Professional Documents
Culture Documents
Tachdjian’s
Pediatric
Orthopaedics
From the Texas Scottish Rite Hospital for Children
ERRNVPHGLFRVRUJ
John A. Herring, MD
Chief of Staff Emeritus
Department of Orthopaedic Surgery
Texas Scottish Rite Hospital for Children
Professor
Department of Orthopaedic Surgery
University of Texas Southwestern Medical Center
Dallas, Texas
Sixth Edition
Volume Two
Tachdjian’s
Pediatric
Orthopaedics
From the Texas Scottish Rite Hospital for Children
ERRNVPHGLFRVRUJ
John A. Herring, MD
Chief of Staff Emeritus
Department of Orthopaedic Surgery
Texas Scottish Rite Hospital for Children
Professor
Department of Orthopaedic Surgery
University of Texas Southwestern Medical Center
Dallas, Texas
Sixth Edition
Elsevier
1600 John F. Kennedy Blvd.
Ste 1600
Philadelphia, PA 19103-2899
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v
vi Contributors
This edition of Tachdjian’s Pediatric Orthopaedics is the The authors of this book are experienced clinicians
fourth that has been written and edited by the staff of the with expertise and training in pediatric orthopaedics,
Texas Scottish Rite Hospital for Children. As we research and most have subspeciality interests and expertise. They
and reevaluate each chapter, we are usually surprised to are leaders in their fields and base their discussions and
see how many things have changed between editions. recommendations on a very rich clinical experience in
For example, in recent years we have seen considerable an academic practice. An important feature of our aca-
growth in the knowledge and practice in the field of demic environment is the vigorous preoperative group
pediatric sports subspecialization. In recognition of this discussion of surgical procedures. As academic leaders,
growth, we have added a new chapter dedicated to pedi- they regularly present their research at national and inter-
atric and adolescent sports conditions, which includes national meetings. Their work is widely published and
the most recent developments in the management of broadly respected.
concussion. In the scoliosis chapter, exciting new infor- Users of the text include students from all levels from
mation about the rapidly evolving management of early medical school, residency, fellowship, new and estab-
onset scoliosis has been added, including important non- lished physicians, and non-physician practitioners, as well
operative measures such as serial casting and bracing, as as established professors as they augment their publica-
well as the use of tethering. The field of genetics is con- tions. The text of this edition is fully produced in two print
tinually expanding, and genetics-related content, which volumes. To lighten the load of the textbook, a compre-
appears in many of our chapters, has been updated to hensive bibliography is available in the online version. This
reflect current understanding. placement facilitates Internet access to other resources.
Twenty years ago, we took on the challenge to build As in prior editions, our popular surgical videos are
on the groundwork laid by Dr. Mirhan Tachdjian in his available online. These videos present the important steps
two editions. Our goal has been to produce a textbook of actual surgical cases and are narrated by the operating
that fully encompasses the broad field of pediatric ortho- surgeons. We receive frequent positive comments from
paedics. We have based our descriptions on the best avail- surgeons throughout the world who find these very use-
able published knowledge. We have sought to present the ful for planning their surgical procedures. Other videos in
most current evidence from the literature from level 1 to the collection cover non-operative subjects such as cast
5 in a succinct and readable format. We have augmented application for scoliosis, club foot casting, and Pavlik har-
the discussions with recommendations based on personal ness application.
experiences of a top-level clinical faculty. When presenting
I am sincerely grateful to each of our authors and truly
controversial topics, we prefer to give the reader the evi- appreciate the effort involved in making the sixth edition a
dence from the different arguments so that the reader can reality. We welcome two new authors, Dr. Jane Chung and
make a reasoned decision after reviewing the conflicting Dr. Shane Miller, who are pediatric-trained practitioners
evidence. We carefully avoid the “cookbook” approach in with expertise in sports medicine. We continue to be grate-
which one puts forth their preferred treatment as gospel. ful for the contribution of our Boston colleagues, Professor
We continue to insist that our text be comprehensive, Mark Gebhardt and Dr. Megan Anderson, who are respon-
even though a shorter text would be more convenient to sible for the chapter on malignant tumors. I especially want
handle. We fully present each topic, include the descrip- to thank my administrative assistant, Louise Hamilton, who
tion of a disorder, and discuss appropriate history and had the huge task of putting the whole project together.
physical exam, relevant studies, differential diagnosis, and She was able to devote the time needed for this edition
details of treatment. We believe that it is important to because of coverage by the other administrative assistants,
present the important details of decision making, and we including Stacy Duckworth, Lisa Sherman, Rebecca Fuller,
emphasize the complexity of overall patient care. Our sur- Amy Park, and our administrative director, Laura Griffiths.
gical discussions stress proper preoperative planning and Again, our heartfelt appreciation goes to our families, who
preparation, as well as description of operative details. We are vitally important in every facet of our lives; thanks for
also provide the important postoperative protocols that giving us your support and understanding.
are necessary to ensure the best results.
John A. Herring, MD
vii
PREFACE
This edition of Tachdjian’s Pediatric Orthopaedics is the The authors of this book are experienced clinicians
fourth that has been written and edited by the staff of the with expertise and training in pediatric orthopaedics,
Texas Scottish Rite Hospital for Children. As we research and most have subspeciality interests and expertise. They
and reevaluate each chapter, we are usually surprised to are leaders in their fields and base their discussions and
see how many things have changed between editions. recommendations on a very rich clinical experience in
For example, in recent years we have seen considerable an academic practice. An important feature of our aca-
growth in the knowledge and practice in the field of demic environment is the vigorous preoperative group
pediatric sports subspecialization. In recognition of this discussion of surgical procedures. As academic leaders,
growth, we have added a new chapter dedicated to pedi- they regularly present their research at national and inter-
atric and adolescent sports conditions, which includes national meetings. Their work is widely published and
the most recent developments in the management of broadly respected.
concussion. In the scoliosis chapter, exciting new infor- Users of the text include students from all levels from
mation about the rapidly evolving management of early medical school, residency, fellowship, new and estab-
onset scoliosis has been added, including important non- lished physicians, and non-physician practitioners, as well
operative measures such as serial casting and bracing, as as established professors as they augment their publica-
well as the use of tethering. The field of genetics is con- tions. The text of this edition is fully produced in two print
tinually expanding, and genetics-related content, which volumes. To lighten the load of the textbook, a compre-
appears in many of our chapters, has been updated to hensive bibliography is available in the online version. This
reflect current understanding. placement facilitates Internet access to other resources.
Twenty years ago, we took on the challenge to build As in prior editions, our popular surgical videos are
on the groundwork laid by Dr. Mirhan Tachdjian in his available online. These videos present the important steps
two editions. Our goal has been to produce a textbook of actual surgical cases and are narrated by the operating
that fully encompasses the broad field of pediatric ortho- surgeons. We receive frequent positive comments from sur-
paedics. We have based our descriptions on the best avail- geons throughout the world who find these very useful for
able published knowledge. We have sought to present the planning their surgical procedures. Other videos in the col-
most current evidence from the literature from level 1 to lection cover non-operative subjects such as cast application
5 in a succinct and readable format. We have augmented for scoliosis, club foot casting, and Pavlik harness application.
the discussions with recommendations based on personal I am sincerely grateful to each of our authors and truly
experiences of a top-level clinical faculty. When presenting
appreciate the effort involved in making the sixth edition a
controversial topics, we prefer to give the reader the evi- reality. We welcome two new authors, Dr. Jane Chung and
dence from the different arguments so that the reader can Dr. Shane Miller, who are pediatric-trained practitioners
make a reasoned decision after reviewing the conflicting with expertise in sports medicine. We continue to be grate-
evidence. We carefully avoid the “cookbook” approach in ful for the contribution of our Boston colleagues, Professor
which one puts forth their preferred treatment as gospel. Mark Gebhardt and Dr. Megan Anderson, who are respon-
We continue to insist that our text be comprehensive, sible for the chapter on malignant tumors. I especially want
even though a shorter text would be more convenient to to thank my administrative assistant, Louise Hamilton, who
handle. We fully present each topic, include the descrip- had the huge task of putting the whole project together.
tion of a disorder, and discuss appropriate history and She was able to devote the time needed for this edition
physical exam, relevant studies, differential diagnosis, and because of coverage by the other administrative assistants,
details of treatment. We believe that it is important to including Stacy Duckworth, Lisa Sherman, Rebecca Fuller,
present the important details of decision making, and we Amy Park, and our administrative director, Laura Griffiths.
emphasize the complexity of overall patient care. Our sur- Again, our heartfelt appreciation goes to our families, who
gical discussions stress proper preoperative planning and are vitally important in every facet of our lives; thanks for
preparation, as well as description of operative details. We giving us your support and understanding.
also provide the important postoperative protocols that
are necessary to ensure the best results. John A. Herring, MD
vii
CHAPTER 1
ERRNVPHGLFRVRUJ
4 SECTION I Disciplines
Examiner:
DENVER ll Date:
Name:
Birthdate:
ID#:
Months 2 4 6 9 12 15 18 24 Years 3 4 5 6
prepare cereal
brush teeth, no help
Percent of children passing
play board/card games
25 50 75 90
dress, no help
test item put on t-shirt
name friend
86%
copy
wash and dry hands
draw person, 6 parts
brush teeth with help
copy , demonstrate
put on clothes
pick longer line
feed doll
copy +
remove garment
draw person, 3 parts
use spoon/fork
copy
help in house
wiggle thumb
88%
drink from cup define 7 words
tower of 8 cubes
initate activites name 2 opposites
imit. vert. line
play ball with examiner count 5 blocks
tower of 6 cubes
wave bye-bye tower of 4 cubes know 3 adjectives
indicate wants define 5 words
tower of 2 cubes
play pat-a-cake name 4 colors
dump raisin, demonstrated
feed self understand 4 prepostitions
scribbles
Personal–Social
heel-to-toe walk
regard raisin speech half understandable
balance each foot 5 sec
follow 180° name 4 pictures
balance each foot 4 sec
hands name 6 body parts
together balance each foot 3 sec
name 1 picture
grasp hops
rattle combine words
balance each foot
follow past point to pictures 2 sec
midline
6 words balance each
follow foot 1 sec
to midln. 3 words
broad jump
2 words
throw ball overhand
1 word
jump up
Dada/Mama specific
kick ball forward
jabbers
walk up steps
combine syllables
runs
Dada/Mama
nonspecific walk backward
imitate speech sounds walk well
single syllables stoop and recover
turn to voice stand alone
turn to stand 2 sec
rattling sound get to
squeals sitting
Language
laughs pull to
stand
"Ooo/aah" stand
vocalizes holding on
respond sit–no
to bell support
pull to stand no head lag
roll over
chest up
arm support
wear wt. on legs
sit-head steady
Gross Motor
head up 90°
head up 45°
lift head
equal
movements
Months 2 4 6 9 12 15 18 24 Years 3 4 5 6
FIG. 1.1 The revised Denver Developmental Screening Test showing the range of age when a child should achieve milestones in the de-
velopment of gross motor skills, fine motor–adaptive skills, language, and personal-social skills. (Modified from Frankenburg WK, Dodds JB.
The Denver Developmental Screening Test. J Pediatr. 1967;71:181; Hensinger RN. Standards in Pediatric Orthopedics. New York: Raven Press;
1986.)
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 5
gestation. Examples include myelomeningocele, syndactyly, either by eliminating the deforming force or by counteract-
preaxial polydactyly, Poland syndrome, and proximal focal ing the force with stretching, casting, or bracing.
femoral deficiency (congenital femoral deficiency).
Disruptions
Deformations
Disruptions are morphologic abnormalities that result from
Deformations are defects in the form, shape, or site of body an extrinsic interference with or breakdown of the nor-
parts caused by mechanical stress. The mechanical stress, mal growth and development process. Disruptions can be
which may be intrinsic or extrinsic, alters or distorts tissues. caused by drugs or toxic materials. These structural defects
Because the fetus grows considerably faster than the infant, may affect organs or systems that were normal during
fetuses are more vulnerable to deformations. Examples organogenesis. A congenital constriction band in the limb is
include supple metatarsus adductus, calcaneovalgus feet, con- an example of a disruption.
genital knee hyperextension, and physiologic bowing of the
tibia.
Dysplasias
Differentiating deformations from malformations is
important. During a cursory examination, severe deforma- Dysplasias are structural defects caused by abnormal tis-
tions may look like malformations.3 Careful assessment is sue differentiation as cells organize into tissues. Examples
essential if the child is to receive appropriate care for the include osteogenesis imperfecta, achondroplasia, and spon-
condition. Malformations cannot be corrected directly, dyloepiphyseal dysplasia.
whereas deformations can often be reversed relatively easily
Physical Growth
FIG. 1.2 Typical position of the neonate with vertex presentation. Head Circumference
The hips and knees are flexed, the lower legs are rotated internally,
and the feet are rotated further inward on the lower leg. The lower
During infancy it is essential to obtain individual or serial
limbs are contracted into this position for a variable period after measurements of the patient’s head circumference to deter-
birth. mine whether head growth is slower or faster than normal.
ERRNVPHGLFRVRUJ
6 SECTION I Disciplines
Head circumference should be measured at every physical The approximate ages at which children should normally
examination during the first 2 years and at least biennially attain various gross motor skills are given in Table 1.1.
thereafter. With the child supine, the examiner places a cen- By 3 months of age, infants should be able to hold their
timeter tape over the occipital, parietal, and frontal promi- heads above the plane of the body when they are supported
nences of the head. The tape should be stretched and the in a prone position. By 6 months of age, the head should not
reading noted at the point of greatest circumference. Possible lag when infants are pulled from a supine to a sitting posi-
conditions that can affect head circumference and growth tion. Normally, infants will begin to roll over between 4 and
include microcephaly, premature closure of the sutures, 6 months of age and can sit with minimal external support
hydrocephalus, subdural hematoma, and brain tumor. Head at 6 to 7 months. They should be able to pull up to a stand-
circumference should be charted for age and percentile, as ing position by holding onto furniture at 9 to 12 months and
noted in Fig. 1.4. stand without support by 14 months.
The average milestones of development of locomotion
are as follows: the infant should be able to crawl by 7 to 9
Height and Weight
months of age, cruise and walk with assistance at 12 months,
A child’s growth, as demonstrated by an increase in body walk forward without support by 12 to 16 months, and run
height and weight within predetermined normal limits, is at 18 months of age.1,2,11 Children should be able to ascend
one of the best indicators of health during infancy and child- stairs with support by 18 months of age and without sup-
hood. The child’s height and weight should be plotted on port by 2 years of age. They should be able to descend stairs
a standard growth chart to verify that normal progress is with support at approximately 3 years of age and without
being made. Numerous tables, charts, and graphs depict- support by 4 years.
ing pediatric growth standards are available in Hensinger’s On gross inspection the independent gait of the infant has
Standards in Pediatric Orthopedics7 and in Proceedings of a wide base, the hips and knees are hyperflexed, the arms are
the Greenwood Genetic Center: Growth References.10 The held in flexion, and the movements are abrupt. With matura-
World Health Organization published an extensive study of tion of the neuromuscular system, the width of the base gradu-
child growth standards for length and height for age, weight ally diminishes, the movements become smoother, reciprocal
for age, weight for length, weight for height, and body mass swing of the upper limbs begins, and step length and walking
index for age.18 Height and weight should be charted for velocity increase.13 The adult pattern of gait develops between
age and percentile, as noted in Fig. 1.5. If growth measure- 3 and 5 years of age.14 A more complete description of normal
ments are lower than the 3rd percentile or higher than the pediatric gait patterns is provided in Chapter 5.
97th percentile, or if a recent deviation from previously
stable percentile rankings is noted, further investigation is
Fine Motor Skills
warranted.
The approximate ages at which children normally attain
various fine motor skills are listed in Table 1.2. A child’s
Epiphyseal Growth and Closure
exploration of the environment by touch and the devel-
During normal growth and development, the pattern in the opment of manual skills should emerge in an orderly and
appearance of centers of ossification and fusion of epiphy- sequential manner. At 3 months of age, infants can apply
ses in the upper and lower limbs is orderly. This pattern lip pressure and coordinate sucking and swallowing during
varies among individuals and is different for boys and girls feeding (the sucking reflex is present at birth in all normal
(Figs. 1.6–1.9). Thus the orthopaedist must understand full-term neonates but usually disappears at 3–4 months of
the ranges of normal when treating the pediatric patient, age). By 6 months of age, children are able to feed them-
particularly when interpreting radiographs. The percentage selves from hand to mouth. By 9 months, children can feed
contribution of each epiphysis to longitudinal growth of the themselves food such as cookies. By 12 months of age, chil-
upper and lower extremity long bones is shown in Figs. 1.10 dren can pick up a spoon from the table, chew cookies or
and 1.11. toast, and drink milk from a cup if assisted. Between 12
and 18 months, they are able to feed themselves (messily)
with a spoon and drink from a cup by using one or two
Tanner Stages of Development
hands. By 24 months, they can feed themselves semisolid
The physical maturation of a child can also be compared food with a spoon and drink holding the cup in one hand
with his or her chronologic age by using the pubertal or using a straw.
stages of development as described by Tanner (Figs. 1.12 Children should be able to purposefully grasp objects
and 1.13).15,16 The Tanner stages of maturation are based such as a bottle or toy rattle by 6 months of age. At 9
on breast size in girls, genital size in boys, and pubic hair months of age, children use their fingers and thumb to grasp
stages for both girls and boys. The onset of menstruation objects and are able to transfer objects from one hand to
is also an important milestone in the physical maturation the other. By 12 months, children’s hand skills are such that
of girls. they are able to hit two objects together, voluntarily release
objects, manipulate and throw objects on the floor, and hold
crayons and imitate scribbling. Between 18 and 24 months
Developmental Milestones of age, their hand skills evolve to the point that they can
build block towers, turn pages one at a time, and throw a
Gross Motor Skills
ball (but inaccurately). Between 2 and 3 years of age, their
The development of gross motor skills depends on maturation writing skills evolve from imitating vertical, horizontal, and
of the CNS, which proceeds in a cephalocaudal direction.8 circular strokes to copying circles.
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 7
B 3 6 9 12 15 18 21 24 27 30 33 36
54 ( t 54
21 21
53 53
95
Head circumference
52 90 52
75
20 51 51 20
50
50 50
25
49 10 49
19 5
48 48 19
47 47
46 46
18
cm in
45
44
17 43 21 46
42 20 44
41 19 42
16
40 18 40
95
39 90 17 38
75 36
15 38 16
50
34
37 25 15
10 32
36 5 14
14 30
35 13
28
34 12
26
13 33 11 24
32 10 22
31 9 20
12
8 18
Weight
in cm 16
7
14
6 6
12 12
5 5
10 10
4 4
8 8
3 3
6 6
2 2 4
4
Length
lb kg kg lb
cm 50 55 60 65 70 75 80 85 90 95 100
in 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
A
FIG. 1.4 Normal head circumference parameters for boys and girls from birth to 36 months. (A) Boys, birth to 36 months.
Continued
ERRNVPHGLFRVRUJ
8 SECTION I Disciplines
B 3 6 9 12 15 18 21 24 27 30 33 36
54 ( t 54
21 21
53 53
52 Head circumference 52
51 95 51
20 90 20
50 75 50
49 50 49
19 25
19
48 10
48
5
47 47
46 46
18
cm in
45
44
17 43 21 46
42 20 44
41 19 42
16
40 18 40
39 17 38
95
15 90 36
38 16
75 34
37 50
15
32
36 25 14
14 10 30
35 5 13
28
34 12
26
13 33 11 24
32 10 22
31 9 20
12 Weight 8 18
in cm 16
7
14
6 6
12 12
5 5
10 10
4 4
8 8
3 3
6 6
2 2 4
4
Length
lb kg kg lb
cm 50 55 60 65 70 75 80 85 90 95 100
in 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
B
FIG. 1.4, cont’d (B) Girls, birth to 36 months. NCHS, National Center for Health Statistics. (From the National Center for Health Statistics.)
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 9
B 3 6 9 12 15 18 21 24 27 30 33 36
42 42
105 105
41 Age o t s 41
95
40 40
90
100 100
39 39
75
38 50 38
95 95
37
Length
25
cm in
36 10
5
90
35
41
34 40
85 18
33 39
32 38
80 95 17
31 37
90 36
30
75 16 35
29
75 34
28
70 15 33
27
50 32
26
65 14 31
25 30
25
24 29
60 13
23 28
10
22 5 27
55 12
21 26
25
20
50 11 24
19
23
18 45 22
10
17
Weight
21
16 20
40 9
15 19
18
8
in cm 17
16
7 Age (months)
15 kg lb
14 12 15 18 21 24 27 30 33 36
13 6
Mother's stature Gestational
12
Father's stature age weeks
11 5
10 Date Age Length Weight Head circ. Comment
9 Birth
4
8
7
3
6
5
2
4
lb kg
B 3 6 9
A
FIG. 1.5 Normal length and weight parameters for boys and girls from birth to 18 years. (A) Boys, birth to 36 months.
Continued
ERRNVPHGLFRVRUJ
10 SECTION I Disciplines
B 3 6 9 12 15 18 21 24 27 30 33 36
42 42
105 105
41 Age o t s 41
40 40
95
100 100
39 90 39
75
38 38
95 50 95
37
Length
25
cm in
36
90 10
35 5
41
34 40
85 18
33 39
32 38
80 17
31 37
30 95 36
75 16 35
29 90
34
28
70 15 33
27 75
32
26
65 14 31
25 50
30
24 29
60 13
25
23 28
22 27
55 10 12
21 26
5 25
20
50 11 24
19
23
18 45 22
10
17
Weight
21
16 20
40 9
15 19
18
8
in cm 17
16
7 Age (months)
15 kg lb
14 12 15 18 21 24 27 30 33 36
13 6
Mother's stature Gestational
12
Father's stature age weeks
11 5
10 Date Age Length Weight Head circ. Comment
9 Birth
4
8
7
3
6
5
2
4
lb kg
B 3 6 9
B
FIG. 1.5, cont’d (B) Girls, birth to 36 months.
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 11
Boys: 2 to 18 years
Physical growth
Name Record #
NCHS percentiles
57 145 95 210
56 95
140 90 200
55
54
190
53 135 90 85
52 180
51 130 80
50 170
49 125 75 75
48 160
47 120 70
150
46 50
45 115 65
140
44
25
43 110 60
130
42 10
55
41 105 120
5
40
50
39 100 110
38
95 45 100
37
36 90
90 40
35
34 80
85 35
33
32 70
80 30
Weight
31
60
30
75 25
29
50
in cm
20
40 40
15 15
30 Age (years) 30
lb kg kg lb
C 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
FIG. 1.5, cont’d (C) Boys, 2 to 18 years.
Continued
ERRNVPHGLFRVRUJ
12 SECTION I Disciplines
Girls: 2 to 18 years
Physical growth
Name Record #
NCHS percentiles
57 145 95 210
56
140 90 200
55
54
190
53 135 85
52 95 180
51 130 80
50 170
49 125 75
48 90
160
47 120 70
150
46
45 115 65
140
75
44
43 110 60
130
42 50
55
41 105 120
40 25
50
39 100 110
38 10
95 5 45 100
37
36 90
90 40
35
34 80
85 35
33
32 70
80 30
Weight
31
60
30
75 25
29
50
in cm
20
40 40
15 15
30 Age (years) 30
lb kg kg lb
D 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
FIG. 1.5, cont’d (D) Girls, 2 to 18 years.
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 13
Boys: prepubescent
Physical growth
Name Record #
NCHS percentiles
42
90
41 90
40
39
85
75 38
37
80
36
35
50
34 75
33
25 32 70
31
10
65 30 30 65
5
29 29
28 28
60 60
27 27
26 26
55 25 25 55
24 24
50 23
Weight 23 50
22 22
21 21
45 45
20 20
19 19
40 40
18 18
17 17
35 16 16 35
15 15
30 14 14 30
13 13
12 12
25 25
Stature
lb kg kg lb
cm 85 90 95 100 105 110 115 120 125 130 135 140 145
in 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58
E
FIG. 1.5, cont’d (E) Boys, prepubescent.
Continued
ERRNVPHGLFRVRUJ
14 SECTION I Disciplines
Girls: prepubescent
Physical growth
Name Record #
NCHS percentiles
75
35
34 75
33
32 70
50
31
65 30 30 65
29 25 29
28 28
60 10
60
27 27
5
26 26
55 25 25 55
24 Weight 24
50 23 23 50
22 22
21 21
45 45
20 20
19 19
40 40
18 18
17 17
35 16 16 35
15 15
30 14 14 30
13 13
12 12
25 25
Stature
lb kg kg lb
cm 85 90 95 100 105 110 115 120 125 130 135 140 145
in 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58
F
FIG. 1.5, cont’d (F) Girls, prepubescent. NCHS, National Center for Health Statistics. (From the National Center for Health Statistics.)
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 15
Acromion Clavicle
appears 15–18 yr appears 17 yr
Humerus, head
appears birth–3 mo Coracoid process (main center)
appears 1 yr
Greater tuberosity
appears 6 mo–2 yr Scapula
3 mo–1.5 yr appears 1 FW
Lesser tuberosity
appears 3–5 yr Subcoracoid element
appears 10–12 yr
Glenoid cavity
appears 18 yr
Trochlea
appears 9 yr 8 yr Medial epicondyle
range 8–10 yr 7–9 yr appears 7 yr 5 yr
range 5–7 yr 3–6 yr
Lateral epicondyle
appears 12 yr 11 yr
Olecranon
appears 10 yr 8 yr
Capitulum
appears 5 mo 4 mo Navicular
range 6 wk–8 mo appears 5.5 yr 4.5 yr
1–6 mo range 2.5–9 yr
Radius, head
Trapezium
appears 5 yr 4 yr
appears 5 yr 4 yr
range 3–6 yr range 1.5–10 yr
ERRNVPHGLFRVRUJ
16 SECTION I Disciplines
Subcoracoid Coracoid
closure 18 yr closure 18–21 yr
Humerus, capitulum,
lateral epicondyle, and trochlea
fuse together at puberty
fuse to shaft 17 yr 14 yr
Medial epicondyle
closure 18 yr 15 yr
Olecranon
Radius, head closure 14–17 yr
closure 15–17 yr 14–15 yr
14–15 yr
Radial tuberosity
closure 14–18 yr
Ulna, styloid
Radius, styloid closure 18–20 yr
closure variable
FIG. 1.7 Average age at closure of growth plates (physes) in the epiphyses of the upper extremity, with ages for boys (blue) and girls (pink).
(Adapted from von Lanz T, Wachsmuth W. Praktische Anatomie. Berlin: Julius Springer; 1938:28.)
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 17
Iliac crest
Ischial spine appears at puberty
appears 13–15 yr
Iliac tubercle
Head of femur appears 13–15 yr
appears 4 mo
Tubercle of pubis
appears 18–20 yr
Greater trochanter
appears 3 yr
Acetabulum
appears 10–13 yr
Lesser trochanter
appears 12 yr 11 yr Tubercle of ischium
appears 13–15 yr
Patella
appears 4–5 yr 3 yr
Tibial tuberosity
appears 7–15 yr
FIG. 1.8 Average age at appearance of secondary centers of ossification in the epiphyses of the lower extremity, with ages for boys (blue)
and girls (pink). FW, Fetal week. (Adapted from von Lanz T, Wachsmuth W. Praktische Anatomie. Berlin: Julius Springer; 1938:28.)
ERRNVPHGLFRVRUJ
18 SECTION I Disciplines
Iliac crest
Head of femur closure 20 yr
closure 17–18 yr
16–17 yr
Greater trochanter
closure 16–17 yr
Closure variable
Distal phalanges
closure 18 yr (begins proximally)
FIG. 1.9 Average age at closure of growth plate (physis) in the epiphyses of the lower extremity, with ages for boys (blue) and girls (pink).
(Adapted from von Lanz T, Wachsmuth W. Praktische Anatomie. Berlin: Julius Springer; 1938:29.)
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 19
Humerus
Proximal 80%
Distal 20%
1 2 3
4 5
FIG. 1.12 Tanner stages of development of secondary sexual char-
Radius Ulna acteristics: male.
Proximal 25% Proximal 80%
Distal 75% Distal 20% Ambidexterity (i.e., lack of hand preference) is normal
during the first 18 to 24 months of age. If an infant demon-
strates evidence of hand preference during this time, it may
be caused by some defect in the hand and arm not being
used, and attention should be directed to that limb’s status.
FIG. 1.10 Average percentage contribution of the proximal and This may be the first sign of spastic hemiplegia.
distal physes to the longitudinal growth of the upper extremity
long bones.
Personal, Social, and Verbal Skills
The approximate ages at which children should normally
acquire various personal, social, and verbal skills are provided in
Table 1.3. At 2 to 3 months of age, infants smile when spo-
ken to and vocalize without crying. By 4 months, children
Femur turn their head to sound and recognize their mother, and at
Proximal 30% 6 months, they are laughing and smiling. At 8 to 10 months,
Distal 70% infants respond to “no.” By 10 months, they wave bye-bye,
ERRNVPHGLFRVRUJ
20 SECTION I Disciplines
Anterior
1 2 3 4 5
Lateral
1 2 3 4 5
A
B 1 2 3 4 5
FIG. 1.13 Tanner stages of development of secondary sexual characteristics: female. (A) Breast development. (B) Genital development.
2 mo Able to maintain head in plane of body when prone; partial head control when pulled from supine to sitting position
6 mo Able to lift head and chest off bed with weight on hands; head does not lag when pulled from supine to sitting position;
sits with support; head held steady when sitting; turns head side to side; rolls over; almost full weight on legs when held in
standing position
9 mo Sits without support, legs extended; sits “tailor fashion”—external rotation; sits with legs in internal rotation; pulls self to
stand; stands with two-hand support; crawls
12 mo Leans and recovers balance when sitting; walks with one-hand support
14 mo Stands without support; walks forward without support; stoops and recovers balance
3 yr Ascends stairs without support, foot over foot; descends stairs with support, one foot at a time; able to stand briefly on one
foot; pedals tricycle
4 yr Descends stairs without support, foot over foot; beginning to balance on one foot; hops on one foot; able to climb well
5 yr Hops on one foot without support; skips one foot at a time; forward heel-toe walk
6 yr Backward heel-toe walk; throws ball up and catches it with one hand
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 21
6 mo Purposefully reaches out and touches objects; palmar grasp of bottle or toy; involuntary release of bottle or toy; hand-to-
mouth feeding
9 mo Extended reach and grasp; uses fingers and thumb to grasp objects; releases object with flexed wrist; transfers object from
hand to hand; can feed self cookies; can protrude tongue during feeding
12 mo Attempts to stack one block on another (brings over and drops); hits two objects together; can voluntarily release object;
rolls ball imitatively; puts round block into round hole; puts cube into container; can hold crayon and imitate scribbling;
picks spoon up from table; chews cookies or toast; drooling controlled at all times; drinks milk from cup, if cup is held
18 mo Builds three-block tower (1-in cube); turns pages (two or three at a time); puts pegs into hole (1-in diameter); pounds;
hurls ball; points to nose, eyes, ears; drinks from cup (one- or two-handed); feeds self with spoon, but messily
2 yr Builds six-block tower; turns pages one at a time; throws bean bags; strings beads (1 in); throws ball, but inaccurately;
feeds self-semisolid food with spoon; drinks from cup or glass with one hand or straw; imitates vertical, horizontal, and
3 yr Builds nine-block tower; creases paper neatly; rides tricycle; feeds self with fork; tries to use scissors, but cannot follow line
5 yr Bounces ball and catches it; performs three simple directions in sequence; draws recognizable person; colors within 1-inch
6 yr Able to cut food with knife and eat with fork; copies printing (A, B, C)
Table 1.3 Developmental Milestones for Personal, Social, and Verbal Skills.
10 mo Responds to “no”; waves bye-bye; plays pat-a-cake; vocalizes “da-da” and “ma-ma” (nonspecific)
12 mo Begins to show interest in picture books; recognizes familiar objects; starts cooperating with dressing (extends arm for
sleeve); able to speak two or more words other than “da-da” or “ma-ma”
3 yr Unlaces and removes shoes; learns to lace shoes; takes off pants; dresses self with supervision; puts on shoes (not necessarily
on correct foot); tries to wash and dry hands; knows age and sex
4 yr Puts shoes on correct feet; laces shoes, but does not tie bow; dresses, knows back and front of clothes; manages buttons;
washes and dries face; brushes and combs hair; brushes teeth; counts three objects correctly
5 yr Dresses and undresses self completely (except for back fasteners); names four colors; names penny, nickel, dime; counts 10
objects correctly
6 yr Buttons small buttons on shirt; ties bows on shoes; combs and brushes hair
References
For references, see expertconsult.com.
ERRNVPHGLFRVRUJ
CHAPTER 1 Growth and Development 21.e1
1. Burnett CN, Johnson EW. Development of gait in childhood. I. Third Trimester to Adulthood. Greenwood, SC: Keys Printing;
Method. Dev Med Child Neurol. 1971;13(2):196–206. 1988.
2. Burnett CN, Johnson EW. Development of gait in childhood. II. 11. Sheridan MD. The Developmental Progress of Infants and Young
Method. Dev Med Child Neurol. 1971;13(2):207–215. Children Ministry of Health Report. London: Her Majesty’s Sta-
3. Chapple CC, Davidson DT. A study of the relationship be- tionery Office; 1960.
tween fetal position and certain congenital deformities. J Pediatr. 12. Spranger J, Benirschke K, Hall JG, et al. Errors of morphogenesis:
1941;18:483. concepts and terms. Recommendations of an international working
4. Dunne KB, Clarren SK. The origin of prenatal and postnatal de- group. J Pediatr. 1982;100(1):160–165.
formities. Pediatr Clin N Am. 1986;33(6):1277–1297. 13. Statham L, Murray MP. Early walking patterns of normal children.
5. Frankenburg WK, Dodds JB. The Denver Developmental Screen- Clin Orthop Relat Res. 1971;79:8–24.
ing Test. J Pediatr. 1967;71(2):181–191. 14. Sutherland DH, Olshen R, Cooper L, et al. The development of
6. Frankenburg WK, Fandal AW, Sciarillo W, et al. The newly ab- mature gait. J Bone Joint Surg Am. 1980;62(3):336–353.
breviated and revised Denver Developmental Screening Test. J 15. Tanner J. Growth and endocrinology of the adolescent. In:
Pediatr. 1981;99(6):995–999. Gardner L, ed. Endocrine and Genetic Diseases of Childhood. 2nd
7. Hensinger RN. Standards in Pediatric Orthopedics: Tables, Charts, ed. Philadelphia: Saunders; 1975.
and Graphs Illustrating Growth. New York: Raven Press; 1986. 16. Tanner JM. Growth at Adolescence. 13th ed. New York: Blackwell
8. Illingworth RS. The Development of the Infant and Young Child: Scientific; 1982.
Normal and Abnormal. New York: Churchill Livingstone; 1987. 17. Vaughan VG, Litt I. Developmental pediatrics: growth and devel-
9. Prechtl HFR, Connolly KJ. Maturation and development: an in- opment. In: Behrman RE, Vaughan VC, Nelson W, eds. Nelson
troduction. In: Connolly KJ, Prechtl HFR, eds. Maturation and Textbook of Pediatrics. 13th ed. Philadelphia: Saunders; 1987:6.
Development: Biologic and Physiologic Perspectives. Philadelphia: 18. World Health Organization. WHO Child Growth Standards. Ge-
JB Lippincott & Co; 1981. neva: World Health Organization Press; 2006.
ERRNVPHGLFRVRUJ
CHAPTER 2
Family History 22
cerned, and the secondary gains the child (or other individu-
Birth History 22
als) may acquire from the illness.
Family History
The comprehensive pediatric orthopaedic history includes The information sought in the family history should be
questions that are not normally asked as part of routine relevant to the patient’s present illness and appropriate to
history taking in adult patients. A history of the mother’s the patient’s age. The age and health, or age and cause of
pregnancy, the neonatal period, the child’s neurologic devel- death, of parents and siblings may be pertinent. Relevant
opment, and the family history often have a much greater health information about other relatives that may have an
impact on the subsequent physical examination and diagnosis impact on the patient’s complaint should also be obtained.
in children than in adults. An outline of pertinent historical The presence of scoliosis, clubfeet, developmental dysplasia
features included in the initial history and physical examina- of the hip, skeletal dysplasias, repeated fractures, genetic
tion used at Texas Scottish Rite Hospital for Children in Dal- conditions, and neuromuscular disorders in family members
las is presented in Chapter 3 (see Appendix 3.1). should be specifically obtained.
Prenatal History
History of Present Illness
During the first trimester of pregnancy, embryogenesis
Next the examiner should develop a clear, chronologic (development of the embryo) and organogenesis (genera-
narrative of the present problem, including its onset, tion of the early organ systems during the end of the embry-
the setting in which it developed, its manifestations, and onic period of gestation) proceed at a rapid rate. By the end
any previous treatments. The principal symptoms should of the embryonic period, all the major body systems have
be described according to their location, quality, quan- been established and the principal body structure is com-
tity or severity, timing (onset, duration, frequency), set- plete. Any extrinsic interruption of normal organogenesis
ting, aggravating or relieving factors, and any associated during the embryonic period can result in significant mal-
manifestations. formations (e.g., myelomeningocele, syndactyly, preaxial
Because the musculoskeletal system is involved with sup- polydactyly). Thus any unusual incident during this period
port and locomotion, many related symptoms are caused by may be of clinical significance.
physical stress and motion. Thus it is important to deter- • Was there any history of vaginal bleeding to indicate
mine whether the patient’s symptoms are related to physi- threatened abortion?
cal activity. If the patient has any history of injury, details of • Did the mother have any infections during the first tri-
22
ERRNVPHGLFRVRUJ
CHAPTER 2 The Orthopaedic History 23
diabetes mellitus during this period? noted? How was it treated (observation at home, obser-
• These conditions are also associated with a high inci-
vation in the hospital, phototherapy, or exchange transfu-
dence of abnormalities in the newborn. sion)? When did it disappear?
• Did the mother have genital herpes or herpes simplex?
• Was there any asymmetry of the face or limbs?
medications that could harm the fetus? Specifically, is • Were there any infections, injuries, or evidence of trauma?
there a history of illicit drug use or alcohol abuse during • Was the infant’s muscle tone flaccid, tight, or normal?
the pregnancy? • What was the nature of bonding with the mother?
dominal wall was struck or in which there was excessive • Did the newborn have to be tube fed?
blood loss with critical lowering of her blood pressure? • When was the infant discharged from the hospital? Did
in prolonged labor, resulting in a greater potential for toy, and transfer objects from hand to hand?
anoxic episodes and other fetal distress. • When did the child offer his or her arm for a coat or foot
The condition of the newborn during the neonatal period is • When did the child begin to show an interest in picture
particularly important in children with congenital disorders books and recognize familiar objects?
or neurologic impairments. • At what age was the child able to speak a few words, and
• How long did it take for the infant’s first breath and first
when did he or she achieve three-word sentences?
cry? What was the nature of the cry? • The examiner should also inquire about the following:
quire any time in an incubator? Was oxygen provided? • Age of toilet training (stool and urine)
Did the infant need to be intubated or otherwise resusci- • When hand dominance was noted
when first seen by the parents? and what characterizes his or her scholastic perfor-
• Was there any cyanosis?
mance
ERRNVPHGLFRVRUJ
CHAPTER 3
Angular Deformity
Chapter Contents The clinician first needs to know and recognize the normal
Recognizing Deformities 24 alignment and deviations of the limbs of the growing child.
Infants usually appear to have bowed and internally rotated
Range of Motion 24
lower extremities which gradually straighten with growth.
Muscle Strength 38
Parents need education and reassurance relative to normal
Neurologic Assessment 39
deviations, and clinicians need to recognize more significant
deviations from normal.
Alignment deviations in the coronal plane are described
as valgus, in which the apex of angulation points to the mid-
This chapter covers many aspects of the general musculo- line, and varus, in which the apex points away from the mid-
skeletal and neuromuscular examination of the neonate, line (Figs. 3.1 and 3.2). Thus, “knock knee” is called genu
infant, child, and adolescent. Because proper function valgus and the term for bowlegs is genu varus (Fig. 3.3).
of the musculoskeletal system depends on proper func- Deviations in the sagittal plane are termed procurvatum in
tioning of the neurologic system, the boundary between which the apex of the bow is anterior and recurvatum with
orthopaedics and neurology is often blurred at the diag- the angulation pointing posteriorly (Fig. 3.4).
nostic level. While some children present to the orthopae- Most clinicians describe angulation by a visual estimate.
dic team with obvious deformities or disabilities, a great A hinged goniometer may be used for greater accuracy.6,48,56
many children come in for minor deviations which are Clinical photographs are especially useful to determine if
concerning to parents, and sometimes especially grand- deformities are improving or worsening over time.
parents. Many of these can be easily diagnosed as normal So-called “normal” alignment variations have been stud-
variations, but the clinician must be able to recognize and ied extensively.3,17,49 With the elbow in full extension, the
accurately describe findings which may be indicators of angle at the elbow, called the carrying angle, is approxi-
more serious problems. It is especially imperative that mately 15 degrees of valgus.3 Normal variations range from
the examiner be familiar with the normal sequence of a near zero degrees of valgus to 20 degrees or more. Mal-
neuro-developmental milestones which occur through- united elbow fractures often result in a varus deformity.
out childhood. It is also the obligation of the orthopaedic The lower extremity alignment in infancy is usually 10 to 15
practitioner to fully evaluate the child in order to recog- degrees of varus angulation. Between ages 14 and 22 months
nize symptoms and signs of syndromic disorders which the knee is usually straight, or at zero degrees of angulation. By
may have been missed by others. age 3 there is approximately 10 to 15 degrees of valgus angula-
tion. This angulation decreases such that by age 7 or 8 the adult
alignment of 5 to 7 degrees of valgus has been reached.17,49
Recognizing Deformities Most clinicians describe angulation as visual estimates,
and for greater accuracy a hinged goniometer may be used.
The examination of a child begins with an overall Clinical photographs are very useful to determine if defor-
assessment. While beyond the scope of this chapter, mities are improving or worsening over time.
abnormalities of any part of the body may give clues
to an orthopaedic diagnosis. Examples are numerous
and include facial features of osteogenesis imperfecta, Range of Motion
the body habitus of Marfan syndrome, or the café o
lait skin lesions of neurofibromatosis. Musculoskeletal Joint motion is judged in several ways (Box 3.1). First, pas-
abnormalities may present with asymmetries of body sive range is recorded, and a number of conditions may influ-
proportion, abnormalities of gait, visible angular defor- ence the evaluation of actual joint motion. When the patient
mities, and missing parts. The examiner should strive has a neurologic abnormality such as spasticity, the rate with
for accuracy and specificity in making a description of which the joint is moved alters the response of the oppos-
findings. ing muscle. If the joint is moved quickly, the spastic muscle
will fire quickly limiting that motion. If moved slowly, the
joint motion will be greater. Another type of neuromuscu-
The author wishes to acknowledge the contribution of John G. Birch lar dysfunction produces rigidity in which movements in all
for his work in the previous edition version of this chapter. directions are limited by opposing muscle firing.
24
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 25
ERRNVPHGLFRVRUJ
26 SECTION I Disciplines
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 27
180°
180°
180°
90° 90°
90°
A 0°
B C
0° 0°
FIG. 3.5 Total shoulder motion is a combination of scapulothoracic and glenohumeral movement. Stabilizing the scapula (A) allows the ex-
aminer to assess glenohumeral motion (B). Leaving the scapula free allows the examiner to assess total shoulder motion (C). Scapulothoracic
motion is responsible for the difference between the motion measured in B and C. (Adapted from Committee for the Study of Joint Motion.
Joint Motion: Method of Measuring and Recording. Chicago: American Academy of Orthopaedic Surgeons; 1965.)
0° 0°
90°
40°
forearm is the indicator of motion (Fig. 3.9A). The normal external rotation, the shoulder is moved superiorly toward
range of internal shoulder rotation is 50 to 60 degrees (the the ceiling, with the average external rotation approximately
chest wall blocks its motion), and the normal range of exter- 100 degrees.
nal shoulder rotation is 40 to 45 degrees. There are a number of quick and easy methods of clini-
Shoulder rotation may also be assessed with the neutral cally estimating active shoulder range of motion. To mea-
zero position of the shoulder at 90 degrees of elevation and sure shoulder elevation, the patient should stand with
90 degrees of abduction, and with the forearm parallel to elbows straight and forearms fully supinated, and then raise
the floor (see Fig. 3.9B). In internal rotation, the arm is both arms vertically and touch the fingers over the head
moved inferiorly toward the floor, with the average internal (Fig. 3.10A). To measure horizontal abduction and exter-
rotation approximately 70 degrees. Restricted internal rota- nal rotation, the patient should place both hands behind
tion in this position may be due to shoulder instability.23 In the neck and push the elbows posteriorly (see Fig. 3.10B).
D o w n l o a d e d f o r T i m e C e a l ( j i n z h a o
F o r p e r ERRNVPHGLFRVRUJ
s o n a l u s e o n l y . N o o t h e r
28 SECTION I Disciplines
The Elbow
The elbow is a joint with both a hinge component between
the humerus and the radial head and the ulna, and a rotary
component between the capitellum and the radial head (Fig.
0° 3.11).2,9 The hinge component allows flexion to around 160
FIG. 3.7 Abduction and adduction of the shoulder in the horizontal degrees and extension to neutral or zero degrees. In some
plane from the midsagittal zero position of the body. individuals hyperextension to 10 or 15 degrees is found.8,59
90°
20° 2:1
A B C
180°
120°
D E
FIG. 3.8 (A) When the shoulder is elevated, the first 20 degrees of movement represents pure glenohumeral joint motion; the scapula does
not move. (B) From this point, continued elevation of the arm results in combined movement of the glenohumeral and scapulothoracic
articulations in a 2:1 ratio. (C) When the scapula is immobilized, pure glenohumeral elevation is approximately 90 degrees. (D) At approxi-
mately 120 degrees of combined shoulder elevation, the surgical neck of the humerus abuts the acromion process. (E) Complete elevation
of the shoulder (i.e., 180 degrees) is a combined glenohumeral and scapulothoracic movement and is made possible by external rotation
of the shoulder, which turns the surgical neck of the humerus away from the tip of the acromion and increases the articular surface of the
humeral head.
ERRNVPHGLFRVRUJ
90°
45°
0°
0°
45° 45°
45°
90° 90°
A B
90°
FIG. 3.9 (A) Internal and external rotation of the shoulder measured with the arm at the side of the body. Normal range of internal rotation
is 50 to 60 degrees; normal range of external rotation is 40 to 45 degrees. (B) Internal and external rotation measured with the shoulder
in neutral zero position at 90 degrees of elevation and 90 degrees of abduction (i.e., the forearm is parallel to the floor). Internal rotation
moves the arm inferiorly toward the floor; external rotation moves the shoulder superiorly toward the ceiling.
A B C
D E F
FIG. 3.10 Quick method of clinically assessing active shoulder range of motion. (A) Elevation of both shoulders. (B) Horizontal abduction
and external rotation. (C) Adduction and internal rotation. (D) Extension, internal rotation, and adduction. (E) Elevation, internal rotation,
and adduction. (F) Extension, adduction, and internal rotation.
ERRNVPHGLFRVRUJ
30 SECTION I Disciplines
90° 90°
150° 150°
30°
180° 0° 180° 0°
Neutral Neutral
15°
Hyperextension
0°
90° 90°
0°
Supination Pronation
FIG.. 3.13 Assessment of lateral bending of the cervical spine.
FIG. 3.12 Supination is turning of the palm forward or anteriorly,
such that the palm faces up. Pronation is turning of the palm back- over the midline. Head motions are termed tilt, or lateral
ward or posteriorly, such that the palm faces down.
bending (Fig. 3.13) as the ear approaches the shoulder in
the coronal plane, rotation as the head moves in the horizon-
The Forearm tal plane with the chin approaching the shoulder (Fig. 3.14),
flexion and extension as the chin moves toward and away
The rotary motion of the forearm is termed pronation as from the sternum in the sagittal plane (Fig. 3.15). Right and
the hand is rotated to the palm down position. The opposite left tilt occur to around 50 degrees, right and left rotation
motion of turning the hand upward is termed supination. to 90 degrees, and flexion usually allows the chin to touch
This motion of the forearm involves the humerocapitellar the sternum and extension to approximately 70 degrees.b
joint, the proximal radioulnar joint, and the distal radioulnar The vertebral levels involved in cervical motions are noted
joint. The neutral position is when the palm is parallel to the in Boxes 3.2 and 3.3.
sagittal plane, and pronation usually reaches 80 degrees and
supination 90 degrees (Fig. 3.12).5,24,55
Motion of the Spine
The Cervical Spine Spinal motion occurs through the many interverte-
bral joints, and specific motion levels are difficult to
In the neutral position the head is level with the ears parallel
to the ground, the orbits facing ahead, and the chin centered bReferences 1, 12, 13, 14, 30, 43, 44.
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 31
0°
Left Right
rotation rotation
90° 90°
0°
Extension Flexion
Occiput to C5: Flexion is coupled with rotation. grees.19,25,28,51,57 The neonatal hip also has more external
C5–7: Extension is combined with rotation.
rotation than internal rotation.19,25 By 4 to 6 months of
Upper cervical spine: Lateral bending goes in opposite age, the hip and knee usually can be extended to neu-
direction of rotation. tral positions, and by 1 year of age, the hip flexion con-
Lower cervical spine: Bending goes in same direction as tracture and excessive external rotation have gradually
rotation.
resolved.10,45
ERRNVPHGLFRVRUJ
32 SECTION I Disciplines
FIG. 3.19 In the double inclinometer test for lumbar extension, one
inclinometer is placed over the midsacrum and the other is placed
FIG. 3.17 Visual inspection of thoracolumbar flexion. Normal
over T12. With the patient in maximum extension, the degree of
lumbar lordosis disappears with flexion and a slight lumbar kyphosis
extension is obtained by subtracting the sacral inclinometer reading
is seen. When the patient is at maximum flexion, the examiner meas-
from the reading of the T12 inclinometer.
ures the distance between the patient’s fingertips and the floor.
T12
Midsacrum
Newborns also have a greater range of hip rotation (aver- Hip range of motion is usually first measured in the supine
age, 170 degrees19) than children 1 year of age or older (aver- position. The examiner stabilizes the pelvis with a hand over
age range, 90–100 degrees). This increase in hip rotation the anterior superior iliac spines. The examiner’s hand cre-
may be due to the associated flexion contracture, insofar as ates a reference line for the position of the lower extremity,
rotation is greater when the hip is flexed. With increasing especially in the coronal plane. The contralateral hip is fully
age, hip rotation decreases by 15 to 20 degrees each decade flexed to flatten the lumbar spine, and the hip being exam-
during the first 20 years, and by approximately 5 degrees ined is in the zero or neutral position when the leg remains
per decade thereafter. Hip abduction decreases on average flat on the exam surface. The hip is flexed until the pelvis
by 10 to 15 degrees per decade for the first 20 years. starts to tilt and that degree is the recorded maximal flexion,
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 33
usually around 120 (Fig. 3.23). The degree of extension is neutral positions, and by 1 year of age the hip flexion contrac-
determined by the Thomas test in which the contralateral hip tures and excess external rotation have gradually resolved.
is maximally flexed and the degree to which the examined Hip rotation in flexion is measured supine with the hip
hip lifts from the surface is the degree of flexion contrac- and knee flexed to 90 degrees (Fig. 3.27). Moving the foot
ture (Fig. 3.24). To measure for hyperextension the patient away from the patient measures internal or medial rotation.
is placed prone and the lower extremity is lifted until the Moving the foot toward the midline measures external or
pelvis starts to rise, and that is the degree of hyperextension. lateral rotation. Hip rotation in extension is measured prone
Hip flexion contracture may also be measured in the prone with the knee flexed to 90 degrees (Fig. 3.28). Internal or
position, and the degree of flexion contracture is the degree medial rotation is done by moving the foot away from the
of flexion noted when the lumbar lordosis starts to increase midline, while external or lateral rotation is done by moving
as the limb is raised toward neutral (Figs. 3.25 and 3.26).52 the foot toward the midline.
The normal range of motion for children of all ages has been Hip abduction is measured supine with a hand on the
published by many authors. Newborn babies usually have hip anterior superior spines of the pelvis to determine the
flexion contractures up to around 30 degrees. The neonatal neutral or zero position (Fig. 3.29). The lower extremity
hip also has more external rotation than internal rotation. By is moved laterally to measure abduction, and moved medi-
4 to 6 months of age the hip and knees can be extended to ally under the other lower extremity to measure adduction.
Both hips moved laterally measures combined abduction
and can elicit differences between the two. Hip abduction
may also be determined with the hips and knees flexed to
90 and the knees moved apart, taking care to keep the pelvis
level (Fig. 3.30).
Hip adduction can be assessed by passing the examined
leg over the opposite leg (Fig. 3.31).
45°
0° 0°
45°
Table 3.1 Normal Range of Hip Motion in Children at Different Ages (in Degrees).
Age
Motion Newborn 4 Years 8 Years 11 Years
Flexion 128 ± 4.8 150 ± 12.5 146 ± 11.3 138 ± 14.5
ERRNVPHGLFRVRUJ
34 SECTION I Disciplines
Trendelenburg Test and to hold that posture for 10 seconds. The patient
The Trendelenburg test is an important evaluation of hip should not use a hand for support. A positive Tren-
function. It is based on the concept that normal stance delenburg sign is present when the pelvis drops as the
and gait require a biomechanical couple of abductor and standing hip adducts. In a negative test the pelvis either
extensor muscle function acting on an anatomically cor- stays level or elevates slightly. Each side is tested in turn
rect hip and proximal femur. The examiner should con- (Fig. 3.32).
sider that when a person lifts one foot to take a step, the
entire body weight is being held up by the contralateral
muscle complex which is affixed to the pelvis on one side
and upper femur on the other. Weakness of the relevant
muscles, anatomic abnormalities of the femur or acetabu-
lum, or painful conditions of the hip may disrupt this A
function.
To perform the test the examiner stands behind the
patient and should be able to see the pelvis and dimples
of the posterior iliac spines. The patient is asked to lift
one foot off the floor by flexing the hip and the knee, B
C
FIG. 3.24 The Thomas test. (A) In the supine position, normal
lumbar lordosis is present in fully extended hips. (B) If flexion
contracture is present, the legs still lie on the examining surface,
but there is increased lumbar lordosis. (C) The Thomas test is per-
formed by first flexing both hips until the lumbar spine is flattened,
then extending the affected hip. The amount of flexion contracture
is represented by the angle between the thigh and the examining
surface.
30°
0° FIG. 3.25 The amount of hip flexion deformity can also be deter-
mined with the patient prone. The pelvis is stabilized, the patient’s
thigh is raised toward the ceiling, and the tested hip is extended.
FIG. 3.23 Normal range of hip flexion. Normal extension is 30 degrees.
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 35
A provocative version of the test is to have the patient The Ober test is used to detect an abduction contracture
hold the elevated leg for a minute. When this produces a of the hip (Fig. 3.34). With the patient lying on one side,
positive test it is termed a “delayed” positive Trendelen- the down hip and knee are maximally flexed. The upper
burg test. Another method to discover mild weakness hip is flexed to 90 degrees with the knee flexed to 90 as
is for the examiner to press down on the contralateral well. The hip and knee are then abducted fully, and then
shoulder while the patient is holding the extremity up extended fully. The examiner then allows the hip to adduct
(Fig. 3.33). toward a neutral position. A normal hip will adduct to neu-
The gait abnormality which accompanies this test is tral, while an abduction contracture will block the adduc-
termed a Trendelenburg gait. In the classic gait, the com- tion. The degree of remaining adduction is the degree of the
pensated Trendelenburg gait, the patient leans over the hip abduction contracture.
laterally in stance phase to stabilize the hip. In the uncom-
pensated version the patient does not lean over but allows
the pelvis to drop markedly on the opposite side. A slight
drop of the pelvis in midstance is part of normal gait. 0°
External Internal
rotation rotation
20°
FIG. 3.26 The degree by which the hip fails to reach neutral posi- FIG. 3.28 Rotation of the hip in extension is assessed with the
tion is the degree of deformity. patient prone and the knee flexed 90 degrees.
90° 90°
45°
90° 90°
45°
0°
0° 30°
FIG. 3.29 Abduction of the hip. The child is placed supine with the
FIG.. 3.27 Rotation of the hip in flexion is assessed with the patient pelvis held in a fixed position by abducting the opposite hip and
supine and the hip and knee flexed 90 degrees. steadied by the examiner’s hand.
ERRNVPHGLFRVRUJ
36 SECTION I Disciplines
The Ankle
The ankle is a hinge joint and is in the neutral position
when the foot is perpendicular to the tibia. Moving the foot
upward is termed dorsiflexion and downward is plantar
0°
A Normal B Positive
FIG. 3.32 Trendelenburg test. (A) Normal; Trendelenburg sign is
not elicited. (B) Positive test; Trendelenburg sign is elicited.
90°
FIG. 3.30 Hip abduction assessed with the patient’s knees and hips
in 90 degrees of flexion.
ERRNVPHGLFRVRUJ
CHAPTER 3 The Orthopaedic Examination: A Comprehensive Overview 37
A B
C D
E
FIG. 3.34 Ober test for determining the presence and degree of abduction contracture of the hip. (A) The lumbar spine is flattened by acute
flexion of the hip below. (B) Flex the hip 90 degrees. (C) Abduct the hip fully. (D) Extend the hip. (E) Adduct the hip maximally; note the
20-degree abduction contracture.
Flexion
20°
50°
FIG. 3.36 Measurement of dorsiflexion and plantar flexion of the
FIG. 3.35 Assessment of knee range of motion. ankle.
ERRNVPHGLFRVRUJ
38 SECTION I Disciplines
0° 0°
Inversion Eversion
FIG. 3.37 Zero starting position for testing foot motion. The
patient is prone, the knee is flexed, and the ankle is in gentle dor-
siflexion. (Reproduced from Greene WB, Heckman JD. The Clinical
A B
Measurement of Joint Motion. Rosemont, IL: American Academy of
Orthopaedic Surgeons; 1994.)
FIG. 3.38 Assessment of inversion (A) and eversion (B) of the ankle.
(Reproduced from Greene WB, Heckman JD. The Clinical Measure-
The Foot ment of Joint Motion. Rosemont, IL: American Academy of Ortho-
The subtalar or talocalcaneal joint is a complex joint with a paedic Surgeons; 1994.)
sliding, rotating type of movement. It is tested by holding
the heel in one hand, with the foot slightly dorsiflexed. The
examiner tilts the heel inward to produce inversion, and tilts
the heel outward to produce eversion (Fig. 3.38). Deformi-
ties, or fixed positions in these directions are termed varus
and valgus.
Supination and pronation are more complex, and some-
what confusing, terms for a more global foot motion (Fig.
3.39). The foot is grasped at the midfoot and is tilted and
rotated inward and plantar flexed to produce supination.
To produce pronation the foot is tilted outward and rotated
laterally, with some ankle dorsiflexion.
The motions of the midfoot involve the talonavicular,
calcaneocuboid, naviculocunieform, and tarsometatarsal
joints.24,35,37 The predominant motions are abduction and
adduction which are horizontal motions away from and 0° 0°
toward the midline in a standing position. There is a small A B
Supination Pronation
amount of rotation in these joints as well, with downward (inversion, adduction, (eversion, abduction,
rotation of the first metatarsal toward the ground being and plantar flexion) and dorsiflexion)
pronation and rotation upward and laterally being part of FIG. 3.39 Assessment of supination (A) and pronation (B) of the
supination. ankle. (Reproduced from Greene WB, Heckman JD. The Clinical
Distally, the toes flex downward at the metatarsopha- Measurement of Joint Motion. Rosemont, IL: American Academy of
langeal joints, and extend upward at the same joints. Each Orthopaedic Surgeons; 1994.)
of these joints will also abduct away from the midline and
adduct toward the midline to a small degree, with the great examiner can get a great deal of information quickly and
toe having the greatest degree of mobility. The interphalan- efficiently.11,29,31
geal joints of the toes allow only flexion and extension. There are two basic ways to examine a specific mus-
cle. The static test is done by having the patient hold
the extremity in one position and the examiner tries to
Muscle Strength move the joint. The examiner estimates whether the
amount of resistance was in the normal range or not. For
In almost every examination the practitioner will need to example the examiner may ask the patient to hold the
evaluate the child’s muscular strength (Tables 3.2 and 3.3). arms elevated to horizontal and not allow the examiner
The needs range from determining overall fitness to eval- to move the arms in any direction. In the lower extremity
uating individual muscles and patterns of weakness, and the examiner tells the patient to extend the knee and not
the patients range from premature newborns to skeletally allow it to be flexed.
mature adolescents. The more specific examination will A more sensitive examination is the dynamic or kinetic
test the majority of muscle groups and the experienced exam. The patient is asked to move the joint through the
ERRNVPHGLFRVRUJ
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sen, jota sanotaan elämäntehtäväksi. —"
"Kaikesta siitä mitä minulla on, kiitän teitä, — kiitän teitä vaan!"
virkkoi Helvi lämpimästi ja salataksensa mielenliikutustaan kääntyi
hän nopeasti taloon vievälle puistotielle.
Suurin osa siitä opista, jota hän koulun penkillä oli päähänsä
puinut, näytti niin tuiki tarpeettomalta, tyhjältä. — — Sen sijaan että
sielläkin olisi opastettu kaikkeen siihen, elävään välttämättömyyteen,
innostutettu suuriin aatteisiin, hyviin töihin ja käytännöllisyyteen,
pantiin pääpaino kuolleisiin, homehtuneisiin numeroihin ja
ijänikuisten tapausten häirähtämättömään muistamiseen, joista henki
ei kohonnut, eikä järki avartunut.
Miksei ollut kotikaan antanut hänelle niitä aatteita, joita hän oli
tietämättään janonnut?
(Koskenlaskijan morsiamet).
"Petturi!"
"Kätke kaikkien katseilta se, joka kirveltää, moni muu ennen sinua
on tehnyt niin…"
Sydänmaan rakkautta.
"No ei sinne niin pitkä matka ole", vastasi hän sitten lapselle,
yhtäkkiä rohkaistuen ja ottaen tämän syliinsä.
"Anna toki pojan istua… Tämähän on niin hyvä poika tämä pikku
Kaapro."
Tuskin oli Jaakko päässyt ovesta ulos, kun kalvava kaiho täytti
hänen rintansa ja hän olisi tahtonut jälleen lämpimään, armaaseen
tupaan katselemaan Hiljaa ja pitelemään poikaa polvillansa…
*****
Sitten alkoi siellä ja täällä kuulua lisäksi ääniä, että isäntä aikoo
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oli Kaapro Kalposen kuoleman viesti saapunut, — tunsi hän suurta
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*****
Miina.
Miinalla oli tapana iltasin, kun tupa oli lämmitetty ja pelti pantu
kiinni, lähteä sukanneuleineen vähäksi aikaa kylään "häkää pakoon."
Niitä varten pani Miina aina oluen, keitti lämpimät ruuat ja kahvin
— ja jos sattui olemaan jouluinen aika, saattoi hänellä toisinaan olla
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