Group 1 Medsurg
Group 1 Medsurg
Group 1 Medsurg
ORU IJEBU
MEDICAL SURGICAL NURSING II
PRESENTATION FOR GROUP 1
Names of group members Matric no
1.AWOBAYIKUN OYINDAMOLA JCONS/22B/020
2.ILELADEWA IMOLEAYO JCONS/22B/032
3.KALEJAYE OREOLUWA JCONS/22B/035
4.ABASS OYINKANSOLA JCONS/23A/001
5.ABDULAZEEZ SAVIOUR JCONS/23A/002
6.ABEEB ABIBAT JCONS/23A/003
7.ADEBANJO TAIWO JCONS/23A/004
8.ADEBAYO AYOMIDE JCONS/23A/005
9.ADETUNJI WALIYAT JCONS/23A/006
10.ADEYEMI CHAMPION JCONS/23A/007
LECTURER IN CHARGE:
MRS. AGHOLOR M.O
TABLE OF CONTENTS
ILELADEWA IMOLEAYO
JCONS/22B/032
Assessment of patient with
cardiovascular system
General examination Introduction The
purpose of examining the cardiovascular
system is to assess the function of the
heart as a pump and arteries and veins
throughout the body in transporting oxygen
and nutrients to the tissues and
transporting waste products and carbon
dioxide from the tissues. Your assessment
of the cardiovascular system is important
because cardiovascular disease is the
most prevalent health care problem in the
United Kingdom. Over 250 000 deaths per
year are attributed to cardiovascular
disease [13]. History taking The patient’s
history is his health status major subjective
data source. Physiological, psychological,
and psychosocial information (including
family relationships and cultural
influences) can be obtained which will
inform you about the patient’s perception of
his current health status and lifestyle [14].
It will give insight into actual and potential
problems as well as provide a guide for the
physical examination. It is important to use
open questioning to elicit the patient’s
presenting complaint [15]. Provides the
diagnosis most often: history, physical,
or diagnostic tests [16]. ▪ History: 70%. ▪
Physical: 15% to 20%. ▪ Diagnostic tests:
10% to 15%. Components of the health
history 1. Biographical data Begin by
asking the patient his name, address,
telephone number, birth date, age,
birthplace, Social Security number, race,
nationality, religion, and marital status. Also,
find out the names of anyone living with
the patient, the name and telephone
number of the person to call in an
emergency, and the patient usual source of
health care
KALEJAYE OREOLUWA
JCONS/22B/035
DYSRHYTHMIA
Dysrhythmia, also known as arrhythmia,
refers to abnormalities in the heart's rhythm,
which can lead to irregular heartbeats.
These irregularities can manifest as the
heart beating too fast (tachycardia), too
slow (bradycardia), or with an irregular
pattern.
History
• Not all symptoms may be present
• Client may note irregular heartbeat
• Palpitations
• Chest discomfort
• Shortness of breath
• Dizziness
• Diaphoresis
• Weakness
• Syncope
• Nausea
Physical Findings
Sinus bradycardia: ECG normal, heart rate
< 60 bpm. A heart rate below 40 bpm is
usually a
junctional rhythm originating in the ventricle.
Look for irregular PR intervals to determine
heart
block or sick sinus syndrome.
Sinus tachycardia: ECG normal, heart rate >
100
bpm, blood pressure constant
PSVT (Atrioventricular nodal re-entrant
tachycardia): ECG abnormal - rhythm
regular,
fast, atrioventricular block usual as seen by
a
prolonged PR interval, systolic BP constant,
electrical alternans rare
SVT (Orthodromic atrioventricular re-
entrant
tachycardia): ECG abnormal - rhythm
regular,
atrioventricular block not present, systolic
BP
constant, electrical alternans common
especially at
high heart rates
Atrial fibrillation: ECG abnormal, rhythm
irregular, P waves not visible, systolic BP
changing. At high rates there is risk of
developing
Wolfe-Parkinson-White syndrome in some
individuals - look for delta waves on the Q
wave
(slurred QRS)
Atrial flutter: ECG abnormal, ventricular
rhythm
is usually regular, P waves have a well
defined
saw-tooth pattern. If rate is
< 120 bpm, there may be no symptoms, if >
120
bpm, there may be hemodynamic instability
Premature ventricular contractions (PVC):
ECG
normal with occasional wide and bizarre
QRS
complexes. Pulse volume is diminished or
absent
during PVC
Ventricular tachycardia: ECG abnormal,
rhythm
may be regular or irregular. There are no
comprehensive ECG criteria for diagnosing
VT,
but the presence of a rate
> 150 bpm, wide and bizarre QRS
complexes,
atrioventricular dissociation and presence
of
fusion beats, suggest ventricular
tachycardia.
Hypotension, dyspnea, diaphoresis may
also be
present.
Torsades de pointe: ECG abnormal, rhythm
regular or irregular. QRS complexes appear
to
change appearance and size, looks like they
are
twisting. Hypotension, dyspnea, diaphoresis
may
also be present.
Ventricular fibrillation: ECG abnormal,
unintelligible, no identifiable waves,
complexes or
rhythms. No heart rate detectable,
hemodynamically very unstable.
Differential Diagnosis
• Multifocal atrial tachycardia
• Sinus tachycardia with multiple premature
atrial
contractions
• Sick sinus syndrome
• Wolfe-Parkinson-White syndrome
• Atrioventricular block
Complications
• Heart failure
• Myocardial infarction
• Cerebrovascular accident
• Thromboembolism
• Wolff-Parkinson-White syndrome
• Cardiac arrest
Diagnostic Tests
• 12 lead ECG
• Arrange for 24-hour Holter monitoring
• Bloodwork - TSH, CBC, INR, PTT CK,
Troponin T
Torsades de Pointes
This is a variant of VT. The complexes are
wide
and bizarre and look like the axis is
changing
(QRS from positive to negative and back).
Usually associated with drugs or conditions
that
increase the QT interval. (Ernoehazy, W. Jnr.,
2001, eMedecine Journal, 2:12)
Ventricular fibrillation (VF)
VF is a pulseless arrhythmia that is irregular
and
chaotic. The heart can no longer pump
blood
around the body. VF is the primary cause of
sudden cardiac death. VF is most
commonly seen
following an MI. VF can be coarse or fine.
The
heart rate is irregular, usually > 300 bpm,
and a
waveform that resembles a squiggle that
fades to a
flat line. (Kazzi, A., 2001 eMedecine Journal,
2:8)
Pulseless Electrical Activity (PEA)
A clinical condition "characterized by loss
of
palpable pulse (or ventricular contraction)
in the
presence of recordable cardiac electrical
activity."
ECG recording may show myocardial
infarction,
signs of hyperkalemia, prolonged QT
interval
related to tricyclic drug overdose. PEA is
caused
by an inability to generate a strong
contraction in
spite of adequate electrical impulse. "PEA is
always caused by a profound global cardiac
insult."
Symptoms of Dysrhythmias
Symptoms of dysrhythmias can vary
depending on the type and severity but may
include:
Pathophysiology of dysrhythmias
Etiology of dysrhythmias
Implantation of a cardioverter-defibrillator
(ICD) to monitor the heart's rhythm and
deliver shocks to restore normal rhythm if
dangerous arrhythmias occur
Catheter ablation to destroy abnormal heart
tissue responsible for causing
dysrhythmias
Coronary artery bypass grafting (CABG) to
improve blood flow to the heart in cases
where coronary artery disease contributes
to dysrhythmias
Pharmacologic Interventions
Initial treatment prescribed only by a
physician.
Selection of treatment modality should be
based
on underlying pathophysiology.
Chronic atrial fibrillation is also treated with
anticoagulants such as warfarin.
Therapy is started as soon as possible if
there is a
history of underlying heart disease.
Monitoring and Follow-Up
• For clients taking antiarrhythmic agents,
liver
enzyme levels should be measured during
first
4-8 weeks of therapy
• Clients with risk factors for cardiac
complications of therapy should undergo
ECG
during first weeks of therapy and every 3-6
months thereafter
• Clients taking digoxin should be monitored
carefully for toxic effects
• Evaluate INR on a regular basis to monitor
therapeutic response to warfarin
Referral
Medevac clients with hemodynamic
instability
ABASS OYINKANSOLA
JCONS/23A/002
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Symptoms and Causes
Is it genetic?
Blood tests.
Cardiac catheterization.
Computed tomography (CT) coronary
angiogram.
Heart MRI (magnetic resonance imaging).
Coronary calcium scan.
Echocardiogram (echo).
Electrocardiogram (EKG/ECG).
Exercise stress test.
Chest X-ray.
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Management and Treatment
Lifestyle changes
Bleeding.
Diarrhea.
Dizziness.
Cough.
Blood clot.
Coronary artery puncture.
Infection.
Abnormal heart rhythms.
Cardiac tamponade.
How long does it take to recover from this
treatment?
Make an Appointment
Prevention
Can coronary artery disease be prevented?
Living With
Structural Infections:
1. Myocarditis (autoimmune):An
autoimmune response where the immune
system attacks the heart muscle, leading to
inflammation and damage. Giant cell
myocarditis and cardiac sarcoidosis are
examples of autoimmune myocarditis.
2. Cardiac Sarcoidosis: A condition where
inflammatory cells called granulomas form
in the heart muscle, leading to scarring and
potentially heart block, arrhythmias, or heart
failure.
3. Giant Cell Myocarditis: A rare
autoimmune disorder where large
inflammatory cells damage the heart
muscle, leading to rapid heart failure and
potentially death.
4. Takotsubo Cardiomyopathy: A condition
where extreme physical or emotional stress
triggers inflammation and heart muscle
weakness, mimicking a heart attack.
5. Cardiovascular Manifestations of
Systemic Rheumatic Diseases:Conditions
like rheumatoid arthritis, lupus, or
scleroderma can cause inflammation and
damage to the heart and blood vessels,
leading to cardiac complications.
Risk factors
- Bacterial, viral, or fungal infections
- Autoimmune disorders (e.g., rheumatoid
arthritis, lupus)
- Genetic predisposition
- Previous heart surgery or catheterization
- Injecting drug use
- Poor dental hygiene
- Weakened immune system
* Symptoms:
*Diagnosis:
- Physical examination
- Electrocardiogram (ECG)
- Echocardiogram
- Cardiac MRI or CT scan
- Blood tests (e.g., troponin, CRP, blood
cultures)
- Endomyocardial biopsy (in some cases)
*Treatment:
NEOPLASM
A neoplasm is a type of abnormal and
excessive growth of tissue. The process
that occurs to form or produce a neoplasm
is called neoplasia. The growth of a
neoplasm is uncoordinated with that of the
normal surrounding tissue, and persists in
growing abnormally, even if the original
trigger is removed. This abnormal growth
usually forms a mass, which may be called
a tumour or tumor.
Classification of neoplasm:
Benign neoplasms
in situ neoplasms
malignant neoplasms
neoplasms of uncertain or unknown
behavior.
Malignant neoplasms are also simply
known as cancers and are the focus
of oncology.
Prior to the abnormal growth of tissue, such
as neoplasia, cells often undergo an
abnormal pattern of growth, such
as metaplasia or dysplasia. However,
metaplasia or dysplasia does not always
progress to neoplasia and can occur in
other conditions as well. The word
neoplasm is from Ancient Greek 'new' and
plasma 'formation, creation'.
A neoplasm can be benign, potentially
malignant, or malignant (cancer).
Benign tumors include uterine
fibroids, osteophytes , and melanocytic
nevi (skin moles). They are circumscribed
and localized and do not transform into
cancer.[8]
Potentially-malignant neoplasms
include carcinoma in situ. They are
localized, and do not invade and destroy but
in time, may transform into cancer.
Malignant neoplasms are commonly called
cancer. They invade and destroy the
surrounding tissue, may
form metastases and, if untreated or
unresponsive to treatment, will generally
prove fatal.
Secondary neoplasm refers to any of a
class of cancerous tumor that is either a
metastatic offshoot of a primary tumor, or
an apparently unrelated tumor that
increases in frequency following certain
cancer treatments such
as chemotherapy or radiotherapy.
Rarely there can be a metastatic neoplasm
with no known site of the primary cancer
and this is classed as a cancer of unknown
primary origin.
CARDIAC TUMOR
Cardiac tumors (also called heart tumors)
are growths that form in your heart. They
can be either benign (noncancerous) or
malignant (cancerous). Some are harmless
or easily treatable, but others can be fatal.
In general, an earlier diagnosis can lead to
prompt treatment and better outcomes for
people with cardiac tumors.
Cardiac tumors range in size and shape.
Some are pedunculated, meaning they grow
on a stalk. Heart tumors may be smaller
than 1 centimeter in diameter or as big as
15 centimeters. Their size and location
within your heart impact your symptoms
and need for treatment.
Types of cardiac tumor
Noncancerous primary cardiac tumor:
About 75% to 95% of all primary heart
tumors are noncancerous. But they can still
be dangerous if they interfere with your
heart function and can pose a risk of stroke
if left untreated.
Noncancerous primary heart tumors that
develop in adults include.
Myxoma. This is the most common
noncancerous primary heart tumor (about
50% of all cases). It needs to be removed
through surgery to prevent serious
complications like an embolism. Myxomas
usually develop in your left atrium.
Papillary fibroelastoma. This is the second
most common noncancerous primary heart
tumor. It can affect people at any age, but
it’s usually diagnosed in people over age 60.
About 80% of the time, this tumor grows on
heart valves (usually your aortic or mitral
valve). Even if you don’t have symptoms,
your provider will recommend surgery to
reduce your risk of an embolism.
Lipoma. This tumor affects people of many
different ages. The tumor itself varies in its
presentation. It may be small, or it may be
very large. Lipomas usually develop in your
left ventricle, right atrium, or atrial septum
(the wall that separates the top chambers
of your heart)
Hemangioma. These tumors have been
diagnosed across the lifespan, from infants
to people 65 years old. They usually don’t
cause symptoms. So, they’re often
diagnosed through tests for other issues.
Hemangiomas often occur along with
tumors in your gastrointestinal tract or skin.
Noncancerous primary heart tumors that
develop in infants and children include:
Cardiac rhabdomyoma. This is the most
common type of heart tumor in infants and
children. Rhabdomyomas grow in clusters
and usually go away on their own without
treatment.
Teratoma. This tumor typically develops on
the pericardium (the sac that surrounds
your child’s heart). It can also grow from
the base of the major blood vessels
connected to their heart.
Fibroma. Unlike a rhabdomyoma, a fibroma
appears as a single tumor. It usually grows
within the muscle of your child’s ventricles.
Your child will likely need surgery to remove
this tumor since it can cause serious heart
problems.
Hamartoma. This tumor is also called
histiocytoid cardiomyopathy or Purkinje cell
hamartoma. It may affect your child’s heart
rhythm.
Cancerous primary heart tumor
About 5% to 25% of all primary heart tumors
are cancerous. Among those, the most
common form is sarcoma.
Sarcoma affects 50% to 75% of people
with Heart cancer. Sarcoma has many
subtypes. Two of the most common
include:
Angiosarcoma. This is the most common
subtype in adults. An angiosarcoma often
develops in your right atrium or pericardium.
Rhabdomyosarcoma. This is the most
common subtype in infants and children.
But it can also affect adults.
Rhabdomyosarcomas often form in groups
and can develop in any heart chamber.
Less common forms of cancerous primary
heart tumors include:
Malignant fibrous histiocytoma. This tumor
often develops in your left atrium and may
block your mitral valve, causing impaired
blood flow in the chambers of your heart.
Lymphoma. Usually, lymphoma (a cancer of
white blood cells) develops in your lymph
nodes, spleen, or bone marrow. Rarely, it
develops in your heart. This usually
happens in people who have AIDS.
Clinical manifestation of cardiac tumor
The symptoms of cardiac heart tumors are
across the board. They vary based on the
form of tumor you have and where it’s
located in your heart. Some people have no
symptoms or very mild symptoms. Others
have symptoms that signal life-threatening
heart problems.
Chest discomfort.
Dizziness and fainting.
Fatigue.
Fever and chills
Heart palpation.
Joint pain.
Loss of appetite.
Night sweats.
Shortness of breath.
Weight loss without another cause.
Causes of cardiac tumors
It’s not always clear what causes primary
heart tumors. Genetic syndromes (like
Carney complex) may play a role in causing
some noncancerous primary heart tumors.
The spread of cancer from one part of your
body (like lungs or skin) to your heart
causes metastatic heart tumors.
Diagnosis and test
Transthoracic echocardiogram.
Transesophageal echocardiogram.
Cardiac MRI.
Contrast enhanced cardiac CT scans.
PET scan.
Management and treatment
Treatment options of cardiac tumors vary
based on the type of tumor.
Noncancerous primary heart
tumors: Surgery is very successful at
removing these tumors if they’re small.
Larger tumors may be impossible to
remove. Your provider or your child’s
provider will recommend surgery if the
tumor interferes with heart function.
Children who have surgery to remove a
fibroma may also need reconstructive
surgery to fix damage to their heart.
Cancerous primary heart tumors: These
tumors can’t be removed and are often fatal.
Chemotherapy or radiation may be used to
slow the cancer’s progression. Your
provider may also provide medications to
manage complications.
Metastatic heart tumors: Treatment
depends on the source of the cancer. It may
include chemotherapy or surgical removal
of the tumor. Your provider may insert
tubes in your chest to drain excess fluid
from the tumor. They may also inject
medications into your heart to slow tumor
growth or combat fluid buildup.
Conclusion
A neoplasm is a type of abnormal and
excessive growth of tissue. The process
that occurs to form or produce a neoplasm
is called neoplasia. The growth of a
neoplasm is uncoordinated with that of the
normal surrounding tissue, and persists in
growing abnormally, even if the original
trigger is removed. Malignant neoplasms
are also simply known as cancers and are
the focus of oncology. Prior to the
abnormal growth of tissue, such as
neoplasia, cells often undergo an abnormal
pattern of growth, such
as metaplasia or dysplasia. However,
metaplasia or dysplasia does not always
progress to neoplasia and can occur in
other conditions as well. The word
neoplasm is from Ancient Greek 'new' and
plasma 'formation, creation'.
Cardiac tumors range in size and shape.
Some are pedunculated, meaning they grow
on a stalk. Heart tumors may be smaller
than 1 centimeter in diameter or as big as
15 centimeters. Their size and location
within your heart impact your symptoms
and need for treatment.
ADEBANJO TAIWO
JCONS/23A/004
VASCULAR DISORDERS AND PROBLEM OF
PERIPHERAL CIRCULATION
VASCULAR DISORDERS
Prevention
You can’t do anything about your age, family
history or genetics, but you can:
Manage your diabetes, high cholesterol and
high blood pressure.
Exercise regularly.
Eat healthier foods.
Move around once an hour if you have to sit
or stand for hours.
Stay at a healthy weight.
Reduce your stress level.
Avoid tobacco products.
reduction techniques.
of recovery.
6. Collaboration with Interdisciplinary Team:
Nurses collaborate with other healthcare
community centers.
Conclusions
2.ELECTROCARDIOGRAM TEST
An electrocardiogram (ECG or EKG) test is a
non-invasive, painless procedure that
records the electrical activity of the heart. It
provides valuable information about the
heart’s rhythm, rate, and performance.
Doctors often use ECG tests to diagnose
and monitor various heart conditions,
including:
Arrhythmias (abnormal heart rhythms)
Coronary heart disease
Heart attacks
Cardiomyopathy (disease of the heart
muscle)
Electrolyte imbalances
Congenital heart defects
5.COMPUTED TOMOGRAPHY
Computed Tomography (CT) is a non-
invasive medical imaging technique that
uses X-rays and computer algorithms to
generate detailed, cross-sectional images
of the body's internal structures. CT scans
provide valuable diagnostic information and
can help detect various diseases and
abnormalities in soft tissues, bones, and
blood vessels. Here's a comprehensive
overview of CT scans, their applications,
and the benefits and risks associated with
the procedure:
How CT Works
During a CT scan, the patient lies on a table
that slides through a donut-shaped
machine called a gantry. The X-ray tube and
detectors rotate around the patient,
emitting and detecting X-rays as the table
moves. The data collected is then
processed by a computer, which generates
detailed, cross-sectional images of the
scanned body part.
Benefits of CT
Non-invasive and relatively quick procedure
High spatial resolution and excellent tissue
contrast
Ability to visualize various body structures,
including soft tissues, bones, and blood
vessels
Useful for diagnosing a wide range of
medical conditions and guiding treatment
decisions
Can be performed with or without contrast
agents, depending on the clinical indication