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PERSONAL DATA
The daughter of the patient reported that the patient already has diabetes and
hypertension during her 30’s and has no other sickness other than those. Visual problems were
also verbalized by the patient. Also, the daughter verbalized of no surgery was done to the
patient.
Prior to admission, patient is having a slurred speech and an elevated blood pressure.
According to her daughter, the patient suddenly fell from her seat and speech became
incomprehensive, hand and feet movements became imprecise.
Patient was then admitted in General Faustino M. Dy, Sr, Memorial Hospital by her
attending physician, Dr. Paguirigan, at exactly 08:50 in the afternoon of July 7, 2009. She was
admitted with the admitting diagnosis of CVA probable infarct vs. hemorrhage.
Page 1 of 41
IV. BRIEF DESCRIPTION OF THE DISEASE
Cerebrovascular Accident
Definition:
Causes:
Risk Factor:
1. Hypertension – leading risk factor for coronary heart disease and stroke
– treatable and can be controlled.
Page 2 of 41
b. Subarachnoid (5%) – result from aneurismal rupture of a cerebral artery
with blood loss into space surrounding the brain; evolve over 1 –2
hours.
3. Stroke in Evolution
- describe an unstable ischemic event characterized by the progressive
development of more severe neurologic impairment
- often associated with active occlusive thrombosis of a major cerebral artery.
- Once stable called Complete Stroke
- Most important sign – Intellectual Regression
Page 3 of 41
Different Pathogenesis of Stroke
FLEXION EXTENSION
Scapula Retraction / elevation or hypertension Protraction
Shoulder Abduction, external rotation Abduction, internal rotation
Elbow Flexion Extension
Forearm Supination Pronation
Wrist and fingers Flexion Flexion
FLEXION EXTENSION
Hip Flexion; abduction; external notation Extension, adduction; internal rotation
Knee Flexion Extension
Ankle Dorsiflexion; inversion Plantarflexion; inversion
Toe dorsiflexion
Thrombotic Stroke
Page 5 of 41
Thrombi tend to form in large arteries that bifurcate and have narrowed lumens as a
result of deposits of atherosclerotic plaque.
The most common locations of thrombi are the internal carotid artery, the vertebral
arteries and the junction of the vertebral and basilar arteries.
Occurs rapidly but progresses slowly.
EARLY LATE
Urinary tract infection Spasticity
Pressure sore Contracture
Dehydration Central post-stroke pain syndrome
Malnutrition Falls and injuries
Dysphagia Medication overuse
The basal ganglia (or basal nuclei) are a group of nuclei in the brain
interconnected with the cerebral cortex, thalamus and brainstem. The mammalian basal
ganglia are associated with a variety of functions, including motor control and learning.
Page 6 of 41
Currently popular theories implicate the basal ganglia in action selection, that is,
the decision of which of several possible behaviors to execute at a given time.
Anatomical studies show that the basal ganglia exert an inhibitory influence on a
number of motor systems, and physiological studies show that a release of this
inhibition permits a motor system to become active. The "behavior switching" that takes
place within the basal ganglia is influenced by signals from many parts of the brain,
including the prefrontal cortex, which is widely believed to play a key role in executive
functions.
The main components of the basal ganglia are the striatum, pallidum, substantia
nigra, and subthalamic nucleus. The striatum, a large neural mass at the base of the
forebrain, receives input from many brain areas but sends output only to other
components of the basal ganglia. The pallidum receives its most important input from
the striatum (either directly or indirectly), and sends inhibitory output to a number of
motor-related areas, including the part of the thalamus that projects to the motor-
related areas of the cortex. The substantia nigra consists of two parts, one that
functions similarly to the pallidum, and another that is the source of dopamine input to
the striatum. The subthalamic nucleus receives input mainly from the striatum and
cortex, and projects to the pallidum. Each of these areas—the striatum in particular—
also has a very complex internal anatomical and neurochemical organization.
The basal ganglia have a limbic sector whose components are assigned distinct
names: the nucleus accumbens (ventral striatum), ventral pallidum, and ventral
tegmental area (VTA). The VTA supplies dopamine to the nucleus accumbens and
prefrontal cortex. This dopaminergic projection has attracted a great deal of attention,
because there is much evidence that it plays a central role in reward learning. A number
of highly addictive drugs, including cocaine, amphetamines, and nicotine, act to increase
the efficacy of the VTA dopamine signal. There is also evidence implicating overactivity
of the VTA dopaminergic projection in schizophrenia.
Terminology
The nomenclature of the basal ganglia system and its components has always
been problematic. Early anatomists, seeing the macroscopic structure but knowing
nothing of the cellular architecture or functional organization, grouped together
components that are now believed to have distinct functions (such as the internal and
external segments of the globus pallidus), and give distinct names to components that
are now thought to be functionally parts of a single structure (such as the caudate
nucleus and putamen).
The term "basal" comes from the fact that most of its elements are located in
the basal part of the forebrain. The term ganglia is an anomaly: in modern usage, neural
clusters are only called "ganglia" in the peripheral nervous system; in the central
nervous system they are referred to as "nuclei". For this reason, the basal ganglia are
also occasionally known as the "basal nuclei". Terminologia anatomica (1998), the
Page 7 of 41
international authority for anatomical naming, retained "nuclei basales", which is not
commonly used.
The International Basal Ganglia Society (IBAGS) informally considers the basal
ganglia to be made up of the striatum, the pallidum (with two nuclei), the substantia
nigra (with its two distinct parts) and the subthalamic nucleus. Percheron et al. in 1991
and Parent and Parent in 2005 included the central region (centre median-
parafascicular) of the thalamus as part of the basal ganglia, while Mena-Segovia et al. in
2004 included the pedunculopontine complex as well.
Anatomy
Coronal slices of human brain showing the basal ganglia. White matter is shaded darkly, gray matter lightly.
ANTERIOR: striatum, globus pallidus (GPe and GPi)
POSTERIOR: subthalamic nucleus (STN), substantia nigra (SN)
Main article: Anatomical subdivisions and connections of the basal ganglia
At the highest level, the basal ganglia are divided by anatomists into four distinct
structures. Two of them, the striatum and pallidum, are relatively large; the other two,
the substantia nigra and subthalamic nucleus, are smaller. In the illustration to the right,
two coronal sections of the human brain show the location of the basal ganglia. The
subthalamic nucleus and substantia nigra lie farther back in the brain than the striatum
and pallidum.
Connections
Page 8 of 41
The flow of neural signals through the basal ganglia is strongly directional. The
striatum is the primary recipient of input from other brain areas, most notably the
cerebral cortex. The internal segment of the globus pallidus (GPe), together with the
reticular part of the substantia nigra (SNr), give rise to the primary output, most notably
to the thalamus. The striatum projects to the pallidum both directly and indirectly via
the subthalamic nucleus, which also receives cortical input. The substantia nigra consists
of two parts, one of which functions similarly to the pallidum, the other of which sends a
modulatory dopaminergic input to the striatum and other structures.
The adjoining figure shows some of the most important connections between
components. On the largest scale, the basal ganglia form a loop that begins and ends in
the cortex. Anatomists have distinguished two main circuits, known as the "direct" and
"indirect" pathways. The direct pathway runs
cortex→striatum→GPi→thalamus→cortex. Two of these links are excitatory, and two
inhibitory, so the net effect of the whole sequence is excitatory: the cortex excites itself
via the direct pathway. The indirect pathway runs
cortex→striatum→GPe→STN→GPi→thalamus→cortex. Three of these links are
inhibitory and two excitatory, so the net effect of the sequence is inhibitory: the cortex
inhibits itself via the indirect pathway. The total effect of basal ganglia upon the cortex
is believed to result from a complex interplay between these two pathways.
Striatum
The striatum is the largest component of the basal ganglia. The term "striatum"
comes from the observation that this structure has a striped appearance when sliced in
certain directions, arising from numerous large and small bundles of nerve fibers (white
matter) that traverse it. Early anatomists, examining the human brain, perceived the
striatum as two distinct masses of gray matter separated by a large tract of white
matter called the internal capsule. They named these two masses the "caudate nucleus"
and "putamen". More recent anatomists have concluded, on the basis of microscopic
and neurochemical studies, that it is more appropriate to consider these masses as two
separated parts of a single entity, the "striatum", in the same way that a city may be
separated into two parts by a river. Numerous functional differences between the
caudate and putamen have been identified, but these are taken to be consequences of
the fact that each sector of the striatum is preferentially connected to specific parts of
the cerebral cortex.
Numerous studies have shown that the connections between cortex and
striatum are generally topographic; that is, each part of the cortex sends stronger input
to some parts of the striatum than to others. The nature of the topography has been
difficult to understand, however—perhaps in part because the striatum is organized in
three dimensions whereas the cortex, as a layered structure, is organized in two. This
dimensional discrepancy entails a great deal of distortion and discontinuity in mapping
one structure to the other.
Page 9 of 41
Pallidum
The pallidum consists of a large structure called the globus pallidus ("pale globe")
together with a smaller ventral extension called the ventral pallidum. The globus
pallidus appears as a single neural mass, but can be divided into two functionally distinct
parts, called the internal (sometimes "medial") and external (sometimes "lateral")
segments, abbreviated GPi and GPe. Both segments contain primarily GABAergic
neurons, which therefore have inhibitory effects on their targts. The two segments
participate in distinct neural circuits. The external segment, or GPe, receives input
mainly from the striatum, and projects to the subthalamic nucleus. The internal
segment, or GPi, receives signals from the striatum via two pathways, called "direct" and
"indirect". The direct pathway consists of direct projections from the striatum to the
GPi. The indirect pathway consists of projections from the striatum to the GPe, followed
by projections from the GPe to the subthalamic nucleus (STN), followed by projections
from the STN to the GPi. These pathways have opposite net effects: striatal activity
inhibits the GPi via the direct pathway because striatal outputs are GABAergic, but has a
net excitatory effect on the GPi via the indirect pathway because this three-link pathway
consists of two inhibitory links plus one excitatory link.
Subthalamic nucleus
Function
The greatest source of insight into the functions of the basal ganglia has come
from the study of two neurological disorders, Parkinson's disease and Huntington's
disease. For both of these disorders, the nature of the neural damage is well understood
and can be correlated with the resulting symptoms. Parkinson's disease involves major
loss of dopaminergic cells in the substantia nigra; Huntington's disease involves massive
loss of medium spiny neurons in the striatum. The symptoms of the two diseases are
virtually opposite: Parkinson's disease is characterized by gradual loss of the ability to
initiate movement, while Huntington's disease is characterized by an inability to prevent
parts of the body from moving unintentionally. It is noteworthy that although both
diseases have cognitive symptoms, especially in their advanced stages, the most salient
symptoms relate to the ability to initiate and control movement. Thus, both are
classified primarily as movement disorders. A different movement disorder, called
hemiballismus, may result from damage restricted to the subthalamic nucleus.
Hemiballismus is characterized by violent and uncontrollable flinging movements of the
arms and legs.
Role in motivation
Although the role of the basal ganglia in motor control is clear, there are also
many indications that it is involved in the control of behavior in a more fundamental
way, at the level of motivation. In Parkinson's disease, the ability to execute the
components of movement is not greatly affected, but motivational factors such as
hunger fail to cause movements to be initiated or switched at the proper times. The
immobility of Parkinsonian patients has sometimes been described as a "paralysis of the
will". These patients have occasionally been observed to show a phenomenon called
Page 10 of 41
kinesia paradoxica, in which a person who is otherwise immobile responds to an
emergency in a coordinated and energetic way, then lapses back into immobility once
the emergency has passed.
The role in motivation of the "limbic" part of the basal ganglia—the nucleus
accumbens (NA), ventral pallidum, and ventral tegmental area (VTA)—is particularly well
established. Thousands of experimental studies combine to demonstrate that the
dopaminergic projection from the VTA to the NA plays a central role in the brain's
reward system. Animals with stimulating electrodes implanted along this pathway will
bar-press very energetically if each press is followed by a brief pulse of electrical
current. Numerous things that people find rewarding, including addictive drugs, good-
tasting food, and sex, have been shown to elicit activation of the VTA dopamine system.
Damage to the NA or VTA can produce a state of profound torpor.
The basal ganglia form one of the basic components of the forebrain, and can be
recognized in all species of vertebrates. Even in the lamprey (generally considered one
of the most primitive of vertebrates), striatal, pallidal, and nigral elements can be
identified on the basis of anatomy and histochemistry.
The names given to the various nuclei of the basal ganglia are different in different
species:
For example, the "internal segment of the globus pallidus" in primates is called
the "entopenduncular nucleus" in rodents.
The "striatum" and "external segment of the globus pallidus" in primates are
called the "paleostriatum augmentatum" and "paleostriatum primitivum"
respectively in birds.
Page 11 of 41
Neurotransmitters
In most regions of the brain, the predominant classes of neurons use glutamate
as neurotransmitter and have excitatory effects on their targets. In the basal ganglia,
however, the great majority of neurons use GABA as neurotransmitter and have
inhibitory effects on their targets. The inputs from the cortex and thalamus to the
striatum and STN are glutamatergic, but the outputs from the striatum, pallidum, and
substantia nigra pars reticulata all use GABA. Thus, following the initial excitation of the
striatum, the internal dynamics of the basal ganglia are dominated by inhibition and
disinhibition.
History
The acceptance that the basal ganglia system constitutes one major cerebral
system took long to arise. The first anatomical identification of distinct subcortical
structures was published by Thomas Willis in 1664. For many years, the term corpus
striatum was used to describe a large group of subcortical elements, some of which
were later discovered to be functionally unrelated. For many years, the putamen and
the caudate nucleus were not associated with each other. Instead, the putamen was
associated with the pallidum in what was called the nucleus lenticularis or nucleus
lentiformis.
A thorough reconsideration by Cécile and Oskar Vogt Cécile and Oskar Vogt
(1941) simplified the description of the basal ganglia by proposing the term striatum to
describe the group of structures consisting of the caudate nucleus, the putamen and the
Page 12 of 41
mass linking them ventrally, the nucleus accumbens. The striatum was named on the
basis of the striated (striped) appearance created by radiating dense bundles of striato-
pallido-nigral axons, described by anatomist Samuel Alexander Kinnier Wilson (1912) as
"pencil-like".
The anatomical link of the striatum with its primary targets, the pallidum and the
substantia nigra was discovered later. The name globus pallidus was attributed by
Déjerine to Burdach (1822). For this, the Vogts proposed the simpler "pallidum". The
term "locus niger" was introduced by Félix Vicq-d'Azyr as tache noire in (1786), though
that structure has since become known as the substantia nigra, due to Von Sömmering
in 1788. The structural similarity between the substantia nigra and globus pallidus was
noted by Mirto in 1896. Together, the two are known as the pallidonigral ensemble,
which represents the core of the basal ganglia. Altogether, the main structures of the
basal ganglia are linked to each other by the striato-pallido-nigral bundle, which passes
through the pallidum, crosses the internal capsule as the "comb bundle of Edinger",
then finally reaches the substantia nigra.
Additional structures that later became associated with the basal ganglia are the
"body of Luys" (1865) (nucleus of Luys on the figure) or subthalamic nucleus, whose
lesion was known to produce movement disorders. More recently, other areas such as
the central complex (centre médian-parafascicular) and the pedunculopontine complex
have been thought to be regulators of the basal ganglia.
Near the beginning of the 20th century, the basal ganglia system was first
associated with motor functions, as lesions of these areas would often result in
disordered movement in humans (chorea, athetosis, Parkinson's disease).
Page 13 of 41
V. ANATOMY AND PHYSIOLOGY
The Brain
BRAIN
Made up of 1000 billion neurons and is one of the largest organs of the body, weighing
about 1300 kg (3 lbs).
It is a mushroom shaped
4 Principal Parts
1. Brain Stem
Stalk of the mushroom
Consist of medulla oblongata, pons and midbrain
2. Diencephalon
Consisting primarily of the thalamus and hypothalamus
3. Cerebrum
Spreads over the diencephalons
Constitute about seven-eights of the total weight of the brain and occupies most
of the cranium.
4. Cerebellum
Inferior to the cerebrum and posterior to the brain stem
The brain is protected by the cranial bones. Like the spinal cord. The brain is also protected
by meninges. The cranial meninges surround the brain are continues with the spinal meaninges
and have the same basic structure and bear the same names as the spinal meninges.
5. Calcarine Sulcus
This sulcus is surrounded by the visual receptive area.
The function of the cerebral cortex has been mapped out into areas by Broadmann.
These two major types of cortical areas are:
1. Frontal Lobe
Area 4 - primary motor area
Area 6 - premotor area
Area 8 - frontal eye movement and papillary change area
Area 44 - motor speech (Brocas Area)
2. Parietal Lobe
Area 3, 1, 2 - primary sensory areas
Area 5, 7 - sensory association areas
Area 39 – 40 - Wernicke’s area
Area 5, 7, 39 – 40 - Gnostic area
Area 43 - primary gustatory area
3. Occipital Lobe
Area 17 - primary visual cortex
Area 18 – 29 - visual association areas
4. Temporal Lobe
Area 41 - primary auditory cortex
Area 42 & 22 - auditory association areas
Page 15 of 41
Function : Programming and planning of motor activities and perhaps their
imitation.
Has presentation for both right and left sides as well as proximally and
distally.
PARTS FUNCTION
BRAIN STEM
Page 17 of 41
CEREBELLUM 1. Controls subconscious skeletal muscle
contraction’s required for coordination, posture
and balance.
2. Assume a role in emotional development,
modulating sensations of anger and pleasure.
Vascular Anatomy
Blood
CEREBRAL ARTERIES
Page 18 of 41
VI. LABORATORY
Non –contrast CT scan using 5mm in the posterior fossa and 10mm
contiguous slices in the supratentorial region show the following findings:
- There is a focus of low attenuation density seen in the right basal ganglia
extending into the ispilateral internal capsule. Hypodense focus is seen on
the right frontal perventricular white matter region.
- Small foci on low attenuation density are also noted on the left basal
ganglia.
- No definite evidence of intracranial hemorrhage noted.
- Midline stuctures are not displaced.
- Ventricles are not dilated or displaced.
- Cortical sulci and cisterns are not unusual.
- Posterior fossa structures are remarkable.
- Visualized osseous structures are intact.
- Both frontal sinus are aplastic. There is opacification of the left ethmoid
sinus.
- Calcifications are seen in the pineal gland which are physiologic in nature.
- Paucity of pnuemonized air cells are noted on the right mastoid compared
to the cotralateral side.
IMPRESSION:
Impression of the CT scan: Acute to subacute infarcts, right basal
ganglia periventricular white matter region as described.
Lacunar infarcts, left basal ganglia.
Negative intracranial hemorrhage. Aplastic frontal sinus, bilateral.
Opacified left ethmoid sinus, left which can be due to sinusitis.
Sclerotic mastoid, right.
Interpretation:
From the result of the CT scan and from its plain study, it shows that there is a sub acute
infarct at the right basal ganglia periventricular white matter region as described and a lacunar
infarcts on the left basal ganglia. This causes the slurred speech symptom of the patient as well
as its decreased motor responses. The plain study also indicates that there is a negative
intracranial hemorrhage thus proving the diagnosis “CVA probable infarct vs hemorrhage.” It
also shows a sclerosis on the right mastoid.
Nursing consideration:
1. Ensure a signed consent and explain the procedure to the patient as well with the
SO’s.
2. Check hospital policy on withholding food and fluids. Clients are usually on NPO
status
3. (Except for medications ordered as part of the test) for 8 hours before the test if it’s
done in the morning. If the test is done in the afternoon the client may have a liquid
breakfast.
4. Give medications up to 2 hours before test.
5. Asses for possible reaction to iodine dye (by asking about allergy to seafood).
Document any allergy and inform the physician and radiography department.
6. Remove metal hairpins, clips and earrings.
Page 19 of 41
URINALYSIS
Date: July 13, 2009
COLOR Lt. Yellow PROTEIN
TRANSPARENCY Sl. Turbid SUGAR
PH/REACTION 6.5 (4.5-8.0) ACETONE
SPECIFIC GRAVITY 1.015 (1.005-1.030) BILE PIGMENTS
CAST/LFP CRYSTALS
Hayline Cast Amorp. Urate/Phospates Few
CELLS/HPF EPITHELIAL CELLS
WBC/Pus Cell 3-6 (0-4) Squamous Rare
RBC/Red Blood Cell >50 (<2) Renal
Yeast Cells MUCUS THREADS Rare
Pregnancy Test Bacteria Occasional
Interpretation:
The urinalysis of the above patient shows that there is an increase in RBC. This suggest
that RBC cast indicates hemorrhage in the nephron thus suggesting acute glomerolonephritis.
This might be due to the prolonged catheterization, increasing the ascending infection causing
damage to the nephron. With regards to this, it indicates that there is an acute bacterial
infection within the urinary tract, supported by the U/A laboratory result with an increase WBC.
HEMATOLOGY
Date: July 7, 2009
EXAMINATIONS REFERENCE VALUES
HEMOGLOBIN 132 120-160 g/L
HEMATOCRTI (HCT) 39 34-47 vol %
LEUKOCYTE COUNT (WBC) 13.1 5.0-10.0
DIFFERENTIAL COUNT:
Nuetrophils 84 50-70 %
Lymphocytes 15 20-40 %
Eosinophils 1 1-3 %
Toxic Granules Negative
Clotting Time 2-6 minutes
Bleeding Time 1-4 minutes
Malarial Smear No Malarial Parasite Seen (NMPS)
Intrepretation:
Leukocytosis is a raised white blood cell count (the leukocyte count) above the normal
range. This increase in leukocytes (primarily neutrophils) is usually accompanied by a "left shift"
in the ratio of immature to mature neutrophils. The increase in immature leukocytes increases
due to proliferation and release of granulocyte and monocyte precursors in the bone marrow
which is stimulated by several products of inflammation including C3a and G-CSF. Although it
may be a sign of illness, leukocytosis in-and-of itself is not a disorder, nor is it a disease. It is
simply a laboratory finding. A leukocyte count above 25 to 30 x 109/L is termed a leukemoid
reaction, which is the reaction of a healthy bone marrow to extreme stress, trauma, or
infection. (It is different from leukemia and from leukoerythroblastosis, in which immature
blood cells are present in peripheral blood.) Leukocytosis is very common in acutely ill patients.
It occurs in response to a wide variety of conditions, including viral, bacterial, fungal, or
parasitic infection, cancer, hemorrhage, tissue necrosis (for this case, brain tissue death or
infarct) and exposure to certain medications or chemicals including steroids. Leukocytosis can
also be the first indication of neoplastic growth of leukocytes.
Page 20 of 41
Nursing consideration:
1. Explain the procedure and the purpose of the test.
2. Assess the client’s knowledge of the test.
3. Adhere standard precaution.
4. Apply pressure to the venipuncture site.
5. Explain that some bruising, discomfort, and swelling may appear at the site and
that moist compress can alleviate this.
6. Monitor signs of infections.
BLOOD CHEMISTRY
Date: July 8, 2009
EXAMINATIONS RESULT S.I. UNITS NORMAL VALUES
Glucose (Fasting) 3.26 mmol/L 3.85-6.05
Total Cholesterol 7.52 mmol/L 3.9-5.1
Blood Urea Nitrogen 9.0 mmol/L 1.7-9.3
Serum Creatinine 167.4 µmol/L 53-106
Interpretation:
Too much cholesterol in the blood, however, can cause deposits of cholesterol inside
arteries. These plaques can narrow the artery enough to block blood flow. This process known
as atherosclerosis commonly occurs in the coronary arteries which nourish the heart. For this
case, an increase in the Total Cholesterol is just a proof supporting the atherosclerosis and the
CT scan result having an impression of a sclerotic right mastoid.
Measuring serum creatinine is a simple test and it is the most commonly used indicator
of renal function. A rise in blood creatinine levels is observed only with marked damage to
functioning nephrons. Therefore, this test is not suitable for detecting early stage kidney
disease. The increase serum createnine is only indicative that due to the ischemic stroke there
is a renal failure and the damaged nephrones are caused by bacterial infections.
Nursing Considerations:
1. Explain the procedure and the purpose of the test.
2. Assess the client’s knowledge of the test.
3. Adhere standard precaution.
4. Apply pressure to the venipuncture site.
5. Explain that some bruising, discomfort, and swelling may appear at the site and
that moist compress can alleviate this.
6. Monitor signs of infections.
Page 21 of 41
VII. PATHOPHYSIOLOGY
Deposition of atherosclerotic
Plaque in intima of arteries
Thrombus form
Page 22 of 41
VIII. PHYSICAL ASSESSMENT
Page 23 of 41
REST AND ACTIVITY
Current activity level Lie and sit on bed Patient moment varies due to body
weakness
Sleep 8-9 hours a day during the
confinement period
Pain/relief measures Patient tries to position himself Patient usually positions himself on his
on a comfortable position. back and sometimes lie left laterally or
right laterally, depending on patients
choice of comfort.
Patient also verbalized that Patient assumes analgesics for pain
upon having a headache she relief measure in addressing headache.
takes Biogesic. Sudden headache is one of the s/sx of
CVA.
SAFETY
Allergic Reaction Sea foods
Medications Gentamicin 160 mg IV OD Antibiotics were administered so as to
Cefuroxime 750 mg IV q8h stop, or if not, lessen infection which
Clonidine 1 tab SL now caused the disease.
Imidapril 1 tab OD/ NGT CV agent drugs were ordered to lower
the blood pressure of the patient.
Bactoban ointment to wound Antibacterial ointment was ordered to
TID prevent infection of the wound.
Eye/vision
Glasses: With a 120 reading glass
Pupils: Right pupil is dilated non- Due to an infarct in the brain, vision
reactive to light. Left Pupil and normal eye function can be
constricted with minimal affected.
reaction to light.
Color
Skin Pale Patient has a low hemoglobin count.
Nails Pinkish
Lips Somewhat dry
Page 24 of 41
Site Left posterior forearm
Tissue turgor Good skin turgor
Ability to:
Chew Able
Swallow Able
Feed self With SO’s assistance Due to decreased hand movement
accuracy.
Page 25 of 41
IX. DRUG ANALYSIS
Date consumed:
-July 14, 2009
Page 26 of 41
DRUG INDICATION CONTRAINDICATION ADVERSE REACTION NURSING CONSIDERATION
Generic Name: -Elevated systolic and -Hypersensitivity to drug -CV: Hypotension, peripheral -Monitor BP frequently
- Captopril diastolic BP regimen edema, ECG changes,
tachycardia, bradycardia -Instruct client to change
Brand Name: -Pregnancy position slowly.
- Capoten, Captale, Captril -GI: Dry mouth, constipation,
ACTION -Lactation N/V, hepatitis
Classification: - Central-acting anti- -Instruct patient to avoid
-Cardiovascular Drug adrenergic derivative. -CNS: drowsiness, sedation, potentially hazardous
Stimulates alpha2-adrenergic dizziness, headache, fatigue, activities until reaction to
Stock: receptors in CNS to inhibit weakness, sluggishness, drug has been determined
- 25mg tab sympathetic vasomotor nervousness
centers. Also inhibits rennin -Instruct patient not to omit
Doctor’s order: release from kidneys. -Skin: rashes, pruritus doses without consulting the
- 25mg tab BID physician
-UG: impotence, loss of libido
Date started: -Instruct patient not to
-July 7, 2009 breastfeed while taking this
drug(for mothers)
Date consumed:
-July 14, 2009
Page 27 of 41
DRUG INDICATION CONTRAINDICATION ADVERSE REACTION NURSING CONSIDERATIONS
Generic name: Reduction of elevated -Contraindicated in patients -CNS: dizziness, headache, -Assess patient’s blood
-Mannitol intracranial pressure, hypersensitive to drug fever pressure history before
cerebral edema or increased therapy. Monitor pulse and
Brand name: intraocular pressure. -Contraindicated in patients -CV: edema, hypotension, blood pressure regularly
-Osmofundan 20% with anuria, severe tachycardia, vascular
ACTION pulmonary congestion, frank overload -Check weight, renal function,
Classification: Elevates blood plasma pulmonary edema, severe fluid balance and serum urine
-Osmotic Diuretic osmolality, resulting in heart failure, severe -EENT: blurred vision, rhinitis sodium and potassium daily
enhanced flow of water dehydration, metabolic
Doctor’s order: from tissues, including the edema or active intracranial -GI: thirst, dry mouth, -Monitor CNS symptoms and
-Manitol 100cc IV q8 / IV q4 brain and cerebrospinal bleeding. nausea, vomiting, diarrhea changes in mental status.
fluid, into interstitial fluid
Date started : and plasma. -GU: urine retention -To relieve thirst, give
-July 8, 2009 (IV q8) frequent mouth care or fluids
-July 10, 2009 (IV q4) -Metabolic: dehydration -monitor allergic reaction:
rash,fever, pruritus,and
Date Consumed: -Other: chills urticaria.
-July 14, 2009
Page 28 of 41
DRUG INDICATION CONTRAINDICATION ADVERSE REACTION NURSING CONSIDERATIONS
Drug name Cerebrovascular accident in -Must not be administered to -Gastrointestinal disorders -May be taken with or without
-Citicholine acute recovery phase, patients with hypertonia of food
symptoms and signs of the parasympathetic. -Fleeting and discrete
Brand name: cerebral insufficiency such as hypotensive effect -Should be administered slowly
-Somazine dizziness, memory loss, poor for patients with intracranial
concentration, -Elevated body temperature hemorrhage
Classification: disorientation and recent
-Belongs to the class of cranial traumatism and their -Restlessness -Monitor vital signs specifically
other agents used as CNS sequelae. the BP
stimulant.
ACTION -Provide frequent rest periods
Doctor’s order: It increases the
-Citicoline 1gm IV q8 neurotransmission levels
because it favors the
Date started: synthesis and production
-July 7, 2009 speed of dopamine in the
striatum, acting then as a
Date consumed: dopaminergic agonist thru
-July 14, 2009 the inhibition of tyrosine-
hydroxylase.
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DRUG INDICATION CONTRAINDICATION SIDE EFFECTS NURSING CONSIDERATIONS
Drug name: -Secondary bacterial -Contraindicated in patients -CV: phlebitis, -Ask patient if he is allergic
-Cefuroxime sodium infection of acute hypersensitive to drug or thrombophlebitis to penicillins or
bronchitis. other cepghalosporins. cephalosporins.
Brand name: -GI: nausea, anorexia,vomiting,
-Zinacef ACTION -Use cautiously in patients diarrhea -Obtain specimen for culture
-Second generation hypersensitive to penicillin and sensitivity test before
Doctor’s order: cephalosporin that inhibits because of possible cross- -Hematologic: giving first dose.
-Cefuroxime 750 mg IV q8 cell wall synthesis, sensitivity with other beta- Eosinophilia, hemolytic anemia,
ANST promoting osmotic lactam antibiotics thrombocytopenia -Tablet and suspension
instability; usually aren’t bioequivalent and
Date started: bactericidal. -Skin: urticaria, maculopapular can’t be substituted
-July 7, 2009 and erythematous rashes, milligram-for-milligram.
temperature elevation
Date consumed: -monitor patient for signs
-July 14, 2009 -Other: and symptoms of
Hypersensitivity reactions, superinfection.
serum sickness, a
naphylaxis -tell pt. to take drug as
prescribed even after he
feels better
Page 30 of 41
DRUG INDICATION SIDE EFFECTS ADVERSE EFFECTS NURSING CONSIDERATION
Generic Name: -Active duodenal and gastric -Headache, malaise, -Bradycardia, -Assess patient for abdominal
-Ranitidine Hydrochloride ulcer nausea, vomiting, constipation, diarrhea, pain.
-Gastro-esophageal reflux dizziness, skin rash. blurred vision, cardiac
Brand Name: disease (GERD) arrhythmias, burning and -Remind patient to take once daily
-Zantac -Heartburn itching at injection site, prescription drug at bedtime for
headache and fatigue. best results.
Classification: ACTION
-H2 receptor blocker Competitively inhibits -Take the drug with foods.
action of histamine on the
Doctor’s order: h2 at receptor sites of -Advice patient to report
-Ranitidine 50mg IV q8 parietal cells, decreasing abdominal pain and blood in stool
gastric acid secretion. or emesis.
Date started:
-July 7, 2009 -Assess potential for interactions
with other pharmacological
Date consumed: agents the patient may be taking.
-July 14, 2009
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X. COURSE IN THE WARD
ADMISSION DAY
July 7, 2009
Emergency Room
At 08:50 pm, a 49- year old female patient was admitted with history of slurred speach
and body weakness few hours prior to admission. She was assessed to have a BP of 150/100
mmHg. She was then seen and examined by Dr. Paguirigan with orders made and carried out by
the nurse on duty. A request of CXR, ECG, CBS, U/A, BUN, Total Cholesterol, Createnin and FBS
was sent to the Laboratory and for a Cranial CT Scan. IFC was inserted aseptically and
connected to urine bag. An IVF of PNSS 1L x 12° was also inserted at left hand. Stat medications
were given. An ECG was done immediately.
At 9:35 pm, she was sent to the medical ward per wheelchair with same IVF on.
At 9:40 pm, patient was received at the medical ward per wheelchair with an IVF of
same. She was placed on bed comfortable and was assessed to be conscious, weak and with
slurred speech with a v/s of q 1°
At 7 am, patient was received on bed with same IVF at left hand. He was seen to have
an intact IFC which is connected to a urine bag. Seen and examined by Dr. Paguirigan at around
8:00 am, with new orders and carried out. Manitol was increase from q8 to q4 with TF of PNSS.
A Cranial CT scan and neurologist referral was ordered by Dr. Paguirigan.
At 1:20 am, the patient was given a Catapres due to a recorded BP of 200/110.
At 5:15pm a Blood serum result was also attached and referred to AP but with no
further orders. BP as of this time is 180/110.
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3rd DAY OF HOSPITALIZATION
July 9, 2009
At 8:00 in the morning patient was received with an IVF of PNSS 1L X 20gtt/min at 80cc
level and with a patent IFC draining to approximately 300cc of yellowish urine.
At 9:00am, patient was seen and examined by Dr. Salvador with orders carried out.
Patients BP as of this time is 190/110.
At 9:50am, above IVF was consumed. Due to infiltration, IFV was reinserted on the right
radial vein with D5NSS 1L x q 12° regulated at 20-21 gtt/min.
For additional care and second opinion the patient was then referred to Dr. Salvador
with orders carried out. Manitol was decrease from q4 to q8. At 12:15pm a side drip of D5W ½L
+ 4 amp Hydralzine was hooked regulated at 20 µgtt/min.
Monitoring of v/s is carried all throughout the day as well as due meds were given.
Patient is still for CT scan and still for referral to a neurologist.
At 8:00 in the morning patient was received with an IVF of D5NSS 1L X 20gtt/min at
920cc level, side drip of D5W ½L x 20 µgtt/min + 4 amps Hydralazine and with a patent IFC
draining to approximately 560cc of yellowish urine.
At 11:00am, patient was seen and examined by Dr. Salvador with orders carried out.
Monitoring of v/s is carried all throughout the day as well as due meds were given.
Patient is still for CT scan and still for referral to a neurologist.
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5th DAY OF HOSPITALIZATION
July 11, 2009
At 8:00 in the morning patient was received with an IVF of D5NSS 1L X 20gtt/min at
600cc level, side drip of D5W ½L x 20 µgtt/min + 4 amps Hydralazine at 450cc and with a patent
IFC draining to approximately 500cc of yellowish urine.
At 9:30am, patient was seen and examined by Dr. Salvador with orders carried out.
Monitoring of v/s is carried all throughout the day as well as due meds were given.
Patient is still for CT scan and still for referral to a neurologist.
At 8:00 in the morning patient was received with an IVF of D5NSS 1L X 20gtt/min at
700cc level, side drip of D5W ½L x 20 µgtt/min + 4 amps Hydralazine at 100cc and with a patent
IFC draining to approximately 1300cc of yellowish urine.
At 9:30am, patient was seen and examined by Dr. Paguirigan with orders to continue
medications.
At 5:00pm the student nurse, Emmanuel D. Mania, noted, upon assessment, that the
right pupil is dilated and non reactive to light while the left eye pupil is reactive to light. Then at
around 6:15pm the student also observed that the IV line is already sludge. With the
supervision of his clinical instructor, Ms. Arcalyd Rose A. Romos, RN, the IV catheter is removed
aseptically and temporarily stopped. Hot compress was applied to the affected site as to reduce
swelling and pain. At 6:30, IV line was reinserted on the right arm with same solution of D5NSS
1L properly regulated at 20 gtt/min.
At 9:00pm the student again observed that the IV line is again sludge. With the
supervision of his CI, Ms. Arcalyd Rose A. Romos, RN, the IV catheter is removed aseptically and
temporarily stopped. Hot compress was applied on both hands to reduce swelling and pain. At
9:30pm, IV line was reinserted on the left posterior forearm with same solution of D5NSS 1L
properly regulated at 20 gtt/min.
At 10:30pm, above IVF was consumed and replaced with PNSS 1L regulated properly at
20gtt/min.
Monitoring of v/s is carried all throughout the day as well as due meds were given.
Patient is still for CT scan and still for referral to a neurologist and a physical therapist.
Page 34 of 41
MEDICATIONS INTRAVENOUS FLUIDS
Captopril 25mg tab BID D5NSS 1L x q 12°
Catapres 75mg SL q8 x BP >150/100 D5W ½L x 20 µgtt/min + 4 amps Hydralazine
Cefuroxime 750mg IV q8 PNSS 1L x q12°
Citicholine 1g IV q8
Manitol 100cc IV now then q8
Ranitidine 50mg IV q8
At 8:00 in the morning patient was received with an IVF of PNSS 1L X 20gtt/min at
780cc level, side drip of D5W ½L x 20 µgtt/min + 4 amps Hydralazine at 480cc, replaced before
the 8:00am-4:00pm shift, and with a patent IFC draining to approximately 1215cc of yellowish
urine.
At 2:30 pm, patient was out for CT scan. CT scan results are available at this date.
At around 4:00pm, the patient is still having slurred speech, no disease progression and
still appears weak.
At 8:30pm, above IVF consumed and replaced with D5NSS 1L properly regulated at 20
gtt/min.
Monitoring of v/s is carried all throughout the day as well as due meds were given, v/s
q8 until stable. Patient is still for CT scan and still for referral to a neurologist and a physical
therapist.
At 8:00 in the morning patient was received with an IVF of D5NSS 1L x 20gtt/min at
850cc level, side drip of D5W ½L x 20 µgtt/min + 4 amps Hydralazine at 250cc and with a patent
IFC draining to approximately 520cc of yellowish urine.
At 2:30 pm, patient was out for CT scan. CT scan results are available at this date.
Page 35 of 41
At around 4:00pm, the patient is still having slurred speech, no disease progression and
still appears weak.
At 8:30pm, above IVF consumed and replaced with D5NSS 1L properly regulated at 20
gtt/min.
At 9:30am, patient was seen and examined by Dr. Salvador with new orders and carried
out.
At 10:00am SD was temporarily stopped due to a recording of a BP of 150/100mmHg.
Monitoring of v/s is carried all throughout the day as well as due meds were given, v/s
q8 until stable. Patient is still for CT scan and still for referral to a neurologist and a physical
therapist.
Page 36 of 41
XI. COMPREHENSIVE NURSING CARE PLAN
ASSESSMENT NURSING DIAGNOSIS SCIENTIFIC ANALYSIS NURSING GOAL INTERVENTION RATIONALE EVALUATION
SUBJECTIVE: Ineffective cerebral tissue Deposition of fatty SHORT-TERM GOAL: INDEPENDENT: SHORT-TERM GOAL:
“hindi namin maintindihan perfusion r/t interruption of materials on vessel walls After 8 hours of nursing 1. Establish rapport to the -To gain the patient’s and After 8 hours of nursing
ang sinasabi niya” as blood flow in the brain intervention, the patient patient and S. O.’s S.O.’s trust and cooperation intervention, goal was met
verbalized by the daughter. secondary to presence of will be able to: during the nursing care and as evidenced by:
subacute infarcts of the Plaque formation a) Manifest an improved procedures. a) Patient having an
OBJECTIVE: right basal ganglia and nail beds from pale to 2. Monitor V/S every 30 -To gather baseline data improved nail beds from
Inspection: lacunar infarct of the left pinkish minutes and monitor any further pale to pinkish in color
-With slurred speech basal ganglia of the brain. Narrowing of b) Manifest a normal complications/ deviations b) Patient having a normal
-Right eye dilated atherosclerosis plaque papillary response from normal. papillary response
-↓ in muscle strength: 3. Evaluate pupils, noting -To gather baseline data
-Arms: LONG-TERM GOAL: size, shape and equity and monitor any further LONG-TERM GOAL:
L= 3/5 Aneurysm formation After 1 week of nursing complications/ deviations After 1 week of nursing
R= 1/5 intervention, the patient from normal. intervention, goal was met
-Legs: will be able to: 4. Elevate HOB (15 degrees) -To promote circulation and as evidenced by:
L= 3/5 Rupture of artery supplying a) Manifest an improved and maintain head or neck venous drainage and to a) Patient having an
R= 1/5 the brain participation in performing in midline maintain a patent airway. improved participation in
-GCS: ADL’s with or without 5. Provide quiet and restful -For conservation of energy performing ADL’s with or
E= 3 support. atmosphere and lowers oxygen demand without support.
V=2 deprivation of blood supply b) Manifest an improved 6. Reposition pt every 2 -To promote circulation and b) Patient having an
M=4 in the brain speech hours oxygen distribution improved speech with
-With poor muscle tone on c) Manifest an increase in 7. Patient in comfortable -To promote optimal level diminished slurred
the right and left hand and muscle strength of both position of functioning characteristics.
foot Cerebral infarction arms and legs of the 8. Provide support on -To maintain position of c) Patient having an
- Limited ROM on the right patient. affected body part such as function and reduce increased muscle strength
hand and foot(only able to d) Maintain functional pillows and assistance to do discomforts. with a scale of:
carry out passive ROM on Impaired function of the abilities of the right and left ADL’s as needed. Arms
this area) brain side of the body 9. Provide safety -To prevent fall and injury L=4/5 R=2/5
-Unable to carry out e) Improved physical precautions by raising up Legs
activities without mobility from level 3 to the side rails. L=4/5 R=2/5
assistance such as feeding Ineffective tissue perfusion level 2 and improved GCS 10. Encourage the patient -These factors may affect d) Patient having an
and changing clothes. scale and S.O.’s to avoid them in developing various improved functional ability
-Difficulty in chewing and sedentary lifestyle such as diseases as what like the of the right and left side of
swallowing drinking liquor, smoking, patient is suffering now. the body.
-With pale nail beds improper exercise and too e) Patient having level 2
-Level 3 physical mobility much fatty foods. physical mobility and a GCS
scale of E=4, V=4, M=5.
Lab/Diagnostic Tests: COLLABORATIVE:
CT Scan: HEMORRHAGE IN 1. Administer -It restores the activity and
THE LEFT AND RIGHT medications as ordered: functions of the brain. It
BASAL GANGLIA - Citicoline 2 drops BID / improves neuromuscular
1gm IV q8 function.
Page 37 of 41
ASSESSMENT NURSING DIAGNOSIS SCIENTIFIC ANALYSIS NURSING GOAL INTERVENTION RATIONALE EVALUATION
SUBJECTIVE: Impaired physical mobility Deposition of fatty SHORT-TERM GOAL: INDEPENDENT: SHORT-TERM GOAL:
“Hindi siya ganong r/t subacute infarcts of the materials on vessel walls After 8 hours of nursing 1. Establish rapport to the -To gain the pt’s & S.O.’s After 8 hours of nursing
magkagalaw” as verbalized right basal ganglia and intervention, the patient patient and S. O.’s trust & cooperation during intervention, goal was met
by the daughter. lacunar infarct of the left will be able to: the nsg care & procedures. as evidenced by:
basal ganglia of the brain. Plaque formation a) Participate in 2. Assess and determine -To identify contributing a) Patient participated in
OBJECTIVE: performing ADL’s with factors that contribute to factors that enable the performing ADL’s with
-Weak in appearance minimal assistance from physical immobility nurse to focus on minimal assistance
-↓ in muscle strength: Narrowing of others appropriate interventions b) Patient having an active
-Arms: atherosclerosis plaque b) Do active and passive 3. Determine degree of -To assess functional ability and passive ROM exercise
L= 3/5 ROM exercise on the right immobility & muscle within physical limitations
R= 1/5 side of his body within strength after hours of sleep
Legs: Aneurysm formation physical limitations after 4. Assist patient in -To promote optimal level c) Patient having an
L= 3/5 hours of sleep. comfortable position of functioning adequate sleep of 4 hours
R= 1/5 c) Have an adequate rest 5. Provide support on -To maintain position of
-GCS: Rupture of artery supplying and sleep of about 4-5 affected body parts such as function and reduce LONG-TERM GOAL:
E= 3 the brain hours. pillow discomfort After 1 week of nursing
V=2 6. Provide safety -To prevent injury and fall intervention, goal was met
M=4 LONG-TERM GOAL: precautions by raising up as evidenced by:
-Unable to carry out Intracranial hemorrhage After 1 week of nursing the side rails.
activities without intervention, the patient 7. Provide environment -To have a good a) Patient having an
assistance such as feeding will be able to: free from noise and atmosphere conducive to improved participation in
and changing clothes. Deprivation of blood supply a) Manifest an improved disturbances the recovery of the patient performing ADL’s with or
-With poor muscle tone on in the brain participation in performing 8. Change position every 2 -To reduce risk of tissue without
the right hand and foot ADL’s with or without hours and possibly more ischemia or injury and support.
-Difficulty in chewing and support. often if placed on the to prevent pressure sores b) Patient having an
swallowing Cerebral b) Maintain functional affected part improved functional
-Limited ROM on the right haemorrhage in the motor abilities of the right side of 9. Massage pressure points -To promote circulation and abilities of the right side of
hand and foot(only able to area the body. after each position changes oxygen distribution the body
carry out passive ROM on c) Manifest an increase 10. Assist in performing -To promote optimal level c) Patient having an
this area) in muscle strength of both ADL of functioning increased muscle strength
-Needs assistance when Impairment of gross and arms and legs of the 11. Assist in performing -To minimize muscle with a scale of:
turning motor function of the brain patient. ROM exercise after hours of atrophy and promote Arms
-Level 3 physical mobility d) Manifest an sleep & within physical circulation L=4/5
improvement in chewing limitations. -These factors may affect R=2/5
Lab/Diagnostic Tests: Impaired physical mobility and swallowing abilities 12. Encourage the pt and them in developing various Legs
-CT Scan: HEMORRHAGE e) Improved physical S.O.’s to avoid sedentary diseases as what like the L=4/5
IN THE LEFT AND RIGHT mobility from level 3 to lifestyle such as drinking patient is suffering now. R=2/5
BASAL GANGLIA level 2 improved GCS scale liquor, smoking, improper d) Patient having an
exercise and too much fatty improved chewing and
foods. swallowing abilities
COLLABORATIVE: e) Patient having level 2
1. Administer medications -It restores the activity and physical mobility and a GCS
as ordered: functions of the brain. It scale of E=4, V=4, M=5.
- Citicoline 2 drops BID / improves neuromuscular
1gm IV q8 function.
Page 38 of 41
SCIENTIFIC NURSING
ASSESSMENT DIAGNOSIS PLANNING RATIONALE EVALUATION
EXPLANATION INTERVENTION
OBJECTIVE Risk for infection r/t Inadequate protective of After 8hr. shift of nursing INDEPENDENT: After 8hr. shift of nursing
>not changing of IV site prolonged catheterization defense mechanism interventions, the patient interventions,
within 24-36hrs. will: -Monitor and teach the pt. - Any suspicious drainage GOAL MET, the patient
to the signs of infection should be cultured was:
- know the proper hand
Bacterium, virus, fungus, or washing as well as the -encouraged the pt. to wash - Washing between - know the proper hand
other parasites invades the significant others. hands before contact with procedures reduces the washing as well as the
susceptible pt. the patient risk of transmitting significant others.
- know the sign and pathogens from one area
symptoms of infection and of the body to another - know the sign and
Breaks in the integument when to report these to the symptoms of infection and
physician or nurse - Encourage intake of - This maintains optimal when to report these to the
protein- and calorie-rich nutritional status physician or nurse
Invasion of pathogens -able to know what food he foods
carried through bld. Stream must eat -able to know what food he
or lymphatic system - Encourage fluid intake of - Fluids promote diluted must eat especially in
-able to increase his fluid 2000 ml to 3000 ml of water urine and frequent taking of protein and
intake at the range of 8-10 per day emptying of bladder; calorie rich foods.
Risk for infection glasses of water reducing stasis of urine, in
turn, reduces risk of -able to consumed 9glasses
bladder infection or of water
urinary tract infection
-able to take antibiotics as (UTI).
prescribed
- Teach patient to take - Most antibiotics work -instructed to take
antibiotics as prescribed best when a constant antibiotics as prescribed
blood level is maintained;
a constant blood level is
maintained when
medications are taken as
prescribed. The
absorption of some
antibiotics is hindered by
certain foods; patient
should be instructed
accordingly.
Page 39 of 41
ASSESSMENT NURSING DIAGNOSIS SCIENTIFIC ANALYSIS NURSING GOAL INTERVENTION RATIONALE EVALUATION
SUBJECTIVE: Fluid volume excess r/t Deposition of fatty SHORT-TERM GOAL: INDEPENDENT: SHORT-TERM GOAL:
“Nagmamanas ang paa accumulation of fluids at materials on vessel walls After 8 hours of nursing 1. Establish rapport to the -To gain the patient’s and After 8 hours of nursing
nya” as verbalized by the interstitial spaces as intervention, the patient patient and S. O.’s S.O.’s trust and intervention, goal was met
niece. evidenced by bipedal will be able to: cooperation during the as evidenced by:
swelling of patient’s skin Plaque formation a) Exhibit normal skin and nursing care and a) Patient having a normal
OBJECTIVE: above the ankle with skin body condition particularly procedures. skin and body condition
-The patient has a skin indentation of 1+(about ↓ puffiness of the area 2. Monitor V/S every 30 -To gather baseline data puffiness of the area
indentation of about 2mm deep) Stenosis of the artery above the ankle minutes and monitor any further above the ankle.
2mm deep (1+) complications/ deviations
-Swelling of skin above LONG-TERM GOAL: from normal. LONG-TERM GOAL:
the ankle Alteration of usual smooth After 1 week of nursing -To relieve patient After 1 week of nursing
-Area shiny flow of blood through the intervention, the patient intervention, goal was met
-Cold to touch artery will be able to: 3. Clean edematous ankle -To avoid further fluid as evidenced by:
-Skin area is pale in color a) Have a skin indentation of patient with warm accumulation a) Patient having an skin
on normal limits and will saline wiper -To avoid to much indentation on normal
Swirling of blood aroung be free from puffiness of 4. Regulate fluid intake expenditure of energy limits and negative for
the irregular surface of the the area affected carefully puffiness of the area
plaques 5. Advise patient to -To allow good venous affected.
promote bed rest circulation
6. Elevate patient’s legs for -Because wearing
Vessel lumens become about half an hour constrictive clothes
obstructed and occluded 7. Instruct the patient and impedes lower
S.O.’s that constrictive extremities’ circulation of
clothes should be avoided venous return
↑ blood volume in the to the patient
area proximal to the
obstructed vessel
COLLABORATIVE:
1.Administer medications -For diuresis and
↑ hydrostatic pressure as ordered: subsequent mobilization
Manitol 100cc IV q8 of excess fluid
(Osmotic Diuretic)
Fluid extravasates from
intravascular to interstitial
spaces.
Edema
Page 40 of 41
XII. BIBLIOGRAPHY
Book Sources:
Internet Sources:
http://www.siumed.edu/~dking2/ssb/neuron.htm#neuron
http://www.dls.ym.edu.tw/neuroscience/nsdivide.html
http://en.wikipedia.org/wiki/Human_brain
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