ACLS Provider Manual Supplementary Material: © 2016 American Heart Association

ACLS Provider Manual
Supplementary Material
2016 American Heart Association

Contents
Airway Management ...................................................................................................................4

Basic Airway Management ..................................................................................................4
Devices to Provide Supplementary Oxygen .................................................................4
Overview ..............................................................................................................4
Oxygen Supply ....................................................................................................4
Nasal Cannula .....................................................................................................5
Simple Oxygen Face Mask ..................................................................................6
Venturi Mask ........................................................................................................6
Face Mask With Oxygen Reservoir ......................................................................6
Giving Adult Mouth-to-Mask Breaths ....................................................................7
Bag-Mask Ventilation ...................................................................................................8
Overview ..............................................................................................................8
Tips for Performing Bag-Mask Ventilation ............................................................9
Ventilation With an Advanced Airway and Chest Compressions ........................ 11
Advanced Airway Management .........................................................................................11
Advanced Airway Adjuncts: Laryngeal Mask Airway ..................................................11
Overview ............................................................................................................11
Insertion of the Laryngeal Mask Airway ..............................................................12
Advanced Airway Adjuncts: Laryngeal Tube ..............................................................13
Overview ............................................................................................................13
Insertion of the Laryngeal Tube..........................................................................13
Advanced Airway Adjuncts: Esophageal-Tracheal Tube ............................................ 14
Overview ............................................................................................................14
Insertion of the Esophageal-Tracheal Tube........................................................16
Advanced Airway Adjuncts: ET Intubation .................................................................17
Overview ............................................................................................................17
Technique of ET Intubation ................................................................................19
Indications for ET Intubation ..............................................................................21
Ventilating With an ET Tube in Place During Chest Compressions .................... 21
Tube Trauma and Adverse Effects.....................................................................22
Insertion of ET Tube Into One Bronchus ............................................................22
Confirmation of ET Tube Placement: Physical Exam ......................................... 23
Confirmation of ET Tube Placement: Qualitative and Quantitative Devices........ 24
Waveform Capnography ....................................................................................24
Quantitative End-Tidal CO2 Monitors (Capnometry) ........................................... 26
Exhaled (Qualitative) CO2 Detectors ..................................................................26
Esophageal Detector Devices ............................................................................26
ACLS Core Rhythms .................................................................................................................29
Recognition of Core Electrocardiogram Arrest Rhythms ....................................................29
The Basics .........................................................................................................29
Cardiac Arrest Rhythms and Conditions ............................................................29
Recognition of Selected Nonarrest ECG Rhythms.............................................................33
Recognition of Supraventricular Tachyarrhythmias (SVTs) ........................................ 33
Recognition of Ventricular Tachyarrhythmias .............................................................37
Recognition of Sinus Bradycardia ..............................................................................41
Recognition of AV Block ............................................................................................42
VF Treated With CPR and Automated External Defibrillator ..............................................47
Defibrillation ..............................................................................................................................48
Automated External Defibrillator Operation ........................................................48
Know Your AED .................................................................................................48
Universal Steps for Operating an AED ...............................................................48
Troubleshooting the AED ...................................................................................50
2016 American Heart Association 2

Shock First vs CPR First ....................................................................................51

AED Use in Special Situations...........................................................................................51
Introduction ........................................................................................................51
Hairy Chest ........................................................................................................51
Water .................................................................................................................51
Implanted Pacemaker ........................................................................................52
Transdermal Medication Patches .......................................................................52
Defibrillation and Safety.....................................................................................................52
Manual Defibrillation ..................................................................................................52
Using a Manual Defibrillator/ Monitor .................................................................52
Safety and Clearing the Patient .................................................................................54
Clearing: You and Your Team ............................................................................54
A Final Note About Defibrillators ........................................................................54
Access for Medications .............................................................................................................55
Intravenous Access ...........................................................................................................55
Using Peripheral Veins for IV Access .................................................................55
General IV Principles .........................................................................................57
Intraosseous Access .........................................................................................................57
Introduction ........................................................................................................57
Needles .............................................................................................................57
Sites...................................................................................................................58
Indications and Administration ...........................................................................58
Contraindications ...............................................................................................58
Complications ....................................................................................................58
Equipment Needed ............................................................................................58
Procedure ..........................................................................................................59
Follow-up ...........................................................................................................61
Acute Coronary Syndromes ......................................................................................................62
ST-Elevation Myocardial Infarction Location and AV Block ................................................62
Right Ventricular Infarction .................................................................................62
AV Block With Inferior MI ...................................................................................62
Fibrinolytic Checklist for STEMI .........................................................................................63
Human, Ethical, and Legal Dimensions of ECC and ACLS .......................................................64
Rescuer and Witness Issues .............................................................................................64
How Often Will CPR, Defibrillation, and ACLS Succeed?................................... 64
Take Pride in Your Skills as an ACLS Provider ..................................................65
Stress Reactions After Resuscitation Attempts ..................................................65
Techniques to Reduce Stress in Rescuers and Witnesses ................................ 66
Psychological Barriers to Action .........................................................................66
Legal and Ethical Issues....................................................................................................67
The Right Thing to Do ........................................................................................67
Principle of Futility ..............................................................................................68
Terminating Resuscitative Efforts.......................................................................69
When Not to Start CPR ......................................................................................69
Withholding vs Withdrawing CPR.......................................................................70
Withdrawal of Life Support .................................................................................70
Advance Directives, Living Wills, and Patient Self-Determination....................... 71
Out-of-Hospital DNAR Orders ............................................................................72
EMS No-CPR Programs ....................................................................................72
Legal Aspects of AED Use .................................................................................73
Providing Emotional Support for the Family .......................................................................74
Conveying News of a Sudden Death to Family Members................................... 74
Family Presence During Resuscitation...............................................................74
Organ and Tissue Donation ...............................................................................75

Airway Management
Basic Airway Management
Devices to Provide Supplementary Oxygen
Overview Oxygen administration is often necessary for patients with acute coronary
syndromes, pulmonary distress, or stroke. Various devices can deliver
supplementary oxygen from 21% to 100% (Table 1). This section
describes 4 devices to provide supplementary oxygen:
Nasal cannula
Simple oxygen face mask
Venturi mask
Face mask with oxygen reservoir
Whenever you care for a patient receiving supplementary oxygen, quickly

verify the proper function of the oxygen delivery system in use.
Table 1. Delivery of Supplementary Oxygen: Flow Rates and Percentage of

Oxygen Delivered
Flow Rates Delivered
Device
(L/min) Oxygen (%)*
Nasal cannula 1 21-24
2 25-28
3 29-32
4 33-36
5 37-40
6 41-44
Simple oxygen face mask 6-10 35-60
Venturi mask 4-8 24-40
10-12 40-50
Face mask with oxygen 10-15 95-100
reservoir (nonrebreathing mask)
*Percentages are approximate.
Oxygen Supply Oxygen supply refers to an oxygen cylinder or wall unit that connects to
an administration device to deliver oxygen to the patient. When the
patient is receiving oxygen from one of these systems, be sure to check
the following equipment:
Oxygen administration device

Valve handles to open the cylinder
Pressure gauge
Flow meter
Tubing that connects the oxygen supply to the patients oxygen
administration device

Trained advanced cardiovascular life support (ACLS) providers should be

sure they are familiar with all emergency equipment before an
emergency arises.
Nasal Cannula Traditionally, the nasal cannula (Figure 1) is classified as a low-flow

oxygen administration system designed to add oxygen to room air when
the patient inspires. The ultimate inspired oxygen concentration is
determined by the oxygen flow rate through the cannula and by how
deeply and rapidly the patient breathes (minute ventilation), but the nasal
cannula can provide up to 44% oxygen as inspired air mixes with room
air. Increasing the oxygen flow by 1 L/min (starting with 1 L/min and
limited to about 6 L/min) will increase the inspired oxygen concentration
by approximately 4%.
Recent years have seen the advent of high-flow nasal cannula systems,
which allow for flow rates up to (and sometimes exceeding) 60 L/min.
Inspired oxygen concentration can be set up to 100%.
Note that the use of the nasal cannula requires that the patient have
adequate spontaneous respiratory effort, airway protective mechanism,
and tidal volume.
Indications
Patients with arterial oxyhemoglobin saturation less than 94% (less
than 90% for acute coronary syndromes [ACS] patients)
Patients with minimal respiratory or oxygenation problems
Patients who cannot tolerate a face mask
Figure 1. A nasal cannula used for supplementary oxygen delivery in

spontaneously breathing patients.

Simple Oxygen The simple oxygen face mask delivers low-flow oxygen to the patients
Face Mask nose and mouth. It can supply up to 60% oxygen with flow rates of 6 to
10 L/min, but the final oxygen concentration is highly dependent on the
fit of the mask (Table 1). Oxygen flow rate of at least 6 L/min is needed
to prevent rebreathing of exhaled carbon dioxide (CO2) and to maintain
increased inspired oxygen concentration.
Venturi Mask A Venturi mask enables a more reliable and controlled delivery of
oxygen concentrations from 24% to 50% (Table 1). Delivered oxygen
concentrations can be adjusted to 24%, 28%, 35%, and 40% by using a
flow rate of 4 to 8 L/min and 40% to 50% by using a flow rate of 10 to 12
L/min. Observe the patient closely for respiratory depression. Use a
pulse oximeter to titrate quickly to the preferred level of oxygen
administration as long as peripheral perfusion is adequate and no
shunting has occurred.
A Venturi mask can accurately control the inspired oxygen

concentration. Patients with chronic obstructive pulmonary disease
(COPD), who usually have chronic hypercarbia (high CO2) and mild
to moderate hypoxemia, may benefit from this device.
Administration of high oxygen concentrations to patients with COPD
may produce respiratory depression because the increase in PaO2
eliminates the stimulant effect of hypoxemia on the respiratory
centers.
Never withhold oxygen from patients who have respiratory distress
and severe hypoxemia simply because you suspect a hypoxic
ventilatory drive. If oxygen administration depresses respiration,
support ventilation.
Face Mask With The face mask below (figure 2) is a partial rebreathing mask that
Oxygen Reservoir consists of a face mask with an attached oxygen reservoir bag. A
nonrebreathing face mask with an oxygen reservoir provides up to 95%
to 100% oxygen with flow rates of 10 to 15 L/min (Table 1). In this
system, a constant flow of oxygen enters an attached reservoir.

Figure 2. A face mask with oxygen reservoir used for supplementary

oxygen delivery in spontaneously breathing patients.
Use of a face mask with a reservoir is indicated for patients who
Are seriously ill, responsive, spontaneously breathing, have

adequate tidal volume, and require high oxygen concentrations
May avoid endotracheal (ET) intubation if acute interventions
produce a rapid clinical effect (eg, patients with acute pulmonary
edema, COPD, or severe asthma)
Have relative indications for advanced airway management but
maintain intact airway protective reflexes, such as gag and cough
Are being prepared for advanced airway management
Caution
The above patients may have a diminished level of consciousness and
be at risk for nausea and vomiting. A tight-fitting mask always requires
close monitoring. Suctioning devices should be immediately available.
Giving Adult To use a pocket mask, a healthcare provider who is alone should be
Mouth-to-Mask positioned at the patients side. This position is ideal when performing 1-
Breaths rescuer cardiopulmonary resuscitation (CPR) because you can give
breaths and perform chest compressions effectively without
repositioning yourself every time you change from giving compressions
to giving breaths. Follow these steps to open the airway with a head tilt
chin lift maneuver (use the jaw thrust method in patients with suspected
neck or spinal cord injury) to give breaths to the patient:
1. Position yourself at the patients side.

2. Place the pocket mask on the patients face, using the bridge of the
nose as a guide for correct position.

3. Seal the pocket mask against the face.

4. Using your hand that is closer to the top of the patients head, place
the index finger and thumb along the edge of the mask.
5. Place the thumb of your other hand along the edge of the mask.
6. Place the remaining fingers of your second hand along the bony
margin of the jaw and lift the jaw. Perform a head tiltchin lift to open
the airway (Figure 3).
7. While you lift the jaw, press firmly and completely around the outside
edge of the mask to seal the pocket mask against the patients face.
8. Deliver each breath over 1 second, enough to make the patients
chest rise.
Figure 3. Mouth-to-mask ventilation, 1 rescuer. The single rescuer

performs CPR from a position at the patients side. Perform a head tilt
chin lift to open the airway while holding the mask tightly against the
face.
Bag-Mask Ventilation
Overview The bag-mask device typically consists of a self-inflating bag and a

nonrebreathing valve; it may be used with a face mask or an advanced
airway. Masks are made of transparent material to allow detection of
regurgitation. They should be capable of creating a tight seal on the
face, covering both mouth and nose. Bag-mask devices are available in
adult and pediatric sizes. These devices are used to deliver high
concentrations of oxygen by positive pressure to a patient who is not
breathing effectively. Some devices allow the addition of a positive end-
expiratory pressure valve.
Bag-mask ventilation is a challenging skill that requires considerable

practice for competency. It is easier to provide by 2 trained and
experienced rescuers. One rescuer opens the airway and seals the
mask to the face while the other squeezes the bag, with both rescuers
watching for visible chest rise. Healthcare providers can provide bag-
mask ventilation with room air or oxygen if they use a self-inflating bag.

This device provides positive-pressure ventilation when used without

an advanced airway and, therefore, may produce gastric inflation and
its consequent complications.
Tips for Insert an oropharyngeal airway as soon as possible if the patient has
Performing Bag- no cough or gag reflex to help maintain an open airway.
Mask Ventilation Use an adult (1- to 2-L) bag to deliver approximately 500- to 600-mL
(6- to 7-mL/kg) tidal volume for adult patients. This amount is usually
sufficient to produce visible chest rise and maintain oxygenation and
normal carbon dioxide levels in apneic patients.
To create a leak-proof mask seal, perform and maintain a head tilt,
and then use the thumb and index finger to make a C, pressing the
edges of the mask to the face. Next, use the remaining fingers to lift
the angle of the jaw and open the airway (Figure 4A).
To create an effective mask seal, the hand holding the mask must
perform multiple tasks simultaneously: maintaining the head-tilt
position, pressing the mask against the face, and lifting the jaw
Two well-trained, experienced healthcare providers are preferred
during bag-mask ventilation (Figure 4B).
The seal and volume problems do not occur when the bag-mask device
is attached to the end of an advanced airway device (eg, laryngeal mask
airway, laryngeal tube, esophageal-tracheal tube, or ET tube).

Figure 4. A, E-C clamp technique of holding the mask while lifting the
jaw. Position yourself at the patients head. Circle the thumb and first
finger around the top of the mask (forming a C) while using the third,
fourth, and fifth fingers (forming an E) to lift the jaw. B, Two-rescuer
use of the bag-mask. The rescuer at the patients head tilts the patients

head and seals the mask against the patients face with the thumb and
first finger of each hand (creating a C) to provide a complete seal
around the edges of the mask. The rescuer uses the remaining 3 fingers
(the E) to lift the jaw (this holds the airway open). The second rescuer
slowly squeezes the bag over 1 second until the chest rises. Both
rescuers should observe chest rise.
Ventilation With an When the patient has an advanced airway in place during CPR,
Advanced Airway provide continuous compressions and asynchronous ventilations
and Chest once every 6 seconds.
Compressions Avoid excessive ventilation (too many breaths or too large a volume).
Advanced Airway Management
Advanced Airway Adjuncts: Laryngeal Mask Airway
Overview The laryngeal mask airway is composed of a tube with a cuffed, mask-
like projection at the end of the tube (Figure 5). The laryngeal mask
airway is an advanced airway device that is considered an acceptable
alternative to the ET tube. When compared with the ET tube, the
laryngeal mask airway provided equivalent ventilation during CPR in
72% to 97% of patients. A small proportion of patients cannot be
ventilated with the laryngeal mask airway. Therefore, it is important for
providers to have an alternative strategy for airway management.
The advantages of laryngeal mask airway are as follows:
Regurgitation is less likely with the laryngeal mask airway than with
the bag-mask device.
Because insertion of the laryngeal mask airway does not require
laryngoscopy and visualization of the vocal cords, training in its
placement and use is simpler than for ET intubation.
Laryngeal mask airway insertion is easier than ET tube insertion
when access to the patient is limited, there is a possibility of unstable
neck injury, or appropriate positioning of the patient for ET intubation
is impossible.
Figure 5. Laryngeal mask airway.

Insertion of the The steps for insertion of the laryngeal mask airway (Figure 6) are as
Laryngeal Mask follows:
Airway
Step Action
1 Patient preparation: Provide oxygenation and ventilation, and
position the patient.
2 Equipment preparation: Check the integrity of the mask and
tube according to the manufacturers instructions. Lubricate
only the posterior surface of the cuff to avoid blocking the
airway aperture.
3 Insertion technique:
Introduce the laryngeal mask airway into the pharynx and
advance it blindly until you feel resistance. Resistance
indicates that the distal end of the tube has reached the
hypopharynx.
Inflate the cuff of the mask. Cuff inflation pushes the mask
up against the tracheal opening, allowing air to flow through
the tube and into the trachea.
Ventilation through the tube is ultimately delivered to the
opening in the center of the mask and into the trachea.
To avoid trauma, do not use force at any time during
insertion of the laryngeal mask airway.
Avoid overinflating the cuff. Excessive intracuff pressure can
result in misplacement of the device. It also can cause
pharyngolaryngeal injury (eg, sore throat, dysphagia, or
nerve injury).
4 Insert a bite-block (if the laryngeal mask airway does not have
intrinsic bite-block), provide ventilation, and continue to monitor
the patients condition and the position of the laryngeal mask
airway. A bite-block reduces the possibility of airway
obstruction and tube damage. Keep the bite-block in place until
you remove the laryngeal mask airway.
Figure 6. Insertion of the laryngeal mask airway.
Cautions/Additional Information
Do not apply cricoid pressure because it may hinder the insertion of

the laryngeal mask airway. Studies in anesthetized adults have shown
that when cricoid pressure is used before insertion of a laryngeal mask
airway, the proportion of tubes correctly positioned is reduced, and the

incidence of failed insertion and impaired ventilation once the laryngeal

mask airway had been placed is increased.
In general, size 5 fits men and size 4 fits women.
You may note a smooth swelling at the level of the cricoid cartilage in
the neck. This is normal, and it confirms the proper positioning of the
device.
If you hear an air leak during ventilation with a bag for the next 3 or 4
breaths, reevaluate the position of the laryngeal mask airway for
possible misplacement.
To avoid displacement, limit the patients head movement and avoid
suctioning secretions in the pharynx once the laryngeal mask airway is
in place.
Advanced Airway Adjuncts: Laryngeal Tube
Overview The laryngeal tube (Figure 7) is a supraglottic airway device that is

considered an acceptable alternative to an ET tube. The laryngeal tube
is available in single- and dual-lumen versions. Only experienced
providers should perform laryngeal tube insertion.
The advantages of the laryngeal tube are ease of training and ease of
insertion due to its compact size. In addition, it isolates the airway,
reduces the risk of aspiration compared with bag-mask ventilation, and
provides reliable ventilation. Trained healthcare professionals may
consider the laryngeal tube as an alternative to bag-mask ventilation or
ET intubation for airway management in cardiac arrest.
Figure 7. Laryngeal tube.
Insertion of the The steps for insertion of a laryngeal tube are as follows:
Laryngeal Tube
Step Action
position the patient.
2 Equipment preparation: Check the integrity of the laryngeal
tube according to the manufacturers instructions.
Inspect the mouth and larynx of the patient before insertion
of the laryngeal tube.

Open the mouth of the patient approximately 2 to 3 cm by

using the thumb-and-index-finger technique.
Insert the laryngeal tube in the midline of the mouth along
the palate until a slight resistance is felt (Figure 8).
In some cases, a slight head extension can facilitate mouth
opening and tube placement.
Ensure that the ventilation holes of the laryngeal tube lie in
front of the laryngeal inlet.
The insertion depth can be verified according to the teeth
marks at the upper end of the tube.
The laryngeal tube is available in different sizes.
Figure 8. Positioning of the laryngeal tube.
Advanced Airway Adjuncts: Esophageal-Tracheal Tube
Overview The esophageal-tracheal tube (Figures 9 and 10) is an advanced airway

that is an acceptable alternative to the ET tube. The esophageal-
tracheal tube is an invasive airway device with 2 inflatable balloon cuffs.
The tube is more likely to enter the esophagus than the trachea, thereby
allowing ventilation to occur through side openings in the device
adjacent to the vocal cords and trachea. If the tube enters the trachea,
ventilation can still occur by an opening in the end of the tube.
Studies show that healthcare providers with all levels of experience can
insert the esophageal-tracheal tube and deliver ventilation comparable
to that achieved with ET intubation. Compared with bag-mask
ventilation, the esophageal-tracheal tube is advantageous because it
isolates the airway, reduces the risk of aspiration, and provides more
reliable ventilation. The advantages of the esophageal-tracheal tube are

chiefly related to ease of training when compared with the training

needed for ET intubation. Only providers trained and experienced with
the use of the esophageal-tracheal tube should insert the device
because fatal complications are possible if the position of the distal
lumen of the esophageal-tracheal tube in the esophagus or trachea is
identified incorrectly. Other possible complications related to the use of
the esophageal-tracheal tube are esophageal trauma, including
lacerations, bruising, and subcutaneous emphysema. The esophageal-
tracheal tube is supplied in 2 sizes: the smaller size (37F) is used in
patients 4 to 5.5 feet tall, and the larger size (41F) is used in patients
more than 5 feet tall.
Contraindications
Responsive patients with cough or gag reflex

Age 16 years or younger
Height 4 feet or shorter
Known or suspected esophageal disease
Ingestion of a caustic substance
Figure 9. Esophageal-tracheal tube.

Figure 10. Esophageal-tracheal tube inserted in esophagus.
At the H point on Figures 9 and 10, rescuers hands should be

holding/anchoring the tube in place. With the bag-mask squeeze,
potential movement of the invasive airways may occur.
Insertion of the The steps for blind insertion of a esophageal-tracheal tube are as follows:
Esophageal-
Tracheal Tube Step Action
position the patient. Rule out the contraindications to
insertion of the esophageal-tracheal tube.
2 Equipment preparation: Check the integrity of both cuffs
according to the manufacturers instructions, and lubricate
the tube.
Hold the device with cuffs deflated so that the curvature of
the tube matches the curvature of the pharynx.
Lift the jaw and insert the tube gently until the black lines
(H) on the tube (Figures 9 and 10) are positioned between
the patients upper teeth. Do not force insertion and do not
attempt for more than 30 seconds.
Inflate the proximal/pharyngeal (blue) cuff with 100 mL of
air; inflate with 85 mL for the smaller esophageal-tracheal
tube. Then inflate the distal (white or clear) cuff with 15
mL of air; inflate with 12 mL for the smaller esophageal-
tracheal tube.
4 Confirm tube location and select the lumen for ventilation. To
select the appropriate lumen for ventilation, you must
determine where the tip of the tube is located. The tip of the
tube can rest in either the esophagus or the trachea.

Esophageal placement: To confirm esophageal

placement, attach the bag-mask to the blue
(proximal/pharyngeal) lumen. Squeezing the bag provides
ventilation by forcing air through the openings in the tube
between the 2 inflated cuffs. This action produces bilateral
breath sounds. Epigastric sounds do not occur because
the distal cuff, once inflated, obstructs the esophagus,
thereby preventing airflow into the stomach. Because the
tip of the tube rests in the esophagus, do not use the
distal (white or clear) tube for ventilation.
Tracheal placement: If squeezing the bag attached to the
blue (proximal/pharyngeal) lumen does not produce
breath sounds, immediately disconnect the bag and
reattach it to the distal (white or clear) lumen. Squeezing
the bag should now produce breath sounds because this
lumen goes to the trachea. With ET placement of the tube,
the distal cuff performs the same function as a cuff on an
ET tube. Detection of exhaled CO2 (through the ventilating
lumen) should be used for confirmation, particularly if the
patient has a perfusing rhythm.
Unknown placement: If you are unable to hear breath
sounds, deflate both cuffs and withdraw the tube slightly.
Reinflate both cuffs (see previous steps) and attempt to
ventilate the patient. If breath sounds and epigastric
sounds are still absent, remove the tube. Make sure you
have suction equipment available in case tube removal
causes vomiting.
Do not apply cricoid pressure during insertion because it may hinder the
insertion of the esophageal-tracheal tube.
Disadvantages
Insertion of an esophageal-tracheal tube may cause esophageal

trauma, including lacerations, bruising, and subcutaneous
emphysema.
Esophageal-tracheal tubes are available in only 2 sizes and cannot be
used in any patient less than 4 feet tall.
Advanced Airway Adjuncts: ET Intubation
Overview An ET tube is a single-use, cuffed tube that facilitates delivery of a high

concentration of oxygen and selected tidal volume to maintain adequate
ventilation; placement requires visualization of the patients vocal cords.
The advantages of ET tube insertion are
Maintains patent airway

May protect the airway from aspiration of stomach contents or other
substances in the mouth, throat, or upper airway

Permits effective suctioning of the trachea

Facilitates delivery of positive end-expiratory pressure
Provides an alternative route for administration of some resuscitation
medications when intravenous (IV) or intraosseous (IO) access
cannot be obtained
Is ideal if longer-term ventilation is needed
Provides the greatest compliance in situations that require higher
airway pressure
There are several emergency medications that can be administered by

ET tube, including naloxone, atropine, epinephrine, and lidocaine.
The dose is approximately 2 to 2.5 times higher for ET tube

administration than for IV/IO administration.
Mix the dose of the drug with 5 to 10 mL of normal saline or sterile
water. Studies with epinephrine and lidocaine showed that dilution
with sterile water instead of 0.9% saline may achieve better drug
absorption.
After the medication has been administered through the ET tube,
perform 1 to 2 ventilations to facilitate deposition of the drug into the
airways.
Hold chest compressions very briefly during the instillation of the drug
into the ET tube because compressions will cause contents to come
out of the ET tube if the bag-mask device is not reconnected.
There were no efficacy and safety data regarding ET administration of

amiodarone at the time of writing the 2015 American Heart Association
(AHA) Guidelines Update for CPR and Emergency Cardiac Care (ECC).
Note that for drugs that can be administered by the ET route, optimal ET
doses have not been established. IV/IO administration is preferred
because it provides a more reliable drug delivery and pharmacologic
effect.
ET tube insertion was once considered the optimal method of managing

the airway during cardiac arrest. However, intubation attempts by
unskilled providers can produce complications. Therefore, esophageal-
tracheal tubes, laryngeal mask airways, and laryngeal tubes are now
considered acceptable alternatives to the ET tube for advanced airway
management.
Misplacement of an ET tube can result in severe, even fatal,

complications. For this reason, only skilled, experienced personnel
should perform ET intubation. In most states, medical practice acts
specify the level of personnel allowed to perform this procedure. For
clinical reasons, intubation should be restricted to healthcare providers
who meet all of the following criteria:
Personnel are well trained.

Personnel perform intubations frequently.
Personnel receive frequent refresher training in this skill.

ET tube placement is included in the scope of practice defined by

governmental regulations.
Personnel participate in a process of continuous quality improvement
to detect frequency of complications and minimize those
complications.
Placement of an ET tube is an important part of a resuscitation attempt.

But it is a much lower priority than providing high-quality continuous
chest compressions with few interruptions and delivering defibrillation.
Technique of Many ACLS providers do not perform intubation because of the

ET Intubation professional restrictions noted above. Nonetheless, all members of the
resuscitation team must understand the concept of ET intubation. Team
members may assist with ET intubation and must know how to integrate
compressions and ventilations when an ET tube is placed. This
knowledge is often more important than knowing how to perform the
procedure itself.
Step Action
1 Patient preparation: Provide oxygenation and ventilation,
and position the patient. Assess the likelihood of difficult ET
tube placement based on the patients anatomy.
2 Equipment preparation: Assemble and check all necessary
equipment (ET tube and laryngoscope).
Choose an appropriate size of ET tube. In general, a 7.5-
to 8.00-mm internal diameter tube is used for adult
males, and a 7.0- to 7.5-mm internal diameter tube is
used for adult females.
Choose the appropriate type (straight or curved) and size
of laryngoscope blade (Figures 11A and B).
Test the ET tube cuffs integrity.
Secure the stylet inside the ET tube.
Lubricate the ET tube.
Place the head in the sniffing position.
Open the mouth of the patient by using the thumb-and-
index-finger technique.
Insert the laryngoscope blade and visualize the glottic
opening (Figure 12).
Clear the airway if needed.
Insert the ET tube and watch it pass through the vocal
cords.
Inflate the ET tube cuff to achieve a proper seal.
Remove the laryngoscope blade from the mouth.
Hold the tube with one hand and remove the stylet with
the other hand.
Insert a bite-block.
Attach a bag to the tube.

Squeeze the bag to give breaths (1 second each) while

watching for chest rise.
Assess proper placement by both a clinical assessment
and device confirmation:
Auscultate for breath sounds.
Confirm correct positioning of the ET tube by
continuous quantitative waveform capnography or, if
not available, qualitative partial-pressure end-tidal
CO2 (PETCO2) or esophageal detector device (EDD).
Secure the ET tube in place (eg, with a tube holder).
Provide ventilation, and continue to monitor the patients
condition and the position of the ET tube by using
continuous waveform capnography.
Figure 11. A, Curved laryngoscope blades. B, Straight laryngoscope

blades.

Figure 12. View of the vocal cords.
Indications for Cardiac arrest when bag-mask ventilation is not possible or is

ET Intubation ineffective, or if a protected airway is needed
Responsive patient in respiratory distress or compromise
Patient unable to protect airway (eg, coma, areflexia, or cardiac
arrest)
The incidence of complications is unacceptably high when intubation
is performed by inexperienced providers or monitoring of the tube
placement is inadequate.
Detailed assessment of out-of-hospital intubation attempts has
concluded that ET tubes are much more difficult to place properly in
that setting and highly susceptible to dislodgment.
Healthcare providers can minimize interruptions in chest
compressions for ET intubation with advanced preparation. Insert the
laryngoscope blade with the tube ready at hand as soon as
compressions are paused. Interrupt compressions only to visualize
the vocal cords and insert the tube; this is ideally less than 10
seconds. Resume chest compressions immediately after passing the
tube between the vocal cords. Verify the tubes placement. If the
initial intubation attempt is unsuccessful, healthcare providers may
make a second attempt, but they should consider using a supraglottic
airway.
Ventilating With an During cardiac arrest, provide the following:

ET Tube in Place
During Chest Volume: The volume should cause visible chest rise.
Compressions
When practicing this skill, try to get a sense of what such a volume
feels like when squeezing the ventilation bag.

Provide slightly more volume for very obese patients.
Rate: Provide approximately 1 breath every 6 seconds when delivering

ventilation during CPR or respiratory arrest.
Compression-ventilation cycles: Once an advanced airway is in place, the

healthcare provider should provide continuous compressions and
asynchronous ventilations once every 6 seconds. Providers should switch
compressors about every 2 minutes.
Airway Ventilations During Ventilations During

Devices Cardiac Arrest Respiratory Arrest
Any advanced Ventilate once every 6 Once every 5 to 6 seconds
airway seconds
Take care to avoid air trapping in patients with conditions associated with
increased resistance to exhalation, such as severe obstructive lung
disease and asthma. Air trapping could result in a positive end-expiratory
pressure effect that may significantly lower blood pressure. In these
patients, use slower ventilation rates to allow more complete exhalation.
In cases of hypovolemia, restore intravascular volume.
Tube Trauma and ET intubation can cause significant trauma to a patient, including
Adverse Effects
Brain damage or death
If the ET tube is inserted into a patients esophagus, the patient
will receive no ventilation or oxygenation unless he or she is still
breathing spontaneously. If you or your team fails to recognize
esophageal intubation, the patient could suffer permanent brain
damage or die.
Lacerated lips or tongue from forceful pressure between the
laryngoscope blade and the tongue or cheek
Chipped teeth
Lacerated pharynx or trachea from the end of the stylet or ET tube
Injury to the vocal cords
Pharyngeal-esophageal perforation
Vomiting and aspiration of gastric contents into the lower airway
Insertion of ET Insertion of the ET tube into the right (most common) or left main
Tube Into One bronchus is a frequent complication. Unrecognized and uncorrected
Bronchus intubation of a bronchus can result in hypoxemia due to underinflation of
the uninvolved lung or overinflation of the ventilated lung.
To determine if the ET tube has been inserted into a bronchus, listen to

the chest for bilateral breath sounds. Also, look for equal expansion of
both sides during ventilation. Waveform capnography is not sensitive
enough to detect main bronchus intubation.

If you suspect that the tube has been inserted into either the left or right
main bronchus, take these actions:
Deflate the tube cuff.

Withdraw the tube back 1 to 2 cm.
Confirm correct tube placement by both clinical assessment and
device confirmation.
Reinflate the cuff and secure the ET tube in place.
Recheck the patients clinical signs, including chest expansion, breath
sounds, and evidence of oxygenation.
Even when the ET tube is seen to pass through the vocal cords and the
tube position is verified by chest expansion and auscultation during
positive-pressure ventilation, you should obtain additional confirmation of
placement by using continuous quantitative waveform capnography or a
qualitative device like a colorimetric PETCO2 detector or EDD.
Once the patient is more stable, an x-ray may be obtained to optimize

the ET tube position and assess lung pathology. An x-ray takes too long
to be used as a means of confirming tracheal placement of an ET tube.
Recognizing misplacement of an ET tube is a clinical responsibility.
After inserting and confirming the correct placement of an ET tube, you

should record the depth of the tube as marked at the front teeth or gums
and secure it. Because there is significant potential for ET tube
movement with head flexion and extension and when the patient is
moved from one location to another, secure the ET tube with tape or a
commercial device. Devices and tape should be applied in a manner that
avoids compression of the front and sides of the neck to protect against
impairment of venous return from the brain.
Confirmation of ET Confirm tube placement immediately, assessing the first breath

Tube Placement: delivered by the bag-mask device. You should use both clinical
Physical Exam assessment and confirmation devices to verify tube placement
immediately after insertion and again when the patient is moved.
However, because no single confirmation technique is completely
reliable, particularly when cardiac arrest is present, the AHA
recommends the use of continuous waveform capnography, in addition
to clinical assessment, as the most reliable method of confirming and
monitoring the correct placement of an ET tube. If waveform
capnography is not available, EDD or nonwaveform PETCO2 monitor, in
addition to clinical assessment, should be used to confirm ET tube
placement.
Assessment by physical examination consists of visualizing chest

expansion bilaterally and listening over the epigastrium (breath sounds
should not be heard) and the lung fields bilaterally (breath sounds
should be equal and adequate).
As the bag is squeezed, listen over the epigastrium and observe the
chest wall for movement. If you hear stomach gurgling and see no chest-

wall expansion, you have intubated the esophagus. Stop ventilations.

Remove the ET tube at once. Then do the following:
Continue chest compressions if CPR is in progress.

Resume bag-mask ventilation or consider an alternate advanced
airway.
Reattempt intubation only after reoxygenating the patient
(approximately 30 seconds of bag-mask ventilations with 100%
oxygen).
If, after intubation, the chest wall rises appropriately and stomach
gurgling is not heard, listen to the lung fields with 5-point auscultation:
over the stomach, left and right anterior lung fields, and left and right
midaxillary lung fields. Document the location of breath sounds in the
patients medical record. If you have any doubt, stop ventilations
through the tube, and use the laryngoscope to see if the tube is
passing through the vocal cords.
If still in doubt, remove the tube and provide bag-mask ventilation
until the tube can be replaced.
If the tube seems to be in place, reconfirm the tube mark at the front
teeth (previously noted after inserting the tube 1 to 2 cm past the
vocal cords).
Secure the tube (ideally with a commercial device designed for this
purpose), avoiding compression of the front and sides of the neck.
Once the tube is secured, insert a bite-block if the commercial device
used to secure the tube does not prevent the patient from biting down
and occluding the airway.
Confirmation of ET The 2015 AHA Guidelines for CPR and ECC recommend confirmation of
Tube Placement: the ET tube with both clinical assessment and a device. If the device is
Qualitative and attached to the bag before it is joined to the tube, it will increase
Quantitative efficiency and decrease the time in which chest compressions must be
Devices interrupted.
Detailed assessment of out-of-hospital intubation attempts has

concluded that ET tubes are much more difficult to place properly in that
setting and highly susceptible to misplacement and displacement.
Proper training, supervision, frequent clinical experience, and a process
of quality improvement are the keys to achieving successful intubation.
Waveform Continuous waveform capnography, in addition to physical assessment,

Capnography is recommended as the most reliable method of confirming and
monitoring correct placement of an ET tube. Providers should observe a
persistent capnographic waveform with ventilation to confirm and
monitor ET tube placement in the field, in the transport vehicle, on arrival
at the hospital, and after any patient transfer to reduce the risk of
unrecognized tube misplacement or displacement. Studies of waveform
capnography to verify ET tube position in patients in cardiac arrest have
shown high sensitivity and specificity in identifying correct ET tube
placement (Figures 13 and 14A-C).

The use of capnography to confirm and monitor correct placement of

supraglottic airways has not been studied. However, effective ventilation
through a supraglottic airway device should result in a capnographic
waveform during CPR and after return of spontaneous circulation
(ROSC).
Figure 13. Waveform capnography with ET tube.
C
Figure 14. Waveform capnography. A, Normal range (approximately 35
to 45 mm Hg). B, Expected waveform with adequate chest
compressions in cardiac arrest (approximately 20 mm Hg). C, ET tube
incorrectly placed or dislodged (0 mm Hg).

Quantitative End- The quantitative end-tidal CO2 monitor or capnometer provides a single
Tidal CO2 Monitors quantitative readout of the concentration of CO2 at a single point in time.
(Capnometry) The device provides a continuous display of the level of CO2 as it varies
throughout the ventilation cycle.
These monitors can help confirm successful ET tube placement within

seconds of an intubation attempt. They also can detect a patients
deterioration associated with declining clinical status or ET tube
displacement. ET tube displacement is an adverse event that is
alarmingly common during out-of-hospital transport of a patient.
Exhaled A number of commercial devices can react, usually with a color change
(Qualitative) CO2 (different colors for different CO2 detectors), to CO2 exhaled from the
Detectors lungs. This simple method, when used by an experienced operator, can
be a reasonable alternative for detecting correct tube placement if
continuous waveform capnography is not available. There is, however,
no evidence that these devices are accurate for continued monitoring of
ET tube placement.
Note that the carbon dioxide detection cannot ensure proper depth of
tube insertion. The tube should be held in place and then secured once
correct position is verified. Different manufacturers may use different
color indicators.
Esophageal EDDs use simple anatomical principles to determine the location of the
Detector Devices distal end of the ET tube. Unlike the end-tidal CO2 detector, the EDD
does not depend on blood flow. Providers should completely compress
the bulb-style EDD before attaching it to the ET tube. The EDD should be
used before any breaths are given. After the provider releases the bulb, if
the tube is resting in the esophagus, reinflation of the bulb produces a
vacuum, which pulls the esophageal mucosa against the tip of tube. This
results in slow or no reexpansion of the bulb.
With the syringe-style EDDs, the vacuum occurs when the rescuer pulls
back on the syringe plunger. Esophageal placement results in the inability
of the rescuer to pull back on the plunger.
If the tube rests in the trachea, the vacuum will allow smooth reexpansion
of the bulb or aspiration of the syringe.
If continuous waveform capnography is not available, an EDD used by an

experienced operator is also a reasonable alternative for confirming
correct ET tube placement. However, while observational studies and a
small randomized controlled trial of these devices report a low false-
positive rate for confirming tracheal placement, there is no evidence that
an EDD is accurate or practical for the continued monitoring of ET tube
placement.
Note that the EDD may yield misleading results in patients with morbid
obesity, late pregnancy, or status asthmaticus.

Table 2 lists correct responses plus the most common causes of

misleading results from using end-tidal CO2 detector devices and EDDs to
confirm the correct placement of the ET tube. The tables columns
(vertical) indicate the reading and actual location of the ET tube. The rows
(across) indicate the expected results from using either a colorimetric
end-tidal CO2 detector (A) or bulb-type esophageal detector device (B).
With both devices, assume that the rescuer made a conscientious
intubation effort and thinks the ET tube is in the trachea.
Table 2. Comparison of Qualitative Performance: EDD and PETCO2 Devices

A: Colorimetric End-Tidal CO2 Detector
Actual Location of ET
Actual Location of ET
Reading Tube: Esophagus (or
Tube: Trachea
Hypopharynx)
Carbon dioxide ET tube in trachea Reasons for apparent
detected CO2 detection despite
Proceed with tube in esophagus
Color change: ventilations. Causes: Distended
positive = CO2 stomach, recent ingestion
present (or as of carbonated beverage,
specified by nonpulmonary sources of
manufacturer) CO2
Consequences:
Unrecognized esophageal
intubation; can lead to
iatrogenic death
No CO2 No CO2 detection with No CO2 detection and
detected tube in trachea tube is not in trachea (ie,
Causes: Low or no blood tube is in esophagus)
No color flow state (eg, cardiac Causes: Rescuer has
change: arrest); any cardiac inserted ET tube in
negative = CO2 arrest with no, esophagus/hypopharynx.
absent (or as prolonged, or poor CPR A life-threatening adverse
specified by Consequences: Leads to event has been detected.
manufacturer) unnecessary removal of Consequences: Rescuer
properly placed ET tube; recognizes ET tube is not
reintubation attempts in trachea; properly and
increase chances of rapidly identified; tube is
other adverse removed at once; patient
consequences is reintubated.
B: Esophageal Detector Device
Actual Location of ET Actual Location of ET
Reading
Tube: Esophagus Tube: Trachea
Consistent with Device suggests tube in Device suggests tube in
tube in esophagus when it is in esophagus when it is in
esophagus esophagus trachea
Bulb does not Causes: Rescuer has Causes: Secretions in

refill or refills inserted tube in trachea (mucus, gastric
slowly (>10 esophagus/hypo- contents, acute
seconds 2), pharynx. A potentially pulmonary edema);
or syringe insertion in right main

cannot be life-threatening adverse bronchus; pliable trachea

aspirated event has been detected. (morbid obesity, late-term
Consequences: Rescuer pregnancy)
correctly recognizes ET Consequences: This
tube is in esophagus; ET leads to unnecessary
tube is removed at once; removal of properly
patient is reintubated. placed ET tube.
Reintubation attempts
increase chances of other
adverse consequences.
Consistent with Results suggest that Results suggest that tube
tube in trachea tube is not in esophagus is not in the esophagus
(ie, that it is in trachea) (ie, that it is in the
Bulb fills when tube is in trachea) when it is in the
immediately or esophagus. trachea.
syringe can be Causes:
aspirated Conditions that cause Esophageal detector
increased lung device indicates ET tube
expansion (eg, is in trachea.
COPD, status Proceed with ventilations.
asthmaticus)
Conditions that fill
stomach with air (eg,
recent bag-mask
ventilation, mouth-to-
mask or mouth-to-
mouth breathing)
Conditions that cause
poor tone in
esophageal sphincter
or increased gastric
pressure (late
pregnancy)
Consequences:
Unrecognized
esophageal intubation
can lead to death.

ACLS Core Rhythms
Recognition of Core Electrocardiogram Arrest Rhythms
The Basics Figure 15 shows the anatomy of the cardiac conduction system and its
relationship to the electrocardiogram (ECG) cardiac cycle.
A B
Figure 15. Anatomy of the cardiac conduction system: relationship to the ECG cardiac cycle.
A, Heart: anatomy of conduction system. B, Relation of cardiac cycle to conduction system
anatomy.
Cardiac Arrest The ECG rhythms/conditions for patients who are in cardiac arrest are
Rhythms and ventricular fibrillation (VF; Figure 16A and B), pulseless ventricular
Conditions tachycardia (VT), asystole (Figure 17), or pulseless electrical activity
(PEA), which presents with a variety of rhythms.
These ECG rhythms are shown below:
Ventricular Fibrillation
Pathophysiology Ventricles consist of areas of normal
myocardium alternating with areas of
ischemic, injured, or infarcted myocardium,
leading to a chaotic asynchronous pattern of
ventricular depolarization and repolarization.
Without organized ventricular depolarization,
the ventricles cannot contract as a unit, and

they produce no cardiac output. The heart

quivers and does not pump blood.
Defining Criteria per Rate/QRS complex: Unable to determine;
ECG no recognizable P, QRS, or T waves;
baseline undulations occur between 150 and
500 per minute
Rhythm: Indeterminate; pattern of sharp up
(peak) and down (trough) deflections
Amplitude: Measured from peak to trough;
often used subjectively to describe VF as
fine (peak to trough 2 to <5 mm), medium or
moderate (5 to <10 mm), coarse (10 to <15
mm), or very coarse (>15 mm)
Clinical Pulse disappears with onset of VF
Manifestations The pulse may disappear before the
onset of VF if a common precursor to VF,
rapid VT, develops before the VF.
Collapse, unresponsiveness
Agonal gasps or apnea
Sudden death
Common Etiologies ACS leading to ischemic areas of
myocardium
Stable to unstable VT, untreated
Premature ventricular complexes (PVCs)
with R-on-T phenomenon
Multiple drug, electrolyte, or acid-base
abnormalities that prolong the relative
refractory period
Primary or secondary QT prolongation
Electrocution, hypoxia, many others

B
Figure 16. A, Coarse VF. Note high-amplitude waveforms, which vary in
size, shape, and rhythm, representing chaotic ventricular electrical activity.
B, Fine VF. Note the complete absence of QRS complexes.
The ECG criteria for VF are as follows:
QRS complexes: No normal-looking QRS complexes are recognizable;

a regular negative-positive-negative pattern (Q-R-S) cannot be seen.
Rate: Uncountable; electrical deflections are very rapid and too
disorganized to count.
Rhythm: No regular rhythmic pattern can be discerned; the electrical
waveforms vary in size and shape; the pattern is completely
disorganized.
In comparison with Figure 16A, the amplitude of electrical activity in Figure

16B is much reduced. In terms of electrophysiology, prognosis, and the
likely clinical response to attempted defibrillation, adrenergic agents, or
antiarrhythmics, this rhythm pattern may be difficult to distinguish from that
of asystole.
Pulseless Electrical Activity

Pathophysiology Cardiac conduction impulses occur in an
organized pattern but do not produce
myocardial contraction (this condition was
formerly called electromechanical
dissociation), insufficient ventricular filling
during diastole, or ineffective contractions.
Defining Criteria per Rhythm that displays organized electrical
ECG activity (not VF/pulseless VT)
Usually not as organized as normal sinus
rhythm
Can be narrow (QRS <0.12 second) or wide
(QRS 0.12 second); fast (>100 beats per
minute) or slow (<60 beats per minute)

Narrow QRS and fast heart rate mostly

caused by noncardiac etiology; wide QRS
and slow heart rate mostly caused by
cardiac etiology
Clinical Collapse, unresponsiveness
Manifestations Agonal gasps or apnea
No pulse detectable by palpation
Very low systolic blood pressure could
still be present in such cases.
Common Etiologies Use the Hs and Ts mnemonic to recall
possible underlying causes:
Hypovolemia
Hypoxia
Hydrogen ion (acidosis)
Hypo-/hyperkalemia
Hypothermia
Tension pneumothorax
Tamponade, cardiac
Toxins (ie, drug overdose, ingestion)
Thrombosis, pulmonary (embolism)
Thrombosis, coronary (ACS)
Asystole
Defining Criteria per Rate: No ventricular activity seen; so-called
ECG P-wave asystole occurs with only atrial
Classically, asystole impulses present (P waves)
presents as a flat Rhythm: No ventricular activity seen
line; defining criteria PR: Cannot be determined; occasionally P
are virtually wave is seen, but by definition R wave must
nonexistent. be absent
QRS complex: No deflections seen that are
consistent with a QRS complex
Clinical Collapse; unresponsiveness
Manifestations Agonal gasps (early) or apnea
No pulse or blood pressure
Death
Common Etiologies End of life (death)
Cardiac ischemia
Acute respiratory failure/hypoxia from many
causes (no oxygen, apnea, asphyxiation)
Massive electrical shock (eg, electrocution,
lightning strike)
May represent stunning of the heart
immediately after defibrillation (shock
delivery that eliminates VF) before
resumption of spontaneous rhythm

Figure 17. The rhythm of ventricular asystole. This patient is pulseless

and unresponsive. Note the 2 QRS-like complexes at the start of this
rhythm display. These complexes represent a minimum of electrical
activity, probably ventricular escape beats. Note the long section in
which electrical activity is completely absent. This patient is in asystole
at this point.
Recognition of Selected Nonarrest ECG Rhythms
Recognition of Supraventricular Tachyarrhythmias (SVTs)
Sinus Tachycardia (Figure 18)

Pathophysiology More of a physical response or sign than an
actual arrhythmia or pathologic condition
Normal impulse formation and conduction
Defining Criteria Rate: >100 beats per minute
and ECG Rhythm: Sinus
Features PR: Usually <0.20 second
P for every QRS complex
QRS complex: May be normal or wide if there
is an underlying abnormality
Clinical None specific for the tachycardia
Manifestations Symptoms may be present due to the cause of
the tachycardia (fever, hypovolemia, etc)
Common Normal exercise
Etiologies Hypoxemia
Fever
Hypovolemia
Adrenergic stimulation, anxiety
Hyperthyroidism
Anemia
Pain

Figure 18. Sinus tachycardia.
Atrial Fibrillation (Figure 19) and Atrial Flutter (Figure 20)

Pathophysiology Atrial impulses are faster than sinoatrial (SA
node) impulses.
Atrial fibrillation: Impulses take multiple chaotic,
random pathways through atria.
Atrial flutter: Impulses take a circular course
around atria, setting up flutter waves.
Defining Criteria Atrial Fibrillation Atrial Flutter
and ECG Rate Wide-ranging Atrial rate is 220
Features ventricular to 350 beats per
Distinctions response to minute.
between atrial atrial Ventricular
fibrillation and undulations response is a
atrial flutter; all that occur function of AV
other between 300 node block or
characteristics and 400 per conduction of
are the same minute atrial impulses.
May be Ventricular
Atrial Fibrillation normal or response is rarely
Key: A classic slow if >150 to 180
clinical axiom is atrioventricula beats because of
Irregularly r (AV) nodal AV nodal
irregular rhythm conduction is conduction limits.
with variation in abnormal (eg,
both interval and sick sinus
amplitude from R syndrome)
wave to R wave Rhythm Irregular (classic Regular
is atrial irregularly Ventricular
fibrillation. This irregular) rhythm often
one is usually regular
dependable and Set ratio to atrial
can also be rhythm, eg, 2:1 or
observed in 4:1
multifocal atrial
P Chaotic atrial No true P waves
tachycardia
waves fibrillatory seen
(MAT).
waves only

Atrial Flutter Creates Flutter waves in

Key: Flutter variable classic sawtooth
waves in classic baseline pattern
sawtooth PR Cannot be measured
pattern
QRS Remains <0.12 second unless QRS
complex is distorted by fibrillation or
flutter waves or by conduction
defects through ventricles
Clinical Signs and symptoms are a function of the rate
Manifestations of ventricular response to atrial fibrillation
waves; atrial fibrillation with rapid ventricular
response may be characterized by dyspnea on
exertion, shortness of breath, and sometimes
acute pulmonary edema.
Loss of atrial kick may lead to drop in cardiac
output and decreased coronary perfusion.
Irregular rhythm is often perceived as
palpitations.
Atrial fibrillation and atrial flutter can be
asymptomatic.
Common Acute coronary syndromes, coronary artery
Etiologies disease, congestive heart failure
Disease at mitral or tricuspid valve
Hypoxia, acute pulmonary embolism
Drug-induced: digoxin or quinidine; -agonists,
theophylline
Sepsis
Hypertension
Hyperthyroidism
Figure 19. Atrial fibrillation.
Figure 20. Atrial flutter (sawtooth pattern).

Accessory-Mediated SVT (Figure 21)

May include AV nodal reentrant tachycardia or AV reentry tachycardia
Pathophysiology Reentry phenomenon: Impulses recycle
repeatedly in the AV node because an
abnormal rhythm circuit allows a wave of
depolarization to travel in a circle. Usually the
depolarization travels antegrade (forward)
through the abnormal pathway and then
circles back retrograde through the normal
conduction tissue.
Defining Criteria Rate: Exceeds upper limit of sinus
and ECG Features tachycardia at rest (>220 beats per minute),
Key: Regular, seldom <150 beats per minute, often up to
narrow-complex 250 beats per minute
tachycardia without Rhythm: Regular
P waves and P waves: Seldom seen because rapid rate
sudden onset or causes P wave to be hidden in preceding T
cessation waves or to be difficult to detect because the
Note: To merit the origin is low in the atrium
diagnosis of reentry QRS complex: Normal, narrow
SVT, some experts
require capture of
the abrupt onset or
cessation on a
monitor strip.
Clinical Palpitations felt by patient at onset; becomes
Manifestations anxious, uncomfortable
Low exercise tolerance with very high rates
Symptoms of unstable tachycardia may occur
Common Accessory conduction pathway occurs in
Etiologies many SVT patients.
For such otherwise healthy people, many
factors can provoke the reentry SVT:
caffeine, hypoxia, cigarettes, stress, anxiety,
sleep deprivation, numerous medications.
Frequency of SVT increases in unhealthy
patients with coronary artery disease, chronic
obstructive pulmonary disease, and
congestive heart failure.
Figure 21. Sinus rhythm with a reentry SVT.

Recognition of Ventricular Tachyarrhythmias
Monomorphic VT (Figure 22)

Pathophysiology Impulse conduction is slowed around areas
of ventricular injury, infarct, or ischemia.
These areas also serve as sources of
ectopic impulses (irritable foci).
These areas of injury can cause the impulse
to take a circular course, leading to the
reentry phenomenon and rapid repetitive
depolarizations.
Defining Criteria per Rate: Ventricular rate >100 beats per
ECG minute; typically 120 to 250 beats per
Key: The same minute
morphology, or Rhythm: Regular ventricular rhythm
shape, is seen in PR: Absent (rhythm is AV dissociated)
every QRS complex. P waves: Seldom seen but present; VT is a
Notes: form of AV dissociation, a defining
Three or more characteristic for wide-complex tachycardias
consecutive PVCs of ventricular origin versus supraventricular
indicate VT. tachycardias with aberrant conduction
VT of less than 30 QRS complex: Wide and bizarre, PVC-like
seconds duration complexes 0.12 second, with large T wave
is nonsustained of opposite polarity from QRS
VT. Fusion beats: Occasional chance capture
VT of more than of a conducted P wave. Resulting QRS
30 seconds hybrid complex, part normal, part
duration is ventricular
sustained VT. Nonsustained VT: Lasts <30 seconds and
does not require intervention
Clinical Typically, symptoms of decreased cardiac
Manifestations output (orthostasis, hypotension, syncope,
exercise limitations, etc) do develop.
Monomorphic VT can be asymptomatic
despite widespread belief that sustained VT
always produces symptoms.
Untreated and sustained VT will deteriorate
to unstable VT and often to VF.
Common Etiologies An acute ischemic event (see
Pathophysiology) with areas of ventricular
irritability leading to PVCs
Low ejection fraction due to chronic systolic
heart failure
PVCs that occur during relative refractory
period of cardiac cycle (R-on-T
phenomenon)
Drug-induced prolonged QT interval (tricyclic
antidepressants, procainamide, sotalol,
amiodarone, ibutilide, dofetilide, some
antipsychotics, digoxin, some long-acting
antihistamines, certain antibiotics)

Figure 22. Monomorphic VT at a rate of 150 beats per minute; wide QRS
complexes (arrow A) with opposite polarity T waves (arrow B).
Polymorphic VT (Figure 23)

Pathophysiology Impulse conduction is slowed around multiple
areas of ventricular injury, infarct, or ischemia.
These areas also serve as the source of ectopic
impulses (irritable foci); irritable foci occur in
multiple areas of the ventricles and thus are
polymorphic.
These areas of injury can cause impulses to
take a circular course, leading to the reentry
phenomenon and rapid repetitive
depolarizations.
Defining Criteria Rate: Ventricular rate >100 beats per minute;
per ECG typically 120 to 250 beats per minute
Key: Marked Rhythm: Regular or irregular ventricular; no
variation and atrial activity
inconsistency PR: Nonexistent
seen in QRS P waves: Seldom seen but present; VT is a
complexes form of AV dissociation
QRS complexes: Marked variation and
inconsistency seen in QRS complexes
Clinical Typically will rapidly deteriorate to pulseless VT
Manifestations or VF
Symptoms of decreased cardiac output
(orthostasis, hypotension, poor perfusion,
syncope, etc) present before pulseless arrest
Common Acute ischemic event (see Pathophysiology)
Etiologies with areas of ventricular irritability
PVCs that occur during relative refractory period
of cardiac cycle (R-on-T phenomenon)
Drug-induced prolonged QT interval (tricyclic
antidepressants, procainamide, sotalol,
amiodarone, ibutilide, dofetilide, some
antipsychotics, digoxin, some long-acting
antihistamines, certain antibiotics)
Hereditary long QT interval syndromes

Figure 23. Polymorphic VT; QRS complexes display multiple

morphologies.
Torsades de Pointes (a Unique Subtype of Polymorphic VT)

(Figure 24)
Pathophysiology Specific pathophysiology of classic
torsades:
QT interval is abnormally long
(baseline ECG) and leads to an
increase in the relative refractory
period (vulnerable period) of the
cardiac cycle. This increases the
probability that an irritable focus
(PVC) will occur on the T wave
(vulnerable period or R-on-T
phenomenon).
The R-on-T phenomenon often
induces VT.
Defining Criteria per ECG Atrial rate: Cannot be
Key: QRS complexes display a determined
spindle-node pattern, in which Ventricular rate: 150 to 250
VT amplitude increases and complexes per minute
then decreases in a regular Rhythm: Only irregular
pattern, creating the spindle. ventricular rhythm
The initial deflection at the start PR: Nonexistent
of one spindle (eg, negative) will
P waves: Nonexistent
be followed by complexes of
opposite (eg, positive) polarity or QRS complexes: Display classic
deflection at the start of the next spindle-node pattern (see Key at
spindle, creating the node. left)
Clinical Manifestations Tendency toward sudden
deterioration to pulseless VT or
VF
Symptoms of decreased cardiac
output typical (orthostasis,
hypotension, syncope, signs of
poor perfusion, etc)
Stable torsades; sustained
torsades is uncommon

Common Etiologies Most commonly occurs in

patients with prolonged QT
interval, due to many causes:
Drug-induced: tricyclic
antidepressants,
procainamide, sotalol,
amiodarone, ibutilide,
dofetilide, some
antipsychotics, digoxin, some
long-acting antihistamines,
certain antibiotics
Electrolyte and metabolic
alterations (hypomagnesemia
is the prototype)
Inherited forms of long QT
syndrome
Acute ischemic events (see
Pathophysiology)
Figure 24. Torsades de pointes, a unique type of polymorphic VT. A,

Start of a spindle. Note negative initial deflection and increasing QRS
amplitude. B, End of a spindle and start of a node. C, End of a node and
start of the next spindle. Note the positive initial deflection and spindling in
QRS amplitude.

Recognition of Sinus Bradycardia
Sinus Bradycardia (Figure 25)

Pathophysiology Impulses originate at SA node at a slow rate
May be physiologic
Can be a physical sign, as in sinus tachycardia
Defining Criteria Rate: <60 beats per minute (when symptomatic
per ECG and bradycardia is the cause of symptoms, the
Key: Regular P rate is generally <50 beats per minute)
waves followed Rhythm: Regular sinus
by regular QRS PR: Regular, 0.12 to 0.20 second
complexes at rate P waves: Size and shape normal; every P wave
<60 beats per followed by a QRS complex; every QRS
minute complex preceded by a P wave
Note: Often a QRS complex: Narrow; <0.12 second (often
physical sign <0.11 second) in absence of intraventricular
rather than an conduction defect
abnormal rhythm
Clinical Person is usually asymptomatic when at rest.
Manifestations With increased activity and sinus node
dysfunction, a persistent slow rate can lead to
symptoms of easy fatigue, shortness of breath,
dizziness or lightheadedness, syncope,
hypotension, diaphoresis, pulmonary
congestion, and frank pulmonary edema.
The ECG can independently display acute ST-
segment or T-wave deviation or ventricular
arrhythmias.
Common Can be normal for well-conditioned people
Etiologies Vasovagal event, such as vomiting, Valsalva
maneuver, rectal stimuli, inadvertent pressure
on carotid sinus (shavers syncope)
Acute coronary syndromes that affect circulation
to SA node (right coronary artery); most often
inferior acute myocardial infarctions (AMIs)
Adverse drug effects, eg, -blockers or calcium
channel blockers, digoxin, quinidine
Figure 25. Sinus bradycardia.

Recognition of AV Block
First-Degree AV Block (Figure 26)

Pathophysiology Impulse conduction slowed (partial block) at AV
node for a fixed interval
May be a sign of another problem or a primary
conduction abnormality
Defining Criteria Rate: First-degree AV block seen with rhythms
per ECG with both sinus bradycardia and sinus
Key: PR interval tachycardia as well as a normal sinus
>0.20 second mechanism
Rhythm: Sinus, regular, both atria and
ventricles
PR: Prolonged, >0.20 second but does not vary
(fixed)
P waves: Size and shape normal; every P wave
followed by a QRS complex; every QRS
complex preceded by P wave
QRS complex: Narrow, <0.12 second in
absence of intraventricular conduction defect
Clinical Usually asymptomatic
Manifestations
Common Many first-degree AV blocks due to drugs,
Etiologies usually the AV nodal blockers: -blockers,
nondihydropyridine calcium channel blockers,
and digoxin
Any condition that stimulates the
parasympathetic nervous system (eg,
vasovagal reflex)
AMI that affects circulation to the AV node (right
coronary artery); most often inferior AMI
Figure 26. First-degree AV block.
Type I Second-Degree AV Block (Mobitz IWenckebach)

(Figure 27)
Pathophysiology Site of pathology is AV node.
AV node blood supply comes from branches of
right coronary artery (right dominant circulation).
Impulse conduction is progressively slowed at
AV node (causing increasing PR interval) until

one sinus impulse is completely blocked and

QRS complex fails to follow.
Defining Criteria Rate: Atrial rate just slightly faster than
per ECG ventricular (because of dropped conduction),
Key: There is usually within normal range.
progressive Rhythm: Atrial complexes are regular and
lengthening of PR ventricular complexes are irregular in timing
interval until one (because of dropped beats); can show regular P
P wave is not waves marching through irregular QRS.
followed by QRS PR: Progressive lengthening of PR interval
complex (dropped occurs from cycle to cycle; and then one P
beat). wave is not followed by QRS complex (dropped
beat).
P waves: Size and shape remain normal;
occasional P wave is not followed by QRS
complex (dropped beat).
QRS complex: <0.12 second most often, but a
QRS drops out periodically.
Clinical Due to bradycardia
Manifestations Most often asymptomatic
Rate-Related Symptoms: Chest pain, shortness of breath,
decreased level of consciousness
Signs: Hypotension, shock, pulmonary
congestion, congestive heart failure, angina
Common AV nodal blocking agents: -blockers,
Etiologies nondihydropyridine calcium channel blockers,
digoxin
Conditions that stimulate the parasympathetic
nervous system
Acute coronary syndrome that involves right
coronary artery
Figure 27. Type I second-degree AV block. Note the progressive

lengthening of the PR interval until one P wave (arrow) is not followed by
a QRS.
Type II Second-Degree AV Block (Infranodal; Mobitz II) (Figure 28)

Pathophysiology The site of the block is most often below the AV
node (infranodal) at the bundle of His
(infrequent) or at bundle branches.
Impulse conduction is normal through node,
thus no first-degree block and no prior PR
prolongation.

Defining Criteria Atrial rate: Usually 60 to 100 beats per minute

per ECG Ventricular rate: By definition (because of
blocked impulses), slower than atrial rate
Rhythm: Atrial is regular; ventricular is irregular
(because of blocked impulses); ventricular is
regular if there is consistent 2:1 or 3:1 block
PR: Constant and set; no progressive
prolongation as with Type I second-degree AV
block Mobitza distinguishing characteristic
P waves: Typical in size and shape; by
definition, some P waves will not be conducted
and therefore not followed by a QRS complex
QRS complex: Narrow (<0.12 second) implies
high block relative to AV node; wide (0.12
second) implies low block relative to AV node
Manifestations Symptoms: Chest pain, shortness of breath,
Rate-Related decreased level of consciousness
congestion, congestive heart failure, AMI
Common Acute coronary syndrome that involves
Etiologies branches of left coronary artery
B
Figure 28. A, Type II (high block): regular PR-QRS intervals until 2
dropped beats occur; borderline normal QRS complexes indicate high
nodal or nodal block. B, Type II (low block): regular PR-QRS intervals
until dropped beats; wide QRS complexes indicate infranodal block.
Third-Degree AV Block and AV Dissociation (Figure 29)

PathophysiologyPearl Injury or damage to cardiac conduction
AV dissociation is the system so that no impulses (complete
defining class; third- block) pass between atria and ventricles
degree or complete AV (neither antegrade nor retrograde)
block is one type of AV This complete block can occur at several
dissociation. different anatomic areas:

AV node (high-, supra-, or junctional

nodal block)
Bundle of His
Bundle branches (low-nodal or
infranodal block)
Defining Criteria per Atrial rate: Usually 60 to 100 beats per
ECG minute; impulses completely independent
Key: Third-degree (dissociated) from the slower ventricular
block (see rate
Pathophysiology) Ventricular rate: Depends on rate of
causes atria and ventricular escape beats that arise:
ventricles to depolarize Ventricular escape rate slower than
independently, with no atrial rate = third-degree AV block (rate
relationship between = 20 to 40 beats per minute)
the two (AV Ventricular escape rate faster than
dissociation). atrial rate = AV dissociation (rate = 40
to 55 beats per minute)
Rhythm: Both atrial rhythm and
ventricular rhythm regular but independent
(dissociated)
PR: By definition, no relationship between
P wave and R wave
P waves: Typical in size and shape
QRS complex: Narrow (<0.12 second)
implies high block relative to AV node;
wide (0.12 second) implies low block
relative to AV node
ManifestationsRate- Symptoms: Chest pain, shortness of
Related breath, decreased level of consciousness
congestion, congestive heart failure, AMI
Common Etiologies Acute coronary syndrome that involves
branches of left coronary artery
In particular, involves left anterior
descending (LAD) artery and branches to
interventricular septum (supply bundle
branches)
Figure 29. Third-degree AV block. Regular P waves at 50 to 55 beats per

minute; regular ventricular escape beats at 35 to 40 beats per minute;
no relationship between P waves and escape beats.

The electrical cardioversion algorithm (Figure 30) is used for unstable

SVT or unstable monomorphic VT.
Figure 30. Electrical Cardioversion Algorithm.

VF Treated With CPR and Automated External Defibrillator
Figure 31. Adult BLS for Healthcare Provider Algorithm.

Defibrillation
Automated ACLS providers will typically use a manual defibrillator to shock a patient
External in VF or pulseless VT. In some cases, only an automated external
Defibrillator defibrillator (AED) will be available. The information below will discuss
Operation the use of AEDs within the framework of the BLS Healthcare Provider
Adult Cardiac Arrest Algorithm (Figure 31).
Use AEDs only when patients have the following 3 clinical findings:
No response
Absent or abnormal breathing (ie, no breathing or only gasping)
No pulse
In the first few minutes after the onset of sudden cardiac arrest, the
patient may demonstrate agonal gasps, which are not adequate
breathing. A nonresponsive patient with agonal gasping who has no
pulse is in cardiac arrest.
Know Your AED You must be familiar with the AED used in your clinical setting and be
ready to use it at any time. Review the troubleshooting checklist supplied
by the AED manufacturer. Learn to perform daily maintenance checks.
Not only are these checks an effective review of the steps of operation,
but they are also a means of verifying that the AED is ready for use.
Universal Steps After the AED arrives, place it at the patients side, next to the rescuer
for Operating who will operate it. This position provides ready access to the AED
an AED controls and easy placement of electrode pads. It also allows a second
rescuer to perform CPR from the opposite side of the patient without
interfering with AED operation.
AEDs are available in different models. Although there are small

differences from model to model, all AEDs operate in basically the same
way. The following table lists the universal steps for operating an AED:
Step Action
1 Open the carrying case. Power on the AED if needed.
Some devices will power on automatically when you open
the lid or case.
Follow the AED prompts as a guide to next steps.

2 Attach AED pads to the patients bare chest. Choose adult

pads (not child pads or a child system) victims 8 years of age
and older.
Peel the backing away from the AED pads.
Attach the adhesive AED pads to the patients bare chest.
Follow the placement diagrams on the pad (Figure 32). See
Foundational Facts: Alternative AED Electrode Pad
Placement Positions for common placement options.
Attach the AED connecting cables to the AED device (some
AED are already preconnected to the device).
3 Clear the patient and allow the AED to analyze the rhythm.
When the AED prompts you, clear the victim during
analysis. Be sure that no one is touching the patient, not
even the rescuer in charge of giving breaths.
Some AEDs will tell you to push a button to allow the AED
to begin analyzing the heart rhythm; others will do that
automatically. The AED may take a few seconds to analyze.
The AED then tells you if a shock is needed.
4 If the AED advises a shock, it will tell you to clear the victim
and then deliver a shock.
Clear the patient before delivering the shock; be sure that
no one is touching the patient.
Loudly state a clear the patient message, such as
Everybody clear or simply Clear.
Look to be sure that no one is in contact with the victim.
Press the shock button.
The shock will produce a sudden contraction of the patients
muscles.
5 If no shock is needed, and after any shock delivery,
immediately resume CPR, starting with chest compressions.
6 After about 5 cycles or 2 minutes of CPR, the AED will prompt
you to repeat steps 3 and 4.
Immediately resume high-quality CPR, starting with chest compressions,

after
A shock is delivered or
The AED prompts no shock advised
After about 5 cycles or 2 minutes of high-quality CPR, the AED will

prompt you to repeat steps 3 and 4. Continue until advanced life support
providers take over or the patient begins to breathe, move, or otherwise
react.

Figure 32. AED electrode pad placement on the patient.
Alternative AED Electrode Pad Placement Positions

There are 4 acceptable AED electrode pad positions:
Anterolateral
Anteroposterior
Anteriorleft infrascapular
Anteriorright infrascapular
All 4 positions are equally effective in shock success and are reasonable
for defibrillation. For ease of placement, anterolateral is a reasonable
default electrode placement. Providers may consider alternative pad
positions based on individual patient characteristics.
Troubleshooting Studies of AED failures have shown that most problems are caused by
the AED operator error rather than by AED defects. Operator error is less likely if
the operator is experienced in using the AED, has had recent training or
practice with the AED, and is using a well-maintained AED.
If the AED does not promptly analyze the rhythm, do the following:
Resume high-quality chest compressions and ventilations.

Check all connections between the AED and the patient to make sure
that they are intact.
Never delay chest compressions to troubleshoot the AED.

Shock First vs When you care for an adult patient in cardiac arrest, should you attempt
CPR First to shock first with an AED or provide CPR first?
Healthcare providers who treat cardiac arrest in hospitals and other

facilities should provide immediate CPR until the AED/defibrillator is
ready for use. Use the AED as soon as it is available.
At this time, the benefit of delaying defibrillation to perform CPR before

defibrillation is unclear. EMS system medical directors may consider
implementing a protocol that allows EMS responders to provide CPR
while preparing for defibrillation of patients found by EMS personnel to
be in VF. In practice, however, CPR can be initiated while the AED is
being readied.
With in-hospital sudden cardiac arrest (SCA), there is insufficient

evidence to support or refute CPR before defibrillation. However, in
monitored patients, the time from VF to defibrillation should be under 3
minutes. When 2 or more rescuers are present, one rescuer should
begin CPR while the other activates the emergency response system
and prepares the defibrillator.
AED Use in Special Situations
Introduction The following special situations may require the operator to take extra
care in placing the electrode pads when using an AED.
Hairy Chest If the patient has a hairy chest, the AED pads may stick to the hair and
not the skin on the chest. If this occurs, the AED will not properly analyze
the patients heart rhythm. The AED will give a check electrodes or
check electrode pads message. If this happens, complete the following
steps and actions while minimizing interruptions in chest compressions.
Step Action
1 If the pads stick to the hair instead of the skin, press down
firmly on each pad.
2 If the AED continues to prompt you to check pads or check
electrodes, quickly pull off the pads. This will remove much
of the hair.
3 If too much hair remains where you will put the pads, shave
the area with the razor in the AED carrying case, if available.
4 Put on a new set of pads. Follow the AED voice prompts.
Water Do not use an AED in water. If water is present on the patients chest, it
may conduct the shock electricity across the skin of the chest. This will
prevent the delivery of an adequate shock dose to the heart.

If Then
The patient is in the water Pull the patient out of the water.
The patients chest is covered with Wipe the chest quickly before
water attaching the electrodes.
The patient is lying on snow or ice Use the AED.
or in a small puddle
Implanted Patients known to be at high risk for sudden cardiac arrest may have
Pacemaker implanted defibrillators/pacemakers that automatically deliver shocks
directly to the heart muscle if a life-threatening arrhythmia is detected.
You can immediately identify these devices because they create a hard
lump beneath the skin of the upper chest or abdomen. The lump ranges
from the size of a silver dollar to half the size of a deck of cards, with a
small overlying scar. The presence of an implanted defibrillator or
pacemaker is not a contraindication to attaching and using an AED.
Avoid placing the AED electrode pads directly over the device because
the devices may interfere with each other.
If you identify an implanted defibrillator/pacemaker, take the following

steps:
If possible, place the AED electrode pad to either side and not directly
on top of the implanted device.
Follow the normal steps for operating an AED.
Note that a pacemaker spike may confuse the AEDs interpretation of

the patients real heart rhythm. Occasionally, the analysis and shock
cycles of implanted defibrillators and AEDs will conflict. If the implanted
defibrillator is delivering shocks to the patient (the patients muscles
contract in a manner like that observed after an AED shock), allow 30 to
60 seconds for the implanted defibrillator to complete the treatment cycle
before delivering a shock from the AED.
Transdermal Do not place AED electrodes directly on top of a medication patch (eg, a
Medication patch of nitroglycerin, nicotine, pain medication, hormone replacement
Patches therapy, or antihypertensive medication). The medication patch may
block the transfer of energy from the electrode pad to the heart or cause
small burns to the skin. To prevent these complications, remove the
patch and wipe the area clean before attaching the AED electrode pad.
Try to minimize interruptions in chest compressions, and do not delay
shock delivery.
Defibrillation and Safety
Manual Defibrillation
Using a Manual When using a manual defibrillator/monitor, perform a rhythm check as

Defibrillator/ indicated by the ACLS Cardiac Arrest Algorithm. This can be performed
Monitor by attaching the adhesive defibrillator electrode pads or placing the
defibrillator paddles on the chest (with appropriate conduction surface or

gel) to reduce transthoracic impedance, and by using the paddle quick

look feature.
At the time of writing of the 2015 AHA Guidelines Update for CPR and
ECC, there were no data to suggest that one of these modalities is
better than the others are in reducing impedance. Because adhesive
monitor/defibrillator electrode pads are as effective as paddles and gel
pads or paste, and the pads can be placed before cardiac arrest to allow
for monitoring and rapid administration of a shock when necessary,
adhesive pads should be used routinely instead of standard paddles.
For adult defibrillation, both handheld paddles and self-adhesive pads (8

to 12 cm in diameter) perform well, although defibrillation success may
be higher with electrodes 12 cm in diameter than with those 8 cm in
diameter, whereas small electrodes (4.3 cm) may be harmful and may
cause myocardial necrosis. When using handheld paddles and gel or
pads, you must ensure that the paddle is in full contact with the skin.
Even smaller pads have been found to be effective in VF of brief
duration. Use of the smallest (pediatric) pads, however, can result in
unacceptably high transthoracic impedance in larger children.
Early defibrillation is critical to survival from SCA. A common initial

rhythm in out-of-hospital witnessed SCA is VF, the treatment for which is
defibrillation. The probability of successful defibrillation diminishes
rapidly over time, and VF tends to deteriorate to asystole within 10 to 15
minutes. Therefore, whether the adhesive electrode pads or paddles are
being used, you should be very careful not to delay the shock during
CPR to minimize the time between last compression and shock delivery.
Intervals between pausing chest compressions and shock delivery have
been shown to last approximately 20 to 30 seconds, which is no longer
acceptable. If CPR is in progress, chest compressions should continue
until the defibrillator electrode adhesive pads are attached to the chest
and the manual defibrillator is ready to analyze the rhythm.
For every minute that passes between collapse and defibrillation,

survival rates from witnessed VF SCA decrease 7% to 10% if no CPR is
provided. When bystander CPR is provided, the decrease in survival
rates is more gradual and averages 3% to 4% from collapse to
defibrillation. CPR can double or triple survival from witnessed SCA at
most intervals to defibrillation.
When any rescuer witnesses an out-of-hospital arrest and an AED is

immediately available onsite, the rescuer should start CPR and use the
AED as soon as possible. Healthcare providers who treat cardiac arrest
in hospitals and other facilities with AEDs onsite should provide
immediate CPR and should use the AED/defibrillator as soon as it
becomes available.
When you identify VF/pulseless VT, immediately deliver 1 shock, using

the following energy levels:
Biphasic: Device-specific; the first dose is typically a selected energy

of 120 J with a rectilinear biphasic waveform and a first dose selected
energy of 120 J to 200 J with a biphasic truncated exponential

waveform. If you do not know the device or the manufacturers

recommendation regarding the specific dose shown to be effective for
elimination of VF, defibrillation at the maximal dose may be
considered.
Monophasic: 360 J; if VF persists after the first shock, second and
subsequent shocks of 360 J should be given.
After delivering a single shock, immediately resume CPR, pushing hard

and fast at a rate of 100 to 120 compressions per minute. Minimize
interruption of CPR, and allow full chest recoil after each compression.
Safety and Clearing the Patient
Clearing: You and To ensure the safety of defibrillation, whether manual or automated, the
Your Team defibrillator operator must always announce that a shock is about to be
delivered and perform a visual check to make sure no one is in contact
with the patient. The operator is responsible for clearing the patient and
rescuers before each shock is delivered. Whenever you use a
defibrillator, firmly state a defibrillation clearing or warning before each
shock. The purpose of this warning is to ensure that no one has any
contact with the patient and that no oxygen is flowing across the
patients chest or openly flowing across the electrode pads. You should
state the warning quickly to minimize the time from last compression to
shock delivery. For example, state, Clear. Shocking, and then perform
a visual check to make sure you have no contact with the patient, the
stretcher, or other equipment.
You do not need to use those exact words. But it is imperative that you
warn others that you are about to deliver a shock and that everyone
stand clear.
Make sure all personnel step away from the patient, remove their hands
from the patient, and end contact with any device or object touching the
patient. Any personnel in indirect contact with the patient, such as the
team member holding a ventilation bag attached to an ET tube, must
also disconnect the bag and end contact with the patient. The person
responsible for airway support and ventilation should ensure that oxygen
is not openly flowing around the electrode pads (or paddles) or across
the patients chest.
A Final Note About Most modern AEDs and manual defibrillators use biphasic waveforms.
Defibrillators Take the time to learn to operate the defibrillator used in your workplace
and its energy settings. Remember, early defibrillation in the presence of
shockable rhythm increases the patients chance of survival. This
principle holds true regardless of the type of defibrillator or waveform.

Access for Medications
Intravenous Access
Using Peripheral The most common sites for IV access are in the hands and arms.
Veins for IV Favored sites are the dorsum of the hands, the wrists, and the
Access antecubital fossae. The antecubital vein is the preferred location for IV
drug administration during CPR.
Anatomy: Upper Extremities

Starting at the radial side of the wrist, a thick vein, the superficial radial
vein, runs laterally up to the antecubital fossa and joins the median
cephalic vein to form the cephalic vein. Superficial veins on the ulnar
aspect of the forearm run to the elbow and join the median basilic vein to
form the basilic vein. The cephalic vein of the forearm bifurcates into a Y
in the antecubital fossa, becoming the median cephalic (laterally) and
the median basilic (medially).
Technique: Antecubital Venipuncture

The largest surface veins of the arm are in the antecubital fossa. Select
these veins first for access if the patient is in circulatory collapse or
cardiac arrest. Select a point between the junctions of 2 antecubital
veins (Figure 33). The vein is more stable here, and venipuncture is
more often successful.
If peripheral access is impossible, consider central access via the

femoral veins since chest compressions and other resuscitation
interventions should not be interrupted, and potential vascular injuries
can be better controlled at this site.
If upper extremity access is impossible and a central line is not an

option, consider a peripheral leg vein.

Figure 33. Antecubital venipuncture. A, Scene perspective from a

distance. B, Close-up view of antecubital area: anatomy of veins of
upper extremity.

General IV Once you gain vascular access, follow these important principles for
Principles administering IV therapy:
After a cardiac arrest patient becomes stable, remove the cannula

inserted emergently, and replace it with a new one under sterile
conditions. Strict aseptic technique is compromised in most
emergency venipunctures, where speed is essential. This
compromise is particularly likely when emergency vascular access is
established outside the hospital, because personnel and equipment
are limited.
IV solutions are usually packaged in nonbreakable plastic bottles or
bags. Squeeze plastic bags before use to detect punctures that may
lead to contamination of the contents.
Avoid adding drugs that may be adsorbed by the plastic bag or tubing
(eg, IV nitroglycerin). If you must administer these drugs without
specialty infusion systems, allow for drug adsorption when you titrate
the drug administration rate.
Ideally, set the rate of infusion to at least 10 mL/h to keep the IV line
open.
Saline lock catheter systems are particularly useful for patients who
have spontaneous circulation and require drug injections but not IV
volume infusion.
Most contemporary systems use needleless injection sites. These
systems permit drug and flush infusions without the use of needles
and the associated risk of needle sticks.
Avoid letting the arm with the IV access hang off the bed. Place the
arm at the level of the heart, or slightly above the heart, to facilitate
delivery of fluids and medications to the central circulation.
During cardiac arrest, follow all peripherally administered drugs with a
bolus of at least 20 mL of IV flush solution. This flush will facilitate
delivery to the central circulation. Elevate the extremity for 10 to 20
seconds to facilitate drug delivery to the central circulation.
Be aware of complications common to all IV techniques. Local
complications include hematomas, cellulitis, thrombosis, infiltration,
and phlebitis. Systemic complications include sepsis, pulmonary
thromboembolism, air embolism, and catheter fragment embolism.
Intraosseous Access
Introduction IO access can serve as a rapid, safe, and reliable route for
administration of drugs, crystalloids, and colloids (including blood).
Needles The technique uses a rigid needle, preferably a specially designed IO or

Jamshidi-type bone marrow needle. In the past, the higher bone density
in older children and adults made it difficult for smaller IO needles to
penetrate the bone without bending. With the development of IO cannula
systems and newer, drill-type devices, IO access is now easier to obtain
in older children and adults.

Sites Many sites are appropriate for IO infusion. In older children and adults,
these general sites include the humeral head, proximal tibia, medial
malleolus, sternum, distal radius, distal femur, and anterior-superior iliac
spine.
Indications and Resuscitation drugs, fluids, and blood products can be administered
Administration safely by the IO route. Continuous catecholamine infusions can also be
provided by this route.
The onset of action and drug levels after IO infusion during CPR are
comparable to those for vascular routes of administration, including
central venous access. When providing drugs and fluids by the IO route,
remember the following:
Flush all IO medications with normal saline to facilitate delivery into

the central circulation.
Administer viscous drugs and solutions and fluid for rapid volume
resuscitation under pressure by using an infusion pump, pressure
bag, or forceful manual pressure to overcome the resistance of the
emissary veins.
Some have expressed concern that high-pressure infusion of blood
might induce hemolysis, but animal studies have failed to document
this problem.
Contraindications Absolute contraindications to IO access are as follows:
Fractures and crush injuries near or proximal to the access site

Conditions in which the bone is fragile, such as osteogenesis
imperfecta
Previous attempts to establish access in the same bone
Presence of infection of the overlying tissues
Complications Complications of IO infusion include tibial fracture, lower extremity

compartment syndrome or severe extravasation of drugs, and
osteomyelitis. But less than 1% of patients have complications after IO
infusion. Careful technique helps to prevent complications.
Equipment The following equipment is needed to establish IO access:

Needed
Gloves
Skin disinfectant
IO needle (15 to 18 gauge) or bone marrow needle
Tape
Syringe
Isotonic crystalloid fluid
Intravenous tubing

Procedure The steps to establish IO by using the tibial tuberosity as an example of

an access site are described below. Commercial kits (eg, newer, drill-type
IO devices) are currently available, and providers should follow the
manufacturers steps provided with the kit.
Step Action
1 Always use universal precautions when attempting vascular
access. Disinfect the overlying skin and surrounding area
with an appropriate agent.
Identify the tibial tuberosity just below the knee joint. The
insertion site is the flat part of the tibia, 1 or 2 finger widths
below and medial to this bony prominence. Figure 34
shows some of the sites for IO access.
2 The stylet should remain in place during insertion to prevent
the needle from becoming clogged with bone or tissue.
Stabilize the leg to facilitate needle insertion. Do not place
your hand behind the leg.
3 Insert the needle so that it is perpendicular to the tibia.
(When placing an IO needle in other locations, aim slightly
away from the nearest joint space to reduce the risk of
injury to the epiphysis or joint, but keep the needle as
perpendicular to the bone as possible to avoid bending.)
Twist, do not push, the needle.
Use a twisting motion with gentle but firm pressure. Some
IO needles have threads. These threads must be turned
clockwise and screwed into the bone.
4 Continue inserting the needle through the cortical bone until
there is a sudden release of resistance. This release occurs
as the needle enters the marrow space. If the needle is
placed correctly, it will stand easily without support.
5 Remove the stylet and attach a syringe.
Aspiration of bone marrow contents and blood in the hub of
the needle confirms appropriate placement. You may send
this blood to the lab for study. (Note: Blood or bone marrow
may not be aspirated in every case.)
Infuse a small volume of saline and observe for swelling at
the insertion site. Also check the extremity behind the
insertion site in case the needle has penetrated into and
through the posterior cortical bone. Fluid should easily
infuse with saline injection from the syringe with no
evidence of swelling at the site.
If the test injection is unsuccessful (ie, you observe
infiltration/swelling at or near the insertion site), remove the
needle and attempt the procedure on another bone. If the
cortex of the bone is penetrated, placing another needle in
the same extremity will permit fluids and drugs to escape
from the original hole and infiltrate the soft tissues,
potentially causing injury.

6 There are a number of methods to stabilize the needle. Place

tape over the flange of the needle to provide support. Position
gauze padding on both sides of the needle for additional
support.
7 When connecting IV tubing, tape it to the skin to avoid
displacing the needle by placing tension on the tubing.
8 Volume resuscitation can be delivered via a stopcock
attached to extension tubing or by infusion of fluid under
pressure. When using a pressurized fluid bag, take care to
avoid air embolism.
Other methods include the following:
Use a syringe bolus via a medication port in the IV tubing
(3-way stopcock not needed).
Attach a saline lock to the IO cannula, and then provide
syringe boluses through the lock.
9 Any medication that can be administered by the IV route can
be given by the IO route, including vasoactive drug infusions
(eg, epinephrine drip).
All medications should be followed with a saline flush.

B
Figure 34. A, Locations for IO insertion in the distal femur, proximal tibia
and medial malleolus. B, Location for IO insertion in the anterior-superior
iliac spine.
Follow-up Follow-up is important after you establish IO access. Use these

guidelines:
Check the site frequently for signs of swelling.

Check the site often for needle displacement. Delivery of fluids or
drugs through a displaced needle may cause severe complications
(eg, tissue necrosis or compartment syndrome).
Replace the IO access with vascular access as soon as reasonable.
IO needles are intended for short-term use, generally less than 24
hours. Replacement with long-term vascular access is usually done in
the intensive care unit.

Acute Coronary Syndromes
ST-Elevation Myocardial Infarction Location and AV Block
Right Ventricular Patients with inferior or right ventricular (RV) infarction often present with
Infarction excess parasympathetic tone. Inappropriate parasympathetic discharge
can cause symptomatic bradycardia and hypotension. If hypotension is
present, it is usually due to a combination of hypovolemia (decreased
left ventricular [LV] filling pressure) and bradycardia.
Administer normal saline (250 to 500 mL) and reassess the patient.
If there is improvement and no symptoms or signs of heart failure or
volume overload, repeat fluid administration (typically up to 1 to 2 L).
Reassess the patient before each fluid administration.
For patients with RV infarct and hypotension, volume administration
may be lifesaving.
When hypotension is present, a slow heart rate is inappropriate. The

heart rate should be faster in the presence of low blood pressure. The
fluid bolus increases RV filling pressures, which cause an increase in the
strength of RV contractions (Starling mechanism), blood flow through the
lungs, and, ultimately, LV filling pressure and cardiac output.
AV Block With Acute inferior wall myocardial infarction (usually a right coronary artery
Inferior MI event) may result in symptomatic second-degree or third-degree AV
block with a junctional, narrow-complex escape rhythm. However, if the
patient remains asymptomatic and hemodynamically stable,
transcutaneous pacing (TCP) and a transvenous pacemaker are not
indicated. Monitor the patient and prepare for TCP if high-degree block
develops and the patient becomes symptomatic or unstable before
expert cardiology evaluation.
AV block frequently develops from excess vagal tone and

atrioventricular nodal ischemia. The patient may be stable if junctional
pacemaker cells can function and maintain an adequate ventricular
rate. This rhythm usually has a narrow-complex QRS and a
ventricular rate of 40 to 60 beats per minute. Unless a large amount
of myocardium is nonfunctional or comorbid conditions exist, the
patient is often stable.
If the bradycardia is symptomatic, follow the Bradycardia Algorithm.
Prepare for TCP.
Use atropine to increase heart rate and blood pressure if the patient
becomes symptomatic. The initial recommended atropine dose is 0.5
mg IV bolus. Repeat every 3 to 4 minutes, not exceeding the
maximum dose of 3 mg. Use only the dose necessary to stabilize the
patient. Excess atropine may increase ischemia by excessively
increasing heart rate and contractilitymajor determinants of
myocardial oxygen consumption.
If there is no response to atropine in an unstable patient, initiate TCP
or infusion of chronotropic drug, such as epinephrine (2 to 10

mcg/min) or dopamine (2 to 20 mcg/kg per minute). Titrate to patient

response.
If the patient does not respond to drugs or TCP, start transvenous
pacing.
Evaluation of AV block with AMI can be difficult. Obtain immediate

expert consultation for evaluation and recommendation (eg, transvenous
temporary pacemaker).
Fibrinolytic Checklist for STEMI
*Contraindications for fibrinolytic use in STEMI are viewed as advisory for clinical decision-
making and may not be all-inclusive. These contraindications are consistent with the 2004
ACC/AHA Guidelines for the Management of Patients With ST-Elevation Myocardial Infarction.
Consider transport to primary PCI facility as destination hospital.

Figure 35. Fibrinolytic checklist for STEMI.

Human, Ethical, and Legal Dimensions of ECC and ACLS
Rescuer and Witness Issues
How Often Will Cardiac arrest occurs both in and out of the hospital. In the United
CPR, Defibrillation, States, more than 500 000 people per year have a cardiac arrest and
and ACLS undergo a resuscitation attempt. The estimated incidence of out-of-
Succeed? hospital cardiac arrest assessed by emergency medical services (EMS)
in the United States is about 141 adults per 100 000. Extrapolation of the
incidence of in-hospital cardiac arrest reported by Get With The
Guidelines-Resuscitation to the total population of hospitalized patients
in the United States suggests that each year, 209 000 people are treated
for in-hospital cardiac arrest. Cardiac arrest continues to be an all-too-
common cause of premature death, and small, incremental
improvements in survival can translate into thousands of lives saved
every year.
Many public health experts consider CPR training to be the most

successful public health initiative of modern times. Millions of people
have prepared themselves to take action to save the life of a fellow
human being. But despite our best efforts, in most locations, half or more
of out-of-hospital resuscitation attempts do not succeed.
Tragically, even when ROSC occurs, few VF cardiac arrest patients

admitted to the emergency department and hospital survive and go
home. This means that most CPR attempts will be unsuccessful in terms
of neurologically intact survival to hospital discharge. In 2014, survival
after bystander-witnessed VF was 38.6% for patients of any age.
Survival to hospital discharge after nontraumatic, EMS-treated cardiac
arrest with any first recorded rhythm was only 12%. In the hospital
setting, only 24.8% of cardiac arrest patients survived to hospital
discharge. We must consider and plan for the emotional reactions from
rescuers and witnesses to any resuscitation attempt. This is particularly
true when their efforts appear to have failed.
Successful resuscitation after cardiac arrest requires an integrated set of

coordinated actions represented by the links in the AHA Chain of
Survival (Figure 36). The links include the following:
Immediate recognition of cardiac arrest and activation of the

emergency response system
Early CPR with an emphasis on chest compressions
Rapid defibrillation
Effective advanced life support
Integrated postcardiac arrest care
Emergency systems that can effectively implement these links can

achieve witnessed VF cardiac arrest survival to discharge of almost
50%. In most emergency systems, however, survival is lower, indicating
that there is an opportunity for improvement by carefully examining the
links and strengthening those that are weak. The individual links are

interdependent, and the success of each link is dependent on the

effectiveness of those that precede it.
Figure 36. System-specific Chains of Survival.
Take Pride in You should be proud that you are learning to become an ACLS provider.
Your Skills as an Now, you can be confident that you will be better prepared to do the right
ACLS Provider thing when your professional skills are needed. Of course, these
emergencies can have negative outcomes. You and the other
emergency personnel who arrive to help in the resuscitation may not
succeed in restoring life. Some people have a cardiac arrest simply
because they have reached the end of their lives. Your success will not
be measured by whether a cardiac arrest patient lives or dies, but rather
by the fact that you tried and worked well together as a team. Simply by
taking action, making an effort, and trying to help, you will be judged a
success.
Stress Reactions A cardiac arrest is a dramatic and emotional event, especially if the
After Resuscitation patient is a friend or loved one. The emergency may involve
Attempts disagreeable physical details, such as bleeding, vomiting, or poor
hygiene. The emergency can produce strong emotional reactions in
physicians, nurses, bystanders, lay rescuers, and EMS professionals.
Failed attempts at resuscitation can impose even more stress on
rescuers. This stress can result in a variety of emotional reactions and
physical symptoms that may last long after the original emergency.
It is common for a person to experience emotional aftershocks

following an unpleasant event. Usually, such stress reactions occur
immediately or within the first few hours after the event. Sometimes, the
emotional response occurs later. These reactions are frequent and
normal. There is nothing wrong with you or with someone who has such
reactions after an event.

Psychologists working with professional emergency personnel have

learned that rescuers may experience grief, anxiety, anger, and guilt.
Typical physical reactions include difficulty sleeping, fatigue, irritability,
changes in eating habits, and confusion. Many people say they are
unable to stop thinking about the event. Remember that these reactions
are common and normal. They do not mean that you are disturbed or
weak. Strong reactions simply indicate that this particular event had a
powerful impact on you. With the understanding and support of friends
and loved ones, the stress reactions usually pass.
Techniques to Psychologists tell us that one of the most successful ways to reduce
Reduce Stress in stress after a rescue effort is simple: talk about it. Sit down with other
Rescuers and people who witnessed the event and talk it over. EMS personnel who
Witnesses respond to calls from lay rescuer defibrillation sites are encouraged to
offer emotional support to lay rescuers and bystanders. More formal
discussions, called critical event debriefings, should include not only the
lay rescuers but also the professional responders.
In these discussions, you will be encouraged to describe what

happened. Do not be afraid of reliving the event. It is natural and healthy
to talk about the event. Describe what went through your mind during the
rescue effort. Describe how it made you feel at the time. Describe how
you feel now. Be patient with yourself. Understand that many reactions
will diminish within a few days. Sharing your thoughts and feelings with
your companions at work, fellow rescuers, EMS personnel, or friends will
help reduce stress reactions and help you recover.
Other sources of psychological and emotional support are local clergy,

police chaplains, fire service chaplains, and hospital and emergency
department social workers. Your course instructor may be able to tell
you what plans are established for critical event debriefings in your
professional setting.
Psychological Performance Anxiety

Barriers to Action
The ACLS Provider Course helps prepare you to respond appropriately
to a future emergency. ACLS providers have expressed some common
concerns about responding to sudden cardiac emergencies: Will I be
able to take action? Will I remember the steps of the ACLS approach?
Will I remember how to perform the skills of CPR, defibrillation, and
intubation; the details of drug doses; and the steps in the algorithms?
Will I really have what it takes to respond to a true emergency? Any
emergency involving a patient you have grown close to, a friend, or a
family member will produce a strong emotional reaction.
Disagreeable Aspects of CPR

What about the unpleasant and disagreeable aspects of performing CPR
in either the in-hospital or out-of-hospital setting? Will you really be able
to perform mouth-to-mouth rescue breathing on a stranger? What if the
patient is bleeding from facial injuries? Would this not pose a risk of
disease for a rescuer without a CPR barrier device? CPR and
defibrillation require that the rescuer remove clothing from the patients

chest. You cannot attach defibrillation electrodes unless the pads are
placed directly on the skin. The rescuer must open the patients shirt or
blouse and remove the undergarments. Common courtesy and modesty
may cause some people to hesitate before removing the clothing of
strangers, especially in front of many other people in a public location.
Everyone is familiar with the concept of defibrillation shocks as shown in

television shows and movies. These shocks appear painful. Can you
overcome your natural tendency not to hurt others, even in an
emergency when your actions could be lifesaving? Often, friends and
relatives will be at the scene of an emergency. If you respond and take
action, these people will look to you to perform quickly, effectively, and
confidently.
These barriers can hinder a quick emergency response, especially in

settings where such events are rare. There are no easy solutions to help
overcome these barriers. Your instructor will encourage you to anticipate
many of the scenes described above. The case scenarios will include
role-playing and rehearsals. Think through how you would respond when
confronted with such a circumstance. Mental practice, even without
hands-on practice, may help improve your future performance. The best
preparation, however, is frequent practice with manikins in realistic
scenarios and situations.
Leaders of all courses that follow the AHA guidelines are aware of the
mental and emotional challenge of rescue efforts. You will have support
if you ever participate in a resuscitation attempt. You may not know for
several days whether the patient lives or dies. If the person you try to
resuscitate does not live, take comfort from knowing that, in taking
action, you did your best.
Legal and Ethical Issues
The Right Thing The AHA has supported community CPR training for more than 3
to Do decades. Citizen CPR responders have helped save thousands of lives.
The AHA believes that training in the use of CPR and AEDs will
dramatically increase the number of survivors of cardiac arrest.
Studies of lay rescuer AED programs in airports and casinos and of first-
responder programs with police officers have shown survival rates of
41% to 74% from out-of-hospital witnessed VF SCA when immediate
bystander CPR is provided and defibrillation occurred within 3 to 5
minutes of collapse. Other studies have demonstrated decreased time
intervals from collapse to delivery of the first shock when AEDs were
used during adult out-of-hospital cardiac arrest. However, if no decrease
in time to defibrillation is achieved, then high survival rates are not
observed.
Anyone can perform emergency CPR without fear of legal action.
Chest compressions and rescue breathing require direct physical

contact between rescuer and patient. Often, these 2 people are
strangers. Too often, the arrest patient dies. In the United States, people

may take legal action when they think that one person has harmed
another, even unintentionally. Despite this legal environment, CPR
remains widely used and remarkably free of legal issues and lawsuits.
Although attorneys have included rescuers who performed CPR in
lawsuits, no Good Samaritan has ever been found guilty of doing harm
while performing CPR.
All 50 states have Good Samaritan laws that grant immunity to any
volunteer or lay rescuer who attempts CPR in an honest, good faith
effort to save a life. A person is considered a Good Samaritan if the
following apply:
The person is genuinely trying to help.

The help is reasonable (you cannot engage in gross misconduct, ie,
actions that a reasonable person with your training would never do).
The rescue effort is voluntary and not part of the persons job
requirements.
Most Good Samaritan laws protect laypersons who perform CPR even if
they have had no formal training. The purpose of this protection is to
encourage broad awareness of resuscitative techniques and to remove
a barrier to involving more people. As the details of these laws may vary
across states, please check with your state legislation agency for further
information.
Principle of Futility If the purpose of medical treatment cannot be achieved, it is considered

futile. The key determinants of medical futility are length and quality of
life. An intervention that cannot establish any increase in length or quality
of life is futile. An objective criterion for medical futility was defined in
1990 for interventions and drug therapy as imparting a less than 1%
chance of survival. Although this criterion may be controversial, it
remains a basis for current futility research.
Patients or families may ask physicians to provide care that is

inappropriate. However, physicians have no obligation to provide such
care when there is scientific and social consensus that the treatment is
ineffective. An obvious example of an inappropriate or futile intervention
is CPR for patients with signs of irreversible death. Other healthcare
providers also have no obligation to provide CPR or ACLS if no benefit
can be expected (ie, CPR would not restore effective circulation) and/or
in the presence of advance directives, including do not attempt
resuscitation (DNAR) orders or living wills. In the absence of these
clinical circumstances and personal desires, healthcare providers should
attempt resuscitation.
A careful balance of the patients prognosis for both length and quality of
life will determine whether CPR is appropriate. CPR is inappropriate
when survival is not expected.
When the likelihood of survival is borderline, or when the likelihood of

morbidity and burden to the patient is relatively high, rescuers should
support the patients desires. If the patients desires are unknown,
healthcare providers may follow the preferences of the legally authorized

surrogate decision maker. Noninitiation of resuscitation and

discontinuation of life-sustaining treatment during or after resuscitation
are ethically equivalent. When the patients prognosis is uncertain,
consider a trial of treatment while gathering more information to
determine the likelihood of survival and the expected clinical course.
Terminating The decision to stop resuscitative efforts rests with the treating physician
Resuscitative in the hospital. The physician bases this decision on many factors,
Efforts including time to CPR, time to defibrillation, comorbid disease, prearrest
state, initial arrest rhythm, clinical factors, and intra-arrest physiologic
parameters. None of these factors alone is clearly predictive of outcome.
The chance of discharge from the hospital alive and neurologically intact
may diminish as resuscitation time increases but must be considered in
context with the other factors mentioned. The responsible clinician
should stop the resuscitation when he or she determines with a high
degree of certainty that the patient will not respond to further ACLS
efforts.
It is important to consider the circumstances of the cardiac arrest when

deciding whether to continue resuscitative efforts. Resuscitation efforts
may be prolonged beyond what would be appropriate for prolonged
asystole in the following conditions:
Young patient
Presence of toxins or electrolytes abnormalities
Profound hypothermia
Victims of cold water submersion
Therapeutic or illicit drug overdose
Suicide attempt
Nearby family member or loved ones expressing opposition to
stopping efforts
Delayed or token efforts such as so-called slow codes (knowingly

providing ineffective resuscitative efforts) are inappropriate. This practice
compromises the ethical integrity of healthcare providers, uses deception
to create a false impression, and may undermine the provider-patient
relationship. The practice of pseudo-resuscitation was self-reported by
paramedics to occur in 27% of cardiac arrests in a community where a
termination-of-resuscitation protocol was not in place.
When Not to Few criteria can accurately predict the futility of CPR. In light of this
Start CPR uncertainty, all patients in cardiac arrest should receive resuscitation
unless any of the following apply:
The patient has a valid DNAR order.

The patient has signs of irreversible death (eg, rigor mortis,
decapitation, decomposition, or dependent lividity).

No physiologic benefit can be expected because vital functions have

deteriorated despite maximal therapy (eg, progressive septic or
cardiogenic shock).
Withholding vs Basic life support (BLS) training urges the first lay responder at a cardiac
Withdrawing CPR arrest to begin CPR. Healthcare providers are expected to provide BLS
and ACLS as part of their duty to respond. There are a few exceptions to
this rule:
A person lies dead with obvious clinical signs of irreversible death

(eg, rigor mortis, dependent lividity, decapitation, or decomposition).
Attempts to perform CPR would place the rescuer at risk of physical
injury.
The patient or surrogate has indicated that resuscitation is not
desired with an advance directive (DNAR order).
No physiologic benefit can be expected because vital functions have
deteriorated despite maximal therapy (eg, progressive sepsis or
cardiogenic shock).
No rescuer should make a judgment about the present or future quality

of life of a patient of cardiac arrest on the basis of current (ie, during the
attempted resuscitation) or anticipated neurologic status. Such snap
judgments are often inaccurate. Conditions such as irreversible brain
damage or brain death cannot be reliably assessed or predicted during
an emergency.
Out-of-hospital DNAR protocols must be clear to all involved (eg,

physicians, patients, family members, loved ones, and out-of-hospital
healthcare providers). Advance directives can take many forms (eg,
written bedside orders from physicians, wallet identification cards, and
identification bracelets).
The ideal EMS DNAR form is portable in case the patient is transferred.
In addition to including out-of-hospital DNAR orders, the form should
provide direction to EMS about initiating or continuing life-sustaining
interventions for the patient who is not pulseless and apneic.
Withdrawal of Withdrawal of life support is an emotionally complex decision for family

Life Support and staff. Withholding and withdrawing life support are ethically similar.
The decision to withdraw life support is justifiable when it is determined
that the patient is dead, if the physician and patient or surrogate agree
that treatment goals cannot be met, or the burden to the patient of
continued treatment would exceed any benefits.
Patients who are unconscious or unresponsive after cardiac arrest

should be directed to an inpatient critical-care facility with a
comprehensive care plan that includes acute cardiovascular
interventions, use of targeted temperature management (TTM),
standardized medical goal-directed therapies, and advanced
neurological monitoring and care. The earliest time for prognostication in
patients treated with TTM by using clinical examination where sedation

and paralysis could be a confounder may be 72 hours after return to

normothermia. In patients not treated with TTM, the earliest time to
prognosticate a poor neurologic outcome by using clinical examination is
72 hours after cardiac arrest. This time can even be longer if the residual
effect of sedation or paralysis confounds the clinical examination. Many
initially comatose survivors of cardiac arrest have the potential for full
recovery such that they are able to lead normal lives. Between 20% and
50% (or more) of survivors of out-of-hospital cardiac arrest who are
comatose on arrival at the hospital may have good 1-year neurological
outcome. Therefore, it is important to place patients in a hospital critical-
care unit where expert care and neurological evaluation can be
performed and where appropriate testing to aid prognosis is available
and performed in a timely manner.
The following 3 factors are associated with poor outcome:
Absence of pupillary response to light on the third day

Absence of motor response to pain on the third day
Bilateral absence of cortical response to median somatosensory
evoked potentials when used in normothermic patients who are
comatose for at least 72 hours after the cardiac arrest and
resuscitation
Withdrawal of life support is ethically permissible under these

circumstances.
Patients in the end stage of an incurable disease, whether responsive or

unresponsive, should receive care that ensures their comfort and dignity.
The goal of such care is to minimize the suffering associated with pain,
dyspnea, delirium, convulsions, and other terminal complications. It is
ethically acceptable to gradually increase the dose of narcotics and
sedatives to relieve pain and other symptoms, even to levels that might
shorten the patients life. Nursing and comfort care (eg, oral hygiene,
skin care, patient positioning, and measures to relieve pain and
suffering) should be continued.
Advance An advance directive is any expression of a persons thoughts, wishes,

Directives, Living or preferences for his or her end-of-life care. Advance directives can be
Wills, and Patient based on conversations, written directives, living wills, or durable powers
Self-Determination of attorney for health care. The legal validity of various forms of advance
directives varies from jurisdiction to jurisdiction. Courts consider written
advance directives to be more trustworthy than recollections of
conversations.
A living will provides written direction to physicians about medical care

the patient would approve if he or she becomes terminally ill and unable
to make decisions. A living will constitutes clear evidence of the patients
wishes and can be legally enforced in most areas.
Patients should periodically reevaluate their living wills and advance

directives. Desires and medical conditions may change over time. In the
United States, the Patient Self-Determination Act of 1991 requires
healthcare institutions and managed-care organizations to ask if patients

have advance directives. Healthcare institutions are required to facilitate

the completion of advance directives if patients request them.
Out-of-Hospital In many settings, Allow Natural Death is becoming a preferred term to

DNAR Orders replace DNAR, to emphasize that the order is to allow natural
consequences of a disease or injury, and to emphasize ongoing end-of-
life care.
Many patients for whom EMS is called because of cardiac arrest are
chronically ill, have a terminal illness, or have a written advance directive
(DNAR order). Countries, individual states in the United States, and
individual jurisdictions worldwide have different laws for out-of-hospital
DNAR orders and advance directives. Even if a patient has a DNAR
order, it may be difficult to determine whether to start resuscitation. It is
especially difficult if family members have differing opinions. You should
initiate CPR and ACLS if you have reason to believe that
There is reasonable doubt about the validity of a DNAR order or

advance directive
The patient may have changed his or her mind
The best interests of the patient are in question
Sometimes, within a few minutes of initiation of CPR, relatives or other

medical personnel arrive and confirm that the patient had clearly
expressed a wish that resuscitation not be attempted. CPR or other life
support measures may be discontinued, with approval of medical
direction, when further information becomes available.
Some EMS systems in the United States have extended the DNAR
protocol to include verbal requests from family members as grounds to
withhold therapy from cardiac arrest patients with a history of a terminal
illness and under the care of a physician.
The number of patients for whom resuscitation was withheld doubled

after implementation of this law from 45 to 99 patients a year. This is an
important step in expanding the clinical decision rule pertaining to when
to start resuscitation in out-of-hospital cardiac arrest.
When you cannot obtain clear information about the patients

wishes, you should initiate resuscitative measures.
EMS No-CPR In the United States, a number of states have adopted no-CPR
Programs programs. These programs allow patients and family members to call
EMS for emergency care, support, and treatment for end-of-life distress
(ie, shortness of breath, bleeding, or uncontrolled pain). Patients do not
have to fear unwanted resuscitative efforts.
In a no-CPR program, the patient, who usually has a terminal illness,

signs a document requesting no heroics if there is a loss of pulse or if
breathing stops. In some states, the patient must wear a no-CPR
identification bracelet. In an emergency, the bracelet or other

documentation signals rescuers that CPR efforts, including use of an

AED, are not recommended.
If an ACLS provider arrives at the side of a person in apparent cardiac

arrest (unresponsive, no pulse, no breathing) and sees that the person is
wearing a no-CPR bracelet (or has some other indication of no-CPR
status), the provider should respect the persons wishes. Report the
problem as a collapsed, unresponsive person wearing a no-CPR
bracelet. State that you think CPR should not be performed.
Check with your state or ask your instructor to see what the law is in
your jurisdiction regarding no-CPR orders in the out-of-hospital setting.
Legal Aspects of Defibrillators, including many AEDs, are restricted medical devices. In
AED Use the United States, most states have legislation that requires a physician
to authorize the use of restricted medical devices. Lay rescuer CPR and
defibrillation programs that make AEDs available to lay rescuers (and, in
some cases, EMS providers) may be required to have a medical
authority or a healthcare provider who oversees the purchase of AEDs,
treatment protocols, training, and contact with EMS providers. In a
sense, the medical authority prescribes the AED for use by the lay
responder and therefore complies with medical regulations.
In the United States, malpractice accusations and product liability

lawsuits increase every year. In the past, fear of malpractice suits
hindered innovative programs to bring early CPR and early defibrillation
into every community, but such fears have proven unfounded.
To solve this problem of fear of litigation, all states have changed

existing laws and regulations to provide limited immunity for lay rescuers
who use AEDs in the course of attempting resuscitation. These are the
Good Samaritan laws. Many states have amended Good Samaritan
laws to include the use of AEDs by lay rescuers. This means that the
legal system will consider lay rescuers to be Good Samaritans when
they attempt CPR and defibrillation for someone in cardiac arrest. As a
Good Samaritan, you cannot be successfully sued for any harm or
damage that occurs during the rescue effort (except in cases of gross
negligence).
In 2006, the AHA published a statement detailing recommended

legislation to promote lay rescuer AED programs and to assist legislators
and policymakers in removing impediments to these programs. You can
find this statement at
http://circ.ahajournals.org/content/early/2006/01/16/CIRCULATIONAHA.
106.172289.full.pdf.
Lay rescuer CPR and AED programs should implement processes of

continuous quality improvement, including evaluation of the following:
Performance of the emergency response plan, including accurate

time intervals for key interventions (such as collapse to shock or no
shock advisory to initiation of CPR) and patient outcome
Responder performance

AED function
Battery status and function
Electrode pad function and readiness, including expiration date
Providing Emotional Support for the Family
Conveying News Before talking to the family, obtain as much information as possible
of a Sudden Death about the patient and the circumstances surrounding the death. Be
to Family Members ready to refer to the patient by name.
Call the family if they have not been notified. Explain that their loved
one has been admitted to the emergency department or critical care
unit and that the situation is serious. If possible, family members
should be told of the death in person, not over the telephone.
When family members arrive, ask someone to take them to a private
area. Walk in, introduce yourself, and sit down. Address the closest
relative. Maintain eye contact and position yourself at the same level
as family members (ie, sitting or standing).
Enlist the aid of a social worker or a member of the clergy if possible.
Briefly describe the circumstances leading to the death. Summarize
the sequence of events. Avoid euphemisms such as hes passed
on, shes no longer with us, or hes left us. Instead, use the words
death, dying, or dead.
Allow time for family members to process the information. Make eye
contact and touch. Convey your feelings with a simple phrase such
as You have my (our) sincere sympathy.
Determine the patients suitability for and wishes about tissue
donation (use drivers license and patient records). Follow local
protocols on when to discuss with family. Consent for donation should
be requested by a trained individual who is not part of the care team.
(See Organ and Tissue Donation for more information.)
Allow as much time as necessary for questions and discussion.
Review the events several times if needed.
Allow family members the opportunity to see the patient. Prepare the
family for what they will see. If equipment is still connected to the
patient, tell the family. Equipment must be left in place for coroners
cases or when an autopsy is performed.
Determine in advance what happens next and who will sign the death
certificate. Physicians may impose burdens on staff and family if they
fail to understand policies about death certification and disposition of
the body.
Offer to contact the patients attending or family physician and to be
available if there are further questions. Arrange for follow-up and
continued support during the grieving period.
Family Presence According to surveys in the United States and the United Kingdom, most
During family members state that they would like to be present during the
Resuscitation attempted resuscitation of a loved one. Parents and care providers of

chronically ill patients are often knowledgeable about and comfortable

with medical equipment and emergency procedures.
Even family members with no medical background report that it is

comforting to be at the side of a loved one and say goodbye during the
final moments of life. These are those who choose to be at the bedside
and who have a designated support person with them to answer
questions, clarify information, and comfort the family.
Family members often do not ask if they can be present, but healthcare
providers should offer the opportunity whenever possible.
Relatives and friends who are present and are provided counseling
during resuscitation of a loved one report fewer incidences of
posttraumatic avoidance behaviors, fewer grieving symptoms, and less
intrusive imagery.
When family members are present during resuscitative efforts, sensitivity

is heightened among resuscitation team members. A team member who
is knowledgeable about resuscitation practices should be available to
answer questions, provide comfort, and help the family during the
resuscitation. Even when the resuscitation outcome is not optimal,
families feel comforted to know they can be present to say goodbye,
give comfort to their dying loved one, and begin the grieving process.
Organ and Tissue Most communities do not optimize the retrieval of organ and tissue
Donation donations. This has created protracted waiting and greater suffering for
patients awaiting organ transplantation. The ECC community of the AHA
supports efforts to optimize the ethical acquisition of organ and tissue
donations. Studies suggest no difference in functional outcomes of
organs transplanted from patients who are determined to be brain dead
as a consequence of cardiac arrest when compared with donors who are
brain dead from other causes. Therefore, it is reasonable to suggest that
all communities should optimize retrieval of tissues and organ donations
in brain-dead postcardiac arrest patients in-hospital and those
pronounced dead in the out-of-hospital setting.
Most important to this process are advanced planning and infrastructure

support to allow organ donation to occur in a manner sensitive to the
needs of the donors family and without undue burden on the staff.
Medical directors of EMS agencies, emergency departments, and critical
care units should develop protocols and implementation plans with the
regional organ and tissue donation program to optimize donation after a
cardiac arrest death. These include
A process by which permission for organ and tissue donations will be

obtained for in- and out-of-hospital settings
The establishment of clearly defined guidelines for organ and tissue
procurement that will be available to all healthcare providers both in-
and out-of-hospital

Availability of information to address the possible difference between

applicable laws and social values in procedures for organ
procurement
The emotional support to be offered to providers after the event

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What are the different devices that can be used to provide supplementary oxygen?

What are the different devices that can be used to provide supplementary oxygen?

What are the steps involved in bag-mask ventilation?

What are the steps involved in bag-mask ventilation?

ACLS Provider Manual

2016 American Heart Association

Airway Management ...................................................................................................................4

2016 American Heart Association 2

Shock First vs CPR First ....................................................................................51

2016 American Heart Association 3

Basic Airway Management

Devices to Provide Supplementary Oxygen

Whenever you care for a patient receiving supplementary oxygen, quickly

Table 1. Delivery of Supplementary Oxygen: Flow Rates and Percentage of

*Percentages are approximate.

Oxygen administration device

2016 American Heart Association 4

Trained advanced cardiovascular life support (ACLS) providers should be

Nasal Cannula Traditionally, the nasal cannula (Figure 1) is classified as a low-flow

Figure 1. A nasal cannula used for supplementary oxygen delivery in

2016 American Heart Association 5

A Venturi mask can accurately control the inspired oxygen

2016 American Heart Association 6

Figure 2. A face mask with oxygen reservoir used for supplementary

Use of a face mask with a reservoir is indicated for patients who

Are seriously ill, responsive, spontaneously breathing, have

1. Position yourself at the patients side.

2016 American Heart Association 7

3. Seal the pocket mask against the face.

Figure 3. Mouth-to-mask ventilation, 1 rescuer. The single rescuer

Overview The bag-mask device typically consists of a self-inflating bag and a

Bag-mask ventilation is a challenging skill that requires considerable

2016 American Heart Association 8

This device provides positive-pressure ventilation when used without

2016 American Heart Association 9

2016 American Heart Association 10

Advanced Airway Management

Advanced Airway Adjuncts: Laryngeal Mask Airway

The advantages of laryngeal mask airway are as follows:

Figure 5. Laryngeal mask airway.

2016 American Heart Association 11

Figure 6. Insertion of the laryngeal mask airway.

Do not apply cricoid pressure because it may hinder the insertion of

2016 American Heart Association 12

incidence of failed insertion and impaired ventilation once the laryngeal

Advanced Airway Adjuncts: Laryngeal Tube

Overview The laryngeal tube (Figure 7) is a supraglottic airway device that is

Figure 7. Laryngeal tube.

2016 American Heart Association 13

Open the mouth of the patient approximately 2 to 3 cm by

Figure 8. Positioning of the laryngeal tube.

Advanced Airway Adjuncts: Esophageal-Tracheal Tube

Overview The esophageal-tracheal tube (Figures 9 and 10) is an advanced airway

2016 American Heart Association 14

chiefly related to ease of training when compared with the training

Responsive patients with cough or gag reflex

Figure 9. Esophageal-tracheal tube.

2016 American Heart Association 15

Figure 10. Esophageal-tracheal tube inserted in esophagus.