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Conditions in Occupational Therapy Effect On Occupational Performance 5Th Edition PDF Full Chapter PDF
Conditions in Occupational Therapy Effect On Occupational Performance 5Th Edition PDF Full Chapter PDF
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Professor
Department of Occupational Therapy
Western Michigan University
Kalamazoo, Michigan
Ben J. Atchison
Diane Powers Dirette
American Psychiatric Association. (2013). Diagnostic and statistical
manual of mental disorders (5th ed.). Washington, DC: Author.
National Board for Certification of Occupational Therapists. (2012).
Practice analysis of the occupational therapist registered: Executive
summary. Gaithersburg, MD: Author.
Contributors
Preface
1 Thinking Like an OT
Index
Glossary
CHAPTER
1 Thinking Like an OT
Diane Powers Dirette Ben J. Atchison
KEY TERMS
Altruism
Client factors
Context and environment
Core values
Equality
Evidence-based practice
Freedom
Justice
Occupations
Performance patterns
Performance skills
Personalized medicine
Person-first language
Philosophical assumptions
Practice Framework
Prudence
Truth
It is more important to know what kind of person has the disease than what kind of disease the
person has.
—Sir William Osler (Address at Johns Hopkins University, February 1905)
These values are the foundation of the belief system that occupational
therapists (OTs) use as a moral guide when making clinical decisions.
Philosophical Assumptions
The philosophical assumptions of the profession guide OTs in providing
client-centered therapy that meets the needs of the client and society. These
assumptions express our basic beliefs about the client and the context in
which the client functions (Mosey, 1996). These assumptions are as
follows:
Pediatric Conditions
The Pediatric Conditions Unit includes the most common conditions that
children have who are treated by occupational therapists as determined by
the National Board of Certification in Occupational Therapy. These
chapters focus on conditions that are typically diagnosed in childhood, but
many of them affect people throughout their lifespan. Each chapter
provides information about the etiology, incidence and prevalence, signs
and symptoms, course and prognosis, diagnosis, medical/surgical
management, and impact on occupational performance of these conditions.
Case illustrations are used to provide examples of lives affected by the
condition. The conditions included in this unit are the following:
Chapter 2: Cerebral Palsy
Chapter 3: Autism Spectrum Disorders
Chapter 4: Intellectual Disability
Chapter 5: Muscular Dystrophy
Chapter 6: Attention Deficit Disorder/ADHD
Chapter 7: Sensory Processing Disorder
CHAPTER
2 Cerebral Palsy
Mary Steichen Yamamoto
KEY TERMS
Ataxia
Athetoid (dyskinetic)
Clonus
Contracture
Diplegia
Dysarthria
Equinovarus
Equinovalgus
Gastroesophageal reflux
Hemiplegia
Homonymous hemianopsia
Hydrocephalus
Hypertonicity (spasticity)
Hyperreflexia
Hypotonicity
Kyphosis
Lordosis
Nystagmus
Primitive reflexes
Quadriplegia
Scoliosis
Strabismus
Stretch reflex
A couple who had been trying to conceive a child for several years were
thrilled when a family friend asked if they would be interested in adopting
a baby girl that had just been born to a young unmarried woman in her
church. The baby was born 6 weeks early and her weight was 4 lb, but she
appeared to be healthy. After initiating the paperwork for a private
adoption, they brought the baby home and named her Jill. By the time of
Jill’s 6-month well-baby visit, her parents had become concerned. She
appeared to be a bright baby who smiled and cooed and enjoyed reaching
for and playing with toys, but her legs seemed stiff and she was not yet
rolling over. They spoke with their family doctor about their concerns, but
he assured them that Jill was developing normally and they had nothing to
be concerned about. By the time of Jill’s 9-month well-baby visit, her
parents’ concerns were only growing. Jill was still not sitting up and had
not yet learned to roll over or crawl. Her doctor decided to refer Jill to the
county early intervention program for a developmental assessment. Jill was
assessed by the early intervention team consisting of an occupational
therapist, physical therapist, and speech and language pathologist. The
occupational therapist noted some mildly increased tone and incoordination
in her upper extremities and a 2- to 3-month delay in fine motor and self-
help skills. The physical therapist noted that Jill had hypertonicity and
retained primitive reflexes in her lower extremities, which was causing
significant delay in the acquisition of gross motor skills. The speech and
language therapist found Jill’s cognitive, language, and social skills to be at
age level. The team suggested to the parents that they have a pediatric
neurologist assess Jill, as she was demonstrating some of the signs and
symptoms of cerebral palsy. Both the occupational and physical therapist
recommended that therapy services begin as soon as possible. An IFSP
(Individualized Family Service Plan) was developed at a subsequent
meeting, and Jill began receiving weekly physical and occupational therapy
services.Jill’s parents took her to a pediatric neurologist who diagnosed her
with spastic diplegia, a type of cerebral palsy. Her parents were initially
overwhelmed and devastated by the diagnosis. The next year was very
difficult as they grieved the loss of so many dreams that they had for Jill
and faced so much uncertainty about her future. They waded through an
array of possible therapy approaches and medical and surgical
interventions that were recommended trying to decide which would be right
for Jill and their family. They struggled to find time to work on home
exercises that had been prescribed for Jill. The strain became so great that
they even separated for a period but eventually reconciled. By the time Jill
turned 3 years old, she was walking with a walker and able to sit in a chair
independently, although she needed assistance with changing positions. She
was feeding herself but not yet dressing herself. They enrolled her in a
preschool special education classroom where she received therapy services.
By kindergarten, Jill was in a regular education classroom with a
paraeducator for safety and support. Jill was a happy child, who had many
friends and did well academically. Jill most likely will continue to need
some type of additional support in order to be an independent adult, but all
involved were optimistic about her future.
Description and Definition
Sigmund Freud, in his monograph entitled “Infantile Cerebral Paralysis,”
points out that a well-known painting by Spanish painter Jusepe Ribera
(1588–1656), which depicts a child with infantile hemiplegia, proves that
cerebral paralysis existed long before medical investigators began paying
attention to it in the mid-1800s (Freud, 1968). Freud’s work as a
neurologist is not generally well known, and at the time that his monograph
was published in 1897, he was already deep into his work in the area of
psychotherapy. However, he was recognized at the time as the prominent
authority on the paralyses of children. Today, cerebral paralysis is known as
cerebral palsy.
Cerebral palsy is not one specific condition but rather a grouping of
clinical syndromes that affect movement, muscle tone, and coordination as
a result of an injury or lesion of the immature brain. It is not considered a
disease, but is classified as a developmental disability since it occurs early
in life and interferes with the development of motor and sometimes
cognitive skills. Historically, cerebral palsy has been classified as and is
still sometimes diagnostically referred to as a static encephalopathy
(Brooke, 2010). This is now considered inaccurate due to recognition of the
fact that the neurological manifestations of cerebral palsy often change or
progress over time. Static encephalopathy is permanent and unchanging
damage to the brain and includes other developmental problems such as
fetal alcohol syndrome, cognitive impairments, and learning disabilities.
Many individuals with cerebral palsy perform well academically and
vocationally without any signs of cognitive dysfunction associated with the
term encephalopathy (Johnson, 2004).
A child is considered to have cerebral palsy if all of the following
characteristics apply:
The injury or insult occurs when the brain is still developing. It can
occur anytime during the prenatal, perinatal, or postnatal periods. There is
some disagreement about the upper age limit for a diagnosis of cerebral
palsy during the postnatal period. An upper age limit ranging from 2 to 8
years of age is applied to postneonatally acquired brain injury (Smithers-
Sheedy et al., 2009).
1. It is not progressive. Once the initial insult to the brain has occurred,
there is no further worsening of the child’s condition or further
damage to the central nervous system. However, the characteristics
of the disabilities affecting an individual often change over time.
2. It always involves a disorder in sensorimotor development that is
manifested by abnormal muscle tone and stereotypical patterns of
movement. The severity of the impairment ranges from mild to
severe.
3. The sensorimotor disorder originates specifically in the brain. The
muscles themselves and the nerves connecting them with the spinal
cord are normal. Although some cardiac or orthopedic problems can
result in similar postural and movement abnormalities, they are not
classified as cerebral palsy.
4. It is a lifelong disability. Some premature babies demonstrate
temporary posture and movement abnormalities that look similar to
patterns seen in cerebral palsy but resolve typically by 1 year of age.
For children with cerebral palsy, these difficulties persist.
Etiology
Historically, birth asphyxia was considered the major cause of cerebral
palsy. When the British surgeon William Little first identified cerebral
palsy in 1860, he suggested that a major cause was a lack of oxygen during
the birth process (Little, 1862). In 1897, Sigmund Freud disagreed,
suggesting that the disorder might have roots earlier in life. Freud wrote,
“Difficult birth, in certain cases is merely a symptom of deeper effects that
influence the development of the fetus” (Freud, 1968). Although Freud
made these observations in the late 1800s, it was not until the 1980s that
research supported his views (Freeman & Nelson, 1988; Illingsworth,
1985). Only a small percentage of cases of cerebral palsy are a result of
birth complications. The majority of children (70% to 80%) who are
diagnosed with cerebral palsy have congenital cerebral palsy, that is, the
injury to the brain occurred prior to their birth (Johnson, 2004).
There are a large number of risk factors that can result in cerebral
palsy, and the interplay between these factors is often complex, making it
difficult to identify the specific cause (Blickstein, 2003). The presence of
risk factors does not always result in a subsequent diagnosis of cerebral
palsy. The presence of one risk factor may not result in cerebral palsy
unless it is present to an overwhelming degree. Current thought is that
often two or more risk factors may interact in such a way as to overwhelm
natural defenses, resulting in damage to the developing brain. The strongest
risk factors are prematurity and low birth weight (Lawson & Badawi,
2003). During the postpartum period, premature and low birth weight
infants are at greater risk for developing complications, especially in the
circulatory and pulmonary systems. These complications can lead to brain
hypoxia and result in cerebral palsy.
Additional risk factors include intrauterine exposure to infection and
disorders of coagulation (National Institute of Neurological Disorders and
Stroke, 2015). Maternal infection is a critical risk factor for cerebral palsy,
both during prenatal development and at the time of delivery. The infection
does not necessarily produce signs of illness in the mother, which can make
it difficult to detect. In a study conducted in the mid-1990s, it was
determined that mothers with infections at the time of birth had a higher
risk of having a child with cerebral palsy (Grether & Nelson, 1997). Table
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Fig. 343.-Morus alba ♀ inflorescence.
Fig. 344.—Morus nigra fruits.
A. Moreæ. The filaments are incurved in the bud. Leaves folded
in the bud—Morus (Mulberry) (Figs. 342–344). Monœcious. The
inflorescences are catkin-like in appearance, but in reality composed
of many small dichasia. The flowers are similar to those of the Nettle,
but with 2 carpels: in the ♂ with perianth 2 + 2, and stamens 2 + 2
(Fig. 342), in the ♀ , perianth 2 + 2, and 2 carpels in regular
alternation. The small drupes are enveloped by the perianth, which
eventually becomes fleshy, and as all the flowers on the axis very
accurately fit together, the collection of fruits is formed, which we call
a Mulberry (Fig. 344). The leaves are folded in the buds, and have
small stipules. The following are allied to Morus:—Maclura, Broussonetia (the
Paper-mulberry tree) which has spheroid ♀ inflorescences (made up of dichasia),
etc.
Dorstenia presents an interesting transitional form to the Fig in its flat, open,
and, in some instances, lobed inflorescence on which the ♂ and ♀ flowers are
sunk in grooves. Indications of a somewhat similar structure are found in certain
Nettles, the sympodial axes of the dichasia becoming flatly expanded. The fruits
are 1-seeded, but, nevertheless, spring open and eject their seeds.
B. Artocarpeæ. Filaments straight in the bud; foliage-leaves with
convolute vernation. An interpetiolar leaf-sheath (ocrea) formed in
the axil of each leaf by the connate stipules, covers the younger
leaves as a hood. It falls off as the leaf expands, and leaves a ring-
like scar on the stem.—Ficus (the Fig). The inflorescence (the so-
called syconus) has a pear-shaped, fleshy, but hollow axis, on the
interior surface of which the flowers are situated (Fig. 345). It is a
kind of capitulum, with a hollow receptacle, whose “involucral” leaves
close over the entrance to the interior; it is not, however, a simple
capitulum, but a coalescence of cymose inflorescences. The edible
parts are the fleshy stem-portion and perianth-leaves. The ♂-flower
has a 2–6 divided perianth, 1–2 (–6) stamens; the ♀-flower has an
oblique ovary. The fruits are drupes, with thin flesh.—Many species
have aerial roots, and some live as epiphytes on trees. Pollination, in the edible
Fig, is effected by a small Gall-wasp (Cynips psenes L.), which lays its eggs in the
Fig, and hence carries the pollen away. Even in very ancient times it was
customary to hang infected wild Figs on the branches of cultivated ones, so that
the young Gall-wasps, as they emerged, could immediately effect the pollination
(caprification). Ficus carica, and other species, have two kinds of ♀ -flowers,
besides the ♂-flowers. One kind has a short style and no stigmatic hairs, and it is
only in the ovaries of these that the wasps lay their eggs (gall-flowers); the other
kind has a long style and well-developed stigmatic-hairs, but the wasps cannot
reach their ovaries—these are “seed-flowers.” There are, moreover, two kinds of
plants of Ficus carica; ♀-plants, which have only seed-flowers, and bear the edible
Figs, and ♂ -plants (called “Caprificus”), which bear inedible fruits, and have ♂ -
flowers at the upper part of the Fig, but gall-flowers at the base. [The Caprificus, at
Naples, bears three crops of inedible Figs each year, viz. Mamme (April), Profichi
(June), Mamnoni (August). The ♂-flowers are produced especially in June, the first
Figs being almost entirely ♀ , and the last having but few ♂ -flowers. Each crop
produces a new generation of Fig-wasps. The female wasp enters the Figs on the
Caprificus, and lays one egg in each flower, with the result that the flower
developes into a kind of gall. The mother-wasp dies within the Fig. The male wasp
is wingless; it bites a small passage into the ovaries containing the female wasps,
and impregnates them; the female wasps then escape from the Fig, those in the
Profichi carrying pollen away with them as they pass out. They then enter another
Fig, lay their eggs, and die. The edible Fig-tree similarly has three crops in the
year, Fiori di fico, Pedagnuoli, Cimaruoli. The wasps, entering these Figs, are
unable to lay their eggs in the ovary, but, nevertheless, they effect cross-pollination
on entering the Pedagnuoli, which bear fertile seeds.]
Family 7. Curvembryæ.
The plants in this family have a curved ovule, and most frequently
a kidney-shaped seed (generally provided with fine, cuticular,
projecting warts, Fig. 362 B), with a curved, peripheral embryo
enclosing the endosperm which is most frequently floury (Figs. 362
C, 365 H; for exceptions, see Fig. 366); the seeds in all cases are
borne on a centrally-placed, and in most cases free, placenta (they
are “basal” when there is only 1 ovule in the ovary, Fig. 364). The
flower is regular, hypogynous or perigynous (Fig. 364) (only rarely
epigynous) and usually 5-merous. The flower which is most
complete has 5 whorls (S5, P5, A5+5, G2-3–5), as in some genera
of the Caryophyllaceæ (Figs. 360, 361); but from this type it
becomes reduced, the petals and stamens being suppressed, so
that finally 5 perianth-leaves, 5 stamens (opposite the perianth-
leaves), and 2 carpels (Fig. 361 F) only are present; for example, in