9 - ACLS - Part 1
9 - ACLS - Part 1
9 - ACLS - Part 1
(ACLS)
Part One
Advanced Cardiac Life Support (ACLS)
▪ The mask is placed on the face of the patient with the narrow end
over the nose, & the wide end positioned just below the lower lip.
▪ Using the thumb & forefinger of the hand holding the mask (forming
a “C”), the rescuer presses directly down on the mask.
▪ Using the other three fingers of the same hand (forming an “E”), the
rescuer then grasps the bony part of the mandible, pulling the angle
of the jaw up & back.
▪ With 2 providers, one opens the airway & seals the mask to the
face while the other squeezes the bag.
Opening the Airway
• Advantages of ET
– keeps the airway patent, permits suctioning of airway
secretions, enables delivery of a high concentration of
oxygen, provides an alternative route for the administration
of some drugs, facilitates delivery of a selected tidal volume,
&, with use of a cuff, may protect the airway from aspiration.
• Complications of ET intubation
– Trauma—teeth, lips, tongue, mucosa, vocal cords, trachea
– Esophageal intubation, Vomiting & Aspiration
– Arrhythmias
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Advanced Airways/ ET
▪ Capnography:
• Is a noninvasive method attached to ET for monitoring the
level of Carbone dioxide in exhaled breath (End- tidal Co2
ETCo2) to assess ventilation status.
• Capnometer/Capnogram: gives both a numerical reading
value of ETCo2 as well as a waveform.
• The presence of waveform indicates that ET is correctly
placed in the trachea.
Capnography Waveform
Advanced Airways/ET
▪ Sequence of Management
1- When a rhythm reveals VF/VT, the first provider
should resume CPR while the second provider charges
the defibrillator.
2- Once the defibrillator is charged, CPR is paused to
“clear” the patient for shock delivery. After the “clear,”
the second provider gives a single shock as quickly as
possible to minimize the interruption in chest
compressions (“hands-off interval”).
3- The first provider resumes CPR immediately after
shock delivery (without a rhythm or pulse check) &
continues for 2 minutes.
Management of Cardiac Arrest
Pulseless V Tach or V Fib
• Sequence of Management
4- After 2 minutes of CPR the sequence is repeated,
beginning with a rhythm check.
➢ Defibrillation Strategies
– The shorter the time interval between the last
chest compression & shock delivery, the more
likely the shock will be successful.
VF VT
Management of Cardiac Arrest/Pulseless V Tach
or V Fib/ Defibrillation Dose
▪ Biphasic Defibrillator
• Use the manufacturer's recommended energy dose
(eg, initial dose of 120 to 200 J) for terminating VF.
• If the provider is unaware of the effective dose range,
the provider may use the maximal dose.
• Second & subsequent energy levels should be at least
equivalent, & higher energy levels may be considered.
• If VF is terminated by a shock but then recurs later in
the arrest, deliver subsequent shocks at the previously
successful energy level.
• Monophasic Defibrillator
• Deliver an initial shock of 360 J & use that dose for all
subsequent shocks.
Management of Cardiac Arrest
Pulseless V Tach or V Fib
▪ Drug Therapy
• There is insufficient evidence to recommend a specific
timing or sequence (order) of drug administration &
advanced airway placement during cardiac arrest.
• If a shock fails to generate a perfusing rhythm, then giving
a Epinephrine soon after the shock (without interrupting
CPR) will optimize the potential impact of increased
myocardial blood flow before the next shock.
• Vasopressin offers no advantage as a substitute for
Epinephrine in cardiac arrest . Vasopressin has been
removed from adult cardiac arrest algorithm.
• Amiodarone/ Lidocaine may be considered when VF/VT is
unresponsive to CPR, & defibrillation therapy.
Management of Cardiac Arrest
Asystole, PEA
▪ Drug Therapy
– Epinephrine I mg Q 3-5 min IV.
– Atropine during PEA or or asystole is unlikely to
have a therapeutic benefit. For this reason
Atropine has been removed (in 2020) from the
cardiac arrest algorithm.
– Vasopressin offers no advantage as a substitute
for Epinephrine in cardiac arrest . Vasopressin
has been removed (in 2020) from adult
cardiac arrest algorithm.
Management of Cardiac Arrest/Asystole, PEA
▪ Consider:
• Reperfusion strategies such as coronary angiography &
PCI during CPR or emergency cardiopulmonary bypass
• Fibrinolytic therapy with pulmonary thrombosis
• Placement of an advanced airway might be necessary
to achieve adequate oxygenation or ventilation.
• PEA caused by severe volume loss or sepsis will
potentially benefit from administration of IV Crystalloid.
• If tension pneumothorax is clinically suspected as the
cause of PEA, initial management includes needle
decompression.
II-Management of Cardiac Arrest
Monitoring During CPR
▪ Pulse
• No validity of checking pulses during ongoing CPR
• The healthcare provider should take no more than 10
seconds to check for a pulse, & if it is not felt within
that time period chest compressions should be started.
• Upon completion of five cycles of CPR, the patient’s
rhythm is again assessed.
• Pulses are only checked if a perfusing rhythm (ie,
normal sinus rhythm, bradycardia, tachycardia) is
detected after 2 minutes of CPR.
• If the rhythm remains unchanged (VF or PVT), then
there is no pulse check before the next defibrillation.
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II-Management of Cardiac Arrest
Monitoring During CPR
▪ It may be reasonable to use physiologic parameters such as arterial
blood pressure or ETCO2 when feasible to monitor and optimize
CPR quality.
▪ End-Tidal CO2 ETCO2
▪ ETCO2 is the concentration of carbon dioxide in exhaled air at the end
of expiration.
• Under normal conditions ETCO2 is in the range of 35 to 40 mm Hg.
• In general , If PETCO2 is 10 mm Hg, then try to improve CPR quality
by optimizing chest compression parameters.
• If ETCO2 abruptly increases to a normal value (35 to 40 mm Hg),
you may consider that this is an indicator of ROSC (return of
spontaneous circulation).
• An air leak during bag-mask ventilation or ventilation with a
supraglottic airway could result in lower ETCO2 values.
Monitoring During CPR
▪ ABG
– Arterial blood gas monitoring during CPR is
not a reliable indicator of the severity of
tissue hypoxemia, hypercarbia (and
therefore adequacy of ventilation during
CPR).
• Pulse Oximetry
– During cardiac arrest, pulse oximetry
typically does not provide a reliable signal
because pulsatile blood flow is inadequate
in peripheral tissue beds.
Access for Parenteral Medications during
Cardiac Arrest
▪ A peripheral Venous Route
• A drug should be administered by bolus injection & followed
with a 20-mL bolus of IV fluid to facilitate the drug flow from
the extremity into the central circulation.
• Briefly elevating the extremity during & after drug administration
▪ ET
– Lidocaine, Epinephrine, Atropine, & Naloxone are
absorbed via the trachea.
– Administration of resuscitation drugs into the
trachea results in lower blood concentrations than
when the same dose is given intravascularly.
– Typically the dose given by the ET is 2 to 2.5 times
the recommended IV dose.
– Providers should dilute the recommended dose in 5
to 10 mL of sterile water or normal saline & inject
the drug directly into the ET.
II-Management of Cardiac Arrest