Professional Documents
Culture Documents
Bronchoscopy
Bronchoscopy is a procedure to look directly at the airways in the lungs through a thin, lighted tube
(bronchoscope).
Chest Fluoroscopy
Chest fluoroscopy is an imaging test that uses X-rays to look at how well your lungs are working. It can also
look at other parts of your respiratory tract. Your respiratory tract includes your lungs, nose, throat, trachea,
and bronchi.
Chest Ultrasound
Chest ultrasound is a procedure in which sound wave technology is used alone, or along with other types of
diagnostic methods, to examine the organs and structures of the chest.
Chest X-Ray
A chest X-ray is an imaging test that uses X-rays to look at the structures and organs in your chest. It can help
your health care provider see how well your lungs and heart are working. Certain heart problems can cause
changes in your lungs. Certain diseases can cause changes in the structure of the heart or lungs.
Lobectomy
A lobectomy is a surgery to remove one of the lobes of the lungs.
Lung Biopsy
A biopsy is a procedure done to remove a sample of tissue from the body so it can be examined. A lung biopsy
is a procedure to take a small piece of a lung.
Lung Scan
A lung scan is an imaging test to look at your lungs and help diagnose certain lung problems. A lung scan may
also be used to see how well treatment is working.
Lung Transplant
A lung transplant is surgery done to remove a diseased lung and replace it with a healthy lung from another
person.
Mediastinoscopy A mediastinoscopy is a procedure used to examine the mediastinum. This is the space
behind the breastbone (sternum). This area can be examined with a tool called a mediastinoscope. This is a
long, thin, flexible tube that has a light and a tiny camera.
Pleural Biopsy
Pleural biopsy is a procedure to remove a tissue sample from the membrane that surrounds the lungs called
the pleura.
Pulmonary Angiogram
Pulmonary angiogram is an X-ray image of the blood vessels of the lungs.
Pulse Oximetry
Pulse oximetry is a test used to measure the oxygen level (oxygen saturation) of the blood. It is an easy,
painless measure of how well oxygen is being sent to parts of your body furthest from your heart, such as the
arms and legs.
Sinus X-ray
A sinus X-ray is an imaging test that uses X-rays to look at your sinuses. The sinuses are air-filled pockets
(cavities) near your nasal passage.
Sleep Study
The stages of sleep range from light to deep. Each stage has characteristics that can be measured. A sleep
study is a number of tests done at the same time during sleep. The tests measure specific sleep characteristics
and help to diagnose sleep disorders. A sleep study may also be called polysomnogram.
Thoracentesis
Thoracentesis is a procedure to remove fluid or air from around the lungs.
Spirometry
Spirometry (figure 1) is the most important function test it measures vital capacity (VC) and forced expiratory volume in 1 second (FEV1). This permits
differentiation between restrictive and obstructive respiratory diseases. If expired volume is measured by electrical integration of airflow (using a
pneumotachograph), maximum flowvolume curves can also be registered. These tests are used to measure the effect of bronchodilating drugs on reversibility of
obstruction as well as to determine responsiveness to bronchial provocation tests. Simple instruments for patient home use include peak flow meters, which
measure the degree of obstruction.
The total lung capacity can be determined using either gas dilution techniques or body plethysmography. The latter method also allows the measurement of airway
resistance. The forced oscillation technique, which measures the resistance of the total respiratory system, has the advantage that the patient does not need to
perform specific breathing manoeuvres.
Diffusing capacity
The diffusing capacity of the lung for carbon monoxide (also known as transfer factor), which is usually performed as a single-breath test, measures the overall
gas-exchange function of the lung.
Arterial blood gas (ABG) measurement to determine the arterial oxygen tension (PaO2 ) and arterial carbon dioxide tension (PaCO2) is one of the most useful
diagnostic tests: blood can be sampled directly from an artery, or an estimate can be obtained from capillary blood from, for instance, a warmed earlobe. ABG
measurement allows the diagnosis of hypoxaemia (decreased PaO2) with or without hypercapnia (increased PaCO2), a sensitive index of inefficient pulmonary gas
exchange, which is also used for defining respiratory failure. PaO2 measurement after breathing 100% oxygen is sometimes used to estimate the anatomical rightto-left shunt. Arterial oxygen saturation (SaO2) represents the percentage of binding sites on the haemoglobin molecule occupied by oxygen and offers a
noninvasive method of estimating arterial blood oxygenation; it is measured directly by an oximeter with a probe attached to either the finger or the
earlobe.PaCO2 can also be estimated noninvasively, using a transcutaneous electrode but such devices are not yet as widely used as oximeters. ABG
measurement also allows evaluation of acidbase disorders.
Cardiopulmonary exercise testing (CPET), with determination of minute ventilation, cardiac and respiratory frequency, oxygen uptake and carbon dioxide output, is
an objective measure of exercise capacity (spiroergometry). Simpler tests use capillary oxygen partial pressure measurements during exercise on an ergometer or
symptom-limited walking tests, such as the 6-min shuttle walk test, with measurement of SaO2 using an oximeter.
Respiratory muscle function is commonly assessed by measuring maximal pressures generated at the mouth during maximal inspiratory and expiratory efforts
against an occluded airway.
Control of ventilation
Tests of ventilatory control include the hyperoxic rebreathing method and the hypoxia-withdrawal method. Simpler, but less specific, is the measurement of the
mouth occlusion pressure.
The diagnosis of sleep-related respiratory disorders requires special tests. The gold standard is polysomnography, but simpler tests are available for screening
purposes (respiratory polysomnography).
The management of respiratory failure in the intensive care unit requires, in addition to frequent checking of ABGs, the measurement of several special parameters
(e.g. tidal volume, inspiratory and expiratory pressures); in mechanically ventilated patients, these are often measured automatically by the ventilator.
Partial pressure of oxygen (PaO2): Measures the pressure of oxygen dissolved in the blood and how well oxygen is able to move from the airspace of the lungs into the
blood.
Partial pressure of carbon dioxide (PaCO2): Measures how much carbon dioxide is dissolved in the blood and how well carbon dioxide is able to move out of the body.
pH: The pH measures hydrogen ions (H+) in blood. The pH of blood is usually between 7.35 and 7.45. A pH of less than 7.0 is called acid and a pH greater than 7.0 is called
basic (alkaline). So blood is slightly basic.
Bicarbonate (HCO3): Bicarbonate is a chemical (buffer) that keeps the pH of blood from becoming too acidic or too basic.
Oxygen content (O2CT) and oxygen saturation (O2Sat) values: O2 content measures the amount of oxygen in the blood. Oxygen saturation measures how much of the
hemoglobin in the red blood cells is carrying oxygen (O2).Blood for an ABG test is taken from an artery. Most other blood tests are done on a sample of blood taken from a
vein, after the blood has already passed through the body's tissues where the oxygen is used up and carbon dioxide is produced.
Erswhitebook.org,. (2016). Respiratory function tests - ERS. Retrieved 21 January 2016, from
http://www.erswhitebook.org/chapters/principles-of-respiratory-investigation/respiratory-function-tests/
Hopkinsmedicine.org,. (2016). Pulmonary Tests and Procedures | Johns Hopkins Medicine Health Library. Retrieved 21 January 2016, from
http://www.hopkinsmedicine.org/healthlibrary/test_procedures/pulmonary/
shortness of breath.
fever.
Physicians use the examination to help diagnose or monitor treatment for conditions such as:
pneumonia.
emphysema.
lung cancer.
Different parts of the body absorb the x-rays in varying degrees. Dense bone absorbs much of the radiation while soft tissue, such as
muscle, fat and organs, allow more of the x-rays to pass through them. As a result, bones appear white on the x-ray, soft tissue shows
up in shades of gray and air appears black.
On a chest x-ray, the ribs and spine will absorb much of the radiation and appear white or light gray on the image. Lung tissue absorbs
little radiation and will appear dark on the image.
Until recently, x-ray images were maintained as hard film copy (much like a photographic negative). Today, most images are digital files
that are stored electronically. These stored images are easily accessible and are frequently compared to current x-ray images for
diagnosis and disease management.
top of page
Follow-up examinations may be necessary, and your doctor will explain the exact reason why another exam is requested. Sometimes a
follow-up exam is done because a suspicious or questionable finding needs clarification with additional views or a special imaging
technique. A follow-up examination may also be necessary so that any change in a known abnormality can be monitored over time.
Follow-up examinations are sometimes the best way to see if treatment is working or if an abnormality is stable or changed over time.
top of page
X-rays usually have no side effects in the typical diagnostic range for this exam.
X-ray equipment is relatively inexpensive and widely available in emergency rooms, physician offices, ambulatory care centers,
nursing homes and other locations, making it convenient for both patients and physicians.
Because x-ray imaging is fast and easy, it is particularly useful in emergency diagnosis and treatment.
Risks
There is always a slight chance of cancer from excessive exposure to radiation. However, the benefit of an accurate diagnosis
far outweighs the risk.
The effective radiation dose for this procedure varies. See the Safety page for more information about radiation dose.
Women should always inform their physician or x-ray technologist if there is any possibility that they are pregnant.See
the Safety page for more information about pregnancy and x-rays.
(ACR),. (2016). Chest X-ray (Radiography). Radiologyinfo.org. Retrieved 21 January 2016, from
http://www.radiologyinfo.org/en/info.cfm?pg=chestrad
Chest X-rays are a common type of exam. A chest X-ray is often among the first procedures you'll undergo if your doctor
suspects you have heart or lung disease. It can also be used to check how you are responding to treatment.
A chest X-ray can reveal many things inside your body, including:
The condition of your lungs. Chest X-rays can detect cancer, infection or air collecting in the space around a
lung (pneumothorax). They can also show chronic lung conditions, such as emphysema or cystic fibrosis, as well as
complications related to these conditions.
Heart-related lung problems. Chest X-rays can show changes or problems in your lungs that stem from heart
problems. For instance, fluid in your lungs (pulmonary edema) can be a result of congestive heart failure.
The size and outline of your heart. Changes in the size and shape of your heart may indicate heart failure, fluid
around the heart (pericardial effusion) or heart valve problems.
Blood vessels. Because the outlines of the large vessels near your heart the aorta and pulmonary arteries
and veins are visible on X-rays, they may reveal aortic aneurysms, other blood vessel problems or congenital heart
disease.
Calcium deposits. Chest X-rays can detect the presence of calcium in your heart or blood vessels. Its presence
may indicate damage to your heart valves, coronary arteries, heart muscle or the protective sac that surrounds the
heart. Calcium deposits in your lungs are most often from an old, resolved infection.
Fractures. Rib or spine fractures or other problems with bone may be seen on a chest X-ray.
Postoperative changes. Chest X-rays are useful for monitoring your recovery after you've had surgery in your
chest, such as on your heart, lungs or esophagus. Your doctor can look at any lines or tubes that were placed during
surgery to check for air leaks and areas of fluid or air buildup.
A pacemaker, defibrillator or catheter. Pacemakers and defibrillators have wires (leads) attached to your heart
to make sure your heart rate and rhythm are normal. Catheters are small tubes used to deliver medications or for
dialysis. A chest X-ray usually is taken after placement of such medical devices to make sure everything is positioned
correctly.
As mentioned earlier, the image on chest X-ray film is in shades of black and white, similar to a negative of a regular
photograph. The shadows on a chest X-ray test depend on the degree of absorbed radiation by the particular organ based
on its composition. Bony structures absorb the most radiation and appear white on the film. Hollow structures containing
mostly air, such the lungs, normally appear dark. In a normal chest X-ray, the chest cavity is outlined on each side by the
white bony structures that represent the ribs of the chest wall. On the top portion of the chest is the neck and the collar
bones (clavicles). On the bottom, the chest cavity is bordered by the diaphragm under which is theabdominal cavity. On
either side of the chest wall, the bones of the shoulders and arms are easily recognizable.
Inside the chest cavity, the vertebral column can be seen down the middle of the chest, splitting it nearly in equal halves.
On each side of the midline, the dark appearing lung fields are seen. The white shadow of the heart is in the middle of the
field, atop the diaphragm and more to the left side. The trachea (wind pipe), aorta (main blood vessel exiting the heart),
and the esophagus descend down the middle, overlapping the vertebral column.
Abnormal Chest X-ray Test
Many abnormalities can be detected on a chest X-ray test. Common abnormalities seen on a chest X-ray test include:
pneumonia (abnormally white or hazy shadow on the lung fields that would normally look dark);
fluid collection between the lung and the chest wall appearing whiter than the lungs and making the sharp lung borders on the film more hazy
(pleural effusion);
pulmonary edema (fluid build-up in the lung or its blood vessels) seen as diffuse haziness on the lung fields (for example, from congestive
heart failure);
broken ribs or arm bones (irregularity in the structure and shape of any of the ribs or the humerus bone of the arm);
dislocated shoulders;
lung cancer or other lung masses (irregular and abnormal shadow on the lung fields);
abnormal presence of air between the chest wall and the lung creating a distinct black shadow (darker than the lung fields) between the
border of the lung tissue and the inside border of the chest wall (pneumothorax);
hiatal hernia (protrusion of the upper portion of the stomach into the chest cavity); and
aortic aneurysm (dilated aorta - a widening of the midline of the chest overlying the vertebral column).
These are some of the common abnormal findings that can be seen on chest X-ray test. There are many other less
common abnormalities that can be detected on chest X-ray tests.
Bacteriologic examination of sputum material raised from the lungs and bronchi during deep coughing is an
important aid in managing lung disease. The usual method of specimen collection is expectoration. Other
methods include tracheal suctioning and bronchoscopy. A gram stain of expectorated sputum must be
examined to ensure that its representative of secretions from the lower respiratory tract rather than
contaminated by oral flora. Careful examination of an acid-fast sputum smear may provide presumptive
evidence of a mycobacterial infection, such as tuberculosis.
Sputum may be cultured to identify respiratory pathogens. Expectoration, the usual sputum collection method,
may require ultrasonic nebulization, hydration, or chest percussion and postural drainage. Less common
method include tracheal suctioning where in it provides a more reliable diagnostic specimen but generally isnt
used, unless expectoration fails to provide sample.
Purpose
4.
Using aseptic technique, close the container securely and place it in a leak proof bag
before sending it to the laboratory.
Tracheal Suctioning
1.
Give oxygen to the patient before and after the procedure as necessary.
2.
Attach the sputum trap to suction catheter.
3.
Lubricate the catheter with normal saline solution and pass the catheter through the
nostril without suction.
4.
Advance the catheter into the trachea; apply suction while withdrawing the catheter,
not during catheter insertion.
5.
Suction only for 5 to 10 seconds at a time.
6.
Stop suction and remove the catheter.
7.
Discard the catheter in the proper receptacle.
8.
Detach the in-line sputum trap from the suction apparatus and cap the opening.
9.
During the passage through the throat and oropharynx, sputum specimens are
commonly contaminated with indigenous bacterial flora.
10. Label the container with the patients name, the nature and origin of the specimen,
the date and time of collection, the initial diagnosis, and any current antimicrobial
therapy.
11. Send the specimen to the laboratory immediately after collection.
Nursing Interventions
1.
Provide mouth care to the patient.
2.
Monitor his vital signs and respiratory status.
3.
Monitor oxygen saturation with a pulse oximeter.
4.
If the patient becomes hypoxic or cyanotic during suctioning, remove the catheter
immediately and give oxygen while suctioning pulse oximetry.
Interpretation
Normal Results
1.
Common flora includes alpha-hemolytic streptococci. Neisseria, and diptheroid.
2.
Presence of common flora doesnt rule out infection.
Abnormal Results
1.
Because sputum is invariably contaminated with normal oropharyngeal flora, a culture
isolate must be interpreted in light of the patients overall clinical condition.
2.
Isolation of Myobacterium Tuberculosis suggests tuberculosis.
3.
Isolation of pathogenic organisms most often includes Streptococcus pneumonia,
Myobacterium Tuberculosis, Klebsiella pneumoniae (and other Enterobacteriaceae),
Haemophilus influenzae, Staphyloccocus aureus, and Pseudomonas aeruginosa.
Complications
Hypoxemia
Cardiac arrhythmias
Laryngospasm
Bronchospasm
Pneumothorax
Bleeding
Interfering Factors
Obstructive. This is when air has trouble flowing out of the lungs due to resistance. This causes a decreased flow of air.
Restrictive. This is when the chest muscles cant expand enough. This creates problems with air flow.
PFT measures:
Tidal volume (VT). This is the amount of air inhaled or exhaled during normal breathing.
Minute volume (MV). This is the total amount of air exhaled per minute.
Vital capacity (VC). This is the total volume of air that can be exhaled after inhaling as much as you can.
Functional residual capacity (FRC). This is the amount of air left in lungs after exhaling normally.
Residual volume. This is the amount of air left in the lungs after exhaling as much as you can.
Total lung capacity. This is the total volume of the lungs when filled with as much air as possible.
Forced vital capacity (FVC). This is the amount of air exhaled forcefully and quickly after inhaling as much as you can.
Forced expiratory volume (FEV). This is the amount of air expired during the first, second, and third seconds of the FVC test.
Forced expiratory flow (FEF). This is the average rate of flow during the middle half of the FVC test.
Peak expiratory flow rate (PEFR). This is the fastest rate that you can force air out of your lungs.
Normal values for PFTs vary from person to person. The amount of air inhaled and exhaled in your test results are compared to the average for someone
of the same age, height, sex, and race. Results are also compared to any of your previous test results. If you have abnormal PFT measurements or if your
results have changes, you may need other tests.
Allergies
Respiratory infections
Trouble breathing from injury to the chest or a recent surgery
Chronic lung conditions, such as asthma, bronchiectasis, emphysema, or chronic bronchitis
Asbestosis, a lung disease caused by inhaling asbestos fibers
Restrictive airway problems from scoliosis, tumors, or inflammation or scarring of the chest wall
Sarcoidosis, a disease that causes lumps of inflammatory cells around organs such as the liver, lungs, and spleen
Scleroderma, a disease that causes thickening and hardening of connective tissue
PFTs may be used to check lung function before surgery or other procedures in patients who have lung or heart problems, who are smokers, or who have
other health conditions. Another use of PFTs is to assess treatment for asthma, emphysema, and other chronic lung problems. Your healthcare provider
may also have other reasons to advise PFTs.
In some cases, a person shouldnt have PFTs. Reasons for this can include:
Recent eye surgery, because of increased pressure inside the eyes during the procedure
Recent belly (abdominal) or chest surgery
Chest pain, recent heart attack, or an unstable heart condition
A bulging blood vessel (aneurysm) in the chest, belly, or brain
Active tuberculosis (TB) or respiratory infection, such as a cold or the flu
Your risks may vary depending on your general health and other factors. Ask your healthcare provider which risks apply most to you. Talk with him or her
about any concerns you have.
Certain things can make PFTs less accurate. These include:
Stop taking certain medicines before the procedure, if instructed by your healthcare provider
Stop smoking before the test, if instructed by your healthcare provider
Not eat a heavy meal before the test, if instructed by your healthcare provider
Follow any other instructions your healthcare provider gives you
Your height and weight will be recorded before the test. This is done so that your results can be accurately calculated.
Youll be asked to loosen tight clothing, jewelry, or other things that may cause a problem with the procedure.
If you wear dentures, you will need to wear them during the procedure.
Youll need to empty your bladder before the procedure.
Youll sit in a chair. A soft clip will be put on your nose. This is so all of your breathing is done through your mouth, not your nose.
Youll be given a sterile mouthpiece that is attached to a spirometer.
Youll form a tight seal over the mouthpiece with your mouth. Youll be instructed to inhale and exhale in different ways.
You will be watched carefully during the procedure for dizziness, trouble breathing, or other problems.
You may be given a bronchodilator after certain tests. The tests will then be repeated several minutes later, after the bronchodilator has taken
effect.
Next steps
Before you agree to the test or the procedure make sure you know:
To
To
To
To
Pulse oximetry is also used to check the health of a person with any condition that affects blood oxygen levels, such as:
Heart attack
Heart failure
Chronic obstructive pulmonary disease (COPD)
Anemia
Lung cancer
Asthma
Pneumonia
Your healthcare provider may have other reasons to advise pulse oximetry.
Incorrect reading if the probe falls off the earlobe, toe, or finger
Skin irritation from adhesive on the probe
Your risks may vary depending on your general health and other factors. Ask your healthcare provider which risks apply most to you. Talk with him or her
about any concerns you have.
A clip-like device called a probe will be placed on your finger or earlobe. Or, a probe with sticky adhesive may be placed on your forehead or
finger.
The probe may be left on for ongoing monitoring.
Or it may be used to take a single reading. The probe will be removed after the test.
Next steps
Before you agree to the test or the procedure make sure you know:
Hopkinsmedicine.org,. (2016). Pulse Oximetry | Johns Hopkins Medicine Health Library. Retrieved 21 January 2016, from
http://www.hopkinsmedicine.org/healthlibrary/test_procedures/pulmonary/oximetry_92,P07754/
blood, and calculates exact mixed venous oxygen saturation without interference from
surrounding venous blood, skin, connective tissue, or bone.
Equipment
Oximeter
Sensor probe
Alcohol pads
Select a finger (usually index finger) on the patients nondominant hand, if possible for
placement of the probe.
Remove fake fingernail and nail polish from the test finger.
Place the transducer (photoprotector) probe over the patients finger so the light
beams and sensor oppose each other.
Turn on the power switch. If the device is working properly, a beep will sound, a display
will light momentarily, and the pulse search light will flash.
After four to six heartbeats the pulse amplitude indicator will begin tracking the pulse.
Clean the probe per facility policy between patients or, if disposable, discard.
Nursing Interventions
1.
Some machines have a pleth wave. A steady, level, even wave form ensures that the
numerical reading is accurate.
2.
The pulse rate on the oximeter should correspond to the patients actual pulse. If it
doesnt, monitor the patient, check the oximeter, and reposition the probe.
3.
Factors that interfere with accuracy include:
o
Elevated carboxyhemoglobin or methemoglobin levels
o
Lipid emulsions and dyes
o
Excessive light
o
Excessive patient movement
o
Hypothermia
o
Hypotension
o
Vasoconstriction
o
Medications such as dapsone, vasopressors.
Use the bridge of the nose if the patient has compromised circulation in his
extremities.
If patient movement is the problem, move the probe or select a different probe.
KEY WORDS: pulse oximetry, arterial oxygen saturation (SpO or SaO ), arterial blood gas (ABG) analysis, partial oxygen
2
pressure (PaO ), partial carbon dioxide pressure (PaCO ), capnography, oxyhemoglobin dissociation curve
2
Pulse oximetry is a useful tool for assessing oxygen saturation, but it doesn't provide a complete picture of your
patient's respiratory status. Understanding what pulse oximetry can and can't do will help you to use this
technology wisely.
Jump to:
Pulse oximetry is a noninvasive method of monitoring a patient's pulse rate and arterial oxygen saturation. A pulse
oximeter uses a light-emitting diode (LED) and a photodetector to estimate the percentage of total hemoglobin that's
saturated (filled) with oxygen molecules, based on the amounts of red and infrared light that pass through the vascular
bed. Arterial oxygen saturation is represented by the symbol SpO when measured by pulse oximetry or SaO when
2
measured by arterial blood gas (ABG) analysis. For a healthy patient, an SpO of 97% 99% is generally considered
2
normal.
Pulse oximetry is now a part of routine perioperative monitoring, and is widely used to monitor patients in many different
settings, including the ED, OR, ICU, PACU, and med/surg units. However, because it doesn't provide any information
2
about a patient's ventilation, relying on pulse oximetry alone could compromise patient safety, particularly in patients who
are receiving supplemental oxygen or who are at risk of respiratory depression.
Yet, a recent study found that only 35% of nurses (and 39% of physicians) in a major medical center knew that pulse
oximetry monitored oxygen saturation only and did not reflect changes in ventilation. The study also found that an
3
well a patient can exhale carbon dioxide produced by metabolic activities) can be determined by analyzing a patient's
partial carbon dioxide pressure (PaCO ), and the partial pressure of carbon dioxide in exhaled gasthe end-tidal
2
CO (EtCO ).
2
Pulse oximetry can tell you about saturation only; to assess other measures of oxygenation and ventilation, you need to
consider ABG analysis and capnography (which will be discussed below). In some cases, acceptable pulse oximetry
readings ("good sats") have falsely reassured clinicians despite serious deterioration in a patient's respiratory status as
shown by dangerously high levels of PaCO .
2
Taking a more comprehensive approach to respiratory monitoring is especially important for patients at increased risk of
respiratory depression, which can be precipitated by:
altered level of consciousness due to sedation, medications such as opioids, or other conditions;
decreased blood flow to the brain's respiratory centers as the result of increased intracranial pressure, shock, or other
factors;
fatigue associated with the increased work of breathing; or
cardiac or pulmonary diseases that affect oxygenation.
At-risk patients may need not only pulse oximetry but also ABG analysis or capnography. ABG analysis provides a more
complete picture of a patient's respiratory status, including PaO , PaCO , arterial pH, and acid-base balance, but it requires
2
A quicker, noninvasive way to monitor a patient's respiratory status is to use pulse oximetry to evaluate oxygen saturation
together with capnography to measure exhaled carbon dioxide that can provide information about ventilation.
Capnography provides a graphic representation (a capnogram) of the level of exhaled carbon dioxide (CO ). The
2
capnogram gives you breath-to-breath information about the CO that's being exhaled from the lungs. Apnea monitors are
2
an alternative to capnography, but false alarms occur more often with apnea monitors than with
capnography. Capnography devices are now easy to use and available for patients without artificial airways; exhaled
5
CO is collected from a nasal cannula-like device. Monitors are available for bedside use in med/surg, as part of portable
2
monitor-defibrillators for transport, and as cartridges that can be added to the wall-mounted component of central
monitoring systems in critical care areas.
To determine whether a patient has an adequate amount of oxygen in his blood, you need to first interpret his SpO value
2
in the context of his total hemoglobin. Not all patients with the same SpO have the same amount of oxygen in their blood.
6
For example, pulse oximetry may show that two patients, Mr. Thomas and Mr. Martin, both have what appears to be an
acceptable SpO of 97%. However, a complete blood count reveals that Mr. Thomas' total hemoglobin level is normal at 15
2
hemoglobin, such as the patient's temperature, pH, and PaCO . The impact of each of these factors is demonstrated in the
2
oxyhemoglobin dissociation curve in the "The oxyhemoglobin dissociation curve" box. While PaO values shouldn't be
2
ignored, remember: Only 2% to 3% of all oxygen carried in the blood is dissolved in plasma and reflected in the
PaO value. The rest is bound to hemoglobin, which makes saturation all the more importantas long as it's interpreted in
2
artifact." Any motion, but particularly rhythmic movements such as tremors, shivering, or seizures, can affect the accuracy
7
How can you check to see if low perfusion is affecting your readings? One option is to compare the pulse rate displayed
on the pulse oximeter with a palpated pulse or apical heart rate. If they don't match, the oximeter isn't picking up each
arterial pulsation and your readings are probably not reliable. Moving the sensor to the patient's ear lobe, which is least
affected by poor blood flow, or to another digit, may allow you to obtain a more accurate reading.
You should also regularly monitor the pulse oximeter's signal strength indicator. Some monitors provide a waveform,
others a bar of light, and still others provide indicators such as a green light when signal strength is best, yellow when it's
borderline, and red when it's too low for an accurate reading.
Venous pulsationswhich may occur as a result of a rare cardiac defect like tricuspid regurgitationwill cause the
oximeter to record venous oxygen saturation instead of arterial saturation. Often, however, it's not a patient's physical
condition that causes venous pulsations. Taping a clip-on sensor to a toe or finger, for example, can impede venous return
and cause pulsation. To solve this problem, don't use tape, and transfer the sensor to a different extremity on a regular
basis.
Abnormal hemoglobins, such as carboxyhemoglobin or methemoglobin, can also affect how you interpret readings. The
pulse oximeter will accurately measure the percentage of filled binding sites on hemoglobin, but it cannot differentiate
between hemoglobin molecules filled with oxygen and those filled with carbon monoxide (or any other molecule). For
example, hemoglobin binds 200 250 times more readily to carbon monoxide than to oxygen, but because the pulse
oximeter cannot distinguish between the two, the device will give a high SpO reading even if half of the hemoglobin
2
molecules are filled with carbon monoxide and not oxygen. For this reason, pulse oximetry should never be used on
patients suspected of having carbon monoxide exposure; instead use ABG.
Similarly, anemia or polycythemia will not affect the accuracy of the SpO values, but as described above, these factors will
2
affect your interpretation of those values. In this case, you must know the patient's hemoglobin content. An anemic patient
may have a 99% saturation, but because there are fewer hemoglobin molecules, it's easier to fill them up and the total
oxygen content can be significantly decreased despite the "good sats." The jury is still out regarding whether pulse
oximetry readings are reliable in patients with sickle cell disease, in which the hemoglobin is shaped abnormally. Any
abnormalities of hemoglobin have the potential to make SpO readings unreliable.
2
In addition, any discoloration of the nail bed can affect pulse oximetry readings by altering the transmission of light through
the finger. Dark nail polish or bruising under the nail could result in a reading that's artificially low. You can try turning the
1
clip 90 degrees and then placing it on the finger so the light will pass through the finger side-to-side rather than through
the nail bed. Otherwise, move the sensor to the earlobe.
4. Remember ROME
Still, it all boils down to mnemonics. The mnemonic RO-ME.
Respiratory Opposite
When pH is up, PaCO2 is down = Alkalosis
When pH is down, PaCO2 is up = Acidosis
Metabolic Equal
When pH is up, HCO3 is up = Alkalosis
When pH is down, HCO3 is down = Acidosis
5. Tic-Tac-Toe
And yes, ABG problems can be solved work using the tic-tac-toe method. All you have to do is make a
blank chart similar to this:
7. Match it up
In this step, determine at which column matches up with the pH. In the given example, HCO 3goes with pH.
HCO3 is considered Metabolic (shown in step 3), and both are under Acid, so this example implies Metabolic
Acidosis.
8. Determine compensation
The last step is to determine if the ABG is Compensated, Partially Compensated, or Uncompensated. Heres
the trick:
If pH is NORMAL, PaCO2 and HCO3 are both ABNORMAL = Compensated
If pH is ABNORMAL, PaCO2 and HCO3 are both ABNORMAL = Partially Compensated
If pH is ABNORMAL, PaCO2 or HCO3 is ABNORMAL = Uncompensated
Therefore this ABG is METABOLIC ACIDOSIS, PARTIALLY COMPENSATED .
By applying the steps above, interpret the following ABGs:
pH:7.44, PaCO2: 30, HCO3: 21
pH is NORMAL = NORMAL so place pH under Normal
PaCO2 is LOW = BASE so place PaCO2 under Base
HCO3 is LOW = ACID so place HCO3 under Acid
*Since the acidity of the blood is determined by the value of the pH, determine whether the normal pH is
SLIGHTLY ACIDIC or SLIGHTLY BASIC. In this example, pH is NORMAL but SLIGHTLY BASIC therefore it is
ALKALOSIS.
In this case PaCO2 goes with pH. PaCO2 is considered Respiratory (shown in step 3), and both are under
Basic, so this example implies Respiratory Alkalosis. The HCO3 is also abnormal. When pH is NORMAL and
PaCO2 and HCO3 are both ABNORMAL, it indicates FULL COMPENSATION.
Therefore this ABG is RESPIRATORY ALKALOSIS, FULLY COMPENSATED.
Try this problem next:
Interpreting an arterial blood gas (ABG) is a crucial skill for physicians, nurses, respiratory therapists, and other health care personnel.
ABG interpretation is especially important in critically ill patients.
The following six-step process helps ensure a complete interpretation of every ABG. In addition, you will find tables that list commonly
encountered acid-base disorders.
Many methods exist to guide the interpretation of the ABG. This discussion does not include some methods, such as analysis of base
excess or Stewarts strong ion difference. A summary of these techniques can be found in some of the suggested articles. It is unclear
whether these alternate methods offer clinically important advantages over the presented approach, which is based on the anion gap.
6-step approach:
Step 1: Assess the internal consistency of the values using the Henderseon-Hasselbach equation:
[H+] = 24(PaCO2)
[HCO3-]
If the pH and the [H+] are inconsistent, the ABG is probably not valid.
pH
Approximate [H+]
(mmol/L)
7.00
100
7.05
89
7.10
79
7.15
71
7.20
63
7.25
56
7.30
50
7.35
45
7.40
40
7.45
35
7.50
32
7.55
28
7.60
25
7.65
22
Remember: an acidosis or alkalosis may be present even if the pH is in the normal range (7.35 7.45)
You will need to check the PaCO2, HCO3- and anion gap
Step 3: Is the disturbance respiratory or metabolic? What is the relationship between the direction of change in the pH and the
direction of change in the PaCO2? In primary respiratory disorders, the pH and PaCO2 change in oppositedirections; in metabolic
disorders the pH and PaCO2 change in the same direction.
Acidosis
Respiratory
pH
PaCO
Acidosis
Metabolic&
pH
PaCO
Alkalosis
Respiratory
pH
PaCO
Alkalosis
Metabolic
pH
PaCO
Step 4: Is there appropriate compensation for the primary disturbance? Usually, compensation does not return the pH to normal (7.35
7.45).
Disorder
Expected compensation
Correction factor
Metabolic acidosis
Metabolic alkalosis
If the observed compensation is not the expected compensation, it is likely that more than one acid-base disorder is present.
Step 5: Calculate the anion gap (if a metabolic acidosis exists): AG= [Na+]-( [Cl-] + [HCO3-] )-12 2
In patients with hypoalbuminemia, the normal anion gap is lower than 12 meq/L; the normal anion gap in patients with
hypoalbuminemia is about 2.5 meq/L lower for each 1 gm/dL decrease in the plasma albumin concentration (for example, a
patient with a plasma albumin of 2.0 gm/dL would be approximately 7 meq/L.)
If the anion gap is elevated, consider calculating the osmolal gap in compatible clinical situations.
o
Elevation in AG is not explained by an obvious case (DKA, lactic acidosis, renal failure
Step 6: If an increased anion gap is present, assess the relationship between the increase in the anion gap and the decrease in [HCO3-].
Assess the ratio of the change in the anion gap (AG ) to the change in [HCO3-] ([HCO3-]): AG/[HCO3-]
This ratio should be between 1.0 and 2.0 if an uncomplicated anion gap metabolic acidosis is present.
If this ratio falls outside of this range, then another metabolic disorder is present:
If AG/[HCO3-] < 1.0, then a concurrent non-anion gap metabolic acidosis is likely to be present.
It is important to remember what the expected normal anion gap for your patient should be, by adjusting for hypoalbuminemia
(see Step 5, above.)
Table 1: Characteristics of acid-base disturbances
Disorder
pH
Primary problem
Compensation
Metabolic acidosis
in HCO -
in PaCO
Metabolic alkalosis
in HCO -
in PaCO
Respiratory acidosis
in PaCO
in [HCO -]
Respiratory alkalosis
in PaCO
in [HCO -]
Airway obstruction
- Upper
- Lower
COPD
asthma
CNS depression
Neuromuscular impairment
Ventilatory restriction
Increased CO2 production: shivering, rigors, seizures, malignant hyperthermia, hypermetabolism, increased intake of
carbohydrates
CNS stimulation: fever, pain, fear, anxiety, CVA, cerebral edema, brain trauma, brain tumor, CNS infection
Stimulation of chest receptors: pulmonary edema, pleural effusion, pneumonia, pneumothorax, pulmonary embolus
GI loss of H+
Renal loss H+
Loop and thiazide diuretics, post-hypercapnia (especially after institution of mechanical ventilation)
Renal loss of H+: edematous states (heart failure, cirrhosis, nephrotic syndrome), hyperaldosteronism,
hypercortisolism, excess ACTH, exogenous steroids, hyperreninemia, severe hypokalemia, renal artery stenosis,
bicarbonate administration
Methanol intoxication
Uremia
Paraldehyde toxicity
Isoniazid
Lactic acidosisa
a
b
Salicylate intoxication
GI loss of HCO3
proximal RTA
ATN
Distal RTA
Disorder
Respiratory acidosis with metabolic
acidosis
Characteristics
in pH
in HCO
in PaCO
3
Selected situations
Cardiac arrest
Intoxications
Multi-organ failure
in pH
in HCO in PaCO
3
pH in normal range
in PaCO ,
in HCO 2
pH in normal range
in PaCO
in HCO
2
Severe hypokalemia
Sepsis
Salicylate toxicity
pH in normal range
HCO - normal
3
Partial pressure of oxygen (PaO2). This measures the pressure of oxygen dissolved in the blood and how well oxygen is
able to move from the airspace of the lungs into the blood.
Partial pressure of carbon dioxide (PaCO2). This measures the pressure of carbon dioxide dissolved in the blood and how
well carbon dioxide is able to move out of the body.
pH. The pH measures hydrogen ions (H+) in blood. The pH of blood is usually between 7.35 and 7.45. A pH of less than 7.0 is
called acid and a pH greater than 7.0 is called basic (alkaline). So blood is slightly basic.
Bicarbonate (HCO3). Bicarbonate is a chemical (buffer) that keeps the pH of blood from becoming too acidic or too basic.
Oxygen content (O2CT) and oxygen saturation (O2Sat) values. O2 content measures the amount of oxygen in the blood.
Oxygen saturation measures how much of the hemoglobin in the red blood cells is carrying oxygen (O2).
Blood for an ABG test is taken from an artery. Most other blood tests are done on a sample of blood taken from a vein,
after the blood has already passed through the body's tissues where the oxygen is used up and carbon dioxide is
produced.
Why It Is Done
An arterial blood gas (ABG) test is done to:
Check for severe breathing problems and lung diseases, such asasthma, cystic fibrosis, or chronic obstructive pulmonary
disease (COPD).
See how well treatment for lung diseases is working.
Find out if you need extra oxygen or help with breathing (mechanical ventilation).
Find out if you are receiving the right amount of oxygen when you are using oxygen in the hospital.
Measure the acid-base level in the blood of people who have heart failure, kidney failure, uncontrolled diabetes, sleep
disorders, severe infections, or after a drug overdose.