Professional Documents
Culture Documents
IMPERFECTA
CASE PRESENTATION
INTRODUCTION:
We have chosen a case of Osteogenesis
Imperfecta because of its rarity. Aside
from the fact that it is a congenital
disorder, there is also no known
treatment for the said disease.
Osteogenesis imperfecta (OI) is a
genetic disorder characterized by
bones that break easily, often from
little or no apparent cause. Abnormal
collagen composition leads to
brittleness, thus causing the incidences
of fracture higher than average.
A classification system of
different types of OI is commonly
used to help describe how severely a
person with OI is affected.
Prevalence of OI has shown that
6-7 per 100,000 people are affected by
osteogenesis imperfecta worldwide.
Osteogenesis imperfecta is listed as a
"rare disease" by the Office of Rare
Diseases (ORD) of the National
Institutes of Health (NIH).
PERSONAL DATA
Personal Data
• Name: J.M.E
• Age: 13y/o
• Date of Birth: April 20, 1996
• Birthplace: Sorsogon
• Address: 103 Arligue St. Quiapo , Manila
• Sex: Male
• Religion: Roman Catholic
• Nationality: Filipino
• Date of admission: November 5, 2009
History of
Present Illness
History of Present Illness
JME came in due to severe pain of the right
thigh from the moment he fell in a hole
until he was brought to Philippine
Orthopedic Center; he experienced pain
every time he moves his leg. Prior to
admission, the patient was walking home
from school at 1:00 in the afternoon; he
apparently stepped in an open manhole
and fell down. He was brought by his
father to Philippine Orthopedic Center
immediately and was admitted.
Past History
No known allergies to drugs
and foods. Patient JME is fully
immunized. He received 1 dose
of BCG, 3 doses of DPT, 3 doses
of OPV, 3 doses of Hepa B and 1
dose of AMV.
He had 3 previous
hospitalizations.
His first hospitalization was
last 2005 when he was 9 y/o at
Sorsogon Provincial Hospital.
The cause of his hospitalization
was when he fell down in a 4ft
tall niche. He was admitted at
Sorsogon Provincial Hospital
and was seen by Dr. De Castro.
He was fitted with 1½ Hip Spica
due to affection in his right
femur and hips
A year and a half after his first
hospitalization, he was rushed to the
Gubat Hospital due to seizure
episodes secondary to Tetanus. He
had stepped on a broken glass while
walking along the seashore. He
immediately washed it with
seawater. After 3 days, he developed
seizures without any accompanying
signs and symptoms. He was given 2
vials of anti-tetanus.
When he was 11 y/o, he was
hospitalized for the third time
when he slipped on a slippery
surface in their home. He was
brought to POC where he was
examined by Dr. Sy and was
diagnosed with Osteogenesis
Imperfecta.
Family History
Family History
Patient JME has a 39 year
old father and a 40 year old
mother. JME is the 6th child.
His father is a smoker and
always drinks alcohol while
his mother has only just
started to smoke. There is no
heredofamilial disease.
Psychosocial
History
JME is a Grade 4 student from Mabini
Elementary School and tells us of
having no friend and not good social
network. Hobbies include going out
and reading books. His considered
problems are schoolworks such as
projects and assignments and copes
up with stress by sleeping.
Of his parents he is more attached to
his mother and he considers his
mother as a support person.
Activities of
Daily Living
Activities of Daily Living
Activity Before During Analysis
Hospitalization Hospitalization
Fluid & >Drinks 10 glasses of >drinks 5 glasses of >His activities are
Nutrition water/day water/day limited, leading to
>drinks softdrinks >eats 3x a day less consumption of
(coke) and juice >still prefers to eat energy, then to a
(occasionally) but vegetables than meat feeling of full
prefers water >doesn’t take any appetite. With this
>prefers vegetables vitamins feeling, his appetite
than meat >consumes 1 cup of and nutrition is
>eats 3x a day rice, depending on what decreased.
(breakfast, lunch, kind of viand
dinner >on DAT
>doesn’t take any >no IVF
vitamins
>consumes 1 ½ cup
of rice with moderate
viand
Activities of Daily Living
Elimination >voids at least 4 times a >voids at least 4 times a >with his limited
(Bowel and day and defecates at least day and defecates every activities, his peristaltic
Bladder) once a day. other day. movement is decreased
thus slowing down
bowel movement, and
since he is in ward, he
cannot defecate with
lack of privacy. His
urine elimination is
normal.
Rest and Sleep >during schooldays, he >he sleeps most of the >confined to the bed,
sleeps from 8pm to 5am time. When he doesn’t JME has no choice but
>after school, he sleeps have anything to do, he to stay in bed.
for 2 hrs. (2 – 4 pm) just takes a nap.
>during weekends, he >Consumes at least 10hrs.
sleeps from 9:30pm to of sleep at night.
7:00 am
Activities of Daily Living
Activity and >goes to school from > spends most the time at >he cannot do much,
Exercise Monday to Friday the orthopedic bed even exercise and in his
>typical student that does >bed rest condition with OI, his
everything needed in >no exercises instructed by bone are still fragile
school the doctor and is at risk for more
>plays with classmates injuries.
every breaktime
>doesn’t do any exerise
>bathes twice a day > takes a bath thrice a >he lacks privacy, and
Oral and Personal >brushes his teeth 3x a week since he’s in a balanced
Hygiene day after each meal >Brushes his teeth 2x a day skeletal traction, he
>changes clothes every every morning and before cannot clean himself,
time he takes a bath and sleeping especially when his
if necessary mother is away. He
relies instead on the
nursing student to clean
him.
Physical
Assessment
Physical Assessment
General Survey:
DIFFERENTIAL
COUNT
Lymphocytes 0.29 0.2-0.4 Normal
Monocyte 0.04 0-0.07 Normal
Eosinophils 0.01 0-0.05 Normal
Platelet Count 309 150-400x10^g/L Normal
COAGULATION
STUDIES
Prothrombin Time 14.3 11-15 secs Normal
I/O activity 92.2
INR 1.07
Activated PTT 38.0 22-45 secs Normal
Blood Type “O”
RH Typing Postive (+)
CRP:
Peripheral Smear CRP-No Reagent
Component
Indices
MCV 81 82-92 fL Low
MCH 28 28-32 pg Normal
MCHC 35 32-38% Normal
RBC MORPHOLOGY
ESR Westergren
Method
Children 20 0-10mm/hr High
Clotting Time
(lee & white) 5’00” 5-15 mins Normal
Bleeding Time
(ivy’s method) 2’00” 1-7 mins Normal
Anatomy and
Physiology
Anatomy and Physiology
FEMUR
The thigh is the region of the femur. The longest
and strongest bone in the skeleton is almost
perfectly cylindrical in the greater part of its
extent. Looking at the back of the right femur we
see the deep ridge that goes from greater to lesser
trochanter. The greater is the handle for upward
pulling hip abductors (gluteus medius and
minimus). The lesser is the handle for the psoas
tendon. Sitting behind the femoral head, the
flexion action of the psoas is also an outward
rotation force as the lesser trochanter is pulled
forward and upward - spinning and raising the
femur.
The distal end of the femur is one of the four
boney parts of the knee. The others are tibia,
patella, and indirectly (by being a ligament
handle) the fibula.
IMPORTANCE OF COLLAGEN
Collagen is the major protein of the
body’s connective tissue. It is part of the
framework that bones are formed around.
The characteristic feature of a typical
protein molecule is its long, stiff, triple-
stranded helical structure in which three
collagen polypeptide chains (called a [alpha]
chains) are wound around each other forming a
rope-like super helix. Collagen is extremely
rich in the amino acids Proline and Glycine.
Collagen is a natural protein that provides
our bodies with structural support. Twenty-five
per cent of the dry protein weight of the human
body is collagen —the fibrous, elastic,
connective tissue in our bodies that holds us
together. Seventy-five per cent of our skin is
made up of collagen, providing texture,
resiliency, and shape; and in total about 30 per
cent of our body is collagen. As you can see its
part of the natural make-up of our tendons,
ligaments, joints, muscles, hair, skin, etc.
Because glycine is the smallest amino acid
with no side-chain, it plays a unique role in fibrous
structural proteins. In collagen, Gly is required at
every third position because the assembly of the
triple helix puts this residue at the interior (axis) of
the helix, where there is no space for a larger side
group than glycine’s single hydrogen atom. For the
same reason, the rings of the Pro and Hyp must
point outward. These two amino acids help
stabilize the triple helix—Hyp even more so than
Pro—a lower concentration of them is required in
animals such as fish, whose body temperatures are
lower than most warm-blooded animals.
Type I
• Most common and mildest type of OI.
• Bones fracture easily. Most fractures occur before
puberty.
• Normal or near-normal stature.
• Loose joints and muscle weakness.
• Sclera (whites of the eyes) usually have a blue, purple,
or gray tint.
• Triangular face.
• Tendency toward spinal curvature.
• Bone deformity absent or minimal. Brittle teeth
possible.
• Hearing loss possible, often beginning in early 20s or
30s.
• Collagen structure is normal, but the amount is less than
normal.
Type II
• Most severe form.
• Frequently lethal at or shortly after birth, often
due to respiratory problems.
• Numerous fractures and severe bone
deformity.
• Small stature with underdeveloped lungs.
• Tinted sclera.
• Collagen improperly formed.
Type III
• Bones fracture easily. Fractures often present at birth,
and x-rays may reveal healed fractures that occurred
before birth.
• Short stature.
• Sclera have a blue, purple, or gray tint.
• Loose joints and poor muscle development in arms and
legs.
• Barrel-shaped rib cage.
• Triangular face.
• Spinal curvature.
• Respiratory problems possible.
• Bone deformity, often severe.
• Brittle teeth possible.
• Hearing loss possible.
• Collagen improperly formed.
Type IV
• Between Type I and Type III in severity.
• Bones fracture easily. Most fractures occur before
puberty.
• Shorter than average stature.
• Sclera are white or near-white (i.e. normal in color).
• Mild to moderate bone deformity.
• Tendency toward spinal curvature.
• Barrel-shaped rib cage.
• Triangular face.
• Brittle teeth possible.
• Hearing loss possible.
• Collagen improperly formed.
Type V
• Clinically similar to Type IV in appearance and symptoms of
OI.
• A dense band seen on x-rays adjacent to the growth plate of
the long bones.
• Unusually large calluses (hypertrophic calluses) at the sites of
fractures or surgical procedures. (A callus is an area of new
bone that is laid down at the fracture site as part of the healing
process.)
• Calcification of the membrane between the radius and ulna
(the bones of the forearm). This leads to restriction of forearm
rotation.
• White sclera.
• Normal teeth.
• Bone has a “mesh-like” appearance when viewed under the
microscope.
• Dominant inheritance pattern
Type VI
• Clinically similar to Type IV in appearance and
symptoms of OI.
• The alkaline phosphatase (an enzyme linked to
bone formation) activity level is slightly elevated in
OI Type VI. This can be determined by a blood test.
• Bone has a distinctive “fish-scale” appearance when
viewed under the microscope.
• Diagnosed by bone biopsy.
• Whether this form is inherited in a dominant or
recessive manner is unknown, but researchers
believe the mode of inheritance is most likely
recessive.
• Eight people with this type of OI have been
identified.
Type VII
• The first described cases resemble Type IV OI in many
aspects of appearance and symptoms.
• In other instances the appearance and symptoms are
similar to Type II lethal OI, except infants had white
sclera, a small head and a round face.
• Short stature.
• Short humerus (arm bone) and short femur (upper leg
bone)
• Coxa vera is common (the acutely angled femur head
affects the hip socket).
• Results from recessive inheritance of a mutation to the
CRTAP (cartilage-associated protein) gene. Partial
function of CRTAP leads to moderate symptoms while
total absence of CRTAP was lethal in all 4 identified
cases.
Type VIII
• Resembles lethal Type II or Type III OI in
appearance and symptoms except that infants
have white sclera.
• Severe growth deficiency.
• Extreme skeletal under mineralization.
• Caused by a deficiency of P3H1 (Prolyl 3-
hydroxylase 1) due to a mutation to the
LEPRE1 gene.
Disease Entity
Disease Entity
Treatment and
Management
Treatment and Management
Name Classifica- Dose/ Mechanism Indication Contra- Side effects Nursing
tion of action indication responsibility
Frequency
/Route
Generic: Analgesic 250 mg/ prn works by Relief of Hyper- Stomach -Patient should
Mefenami /oral reducing pain on pin sensitivity, upset, take medication
on full stomach
c acid prostaglan- site active dizziness,
-Assess patient’s
din ulceration drowsiness, pain before
hormones or chronic diarrhea, therapy
that cause inflamma- and headach -Monitor for
inflammation tion of e possible drug
and pain in either upper induced adverse
the body or lower reactions:
•Edema;
GIT, blood
•weight gain;
disorders, •altered BP;
poor •chest pain;
platelet •Rash;
function, •Blurred vision;
kidney or •dry mouth;
•Shortness of
liver
breath.
impairment,
children
<14 y/o
Nursing Care
Plan
Nursing Care Plan
CUES BACK- NURSING OBJECTIVE NURSING RATIONALE EVALUATION
GROUND DIAGNOSIS INTERVEN-
KNOW- TIONS
LEDGE
Objective: The main Risk for After 4 hours Independent: Goal was met.
> history of 2 clinical further injury of nursing >refrain from >to promote After 4 hours of
previous manifestation related to intervention performing non- rest nursing
fractures of OI is the masculo- the patient will essential intervention the
> deformity of tendency for skeletal be able procedures patient was able
bones bones to impairment verbalize ways to recite ways in
> bone fracture easily. secondary to in which injury >keep side rails >to promote which he can
brittleness disease can be up and bed in safe prevent injury or
> thinness / process prevented low position environment trauma.
decreased
muscle tone >check for >To check for
> poor bone peripheral pulse circulation in
healing on the affected the affected
area extremity
Subjective:
The patient is Impaired social After 4 hours of Help patient Acceptance of After 4 hours of
“Pinagbabawalan na
po ko maglaro prone to further interaction nursing identify the problem nursing
masyado ng doctor injuries; he related to intervention, behaviours encourages intervention, the
dahil mabilis akong needs to be therapeutic patient will be needing positive improve-ment patient
mabalian ng buto”
as verbalized by the
isolated from isolation able to develop change. developed
patient. kids his age effective social Role-play effective social
Objective: because of the support system. random social support system
Observed
tendency of situations in
discomfort in social
situations their activities therapeutically
Inability to receive to be harmful to controlled
and communicate a the patient. environment.
satisfying sense of
Thus, making Explain the
belonging, interest
and shared history the patient not effects of having
Observed use of able to socialize a good social
unsuccessful social and build social network.
interaction
behaviors
network.
CUES BACKGROUND NURSING NURSING NURSING RATIONALE EVALUATION
KNOWLEDGE DIAGNOSIS OBJECTIVES INTERVENTIONS
Subjective: BST is use to Impaired After 4 hours of •Instruct to use •To increase GOAL MET:
“hindi ko immobilize the physical nursing the overhead mobility or
trapeze facilitates After 4 hours
maigalaw yung patient and to mobility interventions
movement; it of nursing
binti ko, may correct related to BST the patient will also reduces interventions
nakakabit kasi” deformities in secondary to be able: discomfort of
as verbalized by which fractured M3rd >to demonstrate the patient
remaining flat
the patient steinmann’s pin femur the use of in bed. was able to
Objective: is inserted at the assistive device fully
Application of femur thus such as •Provide •Useful in
maximize
footboard maintaining
balance skeletal mobility is overhead body function
functional
traction lessened. trapeze and position of within
Limited ROM support pillow extremities. therapeutic
Reluctance to
move • Assist patient •Increase limitations
Inability to when exercising blood flow to by:
move the unaffected muscle and >demonstrati
extremities bone to
purposefully ng use of
improve
muscle tone, assistive
maintain joint devices such
mobility and
prevent as overhead
contractures trapeze and
support
pillow
Position Prevent
every 2 incidence
hours of skin
complica-
tion
Encourage
participatio
n in
diversional
activities
and
maintain
stimulating
environmen
t like
personal
possessions
, visits from
family or
friends.