke MB, Pflüger H, Rosendahl W, et al. Turner syndrome: spontaneous
growth in 150 cases and review of the literature. Eur J Pediatr. 1983;141(2):81–88
Stevens CA, Hennekam RC, Blackburn BL. Growth in the Rubinstein-Taybi
syndrome. Am J Med Genet Suppl. 1990;6:51–55
Zemel BS, Pipan M, Stallings VA, et al. Growth charts for children with Down
syndrome in the United States. Pediatrics. 2015;135(5):e1204–e1211
Growth 41
95
18 18
90
17 17
75
16 50 16
M 25 M
U U
15 15
A A
C 10 C
3
14 14
13 13
12 12
AGE (MONTHS)
11 11
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
Figure S1. MUAC growth charts based on the LMS data described herein for boys aged 2 months through 2 years.
Abbreviation: MUAC, mid-upper arm circumference.
© 2016, American Society for Parenteral and Enteral Nutrition. All rights reserved.
From Abdel-Rahman SM, Bi C, Thaete K. Construction of lambda, mu, sigma values for
determining mid-upper arm circumference z scores in U.S. children aged 2 months through
18 years. Nutr Clin Pract. 2017;32(1):68–76, with permission.
Growth 43
39 39
38 38
90
37 37
36 36
35 35
75
34 34
33 33
32 32
50
21 21
M 30 30 M
U U
29 29
A 25 A
C 28 28 C
27 10
27
26 26
5
25 3 25
24 24
23 23
22 22
21 21
20 20
19 19
18 18
17 17
16 16
15 15
AGE (YEARS)
14 14
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Figure S2. MUAC growth charts based on the LMS data described herein for boys aged 2 years through 18 years.
Abbreviation: MUAC, mid-upper
© 2016, Americanarm circumference.
Society for Parenteral and Enteral Nutrition. All rights reserved.
From Abdel-Rahman SM, Bi C, Thaete K. Construction of lambda, mu, sigma values for
determining mid-upper arm circumference z scores in U.S. children aged 2 months through
18 years. Nutr Clin Pract. 2017;32(1):68–76, with permission.
44 Reference Range Values for Pediatric Care
cm cm
19 19
2 to 24 months: Girls 97
mid-upper arm circumference-for-age percentiles
95
18 18
90
17 17
75
16 50 16
M M
U 25 U
15 15
A A
C C
10
5
14 14
3
13 13
12 12
AGE (MONTHS)
11 11
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
Figure S3. MUAC growth charts based on the LMS data described herein for girls aged 2 months through 2 years.
Abbreviation: MUAC, mid-upper arm
© 2016, American circumference.
Society for Parenteral and Enteral Nutrition. All rights reserved.
From Abdel-Rahman SM, Bi C, Thaete K. Construction of lambda, mu, sigma values for
determining mid-upper arm circumference z scores in U.S. children aged 2 months through
18 years. Nutr Clin Pract. 2017;32(1):68–76, with permission.
Growth 45
36 36
90
35 35
34 34
33 33
32 75
32
21 21
30 30
29 29
50
28 28
M
U 27 27 M
A 26 U
25 26
C A
25 25 C
24 10 24
23 5 23
3
22 22
21 21
20 20
19 19
18 18
17 17
16 16
15 15
14 14
AGE (YEARS)
13 13
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Figure S4. MUAC growth charts based on the LMS data described herein for boys aged 2 years through 18 years.
© 2016, American Society for Parenteral and Enteral Nutrition. All rights reserved.
Abbreviation: MUAC, mid-upper arm circumference.
From Abdel-Rahman SM, Bi C, Thaete K. Construction of lambda, mu, sigma values for
determining mid-upper arm circumference z scores in U.S. children aged 2 months through
18 years. Nutr Clin Pract. 2017;32(1):68–76, with permission.
46 Reference Range Values for Pediatric Care
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
Growth 49
Forearm Length
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
50 Reference Range Values for Pediatric Care
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
Growth 51
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
52 Reference Range Values for Pediatric Care
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
Growth 53
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
54 Reference Range Values for Pediatric Care
From Rollins JD, Tribble LM, Collins JS, et al, eds. Growth References. 3rd ed. Greenwood, SC:
Greenwood Genetic Center; 2011, with permission.
Growth 55
40
30
Length (mm)
20
10
0
28 30 32 34 36 38 40
Conceptual age (weeks)
Stretched phallic length of 63 normal premature and full-term male infants (closed circle), showing
lines of mean ± 2 SD. Correlation coefficient is 0.80. Superimposed are data for 2 small-for-gestational
age infants (open triangle), 7 large-for-gestation infants (closed triangle), and 4 twins (closed square),
all of which are in the normal range.
Reproduced with permission from Feldman KW, Smith DW. Fetal phallic growth and penile standards
for newborn male infants. J Pediatr. 1975;86(3):395–398.
56 Reference Range Values for Pediatric Care
6.5 1 SD
6.0 Mean
Penile length, cm
5.5 1 SD
5.0 2 SD
2.5 SD
4.5
4.0
3.5
3.0
2.5
0.0–1.0 1.1–3.0 3.1–6.0 6.1–12.0 12.1–24.0 24.1–36.0 36.1–48.0 48.1–60.0
Reproduced with permission from Camurdan AD, Oz MO, Ilhan MN, Camurdan OM, Sahin F, Beyazo
va U. Current stretched penile length: cross-sectional study of 1040 healthy Turkish children aged 0
to 5 years. Urology. 2007;70(3):572–575.
development Growth 57
PRIMARY
Primary TEETH
Teeth eruption ChartERUPTION CHART
Primary Teeth
From: American Dental Association. Tooth eruption: the primary teeth. J Am Dent Assoc. 2005;136(11):1619.
Copyright © American Dental Association. Used with permission.
4. Blood Pressure
BLOOD PRESSURE NOMOGRAMS
Healthy Term Newborns During the First 12 Hours After Birth
A B
80 80
Systolic Systolic
Mean
(torr) 60 (torr) 60
40 40
20 20
0 1 2 3 4 5 0 1 2 3 4 5
80 80
Diastolic Pulse
(torr) 60 (torr) 60
40 40
20 20
0 1 2 3 4 5 0 1 2 3 4 5
Birth Weight (kg) Birth Weight (kg)
A, Linear regressions (broken lines) and 95% confidence limits (solid lines) of systolic (top) and
diastolic (bottom) aortic blood pressures on birth weight in 61 healthy term newborns during the
first 12 hours after birth. For systolic pressure, y = 7.13x + 40.45; r = 0.79. For diastolic pressure,
y = 4.81x + 22.18; r = 0.71. For both, n = 413 and p < .001. B, Linear regressions (broken lines) and
95% confidence limits (solid lines) of mean pressure (top) and pulse pressure (systolic-diastolic
pressure amplitude) (bottom) on birth weight in 61 healthy term newborns during the first 12 hours
after birth. For mean pressure, y = 5.16x + 29.80; n = 443; r = 0.80. For pulse pressure, y = 2.31x +
18.27; n = 413; r = 0.45. For both, p < .001.
From Versmold HT, Kitterman JA, Phibbs RH, Gregory GA, Tooley WH. Aortic blood pressure
during the first 12 hours of life in infants with birth weight 610 to 4,220 grams. Pediatrics.
1981;67(5):607–613.
60 Reference Range Values for Pediatric Care
90
Systolic Blood Pressure (mm Hg)
80
70
60
50
Lower 95% C.L.
40
30
20
10
0
.750 1.000 1.250 1.500 1.750 2.000 2.250 2.500 2.750 3.000 3.250 3.500 3.750 4.000
70
Upper 95% C.L.
60
50
40
30
10
0
.750 1.000 1.250 1.500 1.750 2.000 2.250 2.500 2.750 3.000 3.250 3.500 3.750 4.000
Linear regression of mean systolic and diastolic blood pressures by birth weight on day 1 after birth,
with 95% confidence limits (C.L.s) (upper and lower dashed lines).
From Zubrow AB, Hulman S, Kushner H, Falkner B. Determinants of blood pressure in infants admitted
to neonatal intensive care units: a prospective multicenter study. Philadelphia Neonatal Blood
Pressure Study Group. J Perinatol. 1995;15(6):470–479. Reproduced with permission. Copyright ©
1995 Nature Publishing Group.
Blood Pressure 61
Preterm and Full-term Newborns During the First Day After Birth
(According to Gestational Age)
80
Systolic Blood Pressure (mm Hg)
70
60
50
40
Lower 95% C.L.
30
20
10
0
22 24 26 28 30 32 34 36 38 40 42
70
Diastolic Blood Pressure (mm Hg)
60
Upper 95% C.L.
50
40
30
Lower 95% C.L.
20
10
0
22 24 26 28 30 32 34 36 38 40 42
Linear regression of mean systolic and diastolic blood pressures by gestational age on day 1 after
birth, with 95% confidence limits (C.L.s) (upper and lower dashed lines).
From Zubrow AB, Hulman S, Kushner H, Falkner B. Determinants of blood pressure in infants admitted
to neonatal intensive care units: a prospective multicenter study. Philadelphia Neonatal Blood
Pressure Study Group. J Perinatol. 1995;15(6):470–479. Reproduced with permission. Copyright ©
1995 Nature Publishing Group.
62 Reference Range Values for Pediatric Care
100
Systolic Blood Pressure (mm Hg)
90
80
70
60
Lower 95% C.L.
50
40
30
20
10
0
24 26 28 30 32 34 36 38 40 42 44 46
100
90
Diastolic Blood Pressure (mm Hg)
80
Upper 95% C.L.
70
60
50
40
30
Lower 95% C.L.
20
10
0
24 26 28 30 32 34 36 38 40 42 44 46
Linear regression of mean systolic and diastolic blood pressures by post conceptual age in weeks,
with 95% confidence limits (C.L.s) (upper and lower dashed lines).
From Zubrow AB, Hulman S, Kushner H, et al. Determinants of blood pressure in infants admitted to
neonatal intensive care units: a prospective multicenter study. Philadelphia Neonatal Blood Pressure
Study Group. J Perinatol. 1995;15(6):470–479. Reproduced with permission. Copyright © 1995
Nature Publishing Group.
Blood Pressure 63
115 115
110 95th 110 95th
90th 105 90th
105
100 100
SYSTOLIC BP
75th
SYSTOLIC BP
75th
95 95
50th 90 50th
90
85 85
80 80
75 75
70 70
65 65
0 1 2 3 4 5 6 7 8 9 10 11 12 0 1 2 3 4 5 6 7 8 9 10 11 12
MONTHS MONTHS
75 75
95th
95th
70 90th 70
90th
65 65
DIASTOLIC BP (K4)
DIASTOLIC BP (K4)
75th
75th
60 60
50th
55 55 50th
50 50
45 45
0 1 2 3 4 5 6 7 8 9 10 11 12 0 1 2 3 4 5 6 7 8 9 10 11 12
MONTHS MONTHS
90th Percentile
Systolic BP 87 101 106 106 106 105 105 106 105 105 105 105 105 76 98 101 104 105 106 106 106 106 106 108 105 105
Diastolic BP 68 65 63 63 63 65 66 67 68 68 69 69 69 68 65 64 64 65 66 66 66 66 67 67 67 67
Height CM 51 59 63 66 68 70 72 73 74 75 77 78 80 54 55 56 58 51 63 66 68 70 72 74 75 77
Weight KG 4 4 5 5 6 7 8 9 9 10 10 11 11 4 4 4 5 5 6 7 8 9 9 10 10 11
1 50th 80 81 83 85 87 88 89 34 35 36 37 38 39 39
90th 94 95 97 99 100 102 103 49 50 51 52 53 53 54
95th 98 99 101 103 104 106 106 54 54 55 56 57 58 58
99th 105 106 108 110 112 113 114 61 62 63 64 65 66 66
2 50th 84 85 87 88 90 92 92 39 40 41 42 43 44 44
90th 97 99 100 102 104 105 106 54 55 56 57 58 58 59
95th 101 102 104 106 108 109 110 59 59 60 61 62 63 63
99th 109 110 111 113 115 117 117 66 67 68 69 70 71 71
3 50th 86 87 89 91 93 94 95 44 44 45 46 47 48 48
90th 100 101 103 105 107 108 109 59 59 60 61 62 63 63
95th 104 105 107 109 110 112 113 63 63 64 65 66 67 67
99th 111 112 114 116 118 119 120 71 71 72 73 74 75 75
4 50th 88 89 91 93 95 96 97 47 48 49 50 51 51 52
90th 102 103 105 107 109 110 111 62 63 64 65 66 66 67
95th 106 107 109 111 112 114 115 66 67 68 69 70 71 71
99th 113 114 116 118 120 121 122 74 75 76 77 78 78 79
5 50th 90 91 93 95 96 98 98 50 51 52 53 54 55 55
90th 104 105 106 108 110 111 112 65 66 67 68 69 69 70
95th 108 109 110 112 114 115 116 69 70 71 72 73 74 74
99th 115 116 118 120 121 123 123 77 78 79 80 81 81 82
6 50th 91 92 94 96 98 99 100 53 53 54 55 56 57 57
90th 105 106 108 110 111 113 113 68 68 69 70 71 72 72
95th 109 110 112 114 115 117 117 72 72 73 74 75 76 76
99th 116 117 119 121 123 124 125 80 80 81 82 83 84 84
7 50th 92 94 95 97 99 100 101 55 55 56 57 58 59 59
90th 106 107 109 111 113 114 115 70 70 71 72 73 74 74
95th 110 111 113 115 117 118 119 74 74 75 76 77 78 78
99th 117 118 120 122 124 125 126 82 82 83 84 85 86 86
8 50th 94 95 97 99 100 102 102 56 57 58 59 60 60 61
90th 107 109 110 112 114 115 116 71 72 72 73 74 75 76
95th 111 112 114 116 118 119 120 75 76 77 78 79 79 80
99th 119 120 122 123 125 127 127 83 84 85 86 87 87 88
9 50th 95 96 98 100 102 103 104 57 58 59 60 61 61 62
90th 109 110 112 114 115 117 118 72 73 74 75 76 76 77
95th 113 114 116 118 119 121 121 76 77 78 79 80 81 81
99th 120 121 123 125 127 128 129 84 85 86 87 88 88 89
Blood Pressure 65
1 50th 83 84 85 86 88 89 90 38 39 39 40 41 41 42
90th 97 97 98 100 101 102 103 52 53 53 54 55 55 56
95th 100 101 102 104 105 106 107 56 57 57 58 59 59 60
99th 108 108 109 111 112 113 114 64 64 65 65 66 67 67
2 50th 85 85 87 88 89 91 91 43 44 44 45 46 46 47
90th 98 99 100 101 103 104 105 57 58 58 59 60 61 61
95th 102 103 104 105 107 108 109 61 62 62 63 64 65 65
99th 109 110 111 112 114 115 116 69 69 70 70 71 72 72
3 50th 86 87 88 89 91 92 93 47 48 48 49 50 50 51
90th 100 100 102 103 104 106 106 61 62 62 63 64 64 65
95th 104 104 105 107 108 109 110 65 66 66 67 68 68 69
99th 111 111 113 114 115 116 117 73 73 74 74 75 76 76
4 50th 88 88 90 91 92 94 94 50 50 51 52 52 53 54
90th 101 102 103 104 106 107 108 64 64 65 66 67 67 68
95th 105 106 107 108 110 111 112 68 68 69 70 71 71 72
99th 112 113 114 115 117 118 119 76 76 76 77 78 79 79
5 50th 89 90 91 93 94 95 96 52 53 53 54 55 55 56
90th 103 103 105 106 107 109 109 66 67 67 68 69 69 70
95th 107 107 108 110 111 112 113 70 71 71 72 73 73 74
99th 114 114 116 117 118 120 120 78 78 79 79 80 81 81
6 50th 91 92 93 94 96 97 98 54 54 55 56 56 57 58
90th 104 105 106 108 109 110 111 68 68 69 70 70 71 72
95th 108 109 110 111 113 114 115 72 72 73 74 74 75 76
99th 115 116 117 119 120 121 122 80 80 80 81 82 83 83
7 50th 93 93 95 96 97 99 99 55 56 56 57 58 58 59
90th 106 107 108 109 111 112 113 69 70 70 71 72 72 73
95th 110 111 112 113 115 116 116 73 74 74 75 76 76 77
99th 117 118 119 120 122 123 124 81 81 82 82 83 84 84
8 50th 95 95 96 98 99 100 101 57 57 57 58 59 60 60
90th 108 109 110 111 113 114 114 71 71 71 72 73 74 74
95th 112 112 114 115 116 118 118 75 75 75 76 77 78 78
99th 119 120 121 122 123 125 125 82 82 83 83 84 85 86
Blood Pressure 67
cells (/mcL)
70 Reference Range Values for Pediatric Care
Abbreviations: CSF, cerebrospinal fluid; RBC, red blood cell; WBC, white blood cell.
Calculating the ratio of RBCs to WBCs in CSF
General rule: For every 500 RBCs in CSF, it is acceptable to have 1 WBC.
Normal ratio of RBCs to WBCs in peripheral blood is 1,000 RBCs:1–2 WBCs (106/L).
No. of WBCs introduced into the CSF per liter = [(WBC[peripheral] × RBC[CSF])/RBC(peripheral)] × 106/L.
Compare this number with the actual number of WBCs in the CSF.
1,000 × 106/L RBCs in CSF raises CSF protein concentration by approximately 0.015 g/L.
a
Correction factors should not be used to reassure that meningitis is unlikely.
Reference Range Values
71
72 Reference Range Values for Pediatric Care
BIBLIOGRAPHY
Ahmed A, Hickey SM, Ehrett S, et al. Cerebrospinal fluid values in the term
neonate. Pediatr Infect Dis J. 1996;15(4):298–303
Avery RA, Shah SS, Licht DJ, et al. Reference range for cerebrospinal fluid
opening pressure in children. N Engl J Med. 2010;363(9):891–893
Biou D, Benoist JF, Nguyen-Thi C, Huong X, Morel P, Marchand M.
Cerebrospinal fluid protein concentrations in children: age-related values
in patients without disorders of the central nervous system. Clin Chem.
2000;46(3):399–403
Griffith BP, Booss J. Neurologic infections of the fetus and newborn. Neurol
Clin. 1994;12(3):541–564
Kestenbaum LA, Ebberson J, Zorc JJ, Hodinka RL, Shah SS. Defining cere-
brospinal fluid white blood cell count reference values in neonates and young
infants. Pediatrics. 2010;125(2):257–264
Lipton JD, Schafermeyer RW. Evolving concepts in pediatric bacterial
meningitis—part I: pathophysiology and diagnosis. Ann Emerg Med.
1993;22(10):1602–1615
McMillan JA, Oski FA, Feigin RD, et al, eds. Oski’s Pediatrics: Principles and
Practice. 3rd ed. Philadelphia, PA: JB Lippincott; 1999
Naidoo BT. The cerebrospinal fluid in the healthy newborn infant. S Afr Med J.
1968;42(35):933–935
Nascimento-Carvalho CMC, Moreno-Carvalho OA. Normal cerebrospinal
fluid values in full-term gestation and premature neonates. Arq Neuropsiquiatr.
1998;56(3A):375–380
Shah SS, Ebberson J, Kestenbaum LA, Hodinka RL, Zorc JJ. Age-specific
reference values for cerebrospinal fluid protein concentration in neonates and
young infants. J Hosp Med. 2011;6(1):22–27
Soldin JS, Brugnara C, Gunter KC, et al, eds. Pediatric Reference Ranges. 2nd
ed. Washington, DC: AAAC Press; 1997
Srinivasan L, Shah SS, Padula MA, Abbasi S, McGowan KL, Harris MC.
Cerebrospinal fluid reference ranges in term and preterm infants in the neona-
tal intensive care unit. J Pediatr. 2012;161(4):729–734
Wong M, Schlaggar BL, Buller RS, Storch GA, Landt M. Cerebrospinal fluid
protein concentration in pediatric patients: defining clinically relevant reference
values. Arch Pediatr Adolesc Med. 2000;154(8):827–831
Reference Range Values 73
CLINICAL CHEMISTRY
For Infants, Children, Teens, and Young Adultsa
Alanine Aminotransferase (ALT) (U/L)
Tissues with high concentration: Liver and kidney. There is evidence suggesting
that these c
utoffs are not sensitive enough to detect chronic liver disease in pedi-
atric p
opulations. Note that infants tend to have a broader range of results com-
pared with older children, and girls of all ages tend to have lower levels than boys.
1–<13 y 9–25
13–<19 y Male: 9–24
Female: 8–22
Aldolase (U/L)
Tissues with high concentration: Liver, muscle, and brain.
10–24 mo 3.4–11.8
2–16 y 1.2–8.8
Adult (17–64 y) 1.7–4.9
Alkaline Phosphatase (ALP) (U/L)
Tissues with high concentration: Liver, bone, intestine, and placenta. A substantial
elevation may occur during accelerated bone growth in children and adolescents.
6 mo–1 y 104–455
2–8 y 111–277
9–14 y 76–479
15–18 y Male: 64–310
Female: 37–222
Ammonia (μmol/L)
It is critical that a free-flowing (no tourniquet) venous (or arterial) sample be col-
lected into a heparinized (and preferably chilled) tube, immediately placed onto
ice, and analyzed within 30 min to prevent artifactual elevation of the result.
All ages <51
Amylase (U/L)
0–14 d 3–10
15 d–<13 wk 2–22
13 wk–<1 y 3–50
1 y–<19 y 25–101
74 Reference Range Values for Pediatric Care
Glucose (mg/dL)
0–<1 d Boy: 36–110
Girl: 36–89
1–7 d 47–110
>7 d 54–117
γ-Glutamyltransferase (GGT) (U/L)
Tissues with high concentration: Liver, kidney, pancreas, and prostate.
0–14 d 23–219
15–<1 y 8–127
1–<11 y 6–16
11–<19 y 7–21
Haptoglobin (mg/dL)
Neonates tend to have very low, even unmeasurable, haptoglobin levels.
Haptoglobin is an acute phase reactant.
0–14 d 0–10
15 d–<1 y 7–221
1–<12 y 7–163
12–<19 y 7–179
Hemoglobin A1c (%)
These values are target ranges as determined by the American Diabetes
Association.
Normal 4.5–5.6
At risk for diabetes 5.7–6.4
Diabetes mellitus ≥6.5
Hemoglobin F (% Total Hemoglobin)c
1d 62.7–91.3
5d 65.4–88.2
3 wk 55.7–84.2
6–9 wk 31.3–74.5
3–4 mo <54.6
6 mo <9.0
8–11 mo <3.6
>11 mo <2.0
78 Reference Range Values for Pediatric Care
Lipids (mg/dL)
These are target ranges recommended by the National Lipid Association,
the National Cholesterol Education Program, and the Expert Panel on
Integrated Guidelines for Cardiovascular Health and Risk Reduction in
Children and Adolescents.
Child or
Chemical Adolescent Adult
Cholesterol Optimal: <170 Optimal: <200
Borderline: Borderline: 200–239
170–199 High: ≥240
High: ≥200
Low-density lipoprotein (LDL) Optimal: <110 Optimal: <100
Borderline: Borderline: 130–159
110–129 High: ≥160
High: ≥130
High-density lipoprotein (HDL) >45 >40
Magnesium (mg/dL)
0–14 d 1.99–3.94
15 d–<1 y 1.97–3.09
1–<19 y 2.09–2.84
Methemoglobin (% of Hemoglobin)c
All 0.04–1.50
Osmolality (Serum or Plasma) (mOsm/kg)
Neonates 266–295
All 275–295
Phosphate (mg/dL)
0–14 d 5.6–10.5
15 d–<1 y 4.8–8.4
1–<5 y 4.3–6.8
5–<13 y 4.1–5.9
13–<16 y Boy: 3.5–6.2
Girl: 3.2–5.5
16–<19 y 2.9–5.0
80 Reference Range Values for Pediatric Care
Pyruvate (mg/dL)
All 0.30–0.70
Rheumatoid Factor (RF) (IU/mL)
RF is a heterogenous group of autoantibodies whose levels may be elevated
in response to a wide variety of rheumatic and non-rheumatic inflammatory
conditions.
0–14 d 9.0–17.1
15 d–<19 y 9.0–9.0
Sodium (mEq/L)d
0–<7 d 131–144
7–31 d 132–142
1–<6 mo 132–140
6 mo–1 y 131–140
>1 y 132–141
Total Iron-Binding Capacity (TIBC) (mcg/dL)
Infant 100–400
Adult 250–425
Transferrin (g/L)
9 wk–<1 y 107–324
1–<19 y 220–337
Triglycerides (mg/dL)
Age Male Female
0–7 d 19–174 26–159
8–30 d 37–279 33–270
31–90 d 42–279 34–340
1–3 y 25–119
4–6 y 30–110
7–9 y 26–123
10–11 y 22–131 37–124
12–13 y 22–138 35–124
14–15 y 32–158 36–129
16–<19 y 32–134 35–134
82 Reference Range Values for Pediatric Care
For Newborns
2- to 4-Hour
Analyte Cord Blood Venous Blood
pH 7.25–7.45 7.28–7.44
Pco2 (mm Hg) 28–52 29–57
Hct (%) 38–58 47–67
Hgb (g/L) 1.33–1.97 1.46–2.34
Sodium (mmol/L) 132–144 131–143
Potassium (mmol/L) 2.7–7.9 4.2–6.2
Chloride (mmol/L) 99–115 101–121
Calcium (ionized) (mmol/L) 0.4–1.85 0.97–1.29
84 Reference Range Values for Pediatric Care
BIBLIOGRAPHY
Adeli K, Higgins V, Nieuwesteeg M, et al. Biochemical marker reference values
across pediatric, adult, and geriatric ages: establishment of robust pediatric and
adult reference intervals on the basis of the Canadian Health Measures Survey.
Clin Chem. 2015;61(8):1049–1062
Bailey D, Colantonio D, Kyriakopoulou L, et al. Marked biological variance
in endocrine and biochemical markers in childhood: establishment of pediat-
ric reference intervals using healthy community children from the CALIPER
cohort. Clin Chem. 2013;59(9):1393–1405
Burritt MF, Slockbower JM, Forsman RW, et al. Pediatric reference intervals for
19 biologic variables in healthy children. Mayo Clinic Proc. 1990;65(3):329–336
Colantonio DA, Kyriakopoulou L, Chan MK, et al. Closing the gaps in pedi-
atric laboratory reference intervals: a CALIPER database of 40 biochemical
markers in a healthy and multiethnic population of children. Clin Chem.
2012;58(5):854–868
Gaujoux-Viala C. C-reactive protein versus erythrocyte sedimentation rate in
estimating the 28-joint Disease Activity Score. J Rheumatol. 2013;40(11):
1785–1787
Ghoshal AK, Soldin SJ. Evaluation of the Dade Behring Dimension RxL: inte-
grated chemistry system-pediatric reference ranges. Clin Chim Acta. 2003;
331(1–2):135–146
Reference Range Values 85
GROWTH HORMONES
In children: Spontaneous growth hormone (GH) secretion is pulsatile
and unpredictable throughout the day, with more peaks overnight in
children who have an established diurnal rhythm. Therefore, random
GH values are generally not helpful.
Growth hormone stimulation tests (arginine, insulin-induced
hypoglycemia, levodopa, or clonidine) may be useful, but they are
difficult to perform. There are different stimulated values suggested,
depending somewhat on which assay is used, but commonly it is
thought that GH deficiency can be ruled out with a value of 10 ng/mL
or greater.
88 Reference Range Values for Pediatric Care
Reproduced with permission from Bidlingmaier M, Friedrich N, Emeny RT, et al. Reference intervals
for insulin-like growth factor-1 (IGF-1) from birth to senescence: results from a multicenter study
using a new automated chemiluminescence IGF-1 immunoassay conforming to recent international
recommendations. J Clin Endocrinol Metab. 2014;99(5):1712–1721.
90 Reference Range Values for Pediatric Care
a
All reference ranges are the 2.5–97.5 percentile.
Reproduced with permission from Bidlingmaier M, Friedrich N, Emeny RT, et al. Reference intervals
for insulin-like growth factor-1 (IGF-1) from birth to senescence: results from a multicenter study
using a new automated chemiluminescence IGF-1 immunoassay conforming to recent international
recommendations. J Clin Endocrinol Metab. 2014;99(5):1712–1721.
Reproduced with permission from Soldin OP, Dahlin JR, Gresham EG, King J, Soldin SJ. IMMULITE
2000 age and sex-specific reference intervals for alpha fetoprotein, homocysteine, insulin, insulin-like
growth factor-1, insulin-like growth factor binding protein-3, C-peptide, immunoglobulin E and intact
parathyroid hormone. Clin Biochem. 2008;41(12): 937–942.
Reference Range Values 91
17α-Hydroxyprogesterone (ng/dL)
Age Values
0–<6 mo 25–248
6 mo–<6 y Girl: 3–107
6–<10 y Girl: 6–62 Boy: 7–100
10–<18 y Girl: 15–137
Reproduced with permission from Soldin OP, Sharma H, Husted L, Soldin SJ. Pediatric reference
intervals for aldosterone, 17α-hydroxyprogesterone, dehydroepiandrosterone, testosterone and
25-hydroxy vitamin D3 using tandem mass spectrometry. Clinical Biochem. 2009;42(9):823–827.
Cortisol (mcg/dL)a
Ageb 5:00 to 11:00 am 5:00 to 11:00 pm
0–24 mo 1.0–34.0 1.0–30.0
2–10 y 1.0–33.0 1.0–24.0
11–18 y 1.0–28.0 1.0–22.0
a
Microgram per liter (mcg/L) units from the original source were divided by 10 to convert to
microgram per deciliter (mcg/dL) units used in this table.
b
All en dashes (–) indicate through except, for example, if an age range stops at 24 mo and the next
age range starts at 2 y; the en dash in the former age range indicates up to 24 mo (2 y).
Modified with permission from Soldin SJ, Murthy JN, Agarwalla PK, Oljeifo O, Chea J. P ediatric
reference ranges for creatine kinase, CKMB, Troponin I, iron, and cortisol. Clinical Biochem.
1999;32(1):77–80.
BIBLIOGRAPHY
Growth Hormone Research Society. Consensus guidelines for the diagnosis
and treatment of growth hormone (GH) deficiency in childhood and adoles-
cence: summary statement of the GH Research Society. J Clin Endocrinol Metab.
2000;85(11):3990–3993
92 Reference Range Values for Pediatric Care
For Infants and Toddlers
Hematology Values
HEMATOLOGY AND COAGULATION
Mean
Corpuscular White
Mean Hemoglobin Blood Red Blood
Hemoglobin Hematocrit Corpuscular Concentration Reticulocytes Cells (× Platelets (× Cells (×
Age (g) (%) Volume (fL) (g/dL per RBC) (%) 103/mcL) 10 /mcL)
3
1012/L)
22–25 12.2 (1.6) 38.59 (3.94) 125.10 3.73 247 (59) 3.09 (0.34)
weeks’ (7.84) (2.17)
gestationa
(mean [SD])
26–29 12.91 (1.38) 40.88 (4.40) 118.50 4.08 242 (69) 3.46 (0.41)
weeks’ (7.96) (0.84)
gestationa
(mean [SD])
>30 weeks’ 13.64 (2.21) 43.55 (7.20) 114.38 6.40 232 (87) 3.82 (0.64)
gestationa (9.34) (2.99)
(mean [SD])
1–3 db M: 12.5–16.6 M: 36.4–47.4 M: M: 32.8–36.4 M: 2.2–4.8 M: 7.69– M: M:
F: 12.7–16.4 F: 36.5–47.7 94.0–106.3 F: 31.7–36.3 F: 2.1–3.7 13.12 140–238 3.69–4.75
F: 89.7– F: 7.51– F: 133–255 F: 3.79–4.76
105.4 15.83
4–7 db M: 12.5–16.3 M: 35.9–46.6 M: 87.1–96.5 M: 30.9–33.4 M: 0.4–2.7 M: 6.54– M: M:
F: 12.6–15.3 F: 36.1–44.0 F: 86.5–93.8 F: 30.6–32.3 F: 0.4–2.0 12.32 129–271 3.98–5.08
F: 5.86– F: 95–230 F: 4.05–4.83
12.23
93
94 Reference Range Values for Pediatric Care
MCH (pg/cell)
3–5 26.1–30.7 26.1–30.7
6–15 26.3–31.7 26.3–31.7
>16 27.6–33.3 27.6–33.3
MCHC (g/dL)
3–5 32.4–34.9 32.4–34.9
>6 32.5–35.2 32.5–35.2
Platelets (× 103/mcL)
3–5 187.4–444.6 187.4–444.6
6–9 186.7–400.4 186.7–400.4
10–13 176.9–381.3 176.9–381.3
14–26 138.7–319.6 158.1–361.6
27–79 151.8–324.0 153.2–361.3
MPV (fL)
3–5 6.4–9.5 6.4–9.5
6–11 6.6–9.8 6.6–9.8
>12 7.0–10.3 7.0–10.3
WBCs (× 103/mcL)
3–5 4.4–12.9 4.4–12.9
6–79 3.8–10.4 3.8–10.4
pediatric, adult, and geriatric ages: establishment of robust pediatric and adult reference intervals
on the basis of the Canadian Health Measures Survey. Clin Chem. 2015;61(8):1075–1086.
96 Reference Range Values for Pediatric Care
For Infants and Toddlers
26–29 weeks’ — 8.5 (4.0) — 8.5 (6.0) — 3.0 (2.5) — 4 (3) — 0.5 (1.0) — 21 (67)
gestationa
(mean [SD])
Abbreviations: F, female (girl); M, male (boy); nRBC, nucleated red blood cell.
a
Forestier F, Daffos F, Catherine N, Renard M, Andreux JP. Developmental hematopoiesis in normal human fetal blood. Blood.
1991;77(11):2360–2363.
b
Soldin SJ, Wong EC, Brugnara C, Soldin OP, eds. Pediatric Reference Intervals. 7th ed. Washington, DC: AACC Press; 2011:58.
a
Adeli K, Raizman JE, Chen Y, et al. Complex biological profile of hematologic markers across
pediatric, adult, and geriatric ages: establishment of robust pediatric and adult reference intervals
on the bases of the Canadian Health Measures Survey. Clin Chem. 2015;61(8):1075–1086.
Lymphocyte Subset Countsa in Peripheral Blood
Subsetb N 0 to 3 Months 3 to 6 Months 6 to 12 Months 1 to 2 Years 2 to 6 Years 6 to 12 Years 12 to 18 Years
WBCs 800 10.60 9.20 9.10 8.80 7.10 6.50 6.00
(7.20–18.00) (6.70–14.00) (6.40–13.00) (6.40–12.00) (5.20–11.00) (4.40–9.50) (4.40–8.10)
Lymphocytes 800 5.40 6.30 5.90 5.50 3.60 2.70 2.20
(3.40–7.60) (3.90–9.00) (3.40–9.00) (3.60–8.90) (2.30–5.40) (1.90–3.70) (1.40–3.30)
CD3 699 3.68 3.93 3.93 3.55 2.39 1.82 1.48
(2.50–5.50) (2.50–5.60) (1.90–5.90) (2.10–6.20) (1.40–3.70) (1.20–2.60) (1.00–2.20)
CD19 699 0.73 1.55 1.52 1.31 0.75 0.48 0.30
(0.30–2.00) (0.43–3.00) (0.61–2.60) (0.72–2.60) (0.39–1.40) (0.27–0.86) (0.11–0.57)
CD16/CD56 770 0.42 0.42 0.40 0.36 0.30 0.23 0.19
(0.17–1.10) (0.17–0.83) (0.16–0.95) (0.18–0.92) (0.13–0.72) (0.10–0.48) (0.07–0.48)
CD4 699 2.61 2.85 2.67 2.16 1.38 0.98 0.84
(1.60–4.00) (1.80–4.00) (1.40–4.30) (1.30–3.40) (0.70–2.20) (0.65–1.50) (0.53–1.30)
CD8 699 0.98 1.05 1.04 1.04 0.84 0.68 0.53
(0.56–1.70) (0.59–1.60) (0.50–1.70) (0.62–2.00) (0.49–1.30) (0.37–1.10) (0.33–0.92)
CD4/CD45RA/ 694 2.25 2.23 2.10 1.64 0.96 0.56 0.39
CD62L (1.20–3.60) (1.30–3.60) (1.10–3.60) (0.95–2.80) (0.42–1.50) (0.31–1.00) (0.21–0.75)
CD8/CD45RA/ 696 0.73 0.74 0.70 0.76 0.54 0.41 0.30
CD62L (0.38–1.30) (0.45–1.20) (0.33–1.20) (0.40–1.40) (0.26–0.85) (0.20–0.65) (0.17–0.56)
CD4/CD45RA 694 2.27 2.32 2.21 1.65 0.98 0.57 0.40
(1.20–3.70) (1.30–3.70) (1.10–3.70) (1.00–2.90) (0.43–1.50) (0.32–1.00) (0.23–0.77)
99
100 Reference Range Values for Pediatric Care
Lymphocyte Subset Countsa in Peripheral Blood (continued)
Subsetb N 0 to 3 Months 3 to 6 Months 6 to 12 Months 1 to 2 Years 2 to 6 Years 6 to 12 Years 12 to 18 Years
CD4/HLA-DR 694 0.10 0.15 0.12 0.13 0.09 0.07 0.06
(0.04–0.18) (0.06–0.28) (0.05–0.26) (0.07–0.28) (0.05–0.18) (0.04–0.12) (0.03–0.10)
CD8/HLA-DR 697 0.05 0.08 0.09 0.18 0.14 0.09 0.07
(0.02–0.16) (0.03–0.17) (0.04–0.29) (0.06–0.60) (0.07–0.42) (0.04–0.27) (0.03–0.18)
CD4/CD38 694 2.54 2.77 2.55 2.02 1.21 0.75 0.57
(0.16–3.90) (1.60–4.00) (1.20–4.10) (1.20–3.30) (0.59–2.00) (0.48–1.20) (0.33–1.00)
CD8/CD38 697 0.93 0.94 0.93 0.95 0.67 0.48 0.31
(0.55–1.60) (0.53–1.50) (0.45–1.60) (0.57–1.90) (0.39–1.10) (0.24–0.74) (0.16–5.70)
CD4/CD28 695 2.56 2.65 2.58 2.12 1.33 0.94 0.79
(1.60–3.80) (1.60–4.00) (1.20–4.20) (1.30–3.40) (0.69–2.00) (0.63–1.50) (0.49–1.20)
CD8/CD28 696 0.71 0.73 0.67 0.72 0.50 0.40 0.29
(0.35–1.30) (0.35–1.20) (0.28–1.10) (0.40–1.30) (0.28–0.87) (0.21–0.70) (0.16–0.52)
CD4/CD95 695 0.29 0.41 0.51 0.50 0.42 0.36 0.40
(0.16–0.58) (0.23–0.62) (0.29–0.82) (0.27–0.91) (0.27–0.65) (0.25–0.62) (0.25–0.66)
COAGULATION VALUES
Age-Specific Coagulation Valuesa—Healthy Preterm Infants
(30–36 Weeks)
Common
Coagulation Day 1 After Day 5 After Day 30 Day 90 Day 180
Tests Birth Birth After Birth After Birth After Birth
PT (s) 13.00 (1.43) 12.40 (1.46) 11.80 (1.25) 11.90 (1.15) 12.30 (0.79)
aPTT (s) 42.90 (5.80) 42.60 (8.62) 40.40 (7.42) 37.10 (6.52) 35.50 (3.71)
Thrombin 23.50 (2.38) 23.10 (3.07) 24.30 (2.44) 25.10 (2.32) 25.50 (2.86)
time (s)
Factor I 2.83 (0.58) 3.12 (0.75) 2.70 (0.54) 2.43 (0.68) 2.51 (0.68)
(fibrinogen)
(g/L)
Factor II 0.48 (0.11) 0.63 (0.15) 0.68 (0.17) 0.75 (0.15) 0.88 (0.14)
(prothrom
bin) (U/mL)
Factor V 0.72 (0.18) 0.95 (0.25) 0.98 (0.18) 0.90 (0.21) 0.91 (0.18)
(U/mL)
Factor VII 0.66 (0.19) 0.89 (0.27) 0.90 (0.24) 0.91 (0.26) 0.87 (0.20)
(U/mL)
Factor VIII 1.00 (0.39) 0.88 (0.33) 0.91 (0.33) 0.79 (0.23) 0.73 (0.18)
(U/mL)
vWF (U/mL) 1.53 (0.67) 1.40 (0.57) 1.28 (0.59) 1.18 (0.44) 1.07 (0.45)
Factor IX 0.53 (0.19) 0.53 (0.19) 0.51 (0.15) 0.67 (0.23) 0.86 (0.25)
(U/mL)
Factor X 0.40 (0.14) 0.49 (0.15) 0.59 (0.14) 0.71 (0.18) 0.78 (0.20)
(U/mL)
Factor XI 0.38 (0.14) 0.55 (0.16) 0.53 (0.13) 0.69 (0.14) 0.86 (0.24)
(U/mL)
Factor XII 0.53 (0.20) 0.47 (0.18) 0.49 (0.16) 0.67 (0.21) 0.77 (0.19)
(U/mL)
PK (U/mL) 0.37 (0.16) 0.48 (0.14) 0.57 (0.17) 0.73 (0.16) 0.86 (0.15)
HMWK 0.54 (0.24) 0.74 (0.28) 0.77 (0.22) 0.82 (0.32) 0.82 (0.23)
(U/mL)
Factor XIII A 0.79 (0.26) 0.94 (0.25) 0.93 (0.27) 1.04 (0.34) 1.04 (0.29)
subunit
(U/mL)
106 Reference Range Values for Pediatric Care
Common
Coagulation Day 1 After Day 5 After Day 30 Day 90 Day 180
Tests Birth Birth After Birth After Birth After Birth
Factor XIII B 0.76 (0.23) 1.06 (0.37) 1.11 (0.36) 1.16 (0.34) 1.10 (0.30)
subunit
(U/mL)
Coagulation Inhibitor Tests
ATIII (U/mL) 0.63 (0.12) 0.67 (0.13) 0.78 (0.15) 0.97 (0.12) 1.04 (0.10)
AMG (U/mL) 1.39 (0.22) 1.48 (0.25) 1.50 (0.22) 1.76 (0.25) 1.91 (0.21)
α2PI (U/mL) 0.85 (0.15) 1.00 (0.15) 1.00 (0.12) 1.08 (0.16) 1.11 (0.14)
C1 INH 0.72 (0.18) 0.90 (0.15) 0.89 (0.21) 1.15 (0.22) 1.41 (0.26)
(U/mL)
AAT (U/mL) 0.93 (0.22) 0.89 (0.20) 0.62 (0.13) 0.72 (0.15) 0.77 (0.15)
Protein C 0.35 (0.09) 0.42 (0.11) 0.43 (0.11) 0.54 (0.13) 0.59 (0.11)
(U/mL)
Protein S 0.36 (0.12) 0.50 (0.14) 0.63 (0.15) 0.86 (0.16) 0.87 (0.16)
(U/mL)
Tests of Fibrinolysis
Plasmino 1.95 (0.35) 2.17 (0.38) 1.98 (0.36) 2.48 (0.37) 3.01 (0.40)
gen (U/mL)
Common Coagulation 1 to 6 to 11 to
Tests 5 Years 10 Years 16 Years Adult
PT (s) 11.0 11.1 11.2 12.0
(10.6–11.4) (10.1–12.1) (10.2–12.0) (11.0–14.0)
INR 1.00 1.01 1.02 1.10
(0.96–1.04) (0.91–1.11) (0.93–1.10) (1.00–1.30)
aPTT (s)b 30 (24–36) 31 (26–36) 32 (26–37) 33 (27–40)
Factor I (fibrinogen) (g/L) 2.76 2.79 3.00 2.78
(1.70–4.05) (1.57–4.0) (1.54–4.48) (1.56–4.00)
Common Coagulation 1 to 6 to 11 to
Tests 5 Years 10 Years 16 Years Adult
Coagulation Inhibitor Tests
ATIII (U/mL) 1.11 1.11 1.05 1.00
(0.82–1.39) (0.90–1.31) (0.77–1.32) (0.74–1.26)
AMG (U/mL) 1.69 1.69 1.56 0.86
(1.14–2.23) (1.28–2.09) (0.98–2.12) (0.52–1.20)
C1 INH (U/mL) 1.35 1.14 1.03 1.00
(0.85–1.83) (0.88–1.54) (0.68–1.50) (0.71–1.31)
AAT (U/mL) 0.93 1.00 1.01 0.93
(0.39–1.47) (0.69–1.30) (0.65–1.37) (0.55–1.30)
Heparin cofactor II (U/mL) 0.88 0.86 0.91 1.08
(0.48–1.28) (0.40–1.32) (0.53–1.29) (0.66–1.26)
Protein C (U/mL) 0.66 0.69 0.83 0.96
(0.40–0.92) (0.45–0.93) (0.55–1.11) (0.64–1.28)
Protein S (total) (U/mL) 0.86 0.78 0.72 0.81
(0.54–1.18) (0.41–1.14) (0.52–0.92) (0.60–1.13)
Protein S (free) (U/mL) 0.45 0.42 0.38 0.45
(0.21–0.69) (0.22–0.62) (0.26–0.55) (0.27–0.61)
Tests of Fibrinolysis
Plasminogen (U/mL) 0.98 0.92 0.86 0.99
(0.78–1.18) (0.75–1.08) (0.68–1.03) (0.70–1.22)
tPA (ng/mL) 2.15 2.42 2.16 4.90
(1.00–4.50) (1.00–5.00) (1.00–4.00) (1.40–8.40)
α2PI (U/mL) 1.05 0.99 0.98 1.02
(0.93–1.17) (0.89–1.10) (0.78–1.18) (0.68–1.36)
PAI (U/mL) 5.42 (1.00– 6.79 (2.00– 6.07 (2.00– 3.60
10.00) 12.00) 10.00) (0–11.00)
20 95th 342
High risk zone percentile
Serum bilirubin (mg/dl)
one
isk z
15 mediate r 257
inter one
High risk z
mol/L
iate
intermed
Low
10 171
0 0
0 12 24 36 48 60 72 84 96 108 120 132 144
Postnatal age (hours)
Nomogram for designation of risk in 2840 well newborns at 36 or more weeks’ gestational age with
birth weight of 2000 g or more or 35 or more weeks’ gestational age and birth weight of 2500 g or
more based on the hour-specific serum bilirubin values.
From Bhutani VK, Johnson L, Sivieri EM. Predictive ability of a predischarge hour-specific serum
bilirubin for subsequent significant hyperbilirubinemia in healthy term and near-term newborns.
Pediatrics. 1999;103(1):6–14.
110 Reference Range Values for Pediatric Care
PHOTOTHERAPY NOMOGRAM
ANION GAP
The anion gap is the difference between the positive ions in the serum
(sodium [Na]) and the negative ions (chloride [CI] and bicarbonate
[HCO3−]). It can be calculated using the following formula (note that
some formulas include potassium [K+]):
Anion Gap = Na − (HCO3− + CI)
Does not apply to EnfaCare, Neocate Infant, NeoSure, or EleCare; Enfamil A.R. and Similac For
a
Spit-Up should not be concentrated >24 kcal/oz. Use a packed scoop measure for Nutramigen
and Pregestimil and an unpacked scoop for all other powders.
Data obtained from Mead Johnson Nutrition Web site. https://www.meadjohnson.com/pediatrics/
us-en/product-information/dilutions-and-preparation. Retrieved May 2018.
116 Reference Range Values for Pediatric Care
A. Infantsa
Human Milk (nutrients per 100 kcal)
Term 20 1.65 5.9 10.8 1.2 2.1 41.9 21.5 0.05 286
Preterm 20 2.1 5.8 9.9 1.6 2.2 37 19 0.18 290
Human Milk and Fortifiers Analysis (nutrients per 100 kcal)
EnfamiI HMF Acidified Liquid + 24 4 6 8.1 2.5 2.5 145 80 1.9 326
preterm human milk (1 packet per
25 mL)b
Similac HMF Concentrated Liquid 24 2.95 5.2 10.4 2.1 3.8 172 98 0.59 385
SimiIac HMF Hydrolyzed Protein 24 3.58 5 10.1 2 3.6 152 85 0.59 450
Concentrated Liquid + preterm
utrient Components
human milk (1 packet per 25 mL)
Similac HMF Powder (1 packet per 23 3 5.3 10.6 2.5 4 175 95 0.55 NA
25 mL)
Preterm Formulas (nutrients per 100 kcal)
117
118 Reference Range Values for Pediatric Care
Enteral Formulas, Including Their Main N
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
A. Infantsa (continued)
Preterm Formulas (nutrients per 100 kcal) (continued)
Similac Special Care 24 High Protein 24 3.3 5.43 10 1.9 3.3 180 100 1.8 280
Similac Special Care 30 30 3 6.61 7.73 1.9 NA 3.3 180 100 1.8
Cow’s Milk–Based Formulas (nutrients per 100 kcal)
Enfamil A.R. 20 2.5 5.1 11.3 1.7 2.8 78 53 1.8 230–240
Enfamil for infants, non-GMO Enfam 20 2 5.3 11.3 1.2 2.8 78 43 1.8 300
il, Enfamil NeuroPro
Generic Organic Milk-Based Infant 20 2.2 5.3 10.6 1.2 2.8 78 43 1.8 NA
Formula
Similac Advance, Similac Pro- 19–20 2.07 5.4 11 1.1 2.8 82 44 1.9 310
utrient Components (continued)
Advance, non-GMO Similac
Similac For Spit-Up 19 2.14 5.4 11 1.4 2.8 88 59 1.9 180
Similac Organic 20 2.07 5.4 10.9 1 2.7 78 42 1.8 225
Similac PM 60/40 20 2.2 5.8 10.2 1 2.1 58 28 0.7 280
Similac Sensitive, Similac Pro- 19 2.1 5.4 10.9 1.4 2.8 88 59 1.9 200
Sensitive
Soy-Based Formulas (nutrients per 100 kcal)
Enfamil ProSobee 20 2.5 5.5 10.2 1.9 3 105 69 1.8 170–200
Gerber Good Start Soy 20 2.5 5.1 11.1 1.7 3 105 63 1.8 180
Similac Soy Isomil 19–20 2.45 5.5 10.4 2 2.8 110 79 1.9 200
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
Abbreviations: GMO, genetically modified organism; HMF, Human Milk Fortifier; NA, not applicable.
Other specialized formula information available from manufacturer or specialized registered dietitian.
a
Data obtained from 2018 pediatric nutritional products guide. Abbott Web site. https://static.abbottnutrition.com/cms-prod/abbottnutrition-2016.com/
img/00874%20-%20ANI2017-09-18%20-%20PEDIATRIC%20NUTRITIONAL%20PRODUCTS%20GUIDE_FINAL_EN_Web_tcm1310-72852.pdf. Published January
2018; Pediatric product guide. Mead Johnson Nutrition Web site. https://www.meadjohnson.com/pediatrics/us-en/sites/hcp-usa/files/mjn-2445_lb6_2018_
wo48_lo_09202018.pdf. Updated September 2018; I want the best formula in organic infant.... Earth’s Best Web site. https://www.earthsbest.com/
en/products/category/formula/infant-formula; Nutricia product reference guide. Nutricia Advanced Medical Nutrition Web site. https://www.nutricia-na.com/
2017-US_PRG.pdf. Updated September 2017; and Product guide, 2018. Nestlé Health Science Web site. https://www.nestlehealthscience.ca/en/resources/
documents/2018%20nhs%20product%20guide.pdf. Published May 2018. Retrieved May 2018.
119
120 Reference Range Values for Pediatric Care
Enteral Formulas, Including Their Main N
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
utrient Components (continued)
PediaSurea 30 30 38 139 16.5 38 1,055 844–845 11 450–490
PediaSure 1.5a 45 59 68 160 16.5 42 1,477 1,055 11 370–390
PediaSure Enterala 30 30 38 139 16.5 33.5 1,055 844 11 335–350
Soy-Based Formulas (nutrients per 1 L)
Bright Beginnings Soy Pediatric 30 29 50 108 16 40 1,042 833 15 515
Drink
“Blenderized” Formulas (nutrients per 1 L)
Compleat Pediatric 30 38 38 136 33 44 1,400 1,080 14 400
Compleat Pediatric Reduced 18 30 20 88 33 44 1,400 1,080 14 310
Calorie
Nourish NA 33 39 48 141 48 42 1,076 469 10
PediaSure Harvest 30 38 38 131 25 60 1,392 1,055 11 353
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
121
122 Reference Range Values for Pediatric Care
Enteral Formulas, Including Their Main N
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
utrient Components (continued)
Ensure Plus 44 55 46 211 40 43 1,266 1,266 19 680
Fibersource HN 36 54 40 164 49 49 960 960 16 480
Glucerna 1.0 30 42 54 96 40 40 705 705 13 355
Isosource 1.5 45 68 59 176 56 60 1,200 1,200 18 650
Jevity 1.0 Cal 32 44 35 155 40 40 910 760 14 300
Jevity 1.2 Cal 36 56 39 169 59 47 1,200 1,200 18 450
Jevity 1.5 Cal 45 64 50 216 61 55 1,200 1,200 18 525
Nutren 1.0c 30 40 34 136 38 41 800 800 14 330–340
Nutren 1.5 45 68 60 176 56 62 1,200 1,200 20 530
Nutren 2.0 60 84 92 216 65 54 1,600 1,480 24 780
Osmolite 1.0 Cal 32 44 35 144 40 40 760 760 14 300
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
123
124 Reference Range Values for Pediatric Care
Enteral Formulas, Including Their Main N
Caloric Osmolality
Concentration Protein Fat Carbohydrates Sodium Potassium Calcium Phosphorous Iron (mOsm/kg
(kcal/oz) (g) (g) (g) (mEq) (mEq) (mg) (mg) (mg) H2O)
utrient Components (continued)
Abbreviations: DRI, dietary reference intake; NA, not applicable.
a
Volume to meet 100% of the DRI for micronutrients varies by product. Consult the manufacturer information to ensure a nutritionally
complete regimen.
b
Other specialized formula information available from manufacturer or specialized registered dietitian.
c
Also available with fiber.
Data obtained from Product category: adult. Abbott Web site. https://static.abbottnutrition.com/cms-prod/abbottnutrition-2016. com/img/Adult.
pdf. Updated August 3, 2017; Liquid Hope. Functional Formularies Web site. https://www.functionalformularies.com/media/wysiwyg/Phase_K_
LH_SpecSheet_11x17_GRAMS_2.pdf; Compare formulas. Kate Farms Web site. https://www.katefarms.com/compare-formulas; and Product guide,
2018. Nestlé Health Science Web site. https://www.nestlehealthscience.ca/en/resources/documents/2018%20nhs%20product%20guide.pdf.
Published May 2018. Retrieved May 2018.
Nutrition and Formula Information 125
From Holliday MA, Segar WE. The maintenance need for water in parenteral fluid therapy. Pediatrics.
1957;19(5):823–832.
Data obtained from Morton Plain Table Salt nutritional facts. Morton Salt Web site. https://www.
mortonsalt.com/article/mortonplain-table-salt-nutritional-facts and Morton Lite Salt Mixture
nutritional facts. Morton Salt Web site. https://www.mortonsalt.com/article/morton-lite-salt-
mixture-nutritional-facts. Retrieved May 2018.
126 Reference Range Values for Pediatric Care
Reproduced with permission from Texas Children’s Hospital Pediatric Nutrition Reference Guide. 11th
ed. Houston, TX: Texas Children’s Hospital; 2016:19.
Daily Requirements DRIs for Age: Macronutrients and M
Infants Infants Children Children Males Males Females Females Pregnancy Lactation
0–6 mo 7–12 mo 1–3 y 4–8 y 9–13 y 14–18 y 9–13 y 14–18 y ≤18 y ≤18 y
Carbohydrate (g/day) 60a 95a 130 130 130 130 130 130 175 210
Total fiber (g/day) ND ND 19a 25a 31a 38a 26a 26a 28a 29a
Fat (g/day) 31a 30a ND ND ND ND ND ND ND ND
n-6 Polyunsaturated fatty acids 4.4a 4.6a 7a 10a 12a 16a 10a 11a 13a 13a
(g/day) (linoleic acid)
n-3 Polyunsaturated fatty acids 0.5a 0.5a 0.7a 0.9a 1.2a 1.6a 1.0a 1.1a 1.4a 1.3a
(g/day) (α-linolenic acid)
Vitamin A (μg/day)b 400a 500a 300 400 600 900 600 700 750 1,200
Vitamin C (mg/day) 40 a
50a 15 25 45 75 45 65 80 115
Vitamin D (IU/day)c,d 400a 400a 600 600 600 600 600 600 600 600
Vitamin E (mg/day)e 4a 5a 6 7 11 15 11 15 15 19
Vitamin K (μg/day) 2.0a 2.5a 30a 55a 60a 75a 60a 75a 75a 75a
Thiamin (mg/day) 0.2a 0.3a 0.5 0.6 0.9 1.2 0.9 1.0 1.4 1.4
Riboflavin (mg/day) 0.3a 0.4a 0.5 0.6 0.9 1.3 0.9 1.0 1.4 1.6
icronutrients
Folate (μg/day)g 65a 80a 150 200 300 400 300 400h 600i 500
Vitamin B12 (μg/day) 0.4a 0.5a 0.9 1.2 1.8 2.4 1.8 2.4 2.6 2.8
Pantothenic acid (mg/day) 1.7 a
1.8a 2a 3a 4a 5a 4a 5a 6a 7a
Biotin (μg/day) 5a 6a 8a 12a 20a 25a 20a 25a 30a 35a
Calcium (mg/day) 200 a
260 a
700 a
1,000 a
1,300 a
1,300 1,300 1,300 1,300 1,300
Cholinej (mg/day) 125a 150a 200a 250a 375a 550a 375a 400a 450a 550a
127
128 Reference Range Values for Pediatric Care
Daily Requirements DRIs for Age: Macronutrients and M
Infants Infants Children Children Males Males Females Females Pregnancy Lactation
0–6 mo 7–12 mo 1–3 y 4–8 y 9–13 y 14–18 y 9–13 y 14–18 y ≤18 y ≤18 y
Chromium (μg/day) 0.2a 5.5a 11a 15a 25a 35a 21a 24a 29a 44a
Copper (μg/day) 200a 220a 340 440 700 890 700 890 1,000 1,300
Fluoride (mg/day) 0.01a 0.5a 0.7a 1a 2a 3a 3a 3a 3a 3a
Iodine (μg/day) 110a 130a 90 90 120 150 120 150 220 290
Iron (mg/day) 0.27a 11 7 10 8 11 8 15 27 10
Magnesium (mg/day) 30a 75a 80 130 240 410 240 360 400 360
Manganese (mg/day) 0.003a 0.6a 1.2a 1.5a 1.9a 2.2a 1.6a 1.6a 2.0a 2.6a
Molybdenum (μg/day) 2a 3a 17 22 34 43 34 43 50 50
Phosphorus (mg/day) 100 a
275a 460 500 1,250 1,250 1,250 1,250 1,250 1,250
Selenium (μg/day) 15a 20a 20 30 40 55 40 55 60 70
Zinc (mg/day) 2a 3 3 5 8 11 8 9 12 13
Potassium (g/day) 0.4a 0.7a 3.0a 3.8a 4.5a 4.7a 4.5a 4.7a 4.7a 5.1a
Sodium (g/day) 0.12a 0.37a 1.0a 1.2a 1.5a 1.5a 1.5a 1.5a 1.5a 1.5a
Chloride (g/day) 0.18a 0.57a 1.5a 1.9a 2.3a 2.3a 2.3a 2.3a 2.3a 2.3a
icronutrients (continued)
Note: This data (taken from the Dietary Reference Intake reports; see www.nas.edu) presents recommended dietary allowances (RDAs) in bold
type, and adequate intakes (AIs) are in ordinary type followed by the symbol (a). ND indicates not determined.
Infants Infants Children Children Males Males Females Females Pregnancy Lactation
0–6 mo 7–12 mo 1–3 y 4–8 y 9–13 y 14–18 y 9–13 y 14–18 y ≤18 y ≤18 y
a
RDAs and AIs may both be used as goals for individual intake. RDAs are set to meet the needs of almost all (97%–98%) individuals in a group.
For healthy breastfed infants, the AI is the mean intake. The AI for other life stage and gender groups is believed to cover needs of all individuals
in the group, but lack of data or uncertainty in the data prevents being able to specify with confidence the percentage of individuals covered by
this intake.
b
As retinol activity equivalents (RAEs). 1 RAE = 1 μg retinol, 12 μg β-carotene, 24 μg α-carotene, or 24 μg β-cryptoxanthin in foods. The RAE for
dietary provitamin A carotenoids is twofold greater than retinol equivalents (REs), whereas the RAE for preformed vitamin A is the same as RE.
c
As cholecalciferol. 1 μg cholecalciferol = 40 IU vitamin D.
d
In the absence of adequate exposure to sunlight.
e
As α-tocopherol. α-Tocopherol includes RRR-α-tocopherol, the only form of α-tocopherol that occurs naturally in foods, and the
2R-stereoisomeric forms of α-tocopherol (RRR-, RSR-, RRS-, and RSS-α-tocopherol) that occur in fortified foods and supplements. It does not
include the 2S-stereoisomeric forms of α-tocopherol (SRR-, SSR-, SRS-, and SSS-α-tocopherol), also found in fortified foods and supplements.
f
As niacin equivalents (NEs). 1 mg of niacin = 60 mg of tryptophan; 0–6 mo = preformed niacin (not NEs).
g
As dietary folate equivalents (DFEs). 1 DFE = 1 μg food folate = 0.6 μg of folic acid from fortified food or as a supplement consumed with food =
0.5 μg of a supplement taken on an empty stomach.
h
In view of evidence linking folate intake with neural tube defects in the fetus, it is recommended that all women capable of becoming pregnant
consume 400 μg from supplements or fortified foods in addition to intake of food folate from the diet.
i
It is assumed that women will continue consuming 400 μg from supplements or fortified food until their pregnancy is confirmed and they enter
prenatal care, which ordinarily occurs after the end of the periconceptional period—the critical time for formation of the neural tube.
j
Although AIs have been set for choline, there are few data to assess whether a dietary supply of choline is needed at all stages of the life cycle,
and it may be that the choline requirement can be met by endogenous synthesis at some of these stages.
Copyright © 2018 National Academies of Sciences. All rights reserved.
Nutrition and Formula Information
129
130 Reference Range Values for Pediatric Care
From American Academy of Pediatric Dentistry Liaison With Other Groups Committee, American
Academy of Pediatric Dentistry Council on Clinical Affairs. Guideline on fluoride therapy. Pediatr Dent.
2008–2009;30(7)(suppl):121–124. Reproduced with permission. Copyright © 2008–2009 American
Academy of Pediatric Dentistry.
9. Umbilical Vein and Artery
Catheterization Measurements
USING BIRTH WEIGHT TO MEASURE CATHETER LENGTH
Before placing an umbilical vein or artery catheter into a newborn as
an elective procedure, you can use the following regression formula
to determine the catheter length in centimeters using birth weight:
Umbilical Artery Catheter Length (cm) = [3 × Birth Weight (kg)] + 9 cm
Umbilical Vein Catheter Length (cm) = [Umbilical Artery Catheter
Length (cm) + 1 cm]/2
You can use this formula to approximate the length necessary for
placement of a high-lying line between the vertebral levels T6 and T10
for umbilical artery lines and for umbilical vein lines above the level of
the diaphragm in the inferior vena cava. Correct placement into small
for gestational age and large for gestational age babies may vary
because the formula is only an approximation. Radiographic confir-
mation of line positioning is important to prevent complications.
132 Reference Range Values for Pediatric Care
30
25
20
15
Internal Catheter Length, cm
10
15
10
0
1000 2000 3000 4000 5000 6000
Birth Weight, g
Umbilical catheters (umbilical artery catheter tip inserted between T-6 and T-10; umbilical vein
catheter tip inserted above diaphragm in interior vena cava near or in right atrium). Modified
estimating equations utilizing birth weight (BW) are as follows: umbilical artery length = 2.5*BW +
9.7 (top graph) and umbilical vein length = 1.5*BW + 5.6 (bottom graph), where BW is measured
in kilograms and lengths in centimeters.
From Shukla H, Ferrara A. Rapid estimation of insertional length of umbilical catheters in new
borns. Am J Dis Child. 1986;140(8):786–788. Copyright © 1986 American Medical Association.
All rights reserved.
Umbilical Vein and Artery C
atheterization Measurements 133
28
26
24
lv e
Va
Umbilical Artery Catheter (cm)
22
c
rti
Ao
20
18
m
16
ag
hr
ap
14
Di
12
orta
10 ofA
n
t io
8 ca
ur
Bif
6
4
8 10 12 14 16 18
Shoulder-Umbilical
Length (cm)
134 Reference Range Values for Pediatric Care
13
12
Umbilical Vein Catheter (cm)
11
10 m
triu
f tA
9
Le
ragm
8
ph
Dia
7
4
8 9 10 11 12 13 14 15 16 17
Reproduced with permission from Kempley ST, Moreira JW, Petrone FL. Endotracheal tube length for
neonatal intubation. Resuscitation. 2008;77(3):369–373.
136 Reference Range Values for Pediatric Care
PEDIATRIC
The following tube sizes and depths are based on internal diame-
ter (ID) of the endotracheal tube and apply to children 2 to 10 years
of age.
Tube Size
Uncuffed Endotracheal Tube Size (mm ID) = [Age (y)/4] + 4
Cuffed Endotracheal Tube Size (mm ID) = [Age (y)/4] + 3.5
BIBLIOGRAPHY
de Caen AR, Berg MD, Chameides L, et al. Part 12: Pediatric Advanced Life
Support; 2015 American Heart Association guidelines update for cardiopul
monary resuscitation and emergency cardiovascular care. Circulation. 2015;
132(18)(suppl 2):S526–S542
11. Doses and Levels of Common
Medications Requiring
Therapeutic Drug Monitoring
ANTIBIOTICS ........................................................................................................................... 138
AMIKACIN....................................................................................................................... 138
GENTAMICIN................................................................................................................. 140
TOBRAMYCIN................................................................................................................ 142
VANCOMYCIN............................................................................................................... 144
ANTICONVULSANTS............................................................................................................. 146
FOSPHENYTOIN........................................................................................................... 146
PHENOBARBITAL......................................................................................................... 150
MISCELLANEOUS.................................................................................................................. 153
DIGOXIN.......................................................................................................................... 153
ENOXAPARIN................................................................................................................. 155
WARFARIN...................................................................................................................... 156
138 Reference Range Values for Pediatric Care
ANTIBIOTICS
Amikacin
NEONATAL DOSING
CONVENTIONAL DOSING
• 5 to 7.5 mg/kg per dose every 8 hours
HIGH-DOSE, EXTENDED INTERVAL DOSING (IN PATIENTS WITH NORMAL
RENAL FUNCTION)
• Non–cystic fibrosis: 15 to 20 mg/kg/d every 24 hours
• Cystic fibrosis: 30 mg/kg/d every 24 hours
DOSE ADJUSTMENT REQUIRED FOR RENAL IMPAIRMENT
• Yes
MONITORING
TIMING OF LEVELS
• Peak
—— Conventional dosing: 30 minutes after end of 30-minute infusion
—— High-dose, extended interval dosing: 1 hour after 1-hour
infusion
• Trough: 0 to 30 minutes before next dose
GOAL LEVELS
• Peak
—— Conventional dosing
20 to 25 mcg/mL (neonates)
20 to 30 mcg/mL (infants, children, and adolescents)
—— High-dose, extended interval dosing
Non–cystic fibrosis: 20 to 25 mcg/mL (serious infections) or
15 to 20 mcg/mL (urinary tract infection)
Cystic fibrosis: 80 to 120 mcg/mL (Pseudomonas organisms)
or 25 to 40 mcg/mL (all other organisms)
• Trough
—— Conventional dosing
Less than 5 mcg/mL (neonates)
4 to 10 mcg/mL (infants, children, and adolescents)
—— High-dose, extended interval dosing: less than 8 mcg/mL
140 Reference Range Values for Pediatric Care
Gentamicin
NEONATAL DOSING
CONVENTIONAL DOSING
• Infants and children younger than 5 years: 2.5 mg/kg per dose
every 8 hours
• Children older than 5 years: 2 to 2.5 mg/kg per dose every 8 hours
• For gram-positive synergy: 1 to 2 mg/kg per dose every 8 hours
HIGH-DOSE, EXTENDED INTERVAL DOSING (IN PATIENTS WITH NORMAL
RENAL FUNCTION)
• Non–cystic fibrosis
—— 3 months to younger than 2 years: 9.5 mg/kg/d every 24 hours
—— 2 to 8 years: 8.5 mg/kg/d every 24 hours
—— Older than 8 years: 7 mg/kg/d every 24 hours
• Cystic fibrosis: 10 to 12 mg/kg/d every 24 hours
DOSE ADJUSTMENT REQUIRED FOR RENAL IMPAIRMENT
• Yes
MONITORING
Tobramycin
NEONATAL DOSING
CONVENTIONAL DOSING
• Infants and children younger than 5 years: 2.5 mg/kg per dose
every 8 hours
• Children older than 5 years: 2 to 2.5 mg/kg per dose every 8 hours
HIGH-DOSE, EXTENDED INTERVAL DOSING (IN PATIENTS WITH NORMAL
RENAL FUNCTION)
• Non–cystic fibrosis
—— 3 months to younger than 2 years: 9.5 mg/kg/d every 24 hours
—— 2 to 8 years: 8.5 mg/kg/d every 24 hours
—— Older than 8 years: 7 mg/kg/d every 24 hours
• Cystic fibrosis: 10 to 12 mg/kg/d every 24 hours
DOSE ADJUSTMENT REQUIRED FOR RENAL IMPAIRMENT
• Yes
MONITORING
Vancomycin
NEONATAL DOSING
• Meningitis: 15 mg/kg per dose
• Bacteremia: 10 mg/kg per dose
Dosing Table for Intravenous Administration
Weight (kg) Postnatal Age (d) Interval (h)
<1.2 ≤28 18–24
0–6 12–18
1.2–2
≥7 8–12
0–6 8–12
>2
≥7 6–8
CONVENTIONAL DOSING
• 15 to 20 mg/kg per dose every 6 to 8 hours (Consider every
6 hours for patients >2 months who do not have a history of
cardiac abnormalities.)
DOSE ADJUSTMENT REQUIRED FOR RENAL IMPAIRMENT
• Yes
MONITORING
ANTICONVULSANTS
In the Anticonvulsants section, EEG indicates electroencephalo-
graphic; IM, intramuscular(ly); IV, intravenous(ly).
Fosphenytoin
Note: All dosing is expressed in phenytoin equivalents (PE). 1 mg of
fosphenytoin PE = 1 mg of phenytoin.
NEONATAL DOSING
LOADING DOSE
• 15 to 20 mg PE/kg IM or IV infusion over at least 10 minutes
MAINTENANCE DOSE
• 4 to 8 mg PE/kg/d IM or IV infusion at a rate of 1 to 2 mg
PE/kg/min every 24 hours. Begin maintenance 24 hours after
loading dose.
LOADING DOSE
• Status epilepticus: 15 to 20 mg PE/kg IV
• Non-emergent: 10 to 20 mg PE/kg IV or IM
MAINTENANCE DOSE
• 4 to 6 mg PE/kg/d IV in 2 to 3 divided doses
MONITORING
TIMING OF LEVELS
• Trough: before steady-state dose
GOAL LEVELS
• Total
—— First week after birth: 6 to 15 mcg/mL
—— After 7 days of birth: 10 to 20 mcg/mL
• Free (unbound): 1 to 2 mcg/mL
148 Reference Range Values for Pediatric Care
Levetiracetam (Keppra)
NEONATAL DOSING
Note: Limited data available; dose not established.
• Intravenous: 10 mg/kg/d divided twice daily; increase dosage by
10 mg/kg over 3 days to 30 mg/kg/d. Additional increases up to
45 to 60 mg/kg/d have been used with persistent seizure activity or
clinical EEG findings. For treatment of status epilepticus, loading
doses of 20 to 30 mg/kg per dose have been used by some centers.
• Oral: Initial, 10 mg/kg/d in 1 to 2 divided doses; increase daily by
10 mg/kg to 30 mg/kg/d (maximum reported dosage: 60 mg/kg/d).
STATUS EPILEPTICUS
Note: Limited data available; dose not established.
• Loading dose of 60 mg/kg per dose (maximum dose: 4,500 mg)
given IV, followed by IV or oral maintenance dosing determined
by clinical response; reported IV maintenance dosage is 30 to
55 mg/kg/d divided twice daily; some institutions may choose to
administer lower loading doses.
MONITORING
TIMING OF CONCENTRATIONS
• Trough: are not routinely measured but may be useful in accessing
magnitude of dosing adjustments, drug adherence, or both
GOAL CONCENTRATIONS
• Therapeutic: none established
150 Reference Range Values for Pediatric Care
Phenobarbital
NEONATAL DOSING
ANTICONVULSANT
• Loading dose: 15 to 20 mg/kg IV, given slowly over 10 to
15 minutes.
• Refractory seizures: Additional doses of 5 to 10 mg/kg, up to
a total of 40 mg/kg.
• Maintenance dose: 3 to 4 mg/kg/d, beginning 12 to 24 hours
after the loading dose. Increase to 5 mg/kg/d if needed (usually
by second week of therapy).
• Frequency and route: Every 24 hours. An IV infusion at a rate
of no faster than 1 mg/kg/min (most rapid control of seizures),
IM, orally, or rectally.
NEONATAL ABSTINENCE SYNDROME
• Loading dose: 16 mg/kg IV or orally on day 1.
• Maintenance dose: 1 to 4 mg/kg per dose orally every 12 hours.
• Weaning that is based on abstinence scoring can be achieved by
decreasing dose 20% every other day.
LOADING DOSE
• 15 to 20 mg/kg (maximum: 1,000 mg per dose)
Maintenance Dose
Age Maintenance Dosing
Infant 5–6 mg/kg/d divided in 1–2 doses
Children 1–5 y 6–8 mg/kg/d divided in 1–2 doses
Children 5–12 y 4–6 mg/kg/d divided in 1–2 doses
Adolescents >12 y 1–3 mg/kg/d divided in 1–2 doses
MONITORING
MONITORING
MISCELLANEOUS
In the Miscellaneous section, INR indicates international normalized
ratio; SQ, subcutaneous(ly).
Digoxin
Neonatal, Infant, Child, and Adolescent Dosing
Total Digitalizing Dose (mcg/kg) Maintenance
Maintenance Oral (mcg/
Patient Age Loading IVa Loading Orala IV (mcg/kg/d)b kg/d)b
Preterm 15–25 20–30 4–6 5–7.5
neonate
Term neonate 20–30 25–35 5–8 8–10
1–24 mo 30–50 35–60 9–15 10–15
2–5 y 25–35 30–45 6–9 8–10
5–10 y 15–30 20–35 4–8 5–10
>10 y 8–12 10–15 2–3 2.5–5
8-hour intervals. The first dose is 50% of the total. The second and third doses are 25% of the total dose.
Divide every 12 h.
b
MONITORING
TIMING OF LEVELS
• Loading dose: 12 to 24 hours after loading dose is completed.
• Maintenance dose: Draw trough levels just before next dose
(minimum 6–8 hours after the previous dose).
GOAL LEVELS
• Heart failure: 0.5–0.9 ng/mL
• Toxic: greater than 2 ng/mL
Doses and Levels of Common Medications Requiring T
herapeutic Drug Monitoring 155
Enoxaparin
PROPHYLAXIS
• Neonates and infants younger than 2 months: 0.75 mg/kg per dose
SQ every 12 hours
• Infants 2 months and older, children, and adolescents: 0.5 mg/kg
per dose SQ every 12 hours
TREATMENT
• Neonates and infants younger than 2 months: 1.5 to 2 mg/kg per
dose SQ every 12 hours
• Infants 2 months and older, children, and adolescents: 1 mg/kg per
dose SQ every 12 hours
MONITORING
Warfarin
MONITORING
RESOURCES
Glauser T, Shinnar S, Gloss D, et al. Evidence-based guideline: treatment of
convulsive status epilepticus in children and adults; report of the Guideline
Committee of the American Epilepsy Society. Epilepsy Curr. 2016;16(1):48–61
Lexicomp Online. Hudson, OH: Lexicomp Inc; 2013. http://online.lexi.com.
Accessed February 6, 2019
Mark LF, Solomon A, Northington FJ, Lee CK. Gentamicin pharmacoki-
netics in neonates undergoing therapeutic hypothermia. Ther Drug Monit.
2013;35(2):217–222
12. Appendixes
ACETAMINOPHEN TOXICITY NOMOGRAM................................................................... 158
500 500
200 200
100 100
Po
ssi
50 ble 50
he
pa Probable hepatic toxicity
tic
tox
20 icit 20
y
No hepatic toxicity
10 10
5 25% 5
2 2
4 8 12 16 20 24
Hours after ingestion
Modified from Rumack BH, Matthew H. Acetaminophen poisoning and toxicity. Pediatrics.
1975;55(6):871–876.
Appendixes 159
RABIES GUIDELINES
Rabies Postexposure Prophylaxis Schedule—United States, 2010
Vaccination
Status Intervention Regimena
Not previously Wound All PEP should begin with immediate thorough
vaccinated cleansing cleansing of all wounds with soap and water. If avail
able, a virucidal agent (eg, povidone-iodine solution)
should be used to irrigate the wounds.
HRIG Administer 20 IU per kilogram of body weight. If ana
tomically feasible, the full dose should be infiltrated
around and into the wound(s), and any remaining
volume should be administered at an anatomical
site (IM) distant from vaccine administration. Also,
HRIG should not be administered in the same syringe
as vaccine. Because rabies immunoglobulin might
partially suppress active production of rabies virus
antibody, no more than the recommended dose
should be administered.
Vaccine HDCV or PCECV at 1.0 mL IM (deltoid areab), 1 each
on days 0,c,d 3d, 7d, and 14d
Previously Wound All PEP should begin with immediate thorough
vaccinatede cleansing cleansing of all wounds with soap and water. If
available, a virucidal agent such as povidone-iodine
solution should be used to irrigate the wounds.
HRIG HRIG should not be administered.
Vaccine HDCV or PCECV at 1.0 mL IM (deltoid areab), 1 each
on days 0c,d and 3d
Abbreviations: HDCV, human diploid cell vaccine; HRIG, human rabies immunoglobulin; IM, intramuscularly;
PCECV, purified chick embryo cell vaccine; PEP, postexposure prophylaxis; RVA, rabies vaccine adsorbed.
a
These regimens are applicable for people in all age-groups, including children.
b
The deltoid area is the only acceptable site of vaccination for adults and older children. For younger children,
the outer aspect of the thigh may be used. Vaccine should never be administered in the gluteal area.
c
Day 0 is the day dose 1 of vaccine is administered.
d
For people with immunosuppression, rabies PEP should be administered using all 5 doses of vaccine on days
0, 3, 7, 14, and 28.
e
Any person with a history of pre-exposure vaccination with HDCV, PCECV, or RVA; prior PEP with HDCV,
PCECV, or RVA; or previous vaccination with any other type of rabies vaccine and a documented history of
antibody response to the prior vaccination.
From Rupprecht CE, Briggs D, Brown CM, et al; Centers for Disease Control and Prevention. Use of a reduced
(4-dose) vaccine schedule for postexposure prophylaxis to prevent human rabies: recommendations of the
Advisory Committee on Immunization Practices. MMWR Recomm Rep. 2010;59(RR–2):1–9. Erratum in: MMWR
Recomm Rep. 2010;59(16):493.
160 Reference Range Values for Pediatric Care
Recommended Immunization Schedule for
IMMUNIZATION SCHEDULES
Children and Adolescents Aged 18 Years or Younger, UNITED STATES, 2018
The table below shows vaccine acronyms, and brand names for vaccines routinely recommend-
ed for children and adolescents. The use of trade names in this immunization schedule is for
• Consult relevant ACIP statements for detailed recommendations identification purposes only and does not imply endorsement by the ACIP or CDC.
(www.cdc.gov/vaccines/hcp/acip-recs/index.html). Vaccine type Abbreviation Brand(s)
• When a vaccine is not administered at the recommended age, Diphtheria, tetanus, and acellular pertussis vaccine DTaP Daptacel
Infanrix
administer at a subsequent visit.
Diphtheria, tetanus vaccine DT No Trade Name
• Use combination vaccines instead of separate injections when Haemophilus influenzae type B vaccine Hib (PRP-T) ActHIB
appropriate. Hib (PRP-OMP)
Hiberix
PedvaxHIB
• Report clinically significant adverse events to the Vaccine Adverse Hepatitis A vaccine HepA Havrix
Event Reporting System (VAERS) online (www.vaers.hhs.gov) or by Vaqta
Hepatitis B vaccine HepB Engerix-B
telephone (800-822-7967). Recombivax HB
• Report suspected cases of reportable vaccine-preventable diseases Human papillomavirus vaccine HPV Gardasil 9
to your state or local health department. Influenza vaccine (inactivated) IIV Multiple
• For information about precautions and contraindications, see www. Measles, mumps, and rubella vaccine MMR M-M-R II
Meningococcal serogroups A, C, W, Y vaccine MenACWY-D Menactra
cdc.gov/vaccines/hcp/acip-recs/general-recs/contraindications.html. MenACWY-CRM Menveo
Meningococcal serogroup B vaccine MenB-4C Bexsero
MenB-FHbp Trumenba
Approved by the Pneumococcal 13-valent conjugate vaccine PCV13 Prevnar 13
Pneumococcal 23-valent polysaccharide vaccine PPSV23 Pneumovax
Advisory Committee on Immunization Practices Poliovirus vaccine (inactivated) IPV IPOL
(www.cdc.gov/vaccines/acip) Rotavirus vaccines RV1 Rotarix
RV5 RotaTeq
American Academy of Pediatrics Tetanus, diphtheria, and acellular pertussis vaccine Tdap Adacel
(www.aap.org) Boostrix
Tetanus and diphtheria vaccine Td Tenivac
No Trade Name
American Academy of Family Physicians Varicella vaccine VAR Varivax
(www.aafp.org)
Combination Vaccines
DTaP, hepatitis B and inactivated poliovirus vaccine DTaP-HepB-IPV Pediarix
American College of Obstetricians and Gynecologists
DTaP, inactivated poliovirus and Haemophilus influenzae DTaP-IPV/Hib Pentacel
(www.acog.org) type B vaccine
This schedule includes recommendations in effect as of January 1, 2018. DTaP and inactivated poliovirus vaccine DTaP-IPV Kinrix
Quadracel
Measles, mumps, rubella, and varicella vaccines MMRV ProQuad
Pneumococcal conjugate5
1st dose 2nd dose 3rd dose 4th dose
(PCV13)
Inactivated poliovirus6
1st dose 2nd dose 3rd dose 4th dose
(IPV: <18 yrs)
Measles, mumps, rubella8 (MMR) See footnote 8 1st dose 2nd dose
Meningococcal1 1 (MenACWY-D
See footnote 11 1st dose 2nd dose
>9 mos; MenACWY-CRM ≥2 mos)
See footnote
Human papillomavirus1 4 (HPV) 14
See footnote 12
Meningococcal B1 2
Appendixes
Pneumococcal polysaccharide5
See footnote 5
(PPSV23)
Range of recommended Range of recommended ages Range of recommended ages Range of recommended ages for non-high-risk No recommendation
ages for all children for catch-up immunization for certain high-risk groups groups that may receive vaccine, subject to
individual clinical decision making
NOTE: The above recommendations must be read along with the footnotes of this schedule.
161
162 Reference Range Values for Pediatric Care
FIGURE 2. Catch-up immunization schedule for persons aged 4 months–18 years who start late or who are more than 1 month behind—United States, 2018.
The figure below provides catch-up schedules and minimum intervals between doses for children whose vaccinations have been delayed. A vaccine series does not need to be restarted, regardless of the time that has elapsed between
Hepatitis B1 Birth 4 weeks 8 weeks and at least 16 weeks after first dose.
Minimum age for the final dose is 24 weeks.
6 weeks
Maximum age 4 weeks2
Rotavirus2 for first dose is 4 weeks Maximum age for final dose is 8 months, 0 days.
14 weeks, 6 days
Diphtheria, tetanus, and 6 weeks 4 weeks 4 weeks 6 months 6 months3
acellular pertussis3
4 weeks4
if current age is younger than 12 months and first dose was administered at younger than age 7 months,
4 weeks and at least 1 previous dose was PRP-T (ActHib, Pentacel, Hiberix) or unknown.
if first dose was administered 8 weeks and age 12 through 59 months (as final dose)4
before the 1 birthday.
st
8 weeks (as final dose)
• if current age is younger than 12 months and first dose was administered at age 7 through 11
Haemophilus influenzae 8 weeks (as final dose) months; This dose only necessary for chil-
type b4 6 weeks if first dose was administered at age OR dren age 12 through 59 months
12 through 14 months. who received 3 doses before the 1st
• if current age is 12 through 59 months and first dose was administered before the 1st birthday, and birthday.
No further doses needed if first second dose administered at younger than 15 months;
dose was administered at age 15 OR
months or older.
• if both doses were PRP-OMP (PedvaxHIB; Comvax) and were administered before the 1st birthday.
No further doses needed if previous dose was administered at age 15 months or older.
4 weeks
if first dose administered before the
1st birthday. 4 weeks
if current age is younger than 12 months and previous dose given at <7 months old. 8 weeks (as final dose)
8 weeks (as final dose for healthy
children) 8 weeks (as final dose for healthy children) This dose only necessary for chil-
Pneumococcal dren aged 12 through 59 months
conjugate5 6 weeks if first dose was administered at the if previous dose given between 7-11 months (wait until at least 12 months old);
who received 3 doses before age 12
1 birthday or after.
st
OR months or for children at high risk
No further doses needed if current age is 12 months or older and at least 1 dose was given before age 12 months. who received 3 doses at any age.
for healthy children if first dose was No further doses needed for healthy children if previous dose administered at age 24 months or older.
administered at age 24 months or
older.
4 weeks6 if current age is < 4 years 6 months6 (minimum age 4 years for
Inactivated poliovirus6 6 weeks 4 weeks6
6 months (as final dose) if current age is 4 years or older final dose).
Measles, mumps, rubella8 12 months 4 weeks
Varicella9 12 months 3 months
Hepatitis A10 12 months 6 months
Meningococcal11
(MenACWY-D ≥9 mos; 6 weeks 8 weeks11 See footnote 11 See footnote 11
MenACWY-CRM ≥2 mos)
Children and adolescents age 7 through 18 years
Meningococcal11
Not Applicable 8 weeks11
(MenACWY-D ≥9 mos;
(N/A)
MenACWY-CRM ≥2 mos)
4 weeks
Tetanus, diphtheria; if first dose of DTaP/DT was administered before the 1st birthday. 6 months if first dose of DTaP/DT
tetanus, diphtheria, and 7 years13 4 weeks was administered before the 1st
acellular pertussis13 6 months (as final dose) birthday.
if first dose of DTaP/DT or Tdap/Td was administered at or after the 1st birthday.
Human papillomavirus14 9 years Routine dosing intervals are recommended.14
Hepatitis A10 N/A 6 months
Hepatitis B1 N/A 4 weeks 8 weeks and at least 16 weeks after first dose.
A fourth dose of IPV is indicated if all
6 months6 previous doses were administered
Inactivated poliovirus6 N/A 4 weeks A fourth dose is not necessary if the third dose was administered at age 4 years or older and at least 6 months at <4 years or if the third dose was
after the previous dose. administered <6 months after the
second dose.
Measles, mumps, rubella8 N/A 4 weeks
3 months if younger than age 13
Varicella9 N/A years.
4 weeks if age 13 years or older.
NOTE: The above recommendations must be read along with the footnotes of this schedule.
Figure 3. Vaccines that might be indicated for children and adolescents aged 18 years or younger based on medical indications
HIV infection
CD4+ count†
<15% or ≥15% or
Immunocompromised total CD4 total CD4 Kidney failure, end- CSF leaks/ Asplenia and persistent Chronic
status (excluding HIV cell count of cell count of stage renal disease, on Heart disease, cochlear complement component liver
VACCINE d INDICATION f Pregnancy infection) <200/mm3 ≥200/mm3 hemodialysis chronic lung disease implants deficiencies disease Diabetes
Hepatitis B1
Rotavirus2
SCID*
Diphtheria, tetanus, & acellular pertussis3
(DTaP)
Pneumococcal conjugate5
Inactivated poliovirus6
Influenza7
Varicella9
Hepatitis A1 0
Meningococcal ACWY1 1
Human papillomavirus1 4
Meningococcal B1 2
Pneumococcal polysaccharide5
Appendixes
Recommended for persons with Vaccination is recommended,
Vaccination according to the and additional doses may be
an additional risk factor for which No recommendation Contraindicated Precaution for vaccination
routine schedule recommended the vaccine would be indicated necessary based on medical
condition. See footnotes.
*Severe Combined Immunodeficiency
†
For additional information regarding HIV laboratory parameters and use of live vaccines; see the General Best Practice Guidelines for Immunization “Altered Immunocompetence” at: www.cdc.gov/vaccines/hcp/acip-recs/gener-
al-recs/immunocompetence.html; and Table 4-1 (footnote D) at: www.cdc.gov/vaccines/hcp/acip-recs/general-recs/contraindications.html.
NOTE: The above recommendations must be read along with the footnotes of this schedule.
163
164 Reference Range Values for Pediatric Care
Footnotes — Recommended Immunization Schedule for Children and Adolescents Aged 18 Years or Younger, UNITED STATES, 2018
1. Hepatitis B (HepB) vaccine. (minimum age: birth) • Infants who did not receive a birth dose should Catch-up vaccination:
Birth Dose (Monovalent HepB vaccine only): begin the series as soon as feasible (see Figure 2). • Do not start the series on or after age 15 weeks, 0
• Mother is HBsAg-Negative: 1 dose within 24 • Administration of 4 doses is permitted when a days.
hours of birth for medically stable infants >2,000 combination vaccine containing HepB is used after • The maximum age for the final dose is 8 months, 0
grams. Infants <2,000 grams administer 1 dose at the birth dose. days.
chronological age 1 month or hospital discharge. • Minimum age for the final (3rd or 4th) dose: 24 • For other catch-up guidance, see Figure 2.
• Mother is HBsAg-Positive: weeks.
Give HepB vaccine and 0.5 mL of HBIG (at • Minimum Intervals: Dose 1 to Dose 2: 4 weeks / 3. Diphtheria, tetanus, and acellular pertussis (DTaP)
separate anatomic sites) within 12 hours of Dose 2 to Dose 3: 8 weeks / Dose 1 to Dose 3: 16 vaccine. (minimum age: 6 weeks [4 years for
birth, regardless of birth weight. weeks. (When 4 doses are given, substitute “Dose Kinrix or Quadracel])
Test for HBsAg and anti-HBs at age 9–12 4” for “Dose 3” in these calculations.) Routine vaccination:
months. If HepB series is delayed, test 1–2 Catch-up vaccination: • 5-dose series at 2, 4, 6, and 15–18 months, and 4–6
months after final dose. • Unvaccinated persons should complete a 3-dose years.
• Mother’s HBsAg status is unknown: series at 0, 1–2, and 6 months. Prospectively: A 4th dose may be given as
Give HepB vaccine within 12 hours of birth, • Adolescents 11–15 years of age may use an
regardless of birth weight. early as age 12 months if at least 6 months
alternative 2-dose schedule, with at least 4 months have elapsed since the 3rd dose.
For infants <2,000 grams, give 0.5 mL of HBIG between doses (adult formulation Recombivax
in addition to HepB vaccine within 12 hours of Retrospectively: A 4th dose that was
HB only).
birth. inadvertently given as early as 12 months may
• For other catch-up guidance, see Figure 2.
Determine mother’s HBsAg status as soon as be counted if at least 4 months have elapsed
possible. If mother is HBsAg-positive, give 0.5 2. Rotavirus vaccines. (minimum age: 6 weeks) since the 3rd dose.
mL of HBIG to infants >2,000 grams as soon as Routine vaccination: Catch-up vaccination:
possible, but no later than 7 days of age. Rotarix: 2-dose series at 2 and 4 months. • The 5th dose is not necessary if the 4th dose was
Routine Series: RotaTeq: 3-dose series at 2, 4, and 6 months. administered at 4 years or older.
• A complete series is 3 doses at 0, 1–2, and 6–18 • For other catch-up guidance, see Figure 2.
If any dose in the series is either RotaTeq or
months. (Monovalent HepB vaccine should be
unknown, default to 3-dose series.
used for doses given before age 6 weeks.)
For further guidance on the use of the vaccines mentioned below, see: www.cdc.gov/vaccines/hcp/acip-recs/index.html.
4. Haemophilus influenzae type b (Hib) vaccine. • HIV infection Cerebrospinal fluid leak; cochlear implant:
(minimum age: 6 weeks) 12–59 months Age 2–5 years:
Routine vaccination: Unvaccinated or only 1 dose before 12 • Any incomplete* schedules with:
• ActHIB, Hiberix, or Pentacel: 4-dose series at 2, 4, months: Give 2 doses 8 weeks apart. 3 PCV13 doses: 1 dose of PCV13 (at least 8
6, and 12–15 months. 2 or more doses before 12 months: Give 1 weeks after any prior PCV13 dose).
• PedvaxHIB: 3-dose series at 2, 4, and 12–15 months. dose, at least 8 weeks after previous dose. <3 PCV13 doses: 2 doses of PCV13, 8 weeks
Catch-up vaccination: Unimmunized* persons 5–18 years after the most recent dose and given 8 weeks
• 1st dose at 7–11 months: Give 2nd dose at least 4 Give 1 dose apart.
weeks later and 3rd (final) dose at 12–15 months or • Immunoglobulin deficiency, early component • No history of PPSV23: 1 dose of PPSV23 (at least 8
8 weeks after 2nd dose (whichever is later). complement deficiency weeks after any prior PCV13 dose).
• 1st dose at 12–14 months: Give 2nd (final) dose at 12–59 months Age 6–18 years:
least 8 weeks after 1st dose. Unvaccinated or only 1 dose before 12 • No history of either PCV13 or PPSV23: 1 dose of
• 1st dose before 12 months and 2nd dose before months: Give 2 doses, 8 weeks apart. PCV13, 1 dose of PPSV23 at least 8 weeks later.
15 months: Give 3rd (final) dose 8 weeks after 2nd 2 or more doses before 12 months: Give 1 • Any PCV13 but no PPSV23: 1 dose of PPSV23 at
dose. dose, at least 8 weeks after previous dose. least 8 weeks after the most recent dose of PCV13
• 2 doses of PedvaxHIB before 12 months: Give 3rd • PPSV23 but no PCV13: 1 dose of PCV13 at least 8
(final) dose at 12–59 months and at least 8 weeks *Unimmunized = Less than routine series (through 14
weeks after the most recent dose of PPSV23.
after 2nd dose. months) OR no doses (14 months or older)
Sickle cell disease and other hemoglobinopathies;
• Unvaccinated at 15–59 months: 1 dose.
5. Pneumococcal vaccines. (minimum age: 6 weeks anatomic or functional asplenia; congenital
• For other catch-up guidance, see Figure 2.
[PCV13], 2 years [PPSV23]) or acquired immunodeficiency; HIV infection;
Special Situations: chronic renal failure; nephrotic syndrome;
• Chemotherapy or radiation treatment Routine vaccination with PCV13:
• 4-dose series at 2, 4, 6, and 12–15 months. malignant neoplasms, leukemias, lymphomas,
12–59 months Hodgkin disease, and other diseases associated
Unvaccinated or only 1 dose before 12 months: Catch-up vaccination with PCV13:
with treatment with immunosuppressive drugs
Give 2 doses, 8 weeks apart • 1 dose for healthy children aged 24–59 months
or radiation therapy; solid organ transplantation;
2 or more doses before 12 months: Give 1 dose, with any incomplete* PCV13 schedule
multiple myeloma:
at least 8 weeks after previous dose. • For other catch-up guidance, see Figure 2.
Age 2–5 years:
Doses given within 14 days of starting therapy or Special situations: High-risk conditions:
• Any incomplete* schedules with:
during therapy should be repeated at least 3 months Administer PCV13 doses before PPSV23 if
3 PCV13 doses: 1 dose of PCV13 (at least 8
after therapy completion. possible.
weeks after any prior PCV13 dose).
• Hematopoietic stem cell transplant (HSCT) Chronic heart disease (particularly cyanotic
<3 PCV13 doses: 2 doses of PCV13, 8 weeks
• 3-dose series with doses 4 weeks apart starting 6 to congenital heart disease and cardiac failure);
after the most recent dose and given 8 weeks
12 months after successful transplant (regardless of chronic lung disease (including asthma treated
apart.
Hib vaccination history). with high-dose, oral, corticosteroids); diabetes
mellitus: • No history of PPSV23: 1 dose of PPSV23 (at least 8
• Anatomic or functional asplenia (including sickle
weeks after any prior PCV13 dose) and a 2nd dose
cell disease) Age 2–5 years:
of PPSV23 5 years later.
12–59 months • Any incomplete* schedules with:
Unvaccinated or only 1 dose before 12 months: 3 PCV13 doses: 1 dose of PCV13 (at least 8 Age 6–18 years:
Give 2 doses, 8 weeks apart. weeks after any prior PCV13 dose). • No history of either PCV13 or PPSV23: 1 dose of
PCV13, 2 doses of PPSV23 (1st dose of PPSV23
2 or more doses before 12 months: Give 1 dose, <3 PCV13 doses: 2 doses of PCV13, 8 weeks administered 8 weeks after PCV13 and 2nd dose of
at least 8 weeks after previous dose. after the most recent dose and given 8 weeks
Appendixes
PPSV23 administered at least 5 years after the 1st
Unimmunized* persons 5 years or older apart. dose of PPSV23).
Give 1 dose • No history of PPSV23: 1 dose of PPSV23 (at least 8 • Any PCV13 but no PPSV23: 2 doses of PPSV23 (1st
• Elective splenectomy weeks after any prior PCV13 dose). dose of PPSV23 to be given 8 weeks after the most
Unimmunized* persons 15 months or older Age 6-18 years: recent dose of PCV13 and 2nd dose of PPSV23
Give 1 dose (preferably at least 14 days before • No history of PPSV23: 1 dose of PPSV23 (at least 8 administered at least 5 years after the 1st dose of
procedure). weeks after any prior PCV13 dose). PPSV23).
165
166 Reference Range Values for Pediatric Care
For further guidance on the use of the vaccines mentioned below, see: www.cdc.gov/vaccines/hcp/acip-recs/index.html.
Appendixes
Note: Menactra should be given either before or at • Adolescents 13–18 who have not received Tdap: inadvertently received a dose of HPV vaccine
the same time as DTaP. For MenACWY booster dose 1 dose, followed by a Td booster every 10 years. while pregnant. Delay remaining doses until after
recommendations for groups listed under “Special • Persons aged 7–18 years not fully immunized pregnancy. Pregnancy testing not needed before
populations and situations” above, and additional vaccination.
with DTaP: 1 dose of Tdap as part of the catch-up
meningococcal vaccination information, see *See MMWR, December 16, 2016;65(49):1405–1408,
series (preferably the first dose). If additional doses at www.cdc.gov/mmwr/volumes/65/wr/pdfs/
meningococcal MMWR publications at: www.cdc.gov/
are needed, use Td. mm6549a5.pdf.
vaccines/hcp/acip-recs/vacc-specific/mening.html. CS270457-M
167
Index
A immunization schedules for,
Acetaminophen toxicity, 158 160–167
Achondroplasia, 31 iron levels in, 78
Activity, APGAR score, 7 lactate dehydrogenase (LDH) levels
Activity, FLACC Pain Scale, 10 in, 78
Adolescents lactate (serum) levels in, 78
age-specific leukocyte differential lactate dehydrogenase (LDH) levels
for, 98 in, 78
alanine aminotransferase (ALT) levetiracetam (Keppra) dosing for,
levels in, 73 148
aldolase levels in, 73 lipase levels in, 78
alkaline phosphatase (ALP) levels lymphocyte subset counts in periph-
in, 73 eral blood in, 99–101
amikacin dosing for, 138 magnesium levels in, 79
ammonia levels in, 73 methemoglobin levels in, 79
amylase levels in, 73 osmolality (serum or plasma) levels
aspartate aminotransferase (AST) in, 79
levels in, 74 phenobarbital dosing for, 150
bicarbonate levels in, 74 phosphate levels in, 79
bilirubin (total) levels in, 74 prealbumin levels in, 80
cerebrospinal fluid levels in, 70–71 protein electrophoresis in, 80
calcium (total and ionized) levels pyruvate levels in, 81
in, 74, 75 rheumatoid factor (RF) levels in, 81
chloride levels in, 75 thyroid function values in, 86
creatine kinase levels in, 75 tobramycin dosing for, 142
creatinine (enzymatic) levels in, 76 transferrin levels in, 81
dietary reference intakes (DRIs) triglyceride levels in, 81
for, 126 troponin I levels in, 82
digoxin dosing for, 153 urea nitrogen (BUN) levels in, 82
enoxaparin dosing for, 155 uric acid levels in, 82
ferritin levels in, 76 valproic acid and derivatives dosing
fosphenytoin dosing for, 146 for, 152
gentamicin dosing for, 140 vancomycin dosing for, 144
γ-glutamyltransferase (GGT) levels vitamin A (retinol) levels in, 82
in, 77 vitamin B1 (thiamine) levels in, 82
haptoglobin levels in, 77 vitamin B2 (riboflavin) levels in, 82
hematology values in, 94–95 vitamin B12 (cobalamin) levels in, 82
vitamin C (ascorbic acid) levels
in, 82
170 Index
F G
Face, FLACC Pain Scale, 10 Gentamicin, 140–141
Facial expression, NPASS, 11, 14 γ-glutamyltransferase (GGT), 77
Fahrenheit conversion, 1, 2 Girls
Fenton preterm growth charts blood pressure levels in, 66–68
boys, 21 clinical chemistry in
girls, 22 alanine aminotransferase
Ferritin, 76 (ALT), 73
Fibrinolysis, 104, 106, 108 alkaline phosphatase (ALP), 73
176 Index
H I
Haemophilus influenzae type b vaccine, Immunization schedules, 160–167
161, 162, 163, 165 Inactivated poliovirus (IPV) vaccine,
Haptoglobin, 77 161, 162, 163, 166
HDL. See High-density lipoprotein (HDL) Infants. See also Newborns
Head circumference age-specific leukocyte differential
with Down syndrome, 34, 38 for, 96–97
growth charts, 20, 34, 38 alanine aminotransferase (ALT)
Height levels in, 73
conversion formulas, 1 aldolase levels in, 73
growth charts, 20 alkaline phosphatase (ALP) levels
in pediatric malnutrition indica- in, 73
tors, 46 amikacin dosing for, 138
and weight for children with cere- ammonia levels in, 73
bral palsy, 40 amylase levels in, 73
Hematocrit aspartate aminotransferase (AST)
in children, teens, and young levels in, 74
adults, 94 bilirubin (total) levels in, 74
in infants and toddlers, 92–93 blood pressure nomograms for, 63
Hematology values cerebrospinal fluid levels in, 70–71
in children, teens and young adults, calcium (total and ionized) levels
94–95 in, 74, 75
in infants and toddlers, 92–93 chloride levels in, 75
Hemoglobin coagulation values in, 105–106
in children, teens, and young cow’s milk–based formulas for, 118
adults, 94 creatine kinase levels in, 75
in infants and toddlers, 92–93 creatinine (enzymatic) levels in, 76
Hemoglobin A1c, 77 dietary reference intakes (DRIs)
Hemoglobin F, 77 for, 126
Hepatitis A vaccine, 161, 162, 163, 166 digoxin dosing for, 153
Hepatitis B vaccine, 161, 162, 163, 164 enoxaparin dosing for, 155
High-density lipoprotein (HDL), 79 extensively hydrolyzed casein for-
HIV infection, 165 mulas for, 119
Holliday-Segar method, 125 ferritin levels in, 76
Human milk, 117 formulas for, 117–119
Human papillomavirus (HPV) vaccine, fosphenytoin dosing for, 146
161, 162, 163, 167 gentamicin dosing for, 140
178 Index
Each child and family is unique; therefore, these Recommendations for Preventive Pediatric Health These recommendations represent a consensus by the American Academy of Pediatrics (AAP) The recommendations in this statement do not indicate an exclusive course of treatment or standard
Care are designed for the care of children who are receiving competent parenting, have no and Bright Futures. The AAP continues to emphasize the great importance of continuity of care of medical care. Variations, taking into account individual circumstances, may be appropriate.
manifestations of any important health problems, and are growing and developing in a satisfactory in comprehensive health supervision and the need to avoid fragmentation of care. Copyright © 2019 by the American Academy of Pediatrics, updated March 2019.
fashion. Developmental, psychosocial, and chronic disease issues for children and adolescents may Refer to the specific guidance by age as listed in the Bright Futures Guidelines (Hagan JF, Shaw JS, No part of this statement may be reproduced in any form or by any means without prior written
require frequent counseling and treatment visits separate from preventive care visits. Additional Duncan PM, eds. Bright Futures: Guidelines for Health Supervision of Infants, Children, and Adolescents. permission from the American Academy of Pediatrics except for one copy for personal use.
visits also may become necessary if circumstances suggest variations from normal. 4th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2017).
BLOOD PRESSURE
• Footnote 6 has been updated to read as follows: “Screening should occur per ‘Clinical Practice Guideline for Screening and Management
of High Blood Pressure in Children and Adolescents’ (http://pediatrics.aappublications.org/content/140/3/e20171904). Blood pressure
measurement in infants and children with specific risk conditions should be performed at visits before age 3 years.”
ANEMIA
• Footnote 24 has been updated to read as follows: “Perform risk assessment or screening, as appropriate, per recommendations in the
current edition of the AAP Pediatric Nutrition: Policy of the American Academy of Pediatrics (Iron chapter).”
LEAD
• Footnote 25 has been updated to read as follows: “For children at risk of lead exposure, see ‘Prevention of Childhood Lead Toxicity’
(http://pediatrics.aappublications.org/content/138/1/e20161493) and ‘Low Level Lead Exposure Harms Children:
A Renewed Call for Primary Prevention’ (https://www.cdc.gov/nceh/lead/ACCLPP/Final_Document_030712.pdf ).”
2ND EDITION
tools you’ll use again and again
New in the second edition Save time and simplify clinical problem-
• Expanded sections on antibiotics and anti- solving with a full set of easy-to-use tools.
convulsant medications and other commonly • APGAR and New Ballard newborn scoring
used drugs with recommended serum drug • Blood pressure nomograms
target levels. • Glucose infusion rate calculators
• Preterm and neonatal populations are high-