Chronic Obstructive Pulmonary Disease
Chronic Obstructive Pulmonary Disease
Chronic Obstructive Pulmonary Disease
o cough,
o chest discomfort,
o shortness of breath, and
o wheezing.
o respiratory distress,
o tachypnea,
o cyanosis,
o use of accessory respiratory muscles,
o peripheral edema,
o hyperinflation,
o chronic wheezing,
o abnormal lung sounds,
o prolonged expiration,
o elevated jugular venous pulse, and
o cyanosis.
Risk Factors
The primary cause of chronic obstructive pulmonary disease is cigarette smoking and/or
exposure to tobacco smoke. Other causes include air pollution, infectious diseases, and
genetic conditions. The risk factors of COPD is increased by smoking tobacco,
secondhand smoke, air pollution, alpha-1 antitrypsin deficiency and a few other
conditions. Chronic bronchitis, emphysema, asthma, and infectious diseases can
contribute to the development of chronic obstructive pulmonary disease.
The stages of chronic obstructive pulmonary disease range from stage I to stage IV. As
the stage number increases, the disease progressively becomes worse; stage IV is also
known as "end stage" chronic obstructive pulmonary disease.
Diagnostic Tests/Procedures
The diagnosis of this COPD is by taking the patient's breathing history and exposure to
irritants such as cigarette smoking or other agents. A pulmonologist usually determines
the stage of COPD by their FEV1 level.
Management
The treatment for this health condition includes avoiding any of the risks and causes
of COPD such as cigarette smoke or toxic fumes, medications, or in a small number
of patients, lung surgery or lung transplant.
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BRONCHIAL ASTHMA
Asthma is a complex clinical syndrome of chronic airway inflammation characterized by
recurrent, reversible, airway obstruction. Airway inflammation also leads to airway
hyperreactivity, which causes airways to narrow in response to various stimuli.
Risk Factors
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The many potential triggers of asthma largely explain the different ways in which asthma
can present. In most cases, the disease starts in early childhood from 2-6 years of age.
In this age group, the cause of asthma is often linked to exposure to allergens, such as
dust mites, tobacco smoke, and viral respiratory infections. In very young children, less
than 2 years of age, asthma can be difficult to diagnose with certainty. Wheezing at this
age often follows a viral infection and might disappear later, without ever leading to
asthma. Asthma, however, can develop again in adulthood. Adult-onset asthma occurs
more often in women, mostly middle-aged, and frequently follows a respiratory tract
infection. The triggers in this group are usually nonallergic in nature.
Your doctor may refer to asthma as being "extrinsic" or "intrinsic." A better understanding
of the nature of asthma can help explain the differences between them. Extrinsic, or
allergic asthma, is more common and typically develops in childhood. Approximately
70%-80% of children with asthma also have documented allergies. Typically, there is a
family history of allergies. Additionally, other allergic conditions, such as nasal allergies
or eczema, are often also present. Allergic asthma often goes into remission in early
adulthood. However, in many cases, the asthma reappears later.
Intrinsic asthma represents a small amount of all cases. It usually develops after the age
of 30 and is not typically associated with allergies. Women are more frequently affected
and many cases seem to follow a respiratory tract infection. Obesity also appears to be
a risk factor for this type of asthma. Intrinsic asthma can be difficult to treat and symptoms
are often chronic and year-round.
The classic signs and symptoms of asthma are shortness of breath, cough (often worse
at night), and wheezing (high-pitched whistling sound produced by turbulent airflow
through narrow airways, typically with exhalation). Many patients also report chest
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tightness. It is important to note that these symptoms are episodic, and individuals with
asthma can go long periods of time without any symptoms.
Common triggers for asthmatic symptoms include exposure to allergens (pets, dust mites,
cockroach, molds, and pollens), exercise, and viral infections. Tobacco use or exposure
to secondhand smoke complicates asthma management.
Many of the symptoms and signs of asthma are nonspecific and can be seen in other
conditions as well. Symptoms that might suggest conditions other than asthma include
new symptom onset in older age, the presence of associated symptoms (such as chest
discomfort, lightheadedness, palpitations, and fatigue), and lack of response to
appropriate medications for asthma.
Diagnostic tests
The diagnosis of asthma begins with a detailed history and physical examination.
Primary-care providers are familiar with the diagnosis of asthma, but specialists such as
allergists or pulmonologists may be involved. A typical history is an individual with a family
history of allergic conditions or a personal history of allergic rhinitis who
experiences coughing, wheezing, and difficulty breathing, especially with exercise or
during the night. There may also be a propensity toward bronchitis or respiratory
infections. In addition to a typical history, improvement with a trial of appropriate
medications is very suggestive of asthma.
In addition to the history and exam, the following are diagnostic procedures that can be
used to help with the diagnosis of asthma:
Lung function testing with spirometry: This test measures lung function as the patient
breathes into a tube. If lung function improves significantly following the administration
of a bronchodilator, such as albuterol, this essentially confirms the diagnosis of asthma.
It is important to note, however, that normal lung function testing does not rule out the
possibility of asthma.
Measurement of exhaled nitric oxide (FeNO): This can be performed by a quick and
relatively simple breathing maneuver, similar to spirometry. Elevated levels of exhaled
nitric oxide are suggestive of "allergic" inflammation seen in conditions such as asthma.
Skin testing for common aeroallergens: The presence of sensitivities to environmental
allergies increases the likelihood of asthma. Of note, skin testing is generally more
useful than blood work (in vitro testing) for environmental allergies. Testing for food
allergies is not indicated in the diagnosis of asthma.
Other potential but less commonly used tests include provocation testing such as a
methacholine challenge, which tests for airway hyperresponsiveness.
Hyperresponsiveness is the tendency of the breathing tubes to constrict or narrow in
response to irritants. A negative methacholine challenge makes asthma much less
likely. Specialists sometimes also measure sputum eosinophils, another marker for
"allergic" inflammation seen in asthma. Chest imaging may show hyperinflation, but is
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often normal in asthma. Tests to rule out other conditions, such as cardiac testing, may
also be indicated in certain cases.
Blood testing can sometimes help differentiate between different types of asthma.
Helpful blood tests include checking for the level of allergic antibody (IgE) or
specialized white blood cells called eosinophils, which are often associated with allergic
or extrinsic asthma.
Management
As per widely used guidelines, the treatment goals for asthma are to:
Inhaled corticosteroids (ICS) are the most effective anti-inflammatory agents available for
the chronic treatment of asthma and are first-line therapy per most asthma guidelines. It
is well recognized that ICS are very effective in decreasing the risk of asthma
exacerbations. Furthermore, the combination of a long-acting bronchodilator (LABA) and
an ICS has a significant additional beneficial effect on improving asthma control.
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Numerous additional monoclonal antibodies are also currently being studied and will
likely be available within the next couple of years.
Immunotherapy or allergy shots have been shown to decrease medication reliance in
allergic asthma.
There are no home remedies that have proven benefit for asthma.
There is often concern about potential long-term side effects of inhaled corticosteroids.
Numerous studies have repeatedly shown that even long-term use of inhaled
corticosteroids has very few if any sustained, clinically significant side effects, including
changes in bone health, growth, or weight. However, the goal always remains to treat all
individuals with the least amount of medication that is effective. Patients with asthma
should be routinely reassessed for any appropriate changes to their medical regimen.
Asthma medications can be administered via inhalers either with or without a spacer or
nebulized solution. It is important to note that if an individual has proper technique with
an inhaler, the amount of medication deposited in the lungs is no different than that when
using a nebulized solution. When prescribing asthma medications, it is essential to
provide the appropriate teaching on proper delivery technique.
Smoking cessation and/or minimizing exposure to secondhand smoke are critical when
treating asthma. Treating concurrent conditions such as allergic rhinitis
and gastroesophageal reflux disease (GERD) may also improve asthma
control. Vaccinations such as the annual influenza vaccination
and pneumonia vaccination are also indicated.
Although the vast majority of individuals with asthma are treated as outpatients, treatment
of severe exacerbations can require management in the emergency department or
inpatient hospitalization. These individuals typically require use of supplemental oxygen,
early administration of systemic steroids, and frequent or even continuous administration
of bronchodilators via a nebulized solution. Individuals at high risk for poor asthma
outcomes are referred to a specialist (pulmonologist or allergist). The following factors
should prompt consideration or referral:
The prognosis for asthma is generally favorable. Children experience complete remission
more often than adults. Although adults with asthma experience a greater rate of loss in
their lung function as compared to age-controlled counterparts, this decline is usually not
as severe as seen in other conditions, such as chronic obstructive pulmonary
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disease (COPD) or emphysema. Asthma in the absence of other comorbidities does not
appear to shorten life expectancy. Risk factors for poor prognosis from asthma include
The airway narrowing in asthma may become fixed over time and can resemble COPD
or emphysema. The other main complication of asthma is due to side effects from oral
steroid use, which can include bone loss (osteoporosis), weight gain, and glucose
intolerance.
With the increasing prevalence of asthma, numerous studies have looked for risk factors
and ways to potentially prevent asthma. It has been shown that individuals living on farms
are protected against wheezing, asthma, and even environmental allergies. The role of
air pollution has been questioned in both the increased incidence of asthma and in
regards to asthma exacerbations.
Climate change is also being studied as a factor in the increased incidence of asthma.
Maternal smoking during pregnancy is a risk factor for asthma and poor outcomes.
Tobacco smoke is also a significant risk factor for the development and progression of
asthma. Treatment of environmental allergies with allergen immunotherapy,
or allergy shots, has been shown to decrease a child's risk of developing asthma. The
development of asthma is ultimately a complex process influenced by many
environmental and genetic factors, and currently there is no proven way to decrease an
individual's risk of developing asthma.
CYSTIC FIBROSIS
Cystic fibrosis (CF) is an inherited disease that affects the secretory glands, including
the mucus and sweat glands. Cystic fibrosis mostly affects the lungs,
pancreas, liver, intestines, sinuses, and sex organs.
CF is due to a mutation in the CF gene on chromosome 7. The CF gene encodes a
protein known as the cystic fibrosis transmembrane regulator (CFTR). The abnormal
CFTR protein in patients with CF leads to disruption of chloride channels on the cells.
CF is characterized by the production of abnormal mucus that is excessively thick and
sticky. The abnormal mucus leads to blockages within the lungs and airways. This
leads to repeated, serious lung infections that can damage the lungs.
Lung function often starts to decline in early childhood in people who have cystic
fibrosis. Over time, permanent damage to the lungs can cause severe breathing
problems.
The thick, sticky mucus also can block tubes, or ducts, in the pancreas. As a result,
the digestive enzymes from the pancreas can't reach the small intestine, causing
impaired absorption of fats and proteins. This can cause vitamin deficiency and
malnutrition.
Due to the defect in chloride channels, CF fibrosis also causes the sweat to become
very salty.
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Every person inherits two CFTR genes -- one from each parent. CF is inherited in an
autosomal recessive manner; children who inherit a faulty gene from each parent will
have cystic fibrosis.
Children who inherit one faulty gene and one normal gene will be "CF carriers." Cystic
fibrosis carriers usually have no symptoms of cystic fibrosis, but they can pass the
faulty gene on to their children.
About 30,000 people in the United States have cystic fibrosis. It is one of the most
common inherited diseases among Caucasians. About 1,000 new cases of cystic
fibrosis are diagnosed each year.
The symptoms of cystic fibrosis vary from person to person and over time.
Doctors diagnose cystic fibrosis based on the results from various tests. The most
commonly used test is a sweat chloride test, which measures the concentration of
chloride in sweat. Direct genetic testing to identify the CF mutation is also used. Most
U.S. States screen newborns for cystic fibrosis.
Cystic fibrosis has no cure. However, treatments have greatly improved in recent
years. Treatment may include nutritional and respiratory therapies,
medicines, exercise, and more. Early treatment for cystic fibrosis can improve both
quality of life and lifespan.
As treatments for cystic fibrosis continue to improve, so does life expectancy for those
who have the disease. Today, some people who have cystic fibrosis are living into
their forties, fifties, and older.
EMPHYSEMA
Emphysema is a destructive disease of the lung in which the alveoli (small sacs) that
promote oxygen exchange between the air and the bloodstream are destroyed.
Smoking is the primary cause of emphysema, which makes it a preventable illness.
There are also less common genetic causes of emphysema including alpha-1
antitrypsin deficiency.
The primary symptom of emphysema is shortness of breath. It is a progressive
complaint by affected individuals, worsening over time. Early in the disease, shortness
of breath may occur with exercise and activity but symptoms gradually worsen and
may occur at rest.
Diagnosis of emphysema is based upon history, physical examination, and pulmonary
function studies.
Once present, emphysema is not curable, but its symptoms are controllable.
Medication regimens are available to preserve function for daily activities and quality
of life for an individual with emphysema.
Oxygen supplementation may be required for a person with emphysema.
Exercise training and education are essential components of emphysema therapy and
pulmonary rehabilitation.
Surgical options for individuals with emphysema have been developed and but are
not expected to be available for widespread use.
Emphysema does not affect quantity of life, but rather quality of life. There are no
studies that can predict life-expectancy in individuals with emphysema.
SARCOIDOSIS
Sarcoidosis is a disease that causes inflammation of body tissues.
The cause of sarcoidosis is not known.
Sarcoidosis commonly affects the lungs and skin.
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Gas is exchanged between the alveoli and the pulmonary capillaries via diffusion.
Diffusion of oxygen and carbon dioxide occurs passively, according to their
concentration differences across the alveolar-capillary barrier. These concentration
differences must be maintained by ventilation (air flow) of the alveoli and perfusion
(blood flow) of the pulmonary capillaries.
A balance between the two normally exists but certain conditions can alter this balance,
resulting in Impaired Gas Exchange. Dead space is the volume of a breath that does
not participate in gas exchange. It is ventilation without perfusion.
Related Factors
Here are some factors that may be related to Impaired Gas Exchange:
Altered oxygen supply
Altered oxygen-carrying capacity of blood
Alveolar-capillary membrane changes
Ventilation-perfusion imbalance
Pathophysiologic
Treatment Related
Anesthesia (general or spinal)
Sedating or paralytic effects of medications, drugs, or chemicals
Suppressed cough reflex
Tracheostomy
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Defining Characteristics
The following are the common goals and expected outcomes for Impaired Gas Exchange.
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Nursing Assessment
The patient’s general appearance may give clues to respiratory status. Observing the
individual’s responses to activity are cue points in performing an assessment related
to Impaired Gas Exchange.
Assessment Rationales
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Nursing Interventions
The following are the therapeutic nursing interventions for Impaired Gas Exchange:
Interventions Rationales
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Regularly check the patient’s position so Slumped positioning causes the abdomen to
that he or she does not slump down in compress the diaphragm and limits full lung
bed. expansion.
If patient is acutely dyspneic, consider Leaning forward can help decrease dyspnea,
having patient lean forward over a bedside possibly because gastric pressure allows better
table, if tolerated. contraction of the diaphragm.
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Schedule nursing care to provide rest and The hypoxic patient has limited reserves;
minimize fatigue. inappropriate activity can increase hypoxia.
Assess the home environment for irritants
that impair gas exchange. Help the patient Irritants in the environment decrease the patient’s
to adjust home environment as necessary effectiveness in accessing oxygen during
(e.g., installing air filter to decrease breathing.
presence of dust).
Instruct patient to limit exposure to This is to reduce the potential spread of droplets
persons with respiratory infections. between patients.
Instruct family in complications of disease
Knowledge of the family about the disease is very
and importance of maintaining medical
important to prevent further complications.
regimen, including when to call physician.
Severely compromised respiratory functioning
Support family of patient with chronic causes fear and anxiety in patients and their
illness. families. Reassurance from the nurse can be
helpful.
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Table of Contents
Title Pages
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