chapter 18 analysis and monitoring of gas exchange
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Chapter 18 Analysis and Monitoring of Gas Exchange. Learning Objectives. Describe the difference between monitoring and analysis. Describe the two types of electrochemical oxygen analyzers. Describe calibration and problem-solving techniques for oxygen analyzers. - PowerPoint PPT PresentationTRANSCRIPT
Copyright © 2013, 2009, 2003, 1999, 1995, 1990, 1982, 1977, 1973, 1969 by Mosby, an imprint of Elsevier Inc.
Chapter 18
Analysis and Monitoring of Gas Exchange
Copyright © 2013, 2009, 2003, 1999, 1995, 1990, 1982, 1977, 1973, 1969 by Mosby, an imprint of Elsevier Inc.
Learning Objectives
Describe the difference between monitoring and analysis.
Describe the two types of electrochemical oxygen analyzers.
Describe calibration and problem-solving techniques for oxygen analyzers.
State how to obtain, process, and analyze arterial and capillary blood gas samples.
List the quality control procedures applied to blood gas analysis.
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Learning Objectives (cont.) List the potential advantages of point-of-care
testing. Describe how to obtain and interpret
transcutaneous oxygen and carbon dioxide monitoring.
Describe the basic principles used by an oximeter to monitor oxygen saturation.
State when and how to perform pulse oximetry. Identify true statements related to interpretation
of pulse oximetry results. Describe how to perform capnometry and
interpret capnograms.
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Analysis vs. Monitoring
Laboratory analysis: discrete measurements of fluids or tissue that must be removed from body
Such measurements are made with an analyzer
Monitoring is an ongoing process by which clinicians obtain & evaluate dynamic physiological processes in a timely manner, usually at bedside
This is done with monitor
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Invasive vs. Noninvasive Procedures
Invasive procedures require insertion of sensor or collection device into body
Noninvasive monitoring is means of gathering data externally
Generally, invasive procedures provide more accurate data but carry greater risk
After gradient between invasive & noninvasive method is established, trends in change of noninvasive method can be useful in making clinical decisions
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Measuring FIO2
Most bedside systems to measure FIO2 use electrochemical principles
2 most common:1. Polargraphic (Clark) electrode- needs battery2. Galvanic fuel cell- no battery needed
Response times for Clark electrodes = about 10 to 30 seconds
Response times for galvanic fuel cells = 60 seconds
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Clark Polarographic Analyzer
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Working as a new therapist in the ICU you come across an O2 analyzer that uses battery to only power its alarm system. This analyzer should be classified as a:
A.paramagnetic analyzer
B.polarographic analyzer
C.galvanic fuel cell analyzer
D.zirconum cell analyzer
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Troubleshooting O2 Analyzers
Calibration according to manufacturer’s recommendation must be done before using device
Failure to calibrate or inconsistent readings are signs of malfunctioning
Best way to avoid problems is through preventative maintenance
If analyzer fails to calibrate, problem could be related to: Low batteries, sensor depletion, electronic failure
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All of these may be reasons for a Galvanic fuel cell to malfunction, except:
A.batteries
B.sensor depletion
C.electric failure
D.condensation of water vapor
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Sampling & Analyzing Blood Gases
Analyzing arterial blood samples is important part of diagnosing & treating patients with respiratory failure
Radial artery is most often used because: Near surface & easy to stabilize Collateral circulation usually exists (confirmed with
the Allen test) No large veins are near Radial puncture is relatively pain free
Arterial cannulation can be done if frequent sampling is needed
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Arterial Sampling
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Arterial Sampling (cont.)
Modified Allen’s test: Done prior to radial artery puncture ONLY Normal test indicating collateral circulation - hand
flush pink within 5-10 seconds Cannot be performed on critically ill patients who
are uncooperative or unconscious
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Modified Allen Test
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The RT receives a doctor order to perform an ABG on a 32 year-old patient. Prior to performing the ABG, the RT does a modified Allen’s test on the patient’s right hand that takes more than 10 seconds for patient’s hand to flush pink. What should the RT do next?
A.should not perform an ABG on patient.
B.perform the ABG on the right brachial artery.
C.perform it on the right radial artery.
D.repeat the modified Allen’s test on the left hand.
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Arterial Sampling (cont.)
Sample volume of 0.5 to 1 mL of blood is adequate
Actual volume depends on: Anticoagulant used Requirements of specific analyzer used Whether or not other tests will be performed on
obtained sample
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Arterial Sampling (cont.)
Important transmission-based and safety precautions: Never recap used needle without safety device;
never handle using both hands, & never point it toward any part of body
Never bend, break, or remove used needles from syringes by hand
Always dispose of used syringes, needles, & other sharp items in appropriate puncture-resistant sharps containers
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Indications for Arterial Sampling
Sudden, unexplained dyspnea Acute shortness of breath/tachypnea Abnormal breath sounds Cyanosis Heavy use of accessory muscles Changes in ventilator settings CPR Diffuse infiltrates in chest radiograph New infiltrates in CXR Sudden cardiac arrhythmias Acute hypotenesion
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Blood Sample Analysis Clinicians can avoid most pre-analytical
errors by ensuring that sample is: Obtained anaerobically Properly anticoagulated Analyzed within 10 to 30 minutes
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Interpretation of ABGs
Interpret oxygenation status PaO2 (see below)
SaO2 (normal = 95100%)
CaO2 (normal = 1820 vol%)
• PaO2 6079 mm Hg = mild hypoxemia
• PaO2 4059 mm Hg = moderate hypoxemia
• PaO2 <40 mm Hg = severe hypoxemia
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The RT is called to run an ABG drawn by the unit resident on a patient in a non-rebreather mask. The RT notices visible bubbles at the top of the blood sample. How this may impact the PaO2 and PaCO2 results?
A.it may increase the PaCO2 of the sampleB.it only affects the gas pressures after 1 hr of drawn
C.it may decrease the PaO2 of the sample
D.air bubbles have no impact on the PaO2/PaCO2 values
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Indwelling Catheters
Provides ready access for blood sampling Allow continuous monitoring of vascular
pressures Infection & thrombosis are more likely than
intermittent punctures Normal routes are peripheral arteries (radial,
brachial, pedal), femoral artery, central vein, & pulmonary artery
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Indwelling Catheter (cont.)
Access for sampling blood from most intravascular lines is provided by a three-way stopcock
Pulmonary artery catheter has separate blood sampling and IV infusion ports and balloon at tip
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Brachial Artery Catheter
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3-way Stopcock
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If a indwelling vascular catheter is placed in the brachial artery, what is the sample assessing?
A.pulmonary gas exchange
B.gas exchange at the tissues
C.right ventricular preload
D.right ventricular afterload
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Capillary Blood Gases
Good capillary sample can accurately reflect & provide clinically useful estimates of arterial pH & PCO2 levels
Capillary PO2 is of no value in estimating arterial
oxygenation. SaO2 must be evaluated by pulse
oximetry. Most common technical errors in capillary sampling
are inadequate warming & squeezing of puncture site Squeezing puncture site may result in venous &
lymphatic contamination of sample
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Analyzing
Measures pH, PCO2, & PO2 levels in blood sample
Several secondary values are calculated: Plasma Bicarbonate (HCO3
-) Base excess (BE) or deficit Hemoglobin saturation (HbO2%).
Some may combine blood gas & hemoximetry (total hemoglobin) measurements
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Instrumentation
Can be based on several different types of sensor technology to measure pH, PCO2, & PO2: Electrochemical electrodes Optical fluorescence Photoluminescence
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Instrumentation (cont.)
Electrodes: PaO2: Clark polarographic electrode
PaCO2: Severinghaus electrode
pH: pH electrode actually consists of 2 electrodes or half-cells:
• Measuring electrode
• Reference electrode
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Instrumentation (cont.)
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Quality Assurance
Accurate ABG results depend on rigorous quality control efforts
Components of quality control are: Record keeping (policies & procedures) Performance validation (testing new instrument) Preventative maintenance & function checks Automated calibration & verification Internal statistical quality control External quality control (proficiency testing) Remedial action (to correct errors)
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Quality Assurance
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Quality Control Components
Recordkeeping Performance Validation Preventive maintenance and function checks Automated calibration Calibration verification by control media Internal statistical quality control External quality control Remedial actions
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2-point Calibration
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Changes on procedures, staff training and retraining, closer supervision and increase in maintenance checks are an example of which of the following quality control elements?
A.external quality control
B.remedial action
C.calibration verification
D.performance validation
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Point-of-Care Testing
Performing blood gas analysis from laboratory to patient’s bedside
Reduces turnaround time, thus should improve care & lower costs
Used increasingly in hospitals & physician offices
Used for blood chemistry & hematology parameters
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GEM Premier 4000
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Blood Gas Monitoring
Provides continuous or interval measurements without removing blood from patient
4 systems in current clinical use:1. Transcutaneous blood gas monitor
2. Intra-arterial (in-vivo) blood gas monitor
3. Extra-arterial (ex-vivo) blood gas monitor
4. Tissue oxygen monitor
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Transcutaneous Monitoring Provides continuous, noninvasive estimates of
PO2 and PCO2 using skin sensor Sensor warms underlying skin to increase arterial
blood flow 2 most important factors influencing accuracy of
transcutaneous measurements: age & perfusion status
Low perfusion & increasing age reduce agreement between PtcO2 & PaO2
Agreement between PtcCO2 & PaCO2 is better because CO2 is more diffusible through skin
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Transcutaneous Monitoring (cont.)
Most common sites for electrode placement for infants & children are abdomen, chest & lower back
Should compare monitor readings with those obtained with concurrent ABG
Validation with ABG should be repeated anytime patient’s status undergoes major change
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Transcutaneous Monitoring (cont.)
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Current data in an infant reveals a PTCO2 of 98 mm Hg and a PTCO2 of 22 mm Hg. A stat ABG is ordered showing a PaO2 of 56 mm Hg and a PaCO2 of 49 mm Hg? What could be the cause of this discrepancy?
A.an air leak
B.electrode placement
C.decreased skin perfusion
D.electrode overheating
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Intra-arterial (In Vivo)
Potential benefits of continuous blood gas analysis: Real time monitoring Reduction in therapeutic decision making time Less blood loss Lower infection risk Improved accuracy Elimination of specimen transport
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Blood Gas Catheter
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Extra-arterial (Ex Vivo)
Eliminates all problems associated with indwelling sensors
Provides quick results Unable to provide real-time continuous data Determine further justification of costs &
patient benefits
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Ex vivo Blood Gas Monitor
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Tissue Oxygen (PtO2) Monitor
Tissue oxygen can be measured by probes inserted directly into organs, tissue, & body fluids
Clinical indications: Monitor brain tissue oxygen as an early sign of
ischemia Assess brain blood flow autoregulation Monitor adequacy of brain perfusion in patients
with traumatic brain injury
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Factors that affect transcutaneous blood gas monitoring accuracy includes all of the following, except:
A.variation in skin characteristics
B.temperature
C.electrode placement
D.hematocrit
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Oximetry
Oximetry measures hemoglobin saturation using spectrophotometry
Oximetry works because each substance has its own unique pattern of light absorption
Each form of hemoglobin (e.g., HbO2, HbCO) has its own pattern of light absorption
For example, HbO2 absorbs less red light & more infrared light
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Oximetry (cont.)
Several types used in clinical practice: Hemoximetry (co-oximetry) - laboratory analytical
procedure requiring invasive sampling of arterial blood
Pulse oximetry - noninvasive monitoring technique performed at bedside
Venous oximetry – invasive monitoring through fiberoptic catheter placed in vena cava or pulmonary artery
Tissue oximetry – noninvasive method of measuring saturation of hemoglobin at tissue level
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Tissue Oxygen Probe
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Hemoximetry
Measures blood oxygen levels & hemoglobin saturations using a hemoximeter
Multiple lights pass through sample to measure multiple hemoglobin species such as HbO2, HbCO, & metHb
If good quality assurance measures are used, measurements are very accurate
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Hemoximeter
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Pulse Oximetry
Combines principles of pectrophotometry with photoplethysmography
Noninvasive portable monitoring device providing estimates of SaO2
Results are reported as SpO2
Pulse oximeter uses light absorption patterns to indicate saturation levels of “pulsed” blood (a.k.a., arterial blood)
Results are not as accurate as hemoximetry
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Pulse Oximetry (cont.)
Accurate to within ±3% to 5% of hemoximetry Finger probes are not reliable in patients with
shock Cannot distinguish HbCO from HbO2; thus
reads falsely high in CO poisoning Does not measure CaO2 or PCO2; patients
suspected of having O2 transport issues or hypoventilation should have an ABG
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Pulse Oximetry (cont.)
2 types of sensors:1. Transmission sensor
• Sensor has two sides One side has red & infrared LEDs Other side has photodetector
• Sensor is placed on finger, toe or earlobe
2. Reflectance sensor• Sensor only on one side (containing both LED light
sources & photodetector)
• Sensor is placed on skin surface, usually forehead
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Pulse Oximetry (cont.)
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Pulse Oximetry (cont.)
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Venous Oximetry
Assesses balance between oxygen delivery & utilization as indirect index of global tissue oxygenation & perfusion
Normal values for mixed venous (pulmonary artery oxygen saturation monitoring (SvO2) range between 60 to 80%
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Venous Oximetry (cont.)
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Tissue Oximetry
Oxygen saturation at tissue level (StO2) assesses adequacy of circulation & oxygen delivery
Early detection of low StO2 can be used as an early detection method of tissue hypoperfusion in patients with traumatic injuries
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A patient rescued from a house fire is brought into the ER. The patient is suspected of suffering from carbon monoxide (CO) poisoning, which device can help monitor CO levels:
A.venous oximeter
B.pulse oximeter
C.co-oximeter
D.tissue oximeter
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Capnometry
Measures CO2 in respiratory gases Capnometer measures CO2 levels Capnography is graphic display of CO2 levels
as they change during breathing Most often used in patients undergoing
general anesthesia or mechanical ventilation
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Capnometry (cont.)
Capnometer functions on basis that CO2
absorbs infrared light proportion to amount of
CO2 present
2 techniques:1. Mainstream technique places an analysis
chamber in patients breathing circuit
2. Sidestream technique pumps small volume of gas from circuit into nearby analyzer
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Capnometry (cont.)
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Capnometry (cont.)
Normal capnogram shows PCO2 of zero at
start of expiratory breath (Phase I)
Soon afterward, the PCO2 level rises sharply
(Phase II) & plateaus as alveolar gas is exhaled (Phase III)
End-tidal PCO2 (PETCO2) is used to estimate
deadspace ventilation & normally averages 3 to 5 mm Hg less than PaCO2
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Capnometry (cont.)
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Capnometry (cont.)
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