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CARDIORESPIRATORY
ARREST
FAISAL SOMMENG
Traumatology , FK-UMI 2020
https://quizizz.com/join?gc=842043
DEFINISI
Cardiorespiratory arrest is
The sudden, unexpected cessation of
respiration and functional circulation.
CPCR Principle
4 – 6 minutes
CPCR
During respiratory and cardiac arrest, CPCR may be successful
if performed before biological death of vital tissue develops.
4
CPCR
MATI KLINIK MATI BIOLOGIK
(REVERSIBEL) (IRREVERSIBEL)
4 - 6 menit
PRINSIP CPCR
MENGALIRKAN DARAH YG MENGANDUNG
OKSIGEN KE ORGAN VITAL TERUTAMA
JANTUNG DAN OTAK
5
RESUSITASI JANTUNG PARU
DAN OTAK (RJPO)
ADALAH USAHA UNTUK MENGEMBALIKAN FUNGSI
PERNAPASAN, SIRKULASI DAN ATAU SEREBRAL SERTA
PENANGANAN AKIBAT TERHENTINYA FUNGSI PERNAPASAN,
DENYUT JANTUNG DAN ATAU
AKTIFITAS SEREBRAL PADA :
 ORANG YANG MENGALAMI KEGAGALAN ORGAN
TERSEBUT SECARA TIBA-TIBA
 MASIH MEMUNGKINKAN HIDUP NORMAL
CARDIAC ARREST
1. Ventricular fibrillation or Pulseless VT
Electrical defibrillation is required to
reestablish spontaneous and effective
cardiac electrical activity.
2. Cardiac asystole.
3. Electromechanical dissociation (PEA)
Circulatory collapse that occurs despite
satisfactory electrical complexes on the ECG
CAUSES OF CARDIAC ARREST
1. Low cardiac output.
2. Hyparcapnia.
3. Hyperkalemia.
4. Hypoxia and vagal stimulation.
5. Stimulation of the heart.
6. Coronary occlusion.
7. Overdosage.
8. Hypothermia.
9. Hyperthermia
10. Acidosis
CAUSES OF RESPIRATORY FAILURE
1. Airway obstruction
Vomitus, foreign body, blood, secretions, solid material,
mucous plugs, laryngeal or bronchial spasm, or tumor.
2. CNS depression
Stroke, head trauma, hypercapnia, barbiturates,narcotics,
tranquilizers, or anesthetics.
3. Neuromuscular failure
Secondary to Poliomyelitis, muscular dystrophy,
myasthenia, or muscle relaxant drugs.
4. Lung or Parenchyma Diss..
PRIMARY CAUSES OF
CARDIAC OR RESPIRATORY ARREST.
Flail chest
Pneumothorax
Massive atelectasis
Acute pulmonary embolism
Congestive heart failure
Overwhelming pneumonia
Gram-negative septicemia
Lung burns
Carbon monoxide poisoning
Massive blood loss.
CARDIAC ARREST IS
More frequent in:
1. Geriatric patients.
2. Patients with a history of
arrhythmias, heart block, digitalis
toxicity, myocarditis , myocardial
infarction, congestive heart failure,
electrolyte imbalance , or
dehydration.
3. Massive hemorrhage.
4. During or following heart surgery.
MANAGEMENT
1. The initial goal of therapy is BRAIN oxygenation
2. The second goal is restoration of circulation.
3. Underlying condition must be corrected.
CPCR
CPCR is not indicated for all patients.
Natural death in the aged or in the terminal stages of a
chronic illness
CPCR should be performed in cases of reversible unexpected
death
CPCR.....
1. Basic Life support (BLS):
A: Airway,
B: Breathing,
C: Circulation, + (Defibrillation )
2. Advanced life support (ALS):
D: Drug and Fluid Therapy
E: Electrocardiography.
F: Fibrillation treatment.
3. Bantuan Hidup Jangka Panjang
G: Gauging
H: Human Mentation
I: Intensive Care
R: Rehabilitation
TINJAUAN BUKTI ILMIAH
KONSENSUS ILMIAH
PEDOMAN PENGOBATAN
CPCR GUIDELINES
Organisasi Resusitasi Dunia
2015
RANTAI KEHIDUPAN
2005
2010
2015
2020
Deskripsi Kerja Siloam Semanggi
1. Dokter/RMO ICU
(Leader)
2. RMO ED 4. Perawat ED
5. Perawat Ruangan/ Duty
Manager
3. Nurse leader
(Perawat ICU)
Korban/Pasien Troley
Emergency
1. RMO ICU (Leader) : pemimpin lapangan
2. RMO ED : membantu tindakan resusitasi
3. Nurse leader (Perawat ICU) : kesiapan
peralatan, obat-obatan dan koordinasi
dg farmasi, lab, dll
4. Perawat (ED) : akses intravena dan
obat-obatan
5. Perawat Ruangan atau DM : pencatatan
status kronologis
1. vertically downward 4-5 cm
2. Push hard push fast
3. 100 - 120x/min.
4. Ratio Comp : Vent  30 : 2
External Cardiac Compression
Cardiac Compression 100 -120 x/menit
Assisting Sirkulasi
Mekanikal kompressi
• Autopulse
• LUCAS
2015: Angka survive sama namun gangguan neurologis
lebih banyak pada Autopulse
KOMPRESI DADA YANG
BERKUALITAS
TERAPI ELEKTRIK
DEFIBRILASI
• Sejak awal , kompresi dada jangan
terputus
• Meminimalkan interupsi sebelum
dan setelah kejut
• Lanjutkan kompresi selama
pengisian defibrilasi
DEFIBRILATION
BIFASIK
Rekomendasi :
• Idealnya : energi bifasik awal tidak kurang dari
150 J (120 – 200 J ) untuk semua bentuk
gelombang
• Pemakaian alat mekanikal kompresi dapat
digunakan bila kompressi dada tidak adekuat atau
memerlukan CPR jangka lama
ENERGI DEFIBRILASI
TETAP ATAU ESKALASI ?
2010/2015 :
• Keduanya dapat diterima, bagaimanapun Jika
kejut pertama tidak berhasil dan defibrilasi masih
dapat memungkinkan untuk meningkatkan energi
yang lebih tinggi, maka masih dapat diterima
untuk ditingkatkan
EARLY DEFIBRILLATION
IT IS CRITICAL TO SURVIVAL FROM SUDDEN CARDIAC ARREST (SCA)
FOR SEVERAL REASONS:
(1) The most frequent initial rhythm
in witnessed is ventricular
fibrillation (VF),
(2) The treatment for VF is electrical
defibrillation,
(3) The probability of successful
defibrillation diminishes rapidly
over time, and
(4) VF tends to deteriorate to asystole
within a few minutes.
PADDLE POSITIONS
DEFIBRILLATION OR CARDIOVERSION
DEFIBRILLATION WAVEFORMS
AND ENERGY LEVELS
 Defibrillation  delivery of current through the chest
and to the heart to depolarize myocardial cells and
eliminate VF.
 The energy settings for defibrillators are designed to
provide the lowest effective energy needed to terminate
VF.
 Electrophysiologic event that occurs in 300 to 500
milliseconds after shock delivery.
 Defibrillation (shock success) is typically defined as
termination of VF for at least 5 seconds following the
shock.
SHOCK ENERGIES
• Biphasic defibrillator (initial shock) :
• selected energies of 120 J to 200 J
(biphasic truncated exponential
waveform) or
• 120 J (rectilinear biphasic waveform).
• For second and subsequent shocks, use the
same or higher energy
SHOCK ENERGIES
• Monophasic defibrillator : select a dose of 200-
360 J for all shocks.
• If VF is initially terminated by a shock but
then recurs later in the arrest, No need to
deliver subsequent shocks BUT continous CPR
SYNCHRONIZED
CARDIOVERSION
• Shock delivery that is timed (synchronized) with the QRS
complex.
• The energy (shock dose) used is lower than that used for
unsynchronized shocks (defibrillation).
• These low-energy shocks if delivered as unsynchronized
are likely to induce VF.
• If cardioversion is needed and it is impossible to
synchronize a shock (eg, the patient’s rhythm is
irregular), use high-energy unsynchronized shocks.
SYNCHRONIZED
CARDIOVERSION
• Ventricular tachycardia
• Ventricular tachycardia with a pulse responds
well to cardioversion using initial monophasic
energies of 200 J.
• Use biphasic energy levels of 120—150 J for
the initial shock.
• Give stepwise increases if the first shock fails
to achieve sinus rhythm.
Electrode Position
DRUGS
• Drugs should be considered only after initial
shocks have been delivered (if indicated) and
chest compressions and ventilation have
been started.
• Three groups of drugs relevant to the
management of cardiac arrest (2015
Consensus Conference): vasopressors, anti-
arrhythmics and other drugs.
INOTROPS and VASOPRESSORS
• Adrenaline - the primary sympathomimetic agent
for the management of cardiac arrest for 40 years.
• Alpha-adrenergic actions, vasoconstrictive effects 
systemic vasoconstriction, which increases coronary
and cerebral perfusion pressures.
• Beta-adrenergic actions, (inotropic, chronotropic)
may increase coronary and cerebral blood flow.
ADRENALINE
 Indications
 Adrenaline is the first drug used in cardiac arrest of any
aetiology: it is included in the ALS algorithm for use every
3—5 min of CPR.
 Adrenaline is preferred in the treatment of anaphylaxis.
 Adrenaline is second-line treatment for cardiogenic shock.
 Dose. During cardiac arrest, the initial intravenous dose of
adrenaline is 1 mg.
 When intravascular (intravenous or intra-osseous) access is
delayed or cannot be achieved, give 2—3 mg, diluted to 10 ml
with sterile water, via the tracheal tube. Absorption via the
tracheal route is highly variable.
ANTI-ARRHYTHMICS
• Amiodarone is a membranestabilising anti-arrhythmic
drug that increases the duration of the action
potential and refractory period in atrial and
ventricular myocardium.
• Atrioventricular conduction is slowed, and a similar
effect is seen with accessory pathways.
• Amiodarone has a mild negative inotropic action
and causes peripheral vasodilation through non-
competitive alpha-blocking effects.
AMIODARONE
• Indications.
• refractory VF/VT
• haemodynamically stable ventricular tachycardia (VT) and other
resistant tachyarrhythmias
• Dose. Consider an initial intravenous dose of 300
mg amiodarone, diluted in 5% dextrose to a
volume of 20 ml (or from a pre-filled syringe), if
VF/VT persists after the third shock.
• Amiodarone can cause thrombophlebitis when
injected into a peripheral vein; use a central
venous catheter if one is in situ but,if not, use a
large peripheral vein and a generous flush.
LIDOCAINE
 Indications. Lidocaine is indicated in refractory
VF/VT (when amiodarone is unavailable).
 Dose. an initial dose of 100 mg (1—1.5 mg/kg) for
VF/pulseless VT refractory to three shocks.
 Give an additional bolus of 50 mg if necessary.
 The total dose should not exceed 3 mg/kg during
the first hour.
OTHER DRUG
• Atropine. antagonises the action of the
parasympathetic neurotransmitter
acetylcholine at muscarinic receptors.
• Blocks the effect of the vagus nerve on
both the sinoatrial (SA) node and the
atrioventricular (AV) node, increasing
sinus automaticity and facilitating AV
node conduction.
ATROPINE
• is indicated in:
• Asystole
• pulseless electrical activity (PEA) with a rate
<60/min.
• sinus, atrial, or nodal bradycardia when the
haemodynamic condition of the patient is
unstable.
• The recommended adult dose of atropine for
Asystole or PEA with a rate <60 /min is 3 mg
i.v. in a single bolus.
• Kurangnya penekanan pada
intubasi tracheal sejak awal kecuali
dilakukan oleh tenaga terlatih
dengan interupsi kompresi yang
minimal
• Penekanan yang lebih terhadap pemakaian
kapnograf untuk confirmasi dan secara
berkesinambungan memantau letak tube,
kualitas RJP, dan memantau indikasi awal
tanda-tanda ROSC
ACLS : GELOMBANG KAPNOGRAF
Perubahan :
• Gelombang kapnograf kuantitatif adalah metode yang
lebih reliable untuk mengkonfirmasi letak ET tube
Kenapa :
• Banyaknya insidens yang tidak diinginkan akibat letak
ET tube yang tidak betul
• Kapnograf memiliki sensitivitas dan spesifitas yang
tinggi untuk mengidentifikasi kebenaran letak ETT
pada pasien gagal jantung
ACLS : GELOMBANG KAPNOGRAF
• Setelah intubasi, karbondioksida yang di ekshalasi
akan terdeteksi, sehingga dapat dipakai sebagai
pengkonfirmasi letak selang ETT dan optimalisai CPR
• Nilai yang paling tinggi pada saat akhir ekspirasi
PERUBAHAN ACLS : JALAN NAPAS
• Alat jalan napas supra glottis dapat dipakai tanpa
pemberhentian CPR
• Insersi selang ETT > 10 detik sebaiknya dihindari
kecuali jalan nafas beresiko
• Memerlukan banyak latihan dan kekompakan tim
CPR -1
30 : 2
CALL
FOR
HELP
PASANG
MONITOR
VF / VT
a single shock -II
a single shock -I - a single shock-IV
a single shock-III a single shock-V
2 menit 2 menit 2 menit 2 menit
adrenalin
adrenalin
CPR-3
CPR-2 CPR-5
CPR-4
- AMIODARON
Adrenaline: 1 mg, iv,
repeated every 3-5
minutes
CPR-6
Cardiac
arrest
Or LIDOCAIN 1mg/kg. Can be
repeated. Do not exceed a total dose
of 3 mg/kg,during the first hour.
Amiodaron is the first choice
300 mg, bolus. Repeated 150 mg
for reccurrent VT/VF. Followed by
900 mg infusion over 24 hours
VF/ VT
Intubasi : as soon as possible, without stop CPR Pijat 100 -120 x/menit
Nafas 8 -10 x/menit
Evaluasi CPR : tiap 2 menit
adrenalin
3’
3’
- AMIODARON
ASYST
2 menit 2 menit 2 menit 2 menit
evaluasi
evaluasi
Adrenalin-1
CPR-3
CPR-2 CPR-5
CPR-4 CPR-6
Cardiac
arrest
ASYSTOL/PEA/EMD
Intubasi : as soon as possible, without stop CPR Pijat 100-120 x/menit
Nafas 8-10 x/menit
Evaluasi CPR : tiap 2 menit
evaluasi
evaluasi
CPR -1
30 : 2
CALL
FOR
HELP
PASANG
MONITOR
Adrenalin-2 Adrenalin-3
Adrenaline: 1 mg, iv,
repeated every 3-5
minutes
TERMINATION OF
RESUSCITATION
• CPR must be continued until
• Cardiopulmonary system is stabilized
• The patient is pronounced death
• Alone rescuer is physically unable to
continue
TERIMAH KASIH
ASSESS RHYTHM
• CPR
• Defibrillate mono or
biphasic
• Epinephrine – several
dose options
• Antiarrhythmic agents
• AMIODARON
• Lidocaine
• Magnesium
Ventricular fibrillation
PULSELESS ELECTRICAL
ACTIVITY
• CPR
• Search for reversible causes and treat
• Epinephrine
• Atropine for absolute or relative bradicardia
ASYSTOLE
• CPR
• Epinephrine
• Consider transcutaneous pacing
• Search for reversible causes and
treat if possible
BRADYCARDIA –
PATIENT NOT IN ARREST
 Oxygen
 Atropine
 Dopamine
 Epinephrine
 Transcutaneous pacing
 Transvenous pacing
TACHYCARDIA WITH SERIOUS
SIGNS/SYMPTOMS
 Oxygen
 Immediate cardioversion
 Premedicate when possible
 Synchronized setting
TACHYCARDIA WITHOUT
SERIOUS INSTABILITY
 Narrow-complex
 Adenosine
 Verapamil
 Diltiazem
 -blockers
 Digoxin
 Synchronized cardioversion
TACHYCARDIA WITHOUT SERIOUS
INSTABILITY
• Wide-complex
– Amiodaron
– Lidocaine
• Synchronized cardioversion
Terima kasih

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4. CARDIORESPIRATORY ARREST (FS)2021.ppt

  • 1. CARDIORESPIRATORY ARREST FAISAL SOMMENG Traumatology , FK-UMI 2020 https://quizizz.com/join?gc=842043
  • 2. DEFINISI Cardiorespiratory arrest is The sudden, unexpected cessation of respiration and functional circulation.
  • 3. CPCR Principle 4 – 6 minutes CPCR During respiratory and cardiac arrest, CPCR may be successful if performed before biological death of vital tissue develops.
  • 4. 4 CPCR MATI KLINIK MATI BIOLOGIK (REVERSIBEL) (IRREVERSIBEL) 4 - 6 menit PRINSIP CPCR MENGALIRKAN DARAH YG MENGANDUNG OKSIGEN KE ORGAN VITAL TERUTAMA JANTUNG DAN OTAK
  • 5. 5 RESUSITASI JANTUNG PARU DAN OTAK (RJPO) ADALAH USAHA UNTUK MENGEMBALIKAN FUNGSI PERNAPASAN, SIRKULASI DAN ATAU SEREBRAL SERTA PENANGANAN AKIBAT TERHENTINYA FUNGSI PERNAPASAN, DENYUT JANTUNG DAN ATAU AKTIFITAS SEREBRAL PADA :  ORANG YANG MENGALAMI KEGAGALAN ORGAN TERSEBUT SECARA TIBA-TIBA  MASIH MEMUNGKINKAN HIDUP NORMAL
  • 6. CARDIAC ARREST 1. Ventricular fibrillation or Pulseless VT Electrical defibrillation is required to reestablish spontaneous and effective cardiac electrical activity. 2. Cardiac asystole. 3. Electromechanical dissociation (PEA) Circulatory collapse that occurs despite satisfactory electrical complexes on the ECG
  • 7. CAUSES OF CARDIAC ARREST 1. Low cardiac output. 2. Hyparcapnia. 3. Hyperkalemia. 4. Hypoxia and vagal stimulation. 5. Stimulation of the heart. 6. Coronary occlusion. 7. Overdosage. 8. Hypothermia. 9. Hyperthermia 10. Acidosis
  • 8.
  • 9. CAUSES OF RESPIRATORY FAILURE 1. Airway obstruction Vomitus, foreign body, blood, secretions, solid material, mucous plugs, laryngeal or bronchial spasm, or tumor. 2. CNS depression Stroke, head trauma, hypercapnia, barbiturates,narcotics, tranquilizers, or anesthetics. 3. Neuromuscular failure Secondary to Poliomyelitis, muscular dystrophy, myasthenia, or muscle relaxant drugs. 4. Lung or Parenchyma Diss..
  • 10. PRIMARY CAUSES OF CARDIAC OR RESPIRATORY ARREST. Flail chest Pneumothorax Massive atelectasis Acute pulmonary embolism Congestive heart failure Overwhelming pneumonia Gram-negative septicemia Lung burns Carbon monoxide poisoning Massive blood loss.
  • 11. CARDIAC ARREST IS More frequent in: 1. Geriatric patients. 2. Patients with a history of arrhythmias, heart block, digitalis toxicity, myocarditis , myocardial infarction, congestive heart failure, electrolyte imbalance , or dehydration. 3. Massive hemorrhage. 4. During or following heart surgery.
  • 12. MANAGEMENT 1. The initial goal of therapy is BRAIN oxygenation 2. The second goal is restoration of circulation. 3. Underlying condition must be corrected. CPCR CPCR is not indicated for all patients. Natural death in the aged or in the terminal stages of a chronic illness CPCR should be performed in cases of reversible unexpected death
  • 13. CPCR..... 1. Basic Life support (BLS): A: Airway, B: Breathing, C: Circulation, + (Defibrillation ) 2. Advanced life support (ALS): D: Drug and Fluid Therapy E: Electrocardiography. F: Fibrillation treatment. 3. Bantuan Hidup Jangka Panjang G: Gauging H: Human Mentation I: Intensive Care R: Rehabilitation
  • 14. TINJAUAN BUKTI ILMIAH KONSENSUS ILMIAH PEDOMAN PENGOBATAN CPCR GUIDELINES
  • 16. 2015
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  • 20. 2015
  • 21. 2020
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  • 27. Deskripsi Kerja Siloam Semanggi 1. Dokter/RMO ICU (Leader) 2. RMO ED 4. Perawat ED 5. Perawat Ruangan/ Duty Manager 3. Nurse leader (Perawat ICU) Korban/Pasien Troley Emergency 1. RMO ICU (Leader) : pemimpin lapangan 2. RMO ED : membantu tindakan resusitasi 3. Nurse leader (Perawat ICU) : kesiapan peralatan, obat-obatan dan koordinasi dg farmasi, lab, dll 4. Perawat (ED) : akses intravena dan obat-obatan 5. Perawat Ruangan atau DM : pencatatan status kronologis
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  • 29. 1. vertically downward 4-5 cm 2. Push hard push fast 3. 100 - 120x/min. 4. Ratio Comp : Vent  30 : 2 External Cardiac Compression
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  • 31. Cardiac Compression 100 -120 x/menit
  • 32. Assisting Sirkulasi Mekanikal kompressi • Autopulse • LUCAS 2015: Angka survive sama namun gangguan neurologis lebih banyak pada Autopulse
  • 33.
  • 34. KOMPRESI DADA YANG BERKUALITAS TERAPI ELEKTRIK DEFIBRILASI • Sejak awal , kompresi dada jangan terputus • Meminimalkan interupsi sebelum dan setelah kejut • Lanjutkan kompresi selama pengisian defibrilasi
  • 35. DEFIBRILATION BIFASIK Rekomendasi : • Idealnya : energi bifasik awal tidak kurang dari 150 J (120 – 200 J ) untuk semua bentuk gelombang • Pemakaian alat mekanikal kompresi dapat digunakan bila kompressi dada tidak adekuat atau memerlukan CPR jangka lama
  • 36. ENERGI DEFIBRILASI TETAP ATAU ESKALASI ? 2010/2015 : • Keduanya dapat diterima, bagaimanapun Jika kejut pertama tidak berhasil dan defibrilasi masih dapat memungkinkan untuk meningkatkan energi yang lebih tinggi, maka masih dapat diterima untuk ditingkatkan
  • 37. EARLY DEFIBRILLATION IT IS CRITICAL TO SURVIVAL FROM SUDDEN CARDIAC ARREST (SCA) FOR SEVERAL REASONS: (1) The most frequent initial rhythm in witnessed is ventricular fibrillation (VF), (2) The treatment for VF is electrical defibrillation, (3) The probability of successful defibrillation diminishes rapidly over time, and (4) VF tends to deteriorate to asystole within a few minutes.
  • 39. DEFIBRILLATION WAVEFORMS AND ENERGY LEVELS  Defibrillation  delivery of current through the chest and to the heart to depolarize myocardial cells and eliminate VF.  The energy settings for defibrillators are designed to provide the lowest effective energy needed to terminate VF.  Electrophysiologic event that occurs in 300 to 500 milliseconds after shock delivery.  Defibrillation (shock success) is typically defined as termination of VF for at least 5 seconds following the shock.
  • 40. SHOCK ENERGIES • Biphasic defibrillator (initial shock) : • selected energies of 120 J to 200 J (biphasic truncated exponential waveform) or • 120 J (rectilinear biphasic waveform). • For second and subsequent shocks, use the same or higher energy
  • 41. SHOCK ENERGIES • Monophasic defibrillator : select a dose of 200- 360 J for all shocks. • If VF is initially terminated by a shock but then recurs later in the arrest, No need to deliver subsequent shocks BUT continous CPR
  • 42. SYNCHRONIZED CARDIOVERSION • Shock delivery that is timed (synchronized) with the QRS complex. • The energy (shock dose) used is lower than that used for unsynchronized shocks (defibrillation). • These low-energy shocks if delivered as unsynchronized are likely to induce VF. • If cardioversion is needed and it is impossible to synchronize a shock (eg, the patient’s rhythm is irregular), use high-energy unsynchronized shocks.
  • 43. SYNCHRONIZED CARDIOVERSION • Ventricular tachycardia • Ventricular tachycardia with a pulse responds well to cardioversion using initial monophasic energies of 200 J. • Use biphasic energy levels of 120—150 J for the initial shock. • Give stepwise increases if the first shock fails to achieve sinus rhythm.
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  • 48. DRUGS • Drugs should be considered only after initial shocks have been delivered (if indicated) and chest compressions and ventilation have been started. • Three groups of drugs relevant to the management of cardiac arrest (2015 Consensus Conference): vasopressors, anti- arrhythmics and other drugs.
  • 49. INOTROPS and VASOPRESSORS • Adrenaline - the primary sympathomimetic agent for the management of cardiac arrest for 40 years. • Alpha-adrenergic actions, vasoconstrictive effects  systemic vasoconstriction, which increases coronary and cerebral perfusion pressures. • Beta-adrenergic actions, (inotropic, chronotropic) may increase coronary and cerebral blood flow.
  • 50. ADRENALINE  Indications  Adrenaline is the first drug used in cardiac arrest of any aetiology: it is included in the ALS algorithm for use every 3—5 min of CPR.  Adrenaline is preferred in the treatment of anaphylaxis.  Adrenaline is second-line treatment for cardiogenic shock.  Dose. During cardiac arrest, the initial intravenous dose of adrenaline is 1 mg.  When intravascular (intravenous or intra-osseous) access is delayed or cannot be achieved, give 2—3 mg, diluted to 10 ml with sterile water, via the tracheal tube. Absorption via the tracheal route is highly variable.
  • 51. ANTI-ARRHYTHMICS • Amiodarone is a membranestabilising anti-arrhythmic drug that increases the duration of the action potential and refractory period in atrial and ventricular myocardium. • Atrioventricular conduction is slowed, and a similar effect is seen with accessory pathways. • Amiodarone has a mild negative inotropic action and causes peripheral vasodilation through non- competitive alpha-blocking effects.
  • 52. AMIODARONE • Indications. • refractory VF/VT • haemodynamically stable ventricular tachycardia (VT) and other resistant tachyarrhythmias • Dose. Consider an initial intravenous dose of 300 mg amiodarone, diluted in 5% dextrose to a volume of 20 ml (or from a pre-filled syringe), if VF/VT persists after the third shock. • Amiodarone can cause thrombophlebitis when injected into a peripheral vein; use a central venous catheter if one is in situ but,if not, use a large peripheral vein and a generous flush.
  • 53. LIDOCAINE  Indications. Lidocaine is indicated in refractory VF/VT (when amiodarone is unavailable).  Dose. an initial dose of 100 mg (1—1.5 mg/kg) for VF/pulseless VT refractory to three shocks.  Give an additional bolus of 50 mg if necessary.  The total dose should not exceed 3 mg/kg during the first hour.
  • 54. OTHER DRUG • Atropine. antagonises the action of the parasympathetic neurotransmitter acetylcholine at muscarinic receptors. • Blocks the effect of the vagus nerve on both the sinoatrial (SA) node and the atrioventricular (AV) node, increasing sinus automaticity and facilitating AV node conduction.
  • 55. ATROPINE • is indicated in: • Asystole • pulseless electrical activity (PEA) with a rate <60/min. • sinus, atrial, or nodal bradycardia when the haemodynamic condition of the patient is unstable. • The recommended adult dose of atropine for Asystole or PEA with a rate <60 /min is 3 mg i.v. in a single bolus.
  • 56.
  • 57. • Kurangnya penekanan pada intubasi tracheal sejak awal kecuali dilakukan oleh tenaga terlatih dengan interupsi kompresi yang minimal
  • 58. • Penekanan yang lebih terhadap pemakaian kapnograf untuk confirmasi dan secara berkesinambungan memantau letak tube, kualitas RJP, dan memantau indikasi awal tanda-tanda ROSC
  • 59. ACLS : GELOMBANG KAPNOGRAF Perubahan : • Gelombang kapnograf kuantitatif adalah metode yang lebih reliable untuk mengkonfirmasi letak ET tube Kenapa : • Banyaknya insidens yang tidak diinginkan akibat letak ET tube yang tidak betul • Kapnograf memiliki sensitivitas dan spesifitas yang tinggi untuk mengidentifikasi kebenaran letak ETT pada pasien gagal jantung
  • 60. ACLS : GELOMBANG KAPNOGRAF • Setelah intubasi, karbondioksida yang di ekshalasi akan terdeteksi, sehingga dapat dipakai sebagai pengkonfirmasi letak selang ETT dan optimalisai CPR • Nilai yang paling tinggi pada saat akhir ekspirasi
  • 61. PERUBAHAN ACLS : JALAN NAPAS • Alat jalan napas supra glottis dapat dipakai tanpa pemberhentian CPR • Insersi selang ETT > 10 detik sebaiknya dihindari kecuali jalan nafas beresiko • Memerlukan banyak latihan dan kekompakan tim
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  • 67. CPR -1 30 : 2 CALL FOR HELP PASANG MONITOR VF / VT a single shock -II a single shock -I - a single shock-IV a single shock-III a single shock-V 2 menit 2 menit 2 menit 2 menit adrenalin adrenalin CPR-3 CPR-2 CPR-5 CPR-4 - AMIODARON Adrenaline: 1 mg, iv, repeated every 3-5 minutes CPR-6 Cardiac arrest Or LIDOCAIN 1mg/kg. Can be repeated. Do not exceed a total dose of 3 mg/kg,during the first hour. Amiodaron is the first choice 300 mg, bolus. Repeated 150 mg for reccurrent VT/VF. Followed by 900 mg infusion over 24 hours VF/ VT Intubasi : as soon as possible, without stop CPR Pijat 100 -120 x/menit Nafas 8 -10 x/menit Evaluasi CPR : tiap 2 menit adrenalin 3’ 3’ - AMIODARON
  • 68. ASYST 2 menit 2 menit 2 menit 2 menit evaluasi evaluasi Adrenalin-1 CPR-3 CPR-2 CPR-5 CPR-4 CPR-6 Cardiac arrest ASYSTOL/PEA/EMD Intubasi : as soon as possible, without stop CPR Pijat 100-120 x/menit Nafas 8-10 x/menit Evaluasi CPR : tiap 2 menit evaluasi evaluasi CPR -1 30 : 2 CALL FOR HELP PASANG MONITOR Adrenalin-2 Adrenalin-3 Adrenaline: 1 mg, iv, repeated every 3-5 minutes
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  • 70. TERMINATION OF RESUSCITATION • CPR must be continued until • Cardiopulmonary system is stabilized • The patient is pronounced death • Alone rescuer is physically unable to continue
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  • 137. ASSESS RHYTHM • CPR • Defibrillate mono or biphasic • Epinephrine – several dose options • Antiarrhythmic agents • AMIODARON • Lidocaine • Magnesium Ventricular fibrillation
  • 138. PULSELESS ELECTRICAL ACTIVITY • CPR • Search for reversible causes and treat • Epinephrine • Atropine for absolute or relative bradicardia
  • 139. ASYSTOLE • CPR • Epinephrine • Consider transcutaneous pacing • Search for reversible causes and treat if possible
  • 140. BRADYCARDIA – PATIENT NOT IN ARREST  Oxygen  Atropine  Dopamine  Epinephrine  Transcutaneous pacing  Transvenous pacing
  • 141. TACHYCARDIA WITH SERIOUS SIGNS/SYMPTOMS  Oxygen  Immediate cardioversion  Premedicate when possible  Synchronized setting
  • 142. TACHYCARDIA WITHOUT SERIOUS INSTABILITY  Narrow-complex  Adenosine  Verapamil  Diltiazem  -blockers  Digoxin  Synchronized cardioversion
  • 143. TACHYCARDIA WITHOUT SERIOUS INSTABILITY • Wide-complex – Amiodaron – Lidocaine • Synchronized cardioversion